Edwin H. Cook
1975–2025 年に発表
- 159
- 論文数
- 51,507
- 被引用数
- 110
- h 指数
- 156
- i10 指数
被引用数
引用元
国・地域
機関
分野
- Neuroscience46.2%
- Biochemistry, Genetics and Molecular Biology28.1%
- Medicine14.6%
- Psychology8.2%
- Agricultural and Biological Sciences0.4%
- Environmental Science0.4%
- その他2.1%
トピック
- Autism Spectrum Disorder Research16.6%
- Genetics and Neurodevelopmental Disorders8.9%
- Genomic variations and chromosomal abnormalities3.2%
- Family and Disability Support Research3.1%
- Attention Deficit Hyperactivity Disorder2.8%
- Child Nutrition and Feeding Issues2.6%
- その他62.8%
共著者
- Bennett Leventhal31
- Catherine Lord19
- Jeremy Veenstra‐VanderWeele15
- James S. Sutcliffe13
- Daniel W. Bradley11
- Dongmei Yu11
- Stephan Sanders11
- Karen A. McCaustland9
- Soma Das9
- Benjamin M. Neale8
- Bernie Devlin8
- Camille W. Brune8
- Daniel H. Geschwind8
- James E. Maynard8
- John A. Sweeney8
- Joseph D. Buxbaum8
- Lambertus Klei8
- Matthew W. Mosconi8
- Nancy J. Cox8
- Géraldine Dawson7
- Lea K. Davis7
- Michael T. Murtha7
- O. Joseph Bienvenu7
- Christine Stevens6
全論文
- The Autism Diagnostic Observation Schedule—Generic: A Standard Measure of Social and Communication Deficits Associated with the Spectrum of Autism
著者: Catherine Lord, Susan Risi, Linda Lambrecht, Edwin H. Cook, Bennett Leventhal, Pamela C. DiLavore, Andrew Pickles, Michael Rutter - Journal of Autism and Developmental Disorders 2000 被引用: 7,557
- Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
著者: Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Brie Wamsley, Lambertus Klei, Lily Wang, Stephanie P. Hao, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Catalina Betancur, Alfredo Brusco, Brian Hon‐Yin Chung, Edwin H. Cook, Michael L. Cuccaro, Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, James S. Sutcliffe, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Simona Cardaropoli, Diana Carli, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina De Sanctis Girardi, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Rebecca J. Schmidt, Moyra Smith, Claudia Ismania Samogy Costa, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, Branko Aleksić, Mykyta Artomov, Elisa Benetti, Monica Biscaldi-Schafer, Anders D. Børglum, Ãngel Carracedo, Andreas G. Chiocchetti, Hilary Coon, Ryan N. Doan, Montse Fernández‐Prieto, Christine M. Freitag, Sherif Gerges, Stephen J. Guter, David M. Hougaard, Christina M. Hultman, Suma Jacob, Miia Kaartinen, A lexander Kolevzon, Itaru Kushima, Terho Lehtimäki, Caterina Lo Rizzo, Nell Maltman, Marianna Manara, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Matthew W. Mosconi, Norio Ozaki, Aarno Palotie, Mara Parellada, Kaija Puura, Abraham Reichenberg, Sven Sandin, Stephen W. Scherer, Sabine Schlitt ほか 17 名 - Nature Genetics 2022 被引用: 617
- Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders
