| Year |
Citation |
Score |
| 2022 |
Tian X, Cai R, Browning SR. Estimating the genome-wide mutation rate from thousands of unrelated individuals. American Journal of Human Genetics. 109: 2178-2184. PMID 36370709 DOI: 10.1016/j.ajhg.2022.10.015 |
0.307 |
|
| 2022 |
Granot-Hershkovitz E, Sun Q, Argos M, Zhou H, Lin X, Browning SR, Sofer T. AFA: Ancestry-specific allele frequency estimation in admixed populations: The Hispanic Community Health Study/Study of Latinos. Hgg Advances. 3: 100096. PMID 35300209 DOI: 10.1016/j.xhgg.2022.100096 |
0.318 |
|
| 2021 |
Taliun D, Harris DN, Kessler MD, Carlson J, Szpiech ZA, Torres R, Taliun SAG, Corvelo A, Gogarten SM, Kang HM, Pitsillides AN, LeFaive J, Lee SB, Tian X, Browning BL, ... ... Browning SR, et al. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program. Nature. 590: 290-299. PMID 33568819 DOI: 10.1038/s41586-021-03205-y |
0.351 |
|
| 2020 |
Zhou Y, Browning SR, Browning BL. IBDkin: fast estimation of kinship coefficients from identity by descent segments. Bioinformatics (Oxford, England). PMID 32844204 DOI: 10.1093/Bioinformatics/Btaa569 |
0.309 |
|
| 2020 |
Zhou Y, Browning BL, Browning SR. Population-Specific Recombination Maps from Segments of Identity by Descent. American Journal of Human Genetics. PMID 32533945 DOI: 10.1016/J.Ajhg.2020.05.016 |
0.416 |
|
| 2020 |
Harris DN, Kessler MD, Shetty AC, Weeks DE, Minster RL, Browning S, Cochrane EE, Deka R, Hawley NL, Reupena MS, Naseri T, McGarvey ST, O'Connor TD. Evolutionary history of modern Samoans. Proceedings of the National Academy of Sciences of the United States of America. PMID 32291332 DOI: 10.1073/Pnas.1913157117 |
0.368 |
|
| 2020 |
Zhou Y, Browning SR, Browning BL. A Fast and Simple Method for Detecting Identity by Descent Segments in Large-Scale Data. American Journal of Human Genetics. PMID 32169169 DOI: 10.1016/J.Ajhg.2020.02.010 |
0.369 |
|
| 2020 |
Kessler MD, Loesch DP, Perry JA, Heard-Costa NL, Taliun D, Cade BE, Wang H, Daya M, Ziniti J, Datta S, Celedón JC, Soto-Quiros ME, Avila L, Weiss ST, Barnes K, ... ... Browning SR, et al. De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population. Proceedings of the National Academy of Sciences of the United States of America. PMID 31964835 DOI: 10.1073/Pnas.1902766117 |
0.413 |
|
| 2019 |
Tian X, Browning BL, Browning SR. Estimating the Genome-wide Mutation Rate with Three-Way Identity by Descent. American Journal of Human Genetics. 105: 883-893. PMID 31587867 DOI: 10.1016/J.Ajhg.2019.09.012 |
0.381 |
|
| 2019 |
Grinde KE, Brown LA, Reiner AP, Thornton TA, Browning SR. Genome-wide Significance Thresholds for Admixture Mapping Studies. American Journal of Human Genetics. PMID 30773276 DOI: 10.1016/J.Ajhg.2019.01.008 |
0.428 |
|
| 2018 |
Wang H, Cade BE, Sofer T, Sands SA, Chen H, Browning S, Stilp AM, Louie TL, Thornton TA, Craig Johnson W, Below JE, Conomos MP, Evans DS, Gharib SA, Guo X, et al. Admixture mapping identifies novel loci for obstructive sleep apnea in hispanic/latino americans. Human Molecular Genetics. PMID 30403821 DOI: 10.1093/Hmg/Ddy387 |
0.396 |
|
| 2018 |
Browning BL, Zhou Y, Browning SR. A One-Penny Imputed Genome from Next-Generation Reference Panels. American Journal of Human Genetics. PMID 30100085 DOI: 10.1016/J.Ajhg.2018.07.015 |
0.35 |
