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Bradley P. Coe

2004–2023 年に発表

54
論文数
18,779
被引用数
48
h 指数
53
i10 指数

被引用数

Bradley P. Coe の年別被引用数1955 年: 被引用 2 件1993 年: 被引用 1 件2000 年: 被引用 1 件2002 年: 被引用 3 件2004 年: 被引用 24 件2005 年: 被引用 53 件2006 年: 被引用 39 件2007 年: 被引用 35 件2008 年: 被引用 37 件2009 年: 被引用 28 件2010 年: 被引用 36 件2011 年: 被引用 55 件2012 年: 被引用 181 件2013 年: 被引用 311 件2014 年: 被引用 351 件2015 年: 被引用 415 件2016 年: 被引用 359 件2017 年: 被引用 356 件2018 年: 被引用 317 件2019 年: 被引用 875 件2020 年: 被引用 796 件2021 年: 被引用 802 件2022 年: 被引用 600 件2023 年: 被引用 405 件2024 年: 被引用 551 件2025 年: 被引用 181 件2026 年: 被引用 7 件1956〜1992 年は被引用が無いため表示していません1994〜1999 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 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 2,664 件、この内訳の 26.2%イギリス: 引用元論文 798 件、この内訳の 7.8%中国: 引用元論文 680 件、この内訳の 6.7%カナダ: 引用元論文 545 件、この内訳の 5.4%ドイツ: 引用元論文 508 件、この内訳の 5%オランダ: 引用元論文 470 件、この内訳の 4.6%フランス: 引用元論文 432 件、この内訳の 4.2%イタリア: 引用元論文 372 件、この内訳の 3.7%オーストラリア: 引用元論文 301 件、この内訳の 3%スペイン: 引用元論文 255 件、この内訳の 2.5%日本: 引用元論文 236 件、この内訳の 2.3%スイス: 引用元論文 190 件、この内訳の 1.9%
0%26.2%その他 26.7%

機関

分野

  • Biochemistry, Genetics and Molecular Biology63.4%
  • Neuroscience17.9%
  • Medicine13.3%
  • Agricultural and Biological Sciences2.1%
  • Psychology1.3%
  • Immunology and Microbiology0.6%
  • その他1.4%

トピック

  • Genomic variations and chromosomal abnormalities10.1%
  • Genetics and Neurodevelopmental Disorders9.2%
  • Genomics and Rare Diseases7.5%
  • Autism Spectrum Disorder Research7%
  • Congenital heart defects research3.4%
  • Genomics and Phylogenetic Studies3.4%
  • その他59.4%

共著者

全論文

検索で開く
  1. Genome structural variation discovery and genotyping

    著者: Can Alkan, Bradley P. Coe, Evan E. Eichler - Nature Reviews Genetics 2011 被引用: 1,719

  2. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

    著者: Brian J. O’Roak, Laura Vives, Santhosh Girirajan, Emre Karakoç, Niklas Krumm, Bradley P. Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D. Smith, Emily H. Turner, Ian B. Stanaway, Benjamin Vernot, Maika Malig, Carl Baker, Beau Reilly, Joshua M. Akey, Elhanan Borenstein, Mark J. Rieder, Deborah A. Nickerson, Raphael Bernier, Jay Shendure, Evan E. Eichler - Nature 2012 被引用: 2,241

  3. Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases

    著者: Holly A.F. Stessman, Bo Xiong, Bradley P. Coe, Tianyun Wang, Kendra Hoekzema, Michaela Fencková, Malin Kvarnung, Jennifer Gerdts, Sandy Trinh, Nele Cosemans, Laura Vives, Janice Lin, Tychele N. Turner, Gijs W.E. Santen, Claudia Ruivenkamp, Marjolein Kriek, Arie van Haeringen, Emmelien Aten, Kathryn Friend, Jan Liebelt, Christopher Barnett, Eric Haan, Marie Shaw, Jozef Gécz, Britt-Marie Anderlid, Ann Nordgren, Anna Lindstrand, Charles E. Schwartz, R. Frank Kooy, Geert Vandeweyer, Céline Helsmoortel, Corrado Romano, A Alberti, Mirella Vinci, Emanuela Avola, Stefania Giusto, Eric Courchesne, Tiziano Pramparo, Karen Pierce, Srinivasa Nalabolu, David G. Amaral, Ingrid E. Scheffer, Martin B. Delatycki, Paul J. Lockhart, Fereydoun Hormozdiari, Benjamin Harich, Anna Castells‐Nobau, Kun Xia, Hilde Peeters, Magnus Nordenskjöld, Annette Schenck, Raphael Bernier, Evan E. Eichler - Nature Genetics 2017 被引用: 580

