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Stephen T. Warren

1981–2023 年に発表

103
論文数
35,924
被引用数
88
h 指数
103
i10 指数

被引用数

Stephen T. Warren の年別被引用数1971 年: 被引用 1 件1976 年: 被引用 1 件1981 年: 被引用 1 件1982 年: 被引用 3 件1983 年: 被引用 2 件1985 年: 被引用 2 件1986 年: 被引用 1 件1987 年: 被引用 1 件1988 年: 被引用 2 件1989 年: 被引用 4 件1990 年: 被引用 4 件1991 年: 被引用 38 件1992 年: 被引用 135 件1993 年: 被引用 207 件1994 年: 被引用 184 件1995 年: 被引用 180 件1996 年: 被引用 172 件1997 年: 被引用 192 件1998 年: 被引用 144 件1999 年: 被引用 161 件2000 年: 被引用 255 件2001 年: 被引用 247 件2002 年: 被引用 275 件2003 年: 被引用 323 件2004 年: 被引用 354 件2005 年: 被引用 392 件2006 年: 被引用 321 件2007 年: 被引用 384 件2008 年: 被引用 471 件2009 年: 被引用 393 件2010 年: 被引用 503 件2011 年: 被引用 552 件2012 年: 被引用 479 件2013 年: 被引用 497 件2014 年: 被引用 484 件2015 年: 被引用 414 件2016 年: 被引用 280 件2017 年: 被引用 300 件2018 年: 被引用 252 件2019 年: 被引用 805 件2020 年: 被引用 760 件2021 年: 被引用 692 件2022 年: 被引用 446 件2023 年: 被引用 330 件2024 年: 被引用 429 件2025 年: 被引用 122 件2026 年: 被引用 1 件1972〜1975 年は被引用が無いため表示していません1977〜1980 年は被引用が無いため表示していません1984 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 3,655 件、この内訳の 38.4%イギリス: 引用元論文 702 件、この内訳の 7.4%カナダ: 引用元論文 499 件、この内訳の 5.2%ドイツ: 引用元論文 427 件、この内訳の 4.5%中国: 引用元論文 386 件、この内訳の 4.1%フランス: 引用元論文 368 件、この内訳の 3.9%イタリア: 引用元論文 366 件、この内訳の 3.8%オランダ: 引用元論文 347 件、この内訳の 3.6%オーストラリア: 引用元論文 264 件、この内訳の 2.8%日本: 引用元論文 252 件、この内訳の 2.7%スペイン: 引用元論文 192 件、この内訳の 2%ベルギー: 引用元論文 183 件、この内訳の 1.9%
0%38.4%その他 19.7%

機関

分野

  • Biochemistry, Genetics and Molecular Biology69.5%
  • Neuroscience18.5%
  • Medicine8.5%
  • Agricultural and Biological Sciences0.9%
  • Immunology and Microbiology0.8%
  • Psychology0.6%
  • その他1.2%

トピック

  • Genetics and Neurodevelopmental Disorders13.4%
  • Autism Spectrum Disorder Research6.5%
  • RNA Research and Splicing4%
  • RNA modifications and cancer4%
  • Epigenetics and DNA Methylation3.7%
  • Genetic Neurodegenerative Diseases3.4%
  • その他65%

共著者

全論文

検索で開く
  1. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

    著者: Annemieke J.M.H. Verkerk, Maura Pieretti, James S. Sutcliffe, Ying‐Hui Fu, Derek P.A. Kuhl, Antonio Pizzuti, Orly Reiner, Stephen Richards, M F Victoria, Fuping Zhang, Bert E. Eussen, Gert‐Jan B. van Ommen, Lau A.J. Blonden, Gregory J. Riggins, Jane L. Chastain, Catherine B. Kunst, H. Galjaard, C. Thomas Caskey, David L. Nelson, Ben A. Oostra, Stephen T. Warren - Cell 1991 被引用: 3,524

  2. A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies

    著者: Yunhee Kang, Ying Zhou, Yujing Li, Yanfei Han, Jie Xu, Weibo Niu, Ziyi Li, Shiying Liu, Hao Feng, Wen Huang, Ranhui Duan, Tianmin Xu, Nisha Raj, Feiran Zhang, Juan Dou, Chongchong Xu, Hao Wu, Gary J. Bassell, Stephen T. Warren, Emily G. Allen, Peng Jin, Zhexing Wen - Nature Neuroscience 2021 被引用: 168

  3. Absence of expression of the FMR-1 gene in fragile X syndrome

    著者: Maura Pieretti, Fuping Zhang, Ying‐Hui Fu, Stephen T. Warren, Ben A. Oostra, C. Thomas Caskey, David L. Nelson - Cell 1991 被引用: 1,485

  4. Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function

    著者: Gary J. Bassell, Stephen T. Warren - Neuron 2008 被引用: 1,042

  5. The mGluR theory of fragile X mental retardation

    著者: Mark F. Bear, Kimberly M. Huber, Stephen T. Warren - Trends in Neurosciences 2004 被引用: 1,591

  6. Age-associated DNA methylation in pediatric populations

    著者: Reid S. Alisch, Benjamin G. Barwick, Pankaj Chopra, Leila K. Myrick, Glen A. Satten, Karen N. Conneely, Stephen T. Warren - Genome Research 2012 被引用: 407

  7. Altered synaptic plasticity in a mouse model of fragile X mental retardation

    著者: Kimberly M. Huber, Sean Gallagher, Stephen T. Warren, Mark F. Bear - National Academy of Sciences, Proceedings of the National Academy of Sciences 2002 被引用: 1,341

