| A global reference for human genetic variation TGP Consortium Nature 526 (7571), 68-74, 2015 | 12960* | 2015 |
| A map of human genome variation from population scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010 | 8739 | 2010 |
| An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012 | 8231 | 2012 |
| Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering SR Browning, BL Browning The American Journal of Human Genetics 81 (5), 1084-1097, 2007 | 3442 | 2007 |
| A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals BL Browning, SR Browning The American Journal of Human Genetics 84 (2), 210-223, 2009 | 1872 | 2009 |
| 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 | 1307 | 2021 |
| A one-penny imputed genome from next-generation reference panels BL Browning, Y Zhou, SR Browning The American Journal of Human Genetics 103 (3), 338-348, 2018 | 1288 | 2018 |
| Genotype imputation with millions of reference samples BL Browning, SR Browning The American Journal of Human Genetics 98 (1), 116-126, 2016 | 1079 | 2016 |
| Haplotype phasing: existing methods and new developments SR Browning, BL Browning Nature Reviews Genetics 12 (10), 703-714, 2011 | 811 | 2011 |
| Demographic history and rare allele sharing among human populations S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ... Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011 | 707 | 2011 |
| A recurrent 16p12. 1 microdeletion supports a two-hit model for severe developmental delay S Girirajan, JA Rosenfeld, GM Cooper, F Antonacci, P Siswara, A Itsara, ... Nature genetics 42 (3), 203-209, 2010 | 657 | 2010 |
| Improving the accuracy and efficiency of identity-by-descent detection in population data BL Browning, SR Browning Genetics 194 (2), 459-471, 2013 | 644 | 2013 |
| Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 Data analysis: Bahlo Melanie 2 Brown Matthew A 6 7 Browning Brian L 20 ... Nature genetics 41 (7), 824-828, 2009 | 533 | 2009 |
| Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel O Delaneau, J Marchini Nature communications 5 (1), 3934, 2014 | 434 | 2014 |
| A fast, powerful method for detecting identity by descent BL Browning, SR Browning The American Journal of Human Genetics 88 (2), 173-182, 2011 | 426 | 2011 |
| Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium RN Lemaitre, T Tanaka, W Tang, A Manichaikul, M Foy, EK Kabagambe, ... PLoS genetics 7 (7), e1002193, 2011 | 424 | 2011 |
| Analysis of human sequence data reveals two pulses of archaic Denisovan admixture SR Browning, BL Browning, Y Zhou, S Tucci, JM Akey Cell 173 (1), 53-61. e9, 2018 | 348 | 2018 |
| Genetic diversity and association studies in US Hispanic/Latino populations: applications in the Hispanic Community Health Study/Study of Latinos MP Conomos, CA Laurie, AM Stilp, SM Gogarten, CP McHugh, ... The American Journal of Human Genetics 98 (1), 165-184, 2016 | 301 | 2016 |
| High-resolution detection of identity by descent in unrelated individuals SR Browning, BL Browning The American Journal of Human Genetics 86 (4), 526-539, 2010 | 287 | 2010 |
| Accurate non-parametric estimation of recent effective population size from segments of identity by descent SR Browning, BL Browning The American Journal of Human Genetics 97 (3), 404-418, 2015 | 283 | 2015 |
Sharon R. BrowningResearch Professor of Biostatistics, University of WashingtonVerified email at uw.edu
