Michael J Malasky

发表

Genetic associations of variants in genes encoding HIV-dependency factors required for HIV-1 infection.

Stephen J O'Brien, James J Goedert, J. Goedert, 2010, The Journal of infectious diseases.

Genome-wide association meta-analyses combining multiple risk phenotypes provides insights into the genetic architecture of cutaneous melanoma susceptibility

Blair H. Smith, Jeffrey E. Lee, G. Abecasis, 2020, Nature Genetics.

Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes.

H. Ostrer, D. Goldstein, X. Estivill, 1998, American journal of human genetics.

Dating the Origin of the CCR 5D 32 AIDS-Resistance Allele by the Coalescence of Haplotypes

H. Ostrer, D. Goldstein, X. Estivill, 2007 .

A high-density admixture map for disease gene discovery in african americans.

Scott M. Williams, Jason H. Moore, D. Altshuler, 2004, American journal of human genetics.

Cell-type-specific meQTLs extend melanoma GWAS annotation beyond eQTLs and inform melanocyte gene-regulatory mechanisms.

Michael A. Kovacs, Jianxin Shi, K. Brown, 2021, American journal of human genetics.

Cell-type-specific meQTL extends melanoma GWAS annotation beyond eQTL and 1 informs melanocyte gene regulatory mechanisms 2

K. Brown, M. Iles, A. Goldstein, 2021 .

Whole exome sequencing reveals a C-terminal germline variant in CEBPA-associated acute myeloid leukemia: 45-year follow up of a large family

M. Yeager, B. Luke, J. Mulvihill, 2016, Haematologica.

Association of Aflatoxin and Gallbladder Cancer.

A. Rashid, A. Hildesheim, C. Ferreccio, 2017, Gastroenterology.

Genetic Variants in Nuclear-Encoded Mitochondrial Genes Influence AIDS Progression

J. Goedert, S. O’Brien, L. Kingsley, 2010, PloS one.

Genome-wide association study implicates PARD3B-based AIDS restriction.

Jean-François Zagury, Olivier Delaneau, Sophie Limou, 2011, The Journal of infectious diseases.

The Principal Genetic Determinants for Nasopharyngeal Carcinoma in China Involve the HLA Class I Antigen Recognition Groove

M. Carrington, S. O’Brien, C. Winkler, 2012, PLoS genetics.

Genome-wide association meta-analyses combining multiple risk phenotypes provides insights into the genetic architecture of cutaneous melanoma susceptibility

Blair H. Smith, Jeffrey E. Lee, G. Abecasis, 2020, Nature Genetics.

Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations

S. Chanock, H. Olsson, M. Yeager, 2016, Human Genetics.

An optimized protocol for retina single-cell RNA sequencing

Michael C. Kelly, A. Swaroop, J. Boland, 2020, Molecular vision.

High-density map of short tandem repeats across the human major histocompatibility complex

M. Carrington, M. Cullen, M. Malasky, 2003, Immunogenetics.