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David H. Ledbetter

1980–2025 年に発表

173
論文数
49,459
被引用数
111
h 指数
168
i10 指数

被引用数

David H. Ledbetter の年別被引用数1980 年: 被引用 1 件1981 年: 被引用 2 件1982 年: 被引用 3 件1983 年: 被引用 9 件1984 年: 被引用 27 件1985 年: 被引用 13 件1986 年: 被引用 32 件1987 年: 被引用 18 件1988 年: 被引用 27 件1989 年: 被引用 64 件1990 年: 被引用 153 件1991 年: 被引用 193 件1992 年: 被引用 220 件1993 年: 被引用 200 件1994 年: 被引用 177 件1995 年: 被引用 150 件1996 年: 被引用 130 件1997 年: 被引用 219 件1998 年: 被引用 240 件1999 年: 被引用 226 件2000 年: 被引用 258 件2001 年: 被引用 256 件2002 年: 被引用 233 件2003 年: 被引用 212 件2004 年: 被引用 203 件2005 年: 被引用 198 件2006 年: 被引用 152 件2007 年: 被引用 220 件2008 年: 被引用 367 件2009 年: 被引用 371 件2010 年: 被引用 347 件2011 年: 被引用 367 件2012 年: 被引用 363 件2013 年: 被引用 426 件2014 年: 被引用 389 件2015 年: 被引用 472 件2016 年: 被引用 453 件2017 年: 被引用 462 件2018 年: 被引用 454 件2019 年: 被引用 1,219 件2020 年: 被引用 1,286 件2021 年: 被引用 1,306 件2022 年: 被引用 1,038 件2023 年: 被引用 639 件2024 年: 被引用 1,001 件2025 年: 被引用 437 件2026 年: 被引用 32 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 6,600 件、この内訳の 33%イギリス: 引用元論文 1,818 件、この内訳の 9.1%カナダ: 引用元論文 1,025 件、この内訳の 5.1%ドイツ: 引用元論文 952 件、この内訳の 4.8%中国: 引用元論文 864 件、この内訳の 4.3%オランダ: 引用元論文 747 件、この内訳の 3.7%イタリア: 引用元論文 746 件、この内訳の 3.7%フランス: 引用元論文 694 件、この内訳の 3.5%オーストラリア: 引用元論文 656 件、この内訳の 3.3%日本: 引用元論文 508 件、この内訳の 2.6%スペイン: 引用元論文 436 件、この内訳の 2.2%スウェーデン: 引用元論文 374 件、この内訳の 1.9%
0%33%その他 22.8%

機関

分野

  • Biochemistry, Genetics and Molecular Biology53.1%
  • Medicine27.8%
  • Neuroscience13.3%
  • Psychology1.2%
  • Agricultural and Biological Sciences1%
  • Computer Science0.8%
  • その他2.8%

トピック

  • Genomic variations and chromosomal abnormalities7.4%
  • Genomics and Rare Diseases5.9%
  • Genetics and Neurodevelopmental Disorders5.7%
  • Autism Spectrum Disorder Research4.4%
  • Prenatal Screening and Diagnostics3.2%
  • Congenital heart defects research2.5%
  • その他70.9%

共著者

全論文

検索で開く
  1. ClinGen — The Clinical Genome Resource

    著者: Heidi L. Rehm, Jonathan S. Berg, Lisa Brooks, Carlos D. Bustamante, James P. Evans, Melissa Landrum, David H. Ledbetter, Donna Maglott, Christa Lese Martin, Robert L. Nussbaum, Sharon E. Plon, Erin M. Ramos, Stephen T. Sherry, Michael S. Watson - New England Journal of Medicine 2015 被引用: 1,537

