John D. Overton

2008–2025 年に発表

96
論文数
20,256
被引用数
56
h 指数
94
i10 指数

被引用数

John D. Overton の年別被引用数1955 年: 被引用 1 件1987 年: 被引用 1 件1991 年: 被引用 1 件1994 年: 被引用 2 件2000 年: 被引用 1 件2004 年: 被引用 2 件2005 年: 被引用 1 件2007 年: 被引用 2 件2009 年: 被引用 7 件2010 年: 被引用 3 件2011 年: 被引用 9 件2012 年: 被引用 52 件2013 年: 被引用 140 件2014 年: 被引用 209 件2015 年: 被引用 176 件2016 年: 被引用 207 件2017 年: 被引用 224 件2018 年: 被引用 256 件2019 年: 被引用 726 件2020 年: 被引用 888 件2021 年: 被引用 1,062 件2022 年: 被引用 1,111 件2023 年: 被引用 862 件2024 年: 被引用 1,257 件2025 年: 被引用 594 件2026 年: 被引用 32 件1956〜1986 年は被引用が無いため表示していません1988〜1990 年は被引用が無いため表示していません1992〜1993 年は被引用が無いため表示していません1995〜1999 年は被引用が無いため表示していません2001〜2003 年は被引用が無いため表示していません2006 年は被引用が無いため表示していません2008 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 3,871 件、この内訳の 26.2%イギリス: 引用元論文 1,304 件、この内訳の 8.8%中国: 引用元論文 869 件、この内訳の 5.9%ドイツ: 引用元論文 829 件、この内訳の 5.6%カナダ: 引用元論文 630 件、この内訳の 4.3%イタリア: 引用元論文 574 件、この内訳の 3.9%フランス: 引用元論文 523 件、この内訳の 3.5%オランダ: 引用元論文 507 件、この内訳の 3.4%オーストラリア: 引用元論文 472 件、この内訳の 3.2%スウェーデン: 引用元論文 403 件、この内訳の 2.7%デンマーク: 引用元論文 339 件、この内訳の 2.3%スペイン: 引用元論文 336 件、この内訳の 2.3%
0%26.2%その他 27.9%

分野

  • Medicine45.5%
  • Biochemistry, Genetics and Molecular Biology41.4%
  • Neuroscience6.3%
  • Immunology and Microbiology3.6%
  • Psychology0.8%
  • Computer Science0.5%
  • その他1.9%

トピック

  • Genetic Associations and Epidemiology6.1%
  • Genomics and Rare Diseases4%
  • Genetics and Neurodevelopmental Disorders2.9%
  • Liver Disease Diagnosis and Treatment2.7%
  • Autism Spectrum Disorder Research2.2%
  • Diabetes, Cardiovascular Risks, and Lipoproteins2%
  • その他80.1%

共著者

全論文

検索で開く
  1. Exome sequencing and analysis of 454,787 UK Biobank participants

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , William Salerno, Alan R. Shuldiner, Luca A. Lotta, John D. Overton, Michael Cantor, Jeffrey G. Reid, George D. Yancopoulos, Hyun Min Kang, Jonathan Marchini, Aris Baras, Gonçalo R. Abecasis, Manuel A. R. Ferreira - Nature 2021 被引用: 1,077

