Sharon R. Browning

2006–2024 年に発表

53
論文数
17,985
被引用数
37
h 指数
51
i10 指数

被引用数

Sharon R. Browning の年別被引用数1972 年: 被引用 1 件1996 年: 被引用 1 件2000 年: 被引用 2 件2002 年: 被引用 1 件2006 年: 被引用 1 件2007 年: 被引用 4 件2008 年: 被引用 35 件2009 年: 被引用 54 件2010 年: 被引用 112 件2011 年: 被引用 172 件2012 年: 被引用 223 件2013 年: 被引用 241 件2014 年: 被引用 215 件2015 年: 被引用 218 件2016 年: 被引用 197 件2017 年: 被引用 215 件2018 年: 被引用 220 件2019 年: 被引用 542 件2020 年: 被引用 551 件2021 年: 被引用 532 件2022 年: 被引用 432 件2023 年: 被引用 357 件2024 年: 被引用 515 件2025 年: 被引用 244 件2026 年: 被引用 18 件1973〜1995 年は被引用が無いため表示していません1997〜1999 年は被引用が無いため表示していません2001 年は被引用が無いため表示していません2003〜2005 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 2,204 件、この内訳の 21.6%中国: 引用元論文 801 件、この内訳の 7.9%イギリス: 引用元論文 746 件、この内訳の 7.3%ドイツ: 引用元論文 511 件、この内訳の 5%フランス: 引用元論文 411 件、この内訳の 4%カナダ: 引用元論文 361 件、この内訳の 3.5%オーストラリア: 引用元論文 351 件、この内訳の 3.4%オランダ: 引用元論文 297 件、この内訳の 2.9%スウェーデン: 引用元論文 291 件、この内訳の 2.9%イタリア: 引用元論文 275 件、この内訳の 2.7%デンマーク: 引用元論文 237 件、この内訳の 2.3%スペイン: 引用元論文 227 件、この内訳の 2.2%
0%21.6%その他 34.3%

分野

  • Biochemistry, Genetics and Molecular Biology72.4%
  • Medicine10.7%
  • Agricultural and Biological Sciences7.5%
  • Immunology and Microbiology2.2%
  • Neuroscience1.7%
  • Environmental Science1.5%
  • その他4%

トピック

  • Genetic Mapping and Diversity in Plants and Animals10.3%
  • Genetic and phenotypic traits in livestock10.1%
  • Genetic Associations and Epidemiology9.9%
  • Genetic diversity and population structure4.8%
  • Genomics and Rare Diseases3.1%
  • Forensic and Genetic Research3%
  • その他58.8%

共著者

全論文

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  1. Rapid and Accurate Haplotype Phasing and Missing-Data Inference for Whole-Genome Association Studies By Use of Localized Haplotype Clustering

    著者: , - The American Journal of Human Genetics 2007 被引用: 3,517

  2. Fast two-stage phasing of large-scale sequence data

    著者: , , , - The American Journal of Human Genetics 2021 被引用: 967

  3. Genotype Imputation with Millions of Reference Samples

    著者: , - The American Journal of Human Genetics 2016 被引用: 1,305

  4. Improving the Accuracy and Efficiency of Identity-by-Descent Detection in Population Data

    著者: , - Genetics 2013 被引用: 742

  5. A Unified Approach to Genotype Imputation and Haplotype-Phase Inference for Large Data Sets of Trios and Unrelated Individuals

    著者: , - The American Journal of Human Genetics 2009 被引用: 1,703

  6. Analysis of Human Sequence Data Reveals Two Pulses of Archaic Denisovan Admixture

    著者: , , , , - Cell 2018 被引用: 434

  7. A Fast and Simple Method for Detecting Identity-by-Descent Segments in Large-Scale Data

    著者: , , - The American Journal of Human Genetics 2020 被引用: 202

  8. Accurate Non-parametric Estimation of Recent Effective Population Size from Segments of Identity by Descent

    著者: , - The American Journal of Human Genetics 2015 被引用: 416

  9. Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , George Papanicolaou, Thomas Lumley, Adam A. Szpiro, Kari E. North, Kenneth Rice, Timothy A. Thornton, Cathy C. Laurie - The American Journal of Human Genetics 2016 被引用: 370