  4. 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

  5. Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development

    著者: Raphael Bernier, Christelle Golzio, Bo Xiong, Holly A.F. Stessman, Bradley P. Coe, Osnat Penn, Kali Witherspoon, Jennifer Gerdts, Carl Baker, Anneke T. Vulto-van Silfhout, Janneke Schuurs-Hoeijmakers, Marco Fichera, Paolo Bosco, Serafino Buono, A Alberti, Pinella Failla, Hilde Peeters, Jean Steyaert, Lisenka E.L.M. Vissers, Ludmila Francescatto, Heather C. Mefford, Jill A. Rosenfeld, Trygve E. Bakken, Brian J. O’Roak, Matthew Pawlus, Randall T. Moon, Jay Shendure, David G. Amaral, Ed S. Lein, Julia Rankin, Corrado Romano, Bert de Vries, Nicholas Katsanis, Evan E. Eichler - Cell 2014 被引用: 837

  6. Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders

    著者: Brian J. O’Roak, Laura Vives, Wenqing Fu, Jarrett D. Egertson, Ian B. Stanaway, Ian G. Phelps, Gemma L. Carvill, Akash Kumar, Choli Lee, Katy Ankenman, Jeff Munson, Joseph B. Hiatt, Emily H. Turner, Roie Levy, Diana R. O’Day, Niklas Krumm, Bradley P. Coe, Beth Martin, Elhanan Borenstein, Deborah A. Nickerson, Heather C. Mefford, Dan Doherty, Joshua M. Akey, Raphael Bernier, Evan E. Eichler, Jay Shendure - Science 2012 被引用: 1,300

  7. Refining analyses of copy number variation identifies specific genes associated with developmental delay

    著者: Bradley P. Coe, Kali Witherspoon, Jill A. Rosenfeld, Bregje W.M. van Bon, Anneke T. Vulto‐van Silfhout, Paolo Bosco, Kathryn Friend, Carl Baker, Serafino Buono, Lisenka E.L.M. Vissers, Janneke Schuurs-Hoeijmakers, Alexander Hoischen, Rolph Pfundt, Nik Krumm, Gemma L. Carvill, Deana Li, David G. Amaral, Natasha J. Brown, Paul J. Lockhart, Ingrid E. Scheffer, A Alberti, Marie Shaw, Rosa Pettinato, Raymond C. Tervo, Nicole de Leeuw, Margot R.F. Reijnders, Beth S. Torchia, Hilde Peeters, Elizabeth Thompson, Brian J. O’Roak, Marco Fichera, Jayne Y. Hehir‐Kwa, Jay Shendure, Heather C. Mefford, Eric Haan, Jozef Gécz, Bert B A de Vries, Corrado Romano, Evan E Eichler - Nature Genetics 2014 被引用: 758

  8. A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disorders

    著者: Sébastien Jacquemont, Bradley P. Coe, Micha Hersch, Michael Duyzend, Niklas Krumm, Sven Bergmann, J. Beckmann, Jill A. Rosenfeld, Evan E. Eichler - The American Journal of Human Genetics 2014 被引用: 619

  9. Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity

    著者: Bradley P. Coe, Holly A.F. Stessman, Arvis Sulovari, Madeleine R. Geisheker, Trygve E. Bakken, Allison M. Lake, Joseph D. Dougherty, Ed S. Lein, Fereydoun Hormozdiari, Raphael Bernier, Evan E. Eichler - Nature Genetics 2018 被引用: 371