  2. Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Yan V. Sun, Scott L. DuVall, Kelly Cho, Jennifer S. Lee, J. Michael Gaziano, Lawrence S. Phillips, James B. Meigs, Peter D. Reaven, Peter W.F. Wilson, Todd L. Edwards, Daniel J. Rader, Scott M. Damrauer, Christopher J. O’Donnell, Philip S. Tsao, Mark A. Atkinson, Al C. Powers, Ali Naji, Klaus H. Kaestner, Gonçalo R. Abecasis, Aris Baras, Michael Cantor, Giovanni Coppola, Aris N. Economides, Luca A. Lotta, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Christina Beechert, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Michael Lattari, Alexander Lopez, Thomas D. Schleicher, Maria Sotiropoulos Padilla, Karina Toledo, Louis Widom, Sarah E. Wolf, Manasi Pradhan, Kia Manoochehri, Ricardo H. Ulloa, Xiaodong Bai, Suganthi Balasubramanian, Leland Barnard, Andrew Blumenfeld, Gisu Eom, Lukas Habegger, Alicia Hawes, Shareef Khalid, Evan K. Maxwell, William Salerno, Jeffrey Staples, Ashish Yadav, Marcus B. Jones, Lyndon J. Mitnaul, VA Million Veteran Program, Samuel M. Aguayo, Sunil K. Ahuja, Zuhair K. Ballas, Sujata Bhushan, Edward J. Boyko, David Cohen, John Concato, Joseph I. Constans, Louis J. Dell’Italia, Joseph Fayad, Ronald Fernando, Hermes Flórez, Melinda A. Gaddy, Saib Gappy ほか 82 名 - Nature Genetics 2020 被引用: 801

  3. A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Scott M. Damrauer, Daniel J. Rader, Brian Zambrowicz, William C. Olson, Andrew Murphy, Ingrid B. Borecki, Alan R. Shuldiner, Jeffrey G. Reid, John D. Overton, George D. Yancopoulos, Helen H. Hobbs, Jonathan C. Cohen, Omri Gottesman, Tanya M. Teslovich, Aris Baras, Tooraj Mirshahi, Jesper Gromada, Frederick E. Dewey - New England Journal of Medicine 2018 被引用: 805

  4. Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Laurent F. Thomas, Margo Tuerlings, John Loughlin, Nigel Arden, Fraser Birrell, Andrew Carr, Panos Deloukas, Michael Doherty, Andrew W. McCaskie, William Ollier, Ashok Rai, Stuart H. Ralston, Tim D. Spector, Gillian A. Wallis, Amy E. Martinsen, Cristen J. Willer, Egil A. Fors, Ingunn Mundal, Knut Hagen, Kristian Bernhard Nilsen, Marie Udnesseter Lie, Sigrid Børte, Ben Brumpton, Jonas B. Nielsen, Lars G. Fritsche, Wei Zhou, Ingrid Heuch, Kjersti Storheim, Evangelos Tyrpenou, A. Koukakis, Dimitrios Chytas, Dimitrios Stergios Evangelopoulos, Chronopoulos Efstathios, Spiros G. Pneumaticos, Vasileios S. Nikolaou, Κonstantinos Ν. Malizos, Lydia Anastasopoulou, Gonçalo R. Abecasis, Aris Baras, Michael Cantor, Giovanni Coppola, Andrew Deubler, Aris N. Economides, Luca A. Lotta, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Katia Karalis, Katherine Siminovitch, Christina Beechert, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Michael Lattari, Alexander Lopez, Thomas D. Schleicher, Maria Sotiropoulos Padilla, Louis Widom, Sarah E. Wolf, Manasi Pradhan, Kia Manoochehri, Xiaodong Bai, Suganthi Balasubramanian, Boris Boutkov, Gisu Eom, Lukas Habegger, Alicia Hawes, Olga Krasheninina, Rouel Lanche, Adam J. Mansfield ほか 55 名 - Cell 2021 被引用: 467

  5. Common and rare variant associations with clonal haematopoiesis phenotypes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Raquel P. Deering, Charles Paulding, Alan R. Shuldiner, Gavin Thurston, Adolfo A. Ferrando, Will Salerno, Jeffrey G. Reid, John D. Overton, Jonathan Marchini, Hyun Min Kang, Aris Baras, Gonçalo R. Abecasis, Eric Jorgenson - Nature 2022 被引用: 304

  6. Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kae‐Woei Liang, Xiuqing Guo, Jerome I. Rotter, Yii‐Der I. Chen, William E. Kraus, Svati H. Shah, Scott M. Damrauer, Aeron Small, Daniel J. Rader, Anders Berg Wulff, Børge G. Nordestgaard, Anne Tybjærg‐Hansen, Anita M. van den Hoek, Hans M.G. Princen, David H. Ledbetter, David J. Carey, John D. Overton, Jeffrey G. Reid, William J. Sasiela, Poulabi Banerjee, Alan R. Shuldiner, Ingrid B. Borecki, Tanya M. Teslovich, George D. Yancopoulos, Scott Mellis, Jesper Gromada, Aris Baras - New England Journal of Medicine 2017 被引用: 875

