PubRank

Elizabeth W Pugh

Author PubWeight™ 121.74‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science 2007 43.16
2 Common variants in the GDF5-UQCC region are associated with variation in human height. Nat Genet 2008 7.31
3 A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. Am J Hum Genet 2009 5.62
4 Genomewide association study for susceptibility genes contributing to familial Parkinson disease. Hum Genet 2008 5.04
5 Quality control and quality assurance in genotypic data for genome-wide association studies. Genet Epidemiol 2010 4.83
6 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. Proc Natl Acad Sci U S A 2010 4.30
7 Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nat Genet 2012 3.68
8 A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. Nat Genet 2010 3.63
9 The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions. Genet Epidemiol 2010 3.48
10 Description of the data from the Collaborative Study on the Genetics of Alcoholism (COGA) and single-nucleotide polymorphism genotyping for Genetic Analysis Workshop 14. BMC Genet 2005 3.04
11 Results of a high-resolution genome screen of 437 Alzheimer's disease families. Hum Mol Genet 2003 3.00
12 Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion. Nat Genet 2012 2.55
13 A genome-wide association study on African-ancestry populations for asthma. J Allergy Clin Immunol 2009 2.53
14 Quality control procedures for genome-wide association studies. Curr Protoc Hum Genet 2011 2.48
15 A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14. Diabetes 2004 2.46
16 Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. Hum Mol Genet 2011 2.26
17 Comprehensive association study of type 2 diabetes and related quantitative traits with 222 candidate genes. Diabetes 2008 2.01
18 Screening of 134 single nucleotide polymorphisms (SNPs) previously associated with type 2 diabetes replicates association with 12 SNPs in nine genes. Diabetes 2007 1.74
19 Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap database. Genet Epidemiol 2006 1.74
20 Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate. Genet Epidemiol 2011 1.47
21 Association between the tumor necrosis factor locus and the clinical outcome of Leishmania chagasi infection. Infect Immun 2002 1.46
22 The development of a highly informative mouse Simple Sequence Length Polymorphism (SSLP) marker set and construction of a mouse family tree using parsimony analysis. Genome Res 2003 1.44
23 Comparison of year-of-exam- and age-matched estimates of heritability in the Framingham Heart Study data. BMC Genet 2003 1.38
24 A graphical assessment of p-values from sliding window haplotype tests of association to identify asthma susceptibility loci on chromosome 11q. BMC Genet 2006 1.33
25 An emerging peri-urban pattern of infection with Leishmania chagasi, the protozoan causing visceral leishmaniasis in northeast Brazil. Scand J Infect Dis 2004 1.27
26 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
27 An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21. Am J Hum Genet 2002 1.20
28 A genome-wide scan for loci predisposing to non-syndromic cleft lip with or without cleft palate in two large Syrian families. Am J Med Genet A 2003 1.10
29 Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2. Eur J Hum Genet 2003 1.10
30 Comparison of single-nucleotide polymorphisms and microsatellite markers for linkage analysis in the COGA and simulated data sets for Genetic Analysis Workshop 14: Presentation Groups 1, 2, and 3. Genet Epidemiol 2005 1.07
31 Imputation-based genomic coverage assessments of current human genotyping arrays. G3 (Bethesda) 2013 1.06
32 Genome-wide association scan of dental caries in the permanent dentition. BMC Oral Health 2012 1.06
33 Linkage analysis of genetic loci for kyphoscoliosis on chromosomes 5p13, 13q13.3, and 13q32. Am J Med Genet A 2006 0.93
34 Genome-wide association analysis of ischemic stroke in young adults. G3 (Bethesda) 2011 0.92
35 Investigation of altering single-nucleotide polymorphism density on the power to detect trait loci and frequency of false positive in nonparametric linkage analyses of qualitative traits. BMC Genet 2005 0.85
36 Application of sex-specific single-nucleotide polymorphism filters in genome-wide association data. BMC Proc 2009 0.79
37 Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white women. J Bone Miner Res 2008 0.78
38 A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma. Am J Hum Genet 2011 0.75