| 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 | 171 | 2016 |
| 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 | 17 | 2022 |
| 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 |
| Benchmarking of Germline Copy Number Variant Callers from Whole Genome Sequencing Data for Clinical Applications FM De La Vega, SA Irvine, P Anur, K Potts, L Kraft, R Torres, P Kang, ... medRxiv, 2024.07. 12.24310338, 2024 | | 2024 |
| 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 |
| 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 |
| 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 |
| 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 | 28 | 2020 |
| Functional refolding of the penetration protein on a non-enveloped virus T Herrmann, R Torres, EN Salgado, C Berciu, D Stoddard, D Nicastro, ... Nature 590 (7847), 666-670, 2021 | 35 | 2021 |
| 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 | 75 | 2018 |
| 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 | 19 | 2012 |
| Indice de la narrativa ecuatoriana RP Torres, SZ Guzman, GJ Buendia Editora Nacional, 1992 | 8 | 1992 |
| NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ... Sequencing of 53, 290-299, 2021 | 84 | 2021 |
| Performance of Copy Number Variant Detection from ShortRead Whole-Genome Sequencing for Clinical Gene-Panel Applications F De La Vega, P Anur, J Han, S Han, S Irvine, P Kang, L Kraft, Y Lee, ... JOURNAL OF MOLECULAR DIAGNOSTICS 25 (11), S147-S147, 2023 | | 2023 |
| Pharmacogenomic insights in psychiatric care: uncovering novel actionability, allele-specific CYP2D6 copy number variation, and phenoconversion in 15,000 … JN Patel, SA Morris, R Torres, B Rhead, C Vlangos, DJ Mueller, LC Brown, ... Molecular Psychiatry, 1-8, 2024 | | 2024 |
| 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 |
| 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 | 1448 | 2021 |
| The Effects of Background Selection and Demography on Patterns of Neutral Variation Within the Genome R Torres University of California, San Francisco, 2018 | | 2018 |
| 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 |
| 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 | 9* | 2017 |
