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David J. Cutler

Active 1978–2025

84
Papers
20,640
Citations
54
h-index
76
i10-index

Citations

Citations per year for David J. Cutler1921: 1 citations1964: 1 citations1967: 2 citations1978: 3 citations1980: 1 citations1981: 2 citations1982: 6 citations1984: 3 citations1985: 1 citations1986: 1 citations1987: 2 citations1989: 6 citations1990: 2 citations1991: 3 citations1992: 2 citations1993: 3 citations1994: 4 citations1995: 1 citations1996: 7 citations1997: 6 citations1998: 1 citations2000: 5 citations2001: 27 citations2002: 31 citations2003: 70 citations2004: 204 citations2005: 302 citations2006: 256 citations2007: 266 citations2008: 308 citations2009: 300 citations2010: 300 citations2011: 255 citations2012: 228 citations2013: 181 citations2014: 180 citations2015: 222 citations2016: 194 citations2017: 210 citations2018: 183 citations2019: 478 citations2020: 487 citations2021: 444 citations2022: 369 citations2023: 302 citations2024: 406 citations2025: 173 citations2026: 11 citations1922–1963: no citations, so these years are not shown1965–1966: no citations, so these years are not shown1968–1977: no citations, so these years are not shown1979: no citations, so this year is not shown1983: no citations, so this year is not shown1988: no citations, so this year is not shown1999: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,552 citing papers, 30.6% of this breakdownUnited Kingdom: 1,007 citing papers, 8.7% of this breakdownChina: 635 citing papers, 5.5% of this breakdownGermany: 562 citing papers, 4.9% of this breakdownCanada: 511 citing papers, 4.4% of this breakdownFrance: 407 citing papers, 3.5% of this breakdownItaly: 399 citing papers, 3.4% of this breakdownNetherlands: 370 citing papers, 3.2% of this breakdownAustralia: 334 citing papers, 2.9% of this breakdownSpain: 297 citing papers, 2.6% of this breakdownJapan: 264 citing papers, 2.3% of this breakdownSweden: 249 citing papers, 2.1% of this breakdown
0%30.6%Other 25.9%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology58.6%
  • Medicine16.6%
  • Neuroscience15.4%
  • Immunology and Microbiology1.8%
  • Computer Science1.6%
  • Agricultural and Biological Sciences1.5%
  • Other4.5%

Topics

  • Genetic Associations and Epidemiology6.5%
  • Genetics and Neurodevelopmental Disorders5%
  • Autism Spectrum Disorder Research4.1%
  • Genomics and Rare Diseases3.6%
  • Genomic variations and chromosomal abnormalities3.5%
  • Genomics and Phylogenetic Studies2.7%
  • Other74.6%

Coauthors

All papers

Open in search
  1. Synaptic, transcriptional and chromatin genes disrupted in autism

    Authors: The DDD Study, Silvia De Rubeis, Homozygosity Mapping Collaborative for Autism, Xin He, Arthur P. Goldberg, Christopher S. Poultney, Kaitlin E. Samocha, A. Ercüment Çiçek, Yan Kou, Li Liu, Menachem Fromer, Susan L. Walker, Tarjinder Singh, Lambertus Klei, Jack A. Kosmicki, Shih‐Chen Fu, Branko Aleksić, Monica Biscaldi, Patrick Bolton, Jessica M. Brownfeld, Jinlu Cai, Nicholas G. Campbell, Ángel Carracedo, Maria H. Chahrour, Andreas G. Chiocchetti, Hilary Coon, Emily L. Crawford, Lucy Crooks, Sarah Curran, Géraldine Dawson, Eftichia Duketis, Bridget A. Fernandez, Louise Gallagher, Evan Geller, Stephen J. Guter, R. Sean Hill, Iuliana Ionita‐Laza, Patricia González, Helena Kilpinen, Sabine M. Klauck, A lexander Kolevzon, Irene Lee, Jing Lei, Terho Lehtimäki, Chiao‐Feng Lin, Avi Ma’ayan, Christian R. Marshall, Alison McInnes, Benjamin M. Neale, Michael J. Owen, Norio Ozaki, Mara Parellada, Jeremy Parr, Shaun Purcell, Kaija Puura, Deepthi Rajagopalan, Karola Rehnström, Abraham Reichenberg, Aniko Sabo, Michael Sachse, Stephan Sanders, Chad Schafer, Martin Schulte‐Rüther, David Skuse, Christine Stevens, Péter Szatmári, Kristiina Tammimies, Otto Valladares, Annette Voran, Li‐San Wang, Lauren A. Weiss, A. Jeremy Willsey, Timothy W. Yu, Ryan K. C. Yuen, Edwin H. Cook, Christine M. Freitag, Michael Gill, Christina M. Hultman, Thomas Lehner, Aarno Palotie, Gerard D. Schellenberg, Pamela Sklar, Matthew W. State, James S. Sutcliffe, Christopher A. Walsh, Stephen W. Scherer, Michael E. Zwick, Jeffrey C. Barrett, David J. Cutler, Kathryn Roeder, Bernie Devlin, Mark J. Daly, Joseph D. Buxbaum - Nature 2014 cited by 2,974

