Item Type | Name |
Concept
|
Alleles
|
Concept
|
Alzheimer Disease
|
Concept
|
Amino Acid Sequence
|
Concept
|
Amyotrophic Lateral Sclerosis
|
Concept
|
Anemia, Sickle Cell
|
Concept
|
Anti-Inflammatory Agents, Non-Steroidal
|
Concept
|
Base Sequence
|
Concept
|
Behavioral Symptoms
|
Concept
|
Binding Sites
|
Concept
|
Brain Diseases
|
Concept
|
Cardiovascular Diseases
|
Concept
|
Charcot-Marie-Tooth Disease
|
Concept
|
Computer Simulation
|
Concept
|
Coronary Artery Disease
|
Concept
|
Cross-Sectional Studies
|
Concept
|
Data Interpretation, Statistical
|
Concept
|
Disease
|
Concept
|
Disease Models, Animal
|
Concept
|
Disease Susceptibility
|
Concept
|
Diseases in Twins
|
Concept
|
DNA, Satellite
|
Concept
|
Drug Synergism
|
Concept
|
Educational Status
|
Concept
|
Endocrine System Diseases
|
Concept
|
Epistasis, Genetic
|
Concept
|
Evaluation Studies as Topic
|
Concept
|
Factor Analysis, Statistical
|
Concept
|
Feasibility Studies
|
Concept
|
Follow-Up Studies
|
Concept
|
Fragile X Syndrome
|
Concept
|
Genes
|
Concept
|
Genes, Dominant
|
Concept
|
Genes, Homeobox
|
Concept
|
Genes, Recessive
|
Concept
|
Multigene Family
|
Concept
|
Health Status
|
Concept
|
Health Surveys
|
Concept
|
Heat-Shock Proteins
|
Concept
|
Hemoglobin, Sickle
|
Concept
|
Hirschsprung Disease
|
Concept
|
Huntington Disease
|
Concept
|
Information Systems
|
Concept
|
Length of Stay
|
Concept
|
Lod Score
|
Concept
|
Longitudinal Studies
|
Concept
|
Major Histocompatibility Complex
|
Concept
|
Marijuana Smoking
|
Concept
|
Mass Screening
|
Concept
|
Mental Status Schedule
|
Concept
|
Mice, Inbred Strains
|
Concept
|
Mice, Mutant Strains
|
Concept
|
Molecular Sequence Data
|
Concept
|
Neonatal Abstinence Syndrome
|
Concept
|
S100 Proteins
|
Concept
|
Synaptic Transmission
|
Concept
|
Organ Specificity
|
Concept
|
Organ Size
|
Concept
|
Parkinson Disease
|
Concept
|
Population Surveillance
|
Concept
|
Prospective Studies
|
Concept
|
Psychiatric Status Rating Scales
|
Concept
|
Psychoses, Substance-Induced
|
Concept
|
Receptors, Cell Surface
|
Concept
|
Receptors, Serotonin
|
Concept
|
Reference Standards
|
Concept
|
Regulatory Sequences, Nucleic Acid
|
Concept
|
Repetitive Sequences, Nucleic Acid
|
Concept
|
Retrospective Studies
|
Concept
|
Saliva
|
Concept
|
Schizophrenia
|
Concept
|
Schizophrenic Psychology
|
Concept
|
Sclerosis
|
Concept
|
Scotland
|
Concept
|
Self-Help Groups
|
Concept
|
Sensitivity and Specificity
|
Concept
|
Serine
|
Concept
|
Severity of Illness Index
|
Concept
|
Sexual Behavior
|
Concept
|
Sex Characteristics
|
Concept
|
Sex Chromosome Aberrations
|
Concept
|
Sex Factors
|
Concept
|
Skin Neoplasms
|
Concept
|
Skinfold Thickness
|
Concept
|
Sleep
|
Concept
|
Smoking
|
Concept
|
Social Environment
|
Concept
|
Socioeconomic Factors
|
Concept
|
Software
|
Concept
|
Solubility
|
Concept
|
Spain
|
Concept
|
Species Specificity
|
Concept
|
Spinal Puncture
|
Concept
|
Spinocerebellar Degenerations
|
Concept
|
Statistics as Topic
|
Concept
|
Stem Cells
|
Concept
|
Street Drugs
|
Concept
|
Stress Disorders, Post-Traumatic
|
Concept
|
Stress, Psychological
|
Concept
|
Structure-Activity Relationship
|
Concept
|
Substance Withdrawal Syndrome
|
Concept
|
Suicide
|
Concept
|
Suicide, Attempted
|
Concept
|
Sulfonylurea Compounds
|
Concept
|
Sweden
|
Concept
|
Switzerland
|
Concept
|
Sympathetic Nervous System
|
Concept
|
United States
|
Concept
|
Waardenburg Syndrome
|
Concept
|
Blotting, Southern
|
Concept
|
Models, Statistical
|
Concept
|
Sulfotransferases
|
Concept
|
Deoxyribonucleases, Type II Site-Specific
|
Concept
|
Cohort Studies
|
Concept
|
Molecular Structure
|
Concept
|
Signal Transduction
|
Concept
|
Trauma Severity Indices
|
Concept
|
Gene Library
|
Concept
|
Substance Abuse, Intravenous
|
Concept
|
Genome, Human
|
Concept
|
Tomography, Emission-Computed, Single-Photon
|
Concept
|
Selection Bias
|
Concept
|
Chi-Square Distribution
|
Concept
|
Least-Squares Analysis
|
Concept
|
Survival Analysis
|
Concept
|
Epidemiologic Studies
|
Concept
|
Case-Control Studies
|
Concept
|
Sequence Tagged Sites
|
Concept
|
Open Reading Frames
|
Concept
|
Sequence Alignment
|
Concept
|
Needle Sharing
|
Concept
|
Genes, Neurofibromatosis 1
|
Concept
|
Smoking Cessation
|
Concept
|
Genome
|
Concept
|
Protein-Serine-Threonine Kinases
|
Concept
|
Sequence Deletion
|
Concept
|
Sequence Homology, Amino Acid
|
Concept
|
Sequence Analysis, DNA
|
Concept
|
Sequence Analysis, RNA
|
Concept
|
Protein Structure, Secondary
|
Concept
|
Protein Structure, Tertiary
|
Concept
|
Marital Status
|
Concept
|
Sex Distribution
|
Concept
|
Machado-Joseph Disease
|
Concept
|
Genes, Reporter
|
Concept
|
Oxidative Stress
|
Concept
|
Sample Size
|
Concept
|
Disease Progression
|
Concept
|
Patient Selection
|
Concept
|
Statistics, Nonparametric
|
Concept
|
Sepsis
|
Concept
|
HSP70 Heat-Shock Proteins
|
Concept
|
Staurosporine
|
Concept
|
Neurodegenerative Diseases
|
Concept
|
Amino Acid Substitution
|
Concept
|
Substance-Related Disorders
|
Concept
|
Calcium Signaling
|
Concept
|
Genetic Predisposition to Disease
|
Concept
|
Catalytic Domain
|
Concept
|
Alcohol-Induced Disorders, Nervous System
|
Concept
|
Alcohol Withdrawal Seizures
|
Concept
|
Oligonucleotide Array Sequence Analysis
|
Concept
|
Stroke
|
Concept
|
Genes, myb
|
Concept
|
Polymorphism, Single Nucleotide
|
Concept
|
RNA Splice Sites
|
Concept
|
Electrophoretic Mobility Shift Assay
|
Concept
|
Metabolic Syndrome X
|
Concept
|
Tumor Suppressor Proteins
|
Concept
|
Amino Acid Transport Systems, Basic
|
Concept
|
Symporters
|
Concept
|
Organic Anion Transporters, Sodium-Dependent
|
Concept
|
Genetic Diseases, Inborn
|
Concept
|
RNA, Small Interfering
|
Concept
|
Siblings
|
Concept
|
Diagnostic and Statistical Manual of Mental Disorders
|
Concept
|
Pluripotent Stem Cells
|
Concept
|
Semaphorins
|
Concept
|
Semaphorin-3A
|
Concept
|
Quantitative Trait Loci
|
Concept
|
DNA Repeat Expansion
|
Concept
|
Receptor, Serotonin, 5-HT2B
|
Concept
|
Unsafe Sex
|
Concept
|
Intracellular Signaling Peptides and Proteins
|
Concept
|
Adaptor Proteins, Signal Transducing
|
Concept
|
Saposins
|
Concept
|
Systems Biology
|
Concept
|
Serotonin Plasma Membrane Transport Proteins
|
Concept
|
STAT6 Transcription Factor
|
Concept
|
Smad3 Protein
|
Concept
|
Smad6 Protein
|
Concept
|
Nitric Oxide Synthase Type I
|
Concept
|
Nitric Oxide Synthase Type III
|
Concept
|
CARD Signaling Adaptor Proteins
|
Concept
|
Amyloid Precursor Protein Secretases
|
Concept
|
Adult Survivors of Child Abuse
|
Concept
|
Genome-Wide Association Study
|
Concept
|
Protein Stability
|
Concept
|
Genetic Loci
|
Concept
|
Sirtuin 1
|
Concept
|
Genetic Association Studies
|
Concept
|
Endosomal Sorting Complexes Required for Transport
|
Concept
|
Nuclear Receptor Subfamily 1, Group F, Member 1
|
Concept
|
Mice, 129 Strain
|
Concept
|
Sorting Nexins
|
Concept
|
Genetic Pleiotropy
|
Concept
|
Molecular Sequence Annotation
|
Concept
|
High-Throughput Nucleotide Sequencing
|
Concept
|
Suicidal Ideation
|
Concept
|
Transcriptome
|
Concept
|
Exome
|
Concept
|
Support Vector Machine
|
Concept
|
Wnt Signaling Pathway
|
Concept
|
Molecular Docking Simulation
|
Concept
|
Sialic Acid Binding Ig-like Lectin 3
|
Concept
|
Sulfonylurea Receptors
|
Academic Article
|
Statement on use of apolipoprotein E testing for Alzheimer disease. American College of Medical Genetics/American Society of Human Genetics Working Group on ApoE and Alzheimer disease.
