Christopher A. Walsh

Active 1983–2025

256
Papers
57,086
Citations
130
h-index
245
i10-index

Citations

Citations per year for Christopher A. Walsh1971: 1 citations1984: 6 citations1985: 7 citations1986: 6 citations1987: 15 citations1988: 12 citations1989: 11 citations1990: 20 citations1991: 16 citations1992: 24 citations1993: 53 citations1994: 50 citations1995: 74 citations1996: 52 citations1997: 70 citations1998: 82 citations1999: 137 citations2000: 170 citations2001: 221 citations2002: 236 citations2003: 320 citations2004: 392 citations2005: 471 citations2006: 501 citations2007: 471 citations2008: 493 citations2009: 530 citations2010: 542 citations2011: 542 citations2012: 607 citations2013: 648 citations2014: 715 citations2015: 795 citations2016: 726 citations2017: 684 citations2018: 696 citations2019: 1,707 citations2020: 1,789 citations2021: 1,695 citations2022: 1,312 citations2023: 1,000 citations2024: 1,455 citations2025: 648 citations2026: 28 citations1972–1983: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 7,334 citing papers, 32.3% of this breakdownUnited Kingdom: 1,781 citing papers, 7.8% of this breakdownGermany: 1,420 citing papers, 6.2% of this breakdownChina: 1,301 citing papers, 5.7% of this breakdownFrance: 1,008 citing papers, 4.4% of this breakdownCanada: 934 citing papers, 4.1% of this breakdownItaly: 879 citing papers, 3.9% of this breakdownJapan: 730 citing papers, 3.2% of this breakdownNetherlands: 713 citing papers, 3.1% of this breakdownAustralia: 635 citing papers, 2.8% of this breakdownSpain: 583 citing papers, 2.6% of this breakdownSwitzerland: 429 citing papers, 1.9% of this breakdown
0%32.3%Other 22%

Fields

  • Biochemistry, Genetics and Molecular Biology52.1%
  • Neuroscience27.9%
  • Medicine15.1%
  • Agricultural and Biological Sciences1.4%
  • Psychology1.1%
  • Immunology and Microbiology0.8%
  • Other1.6%

Topics

  • Genetics and Neurodevelopmental Disorders5.9%
  • Neurogenesis and neuroplasticity mechanisms5.8%
  • Autism Spectrum Disorder Research3.8%
  • Genomic variations and chromosomal abnormalities2.8%
  • Genomics and Rare Diseases2.3%
  • Neuroscience and Neuropharmacology Research2.3%
  • Other77.1%

Coauthors

All papers

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  1. Synaptic, transcriptional and chromatin genes disrupted in autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 2,974

  2. Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 1,547

  3. Innovations present in the primate interneuron repertoire

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Guoping Feng, Steven A. McCarroll - Nature 2020 cited by 386

  4. The ILAE consensus classification of focal cortical dysplasia: An update proposed by an ad hoc task force of the ILAE diagnostic methods commission

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Epilepsia 2022 cited by 341

  5. Aging and neurodegeneration are associated with increased mutations in single human neurons

    Authors: , , , , , , , , , , , , , , , , - Science 2017 cited by 662

  6. Somatic genomic changes in single Alzheimer’s disease neurons

    Authors: , , , , , , , , , , , , , , , , , , , - Nature 2022 cited by 222

  7. Comparative transcriptomics reveals human-specific cortical features

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , William D. Hopkins, Thomas Höllt, C. Dirk Keene, Sten Linnarsson, Steven A. McCarroll, Boudewijn P. F. Lelieveldt, Chet C. Sherwood, Kimberly A. Smith, Christopher A. Walsh, Alexander Dobin, Jesse Gillis, Ed S. Lein, Rebecca D. Hodge, Trygve E. Bakken - Science 2023 cited by 194

  8. Cell-Type-Specific Alternative Splicing Governs Cell Fate in the Developing Cerebral Cortex

    Authors: , , , , , , , , , , , , , - Cell 2016 cited by 391

  9. Rewiring of human neurodevelopmental gene regulatory programs by human accelerated regions

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , - Neuron 2021 cited by 205

