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Nature Genetics|October 16, 2007
A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer riskPeter Broderick, Luis Carvajal-Carmona, Alan M Pittman, et al.American Journal of Human Genetics|May 19, 2015
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaNiccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 16, 2024
NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse PopulationsSara Bandres-Ciga, Faraz Faghri, Elisa Majounie, et al.Genome Biology|February 1, 2017
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencingIris E Jansen, Hui Ye, Sasja Heetveld, et al.Neurobiology of Aging|September 3, 2020
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's diseaseEmmeline E Brown, Cornelis Blauwendraat, Joanne Trinh, et al.Medrxiv : the Preprint Server for Health Sciences|November 21, 2023
NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse PopulationsSara Bandres-Ciga, Faraz Faghri, Elisa Majounie, et al.European Journal of Human Genetics : EJHG|July 17, 2008
Deciphering the genetics of hereditary non-syndromic colorectal cancerEli Papaemmanuil, Luis Carvajal-Carmona, Gabrielle S Sellick, et al.Nature Genetics|December 18, 2007
Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer riskEmma Jaeger, Emily Webb, Kimberley Howarth, et al.Brain : a Journal of Neurology|June 22, 2023
Large-scale rare variant burden testing in Parkinson's diseaseMary B Makarious, Julie Lake, Vanessa Pitz, et al.JAMA Neurology|December 21, 2019
Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal SyndromeEdwin Jabbari, Negin Holland, Viorica Chelban, et al.Pageof 24