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Gregory M. Cooper

2001–2024 年に発表

109
論文数
38,609
被引用数
72
h 指数
102
i10 指数

被引用数

Gregory M. Cooper の年別被引用数1951 年: 被引用 1 件1955 年: 被引用 2 件1960 年: 被引用 1 件1985 年: 被引用 1 件1992 年: 被引用 1 件1996 年: 被引用 1 件1998 年: 被引用 1 件1999 年: 被引用 1 件2000 年: 被引用 1 件2001 年: 被引用 7 件2003 年: 被引用 15 件2004 年: 被引用 67 件2005 年: 被引用 80 件2006 年: 被引用 71 件2007 年: 被引用 87 件2008 年: 被引用 314 件2009 年: 被引用 445 件2010 年: 被引用 466 件2011 年: 被引用 521 件2012 年: 被引用 463 件2013 年: 被引用 473 件2014 年: 被引用 465 件2015 年: 被引用 604 件2016 年: 被引用 536 件2017 年: 被引用 562 件2018 年: 被引用 587 件2019 年: 被引用 1,505 件2020 年: 被引用 1,425 件2021 年: 被引用 1,352 件2022 年: 被引用 1,034 件2023 年: 被引用 638 件2024 年: 被引用 1,091 件2025 年: 被引用 510 件2026 年: 被引用 29 件1952〜1954 年は被引用が無いため表示していません1956〜1959 年は被引用が無いため表示していません1961〜1984 年は被引用が無いため表示していません1986〜1991 年は被引用が無いため表示していません1993〜1995 年は被引用が無いため表示していません1997 年は被引用が無いため表示していません2002 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 6,262 件、この内訳の 25.4%イギリス: 引用元論文 2,085 件、この内訳の 8.5%ドイツ: 引用元論文 1,455 件、この内訳の 5.9%中国: 引用元論文 1,248 件、この内訳の 5.1%カナダ: 引用元論文 1,132 件、この内訳の 4.6%フランス: 引用元論文 1,020 件、この内訳の 4.2%オランダ: 引用元論文 944 件、この内訳の 3.8%イタリア: 引用元論文 908 件、この内訳の 3.7%オーストラリア: 引用元論文 871 件、この内訳の 3.5%スペイン: 引用元論文 650 件、この内訳の 2.6%スウェーデン: 引用元論文 547 件、この内訳の 2.2%日本: 引用元論文 506 件、この内訳の 2.1%
0%25.4%その他 28.4%

機関

分野

  • Biochemistry, Genetics and Molecular Biology61.9%
  • Medicine23.9%
  • Neuroscience5.3%
  • Immunology and Microbiology2.4%
  • Agricultural and Biological Sciences1.4%
  • Engineering1.4%
  • その他3.7%

トピック

  • Genomics and Rare Diseases8.1%
  • Genomic variations and chromosomal abnormalities5.1%
  • Genetic Associations and Epidemiology4.2%
  • Genomics and Phylogenetic Studies3.7%
  • Genetics and Neurodevelopmental Disorders3.1%
  • Genomics and Chromatin Dynamics2.3%
  • その他73.5%

共著者

全論文

検索で開く
  1. A general framework for estimating the relative pathogenicity of human genetic variants

    著者: Martin Kircher, Daniela Witten, Preti Jain, Brian J. O’Roak, Gregory M. Cooper, Jay Shendure - Nature Genetics 2014 被引用: 6,554

  2. Yehudi: An Orchestrated System for the Interoperability of Urban Data and Models

    著者: Philipp Rentzsch, Daniela M. Witten, Gregory M. Cooper, Jay Shendure, Martin Kircher - Nucleic Acids Research, Nucleic Acids Res. 2001 被引用: 3,880

  3. Identifying a High Fraction of the Human Genome to be under Selective Constraint Using GERP++

    著者: Eugene Davydov, David L. Goode, Marina Sirota, Gregory M. Cooper, Arend Sidow, Serafim Batzoglou - PLoS Computational Biology, PLoS Comput. Biol. 2010 被引用: 1,877