著者: Phil H. Lee, Verneri Anttila, Hyejung Won, Yen‐Chen Anne Feng, Jacob Rosenthal, Zhaozhong Zhu, Elliot M. Tucker–Drob, Michel G. Nivard, Andrew D. Grotzinger, Daniëlle Posthuma, Meg M.-J. Wang, Dongmei Yu, Eli A. Stahl, Raymond K. Walters, Richard Anney, Laramie E. Duncan, Tian Ge, Rolf Adolfsson, Tobias Banaschewski, Síntia Belangero, Edwin H. Cook, Giovanni Coppola, Eske M. Derks, Pieter J. Hoekstra, Jaakko Kaprio, Anna Keski‐Rahkonen, George Kirov, Henry R. Kranzler, Jurjen J. Luykx, Luís Augusto Rohde, Clement C. Zai, Esben Agerbo, María J. Arranz, Philip Asherson, Marie Bækvad‐Hansen, Gísli Baldursson, Mark A. Bellgrove, Richard A. Belliveau, Jan K. Buitelaar, Christie L. Burton, Jonas Bybjerg‐Grauholm, Miguel Casas, Felecia Cerrato, Kimberly Chambert, Claire Churchhouse, Bru Cormand, Jennifer Crosbie, Søren Dalsgaard, Ditte Demontis, Alysa E. Doyle, Ashley Dumont, Josephine Elia, Jakob Grove, Ólafur Ó. Guðmundsson, Jan Haavik, Håkon Håkonarson, Christine Søholm Hansen, Catharina A. Hartman, Ziarih Hawi, Amaia Hervás, David M. Hougaard, Daniel P. Howrigan, Hailiang Huang, Jonna Kuntsi, K. Langley, Klaus‐Peter Lesch, Patrick W. L. Leung, Sandra K. Loo, Joanna Martin, Alicia R. Martin, James J. McGough, Sarah E. Medland, Jennifer L. Moran, Ole Mors, Preben Bo Mortensen, Robert D. Oades, Duncan S. Palmer, Carsten Bøcker Pedersen, Marianne G. Pedersen, Triinu Peters, Timothy Poterba, Jesper Buchhave Poulsen, Josep Antoni Ramos‐Quiroga, Andreas Reif, Marta Ribasés, Aribert Rothenberger, Paula Rovira, Cristina Sánchez‐Mora, F. Kyle Satterstrom, Russell Schachar, María Soler Artigas, Stacy Steinberg, Hreinn Stefánsson, Patrick Turley, G. Bragi Walters, Thomas Werge, Tetyana Zayats, Dan E. Arking, Francesco Bettella, Joseph D. Buxbaum ほか 506 名 - Cell 2019 被引用: 1,516
- 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, Ãngel 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
- 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
- Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
著者: Ryan K. C. Yuen, Daniele Merico, Matt Bookman, Jennifer Howe, Bhooma Thiruvahindrapuram, Rohan Patel, J. Andrew Whitney, Nicole Deflaux, Jonathan Bingham, Zhuozhi Wang, Giovanna Pellecchia, Janet A. Buchanan, Susan Walker, Christian R. Marshall, Mohammed Uddin, Mehdi Zarrei, Éric Deneault, Lia D’Abate, Ada J. S. Chan, Stephanie Koyanagi, Tara Paton, Sérgio L. Pereira, Ny Hoang, Worrawat Engchuan, Edward J. Higginbotham, Karen Ho, Sylvia Lamoureux, Weili Li, Jeffrey R. MacDonald, Thomas Nalpathamkalam, Wilson W. L. Sung, Fiona J. Tsoi, John Wei, Lizhen Xu, Anne-Marie Tasse, Emily Kirby, William Van Etten, Simon Twigger, Wendy Roberts, Irene Drmic, Sanne Jilderda, Bonnie MacKinnon Modi, Barbara Kellam, Michael J. Szego, Cheryl Cytrynbaum, Rosanna Weksberg, Lonnie Zwaigenbaum, Marc Woodbury‐Smith, Jessica Brian, Lili Senman, Alana Iaboni, Krissy A.R. Doyle‐Thomas, Ann Thompson, Christina Chrysler, Jonathan Leef, Tal Savion‐Lemieux, Isabel M. Smith, Xudong Liu, Rob Nicolson, Vicki Seifer, Angie Fedele, Edwin H. Cook, Stephen R. Dager, Annette Estes, Louise Gallagher, Beth A. Malow, Jeremy Parr, Sarah Spence, Jacob Vorstman, Brendan J. Frey, James Robinson, Lisa J. Strug, Bridget A. Fernandez, Mayada Elsabbagh, Melissa T. Carter, Joachim Hallmayer, Bartha Maria Knoppers, Evdokia Anagnostou, Péter Szatmári, Robert H. Ring, David Glazer, Mathew T. Pletcher, Stephen W. Scherer - Nature Neuroscience 2017 被引用: 936