  2. Feasibility of blood testing combined with PET-CT to screen for cancer and guide intervention

    著者: Anne Marie Lennon, Adam H. Buchanan, Isaac Kinde, Andrew Warren, Ashley Honushefsky, Ariella Cohain, David H. Ledbetter, Fred Sanfilippo, Kathleen Sheridan, Dillenia Rosica, Christian S. Adonizio, Hee Jung Hwang, Kamel Lahouel, Joshua D. Cohen, Christopher Douville, Aalpen A. Patel, Leonardo N. Hagmann, David D.K. Rolston, Nirav Malani, Shibin Zhou, Chetan Bettegowda, David L. Diehl, Bobbi Urban, Christopher D. Still, Lisa Kann, Julie Woods, Zachary Salvati, Joseph Vadakara, Rosemary Leeming, Prianka Bhattacharya, Carroll N. Walter, Alex Parker, Christoph Lengauer, Alison P. Klein, Cristian Tomasetti, Elliot K. Fishman, Ralph H. Hruban, Kenneth W. Kinzler, Bert Vogelstein, Nickolas Papadopoulos - Science 2020 被引用: 676

  3. Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease

    著者: Frederick E. Dewey, Viktoria Gusarova, Richard L. Dunbar, Colm O’Dushlaine, Claudia Schurmann, Omri Gottesman, Shane McCarthy, Cristopher V. Van Hout, Shannon Bruse, Hayes M. Dansky, Joseph B. Leader, Michael F. Murray, Marylyn D. Ritchie, H. Lester Kirchner, Lukas Habegger, Alex Lopez, John S. Penn, An Sha Zhao, Weiping Shao, Neil Stahl, Andrew Murphy, Sara Hamon, Aurelie Bouzelmat, Rick Zhang, Brad Shumel, Robert Pordy, Daniel A. Gipe, Gary Herman, Wayne Huey‐Herng Sheu, I‐Te Lee, 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

  4. Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

    著者: Stephan Sanders, Xin He, A. Jeremy Willsey, A. Gulhan Ercan‐Sencicek, Kaitlin E. Samocha, A. Ercüment Çiçek, Michael T. Murtha, Vanessa H. Bal, Somer Bishop, Shan Dong, Arthur P. Goldberg, Jinlu Cai, John F. Keaney, Lambertus Klei, Jeffrey D. Mandell, Daniel Moreno‐De‐Luca, Christopher S. Poultney, Elise Robinson, Louw Smith, Tor Solli-Nowlan, Mack Y. Su, Nicole A. Teran, Michael F. Walker, Donna M. Werling, Arthur L. Beaudet, Rita M. Cantor, Éric Fombonne, Daniel H. Geschwind, Dorothy E. Grice, Catherine Lord, Jennifer K. Lowe, Shrikant Mane, Donna M. Martin, Eric M. Morrow, Michael E. Talkowski, James S. Sutcliffe, Christopher A. Walsh, Timothy W. Yu, David H. Ledbetter, Christa Lese Martin, Edwin H. Cook, Joseph D. Buxbaum, Mark J. Daly, Bernie Devlin, Kathryn Roeder, Matthew W. State - Neuron 2015 被引用: 1,547

  5. Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders

    著者: Siddharth Srivastava, Jamie Love‐Nichols, Kira A. Dies, David H. Ledbetter, Christa Lese Martin, Wendy K. Chung, Helen V. Firth, Thomas Frazier, Robin Hansen, Lisa M. Prock, Han G. Brunner, Ny Hoang, Stephen W. Scherer, Mustafa Şahin, David T. Miller - Genetics in Medicine 2019 被引用: 711

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

    著者: Cristopher V. Van Hout, Ioanna Tachmazidou, Joshua Backman, Joshua Hoffman, Daren Liu, Ashutosh Kumar Pandey, Claudia Gonzaga‐Jauregui, Shareef Khalid, Bin Ye, Nilanjana Banerjee, Alexander Li, Colm O’Dushlaine, Anthony Marcketta, Jeffrey Staples, Claudia Schurmann, Alicia Hawes, Evan K. Maxwell, Leland Barnard, Alexander Lopez, John S. Penn, Lukas Habegger, Andrew Blumenfeld, Xiaodong Bai, Sean O’Keeffe, Ashish Yadav, Kavita Praveen, Marcus B. Jones, William Salerno, Wendy K. Chung, Ida Surakka, 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