  4. Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

    著者: Elizabeth T. Cirulli, Brittany N. Lasseigne, Slavé Petrovski, Peter C. Sapp, Patrick A. Dion, Claire S. Leblond, Julien Couthouis, Yifan Lu, Quanli Wang, Brian J. Krueger, Zhong Ren, Jonathan Keebler, Yujun Han, Shawn Levy, Braden Boone, Jack R. Wimbish, Lindsay L. Waite, Angela L. Jones, John P. Carulli, Kelly L. Williams, John F. Staropoli, Winnie Xin, Alessandra Chesi, Alya R. Raphael, Diane McKenna‐Yasek, Janet Cady, J.M.B.V. de Jong, Kevin P. Kenna, Bradley Smith, Simon Topp, Jack W. Miller, Soragia Athina Gkazi, Ammar Al‐Chalabi, Leonard H. van den Berg, Jan H. Veldink, Vincenzo Silani, Nicola Ticozzi, Christopher E. Shaw, Robert H. Baloh, Stanley H. Appel, Ericka Simpson, Clotilde Lagier‐Tourenne, Stefan M. Pulst, Summer Gibson, John Q. Trojanowski, Lauren Elman, Leo McCluskey, Murray Grossman, Neil A. Shneider, Wendy K. Chung, John Ravits, Jonathan D. Glass, Katherine B. Sims, Vivianna M. Van Deerlin, Tom Maniatis, Sebastian Hayes, Alban Ordureau, Sharan Swarup, John E. Landers, Frank Baas, Andrew S. Allen, Richard Bedlack, J. Wade Harper, Aaron D. Gitler, Guy A. Rouleau, Robert H. Brown, Matthew B. Harms, Gregory M. Cooper, Tim Harris, R Myers, David B. Goldstein - Science 2015 被引用: 992

  5. A copy number variation morbidity map of developmental delay

    著者: Gregory M. Cooper, Bradley P. Coe, Santhosh Girirajan, Jill A. Rosenfeld, Tiffany Vu, Carl Baker, Charles A. Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig, Hoda Abdel‐Hamid, Patricia I. Bader, Elizabeth McCracken, Dmitriy Niyazov, Kathleen A. Leppig, Heidi Thiese, Marybeth Hummel, Nora Alexander, Jerome L. Gorski, Jennifer Kussmann, Vandana Shashi, Krys Johnson, Catherine Rehder, Blake C. Ballif, Lisa G. Shaffer, Evan E. Eichler - Nature Genetics 2011 被引用: 1,404

  6. Massively parallel functional dissection of mammalian enhancers in vivo

    著者: Rupali P Patwardhan, Joseph B. Hiatt, Daniela Witten, Mee J. Kim, Robin P. Smith, Dalit May, Choli Lee, Jennifer M. Andrie, Su In Lee, Gregory M. Cooper, Nadav Ahituv, L Pennacchio, Jay Shendure - Nature Biotechnology 2012 被引用: 584