- A framework for the interpretation of de novo mutation in human disease
著者: Kaitlin E. Samocha, Elise Robinson, Stephan Sanders, Christine Stevens, Aniko Sabo, Lauren M. McGrath, Jack A. Kosmicki, Karola Rehnström, Swapan Mallick, Andrew Kirby, Dennis P. Wall, Daniel G. MacArthur, Stacey Gabriel, Mark A. DePristo, Shaun Purcell, Aarno Palotie, Eric Boerwinkle, Joseph D. Buxbaum, Edwin H. Cook, Richard A. Gibbs, Gerard D. Schellenberg, James S. Sutcliffe, Bernie Devlin, Kathryn Roeder, Benjamin M. Neale, Mark J. Daly - Nature Genetics 2014 被引用: 1,123
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
著者: Joseph Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E. Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W. Brune, Jonathan P. Bradfield, Marcin Imieliński, Edward C. Frackelton, Jennifer Reichert, Emily L. Crawford, Jeffrey Munson, Patrick Sleiman, Rosetta Chiavacci, Kiran Annaiah, Kelly Thomas, Cuiping Hou, Wendy Glaberson, James H. Flory, F. George Otieno, Maria Garris, Latha Soorya, Lambertus Klei, Joseph Piven, Kacie J. Meyer, Evdokia Anagnostou, Takeshi Sakurai, Rachel M. Game, Danielle S. Rudd, Danielle Zurawiecki, Christopher J. McDougle, Lea K. Davis, Judith Miller, David J. Posey, Shana M. Michaels, A lexander Kolevzon, Jeremy M. Silverman, Raphael Bernier, Susan E. Levy, Robert T. Schultz, Géraldine Dawson, Thomas Owley, William M. McMahon, Thomas H. Wassink, John A. Sweeney, John I. Nürnberger, Hilary Coon, James S. Sutcliffe, Nancy J. Minshew, Struan F.A. Grant, Maja Bućan, Edwin H. Cook, Joseph D. Buxbaum, Bernie Devlin, Gerard D. Schellenberg, Håkon Håkonarson - Nature 2009 被引用: 1,448
- Patterns and rates of exonic de novo mutations in autism spectrum disorders
著者: Benjamin M. Neale, Yan Kou, Li Liu, Avi Ma’ayan, Kaitlin E. Samocha, Aniko Sabo, Chiao‐Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov, Paz Polak, Seungtai Yoon, Jared Maguire, Emily L. Crawford, Nicholas G. Campbell, Evan Geller, Otto Valladares, Chad Schafer, Han Liu, Tuo Zhao, Guiqing Cai, Jayon Lihm, Ruth Dannenfelser, Omar Jabado, Zuleyma Peralta, Uma Nagaswamy, Donna M. Muzny, Jeffrey G. Reid, Irene Newsham, Yuanqing Wu, Lora Lewis, Yi Han, Benjamin F. Voight, Elaine T. Lim, Elizabeth J. Rossin, Andrew Kirby, Jason Flannick, Menachem Fromer, Khalid Shakir, Tim Fennell, Kiran Garimella, Eric Banks, Ryan Poplin, Stacey Gabriel, Mark A. DePristo, Jack R. Wimbish, Braden Boone, Shawn Levy, Catalina Betancur, Shamil Sunyaev, Eric Boerwinkle, Joseph D. Buxbaum, Edwin H. Cook, Bernie Devlin, Richard A. Gibbs, Kathryn Roeder, Gerard D. Schellenberg, James S. Sutcliffe, Mark J. Daly - Nature 2012 被引用: 1,808