|
Academic Article
|
Apolipoprotein E genotype in patients with Alzheimer's disease: implications for the risk of dementia among relatives.
|
Academic Article
|
Allele epsilon 4 of apolipoprotein E shows a dose effect on age at onset of Pick disease.
|
Academic Article
|
Identification of the genetic locus for keratosis palmaris et plantaris on chromosome 17 near the RARA and keratin type I genes.
|
Academic Article
|
[Mapping the gene for palmoplantar hyperkeratosis (thylosis) to chromosome 17 in the 17q12-q24 region].
|
Academic Article
|
Correlation between CAG repeat length and clinical features in Machado-Joseph disease.
|
Academic Article
|
A contiguous linkage map of chromosome 13q with 39 distinct loci separated on average by 5.1 centimorgans.
|
Academic Article
|
Rate of progression of Alzheimer's disease is associated with genetic risk.
|
Academic Article
|
Machado Joseph disease maps to the same region of chromosome 14 as the spinocerebellar ataxia type 3 locus.
|
Academic Article
|
A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21.
|
Academic Article
|
Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes.
|
Academic Article
|
46,XY/47,XYY male with the fragile X syndrome: cytogenetic and molecular studies.
|
Academic Article
|
Polymorphic microsatellites and Wilson disease (WD).
|
Academic Article
|
A 4.5-megabase yeast artificial chromosome contig from human chromosome 13q14.3 ordering 9 polymorphic microsatellites (22 sequence-tagged sites) tightly linked to the Wilson disease locus.
|
Academic Article
|
Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites.
|
Academic Article
|
Estimating the probability for major gene Alzheimer disease.
|
Academic Article
|
Susceptibility genes for familial Alzheimer's disease on chromosomes 19 and 21: a reality check.
|
Academic Article
|
The normal Huntington disease (HD) allele, or a closely linked gene, influences age at onset of HD.
|
Academic Article
|
Genetic transmission of Alzheimer's disease among families in a Dutch population based study.
|
Academic Article
|
Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population.
|
Academic Article
|
Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.
|
Academic Article
|
A familial factor independent of CAG repeat length influences age at onset of Machado-Joseph disease.
|
Academic Article
|
Presenilin polymorphisms in Alzheimer's disease.
|
Academic Article
|
No genetic effect of alpha1-antichymotrypsin in Alzheimer disease.
|
Academic Article
|
Risk of dementia among relatives of Alzheimer's disease patients in the MIRAGE study: What is in store for the oldest old?
|
Academic Article
|
Linkage of polymorphic congenital cataract to the gamma-crystallin gene locus on human chromosome 2q33-35.
|
Academic Article
|
Evidence for major gene inheritance of Alzheimer disease in families of patients with and without apolipoprotein E epsilon 4.
|
Academic Article
|
A novel mutation in the MITF gene causes Waardenburg syndrome type 2.
|
Academic Article
|
Linkage disequilibrium analysis in Machado-Joseph disease patients of different ethnic origins.
|
Academic Article
|
No association between alpha 1-antichymotrypsin and familial Alzheimer's disease.
|
Academic Article
|
The clinical introduction of genetic testing for Alzheimer disease. An ethical perspective.
|
Academic Article
|
No association or linkage between an intronic polymorphism of presenilin-1 and sporadic or late-onset familial Alzheimer disease.
|
Academic Article
|
Apolipoprotein E epsilon2 does not increase risk of early-onset sporadic Alzheimer's disease.
|
Academic Article
|
Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium.
|
Academic Article
|
Novel ATP7B mutations causing Wilson disease in several Israeli ethnic groups.
|
Academic Article
|
Amyloid-beta-protein isoforms in brain of subjects with PS1-linked, beta APP-linked and sporadic Alzheimer disease.
|
Academic Article
|
Absence of association between Alzheimer disease and the -491 regulatory region polymorphism of APOE.
|
Academic Article
|
Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneity.
|
Academic Article
|
Smoking and risk of Alzheimer's disease. MIRAGE Study Group.
|
Academic Article
|
Association between bleomycin hydrolase and Alzheimer's disease in caucasians.
|
Academic Article
|
An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease.
|
Academic Article
|
Alpha-2 macroglobulin gene in early- and late-onset Alzheimer disease.
|
Academic Article
|
Detecting linkage for a complex disease using simulated extended pedigrees.
|
Academic Article
|
Analysis of the butyrylcholinesterase gene and nearby chromosome 3 markers in Alzheimer disease.
|
Academic Article
|
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations.
|
Academic Article
|
Autosomal dominant orthostatic hypotensive disorder maps to chromosome 18q.
|
Academic Article
|
A family history study of male sexual orientation using three independent samples.
|
Academic Article
|
Evidence for linkage between essential hypertension and a putative locus on human chromosome 17.
|
Academic Article
|
Identification of a polymorphic glutamic acid stretch in the alpha2B-adrenergic receptor and lack of linkage with essential hypertension.
|
Academic Article
|
No association between the HLA-A2 allele and Alzheimer disease.
|
Academic Article
|
Familial risk for Alzheimer disease in ethnic minorities: nondiscriminating genes.
|
Academic Article
|
Power of concordant versus discordant sib pairs at different penetrance levels.
|
Academic Article
|
Stratification techniques to explore genotype environment interactions.
|
Academic Article
|
Association between angiotensin-converting enzyme and Alzheimer disease.
|
Academic Article
|
Intercontinental epidemiology of Alzheimer disease: a global approach to bad gene hunting.
|
Academic Article
|
Highly polymorphic short tandem repeat analyses clarify complex molecular test results.
|
Academic Article
|
Genetic predisposition to stroke in relatives of hypertensives.
|
Academic Article
|
No genetic association between the LRP receptor and sporadic or late-onset familial Alzheimer disease.
|
Academic Article
|
Head injury and the risk of AD in the MIRAGE study.
|
Academic Article
|
Nicastrin modulates presenilin-mediated notch/glp-1 signal transduction and betaAPP processing.
|
Academic Article
|
Reliability of information collected by proxy in family studies of Alzheimer's disease.
|
Academic Article
|
Distinguishable effects of presenilin-1 and APP717 mutations on amyloid plaque deposition.
|
Academic Article
|
The angiotensin-converting enzyme gene as a possible risk or protective factor in Alzheimer's disease.
|
Academic Article
|
Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14.
|
Academic Article
|
Maternal component in the familial aggregation of hypertension.
|
Academic Article
|
Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease.
|
Academic Article
|
The human cationic amino acid transporter (ATRC1): physical and genetic mapping to 13q12-q14.
|
Academic Article
|
Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium.
|
Academic Article
|
Risk of dementia among white and African American relatives of patients with Alzheimer disease.
|
Academic Article
|
Association between apolipoprotein E genotype and Alzheimer disease in African American subjects.
|
Academic Article
|
Genetic and environmental risk factors for Alzheimer's disease in Israeli Arabs.
|
Academic Article
|
Regulatory region variability in the human presenilin-2 (PSEN2) gene: potential contribution to the gene activity and risk for AD.
|
Academic Article
|
Monozygotic twins concordant for late-onset probable Alzheimer disease with suspected Alzheimer disease in four sibs.
|
Academic Article
|
Identification of multiple loci for Alzheimer disease in a consanguineous Israeli-Arab community.
|
Academic Article
|
Comparison of Alzheimer's disease risk factors in white and African American families.
|
Academic Article
|
Genetic variants of WNK4 in whites and African Americans with hypertension.
|
Academic Article
|
Reasons for seeking genetic susceptibility testing among first-degree relatives of people with Alzheimer disease.
|
Academic Article
|
Differences between African Americans and Whites in their attitudes toward genetic testing for Alzheimer's disease.
|
Academic Article
|
Depression as a risk factor for Alzheimer disease: the MIRAGE Study.
|
Academic Article
|
Genetic and environmental epidemiology of Alzheimer's disease in arabs residing in Israel.