|
| 2018 |
Browning SR, Browning BL, Daviglus ML, Durazo-Arvizu RA, Schneiderman N, Kaplan RC, Laurie CC. Ancestry-specific recent effective population size in the Americas. Plos Genetics. 14: e1007385. PMID 29795556 DOI: 10.1371/Journal.Pgen.1007385 |
0.347 |
|
| 2018 |
Browning SR, Browning BL, Zhou Y, Tucci S, Akey JM. Analysis of Human Sequence Data Reveals Two Pulses of Archaic Denisovan Admixture. Cell. PMID 29551270 DOI: 10.1016/J.Cell.2018.02.031 |
0.371 |
|
| 2017 |
Sofer T, Baier LJ, Browning SR, Thornton TA, Talavera GA, Wassertheil-Smoller S, Daviglus ML, Hanson R, Kobes S, Cooper RS, Cai J, Levy D, Reiner AP, Franceschini N. Admixture mapping in the Hispanic Community Health Study/Study of Latinos reveals regions of genetic associations with blood pressure traits. Plos One. 12: e0188400. PMID 29155883 DOI: 10.1371/Journal.Pone.0188400 |
0.394 |
|
| 2017 |
Kerr KF, Avery CL, Lin HJ, Raffield LM, Zhang QS, Browning BL, Browning SR, Conomos MP, Gogarten SM, Laurie CC, Sofer T, Thornton TA, Hohensee C, Jackson RD, Kooperberg C, et al. Genome-wide Association Study of Heart Rate and Its Variability in Hispanic/Latino Cohorts. Heart Rhythm. PMID 28610988 DOI: 10.1016/J.Hrthm.2017.06.018 |
0.331 |
|
| 2017 |
Hodonsky CJ, Jain D, Schick UM, Morrison JV, Brown L, McHugh CP, Schurmann C, Chen DD, Liu YM, Auer PL, Laurie CA, Taylor KD, Browning BL, Li Y, Papanicolaou G, ... ... Browning SR, et al. Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos. Plos Genetics. 13: e1006760. PMID 28453575 DOI: 10.1371/Journal.Pgen.1006760 |
0.426 |
|
| 2017 |
Jain D, Hodonsky CJ, Schick UM, Morrison JV, Minnerath S, Brown L, Schurmann C, Liu Y, Auer PL, Laurie CA, Taylor KD, Browning B, Papanicolaou G, Browning S, Loos RJ, et al. Genome-Wide Association of White Blood Cell Counts in Hispanic/Latino Americans: The Hispanic Community Health Study/Study of Latinos. Human Molecular Genetics. PMID 28158719 DOI: 10.1093/Hmg/Ddx024 |
0.422 |
|
| 2017 |
Brown LA, Sofer T, Stilp AM, Baier LJ, Kramer HJ, Masindova I, Levy D, Hanson RL, Moncrieft AE, Redline S, Rosas SE, Lash JP, Cai J, Laurie CC, Browning S, et al. Admixture Mapping Identifies an Amerindian Ancestry Locus Associated with Albuminuria in Hispanics in the United States. Journal of the American Society of Nephrology : Jasn. PMID 28137830 DOI: 10.1681/Asn.2016091010 |
0.446 |
|
| 2016 |
Fu W, Browning SR, Browning BL, Akey JM. Robust Inference of Identity by Descent from Exome-Sequencing Data. American Journal of Human Genetics. PMID 27745837 DOI: 10.1016/J.Ajhg.2016.09.011 |
0.421 |
|
| 2016 |
Browning SR, Grinde K, Plantinga A, Gogarten SM, Stilp AM, Kaplan RC, Aviles-Santa ML, Browning BL, Laurie CC. Local Ancestry Inference in a large US-Based Hispanic/Latino Study: Hispanic Community Health Study / Study of Latinos (HCHS/SOL). G3 (Bethesda, Md.). PMID 27172203 DOI: 10.1534/G3.116.028779 |
0.416 |
|
| 2016 |
Zhang QS, Browning BL, Browning SR. ASAFE: Ancestry-Specific Allele Frequency Estimation. Bioinformatics (Oxford, England). PMID 27153656 DOI: 10.1093/Bioinformatics/Btw220 |
0.404 |
|
| 2016 |
Schick UM, Jain D, Hodonsky CJ, Morrison JV, Davis JP, Brown L, Sofer T, Conomos MP, Schurmann C, McHugh CP, Nelson SC, Vadlamudi S, Stilp A, Plantinga A, Baier L, ... ... Browning SR, et al. Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans. American Journal of Human Genetics. PMID 26805783 DOI: 10.1016/J.Ajhg.2015.12.003 |
