Yanick J. Crow - Concepedia

Author

Yanick J. Crow

Also Known As

Alberto Martini, Ali Dursun, Buckingham, Kati J., Carolina Uggenti, Crow, YJ, Crow, Yanick, Eric Jeziorski, Eszter Dzsida, G Rice, Gareth Cross

429

Publications

31.3K

Citations

H-Index

197

Concepts

All Affiliations

University of Manchester Manchester Academic Health Science Centre Université Paris Cité Inserm Institut des Maladies Génétiques Imagine

About

Yanick J. Crow is an author at University of Manchester specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	57	97	16.6K
2	Health Sciences	6	6	348
3	Public Health	5	5	772
4	Natural Sciences	4	4	414
5	Social Sciences	3	3	674

Yanick J. Crow

173

Publications

24.8K

Citations

H-Index

Page 1

	Year	Citations
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature Gillian Rice, Paul R. Kasher, Gabriella Forte, Nature Genetics Autoimmune DiseaseGenetic DisorderGeneticsPathogenesisImmunology	2012	916
Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus Yanick J. Crow, Bruce E. Hayward, Rekha Parmar, Nature Genetics Ags1 LocusMendelian DisorderGenetic DisorderMedicineGenetics	2006	876
HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolase David C. Goldstone, Valerie Ennis-Adeniran, Joseph J. Hedden, Nature Human RetrovirusImmunologyAntiviral ResponseMolecular BiologyVirology	2011	803
International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity Capucine Pïcard, H. Bobby Gaspar, Waleed Al–Herz, Journal of Clinical Immunology	2017	779
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response Gillian Rice, Jacquelyn Bond, Aruna Asipu, Nature Genetics AllergyAutoimmune DiseasePathogenesisImmunologyInnate Immune Response	2009	680
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection Yanick J. Crow, Andrea Leitch, Bruce E. Hayward, Nature Genetics Ribonuclease H2Viral EvolutionGenetic DisorderNeurovirologyGenetics	2006	666
Mitochondrial double-stranded RNA triggers antiviral signalling in humans Ashish Dhir, Somdutta Dhir, Lukasz S. Borowski, Nature Viral ReplicationImmunologyAntiviral ResponseVirologyMedicine	2018	597
Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i> Yanick J. Crow, Diana Chase, Johanna L. Schmidt, American Journal of Medical Genetics Part A	2015	589
Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling Gillian Rice, Yoandris del Toro Duany, Emma M. Jenkinson, Nature Genetics	2014	582
ASPM is a major determinant of cerebral cortical size Jacquelyn Bond, Emma Roberts, Ganeshwaran H. Mochida, Nature Genetics NeurophysiologyNeuroanatomyNeurological FunctionCerebral Cortical SizeNeurology	2002	565

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