PubRank

Pamela Whittaker

Author PubWeight™ 216.78‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A second generation human haplotype map of over 3.1 million SNPs. Nature 2007 85.39
2 Integrating common and rare genetic variation in diverse human populations. Nature 2010 32.30
3 Genome-wide detection and characterization of positive selection in human populations. Nature 2007 17.27
4 A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. Nat Genet 2006 15.63
5 Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature 2011 13.23
6 Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat Genet 2007 12.62
7 Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet 2013 7.44
8 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. Nat Genet 2011 5.56
9 Human aging-associated DNA hypermethylation occurs preferentially at bivalent chromatin domains. Genome Res 2010 5.08
10 Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region. Nat Genet 2009 4.61
11 A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose. PLoS Genet 2009 4.32
12 Genome-wide and fine-resolution association analysis of malaria in West Africa. Nat Genet 2009 4.30
13 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. Nat Genet 2010 3.58
14 A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms. Am J Hum Genet 2005 2.85
15 The impact of SNP density on fine-scale patterns of linkage disequilibrium. Hum Mol Genet 2004 2.78
16 A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs. Am J Hum Genet 2009 2.62
17 Common variants in the region around Osterix are associated with bone mineral density and growth in childhood. Hum Mol Genet 2009 1.99
18 Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studies. Diabetes 2008 1.33
19 Phosphodiesterase genes are associated with susceptibility to major depression and antidepressant treatment response. Proc Natl Acad Sci U S A 2006 1.23
20 Variation within the gene encoding the upstream stimulatory factor 1 does not influence susceptibility to type 2 diabetes in samples from populations with replicated evidence of linkage to chromosome 1q. Diabetes 2006 1.04
21 The brain-derived neurotrophic factor rs6265 (Val66Met) polymorphism and depression in Mexican-Americans. Neuroreport 2007 1.01
22 Adaptive low-vision and blindness techniques for blood glucose monitoring. Diabetes Educ 2003 0.88