- 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
- Autism Spectrum Disorders
著者: Catherine Lord, Edwin H. Cook, Bennett Leventhal, David G. Amaral - Neuron 2000 被引用: 553
- A framework for an evidence-based gene list relevant to autism spectrum disorder
著者: Christian P. Schaaf, Catalina Betancur, Ryan K. C. Yuen, Jeremy Parr, David Skuse, Louise Gallagher, Raphael Bernier, Janet A. Buchanan, Joseph D. Buxbaum, Chun‐An Chen, Kira A. Dies, Mayada Elsabbagh, Helen V. Firth, Thomas Frazier, Ny Hoang, Jennifer Howe, Christian R. Marshall, Jacques L. Michaud, Olivia Rennie, Péter Szatmári, Wendy K. Chung, Patrick Bolton, Edwin H. Cook, Stephen W. Scherer, Jacob Vorstman - Nature Reviews Genetics 2020 被引用: 147
- Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p
著者: Daniel J. Weiner, Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove, Jack Fu, Ajay Nadig, Caitlin E. Carey, Nikolas Baya, Jonas Bybjerg‐Grauholm, Preben Bo Mortensen, Thomas Werge, Ditte Demontis, Ole Mors, Merete Nordentoft, Thomas D. Als, Marie Bækvad‐Hansen, Anders Rosengren, Alexandra Havdahl, Anne Hedemand, Aarno Palotie, Aravinda Chakravarti, Dan E. Arking, Arvis Sulovari, Anna Starnawska, Bhooma Thiruvahindrapuram, Christiaan de Leeuw, Caitlin E. Carey, Christine Ladd‐Acosta, Celia van der Merwe, Bernie Devlin, Edwin H. Cook, Evan E. Eichler, Elisabeth Corfield, Gwen Dieleman, Gerard D. Schellenberg, Håkon Håkonarson, Hilary Coon, Isabel Dziobek, Jacob Vorstman, Jessica B. Girault, James S. Sutcliffe, Jinjie Duan, John I. Nürnberger, Joachim Hallmayer, Joseph D. Buxbaum, Joseph Piven, Lauren A. Weiss, Lea K. Davis, Magdalena Janecka, Manuel Mattheisen, Matthew W. State, Michael Gill, Mark J. Daly, Mohammed Uddin, Ole A. Andreassen, Péter Szatmári, Phil Hyoun Lee, Richard Anney, Stephan Ripke, Kyle Satterstrom, Susan L. Santangelo, Susan S. Kuo, Ludger Tebartz van Elst, Thomas Rolland, Thomas Bougeron, Tinca J. C. Polderman, Tychele N. Turner, Jack F. G. Underwood, Veera Manikandan, Vamsee Pillalamarri, Varun Warrier, Alexandra Philipsen, Andreas Reif, Anke Hinney, Bru Cormand, Claiton H.D. Bau, Diego Luiz Rovaris, Edmund Sonuga‐Barke, Elizabeth C. Corfield, Eugênio H. Grevet, Giovanni Abrahão Salum, Henrik Larsson, Jan Buitelaar, Jan Haavik, James J. McGough, Jonna Kuntsi, Josephine Elia, Klaus‐Peter Lesch, Marieke Klein, Mark A. Bellgrove, Martin Tesli, Patrick W. L. Leung, Pedro Mário Pan, Søren Dalsgaard, Sandra K. Loo, Sarah E. Medland, Stephen V. Faraone, Ted Reichborn‐Kjennerud ほか 11 名 - Nature Genetics 2022 被引用: 55
- Common genetic variants on 5p14.1 associate with autism spectrum disorders
