Yanick J. Crow

Research.com Recognitions

• 2024 - Research.com Genetics in France Leader Award
• 2024 - Research.com Genetics and Molecular Biology in France Leader Award
• Fellow of The Academy of Medical Sciences, United Kingdom
• Fellow of The Academy of Medical Sciences, United Kingdom
• Fellow of The Academy of Medical Sciences, United Kingdom
• Fellow of The Academy of Medical Sciences, United Kingdom

Overview

Best Publications

• HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolase

  David C. Goldstone;Valerie Ennis-Adeniran;Joseph J. Hedden;Harriet C. T. Groom

  991
  Citations

• Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature

  Gillian I. Rice;Paul R. Kasher;Gabriella M A Forte;Niamh M. Mannion

  986
  Citations

• Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus.

  Yanick J Crow;Yanick J Crow;Bruce E Hayward;Rekha Parmar;Peter Robins

  982
  Citations

• Aicardi–Goutières syndrome and the type I interferonopathies

  Yanick J. Crow;Nicolas Manel

  939
  Citations

• International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity

  Capucine Picard;H. Bobby Gaspar;Waleed Al-Herz;Aziz Bousfiha

  889
  Citations

• Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response.

  Gillian I Rice;Jacquelyn Bond;Aruna Asipu;Rebecca L Brunette

  818
  Citations

• Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection.

  Yanick J Crow;Yanick J Crow;Andrea Leitch;Bruce E Hayward;Anna Garner

  783
  Citations

• ASPM is a major determinant of cerebral cortical size.

  Jacquelyn Bond;Emma Roberts;Ganesh H. Mochida;Ganesh H. Mochida;Daniel J. Hampshire

  721
  Citations

• Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.

  Yanick J. Crow;Diana S. Chase;Johanna Lowenstein Schmidt;Marcin Szynkiewicz

  638
  Citations

• Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling

  Gillian I Rice;Yoandris del Toro Duany;Yoandris del Toro Duany;Emma M Jenkinson;Gabriella M A Forte

  635
  Citations

• Mitochondrial double-stranded RNA triggers antiviral signalling in humans

  Ashish Dhir;Somdutta Dhir;Lukasz S. Borowski;Lukasz S. Borowski;Laura Jimenez

  597
  Citations

• Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation

  Xianqin Zhang;Dusan Bogunovic;Béatrice Payelle-Brogard;Véronique Francois-Newton

  589
  Citations

• The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.

  Aziz Bousfiha;Leïla Jeddane;Capucine Picard;Fatima Ailal

  582
  Citations

• Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations

  Nadia Jeremiah;Bénédicte Neven;Matteo Gentili;Isabelle Callebaut

  568
  Citations

• Identification of Microcephalin, a Protein Implicated in Determining the Size of the Human Brain

  Andrew P. Jackson;Andrew P. Jackson;Helen Eastwood;Sandra M. Bell;Jimi Adu

  531
  Citations

• Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome

  Gillian Rice;Teresa Patrick;Rekha Parmar;Claire F Taylor

  499
  Citations

• Type I interferonopathies: a novel set of inborn errors of immunity.

  Yanick J. Crow

  479
  Citations

• Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study

  Gillian I Rice;Gabriella M A Gm Forte;Marcin Szynkiewicz;Diana S Chase

  475
  Citations

• Mutations in the Pericentrin (PCNT) Gene Cause Primordial Dwarfism

  Anita Rauch;Christian T. Thiel;Detlev Schindler;Ursula Wick

  449
  Citations

• Heterozygous Mutations in TREX1 Cause Familial Chilblain Lupus and Dominant Aicardi-Goutières Syndrome

  Gillian Rice;William G. Newman;John Dean;Teresa Patrick

  414
  Citations