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Kathryn Roeder

1988–2025 年に発表

124
論文数
39,506
被引用数
80
h 指数
114
i10 指数

被引用数

Kathryn Roeder の年別被引用数1955 年: 被引用 1 件1972 年: 被引用 1 件1978 年: 被引用 1 件1988 年: 被引用 1 件1989 年: 被引用 2 件1990 年: 被引用 3 件1991 年: 被引用 11 件1992 年: 被引用 25 件1993 年: 被引用 10 件1994 年: 被引用 13 件1995 年: 被引用 19 件1996 年: 被引用 19 件1997 年: 被引用 17 件1998 年: 被引用 27 件1999 年: 被引用 34 件2000 年: 被引用 46 件2001 年: 被引用 99 件2002 年: 被引用 92 件2003 年: 被引用 96 件2004 年: 被引用 124 件2005 年: 被引用 157 件2006 年: 被引用 151 件2007 年: 被引用 190 件2008 年: 被引用 223 件2009 年: 被引用 226 件2010 年: 被引用 286 件2011 年: 被引用 265 件2012 年: 被引用 406 件2013 年: 被引用 521 件2014 年: 被引用 638 件2015 年: 被引用 679 件2016 年: 被引用 639 件2017 年: 被引用 659 件2018 年: 被引用 621 件2019 年: 被引用 1,522 件2020 年: 被引用 1,489 件2021 年: 被引用 1,495 件2022 年: 被引用 1,119 件2023 年: 被引用 801 件2024 年: 被引用 1,064 件2025 年: 被引用 458 件2026 年: 被引用 28 件1956〜1971 年は被引用が無いため表示していません1973〜1977 年は被引用が無いため表示していません1979〜1987 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 6,099 件、この内訳の 27.6%イギリス: 引用元論文 1,885 件、この内訳の 8.5%中国: 引用元論文 1,285 件、この内訳の 5.8%ドイツ: 引用元論文 1,053 件、この内訳の 4.8%カナダ: 引用元論文 1,012 件、この内訳の 4.6%オランダ: 引用元論文 903 件、この内訳の 4.1%フランス: 引用元論文 777 件、この内訳の 3.5%オーストラリア: 引用元論文 770 件、この内訳の 3.5%イタリア: 引用元論文 769 件、この内訳の 3.5%スウェーデン: 引用元論文 595 件、この内訳の 2.7%スペイン: 引用元論文 458 件、この内訳の 2.1%デンマーク: 引用元論文 453 件、この内訳の 2%
0%27.6%その他 27.3%

機関

分野

  • Biochemistry, Genetics and Molecular Biology48.8%
  • Neuroscience17.4%
  • Medicine15.8%
  • Computer Science4.5%
  • Psychology4.3%
  • Mathematics2.3%
  • その他6.9%

トピック

  • Genetic Associations and Epidemiology6.8%
  • Genetics and Neurodevelopmental Disorders6.1%
  • Autism Spectrum Disorder Research5.6%
  • Genomics and Rare Diseases3.3%
  • Genomic variations and chromosomal abnormalities3.2%
  • Genetic Mapping and Diversity in Plants and Animals2.1%
  • その他72.9%

共著者

全論文

検索で開く
  1. Identification of common genetic risk variants for autism spectrum disorder

    著者: Jakob Grove, BUPGEN, Stephan Ripke, Thomas D. Als, Manuel Mattheisen, Raymond K. Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A. Andreassen, Richard Anney, Swapnil Awashti, Rich Belliveau, Francesco Bettella, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Felecia Cerrato, Kimberly Chambert, Jane Christensen, Claire Churchhouse, Karin Dellenvall, Ditte Demontis, Silvia De Rubeis, Bernie Devlin, Srdjan Djurovic, Ashley Dumont, Jacqueline I. Goldstein, Christine Søholm Hansen, Mads E. Hauberg, Mads V. Hollegaard, Sigrun Hope, Daniel P. Howrigan, Hailiang Huang, Christina M. Hultman, Lambertus Klei, Julian Maller, Joanna Martin, Alicia R. Martin, Jennifer L. Moran, Mette Nyegaard, Terje Nærland, Duncan S. Palmer, Aarno Palotie, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy dPoterba, Jesper Buchhave Poulsen, Beaté St Pourcain, Per Qvist, Karola Rehnström, Abraham Reichenberg, Jennifer Reichert, Elise Robinson, Kathryn Roeder, Panos Roussos, Evald Sæmundsen, Sven Sandin, F. Kyle Satterstrom, George Davey Smith, Hreinn Stefánsson, Stacy Steinberg, Christine Stevens, Patrick F. Sullivan, Patrick Turley, G. Bragi Walters, Xinyi Xu, Kāri Stefánsson, Daniel H. Geschwind, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum - Nature Genetics 2019 被引用: 2,632

  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. 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

  4. Discovery of target genes and pathways at GWAS loci by pooled single-cell CRISPR screens

    著者: John Morris, Christina M. Caragine, Zharko Daniloski, Júlia Domingo, Timothy Barry, Lu Lu, Kyrie Davis, Marcello Ziosi, Dafni A. Glinos, Stephanie Hao, Eleni P. Mimitou, Peter Smibert, Kathryn Roeder, Eugene Katsevich, Tuuli Lappalainen, Neville E. Sanjana - Science 2023 被引用: 203