  7. Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

    著者: David T. Miller, Margaret P Adam, Swaroop Aradhya, Leslie G. Biesecker, Arthur R. Brothman, Nigel P. Carter, Deanna M. Church, John A. Crolla, Evan E. Eichler, Charles J. Epstein, W. Andrew Faucett, Lars Feuk, Jan M. Friedman, Ada Hamosh, Laird Jackson, Erin B. Kaminsky, Klaas Kok, Ian D. Krantz, Robert M. Kuhn, Charles Lee, James M. Ostell, Carla Rosenberg, Stephen W. Scherer, Nancy B. Spinner, Dimitri J. Stavropoulos, James Tepperberg, Erik C. Thorland, Joris Vermeesch, Darrel Waggoner, Michael S. Watson, Christa Lese Martin, David H. Ledbetter - The American Journal of Human Genetics 2010 被引用: 2,873

  8. Chromosomal Microarray Versus Karyotyping for Prenatal Diagnosis

    著者: Ronald J. Wapner, Christa Lese Martin, Brynn Levy, Blake C. Ballif, Christine M. Eng, Julia Zachary, Melissa Savage, Lawrence D. Platt, Daniel H. Saltzman, William A. Grobman, Susan Klugman, Thomas Scholl, Joe Leigh Simpson, Kimberly McCall, Vimla S. Aggarwal, Brian Bunke, Odelia Nahum, Ankita Patel, Allen N. Lamb, Elizabeth Thom, Arthur L. Beaudet, David H. Ledbetter, Lisa G. Shaffer, Laird Jackson - New England Journal of Medicine 2012 被引用: 1,424

  9. Clinical Genetic Testing for Familial Hypercholesterolemia

    著者: Amy C. Sturm, Joshua W. Knowles, Samuel S. Gidding, Zahid Ahmad, Catherine D. Ahmed, Christie M. Ballantyne, Seth J. Baum, Mafalda Bourbon, Alain Carrié, Marina Cuchel, Sarah D. de Ferranti, Joep C. Defesche, Tomáš Freiberger, Ray E. Hershberger, G. Kees Hovingh, Lala Karayan, Johannes J.P. Kastelein, Iris Kindt, Stacey R. Lane, S. E. A. Leigh, MacRae F. Linton, Pedro Mata, William A. Neal, Børge G. Nordestgaard, Raúl D. Santos, Mariko Harada‐Shiba, Eric J.G. Sijbrands, Nathan O. Stitziel, Shizuya Yamashita, Katherine Wilemon, David H. Ledbetter, Daniel J. Rader - Journal of the American College of Cardiology 2018 被引用: 597

  10. Strong Association of De Novo Copy Number Mutations with Autism

    著者: Jonathan Sebat, B. Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese‐Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, A. Krasnitz, Jude Kendall, Anthony Leotta, Deepa Pai, Ray Zhang, Yoonha Lee, James Hicks, Sarah Spence, Annette T. Lee, Kaija Puura, Terho Lehtimäki, David H. Ledbetter, Peter K. Gregersen, Joel D. Bregman, James S. Sutcliffe, Vaidehi Jobanputra, Wendy K. Chung, Dorothy Warburton, Mary‐Claire King, David Skuse, Daniel H. Geschwind, T. Conrad Gilliam, Kenny Ye, Michael Wigler - Science 2007 被引用: 2,849

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

    著者: Frederick E. Dewey, Viktoria Gusarova, Colm O’Dushlaine, Omri Gottesman, Jesus Trejos, Charleen Hunt, Cristopher V. Van Hout, Lukas Habegger, David G. Buckler, Ka-Man V. Lai, Joseph B. Leader, Michael F. Murray, Marylyn D. Ritchie, H. Lester Kirchner, David H. Ledbetter, John S. Penn, Alexander Lopez, Ingrid B. Borecki, John D. Overton, Jeffrey G. Reid, David J. Carey, Andrew Murphy, George D. Yancopoulos, Aris Baras, Jesper Gromada, Alan R. Shuldiner - New England Journal of Medicine 2016 被引用: 510

