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European Journal of Human Genetics : EJHG|January 21, 2011
Genome-wide association study confirms extant PD risk loci among the DutchJavier Simón-Sánchez, Jacobus J van Hilten, Bart van de Warrenburg, et al.
Acta Neuropathologica Communications|July 7, 2022
Distinct cell type-specific protein signatures in GRN and MAPT genetic subtypes of frontotemporal dementiaSuzanne S M Miedema, Merel O Mol, Frank T W Koopmans, et al.
Nature Neuroscience|September 19, 2018
Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric diseaseXianjun Dong, Zhixiang Liao, David Gritsch, et al.
Science (New York, N.Y.)|September 2, 2017
β2-Adrenoreceptor is a regulator of the α-synuclein gene driving risk of Parkinson's diseaseShuchi Mittal, Kjetil Bjørnevik, Doo Soon Im, et al.
Neurobiology of Aging|February 17, 2009
Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degenerationSara Rollinson, Patrizia Rizzu, Stephen Sikkink, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|May 19, 2010
The Netherlands Twin Register biobank: a resource for genetic epidemiological studiesGonneke Willemsen, Eco J C de Geus, Meike Bartels, et al.
Cell Genomics|March 23, 2023
The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanismElisangela Bressan, Xylena Reed, Vikas Bansal, et al.
American Journal of Human Genetics|January 22, 2013
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminusGea Beunders, Els Voorhoeve, Christelle Golzio, et al.
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