  5. Gene expression elucidates functional impact of polygenic risk for schizophrenia

    著者: Menachem Fromer, Panos Roussos, Solveig K. Sieberts, Jessica Johnson, David H. Kavanagh, Thanneer M. Perumal, Douglas M. Ruderfer, Edwin C. Oh, Aaron Topol, Hardik Shah, Lambertus Klei, Robin S. S. Kramer, Dalila Pinto, Zeynep H. Gümüş, A. Ercüment Çiçek, Kristen K. Dang, Andrew Browne, Cong Lu, Lu Xie, Ben Readhead, Eli A. Stahl, Jianqiu Xiao, Mahsa Parvizi, Tymor Hamamsy, John F. Fullard, Ying‐Chih Wang, Milind Mahajan, Jonathan M.J. Derry, Joel T. Dudley, Scott E. Hemby, Benjamin A. Logsdon, Konrad Talbot, Towfique Raj, David A. Bennett, Philip L. De Jager, Jun Zhu, Bin Zhang, Patrick F. Sullivan, Andrew Chess, Shaun Purcell, Leslie A. Shinobu, Lara M. Mangravite, Hiroyoshi Toyoshiba, Raquel E. Gur, Chang-Gyu Hahn, David A. Lewis, Vahram Haroutunian, Mette A. Peters, Barbara K. Lipska, Joseph D. Buxbaum, Eric E. Schadt, Keisuke Hirai, Kathryn Roeder, Kristen Brennand, Nicholas Katsanis, Enrico Domenici, Bernie Devlin, Pamela Sklar - Nature Neuroscience 2016 被引用: 1,217

  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. Genomic Control for Association Studies

    著者: Bernie Devlin, Kathryn Roeder - Biometrics 1999 被引用: 3,246

  8. 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

  9. A SAS Procedure Based on Mixture Models for Estimating Developmental Trajectories

    著者: Bobby L. Jones, Daniel S. Nagin, Kathryn Roeder - Sociological Methods & Research 2001 被引用: 2,394

  10. 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

  11. APOE and TREM2 regulate amyloid-responsive microglia in Alzheimer’s disease

    著者: Aivi T. Nguyen, Kui Wang, Gang Hu, Xuran Wang, Zhen Miao, Joshua A. Azevedo, EunRan Suh, Vivianna M. Van Deerlin, David Choi, Kathryn Roeder, Mingyao Li, Edward B. Lee - Acta Neuropathologica 2020 被引用: 281

  12. 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

  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. 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

  15. Global spectral clustering in dynamic networks

    著者: Fuchen Liu, David Choi, Lu Xie, Kathryn Roeder - National Academy of Sciences, Proceedings of the National Academy of Sciences 2018 被引用: 147

  16. 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

  17. 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

  18. The huge Package for High-dimensional Undirected Graph Estimation in R

    著者: Tuo Zhao, Han Liu, Kathryn Roeder, John D. Lafferty, Larry A. Wasserman - http://cran.r-project.org/web/packages/huge/vignettes/vignette.pdf, J. Mach. Learn. Res. 2012 被引用: 487

  19. Genome-wide association identifies multiple ulcerative colitis susceptibility loci

    著者: Dermot McGovern, Agnès Gardet, Leif Törkvist, Philippe Goyette, Jonah Essers, Kent D. Taylor, Benjamin M. Neale, Rick Twee‐Hee Ong, Caroline Lagacé, Chun Li, Todd J. Green, Christine Stevens, Claudine Beauchamp, Phillip Fleshner, Marie Carlson, Mauro D’Amato, Jonas Halfvarson, Martin L. Hibberd, Mikael Lördal, Leonid Padyukov, Angelo Andriulli, Elisabetta Colombo, Anna Latiano, Orazio Palmieri, Edmond-Jean Bernard, Colette Deslandres, Daan W. Hommes, Dirk J. de Jong, Pieter Stokkers, Rinse K. Weersma, Yashoda Sharma, Mark S. Silverberg, Judy H. Cho, Jing Wu, Kathryn Roeder, Steven R. Brant, L. Philip Schumm, Richard H. Duerr, Marla C. Dubinsky, Nicole L. Glazer, Talin Haritunians, Andy Ippoliti, Gil Melmed, David S. Siscovick, Eric A. Vasiliauskas, Stephan R. Targan, Vito Annese, Cisca Wijmenga, Sven Pettersson, Jerome I. Rotter, Ramnik J. Xavier, Mark J. Daly, John D. Rioux, Mark Seielstad - Nature Genetics 2010 被引用: 680

  20. 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

  21. Bayesian estimation of cell type–specific gene expression with prior derived from single-cell data

    著者: Jiebiao Wang, Kathryn Roeder, Bernie Devlin - Genome Research 2021 被引用: 115

  22. 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

  23. Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes

    著者: Xin He, Stephan Sanders, Li Liu, Silvia De Rubeis, Elaine T. Lim, James S. Sutcliffe, Gerard D. Schellenberg, Richard A. Gibbs, Mark J. Daly, Joseph D. Buxbaum, Matthew W. State, Bernie Devlin, Kathryn Roeder - PLoS Genetics 2013 被引用: 336

  24. SCEPTRE improves calibration and sensitivity in single-cell CRISPR screen analysis

    著者: Timothy Barry, Xuran Wang, John Morris, Kathryn Roeder, Eugene Katsevich - Genome biology 2021 被引用: 90