Lewis C. Becker

1971–2025 年に発表

別表記
LEWIS C. BECKER
171
論文数
34,383
被引用数
105
h 指数
165
i10 指数

被引用数

Lewis C. Becker の年別被引用数1971 年: 被引用 1 件1972 年: 被引用 5 件1973 年: 被引用 5 件1974 年: 被引用 9 件1975 年: 被引用 12 件1976 年: 被引用 14 件1977 年: 被引用 15 件1978 年: 被引用 15 件1979 年: 被引用 16 件1980 年: 被引用 12 件1981 年: 被引用 48 件1982 年: 被引用 24 件1983 年: 被引用 35 件1984 年: 被引用 24 件1985 年: 被引用 35 件1986 年: 被引用 39 件1987 年: 被引用 62 件1988 年: 被引用 53 件1989 年: 被引用 80 件1990 年: 被引用 91 件1991 年: 被引用 68 件1992 年: 被引用 58 件1993 年: 被引用 65 件1994 年: 被引用 60 件1995 年: 被引用 84 件1996 年: 被引用 77 件1997 年: 被引用 77 件1998 年: 被引用 113 件1999 年: 被引用 109 件2000 年: 被引用 127 件2001 年: 被引用 96 件2002 年: 被引用 107 件2003 年: 被引用 132 件2004 年: 被引用 150 件2005 年: 被引用 160 件2006 年: 被引用 156 件2007 年: 被引用 152 件2008 年: 被引用 158 件2009 年: 被引用 214 件2010 年: 被引用 204 件2011 年: 被引用 259 件2012 年: 被引用 242 件2013 年: 被引用 270 件2014 年: 被引用 222 件2015 年: 被引用 201 件2016 年: 被引用 176 件2017 年: 被引用 188 件2018 年: 被引用 153 件2019 年: 被引用 460 件2020 年: 被引用 595 件2021 年: 被引用 687 件2022 年: 被引用 761 件2023 年: 被引用 641 件2024 年: 被引用 898 件2025 年: 被引用 467 件2026 年: 被引用 33 件

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 4,476 件、この内訳の 28.2%イギリス: 引用元論文 1,280 件、この内訳の 8.1%ドイツ: 引用元論文 890 件、この内訳の 5.6%中国: 引用元論文 760 件、この内訳の 4.8%カナダ: 引用元論文 719 件、この内訳の 4.5%イタリア: 引用元論文 618 件、この内訳の 3.9%オランダ: 引用元論文 570 件、この内訳の 3.6%フランス: 引用元論文 473 件、この内訳の 3%オーストラリア: 引用元論文 469 件、この内訳の 3%スウェーデン: 引用元論文 421 件、この内訳の 2.7%日本: 引用元論文 349 件、この内訳の 2.2%スペイン: 引用元論文 333 件、この内訳の 2.1%
0%28.2%その他 28.3%

分野

  • Medicine57.6%
  • Biochemistry, Genetics and Molecular Biology32%
  • Immunology and Microbiology2.6%
  • Neuroscience2.5%
  • Engineering1.1%
  • Nursing0.9%
  • その他3.3%

トピック

  • Genetic Associations and Epidemiology6.5%
  • Cardiac Imaging and Diagnostics3.7%
  • Cardiovascular Function and Risk Factors2.8%
  • Cardiac Ischemia and Reperfusion2.7%
  • Acute Myocardial Infarction Research1.8%
  • Genetic Mapping and Diversity in Plants and Animals1.6%
  • その他80.9%