  12. The Geisinger MyCode community health initiative: an electronic health record–linked biobank for precision medicine research

    著者: David J. Carey, Samantha N. Fetterolf, F. Daniel Davis, W. Andrew Faucett, H. Lester Kirchner, Uyenlinh L. Mirshahi, Michael F. Murray, Diane T. Smelser, Glenn S. Gerhard, David H. Ledbetter - Genetics in Medicine 2016 被引用: 493

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

    著者: Noura S. Abul‐Husn, Kandamurugu Manickam, Laney K. Jones, Eric A. Wright, Dustin N. Hartzel, Claudia Gonzaga‐Jauregui, Colm O’Dushlaine, Joseph B. Leader, H. Lester Kirchner, D’Andra M. Lindbuchler, Marci L Barr, Monica A. Giovanni, Marylyn D. Ritchie, John D. Overton, Jeffrey G. Reid, Raghu Metpally, Amr H. Wardeh, Ingrid B. Borecki, George D. Yancopoulos, Aris Baras, Alan R. Shuldiner, Omri Gottesman, David H. Ledbetter, David J. Carey, Frederick E. Dewey, Michael F. Murray - Science 2016 被引用: 428

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

    著者: Frederick E. Dewey, Michael F. Murray, John D. Overton, Lukas Habegger, Joseph B. Leader, Samantha N. Fetterolf, Colm O’Dushlaine, Cristopher V. Van Hout, Jeffrey Staples, Claudia Gonzaga‐Jauregui, Raghu Metpally, Sarah A. Pendergrass, Monica A. Giovanni, H. Lester Kirchner, Suganthi Balasubramanian, Noura S. Abul‐Husn, Dustin N. Hartzel, Daniel R. Lavage, Korey A. Kost, Jonathan S. Packer, Alexander Lopez, John S. Penn, Semanti Mukherjee, Nehal Gosalia, Manoj Kanagaraj, Alexander Li, Lyndon J. Mitnaul, Lance J. Adams, Thomas N. Person, Kavita Praveen, 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

  15. Chromosome 17 Deletions and p53 Gene Mutations in Colorectal Carcinomas

    著者: Suzanne J. Baker, Eric R. Fearon, Janice Nigro, Stanley R. Hamilton, Ann C. Preisinger, J. Milburn Jessup, Peter vanTuinen, David H. Ledbetter, David F. Barker, Yusuke Nakamura, R. White, Bert Vogelstein - Science 1989 被引用: 2,084

  16. Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

    著者: Stephan Sanders, A. Gulhan Ercan‐Sencicek, Vanessa Hus, Rui Luo, Michael T. Murtha, Daniel Moreno‐De‐Luca, Su H. Chu, Michael Moreau, Abha R. Gupta, Susanne Thomson, Christopher E. Mason, Kaya Bilgüvar, Patrícia B. S. Celestino-Soper, Murim Choi, Emily L. Crawford, Lea K. Davis, Nicole R. Davis Wright, Rahul M. Dhodapkar, Michael DiCola, Nicholas M. DiLullo, Thomas Fernandez, Vikram Fielding‐Singh, Daniel O. Fishman, Stephanie Frahm, Rouben Garagaloyan, Gerald Goh, Sindhuja Kammela, Lambertus Klei, Jennifer K. Lowe, Sabata C. Lund, Anna D. McGrew, Kyle A. Meyer, William J. Moffat, John D. Murdoch, Brian J. O’Roak, G Ober, Rebecca S. Pottenger, Melanie J. Raubeson, Youeun Song, Qi Wang, Brian L. Yaspan, Timothy W. Yu, Ilana R. Yurkiewicz, Arthur L. Beaudet, Rita M. Cantor, Martin Curland, Dorothy E. Grice, Murat Günel, Richard P. Lifton, Shrikant Mane, Donna M. Martin, Chad A. Shaw, Michael Sheldon, Jay A. Tischfield, Christopher A. Walsh, Eric M. Morrow, David H. Ledbetter, Éric Fombonne, Catherine Lord, Christa Lese Martin, Andrew I. Brooks, James S. Sutcliffe, Edwin H. Cook, Daniel H. Geschwind, Kathryn Roeder, Bernie Devlin, Matthew W. State - Neuron 2011 被引用: 1,292