  7. Single-cell multi-cohort dissection of the schizophrenia transcriptome

    著者: W. Brad Ruzicka, Shahin Mohammadi, John F. Fullard, José Dávila-Velderrain, Sivan Subburaju, Daniel Reed Tso, Makayla Hourihan, Shan Jiang, Hao-Chih Lee, Jaroslav Bendl, Georgios Voloudakis, Vahram Haroutunian, Gabriel E. Hoffman, Panos Roussos, Manolis Kellis, Schahram Akbarian, Alexej Abyzov, Nadav Ahituv, Dhivya Arasappan, José Juan Almagro Armenteros, Brian J. Beliveau, Sabina Berretta, Rahul Bharadwaj, Arjun Bhattacharya, Lucy Bicks, Kristen Brennand, Davide Capauto, Frances A. Champagne, Tanima Chatterjee, Chris Chatzinakos, Yuhang Chen, H. Isaac Chen, Yuyan Cheng, Lijun Cheng, Andrew Chess, Jo-fan Chien, Zhiyuan Chu, Declan Clarke, Ashley Clement, Leonardo Collado‐Torres, Gregory M. Cooper, Gregory E. Crawford, Rujia Dai, Nikolaos P. Daskalakis, Amy Deep‐Soboslay, Chengyu Deng, Christopher P. DiPietro, Stella Dracheva, Shiron Drusinsky, Ziheng Duan, Duc M. Duong, Cagatay Dursun, Nicholas J. Eagles, Jonathan I. Edelstein, Prashant S. Emani, Kiki Galani, Timur R. Galeev, Michael J. Gandal, Sophia C. Gaynor, Mark Gerstein, Daniel H. Geschwind, Kiran Girdhar, Fernando S. Goes, William Greenleaf, Jennifer Grundman, Hanmin Guo, Qiuyu Guo, Chirag Gupta, Yoav Hadas, Joachim Hallmayer, Xikun Han, Natalie Hawken, Chuan He, Ella Henry, Stephanie C. Hicks, Marcus Ho, Li‐Lun Ho, Yi‐Ling Huang, Louise A. Huuki-Myers, Ahyeon Hwang, Thomas M. Hyde, Artemis Iatrou, Fumitaka Inoue, Aarti Jajoo, Matthew L. Jensen, Lihua Jiang, Peng Jin, Ting Jin, Connor Jops, Alexandre Jourdon, Riki Kawaguchi, Joel E. Kleinman, Steven P. Kleopoulos, Alexey Kozlenkov, Arnold R. Kriegstein, Anshul Kundaje, Soumya Kundu, Che-Yu Lee, Donghoon Lee, Junhao Li ほか 119 名 - Science 2024 被引用: 131

  8. Distribution and intensity of constraint in mammalian genomic sequence

    著者: Gregory M. Cooper, Eric A. Stone, George Asimenos, Eric D. Green, Serafim Batzoglou, Arend Sidow - Genome Research 2005 被引用: 1,444

  9. Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

    著者: Sarah Ng, Abigail W. Bigham, Kati J. Buckingham, Mark Hannibal, Margaret J. McMillin, Heidi Gildersleeve, Anita E. Beck, Holly K. Tabor, Gregory M. Cooper, Heather C Mefford, Choli Lee, Emily H. Turner, Joshua D. Smith, Mark J. Rieder, Koh-ichiro Yoshiura, Naomichi Matsumoto, Tohru Ohta, Norio Niikawa, Deborah A. Nickerson, Michael J. Bamshad, Jay Shendure - Nature Genetics 2010 被引用: 1,355

  10. Guidelines for investigating causality of sequence variants in human disease

    著者: Daniel G. MacArthur, Teri A. Manolio, David Dimmock, Heidi L. Rehm, Jay Shendure, Gonçalo R. Abecasis, David R. Adams, Russ B. Altman, Stylianos E. Antonarakis, Euan A. Ashley, Jeffrey C. Barrett, Leslie G. Biesecker, Don F. Conrad, Gregory M. Cooper, Nancy J. Cox, Mark J. Daly, Mark Gerstein, David B. Goldstein, Joel N. Hirschhorn, Suzanne M. Leal, L Pennacchio, J Stamatoyannopoulos, Shamil Sunyaev, David Valle, Benjamin F. Voight, Wendy Winckler, Chris Gunter - Nature 2014 被引用: 1,288

  11. Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

    著者: Tom Walsh, Jon McClellan, Shane McCarthy, Anjené Addington, Sarah B. Pierce, Gregory M. Cooper, Alex S. Nord, Mary Kusenda, Dheeraj Malhotra, Abhishek Bhandari, Sunday M. Stray, Caitlin Rippey, Patricia Roccanova, Vlad Makarov, B. Lakshmi, Robert L. Findling, Linmarie Sikich, T Stromberg, Barry Merriman, Nitin Gogtay, Philip Butler, Kristen Eckstrand, Laila Noory, Peter Gochman, Robert T. Long, Zugen Chen, Sean Davis, Carl Baker, Evan E. Eichler, Paul S. Meltzer, Stanley F. Nelson, Andrew Singleton, Ming K. Lee, Judith L. Rapoport, Mary‐Claire King, Jonathan Sebat - Science 2008 被引用: 1,832

