PubRank

Christopher S Carlson

Author PubWeight™ 106.75‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Population history and natural selection shape patterns of genetic variation in 132 genes. PLoS Biol 2004 7.11
2 Comprehensive assessment of T-cell receptor beta-chain diversity in alphabeta T cells. Blood 2009 7.00
3 Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study. J Am Med Inform Assoc 2011 4.20
4 Pattern of sequence variation across 213 environmental response genes. Genome Res 2004 3.93
5 Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populations. Am J Hum Genet 2004 3.91
6 Association of polymorphisms in the CRP gene with circulating C-reactive protein levels and cardiovascular events. JAMA 2006 3.26
7 Overlap and effective size of the human CD8+ T cell receptor repertoire. Sci Transl Med 2010 3.01
8 The Next PAGE in understanding complex traits: design for the analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study. Am J Epidemiol 2011 2.98
9 Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. Gastroenterology 2012 2.57
10 Quality control procedures for genome-wide association studies. Curr Protoc Hum Genet 2011 2.48
11 Meta-analysis of new genome-wide association studies of colorectal cancer risk. Hum Genet 2011 2.35
12 Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study. PLoS Genet 2011 2.13
13 Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk. Circulation 2013 2.06
14 Genetic ancestry, population sub-structure, and cardiovascular disease-related traits among African-American participants in the CARDIA Study. Hum Genet 2007 1.91
15 Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project. Blood 2013 1.69
16 Efficient selection of tagging single-nucleotide polymorphisms in multiple populations. Hum Genet 2006 1.66
17 Genetic polymorphisms in the catechol estrogen metabolism pathway and breast cancer risk. Cancer Epidemiol Biomarkers Prev 2009 1.62
18 High-throughput genotyping of intermediate-size structural variation. Hum Mol Genet 2006 1.61
19 Multiple independent genetic variants in the 8q24 region are associated with prostate cancer risk. Cancer Epidemiol Biomarkers Prev 2008 1.58
20 Deep sequencing of the human TCRγ and TCRβ repertoires suggests that TCRβ rearranges after αβ and γδ T cell commitment. Sci Transl Med 2011 1.36
21 SNPit: a federated data integration system for the purpose of functional SNP annotation. Comput Methods Programs Biomed 2009 1.33
22 Polymorphisms of the IL1-receptor antagonist gene (IL1RN) are associated with multiple markers of systemic inflammation. Arterioscler Thromb Vasc Biol 2008 1.32
23 Genetic risk factors for BMI and obesity in an ethnically diverse population: results from the population architecture using genomics and epidemiology (PAGE) study. Obesity (Silver Spring) 2013 1.28
24 Fine Mapping and Identification of BMI Loci in African Americans. Am J Hum Genet 2013 1.27
25 Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality. Genet Epidemiol 2011 1.26
26 Genome-wide association of body fat distribution in African ancestry populations suggests new loci. PLoS Genet 2013 1.24
27 Vitamin D related genes, CYP24A1 and CYP27B1, and colon cancer risk. Cancer Epidemiol Biomarkers Prev 2009 1.13
28 C-reactive protein, interleukin-6, and prostate cancer risk in men aged 65 years and older. Cancer Causes Control 2009 1.13
29 High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE. Clin Transl Sci 2012 1.13
30 Cyclooxygenase 1 (COX1) polymorphisms in African-American and Caucasian populations. Hum Mutat 2002 1.08
31 Replication of loci influencing ages at menarche and menopause in Hispanic women: the Women's Health Initiative SHARe Study. Hum Mol Genet 2011 1.07
32 The effects of scale: variation in the APOA1/C3/A4/A5 gene cluster. Hum Genet 2004 1.07
33 Soluble P-selectin, SELP polymorphisms, and atherosclerotic risk in European-American and African-African young adults: the Coronary Artery Risk Development in Young Adults (CARDIA) Study. Arterioscler Thromb Vasc Biol 2008 1.05
34 Dopamine transporter (SLC6A3) 5' region haplotypes significantly affect transcriptional activity in vitro but are not associated with Parkinson's disease. Pharmacogenet Genomics 2005 0.99
35 Confirmation of the reported association of clonal chromosomal mosaicism with an increased risk of incident hematologic cancer. PLoS One 2013 0.98
36 Common coding variants of the HNF1A gene are associated with multiple cardiovascular risk phenotypes in community-based samples of younger and older European-American adults: the Coronary Artery Risk Development in Young Adults Study and The Cardiovascular Health Study. Circ Cardiovasc Genet 2009 0.96
37 Genome-wide search for gene-gene interactions in colorectal cancer. PLoS One 2012 0.96