0.401 |
|
| 2016 |
Conomos MP, Laurie CA, Stilp AM, Gogarten SM, McHugh CP, Nelson SC, Sofer T, Fernández-Rhodes L, Justice AE, Graff M, Young KL, Seyerle AA, Avery CL, Taylor KD, Rotter JI, ... ... Browning SR, et al. Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos. American Journal of Human Genetics. 98: 165-184. PMID 26748518 DOI: 10.1016/J.Ajhg.2015.12.001 |
0.399 |
|
| 2016 |
Browning BL, Browning SR. Genotype Imputation with Millions of Reference Samples. American Journal of Human Genetics. 98: 116-26. PMID 26748515 DOI: 10.1016/J.Ajhg.2015.11.020 |
0.362 |
|
| 2015 |
Browning SR, Browning BL. Accurate Non-parametric Estimation of Recent Effective Population Size from Segments of Identity by Descent American Journal of Human Genetics. 97: 404-418. PMID 26299365 DOI: 10.1016/J.Ajhg.2015.07.012 |
0.387 |
|
| 2015 |
Zhang QS, Browning BL, Browning SR. Genome-wide haplotypic testing in a Finnish cohort identifies a novel association with low-density lipoprotein cholesterol. European Journal of Human Genetics : Ejhg. 23: 672-7. PMID 24896150 DOI: 10.1038/Ejhg.2014.105 |
0.351 |
|
| 2014 |
Qian Y, Browning BL, Browning SR. Efficient clustering of identity-by-descent between multiple individuals Bioinformatics. 30: 915-922. PMID 24363374 DOI: 10.1093/Bioinformatics/Btt734 |
0.337 |
|
| 2013 |
Browning BL, Browning SR. Detecting identity by descent and estimating genotype error rates in sequence data American Journal of Human Genetics. 93: 840-851. PMID 24207118 DOI: 10.1016/J.Ajhg.2013.09.014 |
0.429 |
|
| 2013 |
Nelson SC, Doheny KF, Pugh EW, Romm JM, Ling H, Laurie CA, Browning SR, Weir BS, Laurie CC. Imputation-based genomic coverage assessments of current human genotyping arrays. G3 (Bethesda, Md.). 3: 1795-807. PMID 23979933 DOI: 10.1534/G3.113.007161 |
0.421 |
|
| 2013 |
Browning BL, Browning SR. Improving the accuracy and efficiency of identity-by-descent detection in population data Genetics. 194: 459-471. PMID 23535385 DOI: 10.1534/Genetics.113.150029 |
0.447 |
|
| 2013 |
Myles-Worsley M, Tiobech J, Browning SR, Korn J, Goodman S, Gentile K, Melhem N, Byerley W, Faraone SV, Middleton FA. Deletion at the SLC1A1 glutamate transporter gene co-segregates with schizophrenia and bipolar schizoaffective disorder in a 5-generation family. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 87-95. PMID 23341099 DOI: 10.1002/Ajmg.B.32125 |
0.315 |
|
| 2013 |
Browning SR, Browning BL. Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort Human Genetics. 132: 129-138. PMID 23052944 DOI: 10.1007/S00439-012-1230-Y |
0.423 |
|
| 2012 |
Browning SR, Browning BL. Identity by descent between distant relatives: Detection and applications Annual Review of Genetics. 46: 617-633. PMID 22994355 DOI: 10.1146/Annurev-Genet-110711-155534 |
0.411 |
|
| 2012 |
Browning SR, Thompson EA. Detecting rare variant associations by identity-by-descent mapping in case-control studies Genetics. 190: 1521-1531. PMID 22267498 DOI: 10.1534/Genetics.111.136937 |
0.474 |
|
| 2011 |
Patsopoulos NA, Esposito F, Reischl J, Lehr S, Bauer D, Heubach J, Sandbrink R, Pohl C, Edan G, Kappos L, ... ... Browning SR, et al. Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. Annals of Neurology. 70: 897-912. PMID 22190364 DOI: 10.1002/Ana.22609 |