|
Academic Article
|
The genetics of adult-onset neuropsychiatric disease: complexities and conundra?
|
Academic Article
|
Polymorphisms near a chromosome 6q QTL area are associated with modulation of fetal hemoglobin levels in sickle cell anemia.
|
Academic Article
|
The Machado-Joseph disease locus is different from the spinocerebellar ataxia locus (SCA1).
|
Academic Article
|
Empirically derived phenotypic subgroups - qualitative and quantitative trait analyses.
|
Academic Article
|
Search for genetic factors predisposing to atherogenic dyslipidemia.
|
Academic Article
|
Genome-wide screen for heavy alcohol consumption.
|
Academic Article
|
Differential modulation of endotoxin responsiveness by human caspase-12 polymorphisms.
|
Academic Article
|
Segregation analysis of total nevus density and estimation of lifetime risk and average onset age of melanoma.
|
Academic Article
|
Estimating risk curves for first-degree relatives of patients with Alzheimer's disease: the REVEAL study.
|
Academic Article
|
Who seeks genetic susceptibility testing for Alzheimer's disease? Findings from a multisite, randomized clinical trial.
|
Academic Article
|
Analysis of the glucocerebrosidase gene in Parkinson's disease.
|
Academic Article
|
Postmenopausal hormone therapy and Alzheimer's disease risk: interaction with age.
|
Academic Article
|
Association of single nucleotide polymorphisms in klotho with priapism in sickle cell anaemia.
|
Academic Article
|
Relation between atherogenic dyslipidemia and the Adult Treatment Program-III definition of metabolic syndrome (Genetic Epidemiology of Metabolic Syndrome Project).
|
Academic Article
|
Polymorphisms in the promoter region of catalase gene and essential hypertension.
|
Academic Article
|
Hemolysis-associated priapism in sickle cell disease.
|
Academic Article
|
Estimation of morbid risk and age at onset with missing information.
|
Academic Article
|
Patterns of inheritance of the symptoms of Huntington's disease suggestive of an effect of genomic imprinting.
|
Academic Article
|
Multifactor-dimensionality reduction versus family-based association tests in detecting susceptibility loci in discordant sib-pair studies.
|
Academic Article
|
Whole-genome variance components linkage analysis using single-nucleotide polymorphisms versus microsatellites on quantitative traits of derived phenotypes from factor analysis of electroencephalogram waves.
|
Academic Article
|
Genome-wide linkage analysis for alcohol dependence: a comparison between single-nucleotide polymorphism and microsatellite marker assays.
|
Academic Article
|
Nonsteroidal anti-inflammatory drug use and Alzheimer's disease risk: the MIRAGE Study.
|
Academic Article
|
Complement factor H polymorphism and age-related macular degeneration.
|
Academic Article
|
Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis.
|
Academic Article
|
Rating the severity and character of transient cocaine-induced delusions and hallucinations with a new instrument, the Scale for Assessment of Positive Symptoms for Cocaine-Induced Psychosis (SAPS-CIP).
|
Academic Article
|
Diagnostic reliability of the Semi-structured Assessment for Drug Dependence and Alcoholism (SSADDA).
|
Academic Article
|
Genomewide linkage scan for cocaine dependence and related traits: significant linkages for a cocaine-related trait and cocaine-induced paranoia.
|
Academic Article
|
APOE, vascular pathology, and the AD brain.
|
Academic Article
|
Multiple QTLs influencing triglyceride and HDL and total cholesterol levels identified in families with atherogenic dyslipidemia.
|
Academic Article
|
An alpha satellite DNA polymorphism specific for the centromeric region of chromosome 13.
|
Academic Article
|
Polymorphisms in the PON gene cluster are associated with Alzheimer disease.
|
Academic Article
|
Association of asthma with a functional promoter polymorphism in the IL16 gene.
|
Academic Article
|
The serotonin receptor subtype 2 locus HTR2 is on human chromosome 13 near genes for esterase D and retinoblastoma-1 and on mouse chromosome 14.
|
Academic Article
|
Risk factors for cocaine-induced paranoia in cocaine-dependent sibling pairs.
|
Academic Article
|
Intronic variants in the dopa decarboxylase (DDC) gene are associated with smoking behavior in European-Americans and African-Americans.
|
Academic Article
|
Association studies between the plasmin genes and late-onset Alzheimer's disease.
|
Academic Article
|
Predictive testing for Wilson's disease using tightly linked and flanking DNA markers.
|
Academic Article
|
Predictors of subjective memory complaint in cognitively normal relatives of patients with Alzheimer's disease.
|
Academic Article
|
Education effects on cognitive function in a healthy aged Arab population.
|
Academic Article
|
Genomewide linkage scan for nicotine dependence: identification of a chromosome 5 risk locus.
|
Academic Article
|
Haplotype spanning TTC12 and ANKK1, flanked by the DRD2 and NCAM1 loci, is strongly associated to nicotine dependence in two distinct American populations.
|
Academic Article
|
Diabetes mellitus and risk of developing Alzheimer disease: results from the Framingham Study.
|
Academic Article
|
Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea.
|
Academic Article
|
Genomewide linkage scan for opioid dependence and related traits.
|
Academic Article
|
Association of polymorphisms in the Angiotensin-converting enzyme gene with Alzheimer disease in an Israeli Arab community.
|
Academic Article
|
Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF-beta/BMP pathway.
|
Academic Article
|
Genetic association between endothelial nitric oxide synthase and Alzheimer disease.
|
Academic Article
|
Association of polymorphisms of IGF1R and genes in the transforming growth factor- beta /bone morphogenetic protein pathway with bacteremia in sickle cell anemia.
|
Academic Article
|
Serum heat shock protein 70 level as a biomarker of exceptional longevity.
|
Academic Article
|
Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B.
|
Academic Article
|
The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease.
|
Academic Article
|
Segregation analysis reveals evidence of a major gene for Alzheimer disease.
|
Academic Article
|
The association between genetic variants in SORL1 and Alzheimer disease in an urban, multiethnic, community-based cohort.
|
Academic Article
|
Association of decreased paternal age and late-onset Alzheimer's disease. An example of genetic imprinting?
|
Academic Article
|
Potential ethnic modifiers in the assessment and treatment of Alzheimer's disease: challenges for the future.
|
Academic Article
|
The validity of cocaine dependence subtypes.
|
Academic Article
|
Reliability of DSM-IV diagnostic criteria using the semi-structured assessment for drug dependence and alcoholism (SSADDA).
|
Academic Article
|
A network model to predict the risk of death in sickle cell disease.
|
Academic Article
|
Variation and heritability of Hb F and F-cells among beta-thalassemia heterozygotes in Hong Kong.
|
Academic Article
|
Heritability of magnetic resonance imaging (MRI) traits in Alzheimer disease cases and their siblings in the MIRAGE study.
|
Academic Article
|
Comorbid psychiatric diagnoses and their association with cocaine-induced psychosis in cocaine-dependent subjects.
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Academic Article
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Beta-globin gene cluster polymorphisms are strongly associated with severity of HbE/beta(0)-thalassemia.
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Academic Article
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Association between SORL1 and Alzheimer's disease in a genome-wide study.
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Academic Article
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Further examination of the candidate genes in chromosome 12p13 locus for late-onset Alzheimer disease.
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Academic Article
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Incorporating ethnicity into genetic risk assessment for Alzheimer disease: the REVEAL study experience.
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Academic Article
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Collection of clinical and epidemiological data for linkage studies.
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Academic Article
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Substance dependence low-density whole genome association study in two distinct American populations.
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Academic Article
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Transmission and age-at-onset patterns in familial Alzheimer's disease: evidence for heterogeneity.
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Academic Article
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Estimation of familial risk in Alzheimer's disease.
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Academic Article
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Association of psychiatric and substance use disorder comorbidity with cocaine dependence severity and treatment utilization in cocaine-dependent individuals.
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Academic Article
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Dense genomewide linkage scan for alcohol dependence in African Americans: significant linkage on chromosome 10.
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Academic Article
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Interaction between two independent CNR1 variants increases risk for cocaine dependence in European Americans: a replication study in family-based sample and population-based sample.
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Academic Article
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Association of distinct variants in SORL1 with cerebrovascular and neurodegenerative changes related to Alzheimer disease.
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Academic Article
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Association of variants in MANEA with cocaine-related behaviors.
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Academic Article
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Performance of random forest when SNPs are in linkage disequilibrium.
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Academic Article
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Sources of unreliability in the diagnosis of substance dependence.
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Academic Article
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Correlates of co-occurring ADHD in drug-dependent subjects: prevalence and features of substance dependence and psychiatric disorders.
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Academic Article
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Lack of association between angiotensin-converting enzyme and dementia of the Alzheimer's type in an elderly Arab population in Wadi Ara, Israel.
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Academic Article
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BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies.
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Academic Article
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Wilson's disease in Israel: a genetic and epidemiological study.
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Academic Article
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Magnetic resonance imaging traits in siblings discordant for Alzheimer disease.
