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D Schellenberg

Showing results (271-280 of 467) with videos related to

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Alzheimer'S Research & Therapy|July 24, 2025
Genome-wide association studies of Alzheimer's disease and related disorders stratified by sex, onset age, and Apolipoprotein E genotype reveal novel risk loci in African AmericansRichard Sherva, Congcong Zhu, Rui Zhang, et al.
Journal of Lipid Research|December 7, 2007
A common VLDLR polymorphism interacts with APOE genotype in the prediction of carotid artery disease riskDana C Crawford, Alex S Nord, Michael D Badzioch, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|June 18, 2025
Structural variation detection and association analysis of whole-genome-sequence data from 16,543 Alzheimer's disease sequencing project subjectsHui Wang, Beth A Dombroski, Po-Liang Cheng, et al.
Journal of Alzheimer'S Disease : JAD|December 22, 2006
Effect of statins on Alzheimer's disease biomarkers in cerebrospinal fluidRobert G Riekse, Ge Li, Eric C Petrie, et al.
Archives of Neurology|August 8, 2012
Comprehensive search for Alzheimer disease susceptibility loci in the APOE regionGyungah Jun, Badri N Vardarajan, Jacqueline Buros, et al.
Human Molecular Genetics|December 1, 1996
Homozygous and compound heterozygous mutations at the Werner syndrome locusJ Oshima, C E Yu, C Piussan, et al.
Journal of Alzheimer'S Disease : JAD|January 24, 2022
Alzheimer's Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer's DiseasePavel P Kuksa, Chia-Lun Liu, Wei Fu, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|February 14, 2022
Genome-wide association study of brain arteriolosclerosisLincoln Mp Shade, Yuriko Katsumata, Timothy J Hohman, et al.
Annals of Neurology|December 1, 1996
The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patientsM Ikeda, V Sharma, S M Sumi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 4, 2009
LRRK2 mutations and risk variants in Japanese patients with Parkinson's diseaseCyrus P Zabetian, Mitsutoshi Yamamoto, Alexis N Lopez, et al.
Pageof 47

Showing results (271-280 of 467) with videos related to

Sort By:
Pageof 47
Alzheimer'S Research & Therapy|July 24, 2025
Genome-wide association studies of Alzheimer's disease and related disorders stratified by sex, onset age, and Apolipoprotein E genotype reveal novel risk loci in African AmericansRichard Sherva, Congcong Zhu, Rui Zhang, et al.
Journal of Lipid Research|December 7, 2007
A common VLDLR polymorphism interacts with APOE genotype in the prediction of carotid artery disease riskDana C Crawford, Alex S Nord, Michael D Badzioch, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|June 18, 2025
Structural variation detection and association analysis of whole-genome-sequence data from 16,543 Alzheimer's disease sequencing project subjectsHui Wang, Beth A Dombroski, Po-Liang Cheng, et al.
Journal of Alzheimer'S Disease : JAD|December 22, 2006
Effect of statins on Alzheimer's disease biomarkers in cerebrospinal fluidRobert G Riekse, Ge Li, Eric C Petrie, et al.
Archives of Neurology|August 8, 2012
Comprehensive search for Alzheimer disease susceptibility loci in the APOE regionGyungah Jun, Badri N Vardarajan, Jacqueline Buros, et al.
Human Molecular Genetics|December 1, 1996
Homozygous and compound heterozygous mutations at the Werner syndrome locusJ Oshima, C E Yu, C Piussan, et al.
Journal of Alzheimer'S Disease : JAD|January 24, 2022
Alzheimer's Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer's DiseasePavel P Kuksa, Chia-Lun Liu, Wei Fu, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|February 14, 2022
Genome-wide association study of brain arteriolosclerosisLincoln Mp Shade, Yuriko Katsumata, Timothy J Hohman, et al.
Annals of Neurology|December 1, 1996
The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patientsM Ikeda, V Sharma, S M Sumi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 4, 2009
LRRK2 mutations and risk variants in Japanese patients with Parkinson's diseaseCyrus P Zabetian, Mitsutoshi Yamamoto, Alexis N Lopez, et al.
Pageof 47