| Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ... Nature 590 (7845), 290-299, 2021 | 1391 | 2021 |
| 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 | 159 | 2016 |
| Human demographic history has amplified the effects of background selection across the genome R Torres, ZA Szpiech, RD Hernandez PLoS genetics 14 (6), e1007387, 2018 | 73 | 2018 |
| Case-control admixture mapping in Latino populations enriches for known asthma-associated genes DG Torgerson, CR Gignoux, JM Galanter, KA Drake, LA Roth, C Eng, ... Journal of Allergy and Clinical Immunology 130 (1), 76-82. e12, 2012 | 64 | 2012 |
| The temporal dynamics of background selection in nonequilibrium populations R Torres, MG Stetter, RD Hernandez, J Ross-Ibarra Genetics 214 (4), 1019-1030, 2020 | 29 | 2020 |
| Evaluation and classification of severity for 176 genes on an expanded carrier screening panel A Arjunan, H Bellerose, R Torres, R Ben‐Shachar, JD Hoffman, B Angle, ... Prenatal Diagnosis 40 (10), 1246-1257, 2020 | 26 | 2020 |
| Increased protein-coding mutations in the mitochondrial genome of African American women with preeclampsia D Ding, NM Scott, EE Thompson, T Chaiworapongsa, R Torres, ... Reproductive Sciences 19 (12), 1343-1351, 2012 | 20 | 2012 |
| Population genetic simulations of complex phenotypes with implications for rare variant association tests LH Uricchio, R Torres, JS Witte, RD Hernandez Genetic epidemiology 39 (1), 35-44, 2015 | 17 | 2015 |
| A guidelines-consistent carrier screening panel that supports equity across diverse populations KJ Taber, R Ben-Shachar, R Torres, A Arjunan, D Muzzey, KE Kaseniit, ... Genetics in Medicine 24 (1), 201-213, 2022 | 15 | 2022 |
| Evaluating the efficacy of three carrier screening workflows designed to identify at‐risk carrier couples A Arjunan, R Torres, A Gardiner, KE Kaseniit, J Wootton, R Ben‐Shachar, ... Prenatal Diagnosis 41 (7), 896-904, 2021 | 11 | 2021 |
| Using genotype array data to compare multi-and single-sample variant calls and improve variant call sets from deep coverage whole-genome sequencing data SS Shringarpure, RA Mathias, RD Hernandez, TD O’Connor, ZA Szpiech, ... Bioinformatics 33 (8), 1147-1153, 2017 | 8* | 2017 |
| Consistency of carrier screening guidelines across seven populations and 408, 00 individuals A Arjunan, R Ben-Shachar, R Torres, KJ Taber, KE Kaseniit, D Muzzey EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 28-29, 2020 | | 2020 |
| An evidence-based evaluation of guidelines criteria for condition inclusion on ECS panels: identifying a guidelines-compliant panel KJ Taber, R Torres, R Ben-Shachar, A Arjunan, J Goldberg Fertility and Sterility 114 (3), e360, 2020 | | 2020 |
| The Effects of Background Selection and Demography on Patterns of Neutral Variation Within the Genome R Torres University of California, San Francisco, 2018 | | 2018 |