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Academic Article
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Essential tremor might be less frequent than Parkinson's disease in North Israel Arab villages.
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Academic Article
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Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder.
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Academic Article
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Pro-opiomelanocortin gene variation related to alcohol or drug dependence: evidence and replications across family- and population-based studies.
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Academic Article
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Association of TTR polymorphisms with hippocampal atrophy in Alzheimer disease families.
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Academic Article
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Statin use and the risk of Alzheimer's disease: the MIRAGE study.
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Academic Article
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The Nevada Vital Aging Initiative: a private-public partnership to study early predictors of dementia.
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Academic Article
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Disclosure of APOE genotype for risk of Alzheimer's disease.
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Academic Article
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Subtypes of major depression in substance dependence.
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Academic Article
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Convergence of linkage, gene expression and association data demonstrates the influence of the RAR-related orphan receptor alpha (RORA) gene on neovascular AMD: a systems biology based approach.
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Academic Article
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Transient cocaine-associated behavioral symptoms rated with a new instrument, the scale for assessment of positive symptoms for cocaine-induced psychosis (SAPS-CIP).
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Academic Article
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Homozygote for Huntington disease.
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Academic Article
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Interactive effect of stressful life events and the serotonin transporter 5-HTTLPR genotype on posttraumatic stress disorder diagnosis in 2 independent populations.
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Academic Article
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Hypertension increases the probability of Alzheimer's disease and of mild cognitive impairment in an Arab community in northern Israel.
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Academic Article
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Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
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Academic Article
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Education attenuates the effect of medial temporal lobe atrophy on cognitive function in Alzheimer's disease: the MIRAGE study.
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Academic Article
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Adverse childhood events as risk factors for substance dependence: partial mediation by mood and anxiety disorders.
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Academic Article
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Molecular genetics of familial Alzheimer's disease.
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Academic Article
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Familial Alzheimer's disease: progress and problems.
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Academic Article
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Adolescent cannabis use increases risk for cocaine-induced paranoia.
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Academic Article
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Molecular genetics of familial Alzheimer's disease.
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Academic Article
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Assessment and familial aggregation of psychosis in Alzheimer's disease from the National Institute on Aging Late Onset Alzheimer's Disease Family Study.
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Academic Article
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Confirmation and generalization of an alcohol-dependence locus on chromosome 10q.
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Academic Article
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Genetic modifiers of Hb E/beta0 thalassemia identified by a two-stage genome-wide association study.
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Academic Article
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Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.
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Academic Article
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Interaction of FKBP5 with childhood adversity on risk for post-traumatic stress disorder.
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Academic Article
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Variation in nicotinic acetylcholine receptor genes is associated with multiple substance dependence phenotypes.
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Academic Article
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Head circumference, atrophy, and cognition: implications for brain reserve in Alzheimer disease.
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Academic Article
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Healthy aging and preclinical dementia: the United States-Israel Longitudinal Database project.
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Academic Article
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Meta-analysis of the association between variants in SORL1 and Alzheimer disease.
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Academic Article
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Agitated depression in substance dependence.
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Academic Article
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SORCS1 alters amyloid precursor protein processing and variants may increase Alzheimer's disease risk.
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Academic Article
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Alzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans.
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Academic Article
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Genome-wide analysis of genetic loci associated with Alzheimer disease.
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Academic Article
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Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes.
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Academic Article
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Mild cognitive impairment is associated with mild parkinsonian signs in a door-to-door study.
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Academic Article
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Localization and linkage of three polymorphic DNA sequences on human chromosome 20.
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Academic Article
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Serum paraoxonase activity is associated with variants in the PON gene cluster and risk of Alzheimer disease.
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Academic Article
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Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP data.
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Academic Article
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An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13.
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Academic Article
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A new human RFLP identified by 7D2 places D13S10 proximal to esterase D.
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Academic Article
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Linkage analysis of multiple endocrine neoplasia type 2A (MEN-2A) and three DNA markers on chromosome 20: evidence against synteny.
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Academic Article
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Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage.
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Academic Article
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One large kindred excludes a locus for multiple endocrine neoplasia type 2A from about 25% of the human autosomal genetic map.
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Academic Article
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Predictive testing for Huntington's disease with use of a linked DNA marker.
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Academic Article
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Empirically derived subtypes of opioid use and related behaviors.
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Academic Article
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Power and pitfalls of the genome-wide association study approach to identify genes for Alzheimer's disease.
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Academic Article
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Considerations in using linkage analysis as a presymptomatic test for Huntington's disease.
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Academic Article
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A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression.
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Academic Article
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5-HTTLPR as a potential moderator of the effects of adverse childhood experiences on risk of antisocial personality disorder.
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Academic Article
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Ancestry of African Americans with sickle cell disease.
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Academic Article
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Rare nonsynonymous variants in alpha-4 nicotinic acetylcholine receptor gene protect against nicotine dependence.
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Academic Article
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No association between ADCYAP1R1 and post-traumatic stress disorder in two independent samples.
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Academic Article
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GABRG1 and GABRA2 variation associated with alcohol dependence in African Americans.
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Academic Article
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A CRHR1 haplotype moderates the effect of adverse childhood experiences on lifetime risk of major depressive episode in African-American women.
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Academic Article
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Influence of ROBO1 and RORA on risk of age-related macular degeneration reveals genetically distinct phenotypes in disease pathophysiology.
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Academic Article
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Childhood adversity increases risk for nicotine dependence and interacts with a5 nicotinic acetylcholine receptor genotype specifically in males.
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Academic Article
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Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
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Academic Article
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Association between polymorphisms in catechol-O-methyltransferase (COMT) and cocaine-induced paranoia in European-American and African-American populations.
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Academic Article
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Genetics and genomics of late-onset Alzheimer's disease and its endophenotypes.
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Academic Article
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Magnetic resonance imaging-measured atrophy and its relationship to cognitive functioning in vascular dementia and Alzheimer's disease patients.
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Academic Article
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Hamilton et al. Respond to "Consolidating Data Harmonization"
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Academic Article
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The PhenX Toolkit: get the most from your measures.
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Academic Article
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A genomewide linkage scan of cocaine dependence and major depressive episode in two populations.
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Academic Article
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A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study.
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Academic Article
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Systems biology-based analysis implicates a novel role for vitamin D metabolism in the pathogenesis of age-related macular degeneration.
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Academic Article
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A comprehensive genetic association study of Alzheimer disease in African Americans.
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Academic Article
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ACSL6 is associated with the number of cigarettes smoked and its expression is altered by chronic nicotine exposure.
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Academic Article
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Variation in OPRM1 and risk of suicidal behavior in drug-dependent individuals.
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Academic Article
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High prevalence of mild cognitive impairment and Alzheimer's disease in arabic villages in northern Israel: impact of gender and education.
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Academic Article
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Collection of clinical and epidemiological data for genetic linkage and association studies.
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Academic Article
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Eight closely linked loci place the Wilson disease locus within 13q14-q21.
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Academic Article
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Autosomal linkage scan for loci predisposing to comorbid dependence on multiple substances.
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Academic Article
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Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases.
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Academic Article
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Identification of Alzheimer disease-associated variants in genes that regulate retromer function.
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Academic Article
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Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants.
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Academic Article
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Serotonin transporter 5-HTTLPR genotype moderates the effects of childhood adversity on posttraumatic stress disorder risk: a replication study.
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Academic Article
|
Improved methods to identify stable, highly heritable subtypes of opioid use and related behaviors.
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Academic Article
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Genome-wide association study of Alzheimer's disease.
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Academic Article
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Association of COL25A1 with comorbid antisocial personality disorder and substance dependence.
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Academic Article
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Linkage analysis followed by association show NRG1 associated with cannabis dependence in African Americans.
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Academic Article
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ANKRD7 and CYTL1 are novel risk genes for alcohol drinking behavior.
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Academic Article
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A functional promoter polymorphism of the d-globin gene is a specific marker of the Arab-Indian haplotype.
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Academic Article
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Novel late-onset Alzheimer disease loci variants associate with brain gene expression.
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Academic Article
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Multiple loci influencing hippocampal degeneration identified by genome scan.
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Academic Article
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Comprehensive search for Alzheimer disease susceptibility loci in the APOE region.
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Academic Article
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Prevalence of DSM-IV and DSM-5 alcohol, cocaine, opioid, and cannabis use disorders in a largely substance dependent sample.
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Academic Article
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d-Catenin is genetically and biologically associated with cortical cataract and future Alzheimer-related structural and functional brain changes.
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Academic Article
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Behavioral variant frontotemporal lobar degeneration with amyotrophic lateral sclerosis with a chromosome 9p21 hexanucleotide repeat.
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Academic Article
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Prayer at midlife is associated with reduced risk of cognitive decline in Arabic women.
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Academic Article
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Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis.
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Academic Article
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Initial assessment of the pathogenic mechanisms of the recently identified Alzheimer risk Loci.
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Academic Article
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Seven new loci associated with age-related macular degeneration.
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Academic Article
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Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype.
