Yanick J. Crow

Hôpital Necker-Enfants Malades — France

Immunology and Microbiology · Life Sciences

90h-index31.3kcitations429works6.82yr avg
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Research Topics

interferon and immune responses(160), Inflammasome and immune disorders(90), Systemic Lupus Erythematosus Research(80), RNA regulation and disease(75), Immunodeficiency and Autoimmune Disorders(33)

Publications416 total

Generation of two iPSC lines from patients with Aicardi-Goutières syndrome carrying either biallelic ADAR1 mutations (PC138) or a heterozygous IFIH1 mutation (PC139)
Stem Cell Research·2025Open Access
L’haplotype HAQ de STING n’explique pas à lui seul la pénétrance incomplète du syndrome COPA
La Revue de Médecine Interne·2025
Étude d’une cohorte européenne multicentrique de 38 patients atteints d’une maladie auto-inflammatoire rare, le syndrome COPA
La Revue de Médecine Interne·2025
291 PNPT1 loss-of-function variants in interferon-related psoriasis
Journal of Investigative Dermatology·2025
282 Role of fibroblasts in ADAR1-mediated psoriasis
Journal of Investigative Dermatology·2025
ATRX Deficiency Drives Aberrant Type I Interferon Signalling Through cGAS-Dependent Transcriptional Dysregulation
2025· 2 citedOpen Access
Variants perte de fonction PNPT1 dans le psoriasis associé à une signature interféron
Annales de Dermatologie et de Vénéréologie - FMC·2025
Rôle des fibroblastes dans le psoriasis associé aux variants ADAR1
Annales de Dermatologie et de Vénéréologie - FMC·2025
Insights from a novel monogenic autoinflammatory disease: overview of a multicentric European cohort of 38 patients with COPA syndrome
Annals of the Rheumatic Diseases·2025· 1 citedOpen Access
Human Mendelian disease and <i>in vivo</i> mutagenesis screening define the molecular architecture of the U8 snoRNA
2025Open Access
Two Patients with AGS9: Divergent Clinical Courses of a Rare Metabolic Disease
Neuropediatrics·2025
Spondyloenchondrodysplasia: An enigmatic immuno-osseus type I interferonopathy
Journal of Human Immunity·2025Open Access
NAP1 switches from an activator to a limiter of interferon induction by trapping TBK1 in condensates
2025Open Access
Mutations in <i>RNU4ATAC</i> Are Associated With Chilblain‐Like Lesions and Enhanced Type I Interferon Signalling
European Journal of Immunology·2025Open Access
Author response for "Mutations in &lt;i&gt;RNU4ATAC&lt;/i&gt; Are Associated With Chilblain‐Like Lesions and Enhanced Type I Interferon Signalling"
2025
Distinct pathogenic mutations in ARF1 allow dissection of its dual role in cGAS-STING signalling
EMBO Reports·2025Open Access
Author response for "Mutations in &lt;i&gt;RNU4ATAC&lt;/i&gt; Are Associated With Chilblain‐Like Lesions and Enhanced Type I Interferon Signalling"
2025
Autoinflammatory encephalopathy due to PTPN1 haploinsufficiency: a case series
The Lancet Neurology·2025· 7 citedOpen Access
Baricitinib Treatment in <scp>RNU7</scp>‐1‐Associated Aicardi–Goutières Syndrome in a South African Child: A Case Report
American Journal of Medical Genetics Part A·2025· 1 citedOpen Access
P334: Deep phenotyping of thirty-one cases of Aicardi-Goutières syndrome
Genetics in Medicine Open·2025Open Access
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Frequent Co-authors

Gillian Rice(23), Pierre Lebon(9), Brigitte Bader‐Meunier(8), Mathieu P. Rodero(8), Marie‐Louise Frémond(8), Bénédicte Neven(7), Frédéric Rieux‐Laucat(7), Marcin Szynkiewicz(6), Elisa Fazzi(6), Charles Marques Lourenço(6), Jean‐Laurent Casanova(6), Christine Bodemer(6), Darragh Duffy(6), Tracy A. Briggs(5), Isabelle Desguerre(5), Flore Rozenberg(5), Capucine Pïcard(5), Kate Chandler(5), Alexandre Bélot(5), Isabelle Melki(5)