A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease

Autor: Weixin Wang, Li (Charlie) Xia, Alejandro Nato, D Kalra, Claudia L Satizabal, Mohammad Arfan Ikram, Yuk Yee Leung, Kathryn Lunetta, Jaeyoon Chung, Kim Worley, Elizabeth Blue, Cornelia Van Duijn, Yuning Chen, Sudha Seshadri, Congcong Zhu, William Bush, Yeunjoo Song

Publikováno v: Alzheimer's and Dementia, 15(3), 441-452. Elsevier
Zhang, X, Zhu, C, Beecham, G, Vardarajan, B N, Ma, Y, Lancour, D, Farrell, J J, Chung, J, Alzheimer's Disease Sequencing Project, Mayeux, R, Haines, J L, Schellenberg, G D, Pericak-Vance, M A, Lunetta, K L & Farrer, L A 2019, ' A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease ', Alzheimer's and Dementia, vol. 15, no. 3, pp. 441-452 . https://doi.org/10.1016/j.jalz.2018.10.005

Introduction The genetic architecture of Alzheimer's disease (AD) is only partially understood. Methods We conducted an association study for AD using whole sequence data from 507 genetically enriched AD cases (i.e., cases having close relatives affe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bc9860fbb165b21f9e5e744a9dd31b9
https://ora.ox.ac.uk/objects/uuid:66b506a6-9f82-4eba-93a9-1f030e0d0cb4

The effect of multiple genetic variants in predicting the risk of type 2 diabetes.

Autor: Qing Lu¹ qlu@epi.msu.edu, Yeunjoo Song² yeunjoo.song@case.edu, Xuefeng Wang² xuefeng.wang@case.edu, Sungho Won² sung.won@case.edu, Yuehua Cui³ cui@stt.msu.edu, Elston, Robert C.² robert.elston@cwru.edu

Publikováno v: BMC Proceedings. 2009 Supplement 7, Vol. 3, Special section p1-5. 5p. 1 Chart, 1 Graph.

Association Between Germline Mutation in VSIG10L and Familial Barrett Neoplasia.

Autor: Fecteau, Ryan E., Jianping Kong, Kresak, Adam, Brock, Wendy, Yeunjoo Song, Hisashi Fujioka, Elston, Robert, Willis, Joseph E., Lynch, John P., Markowitz, Sanford D., Guda, Kishore, Chak, Amitabh

Publikováno v: JAMA Oncology; Oct2016, Vol. 2 Issue 10, p1333-1339, 7p, 1 Color Photograph, 1 Black and White Photograph, 2 Diagrams, 1 Graph

Defining genetic determinants of the Metabolic Syndrome in the Framingham Heart Study using association and structural equation modeling methods.

Autor: Nock, Nora L., Wang, Xuefeng, Thompson, Cheryl L., Yeunjoo Song, Baechle, Dan, Raska, Paola, Stein, Catherine M., Gray-McGuire, Courtney

Publikováno v: BMC Proceedings; 2009 Supplement 7, Vol. 3, Special section p1-6, 6p, 1 Diagram, 2 Charts

Assessing the impact of global versus local ancestry in association studies.

Autor: Sun Jung Kang, Emma K. Larkin, Yeunjoo Song, Jill Barnholtz-Sloan, Dan Baechle, Tao Feng, Xiaofeng Zhu

Publikováno v: BMC Proceedings; 2009 Supplement 7, Vol. 3, Special section p1-6, 6p, 3 Charts, 1 Graph