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David J. Cutler

1978–2025 年に発表

84
論文数
20,640
被引用数
54
h 指数
76
i10 指数

被引用数

David J. Cutler の年別被引用数1921 年: 被引用 1 件1964 年: 被引用 1 件1967 年: 被引用 2 件1978 年: 被引用 3 件1980 年: 被引用 1 件1981 年: 被引用 2 件1982 年: 被引用 6 件1984 年: 被引用 3 件1985 年: 被引用 1 件1986 年: 被引用 1 件1987 年: 被引用 2 件1989 年: 被引用 6 件1990 年: 被引用 2 件1991 年: 被引用 3 件1992 年: 被引用 2 件1993 年: 被引用 3 件1994 年: 被引用 4 件1995 年: 被引用 1 件1996 年: 被引用 7 件1997 年: 被引用 6 件1998 年: 被引用 1 件2000 年: 被引用 5 件2001 年: 被引用 27 件2002 年: 被引用 31 件2003 年: 被引用 70 件2004 年: 被引用 204 件2005 年: 被引用 302 件2006 年: 被引用 256 件2007 年: 被引用 266 件2008 年: 被引用 308 件2009 年: 被引用 300 件2010 年: 被引用 300 件2011 年: 被引用 255 件2012 年: 被引用 228 件2013 年: 被引用 181 件2014 年: 被引用 180 件2015 年: 被引用 222 件2016 年: 被引用 194 件2017 年: 被引用 210 件2018 年: 被引用 183 件2019 年: 被引用 478 件2020 年: 被引用 487 件2021 年: 被引用 444 件2022 年: 被引用 369 件2023 年: 被引用 302 件2024 年: 被引用 406 件2025 年: 被引用 173 件2026 年: 被引用 11 件1922〜1963 年は被引用が無いため表示していません1965〜1966 年は被引用が無いため表示していません1968〜1977 年は被引用が無いため表示していません1979 年は被引用が無いため表示していません1983 年は被引用が無いため表示していません1988 年は被引用が無いため表示していません1999 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 3,552 件、この内訳の 30.6%イギリス: 引用元論文 1,007 件、この内訳の 8.7%中国: 引用元論文 635 件、この内訳の 5.5%ドイツ: 引用元論文 562 件、この内訳の 4.9%カナダ: 引用元論文 511 件、この内訳の 4.4%フランス: 引用元論文 407 件、この内訳の 3.5%イタリア: 引用元論文 399 件、この内訳の 3.4%オランダ: 引用元論文 370 件、この内訳の 3.2%オーストラリア: 引用元論文 334 件、この内訳の 2.9%スペイン: 引用元論文 297 件、この内訳の 2.6%日本: 引用元論文 264 件、この内訳の 2.3%スウェーデン: 引用元論文 249 件、この内訳の 2.1%
0%30.6%その他 25.9%

機関

分野

  • Biochemistry, Genetics and Molecular Biology58.6%
  • Medicine16.6%
  • Neuroscience15.4%
  • Immunology and Microbiology1.8%
  • Computer Science1.6%
  • Agricultural and Biological Sciences1.5%
  • その他4.5%

トピック

  • 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%
  • その他74.6%

共著者

全論文

検索で開く
  1. Synaptic, transcriptional and chromatin genes disrupted in autism

    著者: 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 被引用: 2,974

  2. The International HapMap Project

    著者: 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 ほか 83 名 - Nature 2003 被引用: 6,186

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

    著者: 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 ほか 33 名 - Nature Genetics 2022 被引用: 189

  4. Sex differences in brain protein expression and disease

    著者: 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 被引用: 87

  5. Genetic control of the human brain proteome

    著者: 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 被引用: 117

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

    著者: Janis Wigginton, David J. Cutler, Gonçalo R. Abecasis - The American Journal of Human Genetics 2005 被引用: 1,473

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

    著者: 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 被引用: 157

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

    著者: 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 被引用: 367

  9. Recessive gene disruptions in autism spectrum disorder

    著者: 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 被引用: 179

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

    著者: 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 被引用: 122

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

    著者: 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 被引用: 90

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

    著者: 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 ほか 24 名 - Molecular Psychiatry 2020 被引用: 135

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

    著者: 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 被引用: 96

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

    著者: 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 被引用: 44

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

    著者: 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 被引用: 162

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

    著者: 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 被引用: 84

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

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

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

    著者: 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 被引用: 52

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

    著者: 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 被引用: 43

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

    著者: 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 被引用: 28

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

    著者: 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 被引用: 23

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

    著者: 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 被引用: 594

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

    著者: 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 被引用: 95

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

    著者: 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 被引用: 74