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Articles
exaly
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Harvard University
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Program in Medical and Population Genetics
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Top Articles
Program in Medical and Population Genetics
Harvard University
67
Articles
8K
Citations
8.2
avg. Impact Factor
37
h-index
Most Cited Articles of Program in Medical and Population Genetics
Title
Journal
Year
Citations
Genetics of rheumatoid arthritis contributes to biology and drug discovery
Nature
2014
1.4K
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
Nature Genetics
2008
1.1K
Plasma glucose levels and diabetes are independent predictors for mortality and morbidity in patients with SARS
Diabetic Medicine
2006
436
Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms
American Journal of Human Genetics
2002
425
Pervasive sharing of genetic effects in autoimmune disease
PLoS Genetics
2011
413
Defining the role of the MHC in autoimmunity: a review and pooled analysis
PLoS Genetics
2008
400
Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology
PLoS Genetics
2011
383
Using whole-exome sequencing to identify inherited causes of autism
Neuron
2013
297
Impaired autophagy of an intracellular pathogen induced by a Crohn's disease associated ATG16L1 variant
PLoS ONE
2008
261
African origin of modern humans in East Asia: a tale of 12,000 Y chromosomes
Science
2001
225
Common missense variant in the glucokinase regulatory protein gene is associated with increased plasma triglyceride and C-reactive protein but lower fasting glucose concentrations
Diabetes
2008
223
Modern thoughts on an ancyent marinere: function, evolution, regulation
Annual Review of Genetics
1997
203
Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia
Annals of Neurology
2015
183
IL2RA genetic heterogeneity in multiple sclerosis and type 1 diabetes susceptibility and soluble interleukin-2 receptor production
PLoS Genetics
2009
183
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism
PLoS Genetics
2012
134
The role of the Toll receptor pathway in susceptibility to inflammatory bowel diseases
Genes and Immunity
2007
120
Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function
PLoS Genetics
2010
118
Soluble IL-2RA levels in multiple sclerosis subjects and the effect of soluble IL-2RA on immune responses
Journal of Immunology
2009
113
Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load
Proceedings of the National Academy of Sciences of the United States of America
2015
108
Genetic variation in human DNA replication timing
Cell
2014
102
The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease
PLoS Genetics
2015
98
Disentangling the Effects of Colocalizing Genomic Annotations to Functionally Prioritize Non-coding Variants within Complex-Trait Loci
American Journal of Human Genetics
2015
94
Microcephaly Proteins Wdr62 and Aspm Define a Mother Centriole Complex Regulating Centriole Biogenesis, Apical Complex, and Cell Fate
Neuron
2016
82
Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study
BMC Medical Genetics
2007
79
ATG16L1 and IL23R are associated with inflammatory bowel diseases but not with celiac disease in the Netherlands
American Journal of Gastroenterology
2008
77
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