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Academic Article
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GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.
|
Academic Article
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SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians.
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Academic Article
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Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ?4,and the risk of late-onset Alzheimer disease in African Americans.
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Academic Article
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Association of granulomatosis with polyangiitis (Wegener's) with HLA-DPB1*04 and SEMA6A gene variants: evidence from genome-wide analysis.
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Academic Article
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A complex interplay between personality domains, marital status and a variant in CHRNA5 on the risks of cocaine, nicotine dependences and cocaine-induced paranoia.
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Academic Article
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Role of p73 in Alzheimer disease: lack of association in mouse models or in human cohorts.
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Academic Article
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Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairment.
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Academic Article
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Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP).
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Academic Article
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Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics.
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Academic Article
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APOE genotype and MRI markers of cerebrovascular disease: systematic review and meta-analysis.
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Academic Article
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Locating genetic modifiers for inherited neurodegenerative diseases
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Academic Article
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Apolipoprotein E genotyping in Alzheimer’s disease
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Academic Article
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Molecular genetics of autosomal dominant familial Alzheimer's disease
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Academic Article
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Determining the genetic component of a disease
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Academic Article
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Alzheimer’s disease and diet
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Academic Article
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Genetic and environmental risk factors for Alzheimer’s disease in Arabs residing in Israel
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Academic Article
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The genetic component in Parkinson disease is half that of Alzheimer disease
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Academic Article
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DNA markers at 13q14-q22 linked to Wilson's disease
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Academic Article
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Application of database techniques in medical genetics
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Academic Article
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Alzheimer disease and the fronto-temporal dementias: diseases with cerebral deposition of fibrillar proteins
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Academic Article
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Letter to the Editor: Suicide and presymptomatic testing in Huntington disease
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Academic Article
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Book review: Hannah's Heirs: The Quest for the Genetic Origins of Alzheimer's Disease
|
Academic Article
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Age at onset of Alzheimer Disease is influenced by multiple genetic and non-genetic factors: The MIRAGE Study
|
Academic Article
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Effects of smoking, alcohol and APOE genotype on Alzheimer disease: The MIRAGE Study
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Academic Article
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Genetic neurodegenerative disease models for human aging
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Academic Article
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Book review: Alzheimer's Disease and the Environment (Royal Society of Medicine Services, Round Table Series, No. 26)
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Academic Article
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Risk of dementia in first degree relatives of patients with Alzheimer's disease
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Academic Article
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Linkage map of anonymous loci near the CF gene.
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Academic Article
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Molecular genetics of familial Alzheimer's disease and its implications
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Academic Article
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Risk of Alzheimer disease is associated with parental age among apolipoprotein E e4 heterozygotes
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Academic Article
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Reliability of self-reported age at onset of major depression.
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Academic Article
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Assessment of genetic risk for Alzheimer's disease among first-degree relatives.
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Academic Article
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A linkage group of five DNA markers on human chromosome 10.
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Academic Article
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An anthropometric assessment of Huntington's disease patients and families.
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Academic Article
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Suicide and attempted suicide in Huntington disease: implications for preclinical testing of persons at risk.
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Academic Article
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Predictability of phenotype in Huntington's disease.
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Academic Article
|
Diabetes mellitus in Huntington disease.
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Academic Article
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A genetic model for age at onset in Huntington disease.
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Academic Article
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Anthropometric discrimination among affected, at-risk, and not-at-risk individuals in families with Huntington disease.
|
Academic Article
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Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease.
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Academic Article
|
Clinical anthropometry and medical genetics: a compilation of body measurements in genetic and congenital disorders.
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Academic Article
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Evidence for linkage between Wilson disease and esterase D in three kindreds: detection of linkage for an autosomal recessive disorder by the family study method.
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Academic Article
|
Development of a map of chromosome 11p.
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Academic Article
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Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.
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Academic Article
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Managing data for genetic linkage analysis.
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Academic Article
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Automating data manipulation for genetic analysis using a data base management system.
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Academic Article
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Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus.
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Academic Article
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The natural history of Huntington disease: possible role of "aging genes".
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Academic Article
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Inverse relationship between age at onset of Huntington disease and paternal age suggests involvement of genetic imprinting.
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Academic Article
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A test of the hypothesis that age at onset in Huntington disease is controlled by an X-linked recessive modifier.
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Academic Article
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Does the omission of missing information bias the estimates of age-at-onset distributions?
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Academic Article
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Segregation analysis in Alzheimer disease: no evidence for a major gene.
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Academic Article
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Gender equality in Machado-Joseph disease.
|
Academic Article
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Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.
|
Academic Article
|
[A systematic genetic-epidemiologic family study of patients with Alzheimer disease--experience with the MIRAGE study in Germany].
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Academic Article
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Multiple etiologies for Alzheimer disease are revealed by segregation analysis.
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Academic Article
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Linkage of late-onset Alzheimer''s disease with apolipoprotein E type 4 on chromosome 19.
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Academic Article
|
Machado Joseph disease is not an allele of the spinocerebellar ataxia 2 locus.
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Academic Article
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Interrater agreement for diagnosis of Alzheimer's disease: the MIRAGE study.
|
Academic Article
|
Genome-wide association study identifies new susceptibility loci for posttraumatic stress disorder.
|
Academic Article
|
Integrating GWASs and human protein interaction networks identifies a gene subnetwork underlying alcohol dependence.
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Academic Article
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A case of inappropriate apolipoprotein e testing in Alzheimer''s disease due to lack of an informed consent discussion.
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Academic Article
|
Data compatibility in the addiction sciences: an examination of measure commonality.
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Academic Article
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Association of MAPT haplotypes with Alzheimer''s disease risk and MAPT brain gene expression levels.
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Academic Article
|
F-box/LRR-repeat protein 7 is genetically associated with Alzheimer''s disease.
|
Academic Article
|
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.
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Academic Article
|
Genome-wide association study of the rate of cognitive decline in Alzheimer''s disease.
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Academic Article
|
Deep resequencing of 17 glutamate system genes identifies rare variants in DISC1 and GRIN2B affecting risk of opioid dependence.
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Academic Article
|
Structural interactions between inhibitor and substrate docking sites give insight into mechanisms of human PS1 complexes.
|
Academic Article
|
Gene-wide analysis detects two new susceptibility genes for Alzheimer''s disease.
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Academic Article
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Genetic risk prediction and neurobiological understanding of alcoholism.
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Academic Article
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Estimating the risk for conversion from mild cognitive impairment to Alzheimer''s disease in an elderly Arab community.
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Academic Article
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Eye color: A potential indicator of alcohol dependence risk in European Americans.
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Academic Article
|
The ticking clock of Cayo Santiago macaques and its implications for understanding human circadian rhythm disorders.
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Academic Article
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Genome-wide association study of opioid dependence: multiple associations mapped to calcium and potassium pathways.
|
Academic Article
|
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer''s disease.
|
Academic Article
|
Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci.
|
Academic Article
|
Follow-up of loci from the International Genomics of Alzheimer''s Disease Project identifies TRIP4 as a novel susceptibility gene.
|
Academic Article
|
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration.
|
Academic Article
|
Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study.
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Academic Article
|
Evaluating the role of a galanin enhancer genotype on a range of metabolic, depressive and addictive phenotypes.
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Academic Article
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Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans.
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Academic Article
|
Protective variant for hippocampal atrophy identified by whole exome sequencing.
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Academic Article
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Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world.
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Academic Article
|
Variations in opioid receptor genes in neonatal abstinence syndrome.
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Academic Article
|
Evidence of CNIH3 involvement in opioid dependence.
|
Academic Article
|
Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers.
|
Academic Article
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Search for age-related macular degeneration risk variants in Alzheimer disease genes and pathways.
|
Academic Article
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Missense variant in TREML2 protects against Alzheimer''s disease.
|
Academic Article
|
Reply: To PMID 23740775.
|
Academic Article
|
The a-endomannosidase gene (MANEA) is associated with panic disorder and social anxiety disorder.
|
Academic Article
|
FLT1 genetic variation predisposes to neovascular AMD in ethnically diverse populations and alters systemic FLT1 expression.
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Academic Article
|
Genetic risk prediction and neurobiological understanding of alcoholism.
|
Academic Article
|
Genome-wide association meta-analysis of neuropathologic features of Alzheimer''s disease and related dementias.
|
Academic Article
|
Rarity of the Alzheimer disease-protective APP A673T variant in the United States.
|
Academic Article
|
Convergent genetic and expression data implicate immunity in Alzheimer''s disease.
|
Academic Article
|
Which alcohol use disorder criteria contribute to the association of ADH1B with alcohol dependence?
|
Academic Article
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Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease.
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Academic Article
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Polygenic risk for alcohol dependence associates with alcohol consumption, cognitive function and social deprivation in a population-based cohort.
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Academic Article
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Identification of a rare coding variant in complement 3 associated with age-related macular degeneration.
|
Academic Article
|
ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology.
|
Academic Article
|
Nf1 regulates alcohol dependence-associated excessive drinking and gamma-aminobutyric acid release in the central amygdala in mice and is associated with alcohol dependence in humans.
|
Academic Article
|
A novel Alzheimer disease locus located near the gene encoding tau protein.
