Katherine A. High

Active 1989–2025

111
Papers
35,185
Citations
91
h-index
110
i10-index

Citations

Citations per year for Katherine A. High1990: 2 citations1991: 1 citations1993: 1 citations1994: 2 citations1995: 3 citations1996: 4 citations1997: 23 citations1998: 76 citations1999: 101 citations2000: 121 citations2001: 141 citations2002: 135 citations2003: 161 citations2004: 134 citations2005: 150 citations2006: 174 citations2007: 159 citations2008: 239 citations2009: 260 citations2010: 256 citations2011: 296 citations2012: 306 citations2013: 391 citations2014: 371 citations2015: 347 citations2016: 282 citations2017: 543 citations2018: 430 citations2019: 1,238 citations2020: 1,583 citations2021: 1,376 citations2022: 1,068 citations2023: 921 citations2024: 1,203 citations2025: 682 citations2026: 10 citations1992: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,288 citing papers, 36.1% of this breakdownChina: 795 citing papers, 8.7% of this breakdownUnited Kingdom: 662 citing papers, 7.3% of this breakdownGermany: 483 citing papers, 5.3% of this breakdownFrance: 431 citing papers, 4.7% of this breakdownItaly: 354 citing papers, 3.9% of this breakdownCanada: 271 citing papers, 3% of this breakdownNetherlands: 247 citing papers, 2.7% of this breakdownAustralia: 231 citing papers, 2.5% of this breakdownJapan: 215 citing papers, 2.4% of this breakdownSpain: 211 citing papers, 2.3% of this breakdownSwitzerland: 167 citing papers, 1.8% of this breakdown
0%36.1%Other 19.3%

Fields

  • Biochemistry, Genetics and Molecular Biology68.7%
  • Medicine22.3%
  • Neuroscience3.8%
  • Immunology and Microbiology1.6%
  • Engineering1.5%
  • Materials Science0.8%
  • Other1.3%

Topics

  • Virus-based gene therapy research14.7%
  • CRISPR and Genetic Engineering8.6%
  • RNA Interference and Gene Delivery7.6%
  • Retinal Development and Disorders5.9%
  • CAR-T cell therapy research4%
  • Viral Infectious Diseases and Gene Expression in Insects3.3%
  • Other55.9%

Coauthors

All papers

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  1. Efficacy and safety of voretigene neparvovec (AAV2-hRPE65v2) in patients with RPE65 -mediated inherited retinal dystrophy: a randomised, controlled, open-label, phase 3 trial

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Katie Wachtel, Francesca Simonelli, Bart P. Leroy, J. Fraser Wright, Katherine A. High, Albert M. Maguire - The Lancet 2017 cited by 1,889

  2. Gene therapy comes of age

    Authors: , , , , , - Science 2018 cited by 1,378

  3. Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mark A. Kay - Nature Medicine 2006 cited by 2,135

  4. Adenovirus-Associated Virus Vector–Mediated Gene Transfer in Hemophilia B

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Arthur W. Nienhuis, Andrew M. Davidoff - New England Journal of Medicine 2011 cited by 1,843

  5. Long-Term Safety and Efficacy of Factor IX Gene Therapy in Hemophilia B

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2014 cited by 1,250

  6. Immune responses to AAV vectors: overcoming barriers to successful gene therapy

    Authors: , - Blood 2013 cited by 920

  7. Hemophilia B Gene Therapy with a High-Specific-Activity Factor IX Variant

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2017 cited by 759

  8. Gene Therapy

    Authors: , - New England Journal of Medicine 2019 cited by 525

  9. Entering the Modern Era of Gene Therapy

    Authors: , - Annual Review of Medicine 2018 cited by 468

  10. Efficacy, Safety, and Durability of Voretigene Neparvovec-rzyl in RPE65 Mutation–Associated Inherited Retinal Dystrophy

    Authors: , , , , , , , , , , , , , , , , , - Ophthalmology 2019 cited by 391

  11. Safety and Efficacy of Gene Transfer for Leber's Congenital Amaurosis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Katherine A. High, Jean Bennett - New England Journal of Medicine 2008 cited by 2,137

  12. CD8+ T-cell responses to adeno-associated virus capsid in humans

    Authors: , , , , , , , , , , , , - Nature Medicine 2007 cited by 726

  13. Multiyear Factor VIII Expression after AAV Gene Transfer for Hemophilia A

    Authors: , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2021 cited by 253

  14. Long-Term Follow-Up of the First in Human Intravascular Delivery of AAV for Gene Transfer: AAV2-hFIX16 for Severe Hemophilia B

    Authors: , , , , , , , , , , , , , , - Molecular Therapy 2020 cited by 209

  15. Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Bart P. Leroy, Francesca Simonelli, Jean Bennett - The Lancet 2009 cited by 858

  16. Therapeutic in vivo gene transfer for genetic disease using AAV: progress and challenges

    Authors: , - Nature Reviews Genetics 2011 cited by 901

  17. Safety and durability of effect of contralateral-eye administration of AAV2 gene therapy in patients with childhood-onset blindness caused by RPE65 mutations: a follow-on phase 1 trial

    Authors: , , , , , , , , , , , , , , , , , , , , , - The Lancet 2016 cited by 456

  18. Durability of Voretigene Neparvovec for Biallelic RPE65-Mediated Inherited Retinal Disease

    Authors: , , , , , , , , , , - Ophthalmology 2021 cited by 188

  19. Overcoming Preexisting Humoral Immunity to AAV Using Capsid Decoys

    Authors: , , , , , , , , , , , , , , , , - Science Translational Medicine 2013 cited by 344

  20. Effects of transient immunosuppression on adenoassociated, virus-mediated, liver-directed gene transfer in rhesus macaques and implications for human gene therapy

    Authors: , , , , , , , , , , , , - Blood 2006 cited by 320

  21. AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B

    Authors: , , , , , , , , , , , , , , , , , , , - Blood 2003 cited by 747

  22. AAV-1–mediated gene transfer to skeletal muscle in humans results in dose-dependent activation of capsid-specific T cells

    Authors: , , , , , , , , , , - Blood 2009 cited by 284

  23. Clinical development of gene therapy: results and lessons from recent successes

    Authors: , , , , - Molecular Therapy — Methods & Clinical Development 2016 cited by 229

  24. Assessing the potential for AAV vector genotoxicity in a murine model

    Authors: , , , , , , , , , , , - Blood 2010 cited by 228