  10. Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior

    Authors: , , , , , , , , , , , , - Cell 2016 cited by 389

  11. Doublecortin Is a Microtubule-Associated Protein and Is Expressed Widely by Migrating Neurons

    Authors: , , , - Neuron 1999 cited by 1,350

  12. Regulation of Cerebral Cortical Size by Control of Cell Cycle Exit in Neural Precursors

    Authors: , - Science 2002 cited by 1,453

  13. Somatic mutation in single human neurons tracks developmental and transcriptional history

    Authors: , , , , , , , , , , , , , , , - Science 2015 cited by 602

  14. Somatic Mutations Activating the mTOR Pathway in Dorsal Telencephalic Progenitors Cause a Continuum of Cortical Dysplasias

    Authors: , , , , , , , , , , , , , , , , - Cell Reports 2017 cited by 333

  15. Cux1 and Cux2 Regulate Dendritic Branching, Spine Morphology, and Synapses of the Upper Layer Neurons of the Cortex

    Authors: , , , , , , , , , , , - Neuron 2010 cited by 316

  16. Single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements

    Authors: , , , , , , , , , , , , , , , , , , , - Nature Genetics 2022 cited by 105

  17. The Cerebrospinal Fluid Provides a Proliferative Niche for Neural Progenitor Cells

    Authors: , , , , , , , , , , , , , - Neuron 2011 cited by 640

  18. Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Marco Prinz, David D. Limbrick, Christina A. Gurnett, Matthew D. Smyth, Shifteh Sattar, Mark Nespeca, David D. Gonda, Katsumi Imai, Yukitoshi Takahashi, Hsin-Hung Chen, Jin‐Wu Tsai, Valerio Conti, Renzo Guerrini, Orrin Devinsky, Wilson A. Silva, Hélio Rubens Machado, Gary W. Mathern, Alexej Abyzov, Sara Baldassari, Stéphanie Baulac, Joseph G. Gleeson, Marilyn C. Jones, Diane Masser‐Frye, Shifteh Sattar, Mark Nespeca, David D. Gonda, Katsumi Imai, Yukitoshi Takahashi, Hsin-Hung Chen, Jin‐Wu Tsai, Valerio Conti, Renzo Guerrini, Orrin Devinsky, Hélio Rubens Machado, Camila Araújo Bernardino Garcia, Wilson A. Silva, Se Hoon Kim, Hoon‐Chul Kang, Yasemin Alanay, Seema Kapoor, Carola A. Haas, Georgia Ramantani, Thomas J. Feuerstein, Ingmar Blümcke, Robyn M. Busch, Zhong Ying, Vadym Biloshytsky, Kostiantyn Kostiuk, Pedachenko Eg, Gary W. Mathern, Christina A. Gurnett, Matthew D. Smyth, Ingo Helbig, Benjamin C. Kennedy, Judy Liu, Felix Chan, Darcy A. Krueger, Richard E. Frye, Angus A. Wilfong, David L. Adelson, William D. Gaillard, Chima Oluigbo, Anne E. Anderson, Brain Somatic Mosaicism Network, Alice Lee, August Yue Huang, Alissa M. D’Gama, Caroline Dias, Christopher A. Walsh, Eduardo Maury and 105 more - Nature Genetics 2023 cited by 111

  19. Landmarks of human embryonic development inscribed in somatic mutations

    Authors: , , , , , , , , , , , - Science 2021 cited by 122

  20. Somatic mutations in single human cardiomyocytes reveal age-associated DNA damage and widespread oxidative genotoxicity

    Authors: , , , , , , , , , , , , , - Nature Aging 2022 cited by 73

  21. Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 1,292

  22. Single-Neuron Sequencing Analysis of L1 Retrotransposition and Somatic Mutation in the Human Brain

    Authors: , , , , , , , , , , , - Cell 2012 cited by 563

  23. The Genetics of Primary Microcephaly

    Authors: , , - Annual Review of Genomics and Human Genetics 2018 cited by 299

  24. Genetic mosaicism in the human brain: from lineage tracing to neuropsychiatric disorders

    Authors: , - Nature reviews. Neuroscience 2022 cited by 85