  12. Distinct Properties of Cell-Type-Specific and Shared Transcription Factor Binding Sites

    著者: Jason Gertz, Daniel Savic, Katherine E. Varley, E. Christopher Partridge, Alexias Safi, Preti Jain, Gregory M. Cooper, Timothy E. Reddy, Gregory E. Crawford, R Myers - Molecular Cell 2013 被引用: 422

  13. A systematic comparison reveals substantial differences in chromosomal versus episomal encoding of enhancer activity

    著者: Fumitaka Inoue, Martin Kircher, Beth Martin, Gregory M. Cooper, Daniela Witten, Michael T. McManus, Nadav Ahituv, Jay Shendure - Genome Research 2016 被引用: 360

  14. LAGAN and Multi-LAGAN: Efficient Tools for Large-Scale Multiple Alignment of Genomic DNA

    著者: Michael Brudno, Chuong B. Do, Gregory M. Cooper, Michael F. Kim, Eugene Davydov, NISC Comparative Sequencing Program, Eric D. Green, Arend Sidow, Serafim Batzoglou - Genome Research 2003 被引用: 1,154

  15. Massively parallel characterization of regulatory elements in the developing human cortex

    著者: Chengyu Deng, Sean Whalen, Marilyn Steyert, Ryan Ziffra, Pawel F. Przytycki, Fumitaka Inoue, Daniela A. Pereira, Davide Capauto, Scott Norton, Flora M. Vaccarino, Alex A. Pollen, Tomasz J. Nowakowski, Nadav Ahituv, Katherine S. Pollard, Schahram Akbarian, Alexej Abyzov, Nadav Ahituv, Dhivya Arasappan, José Juan Almagro Armenteros, Brian J. Beliveau, Jaroslav Bendl, Sabina Berretta, Rahul Bharadwaj, Arjun Bhattacharya, Lucy Bicks, Kristen Brennand, Davide Capauto, Frances A. Champagne, Tanima Chatterjee, Chris Chatzinakos, Yuhang Chen, H. Isaac Chen, Yuyan Cheng, Lijun Cheng, Andrew Chess, Jo-fan Chien, Zhiyuan Chu, Declan Clarke, Ashley Clement, Leonardo Collado‐Torres, Gregory M. Cooper, Gregory E. Crawford, Rujia Dai, Nikolaos P. Daskalakis, José Dávila-Velderrain, Amy Deep‐Soboslay, Chengyu Deng, Christopher P. DiPietro, Stella Dracheva, Shiron Drusinsky, Ziheng Duan, Duc M. Duong, Cagatay Dursun, Nicholas J. Eagles, Jonathan I. Edelstein, Prashant S. Emani, John F. Fullard, Kiki Galani, Timur R. Galeev, Michael J. Gandal, Sophia C. Gaynor, Mark Gerstein, Daniel H. Geschwind, Kiran Girdhar, Fernando S. Goes, William J. Greenleaf, Jennifer Grundman, Hanmin Guo, Qiuyu Guo, Chirag Gupta, Yoav Hadas, Joachim Hallmayer, Xikun Han, Vahram Haroutunian, Natalie Hawken, Chuan He, Ella Henry, Stephanie C. Hicks, Marcus Ho, Li‐Lun Ho, Gabriel E. Hoffman, Yi‐Ling Huang, Louise A. Huuki-Myers, Ahyeon Hwang, Thomas M. Hyde, Artemis Iatrou, Fumitaka Inoue, Aarti Jajoo, Matthew L. Jensen, Lihua Jiang, Jin Peng, Ting Jin, Connor Jops, Alexandre Jourdon, Riki Kawaguchi, Manolis Kellis, Saniya Khullar, Joel E. Kleinman, Steven P. Kleopoulos, Alexey Kozlenkov ほか 131 名 - Science 2024 被引用: 65

  16. Genomic diagnosis for children with intellectual disability and/or developmental delay

    著者: Kevin M. Bowling, Michelle L. Thompson, Michelle D. Amaral, Candice R. Finnila, Susan M. Hiatt, Krysta L. Engel, J. Nicholas Cochran, Kyle B. Brothers, Kelly M. East, Stacy W. Gray, Whitley V. Kelley, Neil E. Lamb, Edward J. Lose, Carla A. Rich, Shirley Simmons, Jana Whittle, Benjamin T. Weaver, Amy S. Nesmith, R Myers, Gregory S. Barsh, E. Martina Bebin, Gregory M. Cooper - Genome Medicine 2017 被引用: 282

