| Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis Y Liu, MJ Aryee, L Padyukov, MD Fallin, E Hesselberg, A Runarsson, ... Nature biotechnology 31 (2), 142-147, 2013 | 1061 | 2013 |
| Inherited causes of clonal haematopoiesis in 97,691 whole genomes AG Bick, JS Weinstock, SK Nandakumar, CP Fulco, EL Bao, SM Zekavat, ... Nature 586 (7831), 763-768, 2020 | 436 | 2020 |
| Reproducible RNA-seq analysis using recount2 L Collado-Torres, A Nellore, K Kammers, SE Ellis, MA Taub, KD Hansen, ... Nature biotechnology 35 (4), 319-321, 2017 | 382 | 2017 |
| Assembly of a pan-genome from deep sequencing of 910 humans of African descent RM Sherman, J Forman, V Antonescu, D Puiu, M Daya, N Rafaels, ... Nature genetics 51 (1), 30-35, 2019 | 334 | 2019 |
| Confirming genes influencing risk to cleft lip with/without cleft palate in a case–parent trio study TH Beaty, MA Taub, AF Scott, JC Murray, ML Marazita, H Schwender, ... Human genetics 132, 771-781, 2013 | 261 | 2013 |
| Association of DNA methylation differences with schizophrenia in an epigenome-wide association study C Montano, MA Taub, A Jaffe, E Briem, JI Feinberg, R Trygvadottir, A Idrizi, ... JAMA psychiatry 73 (5), 506-514, 2016 | 179 | 2016 |
| 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 EJ Leslie, MA Taub, H Liu, KM Steinberg, DC Koboldt, Q Zhang, ... The American Journal of Human Genetics 96 (3), 397-411, 2015 | 171 | 2015 |
| A continuum of admixture in the Western Hemisphere revealed by the African Diaspora genome RA Mathias, MA Taub, CR Gignoux, W Fu, S Musharoff, TD O'Connor, ... Nature communications 7 (1), 12522, 2016 | 156 | 2016 |
| Overcoming bias and systematic errors in next generation sequencing data MA Taub, H Corrada Bravo, RA Irizarry Genome medicine 2, 1-5, 2010 | 136 | 2010 |
| Measuring cell-type specific differential methylation in human brain tissue CM Montaño, RA Irizarry, WE Kaufmann, K Talbot, RE Gur, AP Feinberg, ... Genome biology 14, 1-9, 2013 | 114 | 2013 |
| Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts A Bureau, MM Parker, I Ruczinski, MA Taub, ML Marazita, JC Murray, ... Genetics 197 (3), 1039-1044, 2014 | 105 | 2014 |
| Genome-wide screen for asthma in Puerto Ricans: evidence for association with 5q23 region S Choudhry, M Taub, R Mei, J Rodriguez-Santana, W Rodriguez-Cintron, ... Human genetics 123, 455-468, 2008 | 88 | 2008 |
| Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations M Daya, N Rafaels, TM Brunetti, S Chavan, AM Levin, A Shetty, ... Nature communications 10 (1), 880, 2019 | 86 | 2019 |
| Challenges and disparities in the application of personalized genomic medicine to populations with African ancestry MD Kessler, L Yerges-Armstrong, MA Taub, AC Shetty, K Maloney, ... Nature communications 7 (1), 12521, 2016 | 75 | 2016 |
| A whole genome long-range haplotype (WGLRH) test for detecting imprints of positive selection in human populations C Zhang, DK Bailey, T Awad, G Liu, G Xing, M Cao, V Valmeekam, ... Bioinformatics 22 (17), 2122-2128, 2006 | 75 | 2006 |
| Genome-wide enrichment of de novo coding mutations in orofacial cleft trios MR Bishop, KKD Perez, M Sun, S Ho, P Chopra, N Mukhopadhyay, ... The American Journal of Human Genetics 107 (1), 124-136, 2020 | 56 | 2020 |
| Evidence of gene− environment interaction for two genes on chromosome 4 and environmental tobacco smoke in controlling the risk of nonsyndromic cleft palate T Wu, H Schwender, I Ruczinski, JC Murray, ML Marazita, RG Munger, ... PloS one 9 (2), e88088, 2014 | 52 | 2014 |
| Using github classroom to teach statistics J Fiksel, LR Jager, JS Hardin, MA Taub Journal of Statistics Education 27 (2), 110-119, 2019 | 49 | 2019 |
| Identifying genetic sources of phenotypic heterogeneity in orofacial clefts by targeted sequencing JC Carlson, MA Taub, E Feingold, TH Beaty, JC Murray, ML Marazita, ... Birth defects research 109 (13), 1030-1038, 2017 | 48 | 2017 |
| A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies Z Li, X Li, H Zhou, SM Gaynor, MS Selvaraj, T Arapoglou, C Quick, Y Liu, ... Nature methods 19 (12), 1599-1611, 2022 | 44 | 2022 |