  2. The International HapMap Project

    Authors: Richard A. Gibbs, John W. Belmont, Paul Hardenbol, T. D. Willis, Fuli Yu, Huanming Yang, Lan-Yang Ch'ang, Wei Huang, Bin Liu, Yan Shen, Paul Kwong Hang Tam, Lap-Chee Tsui, Mary Miu Yee Waye, J. Tze‐Fei Wong, Changqing Zeng, Qingrun Zhang, Illumina, Mark S. Chee, Luana Galver, Semyon Kruglyak, Sarah S. Murray, Arnold Oliphant, Alexandre Montpetit, Thomas J. Hudson, Fanny Chagnon, Vincent Ferretti, Martin Leboeuf, Michael Phillips, Andrei Verner, Pui-Yan Kwok, Shenghui Duan, Denise L. Lind, Raymond D. Miller, John P. Rice, Nancy L. Saccone, Patricia Taillon‐Miller, Ming Xiao, Yusuke Nakamura, Akihiro Sekine, Koki Sorimachi, Toshihiro Tanaka, Yoïchi Tanaka, Tatsuhiko Tsunoda, Eiji Yoshino, David Bentley, Panos Deloukas, Sarah Hunt, Don Powell, David Altshuler, Stacey B. Gabriel, Houcan Zhang, Changqing Zeng, Ichiro Matsuda, Yoshimitsu Fukushima, Darryl Macer, Eiko Suda, Charles N. Rotimi, Clement Adebamowo, Toyin Aniagwu, Patricia A. Marshall, Olayemi Matthew, Chibuzor Nkwodimmah, Charmaine D. M. Royal, Mark Leppert, Missy Dixon, Lincoln D. Stein, Fiona Cunningham, Ardavan Kanani, Guðmundur Á. Þórisson, Aravinda Chakravarti, Peter E. Chen, David J. Cutler, Carl Kashuk, Peter Donnelly, Jonathan Marchini, Gil McVean, Simon Myers, Lon R. Cardon, Gonçalo R. Abecasis, Andrew P. Morris, Bruce S. Weir, James C. Mullikin, Stephen T. Sherry, Michael Feolo, David Altshuler, Mark Daly, Stephen F. Schaffner, Ren-Zong Qiu, Genetic Interest Group, Alastair Kent, Georgia M. Dunston, Kazuto Kato, Norio Niikawa, Bartha Maria Knoppers, Morris W. Foster, Ellen Wright Clayton, Vivian Ota Wang, Wellcome Trust, Jessica Watkin, Richard A. Gibbs and 83 more - Nature 2003 cited by 6,186

