PubRank

Eric K Moses

Author PubWeight™ 61.05‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes. Nat Genet 2007 11.09
2 Identification of common variants associated with human hippocampal and intracranial volumes. Nat Genet 2012 3.73
3 High dimensional endophenotype ranking in the search for major depression risk genes. Biol Psychiatry 2011 2.23
4 Genetic variation at the FTO locus influences RBL2 gene expression. Diabetes 2009 1.91
5 The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging Behav 2014 1.90
6 Inherited thrombophilia polymorphisms and pregnancy outcomes in nulliparous women. Obstet Gynecol 2010 1.90
7 Transcriptomic epidemiology of smoking: the effect of smoking on gene expression in lymphocytes. BMC Med Genomics 2010 1.22
8 The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations. Hum Genet 2009 1.20
9 Chemerin, a novel adipokine in the regulation of angiogenesis. J Clin Endocrinol Metab 2010 1.20
10 A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1). PLoS Genet 2013 1.15
11 A transcriptional profile of the decidua in preeclampsia. Am J Obstet Gynecol 2011 1.14
12 Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study). Eur J Hum Genet 2008 1.08
13 Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene. PLoS One 2012 1.05
14 A chromosome 11q quantitative-trait locus influences change of blood-pressure measurements over time in Mexican Americans of the San Antonio Family Heart Study. Am J Hum Genet 2007 1.04
15 Diverse biological activities of the vascular non-inflammatory molecules - the Vanin pantetheinases. Biochem Biophys Res Commun 2011 1.00
16 Bivariate genetic association of KIAA1797 with heart rate in American Indians: the Strong Heart Family Study. Hum Mol Genet 2010 1.00
17 Endogenous factor VIII synthesis from the intron 22-inverted F8 locus may modulate the immunogenicity of replacement therapy for hemophilia A. Nat Med 2013 0.99
18 Genetic determinants of mitochondrial content. Hum Mol Genet 2007 0.99
19 5 Beta-dihydroprogesterone and steroid 5 beta-reductase decrease in association with human parturition at term. Mol Hum Reprod 2005 0.94
20 Identification of ACOX2 as a shared genetic risk factor for preeclampsia and cardiovascular disease. Eur J Hum Genet 2011 0.93
21 Genotype x adiposity interaction linkage analyses reveal a locus on chromosome 1 for lipoprotein-associated phospholipase A2, a marker of inflammation and oxidative stress. Am J Hum Genet 2006 0.93
22 Genome-wide association study of autistic-like traits in a general population study of young adults. Front Hum Neurosci 2013 0.89
23 Variants in CPT1A, FADS1, and FADS2 are Associated with Higher Levels of Estimated Plasma and Erythrocyte Delta-5 Desaturases in Alaskan Eskimos. Front Genet 2012 0.89
24 An emerging role for comprehensive proteome analysis in human pregnancy research. Reproduction 2005 0.89
25 A critical assessment of the factors affecting reporter gene assays for promoter SNP function: a reassessment of -308 TNF polymorphism function using a novel integrated reporter system. Eur J Hum Genet 2009 0.88
26 Genotype×age interaction in human transcriptional ageing. Mech Ageing Dev 2012 0.88
27 Meta-analysis of human methylation data for evidence of sex-specific autosomal patterns. BMC Genomics 2014 0.87
28 Genetic architecture of carotid artery intima-media thickness in Mexican Americans. Circ Cardiovasc Genet 2013 0.85
29 Genetic dissection of the pre-eclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease. Mol Hum Reprod 2013 0.84
30 Molecular markers of preterm labor in the choriodecidua. Reprod Sci 2009 0.84
31 Genetic variation in PARL influences mitochondrial content. Hum Genet 2009 0.83
32 Novel associations of nonstructural Loci with paraoxonase activity. J Lipids 2012 0.83
33 Proteomic approaches in endometriosis research. Proteomics 2004 0.83
34 Partial correlation network analyses to detect altered gene interactions in human disease: using preeclampsia as a model. Hum Genet 2010 0.82
35 The prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian antenatal population. Aust N Z J Obstet Gynaecol 2008 0.82
36 ADAM28 is elevated in humans with the metabolic syndrome and is a novel sheddase of human tumour necrosis factor-α. Immunol Cell Biol 2012 0.82
37 The 57 kb deletion in cystinosis patients extends into TRPV1 causing dysregulation of transcription in peripheral blood mononuclear cells. J Med Genet 2011 0.82
38 Genetic and molecular functional characterization of variants within TNFSF13B, a positional candidate preeclampsia susceptibility gene on 13q. PLoS One 2010 0.81
39 Plasma levels of soluble interleukin 1 receptor accessory protein are reduced in obesity. J Clin Endocrinol Metab 2014 0.79
40 Inherited thrombophilias and adverse pregnancy outcomes: a case-control study in an Australian population. Acta Obstet Gynecol Scand 2011 0.78
41 Recombinant human zona pellucida proteins ZP1, ZP2 and ZP3 co-expressed in a human cell line. Asian J Androl 2004 0.78
42 Refined phenotyping identifies links between preeclampsia and related diseases in a Norwegian preeclampsia family cohort. J Hypertens 2015 0.78
43 Genome-wide genetic and transcriptomic investigation of variation in antibody response to dietary antigens. Genet Epidemiol 2014 0.77
44 The characterization of Abelson helper integration site-1 in skeletal muscle and its links to the metabolic syndrome. Metabolism 2009 0.77
45 A genome-wide association study for malignant mesothelioma risk. Lung Cancer 2013 0.77
46 The -56T HLA-G promoter polymorphism is not associated with pre-eclampsia/eclampsia in Australian and New Zealand women. Hypertens Pregnancy 2006 0.76
47 Association of the TNF2 allele with eclampsia. Gynecol Obstet Invest 2004 0.76
48 Systems genetics of the nuclear factor-κB signal transduction network. I. Detection of several quantitative trait loci potentially relevant to aging. Mech Ageing Dev 2011 0.75
49 The antihypertensive MTHFR gene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia. J Hypertens 2017 0.75
50 OP004. A SNP associated with susceptibility to preeclampsia near the inhibin, beta B gene, is also associated with cardiovascular disease risk traits. Pregnancy Hypertens 2013 0.75
51 Thrombomodulin Ala455Val dimorphism is not associated with pre-eclampsia in Australian and New Zealand women. Gynecol Obstet Invest 2002 0.75
52 Ethnic differences in the prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian prenatal population. Hum Biol 2006 0.75
53 OP006. A preeclampsia genome-wide linkage scan in norwegian families. Pregnancy Hypertens 2013 0.75