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Academic Article
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Expanding the genomic roadmap of Alzheimer''s disease.
|
Academic Article
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Genome-wide association study of body mass index in subjects with alcohol dependence.
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Academic Article
|
PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation.
|
Academic Article
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A rare mutation in UNC5C predisposes to late-onset Alzheimer''s disease and increases neuronal cell death.
|
Academic Article
|
Global and local ancestry in African-Americans: Implications for Alzheimer''s disease risk.
|
Academic Article
|
Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene.
|
Academic Article
|
Exploring the genetic architecture of alcohol dependence in African-Americans via analysis of a genomewide set of common variants.
|
Academic Article
|
Critical evaluation of transcription factor Atf2 as a candidate modulator of alcohol preference in mouse and human populations.
|
Academic Article
|
Genome-wide association study of copy number variations (CNVs) with opioid dependence.
|
Academic Article
|
Genetic overlap between Alzheimer''s disease and Parkinson''s disease at the MAPT locus.
|
Academic Article
|
BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.
|
Academic Article
|
Genomewide Association Study for Maximum Number of Alcoholic Drinks in European Americans and African Americans.
|
Academic Article
|
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error.
|
Academic Article
|
Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks.
|
Academic Article
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Assessment of the genetic variance of late-onset Alzheimer''s disease.
|
Academic Article
|
Reply: To PMID 25559091.
|
Academic Article
|
Further analyses support the association between light eye color and alcohol dependence.
|
Academic Article
|
Genetic factor common to schizophrenia and HIV infection is associated with risky sexual behavior: antagonistic vs. synergistic pleiotropic SNPs enriched for distinctly different biological functions.
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Academic Article
|
Two novel loci, COBL and SLC10A2, for Alzheimer''s disease in African Americans.
|
Academic Article
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ABCA7 frameshift deletion associated with Alzheimer disease in African Americans.
|
Academic Article
|
Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium.
|
Academic Article
|
Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia.
|
Academic Article
|
Erratum to: Network-driven plasma proteomics expose molecular changes in the Alzheimer''s brain.
|
Academic Article
|
Linkage analyses in Caribbean Hispanic families identify novel loci associated with familial late-onset Alzheimer''s disease.
|
Academic Article
|
Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence.
|
Academic Article
|
Genetic Relationship between Schizophrenia and Nicotine Dependence.
|
Academic Article
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The Interplay Between Risky Sexual Behaviors and Alcohol Dependence: Genome-Wide Association and Neuroimaging Support for LHPP as a Risk Gene.
|
Academic Article
|
Association of maternal and infant variants in PNOC and COMT genes with neonatal abstinence syndrome severity.
|
Academic Article
|
Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer''s disease.
|
Academic Article
|
Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals.
|
Academic Article
|
Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease.
|
Academic Article
|
A protocadherin gene cluster regulatory variant is associated with nicotine withdrawal and the urge to smoke.
|
Academic Article
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Network-driven plasma proteomics expose molecular changes in the Alzheimer''s brain.
|
Academic Article
|
A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia.
|
Academic Article
|
Genomewide Association Study of Alcohol Dependence Identifies Risk Loci Altering Ethanol-Response Behaviors in Model Organisms.
|
Academic Article
|
S100A10 identified in a genome-wide gene × cannabis dependence interaction analysis of risky sexual behaviours.
|
Academic Article
|
Genome-wide association study identifies four novel loci associated with Alzheimer''s endophenotypes and disease modifiers.
|
Academic Article
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Transethnic genome-wide scan identifies novel Alzheimer''s disease loci.
|
Academic Article
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A Common Variant of IL-6R is Associated with Elevated IL-6 Pathway Activity in Alzheimer''s Disease Brains.
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Academic Article
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Genome-wide association study of therapeutic opioid dosing identifies a novel locus upstream of OPRM1.
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Academic Article
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Genetic assessment of age-associated Alzheimer disease risk: Development and validation of a polygenic hazard score.
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Academic Article
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Largest GWAS of PTSD (N=20?070) yields genetic overlap with schizophrenia and sex differences in heritability.
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Grant
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Genetic Basis of Cerebrovascular Mechanisms in Alzheimer’s Disease
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Grant
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Genetic Epidemiological Studies of Alzheimer Disease
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Grant
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Centenarian Offspring and Control for Longitudinal Study
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Grant
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Genetic Factor Underlying Alzheimer Disease
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Grant
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Family Based Studies of Gene-Environment Interactions in Alzheimer’s Disease
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Grant
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Mapping of the Alzheimer’s Disease Susceptibility Gene on Chromosome 12
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Grant
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Biomedical Research Support Program in Genetics
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Grant
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Multi-Ethnic Genome Wide Alzheimer’s Association
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Academic Article
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A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer''s disease.
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Academic Article
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Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer''s disease.
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Academic Article
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Oxytocin receptor gene polymorphisms, attachment, and PTSD: Results from the National Health and Resilience in Veterans Study.
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Academic Article
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Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport.
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Academic Article
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A phased SNP-based classification of sickle cell anemia HBB haplotypes.
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Academic Article
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Genetics of age-related macular degeneration (AMD).
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Academic Article
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Genetics of age-related macular degeneration (AMD).
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Academic Article
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Genome-Wide Association Studies of a Broad Spectrum of Antisocial Behavior.
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Academic Article
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Caspase-8, association with Alzheimer''s Disease and functional analysis of rare variants.
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Academic Article
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Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence.
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Academic Article
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Ancestry-specific and sex-specific risk alleles identified in a genome-wide gene-by-alcohol dependence interaction study of risky sexual behaviors.
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Academic Article
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Genetic Risk Variants Associated With Comorbid Alcohol Dependence and Major Depression.
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Academic Article
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Genome-wide association study identifies a novel locus for cannabis dependence.
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Academic Article
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Exome Sequencing of Extended Families with Alzheimer''s Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function.
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Academic Article
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A putative causal relationship between genetically determined female body shape and posttraumatic stress disorder.
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Academic Article
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The Alzheimer''s Disease Sequencing Project: Study design and sample selection.
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Academic Article
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Genome-wide association study of Alzheimer''s disease endophenotypes at prediagnosis stages.
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Academic Article
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Human induced pluripotent stem cells illuminate pathways and novel treatment targets for age-related macular degeneration.
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Academic Article
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Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer''s disease.
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Academic Article
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Genome-wide Association Study Identifies a Regulatory Variant of RGMA Associated With Opioid Dependence in European Americans.
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Academic Article
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Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer''s Disease Sequencing Project.
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Academic Article
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Tau Phosphorylation is Impacted by Rare AKAP9 Mutations Associated with Alzheimer Disease in African Americans.
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Academic Article
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FUS Phase Separation Is Modulated by a Molecular Chaperone and Methylation of Arginine Cation-p Interactions.
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Academic Article
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One for all and all for One: Improving replication of genetic studies through network diffusion.
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Academic Article
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Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer''s disease.
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Academic Article
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Translational studies support a role for serotonin 2B receptor (HTR2B) gene in aggression-related cannabis response.
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Academic Article
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Analysis of shared heritability in common disorders of the brain.
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Academic Article
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Genome-wide association meta-analysis of age at first cannabis use.