共著者

全論文

検索で開く
  1. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Dan E. Arking, Stella Aslibekyan, Paul L. Auer, John Barnard, R. Graham Barr, Lucas Barwick, Lewis C. Becker, Rebecca Beer, Emelia J. Benjamin, Lawrence F. Bielak, John Blangero, Michael Boehnke, Donald W. Bowden, Jennifer A. Brody, Esteban G. Burchard, Brian E. Cade, James F. Casella, Brandon Chalazan, Daniel I. Chasman, Yii‐Der Ida Chen, Michael H. Cho, Seung Hoan Choi, Mina K. Chung, Clary B. Clish, Adolfo Correa, Joanne E. Curran, Brian Custer, Dawood Darbar, Michelle Daya, Mariza de Andrade, Dawn L. DeMeo, Susan K. Dutcher, Patrick T. Ellinor, Leslie S. Emery, Celeste Eng, Diane Fatkin, Tasha E. Fingerlin, Lukas Forer, Myriam Fornage, Nora Franceschini, Christian Fuchsberger, Stephanie M. Fullerton, Søren Germer, Mark T. Gladwin, Daniel J. Gottlieb, Xiuqing Guo, Michael E. Hall, Jiang He, Nancy L. Heard‐Costa, Susan R. Heckbert, Marguerite R. Irvin, Jill M. Johnsen, Andrew D. Johnson, Robert C. Kaplan, Sharon L. R. Kardia, Tanika N. Kelly, Shannon Kelly, Eimear E. Kenny, Douglas P. Kiel, Robert Klemmer, Barbara A. Konkle, Charles Kooperberg, Anna Köttgen, Leslie A. Lange, Jessica Lasky‐Su, Daniel Levy, Xihong Lin, Keng‐Han Lin, Chunyu Liu, Ruth J. F. Loos ほか 325 名 - Nature 2021 被引用: 2,355

  2. Inherited causes of clonal haematopoiesis in 97,691 whole genomes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sharon L. R. Kardia, Jiang He, Robert C. Kaplan, Nicholas L. Smith, Donna K. Arnett, David A. Schwartz, Adolfo Correa, Mariza de Andrade, Xiuqing Guo, Barbara A. Konkle, Brian Custer, Juan M. Peralta, Hongsheng Gui, Deborah A. Meyers, Stephen T. McGarvey, Ida Yii-Der Chen, M. Benjamin Shoemaker, Patricia A. Peyser, Jai Broome, Stephanie M. Gogarten, Fei Fei Wang, Quenna Wong, May E. Montasser, Michelle Daya, Eimear E. Kenny, Kari E. North, Lenore J. Launer, Brian E. Cade, Joshua C. Bis, Michael H. Cho, Jessica Lasky‐Su, Donald W. Bowden, L. Adrienne Cupples, Angel C. Y. Mak, Lewis C. Becker, Jennifer A. Smith, Tanika N. Kelly, Stella Aslibekyan, Susan R. Heckbert, Hemant K. Tiwari, Ivana V. Yang, John A. Heit, Steven A. Lubitz, Jill M. Johnsen, Joanne E. Curran, Sally E. Wenzel, Daniel E. Weeks, D. C. Rao, Dawood Darbar, Jee‐Young Moon, Russell P. Tracy, Erin Buth, Nicholas Rafaels, Ruth J. F. Loos, Peter Durda, Yongmei Liu, Lifang Hou, Jiwon Lee, Priyadarshini Kachroo, Barry I. Freedman, Daniel Levy, Lawrence F. Bielak, James E. Hixson, James S. Floyd, Eric A. Whitsel, Patrick T. Ellinor, Marguerite R. Irvin, Tasha E. Fingerlin, Laura M. Raffield, Sebastian M. Armasu ほか 314 名 - Nature 2020 被引用: 757

  3. Clonal haematopoiesis and risk of chronic liver disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Raymond T. Chung, Kathleen E. Corey, Daniel Levy, Christie M. Ballantyne, NHLBI TOPMed Hematology Working Group, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Donna K. Arnett, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Larry Bielak, Joshua C. Bis, Thomas W. Blackwell, John Blangero, Nathan R. Blue, Donald W. Bowden, Russell P. Bowler, Jennifer A. Brody, Ulrich Broeckel, Jai Broome, Deborah Brown, Karen Bunting, Esteban G. Burchard, Carlos D. Bustamante, Erin Buth, Brian E. Cade, Jonathan Cardwell, Vincent J. Carey, Julie Carrier, April P. Carson, Cara L. Carty, Richard Casaburi, Juan P. Romero, James F. Casella, Peter J. Castaldi, Mark Chaffin, Christy Chang, Yi‐Cheng Chang, Daniel I. Chasman, Sameer Chavan, Bo-Juen Chen ほか 340 名 - Nature 2023 被引用: 201

