PubRank

G Mark Lathrop

Author PubWeight™ 227.62‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Nat Genet 2008 25.83
2 A genome-wide association study of global gene expression. Nat Genet 2007 22.98
3 Common variants at 30 loci contribute to polygenic dyslipidemia. Nat Genet 2008 20.66
4 Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 2010 20.01
5 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet 2010 17.89
6 Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. Nature 2007 14.43
7 Genome-wide association study identifies eight loci associated with blood pressure. Nat Genet 2009 12.44
8 Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature 2010 12.27
9 Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. Nat Genet 2009 9.45
10 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
11 Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. Am J Hum Genet 2008 7.33
12 Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. PLoS Genet 2009 5.81
13 A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Nat Genet 2012 4.37
14 Genome-wide association study identifies three loci associated with melanoma risk. Nat Genet 2009 3.89
15 Seven new loci associated with age-related macular degeneration. Nat Genet 2013 3.81
16 Genome-wide mapping of human loci for essential hypertension. Lancet 2003 3.53
17 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
18 SNP and haplotype mapping for genetic analysis in the rat. Nat Genet 2008 2.96
19 SLC2A9 is a high-capacity urate transporter in humans. PLoS Med 2008 2.87
20 A variant in the CD209 promoter is associated with severity of dengue disease. Nat Genet 2005 2.31
21 Genome-wide association study identifies three new melanoma susceptibility loci. Nat Genet 2011 2.29
22 Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study. Hum Mol Genet 2005 2.27
23 Genetic and haplotypic structure in 14 European and African cattle breeds. Genetics 2007 2.18
24 Positional cloning of a novel gene influencing asthma from chromosome 2q14. Nat Genet 2003 2.16
25 A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines. Genome Res 2013 1.72
26 A genome-wide association search for type 2 diabetes genes in African Americans. PLoS One 2012 1.72
27 Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity. Diabetes 2004 1.50
28 Angiotensin-1-converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides. Hum Mol Genet 2002 1.24
29 Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16. Nat Genet 2013 1.23
30 A variant in FTO shows association with melanoma risk not due to BMI. Nat Genet 2013 1.17
31 Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension. Hum Mol Genet 2006 1.06
32 Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot. Hum Mol Genet 2013 1.04
33 High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activity. Eur J Hum Genet 2002 1.04
34 Infantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11. PLoS One 2010 1.04
35 Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome. Hum Mol Genet 2004 1.02
36 Integrating pathway analysis and genetics of gene expression for genome-wide association study of basal cell carcinoma. Hum Genet 2011 0.99
37 Duplicating SNPs. Nat Genet 2004 0.97
38 A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis. Hum Mol Genet 2013 0.95
39 Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion. PLoS One 2009 0.92
40 Coordinated conditional simulation with SLINK and SUP of many markers linked or associated to a trait in large pedigrees. Hum Hered 2011 0.85
41 Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions. Int J Cancer 2014 0.84
42 Large-scale genotyping by mass spectrometry: experience, advances and obstacles. Curr Opin Chem Biol 2002 0.82
43 Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls. Circ Cardiovasc Genet 2013 0.82
44 Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension. Am J Hum Genet 2006 0.81
45 Quantitative variation in plasma angiotensin-I converting enzyme activity shows allelic heterogeneity in the ABO blood group locus. Ann Hum Genet 2013 0.76