PubRank

Paul Scheet

Author PubWeight™ 225.92‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Genet Epidemiol 2010 26.41
2 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat Genet 2008 22.35
3 Common variants at 30 loci contribute to polygenic dyslipidemia. Nat Genet 2008 20.66
4 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet 2010 17.89
5 Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nat Genet 2008 15.94
6 Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation. Am J Hum Genet 2005 14.09
7 Genome-wide association study identifies eight loci associated with blood pressure. Nat Genet 2009 12.44
8 Genotype, haplotype and copy-number variation in worldwide human populations. Nature 2008 12.40
9 Variants in MTNR1B influence fasting glucose levels. Nat Genet 2008 10.85
10 Automating sequence-based detection and genotyping of SNPs from diploid samples. Nat Genet 2006 9.04
11 Meta-analysis and imputation refines the association of 15q25 with smoking quantity. Nat Genet 2010 8.55
12 Genotype-imputation accuracy across worldwide human populations. Am J Hum Genet 2009 7.28
13 Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. PLoS Genet 2009 5.81
14 Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia. Nat Genet 2011 4.93
15 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. Circulation 2011 3.68
16 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
17 Rare versus common variants in pharmacogenetics: SLCO1B1 variation and methotrexate disposition. Genome Res 2011 2.52
18 Strengthening the reporting of genetic association studies (STREGA): an extension of the strengthening the reporting of observational studies in epidemiology (STROBE) statement. J Clin Epidemiol 2009 2.45
19 STrengthening the REporting of Genetic Association Studies (STREGA): an extension of the STROBE statement. PLoS Med 2009 2.39
20 A comparison of approaches to account for uncertainty in analysis of imputed genotypes. Genet Epidemiol 2011 2.19
21 Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia. Blood 2012 1.90
22 Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations. Am J Hum Genet 2009 1.87
23 STrengthening the REporting of Genetic Association studies (STREGA)--an extension of the STROBE statement. Eur J Clin Invest 2009 1.82
24 Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. J Natl Cancer Inst 2013 1.81
25 Integrated annotation and analysis of genetic variants from next-generation sequencing studies with variant tools. Bioinformatics 2011 1.73
26 A genome-wide association search for type 2 diabetes genes in African Americans. PLoS One 2012 1.72
27 Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE Statement. Hum Genet 2009 1.47
28 Population structure, migration, and diversifying selection in the Netherlands. Eur J Hum Genet 2013 1.47
29 ARID5B genetic polymorphisms contribute to racial disparities in the incidence and treatment outcome of childhood acute lymphoblastic leukemia. J Clin Oncol 2012 1.39
30 The Young Netherlands Twin Register (YNTR): longitudinal twin and family studies in over 70,000 children. Twin Res Hum Genet 2012 1.36
31 Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE statement. Eur J Epidemiol 2009 1.25
32 Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course. Hum Mol Genet 2013 1.23
33 A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation. PLoS Genet 2012 1.23
34 Nicotinic acetylcholine receptor region on chromosome 15q25 and lung cancer risk among African Americans: a case-control study. J Natl Cancer Inst 2010 1.19
35 STrengthening the REporting of Genetic Association Studies (STREGA)--an extension of the STROBE statement. Genet Epidemiol 2009 1.13
36 STrengthening the REporting of Genetic Association studies (STREGA): an extension of the STROBE Statement. Ann Intern Med 2009 1.11
37 Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Arch Gen Psychiatry 2012 1.08
38 Haplotype-based profiling of subtle allelic imbalance with SNP arrays. Genome Res 2012 1.03
39 The molecular genetic architecture of self-employment. PLoS One 2013 0.96
40 De novo and inherited CNVs in MZ twin pairs selected for discordance and concordance on Attention Problems. Eur J Hum Genet 2012 0.94
41 Somatic mutation load of estrogen receptor-positive breast tumors predicts overall survival: an analysis of genome sequence data. Breast Cancer Res Treat 2014 0.85
42 Association between autozygosity and major depression: stratification due to religious assortment. Behav Genet 2013 0.83
43 Haploscope: a tool for the graphical display of haplotype structure in populations. Genet Epidemiol 2011 0.79