  4. Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Xihao Li, Zilin Li, Elise Lim, D. Y. Lin, Xihong Lin, Simin Liu, Yingchang Lu, JoAnn E. Manson, Lisa W. Martin, Caitlin McHugh, Julie Mikulla, Solomon K. Musani, Maggie Ng, Deborah A. Nickerson, Nicholette Palmer, James A. Perry, Ulrike Peters, Michael Preuß, Qibin Qi, Laura M. Raffield, Laura J. Rasmussen‐Torvik, Alex P. Reiner, Emily M. Russell, Colleen M. Sitlani, Jennifer A. Smith, Cassandra N. Spracklen, Tao Wang, Zhe Wang, Jennifer Wessel, Hanfei Xu, Mohammad Yaser, Sachiko Yoneyama, Kendra A. Young, Jingwen Zhang, Xinruo Zhang, Hufeng Zhou, Xiaofeng Zhu, Sebastian Zoellner, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Allison E. Ashley‐Koch, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Larry Bielak, Joshua C. Bis ほか 360 名 - Nature Genetics 2022 被引用: 359

  5. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mary Susan Burnett, Ian Buysschaert, John F. Carlquist, Li Chen, Sven Cichon, Veryan Codd, R. W. Davies, George Dedoussis, Abbas Dehghan, Serkalem Demissie, Joseph M. Devaney, Patrick Diemert, Ron Do, Angela Doering, Sandra Eifert, Nour Eddine El Mokhtari, Stephen G. Ellis, Roberto Elosúa, James C. Engert, Stephen E. Epstein, Ulf dé Fairé, Marcus Fischer, Aaron R. Folsom, Jennifer Freyer, Bruna Gigante, Domenico Girelli, Sólveig Grétarsdóttir, Vilmundur Guðnason, Jeffrey R. Gulcher, Eran Halperin, Naomi Hammond, Stanley L. Hazen, Albert Hofman, Benjamin D. Horne, Thomas Illig, Carlos Iribarren, Gregory T. Jones, J. Wouter Jukema, Michael Kaiser, Lee M. Kaplan, John J.P. Kastelein, Kay‐Tee Khaw, Joshua W. Knowles, Genovefa Kolovou, Augustine Kong, Reijo Laaksonen, Diether Lambrechts, Karin Leander, Guillaume Lettre, Mingyao Li, Wolfgang Lieb, Christina Loley, Andrew Lotery, Pier Mannuccio Mannucci, Seraya Maouche, Nicola Martinelli, Pascal McKeown, Christa Meisinger, Thomas Meitinger, Olle Melander, Pier Angelica Merlini, Vincent Mooser, Thomas M. Morgan, Thomas W Mühleisen, Joseph B. Muhlestein, Thomas Münzel, Kiran Musunuru, Janja Nahrstaedt, Christopher P. Nelson, Markus M. Nöthen ほか 67 名 - Nature Genetics 2011 被引用: 1,951

  6. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lewis C. Becker, Rebecca Beer, Emelia J. Benjamin, Lawrence F. Bielak, John Blangero, Michael Boehnke, Donald W. Bowden, Jennifer A. Brody, Esteban G. Burchard, Brian E. Cade, James F. Casella, Brandon Chalazan, Yii‐Der Ida Chen, Michael H. Cho, Seung Hoan Choi, Mina K. Chung, Clary B. Clish, Adolfo Correa, Joanne E. Curran, Brian Custer, Dawood Darbar, Michelle Daya, Mariza de Andrade, Dawn L. DeMeo, Susan K. Dutcher, Patrick T. Ellinor, Leslie S. Emery, Diane Fatkin, Lukas Forer, Myriam Fornage, Nora Franceschini, Christian Fuchsberger, Stephanie M. Fullerton, Søren Germer, Mark T. Gladwin, Daniel J. Gottlieb, Xiuqing Guo, Michael E. Hall, Jiang He, Nancy L. Heard‐Costa, Susan R. Heckbert, Marguerite R. Irvin, Jill M. Johnsen, Andrew D. Johnson, Sharon L. R. Kardia, Tanika N. Kelly, Shannon Kelly, Eimear E. Kenny, Douglas P. Kiel, Robert Klemmer, Barbara A. Konkle, Charles Kooperberg, Anna Köttgen, Leslie A. Lange, Jessica Lasky‐Su, Daniel Levy, Xihong Lin, Keng‐Han Lin, Chunyu Liu, Ruth J. F. Loos, Lori Garman, Robert E. Gerszten, Steven A. Lubitz, Kathryn L. Lunetta, Angel C. Y. Mak, Ani Manichaikul, Alisa K. Manning, Rasika A. Mathias, David D. McManus, Stephen T. McGarvey ほか 78 名 - 2019 被引用: 423

