Raveen Basran, DPhil
Assistant Professor
Boston University School of Medicine
Dept of Pathology & Laboratory Medicine

DPhil, University of Oxford
MSc, University of Oxford



Boston Medical Center


Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.

  1. Brzezinski J, Shuman C, Choufani S, Ray P, Stavropoulos DJ, Basran R, Steele L, Parkinson N, Grant R, Thorner P, Lorenzo A, Weksberg R. Wilms tumour in Beckwith-Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelines. Eur J Hum Genet. 2017 Jul 12. PMID: 28699632.
  2. Grafodatskaya D, Choufani S, Basran R, Weksberg R. An Update on Molecular Diagnostic Testing of Human Imprinting Disorders. J Pediatr Genet. 2017 Mar; 6(1):3-17. PMID: 28180023; DOI: 10.1055/s-0036-1593840;.
  3. Cytrynbaum C, Chong K, Hannig V, Choufani S, Shuman C, Steele L, Morgan T, Scherer SW, Stavropoulos DJ, Basran RK, Weksberg R. Genomic imbalance in the centromeric 11p15 imprinting center in three families: Further evidence of a role for IC2 as a cause of Russell-Silver syndrome. Am J Med Genet A. 2016 Oct; 170(10):2731-9. PMID: 27374371; DOI: 10.1002/ajmg.a.37819;.
  4. Gonorazky H, Liang M, Cummings B, Lek M, Micallef J, Hawkins C, Basran R, Cohn R, Wilson MD, MacArthur D, Marshall CR, Ray PN, Dowling JJ. RNAseq analysis for the diagnosis of muscular dystrophy. Ann Clin Transl Neurol. 2016 Jan; 3(1):55-60. PMID: 26783550; DOI: 10.1002/acn3.267;.
  5. Pilozzi-Edmonds L, Maher TA, Basran RK, Milunsky A, Al-Thihli K, Braverman NE, Alfares A. Fraternal twins with Aarskog-Scott syndrome due to maternal germline mosaicism. Am J Med Genet A. 2011 Aug; 155A(8):1987-90.View Related Profiles. PMID: 21739585; DOI: 10.1002/ajmg.a.34094;.
  6. Al-Owain M, Kaya N, Al-Zaidan H, Al-Hashmi N, Al-Bakheet A, Al-Muhaizea M, Chedrawi A, Basran RK, Milunsky A. Novel intragenic deletion in OPHN1 in a family causing XLMR with cerebellar hypoplasia and distinctive facial appearance. Clin Genet. 2011 Apr; 79(4):363-70.View Related Profiles. PMID: 20528889; DOI: 10.1111/j.1399-0004.2010.01462.x;.
  7. Jamal SM, Basran RK, Newton S, Wang Z, Milunsky JM. Novel de novo PCDH19 mutations in three unrelated females with epilepsy female restricted mental retardation syndrome. Am J Med Genet A. 2010 Oct; 152A(10):2475-81.View Related Profiles. PMID: 20830798; DOI: 10.1002/ajmg.a.33611;.
  8. Chen Z, Luo HY, Basran RK, Hsu TH, Mang DW, Nuntakarn L, Rosenfield CG, Patrinos GP, Hardison RC, Steinberg MH, Chui DH. A T-to-G transversion at nucleotide -567 upstream of HBG2 in a GATA-1 binding motif is associated with elevated hemoglobin F. Mol Cell Biol. 2008 Jul; 28(13):4386-93.View Related Profiles. PMID: 18443038; PMCID: PMC2447137; DOI: 10.1128/MCB.00071-08;.
  9. Basran RK, Reiss UM, Luo HY, Ware RE, Chui DH. Beta-thalassemia intermedia due to compound heterozygosity for two beta-globin gene promoter mutations, including a novel TATA box deletion. Pediatr Blood Cancer. 2008 Feb; 50(2):363-6.View Related Profiles. PMID: 16732578.
  10. Schmugge M, Waye JS, Basran RK, Zurbriggen K, Frischknecht H. THE Hb S/beta+ -thalassemia phenotype demonstrates that the IVS-I (-2) (A>C) mutation is a mild beta-thalassemia allele. Hemoglobin. 2008; 32(3):303-7. PMID: 18473247; DOI: 10.1080/03630260802004459;.
Showing 10 of 13 results. Show More

This graph shows the total number of publications by year, by first, middle/unknown, or last author.

Bar chart showing 13 publications over 9 distinct years, with a maximum of 3 publications in 2008

YearPublications
20051
20061
20071
20083
20101
20112
20151
20162
20171
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Boston MA 02118
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