litlas
ログインアカウント作成

Stephan Sanders

1977–2025 年に発表

118
論文数
32,415
被引用数
70
h 指数
107
i10 指数

被引用数

Stephan Sanders の年別被引用数1955 年: 被引用 1 件1978 年: 被引用 3 件1979 年: 被引用 3 件1980 年: 被引用 3 件1981 年: 被引用 1 件1982 年: 被引用 4 件1983 年: 被引用 4 件1984 年: 被引用 1 件1985 年: 被引用 2 件1987 年: 被引用 1 件1988 年: 被引用 8 件1989 年: 被引用 1 件1991 年: 被引用 2 件1992 年: 被引用 2 件1993 年: 被引用 1 件1994 年: 被引用 1 件1995 年: 被引用 1 件1996 年: 被引用 2 件1997 年: 被引用 3 件1998 年: 被引用 1 件1999 年: 被引用 1 件2000 年: 被引用 3 件2001 年: 被引用 2 件2006 年: 被引用 3 件2007 年: 被引用 2 件2008 年: 被引用 1 件2010 年: 被引用 12 件2011 年: 被引用 82 件2012 年: 被引用 172 件2013 年: 被引用 323 件2014 年: 被引用 423 件2015 年: 被引用 495 件2016 年: 被引用 547 件2017 年: 被引用 617 件2018 年: 被引用 612 件2019 年: 被引用 1,490 件2020 年: 被引用 1,519 件2021 年: 被引用 1,619 件2022 年: 被引用 1,201 件2023 年: 被引用 871 件2024 年: 被引用 1,357 件2025 年: 被引用 614 件2026 年: 被引用 44 件1956〜1977 年は被引用が無いため表示していません1986 年は被引用が無いため表示していません1990 年は被引用が無いため表示していません2002〜2005 年は被引用が無いため表示していません2009 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 4,433 件、この内訳の 27.9%イギリス: 引用元論文 1,330 件、この内訳の 8.4%中国: 引用元論文 933 件、この内訳の 5.9%ドイツ: 引用元論文 825 件、この内訳の 5.2%カナダ: 引用元論文 769 件、この内訳の 4.8%フランス: 引用元論文 647 件、この内訳の 4.1%オランダ: 引用元論文 609 件、この内訳の 3.8%イタリア: 引用元論文 608 件、この内訳の 3.8%オーストラリア: 引用元論文 554 件、この内訳の 3.5%スペイン: 引用元論文 365 件、この内訳の 2.3%日本: 引用元論文 331 件、この内訳の 2.1%スウェーデン: 引用元論文 312 件、この内訳の 2%
0%27.9%その他 26.2%

機関

分野

  • Biochemistry, Genetics and Molecular Biology55.7%
  • Neuroscience24.7%
  • Medicine13.4%
  • Psychology2.4%
  • Immunology and Microbiology1.1%
  • Computer Science0.8%
  • その他1.9%

トピック

  • Genetics and Neurodevelopmental Disorders8.7%
  • Autism Spectrum Disorder Research8.4%
  • Genomics and Rare Diseases6%
  • Genomic variations and chromosomal abnormalities4.6%
  • Congenital heart defects research3.7%
  • Genetic Associations and Epidemiology2.6%
  • その他66%

共著者

全論文

検索で開く
  1. Predicting Splicing from Primary Sequence with Deep Learning

    著者: Kishore Jaganathan, Sofia Kyriazopoulou Panagiotopoulou, Jeremy F. McRae, Siavash Fazel Darbandi, David A. Knowles, Yang Li, Jack A. Kosmicki, Juan David Arbelaez, Wenwu Cui, Grace Schwartz, Eric D. Chow, Efstathios Kanterakis, Hong Gao, Amirali Kia, Serafim Batzoglou, Stephan Sanders, Kyle Kai‐How Farh - Cell 2019 被引用: 3,020