  3. Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility

    Authors: Aleksejs Sazonovs, Christine Stevens, Guhan Venkataraman, Kai Yuan, Brandon E. Avila, Maria T. Abreu, Tariq Ahmad, Matthieu Allez, Ashwin N. Ananthakrishnan, Gil Atzmon, Aris Baras, Jeffrey C. Barrett, Nir Barzilai, Laurent Beaugerie, Ashley Beecham, Charles N. Bernstein, Alain Bitton, Bernd Bokemeyer, Andrew Chan, Daniel C. Chung, Isabelle Cleynen, Jacques Cosnes, David J. Cutler, Allan Daly, Oriana M. Damas, Lisa W. Datta, Noor Dawany, Marcella Devoto, Sheila Dodge, Eva Ellinghaus, Laura Fachal, Martti Färkkilâ, William A. Faubion, Manuel A. R. Ferreira, Denis Franchimont, Stacey Gabriel, Tian Ge, Michel Georges, Kyle Gettler, Mamta Giri, Benjamin Gläser, Siegfried Goerg, Philippe Goyette, Daniel B. Graham, Eija Hämäläinen, Talin Haritunians, Graham Heap, Mikko Hiltunen, Marc P. Hoeppner, Julie Horowitz, Peter M. Irving, Vivek Iyer, Chaim Jalas, Judith R. Kelsen, Hamed Khalili, Barbara S. Kirschner, Kimmo Kontula, Jukka Koskela, Subra Kugathasan, Juozas Kupčinskas, Christopher A Lamb, Matthias Laudes, Chloé Lévesque, Adam P. Levine, James D. Lewis, Claire Liefferinckx, Britt-Sabina Loescher, Édouard Louis, John Mansfield, Sandra May, Jacob L. McCauley, Emebet Mengesha, Myriam Mni, Paul Moayyedi, Christopher J. Moran, Rodney D. Newberry, Sirimon O’Charoen, David T. Okou, Bas Oldenburg, Harry Ostrer, Aarno Palotie, Jean Paquette, Joel Pekow, Inga Peter, Marieke Pierik, Cyriel Y. Ponsioen, Nikolas Pontikos, Natalie J. Prescott, Ann E. Pulver, Souad Rahmouni, Daniel L Rice, Päivi Saavalainen, Bruce E. Sands, R. Balfour Sartor, Elena Schiff, Stefan Schreiber, L. Philip Schumm, Anthony W. Segal, Philippe Seksik, Rasha Shawky and 33 more - Nature Genetics 2022 cited by 189

  4. Sex differences in brain protein expression and disease

    Authors: Aliza P. Wingo, Yue Liu, Ekaterina S. Gerasimov, Selina Vattathil, Jiaqi Liu, David J. Cutler, Michael P. Epstein, Gabriëlla A.M. Blokland, Madhav Thambisetty, Juan C. Troncoso, Duc M. Duong, David A. Bennett, Allan I. Levey, Nicholas T. Seyfried, Thomas S. Wingo - Nature Medicine 2023 cited by 87

  5. Genetic control of the human brain proteome

    Authors: Chloe Robins, Yue Liu, Wen Fan, Duc M. Duong, Jacob Meigs, Nadia V. Harerimana, Ekaterina S. Gerasimov, Eric B. Dammer, David J. Cutler, Thomas G. Beach, Eric M. Reiman, Philip L. De Jager, David A. Bennett, James J. Lah, Aliza P. Wingo, Allan I. Levey, Nicholas T. Seyfried, Thomas S. Wingo - The American Journal of Human Genetics 2021 cited by 117

  6. A Note on Exact Tests of Hardy-Weinberg Equilibrium

    Authors: Janis Wigginton, David J. Cutler, Gonçalo R. Abecasis - The American Journal of Human Genetics 2005 cited by 1,473

  7. Blood-Derived DNA Methylation Signatures of Crohn's Disease and Severity of Intestinal Inflammation

    Authors: Hari K. Somineni, Suresh Venkateswaran, Varun Kilaru, Urko M. Marigorta, Angela Mo, David T. Okou, Richárd Kellermayer, Kajari Mondal, Dawayland O. Cobb, Thomas D. Walters, Anne M. Griffiths, Joshua D. Noe, Wallace Crandall, Joel R. Rosh, David Mack, Melvin B. Heyman, Susan S. Baker, Michael C. Stephens, Robert N. Baldassano, James Markowitz, Marla C. Dubinsky, Judy H. Cho, Jeffrey S. Hyams, Lee A. Denson, Greg Gibson, David J. Cutler, Karen N. Conneely, Alicia K. Smith, Subra Kugathasan - Gastroenterology 2019 cited by 157

