Daniel I Chasman

Author PubWeight™ 298.18‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Biological, clinical and population relevance of 95 loci for blood lipids. Nature 2010 28.21
2 Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet 2010 23.08
3 Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 2010 20.01
4 Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature 2011 13.25
5 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat Genet 2010 7.94
6 Population analysis of large copy number variants and hotspots of human genetic disease. Am J Hum Genet 2009 6.79
7 Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3. Ann Intern Med 2009 6.00
8 Sugar-sweetened beverages and genetic risk of obesity. N Engl J Med 2012 5.98
9 New loci associated with kidney function and chronic kidney disease. Nat Genet 2010 5.58
10 Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. Nat Genet 2012 5.48
11 Inactivating mutations in NPC1L1 and protection from coronary heart disease. N Engl J Med 2014 4.94
12 Multiple loci associated with indices of renal function and chronic kidney disease. Nat Genet 2009 4.78
13 Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies. Lancet 2012 4.63
14 Association between a literature-based genetic risk score and cardiovascular events in women. JAMA 2010 4.46
15 Rationale, design, and methodology of the Women's Genome Health Study: a genome-wide association study of more than 25,000 initially healthy american women. Clin Chem 2007 4.45
16 Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study. Am J Hum Genet 2008 4.31
17 Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. N Engl J Med 2016 3.88
18 Genome-wide association studies identify four ER negative-specific breast cancer risk loci. Nat Genet 2013 3.81
19 Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat Genet 2012 3.71
20 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. Circulation 2011 3.68
21 Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein. Am J Hum Genet 2008 3.61
22 Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat Genet 2011 3.40
23 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nat Genet 2010 3.37
24 A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer. Nat Genet 2011 3.37
25 Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat Genet 2013 3.25
26 Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes. Hum Mol Genet 2010 3.24
27 Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. PLoS Genet 2012 3.21
28 Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. Nat Genet 2009 3.06
29 Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nat Genet 2012 3.04
30 Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat Genet 2013 2.92
31 Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women. PLoS Genet 2008 2.85
32 Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. PLoS Genet 2013 2.83
33 FTO genotype is associated with phenotypic variability of body mass index. Nature 2012 2.77
34 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. Circ Cardiovasc Genet 2010 2.76
35 On the use of variance per genotype as a tool to identify quantitative trait interaction effects: a report from the Women's Genome Health Study. PLoS Genet 2010 2.48
36 A statin-dependent QTL for GATM expression is associated with statin-induced myopathy. Nature 2013 2.46
37 A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. Hum Mol Genet 2012 2.45
38 Genome-wide association of lipid-lowering response to statins in combined study populations. PLoS One 2010 2.43
39 Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nat Genet 2012 2.12
40 Fried food consumption, genetic risk, and body mass index: gene-diet interaction analysis in three US cohort studies. BMJ 2014 2.06
41 Novel genetic markers improve measures of atrial fibrillation risk prediction. Eur Heart J 2013 1.93
42 A kinesin family member 6 variant is associated with coronary heart disease in the Women's Health Study. J Am Coll Cardiol 2008 1.92
43 Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study. Circ Cardiovasc Genet 2009 1.92
44 Discovery and replication of novel blood pressure genetic loci in the Women's Genome Health Study. J Hypertens 2011 1.81
45 Rosuvastatin, proprotein convertase subtilisin/kexin type 9 concentrations, and LDL cholesterol response: the JUPITER trial. Clin Chem 2011 1.79
46 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. PLoS Genet 2011 1.77
47 Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study. Circ Cardiovasc Genet 2009 1.71
48 Genome-wide association and functional follow-up reveals new loci for kidney function. PLoS Genet 2012 1.68
49 Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study. PLoS Genet 2008 1.67
50 Detection of protein folding defects caused by BRCA1-BRCT truncation and missense mutations. J Biol Chem 2003 1.61
51 Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals. Hypertension 2011 1.60
52 Informed conditioning on clinical covariates increases power in case-control association studies. PLoS Genet 2012 1.57
53 Tracing sub-structure in the European American population with PCA-informative markers. PLoS Genet 2008 1.56
54 Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. Am J Hum Genet 2013 1.55
55 Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study. Circ Cardiovasc Genet 2009 1.51
56 Gene × physical activity interactions in obesity: combined analysis of 111,421 individuals of European ancestry. PLoS Genet 2013 1.51
57 A genome-wide association study of early menopause and the combined impact of identified variants. Hum Mol Genet 2013 1.50
58 Lifestyle interaction with fat mass and obesity-associated (FTO) genotype and risk of obesity in apparently healthy U.S. women. Diabetes Care 2011 1.44
59 Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake. Am J Clin Nutr 2013 1.35
60 Kinesin-like protein 6 (KIF6) polymorphism and the efficacy of rosuvastatin in primary prevention. Circ Cardiovasc Genet 2011 1.32
61 Loci influencing blood pressure identified using a cardiovascular gene-centric array. Hum Mol Genet 2013 1.27
