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Molecular Systems Biology|September 17, 2009
A simple and efficient algorithm for genome-wide homozygosity analysis in diseaseWei Liu, Jinhui Ding, Jesse Raphael Gibbs, et al.JAMA Neurology|January 16, 2013
Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvementRita João Guerreiro, Ebba Lohmann, José Miguel Brás, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 26, 2021
The Parkinson's Disease DNA Variant BrowserJonggeol J Kim, Mary B Makarious, Sara Bandres-Ciga, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 25, 2019
The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's diseaseSara Bandres-Ciga, Sara Saez-Atienzar, Luis Bonet-Ponce, et al.Neurobiology of Aging|December 14, 2011
Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's diseaseRita João Guerreiro, Ebba Lohmann, Emma Kinsella, et al.Pageof 1