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Nature Genetics|November 17, 2009
Genome-wide association study reveals genetic risk underlying Parkinson's diseaseJavier Simón-Sánchez, Claudia Schulte, Jose M Bras, et al.
Neurobiology of Disease|June 12, 2020
Serum neurofilament light chain levels are associated with white matter integrity in autosomal dominant Alzheimer's diseaseStephanie A Schultz, Jeremy F Strain, Adedamola Adedokun, et al.
Nature Genetics|July 28, 2014
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's diseaseMike A Nalls, Nathan Pankratz, Christina M Lill, et al.
Brain : a Journal of Neurology|February 21, 2018
Left frontal hub connectivity delays cognitive impairment in autosomal-dominant and sporadic Alzheimer's diseaseNicolai Franzmeier, Emrah Düzel, Frank Jessen, et al.
JAMA Neurology|October 16, 2023
Etiology of White Matter Hyperintensities in Autosomal Dominant and Sporadic Alzheimer DiseaseZahra Shirzadi, Stephanie A Schultz, Wai-Ying W Yau, et al.
Acta Neuropathologica Communications|April 26, 2023
Large multi-ethnic genetic analyses of amyloid imaging identify new genes for Alzheimer diseaseMuhammad Ali, Derek B Archer, Priyanka Gorijala, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 2013
Regional variability of imaging biomarkers in autosomal dominant Alzheimer's diseaseTammie L S Benzinger, Tyler Blazey, Clifford R Jack, et al.
Molecular Psychiatry|March 23, 2019
The BDNF<sub>Val66Met</sub> SNP modulates the association between beta-amyloid and hippocampal disconnection in Alzheimer's diseaseNicolai Franzmeier, Jinyi Ren, Alexander Damm, et al.
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