  7. A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Yukinori Okada, Buhm Han, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Donna K. Arnett, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Larry Bielak, Joshua C. Bis, Thomas W. Blackwell, John Blangero, Eric Boerwinkle, Donald W. Bowden, Russell P. Bowler, Jennifer A. Brody, Ulrich Broeckel, Jai Broome, Deborah Brown, Karen Bunting, Esteban Burchard, Carlos D. Bustamante, Erin Buth, Brian E. Cade, Jonathan Cardwell, Vincent J. Carey, Julie Carrier, Cara L. Carty, Richard Casaburi, Juan P. Romero, James F. Casella, Peter J. Castaldi, Mark Chaffin, Christy Chang, Yi‐Cheng Chang, Daniel I. Chasman, Sameer Chavan, Bo‐Juen Chen, Wei‐Min Chen, Seung Hoan Choi, Lee‐Ming Chuang, Mina K. Chung ほか 332 名 - Nature Genetics 2021 被引用: 187

  8. Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael C. Mahaney, Ani Manichaikul, Lisa W. Martin, Rasika A. Mathias, Stephen T. McGarvey, Braxton D. Mitchell, May E. Montasser, Jill E. Moore, Alanna C. Morrison, Jeffrey R. O’Connell, Nicholette D. Palmer, Akhil Pampana, Juan M. Peralta, Patricia A. Peyser, Bruce M. Psaty, Susan Redline, Kenneth Rice, Stephen S. Rich, Jennifer A. Smith, Hemant K. Tiwari, Michael Y. Tsai, Ramachandran S. Vasan, Fei Fei Wang, Daniel E. Weeks, Zhiping Weng, James G. Wilson, Lisa R. Yanek, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan Arking, Donna K. Arnett, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Lawrence F. Bielak, Joshua C. Bis, Thomas W. Blackwell, John Blangero, Eric Boerwinkle, Donald W. Bowden, Russell P. Bowler, Jennifer Brody, Ulrich Broeckel, Jai Broome, Karen Bunting ほか 459 名 - Nature Genetics 2020 被引用: 290

  9. Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lifang Hou, Donald M. Lloyd‐Jones, Susan Redline, Brian E. Cade, Bruce M. Psaty, Joshua C. Bis, Jennifer A. Brody, Edwin K. Silverman, Jeong H. Yun, Dandi Qiao, Nicholette D. Palmer, Barry I. Freedman, Donald W. Bowden, Michael H. Cho, Dawn L. DeMeo, Ramachandran S. Vasan, Lisa R. Yanek, Lewis C. Becker, Sharon L. R. Kardia, Patricia A. Peyser, Jiang He, Michiel Rienstra, Pim van der Harst, Robert C. Kaplan, Susan R. Heckbert, Nicholas L. Smith, Kerri L. Wiggins, Donna K. Arnett, Marguerite R. Irvin, Hemant K. Tiwari, Michael J. Cutler, Stacey Knight, J. Brent Muhlestein, Adolfo Correa, Laura M. Raffield, Yan Gao, Mariza de Andrade, Jerome I. Rotter, Stephen S. Rich, Russell P. Tracy, Barbara A. Konkle, Jill M. Johnsen, Marsha M. Wheeler, J. G. Smith, Olle Melander, Peter M. Nilsson, Brian Custer, Ravindranath Duggirala, Joanne E. Curran, John Blangero, Stephen T. McGarvey, L. Keoki Williams, Shujie Xiao, Mao Yang, C. Charles Gu, Yii‐Der Ida Chen, Wen‐Jane Lee, Gregory M. Marcus, John P. Kane, Clive R. Pullinger, M. Benjamin Shoemaker, Dawood Darbar, Dan M. Roden, Christine M. Albert, Charles Kooperberg, Ying Zhou, JoAnn E. Manson, Pinkal Desai, Andrew D. Johnson, Rasika A. Mathias ほか 418 名 - Nature 2023 被引用: 106