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Award or Honor Receipt
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Alfred P. Sloan Research Fellow
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Award or Honor Receipt
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Who is Who in Science and Engineering (1999 edition)
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Award or Honor Receipt
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Distinguished Alumnus Award
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Award or Honor Receipt
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Distinguished Scientist Award
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Award or Honor Receipt
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Jack Spivack Excellence in Neuroscience Research Award
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Academic Article
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F131. Genome-Wide Association Study Identifies Glutamate Ionotropic Receptor GRIA4 as a Risk Gene for Comorbid Nicotine Dependence and Major Depression
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Academic Article
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NOVEL GENETIC VARIANTS ASSOCIATED WITH FAMILIAL LATE-ONSET ALZHEIMER DISEASE IN THE ALZHEIMER’S DISEASE SEQUENCING PROJECT
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Academic Article
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SEX-SPECIFIC ANALYSIS OF THE ADSP CASE-CONTROL WHOLE-EXOME SEQUENCING DATASET
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Academic Article
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ALZHEIMER'S DISEASE SEQUENCING PROJECT: CASE-CONTROL ANALYSES
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Academic Article
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CEREBROSPINAL FLUID ENDOPHENOTYPES PROVIDE INSIGHT INTO BIOLOGY UNDERLYING ALZHEIMER'S DISEASE
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Academic Article
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BIVARIATE GENOME-WIDE ASSOCIATION STUDY OF NEUROPATHOLOGIC FEATURES OF ALZHEIMER’S DISEASE
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Academic Article
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GENOME-WIDE RARE VARIANT IMPUTATION AND TISSUE-SPECIFIC TRANSCRIPTOMIC ANALYSIS IDENTIFY NOVEL RARE VARIANT CANDIDATE LOCI IN LATE-ONSET ALZHEIMER’S DISEASE: THE ALZHEIMER’S DISEASE GENETICS CONSORTIUM
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Academic Article
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GENOME-WIDE ASSOCIATION STUDY OF ALZHEIMER DISEASE ENDOPHENOTYPES AT PRECLINICAL AND MCI STAGES
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Academic Article
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Genome-Wide Association Study Identifies HTR2B as a Risk Variant of Cannabis-Related Aggression in African Americans
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Academic Article
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FURTHER STRATIFICATION OF APOE E4-NEGATIVE SUBJECTS IDENTIFIES NOVEL GENES FOR ALZHEIMER'S DISEASE
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Academic Article
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HIGH-RESOLUTION IMPUTATION IN GENOME-WIDE ASSOCIATION STUDIES OF LATE-ONSET ALZHEIMER'S DISEASE IDENTIFIES NOVEL RARE VARIANT ASSOCIATIONS
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Academic Article
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A COMMON ALLELE IN SPI1 LOWERS RISK AND DELAYS AGE AT ONSET FOR ALZHEIMER'S DISEASE
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Academic Article
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ALZHEIMER'S DISEASE SEQUENCING PROJECT: SEARCH FOR ALZHEIMER'S DISEASE RESILIENCE GENES THAT MAY MODIFY DISEASE SUSCEPTIBILITY IN SPECIFIC APOE GENOTYPE BACKGROUNDS
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Academic Article
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RARE DELETERIOUS AND LOSS-OF-FUNCTION VARIANTS IN OPRL1 AND GAS2L2 CONTRIBUTE TO THE RISK OF LATE-ONSET ALZHEIMER’S DISEASE: ALZHEIMER’S DISEASE SEQUENCING PROJECT CASE-CONTROL STUDY
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Academic Article
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IDENTIFICATION OF NOVEL CANDIDATE GENES FOR EARLY-ONSET ALZHEIMER'S DISEASE THROUGH INTEGRATED WHOLE-EXOME SEQUENCING AND EXOME CHIP ARRAY ASSOCIATION ANALYSIS
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Academic Article
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Exome array analysis identifies novel risk variants for Alzheimer's disease with onset before 65 years
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Academic Article
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LOW-FREQUENCY VARIANT IMPUTATION IDENTIFIES NOVEL DISEASE-ASSOCIATED LOCI IN A GENOME-WIDE ASSOCIATION STUDY OF LATE-ONSET ALZHEIMER'S DISEASE
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Academic Article
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WHOLE-EXOME SEQUENCING OF HISPANIC EARLY-ONSET ALZHEIMER DISEASE FAMILIES IDENTIFIES RARE VARIANTS IN MULTIPLE ALZHEIMER'S-RELATED GENES
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Academic Article
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A VARIANT IN STK24 ACHIEVES GENOME-WIDE SIGNIFICANCE IN AFRICAN AMERICANS USING A LIABILITY MODEL
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Academic Article
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Ttn as a likely causal gene for QTL of alcohol preference on mouse chromosome 2
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Academic Article
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Genome-wide association study in different clinical stages of Alzheimer’s disease
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Academic Article
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Analyzing pathway specificity of variants associated with Alzheimer’s disease from the scientific literature corpus
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Academic Article
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Speaker 4: Joel Gelernter, USA
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Academic Article
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PM296. SORCS2 regulates alcohol withdrawal severity and excitatory synaptic transmission
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Academic Article
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STRUCTURAL VARIATION (SV) IN HETEROGENOUS WHOLE-GENOME SEQUENCING DATA FROM 111 FAMILIES AT RISK FOR ALZHEIMER'S DISEASE: ALZHEIMER'S DISEASE SEQUENCING PROJECT SV STUDY
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Academic Article
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Transethnic genome-wide meta-analysis for Alzheimer disease
|
Academic Article
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MULTIVARIATE PHENOTYPES ASSOCIATION STUDY OF NEUROPATHOLOGICAL FEATURES OF ALZHEIMER'S DISEASE AND RELATED DEMENTIAS
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Academic Article
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Low-frequency variant imputation identifies rare variant candidate loci in a gwas of late-onset Alzheimer’s disease in the igap consortium
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Academic Article
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ABCA7 deletion associated with Alzheimer's disease in African Americans
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Academic Article
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The role of common and rare variants in risk for Alzheimer's disease across populations
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Academic Article
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Genome-wide association study identifies susceptibility loci associated with the rate of cognitive decline
|
Academic Article
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Protective variant for rate of hippocampal volume loss identified by whole exome sequencing in APOE-e3e3 males with MCI
|
Academic Article
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Genetic variation in PLXNA4 associated with susceptibility of Alzheimer’s disease through tau phosphorylation
|
Academic Article
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Genome-wide association analyses of onset age in late-onset Alzheimer disease (LOAD) demonstrate no strong effect outside of the APOE region
|
Academic Article
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Candidate gene study in the endosome-to-Golgi retrieval pathway reveals association of retromer genes with Alzheimer's disease
|
Academic Article
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Genetic association of variants with late-onset Alzheimer's disease risk and brain gene expression
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Academic Article
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ALCOHOL DEPENDENCE GWAS IN TWO POPULATIONS WITH CONSIDERATION OF SUICIDE-RELATED TRAITS
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Academic Article
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LINKAGE AND ASSOCIATION STUDIES OF CANNABIS DEPENDENCE SUGGEST NRG1 AS A RISK LOCUS
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Academic Article
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Two rare AKAP9 variants are associated with Alzheimers disease in African Americans
|
Academic Article
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ADGC+: An expanded Alzheimer's Disease Genetics Consortium (ADGC) genome-wide association study
|
Academic Article
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The identification of rare variants in late-onset Alzheimer’s disease using extended families
|
Academic Article
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Late-onset Alzheimer’s disease neuropathology genomic screen identifies novel loci for neuritic plaque and other Alzheimer’s neuropathology features
|
Academic Article
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A review of published genetic studies using ADNI multimodality quantitative phenotypes: MRI, PET, fluid biomarkers, cognition and clinical status
|
Academic Article
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Genome-wide association study for cognitive decline
|
Academic Article
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Correction: ACSL6 Is Associated with the Number of Cigarettes Smoked and Its Expression Is Altered by Chronic Nicotine Exposure
|
Academic Article
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Association of TREM2 variants with Alzheimer's disease in African-Americans: For the Alzheimer's Disease Genetics Consortium (ADGC)
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Academic Article
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APP associated with late-onset Alzheimer's disease in an autopsy-confirmed dataset
|
Academic Article
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Structural, functional and molecular imaging as intermediate phenotypes for studies of candidate genes, pathways and GWAS in Alzheimer's disease
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Academic Article
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A rare mutation in the CTNND2 gene is associated with increased Aß42 secretion
|
Academic Article
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Genome-wide association study of Alzheimer's-related brain MRI traits identifies several loci influencing degeneration of the hippocampus
|
Academic Article
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CTNNA3, CAPRIN2 and SPG20 are significantly associated with Alzheimer's disease in preliminary analyses of a genome-wide association study in African-Americans
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Academic Article
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Intracellular Traffic and Neurodegenerative Disorders
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Academic Article
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Clustering Based on Genetic Ancestry
|
Academic Article
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Mild Parkinsonian Signs (MPS) Are Associated with Mild Cognitive Impairment (MCI) but Not Predictive of Progression to Alzheimer's Disease (AD) in a Door-to-Door Study of an Elderly Arab Population
|
Academic Article
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U.S. Alzheimer's Disease Genetics Consortium: Organization and results
|
Academic Article
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Genome-wide Association of Cerebrovascular and Neurodegenerative Quantitative MRI Traits in Alzheimer's Disease
|
Academic Article
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GENETIC MODERATION OF ADVERSE CHILDHOOD EVENTS AND RISK OF DEPRESSION AND SUBSTANCE DEPENDENCE
|
Academic Article
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GENOMEWIDE STUDIES OF ALCOHOL DEPENDENCE
|
Academic Article
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Comparison of Family Based Methods For Genome-Wide Association Study In the Framingham Eye Study
|
Academic Article
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A Genomewide Association Study Of Plasma Total IGE In The Framingham Heart Study Identifies HLA-A As A Susceptibility Locus
|
Academic Article
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Identification of Gene-Gene Interactions in Alzheimer Disease Using CoOperative Game Theory
|
Academic Article
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Genome-Wide Scan Suggested Novel Alzheimer’s Disease Susceptibility Genes by Factoring Influence of APOE
|
Academic Article
|
The ADGC genome browser
|
Academic Article
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Genetic Associations between VPS10 Receptor Genes and Late-Onset Alzheimer's Disease
|
Academic Article
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The genetics of Alzheimer's disease
|
Academic Article
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Using CSF biomarkers to replicate genetic associations in Alzheimer's disease.
