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Journal of Alzheimer'S Disease : JAD|October 16, 2018
Quantitative Genetics Validates Previous Genetic Variants and Identifies Novel Genetic Players Influencing Alzheimer's Disease Cerebrospinal Fluid BiomarkersMafalda Ramos de Matos, Catarina Ferreira, Sanna-Kaisa Herukka, et al.Nature Genetics|March 26, 2015
Loss-of-function variants in ABCA7 confer risk of Alzheimer's diseaseStacy Steinberg, Hreinn Stefansson, Thorlakur Jonsson, et al.Neurology|August 14, 2024
Risk Variants Associated With Normal Pressure Hydrocephalus: Genome-Wide Association Study in the FinnGen CohortJoel Räsänen, Sami Heikkinen, Kiira Mäklin, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 10, 2018
Association of branched-chain amino acids and other circulating metabolites with risk of incident dementia and Alzheimer's disease: A prospective study in eight cohortsJuho Tynkkynen, Vincent Chouraki, Sven J van der Lee, et al.Circulation. Cardiovascular Genetics|March 9, 2012
Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traitsKati Kristiansson, Markus Perola, Emmi Tikkanen, et al.Journal of Alzheimer'S Disease : JAD|November 30, 2020
White Matter Hyperintensities Are No Major Confounder for Alzheimer's Disease Cerebrospinal Fluid BiomarkersLinda J C van Waalwijk van Doorn, Mohsen Ghafoorian, Esther M C van Leijsen, et al.Human Molecular Genetics|February 27, 2018
Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM studyTanya M Teslovich, Daniel Seung Kim, Xianyong Yin, et al.Neurobiology of Aging|January 12, 2011
Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populationsJean-Charles Lambert, Diana Zelenika, Mikko Hiltunen, et al.Molecular Neurodegeneration|April 29, 2025
Monoallelic TYROBP deletion is a novel risk factor for Alzheimer's diseaseHenna Martiskainen, Roosa-Maria Willman, Päivi Harju, et al.Molecular Psychiatry|April 24, 2013
Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairmentK Nho, J J Corneveaux, S Kim, et al.Pageof 121