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Author Details

Bahram Namjou
Cincinnati Children's Hospital
2001
73
30
PMIDPaper TitleJournal TitlePublished Year
36540998Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index.Pac Symp Biocomput2023
37689782Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms.Nat Commun2023
37181728A metadata framework for computational phenotypes.JAMIA Open2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
36746961Author Correction: Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits.Nat Commun2023
34930020Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.Circulation2022
35765100Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations.Genome Med2022
35595084Multiancestral polygenic risk score for pediatric asthma.J Allergy Clin Immunol2022
35594287Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities.PLoS One2022
35388006Lupus enhancer risk variant causes dysregulation of IRF8 through cooperative lncRNA and DNA methylation machinery.Nat Commun2022
36372681Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.Obesity (Silver Spring)2022
36160011Haplotype-specific chromatin looping reveals genetic interactions of regulatory regions modulating gene expression in 8p23.1.Front Genet2022
35915156Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.Nat Med2022
35943490Pathogenic variants in arteriopathy genes detected in a targeted sequencing study: Penetrance and 1-year outcomes after return of results.Genet Med2022
32952152Evaluation of the MC4R gene across eMERGE network identifies many unreported obesity-associated variants.Int J Obes (Lond)2021
33669337Patients with Proliferative Lupus Nephritis Have Autoantibodies That React to Moesin and Demonstrate Increased Glomerular Moesin Expression.J Clin Med2021
33667396Response to Li and Hopper.Am J Hum Genet2021
33729212Genome-wide association studies of low back pain and lumbar spinal disorders using electronic health record data identify a locus associated with lumbar spinal stenosis.Pain2021
34467602Validation of low-coverage whole-genome sequencing for mitochondrial DNA variants suggests mitochondrial DNA as a genetic cause of preterm birth.Hum Mutat2021
33941608Medical Records-Based Genetic Studies of the Complement System.J Am Soc Nephrol2021
34097045A Mendelian Randomization Approach Using 3-HMG-Coenzyme-A Reductase Gene Variation to Evaluate the Association of Statin-Induced Low-Density Lipoprotein Cholesterol Lowering With Noncardiovascular Disease Phenotypes.JAMA Netw Open2021
34282949Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry.Circ Genom Precis Med2021
32307929Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome-Wide Association Study and Inverse Variance-Weighted Meta-Analysis.Arthritis Rheumatol2020
32758450Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk.Am J Hum Genet2020
30298529The eMERGE genotype set of 83,717 subjects imputed to ~40â¿¿million variants genome wide and association with the herpes zoster medical record phenotype.Genet Epidemiol2019
31311600GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.BMC Med2019
30774981A phenome-wide association study to discover pleiotropic effects of <i>PCSK9</i>, <i>APOB</i>, and <i>LDLR</i>.NPJ Genom Med2019
29301385Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience.J Pers Med2018
29912393A plausibly causal functional lupus-associated risk variant in the STAT1-STAT4 locus.Hum Mol Genet2018
30166544A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers.Nat Commun2018
27611488Identification of Four Novel Loci in Asthma in European American and African American Populations.Am J Respir Crit Care Med2017
27472449Electronic Health Record Based Algorithm to Identify Patients with Autism Spectrum Disorder.PLoS One2016
27698673Suboptimal Clinical Documentation in Young Children with Severe Obesity at Tertiary Care Centers.Int J Pediatr2016
27452794Developing an Algorithm to Detect Early Childhood Obesity in Two Tertiary Pediatric Medical Centers.Appl Clin Inform2016
25205108The IRF5-TNPO3 association with systemic lupus erythematosus has two components that other autoimmune disorders variably share.Hum Mol Genet2015
26413716A GWAS Study on Liver Function Test Using eMERGE Network Participants.PLoS One2015
25865496Lupus Risk Variant Increases pSTAT1 Binding and Decreases ETS1 Expression.Am J Hum Genet2015
25620976Lupus risk variants in the PXK locus alter B-cell receptor internalization.Front Genet2015
25824007Autoantibodies targeting glomerular annexin A2 identify patients with proliferative lupus nephritis.Proteomics Clin Appl2015
25566314Imputation and quality control steps for combining multiple genome-wide datasets.Front Genet2014
25477900Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis.Front Genet2014
25545785The effect of inversion at 8p23 on BLK association with lupus in Caucasian population.PLoS One2014
23950893PTPN22 association in systemic lupus erythematosus (SLE) with respect to individual ancestry and clinical sub-phenotypes.PLoS One2013
24348519EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children.Front Genet2013
22231568Evaluation of TRAF6 in a large multiancestral lupus cohort.Arthritis Rheum2012
22472776Identification of novel coding mutation in C1qA gene in an African-American pedigree with lupus and C1q deficiency.Lupus2012
20864496The lupus family registry and repository.Rheumatology (Oxford)2011
21339217The genetics of systemic lupus erythematosus and implications for targeted therapy.Ann Rheum Dis2011
21270825Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort.Genes Immun2011
19919944Interferon-gamma gene polymorphisms associated with susceptibility to systemic lupus erythematosus.Ann Rheum Dis2010
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Collaborators

John B Harley
US Department of Veterans Affairs Medical Center
Co-authored papers 50
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 24
Iftikhar J Kullo
Mayo Clinic
Co-authored papers 17
Joshua C Denny
Vanderbilt University
Co-authored papers 15
Wei-Qi Wei
Vanderbilt University Medical Center
Co-authored papers 15
David R Crosslin
University of Washington Medical Center
Co-authored papers 15
Leah C Kottyan
Cincinnati Children's Hospital Medical Center
Co-authored papers 15
Hakon Hakonarson
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Co-authored papers 14
Patrick M Gaffney
Co-authored papers 12
Kathy L Moser
Co-authored papers 12
Carl D Langefeld
Wake Forest University School of Medicine
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Beth L Cobb
Cincinnati Children's Hospital Medical Center
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Ian B Stanaway
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Joel M Guthridge
Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation
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Michelle Petri
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Marylyn D Ritchie
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Frank D Mentch
Center for Applied Genomics (CAG), Children's Hospital of Philadelphia
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Eric B Larson
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Todd Lingren
Cincinnati Children's Hospital Medical Center
Co-authored papers 9
Timothy J Vyse
Co-authored papers 9
Lindsey A Criswell
Co-authored papers 8
Marc S Williams
University of Washington Medical Center
Co-authored papers 8
Ingrid A Holm
Harvard Medical School
Co-authored papers 8
John J Connolly
Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 8
Krzysztof Kiryluk
Columbia University
Co-authored papers 8
Elisabeth A Rosenthal
University of Washington Medical Center
Co-authored papers 8
John D Reveille
University of Texas
Co-authored papers 8
Barry I Freedman
Co-authored papers 7
Daniel J Schaid
Mayo Clinic
Co-authored papers 7
Adam S Gordon
Northwestern University Feinberg School of Medicine.
Co-authored papers 7
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