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Medrxiv : the Preprint Server for Health Sciences|July 3, 2023
Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinson's Disease in African and African Admixed PopulationsMie Rizig, Sara Bandres-Ciga, Mary B Makarious, et al.
Medrxiv : the Preprint Server for Health Sciences|March 11, 2024
Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and MAPT Sub-haplotypesHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 8, 2025
Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal CellsHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Neuron|September 28, 2011
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDAlan E Renton, Elisa Majounie, Adrian Waite, et al.
Neurology|March 6, 2026
Genetic Determinants of Multiple Sclerosis Susceptibility in People From Diverse Ancestral BackgroundsBenjamin Meir Jacobs, Luisa Schalk, Emily Tregaskis-Daniels, et al.
Breast Cancer Research : BCR|November 30, 2013
Critical research gaps and translational priorities for the successful prevention and treatment of breast cancerSuzanne A Eccles, Eric O Aboagye, Simak Ali, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
Large-scale genetic characterization of Parkinson's disease in the African and African admixed populationsFulya Akçimen, Kimberly Paquette, Peter Wild Crea, et al.
Neuron|May 3, 2024
Genome sequence analyses identify novel risk loci for multiple system atrophyRuth Chia, Anindita Ray, Zalak Shah, et al.
Statistics in Medicine|March 9, 2010
Bayesian methods for meta-analysis of causal relationships estimated using genetic instrumental variablesStephen Burgess, Simon G Thompson, , et al.
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