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JAMA Neurology|July 25, 2018
Frequency of Loss of Function Variants in LRRK2 in Parkinson DiseaseCornelis Blauwendraat, Xylena Reed, Demis A Kia, et al.
Nature Genetics|September 2, 2008
A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemiaMaria Chiara Di Bernardo, Dalemari Crowther-Swanepoel, Peter Broderick, et al.
American Journal of Human Genetics|April 9, 2016
De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal LesionsNiccolò E Mencacci, Erik-Jan Kamsteeg, Kosuke Nakashima, 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.
Brain : a Journal of Neurology|July 5, 2014
Parkinson's disease in GTP cyclohydrolase 1 mutation carriersNiccolò E Mencacci, Ioannis U Isaias, Martin M Reich, et al.
Nature Genetics|November 18, 2008
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer, Richard S Houlston, Emily Webb, et al.
Human Molecular Genetics|August 30, 2008
Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancerAlan M Pittman, Emily Webb, Luis Carvajal-Carmona, et al.
Nature Genetics|April 1, 2008
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3Ian P M Tomlinson, Emily Webb, Luis Carvajal-Carmona, et al.
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