  8. Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples

    Authors: Jack A. Kosmicki, Kaitlin E. Samocha, Daniel P. Howrigan, Stephan Sanders, Kamil Slowikowski, Monkol Lek, Konrad J. Karczewski, David J. Cutler, Bernie Devlin, Kathryn Roeder, Joseph D. Buxbaum, Benjamin M. Neale, Daniel G. MacArthur, Dennis P. Wall, Elise Robinson, Mark J. Daly - Nature Genetics 2017 cited by 367

  9. Recessive gene disruptions in autism spectrum disorder

    Authors: Ryan N. Doan, Elaine T. Lim, Silvia De Rubeis, Catalina Betancur, David J. Cutler, Andreas G. Chiocchetti, Lynne M. Overman, Aubrie Soucy, Susanne Goetze, Christine M. Freitag, Mark J. Daly, Christopher A. Walsh, Joseph D. Buxbaum, Timothy W. Yu - Nature Genetics 2019 cited by 179

  10. Association of Early-Onset Alzheimer Disease With Elevated Low-Density Lipoprotein Cholesterol Levels and Rare Genetic Coding Variants of APOB

    Authors: Thomas S. Wingo, David J. Cutler, Aliza P. Wingo, Ngoc‐Anh Le, Gil D. Rabinovici, Bruce L. Miller, James J. Lah, Allan I. Levey - JAMA Neurology 2019 cited by 122

  11. Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients With Crohn’s Disease

    Authors: Lee A. Denson, Ingrid Jurickova, Rebekah Karns, Kelly Shaw, David J. Cutler, David T. Okou, Anne Dodd, Kathryn Quinn, Kajari Mondal, Bruce J. Aronow, Yael Haberman, Aaron Linn, Adam Price, Ramona Bezold, Kathleen D. Lake, Kimberly Jackson, Thomas D. Walters, Anne M. Griffiths, Robert N. Baldassano, Joshua D. Noe, Jeffrey S. Hyams, Wallace Crandall, Barbara S. Kirschner, Melvin B. Heyman, Scott B. Snapper, Stephen L. Guthery, Marla C. Dubinsky, Neal S. LeLeiko, Anthony Otley, Ramnik J. Xavier, Christine Stevens, Mark J. Daly, Michael E. Zwick, Subra Kugathasan - Gastroenterology 2018 cited by 90

  12. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

    Authors: Isabelle Cleynen, Worrawat Engchuan, Matthew S. Hestand, Tracy Heung, Aaron M. Holleman, H. Richard Johnston, Thomas Monfeuga, Donna M. McDonald‐McGinn, Raquel E. Gur, Bernice E. Morrow, Ann Swillen, Jacob Vorstman, Carrie E. Bearden, Eva W. C. Chow, Marianne B. M. van den Bree, B S Emanuel, Joris Vermeesch, Stephen T. Warren, Michael J. Owen, Pankaj Chopra, David J. Cutler, Richard Duncan, Alex Kotlar, Jennifer G. Mulle, Anna J. Voss, Michael E. Zwick, Alexander Diacou, Aaron Golden, Tingwei Guo, Jhih-Rong Lin, Tao Wang, Zhengdong Zhang, Yingjie Zhao, Christian R. Marshall, Daniele Merico, Andrea Jin, Brenna Lilley, Harold I. Salmons, Oanh Tran, Peter Holmans, Antonio F. Pardiñas, James Walters, Wolfram Demaerel, Erik Boot, Nancy J. Butcher, Gregory Costain, Chelsea Lowther, Rens Evers, Thérèse van Amelsvoort, Esther van Duin, Claudia Vingerhoets, Jeroen Breckpot, Koenraad Devriendt, Elfi Vergaelen, Annick Vogels, T. Blaine Crowley, Daniel E. McGinn, Edward Moss, Robert Sharkus, Marta Unolt, Elaine H. Zackai, Monica E. Calkins, Robert S. Gallagher, Ruben C. Gur, Sunny X. Tang, Rosemarie Fritsch, Claudia Ornstein, Gabriela M. Repetto, Elemi Breetvelt, Sasja N. Duijff, Ania Fiksinski, Hayley Moss, Maria Niarchou, Kieran C. Murphy, Sarah E. Prasad, Eileen Daly, Maria Gudbrandsen, Clodagh M. Murphy, Declan Murphy, Antonio Buzzanca, Fabio Di Fabio, Maria Cristina Digilio, Maria Pontillo, Bruno Marino, Stefano Vicari, Karlene Coleman, Joseph F. Cubells, Opal Ousley, Miri Carmel, Doron Gothelf, Ehud Mekori‐Domachevsky, Elena Michaelovsky, Ronnie Weinberger, Abraham Weizman, Leila Kushan, Maria Jalbrzikowski, Marco Armando, Stéphan Eliez, Corrado Sandini, Maude Schneider and 24 more - Molecular Psychiatry 2020 cited by 135