  10. Impaired Chronotropic and Vasodilator Reserves Limit Exercise Capacity in Patients With Heart Failure and a Preserved Ejection Fraction

    著者: , , , , , , - Circulation 2006 被引用: 690

  11. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Santhi K. Ganesh, Misa Graff, Namrata Gupta, Jiang He, Susan R. Heckbert, Bertha Hidalgo, Chani J. Hodonsky, Marguerite R. Irvin, Andrew D. Johnson, Eric Jorgenson, Robert C. Kaplan, Sharon L. R. Kardia, Tanika N. Kelly, Charles Kooperberg, Jessica Lasky‐Su, Ruth J. F. Loos, Steven A. Lubitz, Rasika A. Mathias, Caitlin McHugh, Courtney G. Montgomery, Jee‐Young Moon, Alanna C. Morrison, Nicholette D. Palmer, Nathan Pankratz, George Papanicolaou, Juan M. Peralta, Patricia A. Peyser, Stephen S. Rich, Jerome I. Rotter, Edwin K. Silverman, Jennifer A. Smith, Nicholas L. Smith, Kent D. Taylor, Timothy A. Thornton, Hemant K. Tiwari, Russell P. Tracy, Tao Wang, Scott T. Weiss, Lu‐Chen Weng, Kerri L. Wiggins, James G. Wilson, Lisa R. Yanek, Sebastian Zöllner, Kari E. North, Paul L. Auer, TOPMed Hematology & Hemostasis Working Group, Laura M. Raffield, Alex P. Reiner, Yun Li - PLoS Genetics 2019 被引用: 322

  12. A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Xiuqing Guo, Rita R. Kalyani, Charles Kooperberg, Brian G. Kral, Leslie A. Lange, Bridget M. Lin, Ani Manichaikul, Alisa K. Manning, Lisa W. Martin, Rasika A. Mathias, James B. Meigs, Braxton D. Mitchell, May E. Montasser, Alanna C. Morrison, Take Naseri, Jeffrey R. O’Connell, Nicholette D. Palmer, Patricia A. Peyser, Bruce M. Psaty, Laura M. Raffield, Susan Redline, Alex P. Reiner, Muagututi‘a Sefuiva Reupena, Kenneth Rice, Stephen S. Rich, Jennifer A. Smith, Kent D. Taylor, Margaret A. Taub, Ramachandran S. Vasan, Daniel E. Weeks, James G. Wilson, Lisa R. Yanek, Wei Zhao, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Nathan R. Blue, Russell P. Bowler, Ulrich Broeckel, Jai Broome, Deborah Brown ほか 413 名 - Nature Methods 2022 被引用: 109

  13. Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Meher Preethi Boorgula, Wei Zhao, Lisa R. Yanek, Kerri L. Wiggins, James E. Hixson, C. Charles Gu, Gina M. Peloso, Dan M. Roden, Muagututi‘a Sefuiva Reupena, Chii‐Min Hwu, Dawn L. DeMeo, Kari E. North, Shannon Kelly, Solomon K. Musani, Joshua C. Bis, Donald M. Lloyd‐Jones, Jill M. Johnsen, Michael Preuß, Russell P. Tracy, Patricia A. Peyser, Dandi Qiao, Pinkal Desai, Joanne E. Curran, Barry I. Freedman, Hemant K. Tiwari, Sameer Chavan, Jennifer A. Smith, Nicholas L. Smith, Tanika N. Kelly, Bertha Hidalgo, L. Adrienne Cupples, Daniel E. Weeks, Nicola L. Hawley, Ryan L. Minster, The Samoan Obesity, Lifestyle and Genetic Adaptations Study (OLaGA) Group, Ranjan Deka, Take Naseri, Lisa de las Fuentes, Laura M. Raffield, Alanna C. Morrison, Paul S. de Vries, Christie M. Ballantyne, Eimear E. Kenny, Stephen S. Rich, Eric A. Whitsel, Michael H. Cho, M. Benjamin Shoemaker, Betty S. Pace, John Blangero, Nicholette D. Palmer, Braxton D. Mitchell, Alan R. Shuldiner, Kathleen C. Barnes, Susan Redline, Sharon L.R. Kardia, Gonçalo R. Abecasis, Lewis C. Becker, Susan R. Heckbert, Jiang He, Wendy S. Post, Donna K. Arnett, Ramachandran S. Vasan, Dawood Darbar, Scott T. Weiss, Stephen T. McGarvey, Mariza de Andrade, Yii‐Der Ida Chen, Robert C. Kaplan, Deborah A. Meyers, Brian Custer ほか 21 名 - Science Advances 2022 被引用: 94