  2. 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

  3. Integrative functional genomic analysis of human brain development and neuropsychiatric risks

    著者: Mingfeng Li, Gabriel Santpere, Yuka Imamura Kawasawa, Oleg V. Evgrafov, Forrest O. Gulden, Sirisha Pochareddy, Susan M. Sunkin, Zhen Li, Yurae Shin, Ying Zhu, André M. M. Sousa, Donna M. Werling, Robert R. Kitchen, Hyo Jung Kang, Mihovil Pletikos, Jinmyung Choi, Sydney K. Muchnik, Xuming Xu, Daifeng Wang, Belén Lorente-Galdós, Shuang Liu, Paola Giusti‐Rodríguez, Hyejung Won, Christiaan de Leeuw, Antonio F. Pardiñas, PsychENCODE Developmental Subgroup, Ming Hu, Fulai Jin, Yun Li, Michael J. Owen, Michael O‘Donovan, James Walters, Daniëlle Posthuma, Mark A. Reimers, Pat Levitt, Daniel R. Weinberger, Thomas M. Hyde, Joel E. Kleinman, Daniel H. Geschwind, Michael Hawrylycz, Matthew W. State, Stephan Sanders, Patrick F. Sullivan, Mark Gerstein, Ed S. Lein, James A. Knowles, Nenad Šestan, A. Jeremy Willsey, Aaron Oldre, Aaron Szafer, Adrian Camarena, Adriana Cherskov, Alexander W. Charney, Alexej Abyzov, Alexey Kozlenkov, Alexias Safi, Allan R. Jones, Allison E. Ashley‐Koch, Amanda Ebbert, Amanda J. Price, Amanda Sekijima, Amira Kefi, Amy Bernard, Anahita Amiri, Andrea Sboner, Andrew E. Clark, Andrew E. Jaffe, Andrew T.N. Tebbenkamp, Andy J. Sodt, Angie Guillozet‐Bongaarts, Angus C. Nairn, Anita Carey, Anita Hüttner, Ann Chervenak, Anna Szekely, Annie W. Shieh, Arif Harmanci, Barbara K. Lipska, Becky C. Carlyle, Ben W. Gregor, Bibi Kassim, Brooke Sheppard, Candace Bichsel, Chang-Gyu Hahn, Chang-Kyu Lee, Chao Chen, Chihchau L. Kuan, Chinh Dang, Chris Lau, Christine Cuhaciyan, Christoper Armoskus, Christopher E. Mason, Chunyu Liu, Cliff Slaughterbeck, Crissa Bennet, Dalila Pinto, Damon Polioudakis, Daniel Franjic, Daniel J. Miller, Darren Bertagnolli ほか 187 名 - Science 2018 被引用: 901

  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. Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

    著者: Sheng Chih Jin, Jason Homsy, Samir Zaidi, Qiongshi Lu, Sarah U. Morton, Steven R. DePalma, Xue Zeng, Hongjian Qi, Wen-I Chang, Michael C. Sierant, Wei-Chien Hung, Shozeb Haider, Junhui Zhang, James Knight, Robert Bjornson, Christopher Castaldi, Irina R Tikhonoa, Kaya Bilgüvar, Shrikant Mane, Stephan Sanders, Seema Mital, Mark W. Russell, J. William Gaynor, John Deanfield, Anna Giardini, George A. Porter, Deepak Srivastava, Cecilia Lo, Yufeng Shen, W. Scott Watkins, Mark Yandell, H. Joseph Yost, Martin Tristani‐Firouzi, Jane W. Newburger, Amy E. Roberts, Richard Kim, Hongyu Zhao, Jonathan R. Kaltman, Elizabeth Goldmuntz, Wendy K. Chung, Jonathan G. Seidman, Bruce D. Gelb, Christine E. Seidman, Richard P. Lifton, Martina Brueckner - Nature Genetics 2017 被引用: 928

  6. De novo mutations revealed by whole-exome sequencing are strongly associated with autism

    著者: Stephan Sanders, Michael T. Murtha, Abha R. Gupta, John D. Murdoch, Melanie J. Raubeson, A. Jeremy Willsey, A. Gulhan Ercan‐Sencicek, Nicholas M. DiLullo, Neelroop Parikshak, Jason L. Stein, Michael F. Walker, G Ober, Nicole A. Teran, Youeun Song, Paul El-Fishawy, Ryan Murtha, Murim Choi, John D. Overton, Robert Bjornson, Nicholas Carriero, Kyle A. Meyer, Kaya Bilgüvar, Shrikant Mane, Nenad Šestan, Richard P. Lifton, Murat Günel, Kathryn Roeder, Daniel H. Geschwind, Bernie Devlin, Matthew W. State - Nature 2012 被引用: 2,183

