Kết quả tìm kiếm - Margaret Pericak‐Vance
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1
A rare missense variant of <i>CASP7</i> is associated with familial late‐onset Alzheimer's disease Bằng Xiaoling Zhang, Congcong Zhu, Gary W. Beecham, Badri N. Vardarajan, Yiyi Ma, Daniel Lancour, John J. Farrell, Jaeyoon Chung, Richard Mayeux, Jonathan L. Haines, Gerard Schellenberg, Margaret Pericak‐Vance, Kathryn L. Lunetta, Lindsay A. Farrer
Được phát hành 2018Artigo -
2
Association of common and rare variants with Alzheimer's disease in more than 13,000 diverse individuals with whole‐genome sequencing from the Alzheimer's Disease Sequencing Projec... Bằng Wan‐Ping Lee, Seung Hoan Choi, Margaret G. Shea, Po‐Liang Cheng, Beth A. Dombroski, Achilleas Pitsillides, Nancy L. Heard‐Costa, Hui Wang, Katia Bulekova, Amanda B Kuzma, Yuk Yee Leung, John J. Farrell, Honghuang Lin, Brian W. Kunkle, Adam C. Naj, Elizabeth Blue, Frederick Nusetor, Dongyu Wang, Eric Boerwinkle, William S. Bush, Xiaoling Zhang, Philip L. De Jager, Josée Dupuis, Lindsay A. Farrer, Myriam Fornage, Eden R. Martin, Margaret Pericak‐Vance, Sudha Seshadri, Ellen M. Wijsman, Li‐San Wang, Gerard D. Schellenberg, Anita L. DeStefano, Jonathan L. Haines, Gina M. Peloso
Được phát hành 2024Artigo
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Các môn học liên quan
Alzheimer's disease
Biology
Disease
Gene
Genetic association
Genetics
Genome-wide association study
Genotype
Medicine
Single-nucleotide polymorphism
Apolipoprotein E
Environmental health
Genetic architecture
Genetic variants
Genome
Internal medicine
Missense mutation
Mutation
PSEN1
Pathology
Population
Presenilin
Quantitative trait locus
Whole genome sequencing