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American Journal of Human Genetics|April 3, 2004
Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic IsolatesRonald G Lafreniere, Marcia L E MacDonald, Marie-Pierre Dube, et al.Cell Metabolism|February 2, 2022
Heterogenous impairment of α cell function in type 2 diabetes is linked to cell maturation stateXiao-Qing Dai, Joan Camunas-Soler, Linford J B Briant, et al.The Clinical Journal of Pain|March 13, 2026
A Systematic Review and Meta-Analysis of the Effectiveness of Process Interventions for Reducing Distress during Vaccine InjectionsAnna Taddio, Vibhuti Shah, C Meghan McMurtry, et al.American Journal of Human Genetics|January 9, 2008
Disruption of neurexin 1 associated with autism spectrum disorderHyung-Goo Kim, Shotaro Kishikawa, Anne W Higgins, et al.Cell|April 30, 2013
Integrated systems approach identifies genetic nodes and networks in late-onset Alzheimer's diseaseBin Zhang, Chris Gaiteri, Liviu-Gabriel Bodea, et al.Nature Human Behaviour|June 26, 2020
Ten considerations for effectively managing the COVID-19 transitionKatrine Bach Habersaat, Cornelia Betsch, Margie Danchin, et al.Cancer Immunology Research|July 27, 2022
Immuno-PET Monitoring of Lymphocytes Using the CD8-Specific Antibody REGN5054Richard Tavaré, Makenzie Danton, Jason T Giurleo, et al.Biorxiv : the Preprint Server for Biology|June 4, 2025
MSH3 is a genetic modifier of somatic repeat instability in X-linked dystonia parkinsonismAlan Mejia Maza, Madison Hincher, Kevin Correia, et al.American Journal of Human Genetics|March 24, 2022
Genetic modifiers of Huntington disease differentially influence motor and cognitive domainsJong-Min Lee, Yuan Huang, Michael Orth, et al.American Journal of Human Genetics|December 24, 2025
MSH3 is a genetic modifier of somatic repeat instability in X-linked dystonia parkinsonismAlan Mejia Maza, Madison Hincher, Kevin Correia, et al.Pageof 133