  17. Diagnostic Yield of Exome Sequencing in Cerebral Palsy and Implications for Genetic Testing Guidelines

    著者: Pedro J. Gonzalez-Mantilla, Yirui Hu, Scott M. Myers, Brenda Finucane, David H. Ledbetter, Christa Lese Martin, Andrés Moreno-De-Luca - JAMA Pediatrics 2023 被引用: 86

  18. The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data

    著者: Sebastian Köhler, Sandra C. Doelken, Chris Mungall, Sebastian Bauer, Helen V. Firth, Isabelle Bailleul‐Forestier, Graeme C. Black, Danielle L. Brown, Michael Brudno, Jennifer Campbell, David Fitzpatrick, Janan T. Eppig, Andrew P. Jackson, Kathleen Freson, Marta Gîrdea, Ingo Helbig, Jane A. Hurst, Johanna Jähn, Laird G. Jackson, Anne M. Kelly, David H. Ledbetter, Sahar Mansour, Christa Lese Martin, Celia Moss, Andrew Mumford, Willem H. Ouwehand, Soo-Mi Park, Erin Rooney Riggs, Richard H. Scott, Sanjay M. Sisodiya, Steven Van Vooren, Ronald J. Wapner, Andrew O.M. Wilkie, Caroline F. Wright, Anneke T. Vulto‐van Silfhout, Nicole de Leeuw, Bert B.A. de Vries, Nicole L. Washingthon, Cynthia L. Smith, Monte Westerfield, Paul N. Schofield, Barbara J. Ruef, Georgios V. Gkoutos, Melissa Haendel, Damian Smedley, Suzanna Lewis, Peter N. Robinson - Nucleic Acids Research, Nucleic Acids Res. 2013 被引用: 837

  19. Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes

    著者: Viktoria Gusarova, Colm O’Dushlaine, Tanya M. Teslovich, Peter N. Benotti, Tooraj Mirshahi, Omri Gottesman, Cristopher V. Van Hout, Michael F. Murray, Anubha Mahajan, Jonas B. Nielsen, Lars G. Fritsche, Anders Berg Wulff, Daníel F. Guðbjartsson, Marketa Sjögren, Connor A. Emdin, Robert A. Scott, Wen‐Jane Lee, Aeron Small, Lydia Coulter Kwee, Om Prakash Dwivedi, Rashmi B. Prasad, Shannon Bruse, Alexander Lopez, John S. Penn, Anthony Marcketta, Joseph B. Leader, Christopher D. Still, H. Lester Kirchner, Uyenlinh L. Mirshahi, Amr H. Wardeh, Cassandra M. Hartle, Lukas Habegger, Samantha N. Fetterolf, Teresa Tusié‐Luna, Andrew P. Morris, Hilma Hólm, Valgerður Steinthórsdóttir, Patrick Sulem, Unnur Thorsteinsdottir, Jerome I. Rotter, Lee‐Ming Chuang, Scott M. Damrauer, David Birtwell, Chad M. Brummett, Amit V. Khera, Pradeep Natarajan, Marju Orho‐Melander, Jason Flannick, Luca A. Lotta, Cristen J. Willer, Oddgeir L. Holmen, Marylyn D. Ritchie, David H. Ledbetter, Andrew Murphy, Ingrid B. Borecki, Jeffrey G. Reid, John D. Overton, Ola Hansson, Leif Groop, Svati H. Shah, William E. Kraus, Daniel J. Rader, Yii‐Der Ida Chen, Kristian Hveem, Nicholas J. Wareham, Sekar Kathiresan, Olle Melander, Kāri Stefánsson, Børge G. Nordestgaard, Anne Tybjærg‐Hansen, Gonçalo R. Abecasis, David Altshuler, José C. Florez, Michael Boehnke, Mark I. McCarthy, George D. Yancopoulos, David J. Carey, Alan R. Shuldiner, Aris Baras, Frederick E. Dewey, Jesper Gromada - Nature Communications 2018 被引用: 153