  17. A data-driven single-cell and spatial transcriptomic map of the human prefrontal cortex

    著者: Louise A. Huuki-Myers, Abby Spangler, Nicholas J. Eagles, Kelsey D. Montgomery, Sang Ho Kwon, Boyi Guo, Melissa Grant‐Peters, Heena R. Divecha, Madhavi Tippani, Chaichontat Sriworarat, Annie B. Nguyen, Prashanthi Ravichandran, Matthew N. Tran, Arta Seyedian, Thomas M. Hyde, Joel E. Kleinman, Alexis Battle, Stephanie C. Page, Mina Ryten, Stephanie C. Hicks, Keri Martinowich, Leonardo Collado‐Torres, Kristen R. Maynard, Schahram Akbarian, Alexej Abyzov, Nadav Ahituv, Dhivya Arasappan, José Juan Almagro Armenteros, Brian J. Beliveau, Jaroslav Bendl, Sabina Berretta, Rahul Bharadwaj, Arjun Bhattacharya, Lucy Bicks, Kristen Brennand, Davide Capauto, Frances A. Champagne, Tanima Chatterjee, Chris Chatzinakos, Yuhang Chen, H. Isaac Chen, Yuyan Cheng, Lijun Cheng, Andrew Chess, Jo-fan Chien, Zhiyuan Chu, Declan Clarke, Ashley Clement, Leonardo Collado‐Torres, Gregory M. Cooper, Gregory E. Crawford, Rujia Dai, Nikolaos P. Daskalakis, José Dávila-Velderrain, Amy Deep‐Soboslay, Chengyu Deng, Christopher P. DiPietro, Stella Dracheva, Shiron Drusinsky, Ziheng Duan, Duc M. Duong, Cagatay Dursun, Nicholas J. Eagles, Jonathan I. Edelstein, Prashant S. Emani, John F. Fullard, Kiki Galani, Timur R. Galeev, Michael J. Gandal, Sophia C. Gaynor, Mark Gerstein, Daniel H. Geschwind, Kiran Girdhar, Fernando S. Goes, William Greenleaf, Jennifer Grundman, Hanmin Guo, Qiuyu Guo, Chirag Gupta, Yoav Hadas, Joachim Hallmayer, Xikun Han, Vahram Haroutunian, Natalie Hawken, Chuan He, Ella Henry, Stephanie C. Hicks, Marcus Ho, Li‐Lun Ho, Gabriel E. Hoffman, Yi‐Ling Huang, Louise A. Huuki-Myers, Ahyeon Hwang, Thomas M. Hyde, Artemis Iatrou, Fumitaka Inoue, Aarti Jajoo, Matthew Jensen, Lihua Jiang, Peng Jin ほか 135 名 - Science 2024 被引用: 65

  18. Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium

    著者: Laura M. Amendola, Gail P. Jarvik, Michael C. Leo, Heather M. McLaughlin, Yassmine Akkari, Michelle D. Amaral, Jonathan S. Berg, Sawona Biswas, Kevin M. Bowling, Laura K. Conlin, Gregory M. Cooper, Michael O. Dorschner, Matthew C. Dulik, Arezou A. Ghazani, Rajarshi Ghosh, Robert C. Green, Ragan Hart, Carolyn Horton, Jennifer J. Johnston, Matthew S. Lebo, Aleksandar Milosavljević, Jeffrey Ou, Christine M. Pak, Ronak Y. Patel, Sumit Punj, Carolyn Sue Richards, Joseph S Salama, Natasha T. Strande, Yaping Yang, Sharon E. Plon, Leslie G. Biesecker, Heidi L. Rehm - The American Journal of Human Genetics 2016 被引用: 580