  7. Exome sequencing and characterization of 49,960 individuals in the UK Biobank

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Cristen J. Willer, Kristian Hveem, Joseph B. Leader, David J. Carey, David H. Ledbetter, Lon R. Cardon, George D. Yancopoulos, Aris N. Economides, Giovanni Coppola, Alan R. Shuldiner, Suganthi Balasubramanian, Michael Cantor, Matthew R. Nelson, John C. Whittaker, Jeffrey G. Reid, Jonathan Marchini, John D. Overton, Robert A. Scott, Gonçalo R. Abecasis, Laura M. Yerges-Armstrong, Aris Baras - Nature 2020 被引用: 636

  8. Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Zhengming Chen, Paraskevi Christofidou, Elizabeth C. Corfield, Christina C. Dahm, Deepika Dokuru, Luke M. Evans, Eco J. C. de Geus, Sudheer Giddaluru, Scott D. Gordon, K. Paige Harden, W. David Hill, Amanda Hughes, Shona M. Kerr, Yongkang Kim, Hyeokmoon Kweon, Antti Latvala, Debbie A. Lawlor, Liming Li, Kuang Lin, Per Magnus, Patrik K. E. Magnusson, Travis T. Mallard, Pekka Martikainen, Melinda C. Mills, Pål R. Njølstad, John D. Overton, Nancy L. Pedersen, David J. Porteous, Jeffrey G. Reid, Karri Silventoinen, Melissa C. Southey, Camilla Stoltenberg, Elliot M. Tucker–Drob, Margaret J. Wright, Hyeokmoon Kweon, Philipp Koellinger, Daniel J. Benjamin, Patrick Turley, Laurence J. Howe, Michel G. Nivard, Tim Morris, Ailin Falkmo Hansen, Humaira Rasheed, Yoonsu Cho, Geetha Chittoor, Rafael Ahlskog, Penelope A. Lind, Teemu Palviainen, Matthijs D. van der Zee, Rosa Cheesman, Massimo Mangino, Yunzhang Wang, Shuai Li, Lucija Klaric, Scott M. Ratliff, Lawrence F. Bielak, Marianne Nygaard, Alexandros Giannelis, Emily A. Willoughby, Chandra A. Reynolds, Jared V. Balbona, Ole A. Andreassen, Helga Ask, Dorret I. Boomsma, Archie Campbell, Harry Campbell, Zhengming Chen, Paraskevi Christofidou, Elizabeth C. Corfield, Christina C. Dahm ほか 96 名 - Nature Genetics 2022 被引用: 393

  9. De novo mutations revealed by whole-exome sequencing are strongly associated with autism

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature 2012 被引用: 2,183

  10. Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Pablo Kuri‐Morales, Jesús Alegre-Díaz, Jason Torres, Jonathan Emberson, Rory Collins, Suganthi Balasubramanian, Alicia Hawes, Marcus Herbert Jones, Brian Zambrowicz, Andrew Murphy, Charles Paulding, Giovanni Coppola, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Michael Cantor, Hyun Min Kang, Gonçalo R. Abecasis, Katia Karalis, Aris N. Economides, Jonathan Marchini, George D. Yancopoulos, Mark W. Sleeman, Judith Y. Altarejos, Giusy Della Gatta, Roberto Tapia-Conyer, Michal L. Schwartzman, Aris Baras, Manuel A. R. Ferreira, Luca A. Lotta - Science 2021 被引用: 276

