Federico Mingozzi

Active 2001–2025

109
Papers
25,079
Citations
74
h-index
106
i10-index

Citations

Citations per year for Federico Mingozzi1984: 1 citations1997: 1 citations1999: 1 citations2001: 1 citations2002: 6 citations2003: 7 citations2004: 21 citations2005: 20 citations2006: 57 citations2007: 78 citations2008: 126 citations2009: 167 citations2010: 161 citations2011: 188 citations2012: 202 citations2013: 322 citations2014: 296 citations2015: 272 citations2016: 216 citations2017: 477 citations2018: 312 citations2019: 1,033 citations2020: 1,330 citations2021: 1,229 citations2022: 1,083 citations2023: 985 citations2024: 1,136 citations2025: 720 citations2026: 8 citations1985–1996: no citations, so these years are not shown1998: no citations, so this year is not shown2000: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,463 citing papers, 36% of this breakdownUnited Kingdom: 518 citing papers, 7.6% of this breakdownChina: 508 citing papers, 7.4% of this breakdownFrance: 377 citing papers, 5.5% of this breakdownGermany: 375 citing papers, 5.5% of this breakdownItaly: 323 citing papers, 4.7% of this breakdownCanada: 213 citing papers, 3.1% of this breakdownNetherlands: 209 citing papers, 3% of this breakdownSpain: 175 citing papers, 2.6% of this breakdownAustralia: 169 citing papers, 2.5% of this breakdownJapan: 152 citing papers, 2.2% of this breakdownSwitzerland: 131 citing papers, 1.9% of this breakdown
0%36%Other 18%

Fields

  • Biochemistry, Genetics and Molecular Biology68.8%
  • Medicine22.7%
  • Neuroscience4.6%
  • Immunology and Microbiology2.2%
  • Engineering0.7%
  • Materials Science0.4%
  • Other0.6%

Topics

  • Virus-based gene therapy research15.8%
  • CRISPR and Genetic Engineering8.8%
  • RNA Interference and Gene Delivery7.1%
  • Retinal Development and Disorders5.3%
  • CAR-T cell therapy research4.2%
  • Viral Infectious Diseases and Gene Expression in Insects3.4%
  • Other55.4%

Coauthors

All papers

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  1. 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

  2. AAV Vector Immunogenicity in Humans: A Long Journey to Successful Gene Transfer

    Authors: , , - Molecular Therapy 2020 cited by 627

  3. Emerging Issues in AAV-Mediated In Vivo Gene Therapy

    Authors: , , - Molecular Therapy — Methods & Clinical Development 2017 cited by 864

  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. IgG-cleaving endopeptidase enables in vivo gene therapy in the presence of anti-AAV neutralizing antibodies

    Authors: , , , , , , , , , , , , , , , , , , , , , - Nature Medicine 2020 cited by 319

  8. 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

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

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

  10. Human Immune Responses to Adeno-Associated Virus (AAV) Vectors

    Authors: , , - Frontiers in Immunology 2020 cited by 344

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

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

  12. Engineering adeno-associated viral vectors to evade innate immune and inflammatory responses

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Matthew J. Pezone, Ru Xiao, Tina Liu, Wei Wang, Henry J. Kaplan, Guangping Gao, Andrew D. Dick, Federico Mingozzi, Maureen A. McCall, Constance L. Cepko, George M. Church - Science Translational Medicine 2021 cited by 207

  13. Antigen-selective modulation of AAV immunogenicity with tolerogenic rapamycin nanoparticles enables successful vector re-administration

    Authors: , , , , , , , , , , , , , , , , , , , - Nature Communications 2018 cited by 254

  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. Pre-existing humoral immunity and complement pathway contribute to immunogenicity of adeno-associated virus (AAV) vector in human blood

    Authors: , , , , , , , , , , , - Frontiers in Immunology 2022 cited by 81

  19. Overcoming Preexisting Humoral Immunity to AAV Using Capsid Decoys

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

  20. Influence of Pre-existing Anti-capsid Neutralizing and Binding Antibodies on AAV Vector Transduction

    Authors: , , , , , , , , , , , , - Molecular Therapy — Methods & Clinical Development 2018 cited by 197

  21. 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

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

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

  24. Unraveling the Complex Story of Immune Responses to AAV Vectors Trial After Trial

    Authors: , , - Human Gene Therapy 2017 cited by 219