Clinical non-penetrance associated with biallelic mutations in the RNase H2 complex

od Crow, Yanick J
izdano v J Clin Immunol (2023)

CNS disease associated with enhanced type 1 interferon signalling

od Crow, Yanick J
izdano v Lancet Neurol (2024)

Aicardi-Goutières syndrome and related phenotypes: linking nucleic acid metabolism with autoimmunity

od Crow, Yanick J., Rehwinkel, Jan
Izdano 2009

cGMP-AMP synthase paves the way to autoimmunity

od Rodero, Mathieu P., Crow, Yanick J.
izdano v Proc Natl Acad Sci U S A (2015)

Type I interferon–mediated monogenic autoinflammation: The type I interferonopathies, a conceptual overview

od Rodero, Mathieu P., Crow, Yanick J.
izdano v J Exp Med (2016)

Cerebral vasculopathy is a common feature in Aicardi–Goutières syndrome associated with SAMHD1 mutations

od du Moulin, Marcel, Nürnberg, Peter, Crow, Yanick J., Rutsch, Frank
Izdano 2011

MDA5-Associated Neuroinflammation and the Singleton–Merten Syndrome: Two Faces of the Same Type I Interferonopathy Spectrum

od Buers, Insa, Rice, Gillian I., Crow, Yanick J., Rutsch, Frank
izdano v J Interferon Cytokine Res (2017)

Familial Blau syndrome: First molecularly confirmed report from India

od Janarthanan, Mahesh, Poddar, Chanchal, Sudharshan, S, Seabra, Luis, Crow, Yanick J
izdano v Indian J Ophthalmol (2019)

Neuromyelitis optica in a child with Aicardi-GoutiÈres syndrome

od Hacohen, Yael, Zuberi, Sameer, Vincent, Angela, Crow, Yanick J., Cordeiro, Nuno
izdano v Neurology (2015)

Teaching NeuroImages: A rare genetic cause of spastic paraparesis

od Bhattacharjee, Shakya, Siripurapu, Rekha, Swale, Andrew, Crow, Yanick J, Kobylecki, Christopher
izdano v Neurology (2024)

Development and Validation of an Ultrasensitive Single Molecule Array Digital Enzyme-linked Immunosorbent Assay for Human Interferon-α

od Llibre, Alba, Bondet, Vincent, Rodero, Mathieu P., Hunt, David, Crow, Yanick J., Duffy, Darragh
izdano v J Vis Exp (2018)

Treatment of Leukoencephalopathy With Calcifications and Cysts With Bevacizumab

od Fay, Alex J., King, Allison A., Shimony, Joshua S., Crow, Yanick J., Brunstrom-Hernandez, Jan E.
izdano v Pediatr Neurol (2017)

Further delineation of the phenotype of severe congenital neutropenia type 4 due to mutations in G6PC3

od Banka, Siddharth, Chervinsky, Elena, Newman, William G, Crow, Yanick J, Yeganeh, Shay, Yacobovich, Joanne, Donnai, Dian, Shalev, Stavit
Izdano 2011

Crossover trial of reverse transcriptase inhibitors in Aicardi-Goutières syndrome

od Crow, Yanick J, Briggs, Tracy A, Eleftheriou, Despina, Parida, Amitav, Battison, Claire, Giddings, Annabel, Kennel, Titouan, Parker, Richard A
izdano v Dev Med Child Neurol (2024)

A Fifth Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 1q31

od Pattison, Lisa, Crow, Yanick J., Deeble, V. Jayne, Jackson, Andrew P., Jafri, Hussain, Rashid, Yasmin, Roberts, Emma, Woods, C. Geoffrey
Izdano 2000

A POT1 mutation implicates defective telomere end fill-in and telomere truncations in Coats plus

od Takai, Hiroyuki, Jenkinson, Emma, Kabir, Shaheen, Babul-Hirji, Riyana, Najm-Tehrani, Nasrin, Chitayat, David A., Crow, Yanick J., de Lange, Titia
izdano v Genes Dev (2016)

The SKIV2L RNA exosome limits activation of the RIG-I-like receptors

od Eckard, Sterling C., Rice, Gillian I., Fabre, Alexandre, Badens, Catherine, Gray, Elizabeth E., Hartley, Jane L., Crow, Yanick J., Stetson, Daniel B.
Izdano 2014

Elevated serum interferon-α2 associates with activity and flare risk in Juvenile-onset Systemic Lupus Erythematosus

od Natoli, Valentina, Crow, Yanick J, Hunt, David PJ, Tharmaratnam, Kukatharmini, Jorgensen, Andrea L, Beresford, Michael W, Hedrich, Christian M, Smith, Eve MD
izdano v Rheumatology (Oxford) (2024)

Modeling of TREX1-dependent autoimmune disease using human stem cells highlights L1 accumulation as a source of neuroinflammation

od Thomas, Charles A., Tejwani, Leon, Trujillo, Cleber A., Negraes, Priscilla D., Herai, Roberto H., Mesci, Pinar, Macia, Angela, Crow, Yanick J., Muotri, Alysson R.
izdano v Cell Stem Cell (2017)

Neuroradiologic patterns and novel imaging findings in Aicardi-Goutières syndrome

od La Piana, Roberta, Uggetti, Carla, Roncarolo, Federico, Vanderver, Adeline, Olivieri, Ivana, Tonduti, Davide, Helman, Guy, Balottin, Umberto, Fazzi, Elisa, Crow, Yanick J., Livingston, John, Orcesi, Simona
izdano v Neurology (2016)