67
Articles
8K
Citations
8.2
avg. Impact Factor
37
h-index

Most Cited Articles of Program in Medical and Population Genetics

TitleJournalYearCitations
Genetics of rheumatoid arthritis contributes to biology and drug discoveryNature20141.4K
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humansNature Genetics20081.1K
Plasma glucose levels and diabetes are independent predictors for mortality and morbidity in patients with SARSDiabetic Medicine2006436
Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphismsAmerican Journal of Human Genetics2002425
Pervasive sharing of genetic effects in autoimmune diseasePLoS Genetics2011413
Defining the role of the MHC in autoimmunity: a review and pooled analysisPLoS Genetics2008400
Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biologyPLoS Genetics2011383
Using whole-exome sequencing to identify inherited causes of autismNeuron2013297
Impaired autophagy of an intracellular pathogen induced by a Crohn's disease associated ATG16L1 variantPLoS ONE2008261
African origin of modern humans in East Asia: a tale of 12,000 Y chromosomesScience2001225
Common missense variant in the glucokinase regulatory protein gene is associated with increased plasma triglyceride and C-reactive protein but lower fasting glucose concentrationsDiabetes2008223
Modern thoughts on an ancyent marinere: function, evolution, regulationAnnual Review of Genetics1997203
Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasiaAnnals of Neurology2015183
IL2RA genetic heterogeneity in multiple sclerosis and type 1 diabetes susceptibility and soluble interleukin-2 receptor productionPLoS Genetics2009183
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autismPLoS Genetics2012134
The role of the Toll receptor pathway in susceptibility to inflammatory bowel diseasesGenes and Immunity2007120
Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain functionPLoS Genetics2010118
Soluble IL-2RA levels in multiple sclerosis subjects and the effect of soluble IL-2RA on immune responsesJournal of Immunology2009113
Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus loadProceedings of the National Academy of Sciences of the United States of America2015108
Genetic variation in human DNA replication timingCell2014102
The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex diseasePLoS Genetics201598
Disentangling the Effects of Colocalizing Genomic Annotations to Functionally Prioritize Non-coding Variants within Complex-Trait LociAmerican Journal of Human Genetics201594
Microcephaly Proteins Wdr62 and Aspm Define a Mother Centriole Complex Regulating Centriole Biogenesis, Apical Complex, and Cell FateNeuron201682
Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart StudyBMC Medical Genetics200779
ATG16L1 and IL23R are associated with inflammatory bowel diseases but not with celiac disease in the NetherlandsAmerican Journal of Gastroenterology200877