  7. Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism

    著者: A. Jeremy Willsey, Stephan Sanders, Mingfeng Li, Shan Dong, Andrew T.N. Tebbenkamp, Rebecca Muhle, Steven K. Reilly, Leon C. W. Lin, Sofia Fertuzinhos, Jeremy A. Miller, Michael T. Murtha, Candace Bichsel, Wei Niu, Justin Cotney, A. Gulhan Ercan‐Sencicek, Jake Gockley, Abha R. Gupta, Wenqi Han, Xin He, Ellen J. Hoffman, Lambertus Klei, Jing Lei, Wenzhong Liu, Li Liu, Cong Lu, Xuming Xu, Ying Zhu, Shrikant Mane, Ed S. Lein, Liping Wei, James P. Noonan, Kathryn Roeder, Bernie Devlin, Nenad Šestan, Matthew W. State - Cell 2013 被引用: 1,000

  8. De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies

    著者: Jason Homsy, Samir Zaidi, Yufeng Shen, James S. Ware, Kaitlin E. Samocha, Konrad J. Karczewski, Steven R. DePalma, David McKean, Hiroko Wakimoto, Josh Gorham, Sheng Chih Jin, John Deanfield, Anna Giardini, George A. Porter, Richard Kim, Kaya Bilgüvar, Francesc López‐Giráldez, Irina Tikhonova, Shrikant Mane, Angela Romano-Adesman, Hongjian Qi, Badri N. Vardarajan, Lijiang Ma, Mark J. Daly, Amy E. Roberts, Mark W. Russell, Seema Mital, Jane W. Newburger, J. William Gaynor, Roger E. Breitbart, Ivan Iossifov, Michael Ronemus, Stephan Sanders, Jonathan R. Kaltman, Jonathan G. Seidman, Martina Brueckner, Bruce D. Gelb, Elizabeth Goldmuntz, Richard P. Lifton, Christine E. Seidman, Wendy K. Chung - Science 2015 被引用: 910

  9. Most genetic risk for autism resides with common variation

    著者: Trent Gaugler, Lambertus Klei, Stephan Sanders, Corneliu Bodea, Arthur P. Goldberg, Ann B. Lee, Milind Mahajan, Dina Manaa, Yudi Pawitan, Jennifer Reichert, Stephan Ripke, Sven Sandin, Pamela Sklar, Oscar Svantesson, Abraham Reichenberg, Christina M. Hultman, Bernie Devlin, Kathryn Roeder, Joseph D. Buxbaum - Nature Genetics 2014 被引用: 1,286

  10. De novo mutations in histone-modifying genes in congenital heart disease

    著者: Samir Zaidi, Murim Choi, Hiroko Wakimoto, Lijiang Ma, Jianming Jiang, John D. Overton, Angela Romano-Adesman, Robert Bjornson, Roger E. Breitbart, Kerry K. Brown, Nicholas Carriero, Yee Him Cheung, John Deanfield, Steven R. DePalma, Khalid A. Fakhro, Joseph Glessner, Håkon Håkonarson, Michael J. Italia, Jonathan R. Kaltman, Juan Pablo Kaski, Richard Kim, Jennie Kline, Teresa Lee, Jeremy Leipzig, Alexander Lopez, Shrikant Mane, Laura E. Mitchell, Jane W. Newburger, Michael Parfenov, Itsik Pe’er, George A. Porter, Amy E. Roberts, Ravi Sachidanandam, Stephan Sanders, Howard Seiden, Mathew W. State, Sai Lakshmi Subramanian, Irina R. Tikhonova, Wei Wang, Dorothy Warburton, Peter S. White, Ismée A. Williams, Hongyu Zhao, Jonathan G. Seidman, Martina Brueckner, Wendy K. Chung, Bruce D. Gelb, Elizabeth Goldmuntz, Christine E. Seidman, Richard P. Lifton - Nature 2013 被引用: 968

  11. 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

  12. Progress in Understanding and Treating SCN2A-Mediated Disorders

    著者: Stephan Sanders, Arthur J. Campbell, Jeffrey R. Cottrell, Rikke S. Møller, Florence F. Wagner, Angie L. Auldridge, Raphael Bernier, William A. Catterall, Wendy K. Chung, James R. Empfield, Alfred L. George, Joerg F. Hipp, Omar Khwaja, Evangelos Kiskinis, Dennis Lal, Dheeraj Malhotra, J Gordon Millichap, Thomas S. Otis, Steven Petrou, Geoffrey S. Pitt, Leah F. Schust, Cora Taylor, Jennifer Tjernagel, John E. Spiro, Kevin J. Bender - Trends in Neurosciences 2018 被引用: 341

