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Author Details

Erin N Smith
Department of Pediatrics and Rady's Children's Hospital, University of California
2002
77
36
PMIDPaper TitleJournal TitlePublished Year
35274923Genome-wide CRISPR Screening to Identify Drivers of TGF-β-Induced Liver Fibrosis in Human Hepatic Stellate Cells.ACS Chem Biol2022
34115965Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.Am J Hum Genet2021
31582554Fibrinogen gamma gene <i>rs2066865</i> and risk of cancer-related venous thromboembolism.Haematologica2020
33311970Friend Support and the Parenting of Latina Adolescent Mothers: The Moderating Role of Maternal Age.J Child Fam Stud2020
32522985Discovery and quality analysis of a comprehensive set of structural variants and short tandem repeats.Nat Commun2020
30659681A large-scale exome array analysis of venous thromboembolism.Genet Epidemiol2019
31668852Association of Human iPSC Gene Signatures and X Chromosome Dosage with Two Distinct Cardiac Differentiation Trajectories.Stem Cell Reports2019
31570892Allele-specific NKX2-5 binding underlies multiple genetic associations with human electrocardiographic traits.Nat Genet2019
31420334Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.Blood2019
31629874Dyadic synchrony among young Latina mothers and their toddlers: The role of maternal and child behavior.Infant Behav Dev2019
30923040Activation of hedgehog signaling associates with early disease progression in chronic lymphocytic leukemia.Blood2019
30773804Effect of prothrombotic genotypes on the risk of venous thromboembolism in patients with and without ischemic stroke. The Tromsø Study.J Thromb Haemost2019
31080113Human iPSC-Derived Retinal Pigment Epithelium: A Model System for Prioritizing and Functionally Characterizing Causal Variants at AMD Risk Loci.Stem Cell Reports2019
30503783Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder.Eur Neuropsychopharmacol2019
29094466Joint effects of prothrombotic genotypes and body height on the risk of venous thromboembolism: the Tromsø study.J Thromb Haemost2018
29964323Discovery of novel plasma biomarkers for future incident venous thromboembolism by untargeted synchronous precursor selection mass spectrometry proteomics.J Thromb Haemost2018
30044985Insights into the Mutational Burden of Human Induced Pluripotent Stem Cells from an Integrative Multi-Omics Approach.Cell Rep2018
30415424Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics.Int J Bipolar Disord2018
30388399Genome Analyses of &gt;200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.Am J Hum Genet2018
30562114Identification of Common and Rare Genetic Variation Associated With Plasma Protein Levels Using Whole-Exome Sequencing and Mass Spectrometry.Circ Genom Precis Med2018
29779052Correction to: Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study.Hum Genet2018
27454887The influence of cultural orientation on associations between Puerto Rican adolescent mothers' parenting and toddler compliance and defiance.Cultur Divers Ethnic Minor Psychol2017
28388874Pgltools: a genomic arithmetic tool suite for manipulation of Hi-C peak and other chromatin interaction data.BMC Bioinformatics2017
28388430Large-Scale Profiling Reveals the Influence of Genetic Variation on Gene Expression in Human Induced Pluripotent Stem Cells.Cell Stem Cell2017
28388429Aberrant DNA Methylation in Human iPSCs Associates with MYC-Binding Motifs in a Clone-Specific Manner Independent of Genetics.Cell Stem Cell2017
28410642iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types.Stem Cell Reports2017
28210534Psychological Adjustment among Young Puerto Rican Mothers: Perceived Partner Support and the Moderating Role of Latino Cultural Orientation.J Lat Psychol2017
28528403Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study.Hum Genet2017
27577874Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans.Hum Mol Genet2016
27479824Joint effects of cancer and variants in the factor 5 gene on the risk of venous thromboembolism.Haematologica2016
27329760Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.Hum Mol Genet2016
27329291Associations Between Common and Rare Exonic Genetic Variants and Serum Levels of 20 Cardiovascular-Related Proteins: The Tromsø Study.Circ Cardiovasc Genet2016
25356967Consanguinity and rare mutations outside of MCCC genes underlie nonspecific phenotypes of MCCD.Genet Med2015
26454205Developmental outcomes of toddlers of young Latina mothers: Cultural, family, and parenting factors.Infant Behav Dev2015
25860294Genetic and epigenetic profiling of CLL disease progression reveals limited somatic evolution and suggests a relationship to memory-cell development.Blood Cancer J2015
23999524Evidence for the role of EPHX2 gene variants in anorexia nervosa.Mol Psychiatry2014
25103687Biased estimates of clonal evolution and subclonal heterogeneity can arise from PCR duplicates in deep sequencing experiments.Genome Biol2014
24787006miR-150 influences B-cell receptor signaling in chronic lymphocytic leukemia by regulating expression of GAB1 and FOXP1.Blood2014
24884706Effective filtering strategies to improve data quality from population-based whole exome sequencing studies.BMC Bioinformatics2014
24560520Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci.Am J Hum Genet2014
24345515Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations.Hum Mol Genet2014
24357391DNA mismatch repair gene MSH6 implicated in determining age at natural menopause.Hum Mol Genet2014
24490717Genetic ancestry of participants in the National Children's Study.Genome Biol2014
22212596Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants.Mol Psychiatry2013
24339474Maternal Depressive Symptoms and Child Behavior Problems among Latina Adolescent Mothers: The Buffering Effect of Mother-reported Partner Child Care Involvement.Merrill Palmer Q (Wayne State Univ Press)2013
24023918Whole transcriptome sequencing enables discovery and analysis of viruses in archived primary central nervous system lymphomas.PLoS One2013
23933821Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.Nat Genet2013
23599027Genome-wide association study of age at menarche in African-American women.Hum Mol Genet2013
23441165High-resolution mutational profiling suggests the genetic validity of glioblastoma patient-derived pre-clinical models.PLoS One2013
23183192Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: a genome-wide association study of 13,372 participants.Heart Rhythm2013
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Collaborators

Kelly A Frazer
University of California, USA Institute for Genomic Medicine
Co-authored papers 28
Nicholas J Schork
University of California San Diego
Co-authored papers 27
Sarah S Murray
University of California San Diego Health System
Co-authored papers 20
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Co-authored papers 18
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Chunyu Liu
Boston University School of Public Health
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William Coryell
University of Iowa
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Melvin G McInnis
University of Michigan ann arbor
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William A Scheftner
Rush Medical College
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William B Lawson
Howard University
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William Byerley
University of California san francisco
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James B Potash
University Hospital Frankfurt
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Pamela B Mahon
Brigham & Women's Hospital, Harvard Medical School
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Bruce M Psaty
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Howard J Edenberg
Indiana University School of Medicine
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Maria Hipolito
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Release 1.2