  13. Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios

    Authors: Madison R. Bishop, Kimberly K. Diaz Perez, Miranda Sun, Samantha Ho, Pankaj Chopra, Nandita Mukhopadhyay, Jacqueline B. Hetmanski, Margaret A. Taub, Lina Moreno‐Uribe, Luz Consuelo Valencia‐Ramirez, Claudia P. Restrepo Muñeton, George L. Wehby, Jacqueline T. Hecht, Frederic W.‐B. Deleyiannis, Seth M. Weinberg, Yah Huei Wu‐Chou, Philip K. Chen, Harrison Brand, Michael P. Epstein, Ingo Ruczinski, Jeffrey C. Murray, Terri H. Beaty, Eleanor Feingold, Robert J. Lipinski, David J. Cutler, Mary L. Marazita, Elizabeth J. Leslie - The American Journal of Human Genetics 2020 cited by 96

  14. Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease

    Authors: Hari K. Somineni, Sini Nagpal, Suresh Venkateswaran, David J. Cutler, David T. Okou, Talin Haritunians, Claire L. Simpson, Ferdouse Begum, Lisa W. Datta, Antonio Quiros, Jenifer Seminerio, Emebet Mengesha, J. Steven Alexander, Robert N. Baldassano, Sharon Dudley‐Brown, Raymond K. Cross, Themistocles Dassopoulos, Lee A. Denson, Tanvi Dhere, Heba Iskandar, Gerald W. Dryden, Jason K. Hou, Sunny Z. Hussain, Jeffrey S. Hyams, Kim L. Isaacs, Howard A. Kader, Michael D. Kappelman, Jeffry Katz, Richárd Kellermayer, John F. Kuemmerle, Mark Lazarev, Ellen Li, Peter Mannon, Dedrick E. Moulton, Rodney D. Newberry, Ashish Patel, Joel Pekow, Shehzad A. Saeed, John F. Valentine, Ming‐Hsi Wang, Jacob L. McCauley, María T. Abreu, Traci Jester, Zarela Molle‐Rios, Sirish Palle, Ellen Scherl, John H. Kwon, John D. Rioux, Richard H. Duerr, Mark S. Silverberg, Michael E. Zwick, Christine Stevens, Mark J. Daly, Judy H. Cho, Greg Gibson, Dermot McGovern, Steven R. Brant, Subra Kugathasan - The American Journal of Human Genetics 2021 cited by 44