  10. Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

    著者: Tianyun Wang, Kendra Hoekzema, Davide Vecchio, Huidan Wu, Arvis Sulovari, Bradley P. Coe, Madelyn A. Gillentine, Amy B. Wilfert, Luis A. Pérez‐Jurado, Malin Kvarnung, Yoeri Sleyp, Rachel K. Earl, Jill A. Rosenfeld, Madeleine R. Geisheker, Lin Han, Bing Du, Chris Barnett, E. A. Thompson, Marie Shaw, Renée Carroll, Kathryn Friend, Rachael Catford, Elizabeth E. Palmer, Xiaobing Zou, Jianjun Ou, Honghui Li, Hui Guo, Jennifer Gerdts, Emanuela Avola, Giuseppe Calabrese, Maurizio Elia, Donatella Greco, Anna Lindstrand, Ann Nordgren, Britt‐Marie Anderlid, Geert Vandeweyer, Anke Van Dijck, Nathalie Van der Aa, Brooke G. McKenna, Miroslava Hančárová, Šárka Bendová, Markéta Havlovicová, Giovanni Malerba, Bernardo Dalla Bernardina, Pierandrea Muglia, Arie van Haeringen, Mariëtte J.V. Hoffer, Barbara Franke, Gerarda Cappuccio, Martin B. Delatycki, Paul J. Lockhart, Melanie A. Manning, Pengfei Liu, Ingrid E. Scheffer, Nicola Brunetti‐Pierri, Nanda Rommelse, David G. Amaral, Gijs W.E. Santen, Elisabetta Trabetti, Zdeněk Sedláček, Jacob J. Michaelson, Karen Pierce, Eric Courchesne, R. Frank Kooy, John Acampado, Andrea J. Ace, Alpha Amatya, Irina Astrovskaya, Asif Bashar, Elizabeth Brooks, Martin E. Butler, Lindsey A. Cartner, Wubin Chin, Wendy K. Chung, Amy M. Daniels, Pamela Feliciano, Chris Fleisch, Swami Ganesan, William B. Jensen, Alex Lash, Richard P. Marini, Vincent J. Myers, Eirene O’Connor, Chris Rigby, B. E. Robertson, Neelay Shah, Swapnil Shah, Emily Singer, LeeAnne Green Snyder, Alexandra N. Stephens, Jennifer Tjernagel, Brianna M. Vernoia, Natalia Volfovsky, L. Casey White, Alexander Hsieh, Yufeng Shen, Xueya Zhou, Tychele N. Turner, Ethan Bahl, Taylor Thomas ほか 135 名 - Nature Communications 2020 被引用: 215

  11. Recent ultra-rare inherited variants implicate new autism candidate risk genes

    著者: Amy B. Wilfert, Tychele N. Turner, Shwetha C. Murali, PingHsun Hsieh, Arvis Sulovari, Tianyun Wang, Bradley P. Coe, Hui Guo, Kendra Hoekzema, Trygve E. Bakken, Lara Winterkorn, Uday S. Evani, Marta Byrska-Bishop, Rachel K. Earl, Raphael Bernier, Xueya Zhou, Pamela Feliciano, Jacob B. Hall, Irina Astrovskaya, Simon Xu, Chang Shu, Joseph Obiajulu, Leo Brueggeman, Jessica Wright, Olena Marchenko, Chris Fleisch, Timothy S. Chang, LeeAnne Green Snyder, Sarah D. Barns, Bing Han, William T. Harvey, Andrew Nishida, Ryan N. Doan, Aubrey Soucy, Brian J. O’Roak, Timothy W. Yu, Daniel H. Geschwind, Jacob J. Michaelson, Natalia Volfovsky, Yufeng Shen, Wendy K. Chung, Michael C. Zody, Evan E. Eichler - Nature Genetics 2021 被引用: 143

  12. Genomic Patterns of De Novo Mutation in Simplex Autism

    著者: Tychele N. Turner, Bradley P. Coe, Diane E. Dickel, Kendra Hoekzema, Bradley J. Nelson, Michael C. Zody, Zev Kronenberg, Fereydoun Hormozdiari, Archana N. Raja, L Pennacchio, Robert B. Darnell, Evan E. Eichler - Cell 2017 被引用: 376

  13. De novo genic mutations among a Chinese autism spectrum disorder cohort

    著者: Tianyun Wang, Hui Guo, Bo Xiong, Holly A.F. Stessman, Huidan Wu, Bradley P. Coe, Tychele N. Turner, Yanling Liu, Wenjing Zhao, Kendra Hoekzema, Laura Vives, Lu Xia, Meina Tang, Jianjun Ou, Biyuan Chen, Yidong Shen, Guanglei Xun, Long Min, Janice Lin, Zev Kronenberg, Yu Peng, Ting Bai, Honghui Li, Xiaoyan Ke, Zhengmao Hu, Jingping Zhao, Xiaobing Zou, Kun Xia, Evan E. Eichler - Nature Communications 2016 被引用: 393

