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Stephen T. Warren

Active 1981–2023

103
Papers
35,924
Citations
88
h-index
103
i10-index

Citations

Citations per year for Stephen T. Warren1971: 1 citations1976: 1 citations1981: 1 citations1982: 3 citations1983: 2 citations1985: 2 citations1986: 1 citations1987: 1 citations1988: 2 citations1989: 4 citations1990: 4 citations1991: 38 citations1992: 135 citations1993: 207 citations1994: 184 citations1995: 180 citations1996: 172 citations1997: 192 citations1998: 144 citations1999: 161 citations2000: 255 citations2001: 247 citations2002: 275 citations2003: 323 citations2004: 354 citations2005: 392 citations2006: 321 citations2007: 384 citations2008: 471 citations2009: 393 citations2010: 503 citations2011: 552 citations2012: 479 citations2013: 497 citations2014: 484 citations2015: 414 citations2016: 280 citations2017: 300 citations2018: 252 citations2019: 805 citations2020: 760 citations2021: 692 citations2022: 446 citations2023: 330 citations2024: 429 citations2025: 122 citations2026: 1 citations1972–1975: no citations, so these years are not shown1977–1980: no citations, so these years are not shown1984: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,655 citing papers, 38.4% of this breakdownUnited Kingdom: 702 citing papers, 7.4% of this breakdownCanada: 499 citing papers, 5.2% of this breakdownGermany: 427 citing papers, 4.5% of this breakdownChina: 386 citing papers, 4.1% of this breakdownFrance: 368 citing papers, 3.9% of this breakdownItaly: 366 citing papers, 3.8% of this breakdownNetherlands: 347 citing papers, 3.6% of this breakdownAustralia: 264 citing papers, 2.8% of this breakdownJapan: 252 citing papers, 2.7% of this breakdownSpain: 192 citing papers, 2% of this breakdownBelgium: 183 citing papers, 1.9% of this breakdown
0%38.4%Other 19.7%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology69.5%
  • Neuroscience18.5%
  • Medicine8.5%
  • Agricultural and Biological Sciences0.9%
  • Immunology and Microbiology0.8%
  • Psychology0.6%
  • Other1.2%

Topics

  • 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%
  • Other65%

Coauthors

All papers

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

    Authors: 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 cited by 3,524

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

    Authors: 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 cited by 168

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

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

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

    Authors: Gary J. Bassell, Stephen T. Warren - Neuron 2008 cited by 1,042

  5. The mGluR theory of fragile X mental retardation

    Authors: Mark F. Bear, Kimberly M. Huber, Stephen T. Warren - Trends in Neurosciences 2004 cited by 1,591

  6. Age-associated DNA methylation in pediatric populations

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

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

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

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

    Authors: Jennifer C. Darnell, Kirk B. Jensen, Peng Jin, Victoria Brown, Stephen T. Warren, Robert B. Darnell - Cell 2001 cited by 956

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

    Authors: 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 cited by 583

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

    Authors: 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 cited by 2,101

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

    Authors: Michael R. Santoro, Steven M. Bray, Stephen T. Warren - Annual Review of Pathology Mechanisms of Disease 2011 cited by 538

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

    Authors: Claude T. Ashley, Keith D. Wilkinson, Daniel Reines, Stephen T. Warren - Science 1993 cited by 739

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

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

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

    Authors: 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 cited by 296

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

    Authors: 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 cited by 97

  16. Fragile X syndrome

    Authors: Kathryn B. Garber, Jeannie Visootsak, Stephen T. Warren - European Journal of Human Genetics 2008 cited by 476

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

    Authors: 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 and 24 more - Molecular Psychiatry 2020 cited by 135

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

    Authors: 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 cited by 1,117

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

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

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

    Authors: Nina Xie, He Gong, Joshua A. Suhl, Pankaj Chopra, Tao Wang, Stephen T. Warren - PLoS ONE 2016 cited by 122

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

    Authors: 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 cited by 332

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

    Authors: 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 cited by 923

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

    Authors: 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 cited by 281

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

    Authors: Kersten M. Small, Jane Iber, Stephen T. Warren - Nature Genetics 1997 cited by 162