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David H. Ledbetter

Active 1980–2025

173
Papers
49,459
Citations
111
h-index
168
i10-index

Citations

Citations per year for David H. Ledbetter1980: 1 citations1981: 2 citations1982: 3 citations1983: 9 citations1984: 27 citations1985: 13 citations1986: 32 citations1987: 18 citations1988: 27 citations1989: 64 citations1990: 153 citations1991: 193 citations1992: 220 citations1993: 200 citations1994: 177 citations1995: 150 citations1996: 130 citations1997: 219 citations1998: 240 citations1999: 226 citations2000: 258 citations2001: 256 citations2002: 233 citations2003: 212 citations2004: 203 citations2005: 198 citations2006: 152 citations2007: 220 citations2008: 367 citations2009: 371 citations2010: 347 citations2011: 367 citations2012: 363 citations2013: 426 citations2014: 389 citations2015: 472 citations2016: 453 citations2017: 462 citations2018: 454 citations2019: 1,219 citations2020: 1,286 citations2021: 1,306 citations2022: 1,038 citations2023: 639 citations2024: 1,001 citations2025: 437 citations2026: 32 citations

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 6,600 citing papers, 33% of this breakdownUnited Kingdom: 1,818 citing papers, 9.1% of this breakdownCanada: 1,025 citing papers, 5.1% of this breakdownGermany: 952 citing papers, 4.8% of this breakdownChina: 864 citing papers, 4.3% of this breakdownNetherlands: 747 citing papers, 3.7% of this breakdownItaly: 746 citing papers, 3.7% of this breakdownFrance: 694 citing papers, 3.5% of this breakdownAustralia: 656 citing papers, 3.3% of this breakdownJapan: 508 citing papers, 2.6% of this breakdownSpain: 436 citing papers, 2.2% of this breakdownSweden: 374 citing papers, 1.9% of this breakdown
0%33%Other 22.8%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology53.1%
  • Medicine27.8%
  • Neuroscience13.3%
  • Psychology1.2%
  • Agricultural and Biological Sciences1%
  • Computer Science0.8%
  • Other2.8%

Topics

  • 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%
  • Other70.9%

Coauthors

All papers

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  1. ClinGen — The Clinical Genome Resource

    Authors: 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 cited by 1,537

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

    Authors: 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 cited by 676

  3. Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease

    Authors: 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 cited by 875

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

    Authors: 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 cited by 1,547

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

    Authors: 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 cited by 711

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

    Authors: 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 cited by 636

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

    Authors: 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 cited by 2,873

  8. Chromosomal Microarray Versus Karyotyping for Prenatal Diagnosis

    Authors: 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 cited by 1,424

  9. Clinical Genetic Testing for Familial Hypercholesterolemia

    Authors: 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 cited by 597

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

    Authors: 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 cited by 2,849

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

    Authors: 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 cited by 510

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

    Authors: 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 cited by 493

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

    Authors: 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 cited by 428

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

    Authors: 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 cited by 607

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

    Authors: 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 cited by 2,084

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

    Authors: 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 cited by 1,292

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

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

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

    Authors: 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 cited by 837

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

    Authors: 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 cited by 153

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

    Authors: 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 cited by 571

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

    Authors: 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 cited by 219

  22. Insufficient Evidence for “Autism-Specific” Genes

    Authors: 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 cited by 169

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

    Authors: 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 cited by 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

    Authors: 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 cited by 65