62 Novel locus including FGF21 is associated with dietary macronutrient intake. Hum Mol Genet 2013 1.27
63 A large-scale candidate gene association study of age at menarche and age at natural menopause. Hum Genet 2010 1.22
64 Common variants in cardiac ion channel genes are associated with sudden cardiac death. Circ Arrhythm Electrophysiol 2010 1.22
65 GOSR2 Lys67Arg is associated with hypertension in whites. Am J Hypertens 2008 1.20
66 Genome-wide association study of relative telomere length. PLoS One 2011 1.16
67 Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation. Circulation 2014 1.11
68 Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci. PLoS Genet 2011 1.10
69 Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels. Arterioscler Thromb Vasc Biol 2010 1.10
70 Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease. Am J Clin Nutr 2013 1.08
71 Genome-wide linkage and association analyses implicate FASN in predisposition to Uterine Leiomyomata. Am J Hum Genet 2012 1.08
72 Functional classification of proteins and protein variants. Proc Natl Acad Sci U S A 2004 1.07
73 Large-scale candidate gene analysis of HDL particle features. PLoS One 2011 1.04
74 The fat-mass and obesity-associated (FTO) gene, physical activity, and risk of incident cardiovascular events in white women. Am Heart J 2010 1.03
75 Lack of association between SLCO1B1 polymorphisms and clinical myalgia following rosuvastatin therapy. Am Heart J 2013 0.95
76 Purinergic receptor P2Y, G-protein coupled, 12 gene variants and risk of incident ischemic stroke, myocardial infarction, and venous thromboembolism. Atherosclerosis 2007 0.93
77 Association of adiposity genetic variants with menarche timing in 92,105 women of European descent. Am J Epidemiol 2013 0.93
78 Physical activity modifies the effect of LPL, LIPC, and CETP polymorphisms on HDL-C levels and the risk of myocardial infarction in women of European ancestry. Circ Cardiovasc Genet 2011 0.91
79 Genetic variants of 11 telomere-pathway gene loci and the risk of incident type 2 diabetes mellitus: the Women's Genome Health Study. Atherosclerosis 2011 0.89
80 Genetic variants in eleven telomere-associated genes and the risk of incident cardio/cerebrovascular disease: The Women's Genome Health Study. Clin Chim Acta 2010 0.89
81 Pharmacogenetic determinants of statin-induced reductions in C-reactive protein. Circ Cardiovasc Genet 2012 0.88
82 Mitochondrial uncoupling protein gene cluster variation (UCP2-UCP3) and the risk of incident type 2 diabetes mellitus: the Women's Genome Health Study. Atherosclerosis 2010 0.88
83 DNA mismatch repair gene MSH6 implicated in determining age at natural menopause. Hum Mol Genet 2013 0.88
84 Reproductive aging-associated common genetic variants and the risk of breast cancer. Breast Cancer Res 2012 0.87
85 Cardiovascular risks associated with incident and prevalent periodontal disease. J Clin Periodontol 2015 0.86
86 Prospective evaluation of B-type natriuretic peptide concentrations and the risk of type 2 diabetes in women. Clin Chem 2013 0.84
87 Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy. Circ Cardiovasc Genet 2012 0.83
88 Genetics, ancestry, and hypertension: implications for targeted antihypertensive therapies. Curr Hypertens Rep 2014 0.83
89 Currently available versions of genome-wide association studies cannot be used to query the common haptoglobin copy number variant. J Am Coll Cardiol 2013 0.82
90 Common variants in Mendelian kidney disease genes and their association with renal function. J Am Soc Nephrol 2013 0.82
91 Tumour necrosis factor gene polymorphisms and migraine: a systematic review and meta-analysis. Cephalalgia 2011 0.81
92 An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12. PLoS One 2012 0.81
93 Genetic determinants of cardiovascular events among women with migraine: a genome-wide association study. PLoS One 2011 0.79
94 Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nat Genet 2016 0.77
95 Physical activity, genes for physical fitness, and risk of coronary heart disease. Med Sci Sports Exerc 2013 0.77
96 Islet amyloid polypeptide gene variation (IAPP) and the risk of incident type 2 diabetes mellitus: the Women's Genome Health Study. Clin Chim Acta 2011 0.76
97 Genetic variation of fifteen folate metabolic pathway associated gene loci and the risk of incident head and neck carcinoma: the Women's Genome Health Study. Clin Chim Acta 2012 0.76
98 Lack of association between genetic variation in 9 innate immunity genes and baseline CRP levels. Ann Hum Genet 2006 0.76
99 Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. PLoS Genet 2016 0.75
100 Age at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sample. Menopause 2016 0.75
101 Correction: Selectivity in Genetic Association with Sub-classified Migraine in Women. PLoS Genet 2015 0.75
102 Getting closer to p-selectin. Clin Chem 2009 0.75
103 Genetics for monitoring prescription practices of commonly used drugs in populations. Clin Chem 2011 0.75
104 Coronary heart disease risk, aspirin use, and apolipoprotein(a) 4399Met allele in the Atherosclerosis Risk in Communities (ARIC) study. Thromb Haemost 2009 0.75
105 New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals. Circ Cardiovasc Genet 2017 0.75
106 Corrigendum: Rare coding variants and X-linked loci associated with age at menarche. Nat Commun 2015 0.75
107 Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Sci Rep 2017 0.75
108 Tryptophanyl-tRNA synthetase gene polymorphisms and risk of incident myocardial infarction. Atherosclerosis 2005 0.75
109 Corrigendum: Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. Nat Genet 2017 0.75
110 Fish intake, genetic predisposition to alzheimer's disease and decline in global cognition and memory in five cohorts of older persons. Am J Epidemiol 2017 0.75
111 Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat Genet 2017 0.75
112 Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. PLoS Genet 2017 0.75