Chad A. Shaw

Active 1986–2024

126
Papers
24,759
Citations
89
h-index
122
i10-index

Citations

Citations per year for Chad A. Shaw1967: 1 citations1972: 1 citations1983: 1 citations1987: 4 citations1988: 1 citations1989: 2 citations1990: 1 citations1991: 3 citations1992: 2 citations1993: 3 citations1994: 2 citations1997: 1 citations1998: 1 citations1999: 1 citations2001: 2 citations2002: 2 citations2003: 10 citations2004: 28 citations2005: 46 citations2006: 64 citations2007: 147 citations2008: 252 citations2009: 320 citations2010: 284 citations2011: 339 citations2012: 378 citations2013: 363 citations2014: 361 citations2015: 382 citations2016: 350 citations2017: 369 citations2018: 316 citations2019: 995 citations2020: 1,002 citations2021: 875 citations2022: 619 citations2023: 394 citations2024: 592 citations2025: 232 citations2026: 4 citations1968–1971: no citations, so these years are not shown1973–1982: no citations, so these years are not shown1984–1986: no citations, so these years are not shown1995–1996: no citations, so these years are not shown2000: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 4,119 citing papers, 32.1% of this breakdownUnited Kingdom: 932 citing papers, 7.3% of this breakdownChina: 827 citing papers, 6.4% of this breakdownGermany: 688 citing papers, 5.4% of this breakdownCanada: 583 citing papers, 4.5% of this breakdownItaly: 504 citing papers, 3.9% of this breakdownFrance: 475 citing papers, 3.7% of this breakdownNetherlands: 474 citing papers, 3.7% of this breakdownSpain: 360 citing papers, 2.8% of this breakdownAustralia: 353 citing papers, 2.8% of this breakdownJapan: 284 citing papers, 2.2% of this breakdownSwitzerland: 224 citing papers, 1.7% of this breakdown
0%32.1%Other 23.5%

Fields

  • Biochemistry, Genetics and Molecular Biology57.6%
  • Medicine24.1%
  • Neuroscience11.6%
  • Immunology and Microbiology3%
  • Agricultural and Biological Sciences1%
  • Computer Science0.8%
  • Other1.9%

Topics

  • Genomic variations and chromosomal abnormalities5.5%
  • Genetics and Neurodevelopmental Disorders5.3%
  • Genomics and Rare Diseases4.1%
  • Autism Spectrum Disorder Research2.9%
  • Epigenetics and DNA Methylation2.7%
  • RNA modifications and cancer2.2%
  • Other77.3%

Coauthors

All papers

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  1. MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription

    Authors: , , , , , , - Science 2008 cited by 1,852

  2. Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation

    Authors: , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2016 cited by 775

  3. The spliceosome is a therapeutic vulnerability in MYC-driven cancer

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature 2015 cited by 524

  4. Aging Hematopoietic Stem Cells Decline in Function and Exhibit Epigenetic Dysregulation

    Authors: , , , , , - PLoS Biology 2007 cited by 796

  5. Reanalysis of Clinical Exome Sequencing Data

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mary Kay Koenig, Andrea M. Lewis, Marvin R. Natowicz, Pedro Mancías, LaKeesha Minor, Fernando Scaglia, Christian P. Schaaf, Haley Streff, Hilary J. Vernon, Crescenda L Uhles, Elaine H. Zackai, Nan Wu, V. Reid Sutton, Arthur L. Beaudet, Donna M. Muzny, Richard A. Gibbs, Jennifer E. Posey, Seema R. Lalani, Chad A. Shaw, Christine M. Eng, James R. Lupski, Yaping Yang - New England Journal of Medicine 2019 cited by 298

  6. Use of Exome Sequencing for Infants in Intensive Care Units

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jianhong Hu, John W. Belmont, Lindsay C. Burrage, Brett H. Graham, V. Reid Sutton, William J. Craigen, Sharon E. Plon, James R. Lupski, Arthur L. Beaudet, Richard A. Gibbs, Donna M. Muzny, Marcus J. Miller, Xia Wang, Magalie S. Leduc, Rui Xiao, Pengfei Liu, Chad A. Shaw, Magdalena Walkiewicz, Weimin Bi, Fan Xia, Brendan Lee, Christine M. Eng, Yaping Yang, Seema R. Lalani - JAMA Pediatrics 2017 cited by 431

  7. 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

  8. Sequence variability of the respiratory syncytial virus (RSV) fusion gene among contemporary and historical genotypes of RSV/A and RSV/B

    Authors: , , , , , - PLoS ONE 2017 cited by 119

  9. MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndrome

    Authors: , , , , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 2015 cited by 316

  10. A Renewable Tissue Resource of Phenotypically Stable, Biologically and Ethnically Diverse, Patient-Derived Human Breast Cancer Xenograft Models

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Cancer Research 2013 cited by 485

  11. Disruption of the circadian clock within the cardiomyocyte influences myocardial contractile function, metabolism, and gene expression

    Authors: , , , , , , , , , , , , , , , , , , - American Journal of Physiology-Heart and Circulatory Physiology 2007 cited by 382

  12. Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles

    Authors: , , , , , , , , , , , , , , , , , - The American Journal of Human Genetics 2018 cited by 233

  13. Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Christine M. Eng - Nature Medicine 2019 cited by 265

  14. Molecular diagnostic experience of whole-exome sequencing in adult patients

    Authors: , , , , , , , , , , , , , , , , , , , , , , - Genetics in Medicine 2015 cited by 242

  15. A SUMOylation-Dependent Transcriptional Subprogram Is Required for Myc-Driven Tumorigenesis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - Science 2011 cited by 440

  16. Hematopoietic stem and progenitor cells confer cross-protective trained immunity in mouse models

    Authors: , , , , , , , , , , , , , , , - iScience 2023 cited by 35

  17. Mus81 and converging forks limit the mutagenicity of replication fork breakage

    Authors: , , , , , , , , - Science 2015 cited by 197

  18. Host Transcriptional Response to Influenza and Other Acute Respiratory Viral Infections – A Prospective Cohort Study

    Authors: , , , , , , , , , , , , - PLoS Pathogens 2015 cited by 156

  19. Early Patterns of Gene Expression Correlate With the Humoral Immune Response to Influenza Vaccination in Humans

    Authors: , , , , , , , , , - The Journal of Infectious Diseases 2011 cited by 233

  20. EMT cells increase breast cancer metastasis via paracrine GLI activation in neighbouring tumour cells

    Authors: , , , , , , , , , , , - Nature Communications 2017 cited by 183

  21. A Protein–Protein Interaction Network for Human Inherited Ataxias and Disorders of Purkinje Cell Degeneration

    Authors: , , , , , , , , , , , , - Cell 2006 cited by 790

  22. Analysis of 13 cell types reveals evidence for the expression of numerous novel primate- and tissue-specific microRNAs

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Charles J. Yeo, Masaya Jimbo, Joseph A. Cozzitorto, Jonathan R. Brody, Kathleen Delgrosso, John S. Mattick, Paolo Fortina, Isidore Rigoutsos - National Academy of Sciences, Proceedings of the National Academy of Sciences 2015 cited by 415

  23. Activation of Multiple Proto-oncogenic Tyrosine Kinases in Breast Cancer via Loss of the PTPN12 Phosphatase

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , - Cell 2011 cited by 279

  24. Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus

    Authors: , , , , - Human Molecular Genetics 2009 cited by 253