Yanick J. Crow

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

Gillian Rice, Paul R. Kasher, Gabriella Forte et al.|Nature Genetics|2012

Cited by 938

Aicardi–Goutières syndrome and the type I interferonopathies

Yanick J. Crow, Nicolas Manel|Nature reviews. Immunology|2015

Cited by 907

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 et al.|Nature Genetics|2006

Cited by 890

HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolase

David C. Goldstone, Valerie Ennis-Adeniran, Joseph J. Hedden et al.|Nature|2011

Cited by 824Open Access

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

Capucine Pïcard, H. Bobby Gaspar, Waleed Al–Herz et al.|Journal of Clinical Immunology|2017

Cited by 793Open Access

Beginning in 1970, a committee was constituted under the auspices of the World Health Organization (WHO) to catalog primary immunodeficiencies. Twenty years later, the International Union of Immunological Societies (IUIS) took the remit of this committee. The current report details the categorization and listing of 354 (as of February 2017) inborn errors of immunity. The growth and increasing complexity of the field have been impressive, encompassing an increasing variety of conditions, and the classification described here will serve as a critical reference for immunologists and researchers worldwide.

Is this you? Claim your profile.

Top publicationsby citations