Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease

Journal: PLOS Genetics

Published: 2019-06-01

DOI: 10.1371/journal.pgen.1008180

Affiliations: 23

Authors: 33

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Institutions Share
Department of Medical Genetics, UBC, Canada 0.20
IRCCS Institute of Experimental Neurology (INSPE), Italy 0.10
Institute of Neurology (CIN), MUW, Austria 0.09
Department of Psychiatry, UBC, Canada 0.08
Red Española de Esclerosis Múltiple (REEM), Spain 0.06
Achucarro Basque Center for Neuroscience, UPV/EHU, Spain 0.06
Institute of Biomedical Research in Malaga (IBIMA), Spain 0.06
Institute of Parasitology and Biomedicine Lopez-Neyra (IPBLN), CSIC, Spain 0.06
Faculty of Medicine, UBC, Canada 0.05
Health Research Institute of San Carlos (IdISSC), Spain 0.03
Toxicology Pharmacology and Cellular Signaling, France 0.03
Department of Pathology and Laboratory Medicine, UBC, Canada 0.03
Hospital Universitario Virgen Macarena, Spain 0.03
Hospital de Cruces, Spain 0.03
National Clinical Research Center for Geriatric Disorders at Xuanwu Hospital, Capital Medical University, China 0.02
Department of Pediatrics, USherbrooke, Canada 0.02
Centre Hospitalier Universitaire de Sherbrooke (CHUS), Canada 0.02
Department of Biomedical Sciences for Health, UNIMI, Italy 0.01
IRCCS Policlinico San Donato, Italy 0.01
Mayo Clinic's Campus in Florida, United States of America (USA) 0.01
Mayo Clinic Department of Clinical Genomics, Florida Campus, United States of America (USA) 0.01
Mayo Clinic Department of Neuroscience, Florida Campus, United States of America (USA) 0.01

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