PubRank

Mark Leppert

Author PubWeight™ 39.86‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Positional cloning of the human quantitative trait locus underlying taste sensitivity to phenylthiocarbamide. Science 2003 4.48
2 Future research directions in acute lung injury: summary of a National Heart, Lung, and Blood Institute working group. Am J Respir Crit Care Med 2003 3.75
3 Identification of a herpes simplex labialis susceptibility region on human chromosome 21. J Infect Dis 2008 2.24
4 Community engagement and informed consent in the International HapMap project. Community Genet 2007 1.73
5 Familial aggregation of abnormal methylation of parental alleles at the IGF2/H19 and IGF2R differentially methylated regions. Hum Mol Genet 2003 1.68
6 Neuropathy target esterase gene mutations cause motor neuron disease. Am J Hum Genet 2008 1.66
7 Interindividual variability and parent of origin DNA methylation differences at specific human Alu elements. Hum Mol Genet 2005 1.65
8 Quantitative-trait loci influencing body-mass index reside on chromosomes 7 and 13: the National Heart, Lung, and Blood Institute Family Heart Study. Am J Hum Genet 2001 1.59
9 Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p. Hum Genet 2003 1.50
10 Ethnicity and human genetic linkage maps. Am J Hum Genet 2004 1.50
11 A frameshift polymorphism in P2X5 elicits an allogeneic cytotoxic T lymphocyte response associated with remission of chronic myeloid leukemia. J Clin Invest 2005 1.33
12 Fine Mapping and Identification of BMI Loci in African Americans. Am J Hum Genet 2013 1.27
13 Linkage analysis of a composite factor for the multiple metabolic syndrome: the National Heart, Lung, and Blood Institute Family Heart Study. Diabetes 2003 1.24
14 A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study. PLoS Genet 2013 1.21
15 C21orf91 genotypes correlate with herpes simplex labialis (cold sore) frequency: description of a cold sore susceptibility gene. J Infect Dis 2011 1.21
16 SNP haplotypes and allele frequencies show evidence for disruptive and balancing selection in the human leukocyte receptor complex. Immunogenetics 2004 1.15
17 Human imprinted chromosomal regions are historical hot-spots of recombination. PLoS Genet 2006 1.12
18 Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Arch Gen Psychiatry 2012 1.08
19 A longitudinal study of X-inactivation ratio in human females. Hum Genet 2004 1.05
20 Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population. PLoS One 2013 1.03
21 Association of adipose and red blood cell lipids with severity of dominant Stargardt macular dystrophy (STGD3) secondary to an ELOVL4 mutation. Arch Ophthalmol 2006 0.96
22 The Arg16Gly polymorphism of the beta2-adrenergic receptor and left ventricular systolic function. Am J Hypertens 2003 0.94
23 From linkage maps to quantitative trait loci: the history and science of the Utah genetic reference project. Annu Rev Genomics Hum Genet 2008 0.90
24 Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genet Epidemiol 2013 0.87
25 Setting priorities for genomic research. Science 2004 0.86
26 Genotype-phenotype analysis of ABCR variants in macular degeneration probands and siblings. Invest Ophthalmol Vis Sci 2002 0.82
27 Genome-wide linkage analysis replicates susceptibility locus for fasting plasma triglycerides: NHLBI Family Heart Study. Hum Genet 2004 0.82
28 Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations. Acta Diabetol 2009 0.76