  10. Haplotype phasing: existing methods and new developments

    著者: , - Nature Reviews Genetics 2011 被引用: 710

  11. Fast, accurate local ancestry inference with FLARE

    著者: , , - The American Journal of Human Genetics 2023 被引用: 103

  12. Identity by Descent Between Distant Relatives: Detection and Applications

    著者: , - Annual Review of Genetics 2012 被引用: 226

  13. Detecting Identity by Descent and Estimating Genotype Error Rates in Sequence Data

    著者: , - The American Journal of Human Genetics 2013 被引用: 216

  14. De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Moustafa Abdalla, Omar Abdul‐Rahman, Gonçalo R. Abecasis, Avinash Abhyankar, Indra Adrianto, François Aguet, Rachel Akers, Rafet Al-Tobasei, Christine M. Albert, Micheala A. Aldred, Laura Almasy, Márcio Rodrigues de Almeida, Álvaro Alonso, Seth A. Ament, Elizabeth Ampleford, Ping An, Christopher D. Anderson, Charlotte Andersson, Pramod Anugu, Elizabeth L. Appelbaum, Kristin Ardlie, Dan Arking, Sebastian M. Armasu, Donna K. Arnett, Heather T Arruda, Marios Arvanitis, Allison E. Ashley‐Koch, Aneel A. Ashrani, Stella Aslibekyan, Tim Assimes, Elizabeth J. Atkinson, Paul L. Auer, Thomas R. Austin, Christy L. Avery, Julián Ávila-Pacheco, Paul Avillach, Abraham Aviv, Dimitrios Avramopoulos, Christie M. Ballantyne, Pallavi Balte, Michael J. Bamshad, Mike Bancks, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Traci M. Bartz, Lucas Barwick, Saonli Basu, Alexis Battle, Michaël Baumann, David Beame, Terri Beaty, Gerald J. Beck, Lewis C. Becker, Diane M. Becker, Rebecca Beer, Ferdouse Begum, Alexa Beiser, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Hanna Berk-Rauch, Zachary M Besich, Marcos Bezerra, Surya P. Bhatt, Wenjian Bi, Alexander G. Bick, Larry Bielak, Mary L. Biggs ほか 1,045 名 - National Academy of Sciences, Proceedings of the National Academy of Sciences 2020 被引用: 112

  15. A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic

    著者: , - PLoS Genetics 2009 被引用: 1,170

  16. Ancestry-specific recent effective population size in the Americas

    著者: , , , , , , - PLoS Genetics 2018 被引用: 194

  17. A neurodegenerative disease landscape of rare mutations in Colombia due to founder effects

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Francisco Lopera, Kenneth S. Kosik - Genome Medicine 2022 被引用: 42

  18. A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Marie McDonald, Joe J. Hoo, Beatrice N. French, Cindy Hudson, John P. Johnson, Jillian R. Ozmore, John B. Moeschler, Urvashi Surti, Luis Escobar, Dima El‐Khechen, Jerome L. Gorski, Jennifer Kussmann, Bonnie Anne Salbert, Yves Lacassie, Alisha Biser, Donna M. McDonald‐McGinn, Elaine H. Zackai, Matthew A. Deardorff, Tamim H. Shaikh, Eric Haan, Kathryn Friend, Marco Fichera, Corrado Romano, Jozef Gécz, Lynn E. DeLisi, Jonathan Sebat, Mary‐Claire King, Lisa G. Shaffer, Evan E. Eichler - Nature Genetics 2010 被引用: 674

  19. Estimating the Genome-wide Mutation Rate with Three-Way Identity by Descent

    著者: , , - The American Journal of Human Genetics 2019 被引用: 92

  20. Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Shabnam Salimi, Wayne H-H Sheu, Alan R. Shuldiner, Kent D. Taylor, Albert V. Smith, Jennifer A. Smith, Adrienne Tin, Dhananjay Vaidya, Robert B. Wallace, Kenichi Yamamoto, Saori Sakaue, Koichi Matsuda, Yoichiro Kamatani, Yukihide Momozawa, Lisa R. Yanek, Betsi A Young, Wei Zhao, Yukinori Okada, Gonzalo Abecasis, Bruce M. Psaty, Donna K. Arnett, Eric Boerwinkle, Jianwen Cai, Ida Yii-Der Chen, Adolfo Correa, L. Adrienne Cupples, Jiang He, Sharon LR Kardia, Charles Kooperberg, Rasika A. Mathias, Braxton D. Mitchell, Deborah A. Nickerson, Steve T Turner, Ramachandran S. Vasan, Jerome I. Rotter, Daniel Levy, Holly Kramer, Anna Köttgen, TOPMed Kidney Working Group, Stephen S. Rich, D. Y. Lin, Sharon R. Browning, Nora Franceschini - EBioMedicine 2021 被引用: 28

  21. Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populations

    著者: , , , , , , , , , , , , , , , , , - Human Genetics and Genomics Advances 2023 被引用: 16

  22. Genome-wide Significance Thresholds for Admixture Mapping Studies

    著者: , , , , - The American Journal of Human Genetics 2019 被引用: 63

  23. Statistical phasing of 150,119 sequenced genomes in the UK Biobank

    著者: , - The American Journal of Human Genetics 2022 被引用: 29

  24. Estimating the genome-wide mutation rate from thousands of unrelated individuals

    著者: , , - The American Journal of Human Genetics 2022 被引用: 20