  15. Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease

    Authors: Steven R. Brant, David T. Okou, Claire L. Simpson, David J. Cutler, Talin Haritunians, Jonathan P. Bradfield, Pankaj Chopra, Jarod Prince, Ferdouse Begum, Archana Kumar, Chengrui Huang, Suresh Venkateswaran, Lisa W. Datta, Zhi Wei, Kelly Thomas, Lisa J. Herrinton, Jan-Micheal A. Klapproth, Antonio Quiros, Jenifer Seminerio, Zhenqiu Liu, J. Steven Alexander, Robert N. Baldassano, Sharon Dudley‐Brown, Raymond K. Cross, Themistocles Dassopoulos, Lee A. Denson, Tanvi Dhere, Gerald W. Dryden, John S. Hanson, Jason K. Hou, Sunny Z. Hussain, Jeffrey S. Hyams, Kim L. Isaacs, Howard A. Kader, Michael D. Kappelman, Jeffry Katz, Richárd Kellermayer, Barbara S. Kirschner, John F. Kuemmerle, John H. Kwon, Mark Lazarev, Ellen Li, David R. Mack, Peter Mannon, Dedrick E. Moulton, Rodney D. Newberry, B. O. Osuntokun, Ashish Patel, Shehzad A. Saeed, Stephan R. Targan, John F. Valentine, Ming‐Hsi Wang, Martin Zonca, John D. Rioux, Richard H. Duerr, Mark S. Silverberg, Judy H. Cho, Håkon Håkonarson, Michael E. Zwick, Dermot McGovern, Subra Kugathasan - Gastroenterology 2016 cited by 162

  16. Identification of Polycystic Kidney Disease 1 Like 1 Gene Variants in Children With Biliary Atresia Splenic Malformation Syndrome

    Authors: John‐Paul Berauer, Anya Mezina, David T. Okou, Aniko Sabo, Donna M. Muzny, Richard A. Gibbs, Madhuri Hegde, Pankaj Chopra, David J. Cutler, David H. Perlmutter, Laura N. Bull, Richard J. Thompson, Kathleen M. Loomes, Nancy B. Spinner, Ramakrishnan Rajagopalan, Stephen L. Guthery, Barry Moore, Mark Yandell, Sanjiv Harpavat, John C. Magee, Binita M. Kamath, Jean P. Molleston, Jorge A. Bezerra, Karen F. Murray, Estella M. Alonso, Philip Rosenthal, Robert H. Squires, Kasper S. Wang, Milton J. Finegold, Pierre Russo, Averell H. Sherker, Ronald J. Sokol, Saul J. Karpen - Hepatology 2019 cited by 84

  17. Profiling non-coding RNA levels with clinical classifiers in pediatric Crohn’s disease

    Authors: Ranjit Pelia, Suresh Venkateswaran, Jason D. Matthews, Yael Haberman, David J. Cutler, Jeffrey S. Hyams, Lee A. Denson, Subra Kugathasan - BMC Medical Genomics 2021 cited by 25

  18. LDL cholesterol is associated with higher AD neuropathology burden independent of APOE

    Authors: Aliza P. Wingo, Selina Vattathil, Jiaqi Liu, Wen Fan, David J. Cutler, Allan I. Levey, Julie A. Schneider, David A. Bennett, Thomas S. Wingo - Journal of Neurology Neurosurgery & Psychiatry 2022 cited by 52

  19. Ileal Derived Organoids From Crohn’s Disease Patients Show Unique Transcriptomic and Secretomic Signatures

    Authors: Barbara Joanna Niklinska-Schirtz, Suresh Venkateswaran, Murugadas Anbazhagan, Vasantha L. Kolachala, Jarod Prince, Anne Dodd, Raghavan Chinnadurai, Gregory Gibson, Lee A. Denson, David J. Cutler, Anil G. Jegga, Jason D. Matthews, Subra Kugathasan - Cellular and Molecular Gastroenterology and Hepatology 2021 cited by 43

  20. Site- and Taxa-Specific Disease-Associated Oral Microbial Structures Distinguish Inflammatory Bowel Diseases

    Authors: Hari K. Somineni, Jordan Weitzner, Suresh Venkateswaran, Anne Dodd, Jarod Prince, Arjuna Karikaran, Cary G. Sauer, Shelly Abramowicz, Michael E. Zwick, David J. Cutler, David T. Okou, Pankaj Chopra, Subra Kugathasan - Inflammatory Bowel Diseases 2021 cited by 28

