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Author Details

Eric M Sobel
1979
79
25
PMIDPaper TitleJournal TitlePublished Year
36610401Unsupervised discovery of ancestry-informative markers and genetic admixture proportions in biobank-scale datasets.2023
36705562Genetic variants of glucose metabolism and exposure to smoking in African American breast cancer.2023
34692549Synergistic Effects of Genetic Variants of Glucose Homeostasis and Lifelong Exposures to Cigarette Smoking, Female Hormones, and Dietary Fat Intake on Primary Colorectal Cancer Development in African and Hispanic/Latino American Women.Frontiers in Oncology2021
34289008A fast data-driven method for genotype imputation, phasing and local ancestry inference: MendelImpute.jl.Bioinformatics2021
33948386Genetically determined elevated C-reactive protein associated with primary colorectal cancer risk: Mendelian randomization with lifestyle interactions.American Journal of Cancer Research (discontinued)2021
33941078Modern simulation utilities for genetic analysis.BMC Bioinformatics2021
33441805Pro-inflammatory cytokine polymorphisms and interactions with dietary alcohol and estrogen, risk factors for invasive breast cancer using a post genome-wide analysis for gene-gene and gene-lifestyle interaction.Scientific Reports2021
32928877Genome-wide Association Analysis of Proinflammatory Cytokines and Gene-lifestyle Interaction for Invasive Breast Cancer Risk: The WHI dbGaP Study.Cancer Prevention Research2021
34572592Molecular Biology Networks and Key Gene Regulators for Inflammatory Biomarkers Shared by Breast Cancer Development: Multi-Omics Systems Analysis.Biomolecules2021
30915546OPENMENDEL: a cooperative programming project for statistical genetics.Hum Genet2020
32491161Iterative hard thresholding in genome-wide association studies: Generalized linear models, prior weights, and double sparsity.Gigascience2020
33614510Genetically Predicted C-Reactive Protein Associated With Postmenopausal Breast Cancer Risk: Interrelation With Estrogen and Cancer Molecular Subtypes Using Mendelian Randomization.Frontiers in Oncology2020
33042629Pro-inflammatory cytokine polymorphisms in ONECUT2 and HNF4A and primary colorectal carcinoma: a post genome-wide gene-lifestyle interaction study.American Journal of Cancer Research (discontinued)2020
32850306Mendelian Randomization Study: The Association Between Metabolic Pathways and Colorectal Cancer Risk.Frontiers in Oncology2020
30936085Breast Cancer Risk and Insulin Resistance: Post Genome-Wide Gene-Environment Interaction Study Using a Random Survival Forest.Cancer Research2019
31554631Post Genome-Wide Gene-Environment Interaction Study Using Random Survival Forest: Insulin Resistance, Lifestyle Factors, and Colorectal Cancer Risk.Cancer Prevention Research2019
30327367Genome-Wide Meta-analysis of Gene-Environmental Interaction for Insulin Resistance Phenotypes and Breast Cancer Risk in Postmenopausal Women.Cancer Prevention Research2019
31246991Post genome-wide gene-environment interaction study: The effect of genetically driven insulin resistance on breast cancer risk using Mendelian randomization.PLoS ONE2019
29074537Genetic Variants in Metabolic Signaling Pathways and Their Interaction with Lifestyle Factors on Breast Cancer Risk: A Random Survival Forest Analysis.Cancer Prevention Research2018
27943406Fast Genome-Wide QTL Association Mapping on Pedigree and Population Data.Genetic Epidemiology2017
28446149Effect of genetic variants and traits related to glucose metabolism and their interaction with obesity on breast and colorectal cancer risk among postmenopausal women.BMC Cancer2017
28478612Interaction of insulin-like growth factor-I and insulin resistance-related genetic variants with lifestyle factors on postmenopausal breast cancer risk.Breast Cancer Res Treat2017
27980643Genome-wide QTL and eQTL analyses using Mendel.BMC Proceedings2016
27377425Obesity and associated lifestyles modify the effect of glucose metabolism-related genetic variants on impaired glucose homeostasis among postmenopausal women.Genetic Epidemiology2016
26567478The Quantitative-MFG Test: A Linear Mixed Effect Model to Detect Maternal-Offspring Gene Interactions.Ann Hum Genet2016
28214848Human Birth Weight and Reproductive Immunology: Testing for Interactions between Maternal and Offspring KIR and HLA-C Genes.Hum Hered2016
26079130Genome-wide ultraconserved elements exhibit higher phylogenetic informativeness than traditional gene markers in percomorph fishes.Mol Phylogenet Evol2015
24955378Next Generation Statistical Genetics: Modeling, Penalization, and Optimization in High-Dimensional Data.Annu Rev Stat Appl2014
25371518Shared molecular pathways and gene networks for cardiovascular disease and type 2 diabetes mellitus in women across diverse ethnicities.Circulation: Cardiovascular Genetics2014
25519348Fast genome-wide pedigree quantitative trait loci analysis using MENDEL.BMC Proceedings2014
23730305The systems genetics resource: a web application to mine global data for complex disease traits.Frontiers in Genetics2013
23386649Common genetic variants in peroxisome proliferator-activated receptor-γ (PPARG) and type 2 diabetes risk among Women's Health Initiative postmenopausal women.Journal of Clinical Endocrinology and Metabolism2013
23610370Mendel: the Swiss army knife of genetic analysis programs.Bioinformatics2013
22143921Quantitative trait Loci association mapping by imputation of strain origins in multifounder crosses.Genetics2012
22954633Mendel-GPU: haplotyping and genotype imputation on graphics processing units.Bioinformatics2012
22218271Shared loci for migraine and epilepsy on chromosomes 14q12-q23 and 12q24.2-q24.3.Neurology2012
21822022Unifying ideas for non-parametric linkage analysis.Human Heredity2011
21121038Penalized regression for genome-wide association screening of sequence data.Pac Symp Biocomput2011
21465549Linkage analysis without defined pedigrees.Genetic Epidemiology2011
22004985Detection of intergenerational genetic effects with application to HLA-B matching as a risk factor for schizophrenia.Hum Hered2011
20422020Intelligence in Williams Syndrome is related to STX1A, which encodes a component of the presynaptic SNARE complex.PLoS One2010
20357198Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC.Invest Ophthalmol Vis Sci2010
20385888A visual migraine aura locus maps to 9q21-q22.Neurology2010
19597142The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies.Proc Natl Acad Sci U S A2009
19176549Genome-wide association analysis by lasso penalized logistic regression.2009
19574904Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene interval.Cornea2009
18791243Mixed effects models for quantitative trait loci mapping with inbred strains.Genetics2008
18986552Integrated weighted gene co-expression network analysis with an application to chronic fatigue syndrome.BMC Syst Biol2008
18674750WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels.Am J Hum Genet2008
18644149Merging microsatellite data: enhanced methodology and software to combine genotype data for linkage and association analysis.BMC Bioinformatics2008
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