  13. Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder

    著者: Joon‐Yong An, Kevin Lin, Lingxue Zhu, Donna M. Werling, Shan Dong, Harrison Brand, Harold Z. Wang, Xuefang Zhao, Grace Schwartz, Ryan L. Collins, Benjamin Currall, Claudia Dastmalchi, Jeanselle Dea, Clif Duhn, Michael C. Gilson, Lambertus Klei, Lindsay Liang, Eirene Markenscoff-Papadimitriou, Sirisha Pochareddy, Nadav Ahituv, Joseph D. Buxbaum, Hilary Coon, Mark J. Daly, Young S. Kim, Gábor Marth, Benjamin M. Neale, Aaron R. Quinlan, John L.R. Rubenstein, Nenad Šestan, Matthew W. State, A. Jeremy Willsey, Michael E. Talkowski, Bernie Devlin, Kathryn Roeder, Stephan Sanders - Science 2018 被引用: 362

  14. The Autism-Associated Gene Scn2a Contributes to Dendritic Excitability and Synaptic Function in the Prefrontal Cortex

    著者: Perry W.E. Spratt, Roy Ben‐Shalom, Caroline M. Keeshen, Kenneth J. Burke, Rebecca L. Clarkson, Stephan Sanders, Kevin J. Bender - Neuron 2019 被引用: 257

  15. Opposing Effects on Na V 1.2 Function Underlie Differences Between SCN2A Variants Observed in Individuals With Autism Spectrum Disorder or Infantile Seizures

    著者: Roy Ben‐Shalom, Caroline M. Keeshen, Kiara N. Berríos, Joon‐Yong An, Stephan Sanders, Kevin J. Bender - Biological Psychiatry 2017 被引用: 296

  16. Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

    著者: iPSYCH-Broad Autism Group, Daniel J. Weiner, Emilie M. Wigdor, Stephan Ripke, Raymond K. Walters, Jack A. Kosmicki, Jakob Grove, Kaitlin E. Samocha, Jacqueline I. Goldstein, Aysu Okbay, Jonas Bybjerg‐Grauholm, Thomas Werge, David M. Hougaard, Jacob Taylor, David Skuse, Bernie Devlin, Richard Anney, Stephan Sanders, Somer Bishop, Preben Bo Mortensen, Anders D. Børglum, George Davey Smith, Mark J. Daly, Elise B Robinson - Nature Genetics 2017 被引用: 556

  17. Leveraging electronic health records and knowledge networks for Alzheimer’s disease prediction and sex-specific biological insights

    著者: Alice Tang, Katherine P. Rankin, Gabriel Cerono, Silvia Miramontes, Hunter Mills, Jacquelyn Roger, Billy Zeng, Charlotte Nelson, Karthik Soman, Sarah Woldemariam, Yaqiao Li, Albert Lee, Riley Bove, M. Maria Glymour, Nima Aghaeepour, Tomiko Oskotsky, Zachary Miller, Isabel Elaine Allen, Stephan Sanders, Sergio E. Baranzini, Marina Sirota - Nature Aging 2024 被引用: 74

  18. Sex and gender differences in autism spectrum disorder: summarizing evidence gaps and identifying emerging areas of priority

    著者: Alycia Halladay, Somer Bishop, John N. Constantino, Amy M. Daniels, Katheen Koenig, Kate Palmer, Daniel S. Messinger, Kevin A. Pelphrey, Stephan Sanders, Alison Singer, Julie Lounds Taylor, Péter Szatmári - Molecular Autism 2015 被引用: 575

  19. An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

    著者: Donna M. Werling, Harrison Brand, Joon‐Yong An, Matthew R. Stone, Lingxue Zhu, Joseph Glessner, Ryan L. Collins, Shan Dong, Ryan M. Layer, Eirene Markenscoff-Papadimitriou, Andrew Farrell, Grace Schwartz, Harold Z. Wang, Benjamin Currall, Xuefang Zhao, Jeanselle Dea, Clif Duhn, Carolyn A. Erdman, Michael C. Gilson, Rachita Yadav, Robert E. Handsaker, Seva Kashin, Lambertus Klei, Jeffrey D. Mandell, Tomasz J. Nowakowski, Yuwen Liu, Sirisha Pochareddy, Louw Smith, Michael F. Walker, Matthew J. Waterman, Xin He, Arnold R. Kriegstein, John L.R. Rubenstein, Nenad Šestan, Steven A. McCarroll, Benjamin M. Neale, Hilary Coon, A. Jeremy Willsey, Joseph D. Buxbaum, Mark J. Daly, Matthew W. State, Aaron R. Quinlan, Gábor Marth, Kathryn Roeder, Bernie Devlin, Michael E. Talkowski, Stephan Sanders - Nature Genetics 2018 被引用: 345