  14. Copy number variation detection and genotyping from exome sequence data

    著者: Niklas Krumm, Peter H. Sudmant, Arthur Ko, Brian J. O’Roak, Maika Malig, Bradley P. Coe, NHLBI Exome Sequencing Project, Aaron R. Quinlan, Deborah A. Nickerson, Evan E. Eichler - Genome Research 2012 被引用: 676

  15. Excess of rare, inherited truncating mutations in autism

    著者: Niklas Krumm, Tychele N. Turner, Carl Baker, Laura Vives, Kiana Mohajeri, Kali Witherspoon, Archana N. Raja, Bradley P. Coe, Holly A.F. Stessman, Zong-Xiao He, Suzanne M. Leal, Raphael Bernier, Evan E. Eichler - Nature Genetics 2015 被引用: 635

  16. Global diversity, population stratification, and selection of human copy-number variation

    著者: Peter H. Sudmant, Swapan Mallick, Bradley J. Nelson, Fereydoun Hormozdiari, Niklas Krumm, John Huddleston, Bradley P. Coe, Carl Baker, Susanne Nordenfelt, Michael J. Bamshad, Lynn B. Jorde, Olga L. Posukh, Hovhannes Sahakyan, W. Scott Watkins, Levon Yepiskoposyan, Muhammad Syafiq Abdullah, Cláudio M. Bravi, Cristian Capelli, Tor Hervig, Joseph Wee, Chris Tyler‐Smith, George van Driem, Irene Gallego Romero, Aashish R. Jha, Sena Karachanak-Yankova, Драга Тончева, David Comas, Brenna M. Henn, Toomas Kivisild, Andrés Ruiz‐Linares, Antti Sajantila, Ene Metspalu, Jüri Parik, Richard Villems, Elena B. Starikovskaya, George Ayodo, Cynthia M. Beall, Anna Di Rienzo, Michael F. Hammer, Р. И. Хусаинова, Э. К. Хуснутдинова, William Klitz, Cheryl A. Winkler, Damian Labuda, Mait Metspalu, Sarah A. Tishkoff, Stanislav Dryomov, R. I. Sukernik, Nick Patterson, David Reich, Evan E. Eichler - Science 2015 被引用: 378

  17. A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP

    著者: Céline Helsmoortel, Anneke T. Vulto-van Silfhout, Bradley P. Coe, Geert Vandeweyer, Liesbeth Rooms, Jenneke van den Ende, Janneke Schuurs-Hoeijmakers, Carlo Marcelis, Marjolein H. Willemsen, Lisenka E.L.M. Vissers, Helger G. Yntema, Madhura Bakshi, Meredith Wilson, Kali Witherspoon, Helena Malmgren, Ann Nordgren, Göran Annerén, Marco Fichera, Paolo Bosco, Corrado Romano, Bert B.A. de Vries, Tjitske Kleefstra, R. Frank Kooy, Evan E. Eichler, Nathalie Van der Aa - Nature Genetics 2014 被引用: 377

  18. Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group

    著者: Ryan J. Schmidt, Marcie Steeves, Pınar Bayrak‐Toydemir, Katherine A. Benson, Bradley P. Coe, Laura K. Conlin, Mythily Ganapathi, John Garcia, Michael H. Gollob, Vaidehi Jobanputra, Minjie Luo, Deqiong Ma, Glenn A. Maston, Kelly McGoldrick, Timothy Blake Palculict, Tina Pesaran, Toni I. Pollin, Emily Qian, Heidi L. Rehm, Erin Rooney Riggs, Samantha L.P. Schilit, Panagiotis I. Sergouniotis, Tatiana Tvrdik, Nicholas Watkins, Lauren Zec, Wenying Zhang, Matthew S. Lebo, Alicia B. Byrne, Amanda B. Spurdle, Blake Palculict, Bradley P. Coe, Ma Deqiong, Elaine Lyon, Emily Groopman, Emily Qian, Erik G. Puffenberger, Erin Rooney Riggs, Fergus J. Couch, Glenn Maston, Hannah Dziadzio, James Harraway, Jessica L. Mester, John Garcia, Jordan Lerner‐Ellis, Katherine A. Benson, Kayleigh Avello, Kelly McGoldrick, Laura K. Conlin, Lauren Zec, Marcie Steeves, Marcy E. Richardson, Matthew S. Lebo, Melissa Kelly, Michael H. Gollob, Minjie Luo, Mythily Ganapathi, Nicholas Watkins, Nifang Niu, Panagiotis I. Sergouniotis, Pınar Bayrak‐Toydemir, Ryan J. Schmidt, Samantha L.P. Schilit, Sarah Richards, Tina Pesaran, Toni I. Pollin, Vaidehi Jobanputra, Wenying Zhang, Wuyan Chen, Yuxin Fan - Genetics in Medicine 2023 被引用: 69