  11. Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Slavé Petrovski, Melissa Miller, Aris Baras, Lyndon J. Mitnaul, Jeffrey G. Reid, Oleg Moiseyenko, Carlos Garcia Rios, Saurabh Saha, Gonçalo R. Abecasis, Nilanjana Banerjee, Christina Beechert, Boris Boutkov, Michael Cantor, Giovanni Coppola, Aris N. Economides, Gisu Eom, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Lukas Habegger, Marcus B. Jones, Rouel Lanche, Michael Lattari, Michelle G. LeBlanc, Dadong Li, Luca A. Lotta, Kia Manoochehri, Adam J. Mansfield, Evan K. Maxwell, Jason Mighty, Mrunali Nafde, Sean O’Keeffe, Max Orelus, Maria Sotiropoulos Padilla, Razvan Panea, Tommy Polanco, Manasi Pradhan, Ayesha Rasool, Thomas D. Schleicher, Deepika Sharma, Alan R. Shuldiner, Jeffrey Staples, Cristopher V. Van Hout, Louis Widom, Sarah E. Wolf, Sally John, Chia‐Yen Chen, David Sexton, Varant Kupelian, Eric Marshall, T. Swan, Susan Eaton, Jimmy Z. Liu, Stephanie Loomis, Megan E. Jensen, Saranya Duraisamy, Jason Tetrault, David Merberg, Sunita Badola, Mark Reppell, Jason Grundstad, Xiuwen Zheng, Aimée M. Deaton, Margaret M. Parker, Lucas D. Ward, Alexander O. Flynn-Carroll, Caroline A. Austin, Ruth March, Menelas N. Pangalos, Adam Platt ほか 11 名 - Nature Genetics 2021 被引用: 427

  12. De novo mutations in histone-modifying genes in congenital heart disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , George A. Porter, Amy E. Roberts, Ravi Sachidanandam, Stephan Sanders, Howard Seiden, Mathew W. State, Sai Lakshmi Subramanian, Irina R. Tikhonova, Wei Wang, Dorothy Warburton, Peter S. White, Ismée A. Williams, Hongyu Zhao, Jonathan G. Seidman, Martina Brueckner, Wendy K. Chung, Bruce D. Gelb, Elizabeth Goldmuntz, Christine E. Seidman, Richard P. Lifton - Nature 2013 被引用: 968

  13. Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations

    著者: , , , , , , , , , , , , , , , , , , , - Nature Communications 2019 被引用: 535

  14. Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alicia Hawes, Marcus B. Jones, Katia Karalis, Shareef Khalid, Olga Krasheninina, Rouel Lanche, Michael Lattari, Dadong Li, Alexander Lopez, Luca A. Lotta, Kia Manoochehri, Adam J. Mansfield, Evan K. Maxwell, Jason Mighty, Lyndon J. Mitnaul, Mona Nafde, Jonas B. Nielsen, Sean O’Keeffe, Max Orelus, John D. Overton, Maria Sotiropoulos Padilla, Razvan Panea, Tommy Polanco, Manasi Pradhan, Ayesha Rasool, Jeffrey G. Reid, William Salerno, Thomas D. Schleicher, Alan R. Shuldiner, Katherine Siminovitch, Jeffrey Staples, Ricardo H. Ulloa, Niek Verweij, Louis Widom, Sarah E. Wolf, Krishna G. Aragam, Kathryn L. Lunetta, Christopher M. Haggerty, Steven A. Lubitz, Patrick T. Ellinor - Nature Genetics 2022 被引用: 173

  15. Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2016 被引用: 510

  16. Germline Mutations in CIDEB and Protection against Liver Disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael Cantor, Brian Zambrowicz, Andrew Murphy, Gonçalo R. Abecasis, Manuel A. R. Ferreira, Ēriks Šmagris, Viktoria Gusarova, Mark W. Sleeman, George D. Yancopoulos, Jonathan Marchini, Hyun Min Kang, Katia Karalis, Alan R. Shuldiner, Giusy Della Gatta, Adam E. Locke, Aris Baras, Luca A. Lotta - New England Journal of Medicine 2022 被引用: 121