  19. Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies

    著者: Gemma L. Carvill, Krysta L. Engel, Aishwarya Ramamurthy, J. Nicholas Cochran, Jolien Roovers, Hannah Stamberger, Nicholas Lim, Amy Schneider, Georgie Hollingsworth, Dylan H. Holder, Brigid M. Regan, James M.J. Lawlor, Lieven Lagae, Berten Ceulemans, E. Martina Bebin, John Nguyen, Gregory S. Barsh, Sarah Weckhuysen, Miriam H. Meisler, Samuel F. Berkovic, Peter De Jonghe, Ingrid E. Scheffer, R Myers, Gregory M. Cooper, Heather C. Mefford, Pasquale Striano, Federico Zara, Ingo Helbig, Rikke S. Møller, Sarah von Spiczak, Hiltrud Muhle, Hande Çağlayan, Katalin Štěrbová, Dana Craiu, Dorota Hoffman, Anna‐Elina Lehesjoki, Kaja Kristine Selmer, Christel Depienne, Johannes R. Lemke, Carla Marini, Renzo Guerrini, Bernd A. Neubauer, Tiina Talvik, Eric Leguern, Peter De Jonghe, Sarah Weckhuysen - The American Journal of Human Genetics 2018 被引用: 122

  20. Genome sequencing as a first-line diagnostic test for hospitalized infants

    著者: Kevin M. Bowling, Michelle L. Thompson, Candice R. Finnila, Susan M. Hiatt, Donald R. Latner, Michelle D. Amaral, James M.J. Lawlor, Kelly M. East, Meagan E. Cochran, Veronica Greve, Whitley V. Kelley, Stacy W. Gray, Stephanie A. Felker, Hannah Meddaugh, Ashley Cannon, Amanda Luedecke, Kelly E. Jackson, Laura G. Hendon, Hillary M. Janani, Marla Johnston, Lee Ann Merin, Sarah Deans, Carly Tuura, Heather Williams, Kelly Laborde, Matthew B. Neu, Jessica Patrick‐Esteve, Anna Hurst, Jegen Kandasamy, Wally Carlo, Kyle B. Brothers, Brian Kirmse, Renate Savich, Duane Superneau, Steven B. Spedale, Sara J. Knight, Gregory S. Barsh, Bruce R. Korf, Gregory M. Cooper - Genetics in Medicine 2021 被引用: 56

  21. University of Kentucky Sanders-Brown Healthy Brain Aging Volunteers: Donor Characteristics, Procedures and Neuropathology

    著者: Frederick A. Schmitt, Peter T. Nelson, Erin L. Abner, Stephen W. Scheff, Gregory A. Jicha, Charles D. Smith, Gregory M. Cooper, Marta Mendiondo, Deborah D. Danner, Linda J. Van Eldik, Allison Caban‐Holt, Mark A. Lovell, Richard J. Kryscio - Current Alzheimer Research 2012 被引用: 192

  22. Long-read genome sequencing for the molecular diagnosis of neurodevelopmental disorders

    著者: Susan M. Hiatt, James M.J. Lawlor, Lori H. Handley, Ryne C. Ramaker, Brianne B. Rogers, E. Christopher Partridge, Lori Beth Boston, Melissa Williams, Christopher Plott, Jerry Jenkins, Stacy W. Gray, James Holt, Kevin M. Bowling, E. Martina Bebin, Jane Grimwood, Jeremy Schmutz, Gregory M. Cooper - Human Genetics and Genomics Advances 2021 被引用: 57

  23. Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

    著者: Sekar Kathiresan, Olle Melander, Candace Guiducci, Aarti Surti, Noël P. Burtt, Mark J. Rieder, Gregory M. Cooper, Charlotta Roos, Benjamin F. Voight, Aki S. Havulinna, Björn Wahlstrand, Thomas Hedner, Dolores Corella, E Shyong Tai, José M. Ordovás, Göran Berglund, Erkki Vartiainen, Pekka Jousilahti, Bo Hedblad, Marja‐Riitta Taskinen, Christopher Newton‐Cheh, Veikko Salomaa, Leena Peltonen, Leif Groop, David Altshuler, Marju Orho‐Melander - Nature Genetics 2008 被引用: 1,407

  24. A general framework for estimating the relative pathogenicity of human genetic variants

    著者: Martin Kircher, Daniela Witten, Gregory M. Cooper, Jay Shendure - F1000Research 2014 被引用: 229