著者: Kai Wang, Haitao Zhang, Deqiong Ma, Maja Bućan, Joseph Glessner, Brett S. Abrahams, Daria Salyakina, Marcin Imieliński, Jonathan P. Bradfield, Patrick Sleiman, Cecilia E. Kim, Cuiping Hou, Edward C. Frackelton, Rosetta Chiavacci, Nagahide Takahashi, Takeshi Sakurai, Eric Rappaport, Clara Lajonchere, Jeffrey Munson, Annette Estes, Olena Korvatska, Joseph Piven, Lisa I. Sonnenblick, Ana I. Alvarez Retuerto, Edward I. Herman, Hongmei Dong, Ted Hutman, Marian Sigman, Sally Ozonoff, Ami Klin, Thomas Owley, John A. Sweeney, Camille W. Brune, Rita M. Cantor, Raphael Bernier, John R. Gilbert, Michael L. Cuccaro, William M. McMahon, Judith Miller, Matthew W. State, Thomas H. Wassink, Hilary Coon, Susan E. Levy, Robert T. Schultz, John I. Nürnberger, Jonathan L. Haines, James S. Sutcliffe, Edwin H. Cook, Nancy J. Minshew, Joseph D. Buxbaum, Géraldine Dawson, Struan F.A. Grant, Daniel H. Geschwind, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, Håkon Håkonarson - Nature 2009 被引用: 975
- Recurrent 16p11.2 microdeletions in autism
著者: Revati Kumar, Samer Karamohamed, Jyotsna Sudi, Donald F. Conrad, Camille W. Brune, Judith A. Badner, T. Conrad Gilliam, Norma J. Nowak, Edwin H. Cook, William B. Dobyns, Susan L. Christian - Human Molecular Genetics 2007 被引用: 744
- Copy-number variations associated with neuropsychiatric conditions
著者: Edwin H. Cook, Stephen W. Scherer - Nature 2008 被引用: 677
- Genome-wide association study of obsessive-compulsive disorder
著者: S. Evelyn Stewart, Dongmei Yu, Jeremiah M. Scharf, Benjamin M. Neale, Jesen Fagerness, Carol A. Mathews, Paul Arnold, Patrick Evans, Eric R. Gamazon, Lisa Osiecki, Lauren M. McGrath, Stephen A. Haddad, Jacquelyn Crane, Dianne M. Hezel, C Illman, C Mayerfeld, Anuar Konkashbaev, Chunyu Liu, Anna Pluzhnikov, А. А. Тихомиров, Christopher K. Edlund, Scott L. Rauch, R. Moessner, Peter Falkai, W. Maier, Stephan Ruhrmann, HJ Grabe, Leonhard Lennertz, Michael Wagner, Laura Bellodi, Maria Cristina Cavallini, Margaret A. Richter, Edwin H. Cook, James L. Kennedy, David Rosenberg, Dan J. Stein, Sian Hemmings, Christine Löchner, Amin Azzam, Denise A. Chavira, Eduardo Fournier, Helena Garrido, Brooke Sheppard, Paula Umaña, Dennis L. Murphy, Jens R. Wendland, Jeremy Veenstra‐VanderWeele, Damiaan Denys, Rianne M. Blom, Dieter Deforce, Filip Van Nieuwerburgh, H.G.M. Westenberg, Susanne Walitza, Karin Egberts, Tobias Renner, Eurı́pedes Constantino Miguel, Carolina Cappi, Ana Gabriela Hounie, Maria Conceição do Rosário, Aline S. Sampaio, Homero Vallada, Humberto Nicolini, Nuria Lanzagorta, Beatríz Camarena, Richard Delorme, Marion Leboyer, Carlos N. Pato, Michele T. Pato, Emanuel Voyiaziakis, Peter Heutink, Daniëlle C. Cath, Daniëlle Posthuma, Johannes H. Smit, Jack Samuels, O. Joseph Bienvenu, Bernadette Cullen, Abby J. Fyer, Marco A. Grados, Benjamin D. Greenberg, James T. McCracken, Mark A. Riddle, Ying Wang, Vladimir Coric, James F. Leckman, Michael H. Bloch, Christopher Pittenger, Valsamma Eapen, Donald W. Black, Roel A. Ophoff, E Strengman, Daniele Cusi, Maurizio Turiel, Francesca Frau, Fabìo Macciardi, J. Raphael Gibbs, M R Cookson, Andrew Singleton, Sampath Arepalli, M R Cookson, Allissa Dillman ほか 32 名 - Molecular Psychiatry 2012 被引用: 391
- Reduced behavioral flexibility in autism spectrum disorders.
