Showing results (351-360 of 477) with videos related to

Sort By:
Pageof 48
Circulation. Cardiovascular Genetics|January 14, 2015
DNA methylation of lipid-related genes affects blood lipid levelsLiliane Pfeiffer, Simone Wahl, Luke C Pilling, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2026
Long-read sequencing maps transposable element variation and its regulatory and epigenetic effects in the human brainAlexis Ayuketah, Melissa Meredith, Cristian Groza, et al.
Science Translational Medicine|July 1, 2026
Alzheimer's disease proteome-wide association study implicates adaptive immunity and identifies risk genes LILRB1 and SIRPAKeenan A Walker, Cassandra Blew, Michael R Duggan, et al.
Human Molecular Genetics|August 16, 2012
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's diseaseMargaux F Keller, Mohamad Saad, Jose Bras, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
CNV-Finder: Streamlining Copy Number Variation DiscoveryNicole Kuznetsov, Kensuke Daida, Mary B Makarious, et al.
Human Molecular Genetics|December 11, 2012
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's diseasePeter Holmans, Valentina Moskvina, Lesley Jones, et al.
Neurology|November 8, 2014
LRRK2 exonic variants and risk of multiple system atrophyMichael G Heckman, Lucia Schottlaender, Alexandra I Soto-Ortolaza, et al.
JAMA Neurology|June 7, 2017
Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune DiseasesAree Witoelar, Iris E Jansen, Yunpeng Wang, et al.
Neurology|February 28, 2020
Disease modification and biomarker development in Parkinson disease: Revision or reconstruction?Alberto J Espay, Lorraine V Kalia, Ziv Gan-Or, et al.
JAMA Neurology|May 12, 2015
Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence ProjectPaul L Auer, Mike Nalls, James F Meschia, et al.
Pageof 48