Genetic risk factors in Parkinson’s disease-Reference-Cited by-同舟云学术

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Genetic risk factors in Parkinson’s disease

Published:2018-03-13 Issue:1 Volume:373 Page:9-20
ISSN:0302-766X
Container-title:Cell and Tissue Research
language:en
Short-container-title:Cell Tissue Res

Author:

Billingsley K. J.,Bandres-Ciga S.,Saez-Atienzar S.,Singleton A. B.

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Histology,Pathology and Forensic Medicine

Link

http://link.springer.com/article/10.1007/s00441-018-2817-y/fulltext.html

Reference85 articles.

1. Abeliovich A, Gitler AD (2016) Defects in trafficking bridge Parkinson’s disease pathology and genetics. Nature 539(7628):207–216

2. Anheim M, Elbaz A, Lesage S, Durr A, Condroyer C, Viallet F, … French Parkinson Disease Genetic Group. (2012). Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers. Neurology, 78(6), 417–420

3. Baker M, Litvan I, Houlden H, Adamson J, Dickson D, Perez-Tur J, … Hutton M (1999). Association of an extended haplotype in the tau gene with progressive supranuclear palsy. Hum Mol Genet, 8(4), 711–715

4. Beilina A, Rudenko IN, Kaganovich A, Civiero L, Chau H, Kalia SK, … Cookson MR (2014). Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease. Proc Natl Acad Sci U S A, 111(7), 2626–2631

5. Berge-Seidl V, Pihlstrøm L, Maple-Grødem J, Forsgren L, Linder J, Larsen JP, … Toft M (2017). The GBA variant E326K is associated with Parkinson’s disease and explains a genome-wide association signal. Neurosci Lett, 658, 48–52

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