0.403 |
|
| 2011 |
Li L, Li Y, Browning SR, Browning BL, Slater AJ, Kong X, Aponte JL, Mooser VE, Chissoe SL, Whittaker JC, Nelson MR, Ehm MG. Performance of genotype imputation for rare variants identified in exons and flanking regions of genes Plos One. 6. PMID 21949800 DOI: 10.1371/Journal.Pone.0024945 |
0.419 |
|
| 2011 |
Browning SR, Browning BL. Haplotype phasing: Existing methods and new developments Nature Reviews Genetics. 12: 703-714. PMID 21921926 DOI: 10.1038/Nrg3054 |
0.358 |
|
| 2011 |
Browning SR, Browning BL. Population structure can inflate SNP-based heritability estimates American Journal of Human Genetics. 89: 191-193. PMID 21763486 DOI: 10.1016/J.Ajhg.2011.05.025 |
0.335 |
|
| 2011 |
Ritchie ME, Liu R, Carvalho BS, Irizarry RA, Bahlo M, Booth DR, Broadley SA, Brown MA, Foote SJ, Griffiths LR, Kilpatrick TJ, Lechner-Scott J, Moscato P, Perreau VM, Rubio JP, ... ... Browning SR, et al. Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips Bmc Bioinformatics. 12. PMID 21385424 DOI: 10.1186/1471-2105-12-68 |
0.341 |
|
| 2011 |
Browning BL, Browning SR. A fast, powerful method for detecting identity by descent American Journal of Human Genetics. 88: 173-182. PMID 21310274 DOI: 10.1016/J.Ajhg.2011.01.010 |
0.446 |
|
| 2010 |
Field J, Browning SR, Johnson LJ, Danoy P, Varney MD, Tait BD, Gandhi KS, Charlesworth JC, Heard RN, Stewart GJ, Kilpatrick TJ, Foote SJ, Bahlo M, Butzkueven H, et al. A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis. Plos One. 5: e13454. PMID 21049023 DOI: 10.1371/Journal.Pone.0013454 |
0.348 |
|
| 2010 |
Browning SR, Weir BS. Population structure with localized haplotype clusters. Genetics. 185: 1337-44. PMID 20457877 DOI: 10.1534/Genetics.110.116681 |
0.38 |
|
| 2010 |
Browning SR, Browning BL. High-Resolution Detection of Identity by Descent in Unrelated Individuals American Journal of Human Genetics. 86: 526-539. PMID 20303063 DOI: 10.1016/J.Ajhg.2010.02.021 |
0.47 |
|
| 2010 |
Bahlo M, Stankovich J, Danoy P, Hickey PF, Taylor BV, Browning SR, Brown MA, Rubio JP. Saliva-derived DNA performs well in large-scale, high-density single-nucleotide polymorphism microarray studies. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 19: 794-8. PMID 20200434 DOI: 10.1158/1055-9965.Epi-09-0812 |
0.329 |
|
| 2010 |
Girirajan S, Rosenfeld JA, Cooper GM, Antonacci F, Siswara P, Itsara A, Vives L, Walsh T, McCarthy SE, Baker C, Mefford HC, Kidd JM, Browning SR, Browning BL, Dickel DE, et al. A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay. Nature Genetics. 42: 203-9. PMID 20154674 DOI: 10.1038/Ng.534 |
0.324 |
|
| 2009 |
Bahlo M, Booth DR, Simon A Broadley, Brown MA, Foote SJ, Griffiths LR, Kilpatrick TJ, Lechner-Scott J, Moscato P, Perreau VM, Rubio JP, Scott RJ, Stankovich J, Stewart GJ, Taylor BV, ... ... Browning SR, et al. Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 Nature Genetics. 41: 824-828. PMID 19525955 DOI: 10.1038/Ng.396 |
0.35 |
|
| 2009 |
Madsen BE, Browning SR. A groupwise association test for rare mutations using a weighted sum statistic Plos Genetics. 5. PMID 19214210 DOI: 10.1371/Journal.Pgen.1000384 |
0.38 |
|
| 2009 |
