Author details

Full Name

Margaret A Taub

Affiliation

ORCID

Career Start Year

2006

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36384317	Damaging Mutations in <b><i>AFDN</i></b> Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate.	Cleft Palate Craniofac J	2024
37489536	Age at Menopause, Leukocyte Telomere Length, and Coronary Artery Disease in Postmenopausal Women.		2023
37679407	Evaluating genomic signatures of aging in brain tissue as it relates to Alzheimer's disease.	Sci Rep	2023
37905118	Determinants of mosaic chromosomal alteration fitness.	medRxiv	2023
37904051	Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing.	Nat Genet	2023
36690926	<i>MUC5B</i>, telomere length and longitudinal quantitative interstitial lung changes: the MESA Lung Study.	Thorax	2023
37496383	Clinically actionable secondary findings in 130 triads from sub-Saharan African families with non-syndromic orofacial clefts.	Mol Genet Genomic Med	2023
34780848	Discovering metabolite quantitative trait loci in asthma using an isolated population.	Journal of Allergy and Clinical Immunology	2022
35451532	Benchmarking statistical methods for analyzing parent-child dyads in genetic association studies.	Genet Epidemiol	2022
35385311	Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.	Sci Adv	2022
35817949	Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate.	Sci Rep	2022
35547202	Multi-Site Observational Study to Assess Biomarkers for Susceptibility or Resilience to Chronic Pain: The Acute to Chronic Pain Signatures (A2CPS) Study Protocol.	Front Med (Lausanne)	2022
35312098	Secondary analyses for genome-wide association studies using expression quantitative trait loci.	Genetic Epidemiology	2022
33119750	A Multiancestry Sex-Stratified Genome-Wide Association Study of Spontaneous Clearance of Hepatitis C Virus.	J Infect Dis	2021
34242216	Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios.	PLoS Genet	2021
33937227	Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft.	Front Cell Dev Biol	2021
33829634	Gene and protein expression in human megakaryocytes derived from induced pluripotent stem cells.	J Thromb Haemost	2021
33094331	Transcriptional profile of platelets and iPSC-derived megakaryocytes from whole-genome and RNA sequencing.	Blood	2021
33116245	Multi-ancestry fine mapping of interferon lambda and the outcome of acute hepatitis C virus infection.	Genes Immun	2020
31848685	Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21.	Hum Genet	2020
31981624	Association of HLA-DRB1â¿¿09:01 with tIgE levels among African-ancestry individuals with asthma.	J Allergy Clin Immunol	2020
32442913	Genomic integrity of human induced pluripotent stem cells across nine studies in the NHLBI NextGen program.	Stem Cell Res	2020
32574564	Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios.	Am J Hum Genet	2020
33230236	Correction: Multi-ancestry fine mapping of interferon lambda and the outcome of acute hepatitis C virus infection.	Genes Immun	2020
31443688	Replicated methylation changes associated with eczema herpeticum and allergic response.	Clin Epigenetics	2019
30455414	Assembly of a pan-genome from deep sequencing of 910 humans of African descent.	Nat Genet	2019
30593799	Multi-Ancestry Genome-Wide Association Study of Spontaneous Clearance of Hepatitis C Virus.	Gastroenterology	2019
30246882	Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants.	Genet Epidemiol	2019
29553866	Targeted deep sequencing of the PEAR1 locus for platelet aggregation in European and African American families.	Platelets	2019
28107356	Integrity of Induced Pluripotent Stem Cell (iPSC) Derived Megakaryocytes as Assessed by Genetic and Transcriptomic Analysis.	PLoS One	2017
28762674	Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing.	Birth Defects Res	2017
28944239	Analysis of sequence data to identify potential risk variants for oral clefts in multiplex families.	Mol Genet Genomic Med	2017
28398307	Reproducible RNA-seq analysis using recount2.	Nat Biotechnol	2017
28019042	Evidence for SNP-SNP interaction identified through targeted sequencing of cleft case-parent trios.	Genet Epidemiol	2017
28035032	Using genotype array data to compare multi- and single-sample variant calls and improve variant call sets from deep coverage whole-genome sequencing data.	Bioinformatics	2017
27725664	Challenges and disparities in the application of personalized genomic medicine to populations with African ancestry.	Nat Commun	2016
27074206	Association of DNA Methylation Differences With Schizophrenia in an Epigenome-Wide Association Study.	JAMA Psychiatry	2016
26473621	Identification of Rare Variants in ATP8B4 as a Risk Factor for Systemic Sclerosis by Whole-Exome Sequencing.	Arthritis Rheumatol	2016
27876072	High-specificity bioinformatics framework for epigenomic profiling of discordant twins reveals specific and shared markers for ACPA and ACPA-positive rheumatoid arthritis.	Genome Med	2016
27725671	A continuum of admixture in the Western Hemisphere revealed by the African Diaspora genome.	Nat Commun	2016
26528484	Identification and functional studies of regulatory variants responsible for the association of NRG3 with a delusion phenotype in schizophrenia.	Mol Neuropsychiatry	2015
25704602	Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci.	Am J Hum Genet	2015
25123830	Analytic power and sample size calculation for the genotypic transmission/disequilibrium test in case-parent trio studies.	Biometrical Journal	2014
25048299	Detecting disease variants in case-parent trio studies using the bioconductor software package trio.	Genetic Epidemiology	2014
24516586	Evidence of gene-environment interaction for two genes on chromosome 4 and environmental tobacco smoke in controlling the risk of nonsyndromic cleft palate.	PLoS One	2014
24793288	Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts.	Genetics	2014
23334450	Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis.	Nat Biotechnol	2013
24000956	Measuring cell-type specific differential methylation in human brain tissue.	Genome Biol	2013
24379823	On multi-marker tests for association in case-control studies.	Frontiers in Genetics	2013
23512105	Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study.	Hum Genet	2013