  17. Genomic Analysis of Non- NF2 Meningiomas Reveals Mutations in TRAF7 , KLF4 , AKT1 , and SMO

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Eric C. Holland, Shrikant Mane, Matthew W. State, Kaya Bilgüvar, Joachim M. Baehring, Philip H. Gutin, Joseph M. Piepmeier, Alexander O. Vortmeyer, Cameron Brennan, M. Necmettin Pamir, Türker Kılıç, Richard P. Lifton, James P. Noonan, Katsuhito Yasuno, Murat Günel - Science 2013 被引用: 904

  18. Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation

    著者: , , , , , , , , , , , , , , - Nature Genetics 2014 被引用: 510

  19. Genetic identification of familial hypercholesterolemia within a single U.S. health care system

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , - Science 2016 被引用: 428

  20. Patients With High Genome-Wide Polygenic Risk Scores for Coronary Artery Disease May Receive Greater Clinical Benefit From Alirocumab Treatment in the ODYSSEY OUTCOMES Trial

    著者: , , , , , , , , , , , , , , , , , , , - Circulation 2019 被引用: 246

  21. Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Anthony Marcketta, Matthew S. Lebo, Christina Austin‐Tse, Heather Mason‐Suares, Shannon Bruse, Scott Mellis, Robert S. Phillips, Neil Stahl, Andrew Murphy, Aris N. Economides, Kimberly A. Skelding, Christopher D. Still, James R. Elmore, Ingrid B. Borecki, George D. Yancopoulos, F. Daniel Davis, W. Andrew Faucett, Omri Gottesman, Marylyn D. Ritchie, Alan R. Shuldiner, Jeffrey G. Reid, David H. Ledbetter, Aris Baras, David J. Carey - Science 2016 被引用: 607

  22. Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Louis Widom, Sarah E. Wolf, Manasi Pradhan, Kia Manoochehri, Ricardo H. Ulloa, Genome Informatics, Xiaodong Bai, Suganthi Balasubramanian, Andrew Blumenfeld, Gisu Eom, Lukas Habegger, Alicia Hawes, Shareef Khalid, Evan K. Maxwell, William Salerno, Jeffrey Staples, Marcus B. Jones, Lyndon J. Mitnaul, Julia Brosnan, Olle Melander, Sofia Carlsson, Ola Hansson, Tiinamaija Tuomi, Leif Groop, Emma Ahlqvist - Nature Genetics 2021 被引用: 175

  23. Genotyping, sequencing and analysis of 140,000 adults from Mexico City

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sebastian Zöllner, Eric Jorgenson, William Salerno, Slavé Petrovski, John D. Overton, Jeffrey G. Reid, Timothy A. Thornton, Gonçalo R. Abecasis, Jaime Berúmen, Lorena Orozco, Rory Collins, RGC Management and Leadership Team, Gonçalo R. Abecasis, Adolfo A. Ferrando, Michael Cantor, Giovanni Coppola, Andrew Deubler, Aris N. Economides, Katia Karalis, Luca A. Lotta, Lyndon J. Mitnaul, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Katherine Siminovitch, Sequencing and Lab Operations, Christina Beechert, Erin D. Brian, Laura M. Cremona, Hang Du, Caitlin Forsythe, Zhenhua Gu, Kristy Guevara, Michael Lattari, Alexander Lopez, Kia Manoochehri, Manasi Pradhan, Raymond Reynoso, Ricardo Schiavo, Maria Sotiropoulos Padilla, Chenggu Wang, Sarah E. Wolf, Amelia Averitt, Nilanjana Banerjee, Dadong Li, Sameer Malhotra, Justin Mower, Mudasar Sarwar, Deepika Sharma, Jeffrey Staples, Jay Sundaram, Sean Yu, Aaron Zhang, Genome Informatics and Data Engineering, Mona Nafde, George Mitra, Sujit Gokhale, Andrew Bunyea, Janice Clauer, Krishna Pawan Punuru, Sanjay Sreeram, Gisu Eom, Benjamin Sultan, Vrushali Mahajan, Eliot Austin, Koteswararao Makkena, Sean O’Keeffe, Tommy Polanco, Ayesha Rasool, William Salerno ほか 483 名 - Nature 2023 被引用: 96

  24. Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - JAMA 2019 被引用: 158