Zeng ISL, Browning SR, Gladding P, Jüllig M, Middleditch M, Stewart RAH. A Multi-feature Reproducibility Assessment of Mass Spectral Data in Clinical Proteomic Studies Clinical Proteomics. 5: 170-177. DOI: 10.1007/S12014-009-9039-Y |
0.317 |
|
| 2008 |
Browning BL, Browning SR. A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals American Journal of Human Genetics. 84: 210-223. PMID 19200528 DOI: 10.1016/J.Ajhg.2009.01.005 |
0.437 |
|
| 2008 |
Browning SR. Missing data imputation and haplotype phase inference for genome-wide association studies Human Genetics. 124: 439-450. PMID 18850115 DOI: 10.1007/S00439-008-0568-7 |
0.427 |
|
| 2008 |
Black J, Browning SR, Collins AV, Phillips JR. A canine model of inherited myopia: Familial aggregation of refractive error in Labrador retrievers Investigative Ophthalmology and Visual Science. 49: 4784-4789. PMID 18566472 DOI: 10.1167/Iovs.08-1828 |
0.329 |
|
| 2008 |
Browning SR. Estimation of pairwise identity by descent from dense genetic marker data in a population sample of haplotypes Genetics. 178: 2123-2132. PMID 18430938 DOI: 10.1534/Genetics.107.084624 |
0.449 |
|
| 2008 |
Browning BL, Browning SR. Haplotypic analysis of Wellcome Trust Case Control Consortium data Human Genetics. 123: 273-280. PMID 18224336 DOI: 10.1007/S00439-008-0472-1 |
0.376 |
|
| 2007 |
Browning SR, Thomas J. Multilocus analysis of GAW15 NARAC chromosome 18 case-control data. Bmc Proceedings. 1: S11. PMID 18466450 DOI: 10.1186/1753-6561-1-S1-S11 |
0.419 |
|
| 2007 |
Wilcox MA, Li Z, Tapper W, Browning S, Curtin K, Ding J, Ding Y, Gagnon F, He Q, Kuo TY, Li M, Matthew G, Mei L, Rao S, Shaw J, et al. Genetic association with rheumatoid arthritis-Genetic Analysis Workshop 15: summary of contributions from Group 2. Genetic Epidemiology. 31: S12-21. PMID 18046771 DOI: 10.1002/gepi.20276 |
0.313 |
|
| 2007 |
Browning SR, Browning BL. Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering American Journal of Human Genetics. 81: 1084-1097. PMID 17924348 DOI: 10.1086/521987 |
0.472 |
|
| 2007 |
Browning BL, Browning SR. Efficient multilocus association testing for whole genome association studies using localized haplotype clustering Genetic Epidemiology. 31: 365-375. PMID 17326099 DOI: 10.1002/Gepi.20216 |
0.432 |
|
| 2006 |
Browning SR. Multilocus association mapping using variable-length Markov chains American Journal of Human Genetics. 78: 903-913. PMID 16685642 DOI: 10.1086/503876 |
0.404 |
|
| 2005 |
Browning SR, Briley JD, Briley LP, Chandra G, Charnecki JH, Ehm MG, Johansson KA, Jones BJ, Karter AJ, Yarnall DP, Wagner MJ. Case-control single-marker and haplotypic association analysis of pedigree data. Genetic Epidemiology. 28: 110-22. PMID 15578751 DOI: 10.1002/Gepi.20051 |
0.439 |
|
| 2003 |
Browning S. Pedigree data analysis with crossover interference Genetics. 164: 1561-1566. PMID 12930760 |
0.31 |
|
| 2000 |
Browning S. A Monte Carlo approach to calculating probabilities for continuous identity by descent data Journal of Applied Probability. 37: 850-864. DOI: 10.1239/Jap/1014842841 |
0.379 |
|
| 1998 |
Browning S. Relationship information contained in gamete identity by descent data Journal of Computational Biology. 5: 323-334. PMID 9672835 DOI: 10.1089/Cmb.1998.5.323 |
0.351 |
|
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