38 Genetic variation in prostaglandin E2 synthesis and signaling, prostaglandin dehydrogenase, and the risk of colorectal adenoma. Cancer Epidemiol Biomarkers Prev 2010 0.94
39 Genetic variation and reproductive timing: African American women from the Population Architecture using Genomics and Epidemiology (PAGE) Study. PLoS One 2013 0.93
40 COX-1 (PTGS1) and COX-2 (PTGS2) polymorphisms, NSAID interactions, and risk of colon and rectal cancers in two independent populations. Cancer Causes Control 2013 0.92
41 USF1 gene variants, cardiovascular risk, and mortality in European Americans: analysis of two US cohort studies. Arterioscler Thromb Vasc Biol 2007 0.92
42 A variational Bayes discrete mixture test for rare variant association. Genet Epidemiol 2014 0.92
43 Estrogen-related genes and their contribution to racial differences in breast cancer risk. Cancer Causes Control 2012 0.89
44 Evaluation of probabilistic and logical inference for a SNP annotation system. J Biomed Inform 2009 0.88
45 T-cell receptor sequencing reveals the clonal diversity and overlap of colonic effector and FOXP3+ T cells in ulcerative colitis. Inflamm Bowel Dis 2015 0.88
46 The influence of obesity-related single nucleotide polymorphisms on BMI across the life course: the PAGE study. Diabetes 2013 0.87
47 5' and 3' region variability in the dopamine transporter gene (SLC6A3), pesticide exposure and Parkinson's disease risk: a hypothesis-generating study. Hum Mol Genet 2006 0.87
48 Associations between common fibrinogen gene polymorphisms and cardiovascular disease in older adults. The Cardiovascular Health Study. Thromb Haemost 2008 0.86
49 Effects of smoking on the genetic risk of obesity: the population architecture using genomics and epidemiology study. BMC Med Genet 2013 0.85
50 Comprehensive genetic variant discovery in the surfactant protein B gene. Pediatr Res 2007 0.85
51 Phospholipase A2G1B polymorphisms and risk of colorectal neoplasia. Int J Mol Epidemiol Genet 2013 0.85
52 Genome-wide association study of age at menarche in African-American women. Hum Mol Genet 2013 0.85
53 Recombination as a mechanism for sporadic mutation in the surfactant protein-C gene. Pediatr Pulmonol 2008 0.84
54 A major deletion in the surfactant protein-B gene causing lethal respiratory distress. Acta Paediatr 2007 0.84
55 Examination of ancestral informative markers and self-reported race with tumor characteristics of breast cancer among Black and White women. Breast Cancer Res Treat 2012 0.84
56 Developmental and genetic regulation of human surfactant protein B in vivo. Neonatology 2008 0.84
57 Genetic variation in the lipoxygenase pathway and risk of colorectal neoplasia. Genes Chromosomes Cancer 2013 0.83
58 Sequence diversity, natural selection and linkage disequilibrium in the human T cell receptor alpha/delta locus. Hum Genet 2006 0.83
59 Agnosticism and equity in genome-wide association studies. Nat Genet 2006 0.83
60 Genetic variability in IL23R and risk of colorectal adenoma and colorectal cancer. Cancer Epidemiol 2011 0.82
61 Sequence variation in the human T-cell receptor loci. Immunol Rev 2002 0.82
62 Genetic variability in EGFR, Src and HER2 and risk of colorectal adenoma and cancer. Int J Mol Epidemiol Genet 2011 0.81
63 Thromboxane synthase (TBXAS1) polymorphisms in African-American and Caucasian populations: evidence for selective pressure. Hum Mutat 2005 0.81
64 Analysis of metabolic syndrome components in >15 000 african americans identifies pleiotropic variants: results from the population architecture using genomics and epidemiology study. Circ Cardiovasc Genet 2014 0.81
65 Genetic variation in the progesterone receptor and metabolism pathways and hormone therapy in relation to breast cancer risk. Am J Epidemiol 2009 0.80
66 Comment on 'Discrepancies in dbSNP confirmations rates and allele frequency distributions from varying genotyping error rates and patterns'. Bioinformatics 2004 0.79
67 Evaluating the accuracy of a functional SNP annotation system. BMC Bioinformatics 2009 0.79
68 Efficient identification of rare variants in large populations: deep re-sequencing the CRP locus in the CARDIA study. Nucleic Acids Res 2013 0.78
69 Polymorphisms predicted to alter function in prostaglandin E2 synthase and prostaglandin E2 receptors. Pharmacogenet Genomics 2007 0.76
70 Common genetic variation in the prothrombin gene, hormone therapy, and incident nonfatal myocardial infarction in postmenopausal women. Am J Epidemiol 2006 0.76
71 Corrigendum: Genome-wide association study of colorectal cancer identifies six new susceptibility loci. Nat Commun 2015 0.76
72 Association between the PTPN2 gene and Crohn's disease: dissection of potential causal variants. Inflamm Bowel Dis 2013 0.76
73 The impact of patents on the development of genome-based clinical diagnostics: an analysis of case studies. Genet Med 2009 0.75