Yanick J. Crow

Also affiliated with Université Paris Cité, Edinburgh Cancer Research, Sorbonne Paris Cité, Institute of Genetics and Cancer, Institut des Maladies Génétiques Imagine, University of Edinburgh

Immunology and MicrobiologyBiochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 10 papers. Top paper: “A partial form of inherited human USP18 deficiency underlies infection and inflammation”.

A partial form of inherited human USP18 deficiency underlies infection and inflammation

The Journal of Experimental Medicine(2022)10.1084/jem.20211273

N/A

0.652DataRank · unranked

76 citations

Sofija Buta, Tom Le Voyer, Zhi Li, Lasse Toftdal Dynesen, Françoise Vuillier +23 more

Biallelic NAA60 variants with impaired N-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications

Nature Communications(2024)10.1038/s41467-024-46354-0

N/A

0.568DataRank · unranked

43 citations

Henriette Aksnes, Reza Maroofian, Lauren C. LaMonica, Luís Seabra, Anette Siggervåg +55 more

Preexisting autoantibodies to type I IFNs underlie critical COVID-19 pneumonia in patients with APS-1

The Journal of Experimental Medicine(2021)10.1084/jem.20210554

N/A

0DataRank · unranked

307 citations

Elizaveta Orlova, Leila Sozaeva, Romain Lévy, Alyssa James, Monica M. Schmitt +60 more

The 2021 European Alliance of Associations for Rheumatology/American College of Rheumatology Points to Consider for Diagnosis and Management of Autoinflammatory Type I Interferonopathies: CANDLE/PRAAS, SAVI, and AGS

Arthritis & Rheumatology(2022)10.1002/art.42087

N/A

0DataRank · unranked

47 citations

Lovro Lamot, Micol Romano, Erkan Demirkaya, David Piskin, Sofia Torreggiani +27 more

Phenotypes associated with genetic determinants of type I interferon regulation in the UK Biobank: a protocol

Wellcome Open Research(2023)10.12688/wellcomeopenres.20385.1

N/A

0DataRank · unranked

1 citations

Michael Chong, Rosie M. Walker, Sarah McGlasson, Kristiina Rannikmäe, Daniel L. McCartney +6 more

Hematopoietic Stem Cell Transplantation for C1q Deficiency: A Study on Behalf of the EBMT Inborn Errors Working Party

Journal of Clinical Immunology(2024)10.1007/s10875-024-01819-1

N/A

0DataRank · unranked

9 citations

Etai Adam, Peter D. Arkwright, Sagar Bhattad, Amir Ali Hamidieh, Maryam Behfar +25 more

Mutations in the non-catalytic polyproline motif destabilize TREX1 and amplify cGAS-STING signaling

Human Molecular Genetics(2024)10.1093/hmg/ddae089

N/A

0DataRank · unranked

10 citations

Xiaohan Luan, Wen Zhou, Yanick J. Crow, John Maciejowski, Abraham Shim

Genetic and phenotypic spectrum associated with IFIH1 gain‐of‐function

Human Mutation(2020)10.1002/humu.23975

N/A

0DataRank · unranked

113 citations

Sehoon Park, Francesco Gavazzi, Laura Adang, Loveline A. Ayuk, Lien Van Eyck +58 more

ATRX Deficiency Drives Aberrant Type I Interferon Signalling Through cGAS-Dependent Transcriptional Dysregulation

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.11.19.685761

N/A

0DataRank · unranked

2 citations

Elsie White, Graeme R. Grimes, Gaofeng Zhu, Andreas Fellas, Tom A Tait +24 more

Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5

Carolina Digital Repository (University of North Carolina at Chapel Hill)(2020)10.17615/x8dg-7b55

N/A

0DataRank · unranked

0 citations

Alan Fryer, Koenraad Devriendt, Richard H. Scott, Jules G. Leroy, Ingrid P.C. Krapels +27 more