著者: Anna-Maria D'Cruz, Michael E. Ragozzino, Matthew W. Mosconi, Sunil Shrestha, Edwin H. Cook, John A. Sweeney - Neuropsychology 2013 被引用: 283
- Combining Information From Multiple Sources in the Diagnosis of Autism Spectrum Disorders
著者: Susan Risi, Catherine Lord, Katherine Gotham, Christina Corsello, Christina Chrysler, Péter Szatmári, Edwin H. Cook, Bennett Leventhal, Andrew Pickles - Journal of the American Academy of Child & Adolescent Psychiatry 2006 被引用: 572
- Autism as a disorder of neural information processing: directions for research and targets for therapy
著者: Matthew K. Belmonte, Edwin H. Cook, George M. Anderson, John L.R. Rubenstein, William T. Greenough, Andrea Beckel‐Mitchener, E Courchesne, Lisa M. Boulanger, Susan B. Powell, Pat Levitt, Emily Perry, Yibo Jiang, Timothy M. DeLorey, Elaine Tierney - Molecular Psychiatry 2004 被引用: 437
- A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data
著者: Quan Wang, Rui Chen, Feixiong Cheng, Qiang Wei, Ying Ji, Yang Hai, Xue Zhong, Ran Tao, Zhexing Wen, James S. Sutcliffe, Chunyu Liu, Edwin H. Cook, Nancy J. Cox, Bingshan Li - Nature Neuroscience 2019 被引用: 154
- Feedforward and Feedback Motor Control Abnormalities Implicate Cerebellar Dysfunctions in Autism Spectrum Disorder
著者: Matthew W. Mosconi, Suman Mohanty, Rachel K. Greene, Edwin H. Cook, David E. Vaillancourt, John A. Sweeney - Journal of Neuroscience 2015 被引用: 150
- Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture
著者: Lea K. Davis, Dongmei Yu, Clare L. Keenan, Eric R. Gamazon, Anuar Konkashbaev, Eske M. Derks, Benjamin M. Neale, Jian Yang, Sang Lee, Patrick Evans, Cathy L. Barr, Laura Bellodi, Fortu Benarroch, Gabriel Bedoya Berrío, O. Joseph Bienvenu, Michael H. Bloch, Rianne M. Blom, Ruth D. Bruun, Cathy L. Budman, Beatríz Camarena, Desmond Campbell, Carolina Cappi, Julio César Cardona Silgado, Daniëlle C. Cath, Maria Cristina Cavallini, Denise A. Chavira, Sylvain Chouinard, David V. Conti, Edwin H. Cook, Vladimir Coric, Bernadette Cullen, Dieter Deforce, Richard Delorme, Yves Dion, Christopher K. Edlund, Karin Egberts, Peter Falkai, Thomas Fernandez, Patience Gallagher, Helena Garrido, Daniel Geller, Simon Girard, Hans J. Grabe, Marco A. Grados, Benjamin D. Greenberg, Varda Gross‐Tsur, Stephen A. Haddad, Gary A. Heiman, Sian Hemmings, Ana Gabriela Hounie, Cornelia Illmann, Joseph Jankovic, Michael A. Jenike, James L. Kennedy, Robert A. King, Bárbara Kremeyer, Roger Kurlan, Nuria Lanzagorta, Marion Leboyer, James F. Leckman, Leonhard Lennertz, Chunyu Liu, Christine Löchner, Thomas L. Lowe, Fabìo Macciardi, James T. McCracken, Lauren M. McGrath, Sandra Catalina Mesa Restrepo, Rainald Moessner, Jubel Morgan, Heike Müller, Dennis L. Murphy, Allan L. Naarden, William Cornejo Ochoa, Roel A. Ophoff, Lisa Osiecki, A.J. Pakstis, Michele T. Pato, Carlos N. Pato, John Piacentini, Christopher Pittenger, Yehuda Pollak, Scott L. Rauch, Tobias Renner, Victor I. Reus, Margaret A. Richter, Mark A. Riddle, Mary M. Robertson, Roxana Romero, Maria Conceição do Rosário, David Rosenberg, Guy A. Rouleau, Stephan Ruhrmann, Andrés Ruiz‐Linares, Aline S. Sampaio, Jack Samuels, Paul Sandor, Brooke Sheppard, Harvey S. Singer, Jan Smit ほか 31 名 - PLoS Genetics 2013 被引用: 344
- A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism
著者: Patrícia B. S. Celestino-Soper, Sara Violante, Emily L. Crawford, Rui Luo, Anath C. Lionel, Elsa Delaby, Guiqing Cai, Bekim Sadiković, Kwanghyuk Lee, Charlene Lo, Kun Gao, Richard Person, Timothy J. M. Moss, Jennifer R. German, Ni Huang, Marwan Shinawi, Diane Treadwell‐Deering, Péter Szatmári, Wendy Roberts, Bridget A. Fernandez, Richard J. Schroer, Roger E. Stevenson, Joseph D. Buxbaum, Catalina Betancur, Stephen W. Scherer, Stephan Sanders, Daniel H. Geschwind, James S. Sutcliffe, Matthew E. Hurles, Ronald J. A. Wanders, Chad A. Shaw, Suzanne M. Leal, Edwin H. Cook, Robin P. Goin‐Kochel, Frédéric M. Vaz, Arthur L. Beaudet - National Academy of Sciences, Proceedings of the National Academy of Sciences 2012 被引用: 142