  20. Implementing genomic medicine in the clinic: the future is here

    著者: Teri A. Manolio, Rex L. Chisholm, Brad Ozenberger, Dan M. Roden, Marc S. Williams, R.T. Wilson, David Bick, Erwin P. Böttinger, Murray H. Brilliant, Charis Eng, Kelly A. Frazer, Bruce R. Korf, David H. Ledbetter, James R. Lupski, Clay B. Marsh, David A. Mrazek, Michael F. Murray, Peter H. O’Donnell, Daniel J. Rader, Mary V. Relling, Alan R. Shuldiner, David Valle, Richard M. Weinshilboum, Eric D. Green, Geoffrey S. Ginsburg - Genetics in Medicine 2013 被引用: 571

  21. Exome Sequencing–Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants

    著者: Kandamurugu Manickam, Adam H. Buchanan, M. Schwartz, Miranda L. G. Hallquist, Janet L. Williams, Alanna Kulchak Rahm, Heather Rocha, Juliann M. Savatt, Alyson Evans, Loren Butry, Amanda L. Lazzeri, D’Andra M. Lindbuchler, Carroll N. Flansburg, Rosemary Leeming, Victor G. Vogel, Matthew S. Lebo, Heather Mason‐Suares, Derick Hoskinson, Noura S. Abul‐Husn, Frederick E. Dewey, John D. Overton, Jeffrey G. Reid, Aris Baras, Huntington F. Willard, Cara Z. McCormick, S. Krishnamurthy, Dustin N. Hartzel, Korey A. Kost, Daniel R. Lavage, Amy C. Sturm, Lauren R. Frisbie, Thomas N. Person, Raghu Metpally, Monica A. Giovanni, Lacy E. Lowry, Joseph B. Leader, Marylyn D. Ritchie, David J. Carey, Anne E. Justice, H. Lester Kirchner, W. Andrew Faucett, Marc S. Williams, David H. Ledbetter, Michael F. Murray - JAMA Network Open 2018 被引用: 219

  22. Insufficient Evidence for “Autism-Specific” Genes

    著者: Scott M. Myers, Thomas D. Challman, Raphael Bernier, Thomas Bourgeron, Wendy K. Chung, John N. Constantino, Evan E. Eichler, Sébastien Jacquemont, David T. Miller, Kevin J. Mitchell, Huda Y. Zoghbi, Christa Lese Martin, David H. Ledbetter - The American Journal of Human Genetics 2020 被引用: 169

  23. Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy

    著者: Andrés Moreno-De-Luca, Francisca Millan, Denis R. Pesacreta, Houda Zghal Elloumi, Matthew T. Oetjens, Claire Teigen, Karen E. Wain, Julie Scuffins, Scott M. Myers, Rebecca I. Torene, Vladimir G. Gainullin, Kevin J. Arvai, H. Lester Kirchner, David H. Ledbetter, Kyle Retterer, Christa Lese Martin - JAMA 2021 被引用: 123

  24. Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology

    著者: Sébastien Jacquemont, Guillaume Huguet, Marieke Klein, Samuel J. R. A. Chawner, Kirsten A. Donald, Marianne B. M. van den Bree, Jonathan Sebat, David H. Ledbetter, John N. Constantino, Rachel K. Earl, Donna M. McDonald‐McGinn, Thérèse van Amelsvoort, Ann Swillen, Anne O’Donnell‐Luria, David C. Glahn, Laura Almasy, Evan E. Eichler, Stephen W. Scherer, Elise Robinson, Anne S. Bassett, Christa Lese Martin, Brenda Finucane, Jacob Vorstman, Carrie E. Bearden, Raquel E. Gur, and the Genes to Mental Health Network - American Journal of Psychiatry 2022 被引用: 65