|
Academic Article
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Statin use is associated with reduced risk of Alzheimer's disease
|
Academic Article
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Polymorphism in the cyclooxygenase-2 (COX-2) and presenilin 2 (PS2) gene promoters: Impact on inflammatory signaling and potential contribution to the etiopathology of Alzheimer's disease (AD)
|
Academic Article
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Genetic polymorphisms associated with fetal hemoglobin response to hydroxyurea in patients with sickle cell anemia
|
Academic Article
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Recent findings from a genomewide linkage scan for cocaine dependence
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Academic Article
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Polymorphisms in paraoxonase genes PON1, PON2 and PON3 are associated with late onset Alzheimer disease
|
Academic Article
|
Modeling genetic polymorhphisms and sickle cell associated vasoocclusive events using classification and regression trees (CART)
|
Academic Article
|
Polymorphisms (Snps) in multiple genes of the Tgf-beta/Bmp pathway are associated with a global measure of sickle cell disease severity
|
Academic Article
|
Modeling Genetic Polymorphisms and Sickle Cell Associated Vasoocclusive Events Using Classification and Regression Trees (CART) and Stochastic Gradient Boosting (SGB)
|
Academic Article
|
P2-060: Comparison of Alzheimer and vascular dementia patients using MRI-based measures of atrophy
|
Academic Article
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Adherence in Internet interventions for anxiety and depression: Systematic review
|
Academic Article
|
CLONING THE WILSON DISEASE GENE
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Academic Article
|
219Cross-national comparison of risk factors for Alzheimer's disease: Same genetic risk in different environments?
|
Academic Article
|
The use of consanguineous families from isolated populations to identify genes for recessive, non-syndromal deafness
|
Academic Article
|
Localization of a gene for blood pressure regulation to human chromosome 18q
|
Academic Article
|
Candidate genes associated with Alzheimer's disease
|
Academic Article
|
Analysis of candidate genes of chromosome 12P
|
Academic Article
|
A genetic linkage study on late-onset familial Alzheimer's disease does not provide strong evidence for linkage to chromosome 1Q22, 9Q21.1, 10Q23, and chromosome 11Q23.3
|
Academic Article
|
Does hypertension affect the risk and age at onset of Alzheimer disease?
|
Academic Article
|
Genetic linkage studies of Alzheimer's disease in Israeli arabs
|
Academic Article
|
The REVEAL study: A new model for susceptibility genotyping. risk assessment and counseling for Alzheimer's disease
|
Academic Article
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Preliminary findings from the REVEAL Study: Genetic risk assessment and counseling for Alzheimer's disease
|
Academic Article
|
Authors' response to commentaries
|
Academic Article
|
Response to Kessler: Suicide and presymptomatic testing in Huntington disease
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Academic Article
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SEARCHING FOR DISEASE MODIFIER GENES IN ß0THALASSEMIA/Hb E
|
Academic Article
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A fine structure linkage map for chromosome 13
|
Academic Article
|
Fetal Hemoglobin In Sickle Cell Anemia: Molecular Characterization of Saudi Patients From the Eastern Province
|
Academic Article
|
Whole exome sequencing study identifies novel rare and common Alzheimer''s-Associated variants involved in immune response and transcriptional regulation.
|
Academic Article
|
Genome-wide association study of cognitive flexibility assessed by the Wisconsin Card Sorting Test.
|
Academic Article
|
Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer''s disease.
|
Academic Article
|
Targeted Sequencing of Alzheimer Disease Genes in African Americans Implicates Novel Risk Variants.
|
Academic Article
|
Risk Locus Identification Ties Alcohol Withdrawal Symptoms to SORCS2.
|
Academic Article
|
Genome-wide association study identifies glutamate ionotropic receptor GRIA4 as a risk gene for comorbid nicotine dependence and major depression.
|
Academic Article
|
An efficient analytic approach in genome-wide identification of methylation quantitative trait loci response to fenofibrate treatment.
|
Academic Article
|
Variation in TMEM106B in chronic traumatic encephalopathy.
|
Academic Article
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Dissecting the genetic relationship between cardiovascular risk factors and Alzheimer''s disease.
|
Academic Article
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Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders.
|
Academic Article
|
Ancestral origin of ApoE e4 Alzheimer disease risk in Puerto Rican and African American populations.
|
Academic Article
|
A rare missense variant of CASP7 is associated with familial late-onset Alzheimer''s disease.
|
Academic Article
|
Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease.
|
Academic Article
|
Comparison of methods for multivariate gene-based association tests for complex diseases using common variants.
|
Academic Article
|
The genetics and epigenetics of Neonatal Abstinence Syndrome.
|
Academic Article
|
Genetic meta-analysis of diagnosed Alzheimer''s disease identifies new risk loci and implicates Aß, tau, immunity and lipid processing.
|
Academic Article
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The Utah Protocol for Postmortem Eye Phenotyping and Molecular Biochemical Analysis.
|
Academic Article
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Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry.
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Academic Article
|
Salivary microRNAs identified by small RNA sequencing and machine learning as potential biomarkers of alcohol dependence.
|
Academic Article
|
CpG-related SNPs in the MS4A region have a dose-dependent effect on risk of late-onset Alzheimer disease.
|
Academic Article
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Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype.
|
Academic Article
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Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes.
|
Academic Article
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A systems biology approach towards understanding and treating non-neovascular age-related macular degeneration.
|
Academic Article
|
Author Correction: Genetic meta-analysis of diagnosed Alzheimer''s disease identifies new risk loci and implicates Aß, tau, immunity and lipid processing.
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Award or Honor Receipt
|
BU Evans Center for Interdisciplinary Biomedical Research Leadership Award
|
Academic Article
|
APOE Promoter Polymorphism-219T/G is an Effect Modifier of the Influence of APOE e4 on Alzheimer''s Disease Risk in a Multiracial Sample.
|
Academic Article
|
International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci.
|
Academic Article
|
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer''s-Associated variants involved in immune response and transcriptional regulation.
|
Academic Article
|
A regulatory variant of CHRM3 is associated with cannabis-induced hallucinations in European Americans.
|
Academic Article
|
Post-GWAS analysis of six substance use traits improves the identification and functional interpretation of genetic risk loci.
|
Academic Article
|
Genome-Wide Association Study of Opioid Cessation.
|
Academic Article
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Exceptionally low likelihood of Alzheimer''s dementia in APOE2 homozygotes from a 5,000-person neuropathological study.
|
Academic Article
|
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.
|
Academic Article
|
Genomic influences on self-reported childhood maltreatment.
|
Academic Article
|
Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium.
|
Academic Article
|
Prefrontal cortex eQTLs/mQTLs enriched in genetic variants associated with alcohol use disorder and other diseases.
|
Academic Article
|
Association of OPRM1 Functional Coding Variant With Opioid Use Disorder: A Genome-Wide Association Study.
|
Academic Article
|
Sex-dependent autosomal effects on clinical progression of Alzheimer''s disease.
|
Academic Article
|
Genome-wide association study of rate of cognitive decline in Alzheimer''s disease patients identifies novel genes and pathways.
|
Academic Article
|
Genetic variants and functional pathways associated with resilience to Alzheimer''s disease.
|
Academic Article
|
Analysis of brain region-specific co-expression networks reveals clustering of established and novel genes associated with Alzheimer disease.
|
Academic Article
|
Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis.
|
Academic Article
|
A large-scale genome-wide association study meta-analysis of cannabis use disorder.
|
Grant
|
The Alzheimer Disease Sequencing Analysis Collaborative
|
Grant
|
Precision Monitoring and Assessment in the Framingham Study: Cognitive, MRI, Genetic and Biomarker Precursors of AD & Dementia
|
Grant
|
Alzheimer Disease Genetic Architecture in African Americans
|
Grant
|
International Alzheimer's Disease Genetics Consortium
|
Grant
|
Alzheimer's Disease Genetics Consortium
|
Grant
|
Coordinating Center for Genetics and Genomics of Alzheimer's Disease
|
Grant
|
Alzheimer's Disease Genetics Consortium
|
Grant
|
Genetic Studies of Alzheimer Disease in Koreans
|
Grant
|
Metabolomic Signatures for Disease Sub-classification and Target Prioritization in AMP-AD
|
Grant
|
Institutional Program Unifying Population and Laboratory Based Sciences Award
|
Grant
|
Genomic and Biological Studies of APOE e2 in Alzheimer's Disease
|
Grant
|
Genetic Mechanisms Shared by Eye and Brain Diseases as Novel Therapeutic Targets for Age-Related macular Degeneration
|
Grant
|
Alzheimer Disease Genetic Architecture in African Americans
|
Grant
|
Personnel Agreement for Research Services of Mark Logue
|
Grant
|
Coordinating Center for Genetics and Genomics of Alzheimer's Disease
|
Grant
|
Identifying Methamphetamine Risk Variants by Extreme Phenotype Exome Sequencing
|
Grant
|
Consortium for Alzheimer Sequencing and Analysis (CASA)
|
Grant
|
Alzheimer Disease Genetics Consortium
|
Academic Article
|
Analysis of telomere length variation and Shelterin complex subunit gene expression changes in ethanol-exposed human embryonic stem cells.
|
Academic Article
|
Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits.
|