Search Results to Kathryn L Lunetta, PhD

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One or more keywords matched the following properties of Lunetta, Kathryn

Research Expertise & Professional Interests Kathryn L. Lunetta, Ph.D. joined the Department of Biostatistics in the fall of 2004 as an Associate Professor. Prior to her arrival, she held positions in the biotechnology industry, and was on the faculty in the Biostatistics department at the Harvard School of Public Health and Dana-Farber Cancer Institute. Dr. Lunetta’s research focuses on statistical problems and study design and analysis issues in human genetics, particularly in the mapping of complex genetic diseases. Dr. Lunetta collaborates as a statistical geneticist on several projects studying the genetic components of complex traits such as Alzheimer Disease, atrial fibrillation, and successful aging/longevity, and the genetic epidemiology of breast cancer.
Self-Described Keywords Statistical genetics

One or more keywords matched the following items that are connected to Lunetta, Kathryn

Item TypeName
Concept Data Interpretation, Statistical
Concept Genetics, Population
Concept Models, Statistical
Academic Article Selected locus and multiple panel models for radiation hybrid mapping.
Academic Article Statistical methods for polyploid radiation hybrid mapping.
Academic Article On the validity of the TDT test in the presence of comorbidity and ascertainment bias.
Academic Article Testing for population subdivision and association in four case-control studies.
Academic Article Expectation maximization algorithm based haplotype relative risk (EM-HRR): test of linkage disequilibrium using incomplete case-parents trios.
Academic Article Demonstrating stratification in a European American population.
Academic Article Combined haplotype relative risk (CHRR): a general and simple genetic association test that combines trios and unrelated case-controls.
Academic Article Estimating the probability of de novo HD cases from transmissions of expanded penetrant CAG alleles in the Huntington disease gene from male carriers of high normal alleles (27-35 CAG).
Academic Article Evaluation of methods accounting for population structure with pedigree data and continuous outcomes.
Academic Article Choice of population structure informative principal components for adjustment in a case-control study.
Academic Article Frailty models: Applications to biomedical and genetic studies.
Academic Article Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairment.
Academic Article Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics.
Academic Article Correction for multiple testing in a gene region.
Academic Article The complex genetics of gait speed: genome-wide meta-analysis approach.
Academic Article Phenotypically Enriched Genotypic Imputation in Genetic Association Tests.
Academic Article Rarity of the Alzheimer Disease-Protective APP A673T Variant in the United States
Academic Article Correction: The complex genetics of gait speed: genome-wide meta-analysis approach.
Academic Article Genome-wide association study of offspring birth weight in 86?577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics.
Academic Article The Epidemiology of Aging
Academic Article The impact of spurious comorbidity and ascertainment bias on genetic association studies
Academic Article RHMAP: Statistical Package for Multipoint Radiation Hybrid Mapping
Academic Article Correction for multiple testing in candidate-gene methylation studies.

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  • Statistical
  • Genetics