  21. Eicosatetraynoic Acid and Butyrate Regulate Human Intestinal Organoid Mitochondrial and Extracellular Matrix Pathways Implicated in Crohn’s Disease Strictures

    Authors: Ingrid Jurickova, Erin Bonkowski, Elizabeth Angerman, Elizabeth Novak, Alex Huron, Grayce Akers, Kentaro Iwasawa, Tzipi Braun, Rotem Hadar, Maria Hooker, Sarah Han, David J. Cutler, David T. Okou, Subra Kugathasan, Anil G. Jegga, James M. Wells, Takanori Takebe, Kevin P. Mollen, Yael Haberman, Lee A. Denson - Inflammatory Bowel Diseases 2022 cited by 23

  22. A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism

    Authors: Dan E. Arking, David J. Cutler, Camille W. Brune, Tanya M. Teslovich, Kristen M. West, Morna Ikeda, Alexis Rea, Moltu Guy, Shin Lin, Edwin H. Cook, Aravinda Chakravarti - The American Journal of Human Genetics 2008 cited by 594

  23. A Statistical Approach for Testing Cross-Phenotype Effects of Rare Variants

    Authors: K. Alaine Broadaway, David J. Cutler, Richard Duncan, Jacob L. Moore, Erin B. Ware, Min A. Jhun, Lawrence F. Bielak, Wei Zhao, Jennifer A. Smith, Patricia A. Peyser, Sharon L. R. Kardia, Debashis Ghosh, Michael P. Epstein - The American Journal of Human Genetics 2016 cited by 95

  24. Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects

    Authors: Yingjie Zhao, Alexander Diacou, H. Richard Johnston, Fadi I. Musfee, Donna M. McDonald‐McGinn, Daniel E. McGinn, T. Blaine Crowley, Gabriela M. Repetto, Ann Swillen, Jeroen Breckpot, Joris Vermeesch, Wendy R. Kates, M. Cristina Digilio, Marta Unolt, Bruno Marino, Maria Pontillo, Marco Armando, Fabio Di Fabio, Stefano Vicari, Marianne B. M. van den Bree, Hayley Moss, Michael J. Owen, Kieran C. Murphy, Clodagh M. Murphy, Declan Murphy, Kelly Schoch, Vandana Shashi, Flora Tassone, Tony J. Simon, Robert J. Shprintzen, Linda Campbell, Nicole Philip, Damián Heine‐Suñer, Sixto García‐Miñáur, Luis C. Fernández, Stylianos E. Antonarakis, Massimo Biondi, Erik Boot, Elemi Breetvelt, Tiffany Busa, Nancy J. Butcher, Antonino Buzzanca, Miri Carmel, Isabelle Cleynen, David J. Cutler, Bruno Dallapiccola, María Angeles de la Fuente Sanches, Michael P. Epstein, Rens Evers, Luis C. Fernández, Rosemarie Fritsch, Fernando García Algas, Tingwei Guo, Raquel E. Gur, Matthew S. Hestand, Tracy Heung, Stephen R. Hooper, Andrea Jin, Leila Kushan, Alejandra Laorden-Nieto, Guido Maria Lattanzi, Christian Marshall, Kathryn McCabe, Elena Michaelovsky, Claudia Ornstein, Candice K. Silversides, Oanh Tran, Esther D.A. van Duin, Elfi Vergaelen, Steve T. Warren, Ronnie Weinberger, Abraham Weizman, Zhengdong Zhang, Michael E. Zwick, Carrie E. Bearden, Claudia Vingerhoets, Thérèse van Amelsvoort, Stéphan Eliez, Maude Schneider, Jacob Vorstman, Doron Gothelf, Elaine H. Zackai, A. J. Agopian, Raquel E. Gur, Anne S. Bassett, Beverly S. Emanuel, Elizabeth Goldmuntz, Laura E. Mitchell, Tao Wang, Bernice E. Morrow - The American Journal of Human Genetics 2019 cited by 74