  14. Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lambertus A. Kiemeney, Oluf Pedersen, Augustine Kong, Unnur Þorsteinsdóttir, Kāri Stefánsson - Nature Genetics 2008 被引用: 1,405

  15. Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jennifer A. Brody, Ming‐Huei Chen, Dhananjay Vaidya, José Manuel Soria, Pierre Suchon, Astrid van Hylckama Vlieg, Karl C. Desch, Ivana Kolčić, Peter K. Joshi, Lenore J. Launer, Tamara B. Harris, Harry Campbell, Igor Rudan, Diane M. Becker, Jun Z. Li, Fernando Rivadeneira, André G. Uitterlinden, Albert Hofman, Oscar H. Franco, Mary Cushman, Bruce M. Psaty, Pierre‐Emmanuel Morange, Barbara McKnight, Michael Chong, Israel Fernández‐Cadenas, Jonathan Rosand, Arne Lindgren, Vilmundur Guðnason, James F. Wilson, Caroline Hayward, David Ginsburg, Myriam Fornage, Frits R. Rosendaal, Juan Carlos Souto, Lewis C. Becker, Nancy S. Jenny, Winfried März, J. Wouter Jukema, Abbas Dehghan, David‐Alexandre Trégouët, Alanna C. Morrison, Andrew D. Johnson, Christopher J. O’Donnell, David P. Strachan, Charles J. Lowenstein, Nicholas L. Smith - Circulation 2019 被引用: 169

  16. Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mary F. Feitosa, Chris Finan, Austin T. Hilliard, Sharon L. R. Kardia, Jason C. Kovacic, Brian G. Kral, Carl D. Langefeld, Lenore J. Launer, Shaista Malik, Firdaus A. A. Mohamed Hoesein, Michal Mokrý, Reinhold Schmidt, Jennifer A. Smith, Kent D. Taylor, James G. Terry, Jeroen van der Grond, Joyce B. J. van Meurs, Rozemarijn Vliegenthart, Jianzhao Xu, Kendra A. Young, Nuno R. Zilhäo, Robert Zweiker, Themistocles L. Assimes, Lewis C. Becker, Daniël Bos, J. Jeffrey Carr, L. Adrienne Cupples, Dominique P.V. de Kleijn, Menno P.J. de Winther, Hester M. den Ruijter, Myriam Fornage, Barry I. Freedman, Vilmundur Guðnason, Aroon D. Hingorani, John E. Hokanson, M. Arfan Ikram, Ivana Išgum, David R. Jacobs, Mika Kähönen, Leslie A. Lange, Terho Lehtimäki, Gerard Pasterkamp, Olli T. Raitakari, Helena Schmidt, P. Eline Slagboom, André G. Uitterlinden, Meike W. Vernooij, Joshua C. Bis, Nora Franceschini, Bruce M. Psaty, Wendy S. Post, Jerome I. Rotter, Johan Björkegren, Christopher J. O’Donnell, Lawrence F. Bielak, Patricia A. Peyser, Rajeev Malhotra, Sander W. van der Laan, Clint L. Miller - Nature Genetics 2023 被引用: 149

  17. 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

  18. Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals

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  19. Sex Differences in Platelet Reactivity and Response to Low-Dose Aspirin Therapy

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  20. Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease

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  21. Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed

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  22. Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

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  23. Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

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  24. Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities

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