  19. Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants

    著者: Santhosh Girirajan, Jill A. Rosenfeld, Bradley P. Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A. Filipink, Juliann McConnell, Brad Angle, Wendy S. Meschino, Marjan M. Nezarati, Alexander Asamoah, Kelly E. Jackson, Gordon C. Gowans, Judith A. Martin, Erin P. Carmany, David W. Stockton, Rhonda E. Schnur, Lynette S. Penney, Donna M. Martin, Salmo Raskin, Kathleen A. Leppig, Heidi Thiese, Rosemarie Smith, Erika Aberg, Dmitriy M. Niyazov, Luis Escobar, Dima El‐Khechen, Kisha Johnson, Robert Roger Lebel, Kiana Siefkas, Susie Ball, Natasha Shur, Marianne McGuire, Campbell K. Brasington, J. Edward Spence, Laura Martin, Carol L. Clericuzio, Blake C. Ballif, Lisa G. Shaffer, Evan E. Eichler - New England Journal of Medicine 2012 被引用: 634

  20. Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID

    著者: Bregje W.M. van Bon, Bradley P. Coe, Raphael Bernier, Cherie Green, Jennifer Gerdts, Kali Witherspoon, Tjitske Kleefstra, Marjolein H. Willemsen, Raman Kumar, Paolo Bosco, Marco Fichera, Denglin Li, David G. Amaral, Francesca Cristofoli, Hilde Peeters, E Haan, Corrado Romano, Heather C. Mefford, Ingrid E. Scheffer, Jozef Gécz, Bert B.A. de Vries, Evan E. Eichler - Molecular Psychiatry 2015 被引用: 207

  21. Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model

    著者: Hui Guo, Tianyun Wang, Huidan Wu, Long Min, Bradley P. Coe, Honghui Li, Guanglei Xun, Jianjun Ou, Biyuan Chen, Guiqin Duan, Ting Bai, Ningxia Zhao, Yidong Shen, Yun Li, Yazhe Wang, Yu Zhang, Carl Baker, Yanling Liu, Nan Pang, Lian Huang, Lin Han, Xiangbin Jia, Cenying Liu, Hailun Ni, Xinyi Yang, Lu Xia, Jingjing Chen, Lu Shen, Ying Li, Rongjuan Zhao, Wenjing Zhao, Jing Peng, Qian Pan, Zhigao Long, Wei Su, Jieqiong Tan, Xiaogang Du, Xiaoyan Ke, Meiling Yao, Zhengmao Hu, Xiaobing Zou, Jingping Zhao, Raphael Bernier, Evan E. Eichler, Kun Xia - Molecular Autism 2018 被引用: 170

  22. Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes

    著者: Hui Guo, Michael Duyzend, Bradley P. Coe, Carl Baker, Kendra Hoekzema, Jennifer Gerdts, Tychele N. Turner, Michael C. Zody, Jennifer S. Beighley, Shwetha C. Murali, Bradley J. Nelson, Michael J. Bamshad, Deborah A. Nickerson, Raphael Bernier, Evan E. Eichler - Genetics in Medicine 2018 被引用: 146

  23. Estimates of penetrance for recurrent pathogenic copy-number variations

    著者: Jill A. Rosenfeld, Bradley P. Coe, Evan E. Eichler, Howard Cuckle, Lisa G. Shaffer - Genetics in Medicine 2012 被引用: 433

  24. Molecular Genetic Anatomy and Risk Profile of Hirschsprung’s Disease

    著者: Joseph M. Tilghman, Albee Y. Ling, Tychele N. Turner, Maria X. Sosa, Niklas Krumm, Sumantra Chatterjee, Ashish Kapoor, Bradley P. Coe, Khanh-Dung H. Nguyen, Namrata Gupta, Stacey Gabriel, Evan E. Eichler, Courtney Berrios, Aravinda Chakravarti - New England Journal of Medicine 2019 被引用: 188