Special Issue “Parkinson’s Disease: Genetics and Pathogenesis”-Reference-Cited by-同舟云学术

Special Issue “Parkinson’s Disease: Genetics and Pathogenesis”

Published:2023-03-17 Issue:3 Volume:14 Page:737
ISSN:2073-4425
Container-title:Genes
language:en
Short-container-title:Genes

Author:

Lesage Suzanne¹,Trinh Joanne²

Affiliation:

1. Sorbonne Université, Institut du Cerveau-Paris Brain Institute, ICM, INSERM U 1127, CNRS UMR 7225, Assistance Publique-Hôpitaux de Paris (AP-HP), 75013 Paris, France

2. Institute of Neurogenetics, University of Lübeck, 23562 Lübeck, Germany

Abstract

Parkinson’s disease (PD) is a common and incurable neurodegenerative disease, affecting 1% of the population over the age of 65 [...]

Funder

Fondation pour la Recherche Médicale

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

Link

https://www.mdpi.com/2073-4425/14/3/737/pdf

Reference15 articles.

1. Jia, F., Fellner, A., and Kumar, K.R. (2022). Monogenic Parkinson’s Disease: Genotype, Phenotype, Pathophysiology, and Genetic Testing. Genes, 13.

2. Elsayed, I., Martinez-Carrasco, A., Cornejo-Olivas, M., and Bandres-Ciga, S. (2021). Mapping the Diverse and Inclusive Future of Parkinson’s Disease Genetics and Its Widespread Impact. Genes, 12.

3. Global Parkinson’s Genetics Program (2021). GP2: The Global Parkinson’s Genetics Program. Mov. Disord., 36, 842–851.

4. Kim, J., Daadi, E.W., Oh, T., Daadi, E.S., and Daadi, M.M. (2022). Human Induced Pluripotent Stem Cell Phenotyping and Preclinical Modeling of Familial Parkinson’s Disease. Genes, 13.

5. Mangone, G., Houot, M., Gaurav, R., Boluda, S., Pyatigorskaya, N., Chalancon, A., Seilhean, D., Prigent, A., Lehéricy, S., and Arnulf, I. (2022). Relationship between Substantia Nigra Neuromelanin Imaging and Dual Alpha-Synuclein Labeling of Labial Minor in Salivary Glands in Isolated Rapid Eye Movement Sleep Behavior Disorder and Parkinson’s Disease. Genes, 13.

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