  20. In Search of Biomarkers to Guide Interventions in Autism Spectrum Disorder: A Systematic Review

    著者: Mara Parellada, Álvaro Andreu-Bernabeu, Mónica Burdeus-Olavarrieta, Antonia San José Cáceres, Elena Urbiola, Linda L. Carpenter, Nina V. Kraguljac, William M. McDonald, Charles B. Nemeroff, Carolyn I. Rodríguez, Alik S. Widge, Matthew W. State, Stephan Sanders - American Journal of Psychiatry 2022 被引用: 110

  21. 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

  22. Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders

    著者: Benxia Hu, Hyejung Won, Won Mah, Royce Park, Bibi Kassim, Keeley Spiess, Alexey Kozlenkov, Cheynna Crowley, Sirisha Pochareddy, Allison E. Ashley‐Koch, Gregory E. Crawford, Melanie E. Garrett, Lingyun Song, Alexias Safi, Graham D. Johnson, Gregory A. Wray, Timothy E. Reddy, Fernando S. Goes, Peter P. Zandi, Julien Bryois, Andrew E. Jaffe, Amanda J. Price, Nikolay A. Ivanov, Leonardo Collado‐Torres, Thomas M. Hyde, Emily E. Burke, Joel E. Kleiman, Ran Tao, Joo Heon Shin, Kiran Girdhar, Yan Jiang, Marija Kundaković, Leanne Brown, Jennifer Wiseman, Elizabeth Zharovsky, Rivka Jacobov, Olivia Devillers, Elie Flatow, Gabriel E. Hoffman, Judson Belmont, Diane M. Del Valle, Nancy Francoeur, Evi Hadjimichael, Dalila Pinto, Harm van Bakel, Panos Roussos, John F. Fullard, Jaroslav Bendl, Mads E. Hauberg, Alexander W. Charney, Vahram Haroutunian, Barbara K. Lipska, David A. Lewis, Chang-Gyu Hahn, Lara M. Mangravite, Mette A. Peters, Yooree Chae, Junmin Peng, Mingming Niu, Xusheng Wang, Maree J. Webster, Thomas G. Beach, Chao Chen, Yi Jiang, Rujia Dai, Yongjun Wang, Yan Xia, Annie W. Shieh, Chunyu Liu, Kay Grennan, Ramu Vadukapuram, Gina Giase, Dominic Fitzgerald, Lijun Cheng, Miguel Brown, Mimi Brown, Tonya M. Brunetti, Thomas Goodman, Majd Alsayed, Kevin P. White, Mohana Ray, Damon Polioudakis, Brie Wamsley, Jiani Yin, Luis de la Torre-Ubieta, Michael J. Gandal, Vivek Swarup, Stephan Sanders, Matthew W. State, Donna M. Werling, Joon‐Yong An, Brooke Sheppard, A. Jeremy Willsey, Amira Kefi, Eugenio Mattei, Michael Purcaro, Zhiping Weng, J. Russell Moore, Henry Pratt, Jack Huey ほか 56 名 - Nature Communications 2021 被引用: 107

  23. The female protective effect against autism spectrum disorder

    著者: Emilie M. Wigdor, Daniel J. Weiner, Jakob Grove, Jack Fu, Wesley K. Thompson, Caitlin E. Carey, Nikolas Baya, Celia van der Merwe, Raymond K. Walters, F. Kyle Satterstrom, Duncan S. Palmer, Anders Rosengren, Jonas Bybjerg‐Grauholm, David M. Hougaard, Preben Bo Mortensen, Mark J. Daly, Michael E. Talkowski, Stephan Sanders, Somer Bishop, Anders D. Børglum, Elise Robinson - Cell Genomics 2022 被引用: 112

  24. The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment

    著者: Justin Cotney, Rebecca Muhle, Stephan Sanders, Li Liu, A. Jeremy Willsey, Wei Niu, Wenzhong Liu, Lambertus Klei, Jing Lei, Jun Yin, Steven K. Reilly, Andrew T.N. Tebbenkamp, Candace Bichsel, Mihovil Pletikos, Nenad Šestan, Kathryn Roeder, Matthew W. State, Bernie Devlin, James P. Noonan - Nature Communications 2015 被引用: 372