  8. Fragile X Mental Retardation Protein Targets G Quartet mRNAs Important for Neuronal Function

    著者: Jennifer C. Darnell, Kirk B. Jensen, Peng Jin, Victoria Brown, Stephen T. Warren, Robert B. Darnell - Cell 2001 被引用: 956

  9. A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergence

    著者: Hsun-Hua Chou, Hiromu Takematsu, Sandra Diaz, Jane Iber, Elizabeth Nickerson, Kerry L. Wright, Elaine A. Muchmore, David L. Nelson, Stephen T. Warren, Ajit Varki - National Academy of Sciences, Proceedings of the National Academy of Sciences 1998 被引用: 583

  10. Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

    著者: Ying‐Hui Fu, Derek P.A. Kuhl, Antonio Pizzuti, Maura Pieretti, James S. Sutcliffe, Stephen Richards, Annemieke J.M.H. Verkert, Jeanette J. A. Holden, Raymond G. Fenwick, Stephen T. Warren, Ben A. Oostra, David L. Nelson, C. Thomas Caskey - Cell 1991 被引用: 2,101

  11. Molecular Mechanisms of Fragile X Syndrome: A Twenty-Year Perspective

    著者: Michael R. Santoro, Steven M. Bray, Stephen T. Warren - Annual Review of Pathology Mechanisms of Disease 2011 被引用: 538

  12. FMR1 Protein: Conserved RNP Family Domains and Selective RNA Binding

    著者: Claude T. Ashley, Keith D. Wilkinson, Daniel Reines, Stephen T. Warren - Science 1993 被引用: 739

  13. Fragile X Mental Retardation Protein: Nucleocytoplasmic Shuttling and Association with Somatodendritic Ribosomes

    著者: Yue Feng, Claire‐Anne Gutekunst, Derek E. Eberhart, Hong Yi, Stephen T. Warren, Steven M. Hersch - Journal of Neuroscience 1997 被引用: 535

  14. Local RNA Translation at the Synapse and in Disease: Figure 1.

    著者: Liqun Liu‐Yesucevitz, Gary J. Bassell, Aaron D. Gitler, Anne C. Hart, Eric Klann, Joel D. Richter, Stephen T. Warren, Benjamin Wolozin - Journal of Neuroscience 2011 被引用: 296

  15. A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium

    著者: Raquel E. Gur, Anne S. Bassett, Donna M. McDonald‐McGinn, Carrie E. Bearden, Eva W.C. Chow, B S Emanuel, Michael J. Owen, Ann Swillen, Marianne B. M. van den Bree, Joris Vermeesch, J.A.S. Vorstman, Stephen T. Warren, Thomas Lehner, Bernice E. Morrow - Molecular Psychiatry 2017 被引用: 97

  16. Fragile X syndrome

    著者: Kathryn B. Garber, Jeannie Visootsak, Stephen T. Warren - European Journal of Human Genetics 2008 被引用: 476

  17. 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

  18. Microarray Identification of FMRP-Associated Brain mRNAs and Altered mRNA Translational Profiles in Fragile X Syndrome

    著者: Victoria Brown, Peng Jin, Stephanie Ceman, Jennifer C. Darnell, William T. O'Donnell, Scott A. Tenenbaum, Xiaokui Jin, Yue Feng, Keith D. Wilkinson, Jack D. Keene, Robert B. Darnell, Stephen T. Warren - Cell 2001 被引用: 1,117

  19. Reversible Inhibition of PSD-95 mRNA Translation by miR-125a, FMRP Phosphorylation, and mGluR Signaling

    著者: Ravi Muddashetty, Vijayalaxmi Nalavadi, Christina Groß, Xiaodi Yao, Lei Xing, Oskar Laur, Stephen T. Warren, Gary J. Bassell - Molecular Cell 2011 被引用: 365

  20. Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X Chromosome

    著者: Nina Xie, He Gong, Joshua A. Suhl, Pankaj Chopra, Tao Wang, Stephen T. Warren - PLoS ONE 2016 被引用: 122

  21. Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia

    著者: Daniel Moreno‐De‐Luca, Jennifer G. Mullé, Erin B. Kaminsky, Stephan Sanders, Scott M. Myers, Margaret P Adam, Amy T. Pakula, Nancy Eisenhauer, Kim Uhas, LuAnn Weik, Lisa Guy, Melanie Care, Chantal F. Morel, Charlotte Boni, Bonnie Anne Salbert, Ashadeep Chandrareddy, Laurie Demmer, Eva W. C. Chow, Urvashi Surti, Swaroop Aradhya, Diane L. Pickering, Denae M. Golden, Warren G. Sanger, Emily Aston, Arthur R. Brothman, Troy J. Gliem, Erik C. Thorland, Todd Ackley, Ram Iyer, Shuwen Huang, John Barber, John A. Crolla, Stephen T. Warren, Christa L. Martin, David H. Ledbetter - The American Journal of Human Genetics 2010 被引用: 332

  22. Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) n

    著者: Eric J. Kremer, Melanie Pritchard, Michael Lynch, Shuancang Yu, K. Holman, Elizabeth Baker, Stephen T. Warren, David Schlessinger, G.R. Sutherland, Robert I. Richards - Science 1991 被引用: 923

  23. Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways †

    著者: Yuhei Nishimura, Christa L. Martin, Araceli Vázquez-López, Sarah Spence, Ana Isabel Alvarez-Retuerto, Marian Sigman, Corinna Steindler, Sandra Pellegrini, N. Carolyn Schanen, Stephen T. Warren, Daniel H. Geschwind - Human Molecular Genetics 2007 被引用: 281

  24. Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeats

    著者: Kersten M. Small, Jane Iber, Stephen T. Warren - Nature Genetics 1997 被引用: 162