Publications:

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Genetics of Multiple System Atrophy and Progressive Supranuclear Palsy: A Systemized Review of the Literature.

International Journal Of Molecular Sciences

Bougea, Anastasia A

Publication Date: 2023-03-09

Variant appearance in text: rs3775444

PubMed Link: 36982356

Variant Present in the following documents:

• Main text
• ijms-24-05281.pdf

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The Genetic Landscape of Parkinsonism-Related Dystonias and Atypical Parkinsonism-Related Syndromes.

International Journal Of Molecular Sciences

Diez-Fairen, Monica M; Alvarez Jerez, Pilar P; Berghausen, Joos J; Bandres-Ciga, Sara S

Publication Date: 2021-07-28

Variant appearance in text: rs3775444

PubMed Link: 34360863

Variant Present in the following documents:

• Main text
• ijms-22-08100.pdf

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A systematic review of associations between common SNCA variants and clinical heterogeneity in Parkinson's disease.

Npj Parkinson'S Disease

Pedersen, Camilla Christina CC; Lange, Johannes J; Førland, Marthe Gurine Gunnarsdatter MGG; Macleod, Angus D AD; Alves, Guido G; Maple-Grødem, Jodi J

Publication Date: 2021-07-01

Variant appearance in text: rs3775444

PubMed Link: 34210990

Variant Present in the following documents:

• 41531_2021_196_MOESM1_ESM.pdf

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MicroRNAs Dysregulation and Metabolism in Multiple System Atrophy.

Frontiers In Neuroscience

Xiang, Chunchen C; Han, Shunchang S; Nao, Jianfei J; Cong, Shuyan S

Publication Date: 2019

Variant appearance in text: rs3775444

PubMed Link: 31680837

Variant Present in the following documents:

• Main text
• fnins-13-01103.pdf

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Cross-examining candidate genes implicated in multiple system atrophy.

Acta Neuropathologica Communications

Katzeff, Jared S JS; Phan, Katherine K; Purushothuman, Sivaraman S; Halliday, Glenda M GM; Kim, Woojin Scott WS

Publication Date: 2019-07-24

Variant appearance in text: rs3775444

PubMed Link: 31340844

Variant Present in the following documents:

• Main text
• 40478_2019_Article_769.pdf

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Functional Variant rs3135500 in NOD2 Increases the Risk of Multiple System Atrophy in a Chinese Population.

Frontiers In Aging Neuroscience

Cao, Bei B; Chen, Yongping Y; Zhou, Qingqing Q; Zhang, Lingyu L; Ou, Ruwei R; Wei, Qianqian Q; Wu, Ying Y; Shang, Hui-Fang HF

Publication Date: 2018

Variant appearance in text: rs3775444

PubMed Link: 29881342

Variant Present in the following documents:

• Main text
• fnagi-10-00150.pdf

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Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson's Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population.

Plos One

Chen, YongPing Y; Wei, Qian-Qian QQ; Ou, RuWei R; Cao, Bei B; Chen, XuePing X; Zhao, Bi B; Guo, XiaoYan X; Yang, Yuan Y; Chen, Ke K; Wu, Ying Y; Song, Wei W; Shang, Hui-Fang HF

Publication Date: 2015

Variant appearance in text: rs3775444

PubMed Link: 26208350

Variant Present in the following documents:

• Main text

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Association of the COQ2 V393A Variant with Parkinson's Disease: A Case-Control Study and Meta-Analysis.

Plos One

Yang, Xinglong X; Xi, Jing J; Zhao, Quanzhen Q; Jia, Hua H; An, Ran R; Liu, Zhuolin Z; Xu, Yanming Y

Publication Date: 2015

Variant appearance in text: rs3775444

PubMed Link: 26098829

Variant Present in the following documents:

• Main text
• pone.0130970.pdf

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The neurogenetics of atypical parkinsonian disorders.

Seminars In Neurology

Fogel, Brent L BL; Clark, Mary C MC; Geschwind, Daniel H DH

Publication Date: 2014-04

Variant appearance in text: rs3775444

PubMed Link: 24963681

Variant Present in the following documents:

• Main text

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Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy.

Plos One

Al-Chalabi, Ammar A; Dürr, Alexandra A; Wood, Nicholas W NW; Parkinson, Michael H MH; Camuzat, Agnes A; Hulot, Jean-Sébastien JS; Morrison, Karen E KE; Renton, Alan A; Sussmuth, Sigurd D SD; Landwehrmeyer, Bernhard G BG; Ludolph, Albert A; Agid, Yves Y; Brice, Alexis A; Leigh, P Nigel PN; Bensimon, Gilbert G; ,

Publication Date: 2009-09-22

Variant appearance in text: rs3775444

PubMed Link: 19771175

Variant Present in the following documents:

• Main text
• pone.0007114.pdf

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