Publications:

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The Impact of SNCA Variations and Its Product Alpha-Synuclein on Non-Motor Features of Parkinson's Disease.

Life (Basel, Switzerland)

Magistrelli, Luca L; Contaldi, Elena E; Comi, Cristoforo C

Publication Date: 2021-08-09

Variant appearance in text: rs7689942

PubMed Link: 34440548

Variant Present in the following documents:

• Main text
• life-11-00804.pdf

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Investigating the relationship between the SNCA gene and cognitive abilities in idiopathic Parkinson's disease using machine learning.

Scientific Reports

Ramezani, Mehrafarin M; Mouches, Pauline P; Yoon, Eunjin E; Rajashekar, Deepthi D; Ruskey, Jennifer A JA; Leveille, Etienne E; Martens, Kristina K; Kibreab, Mekale M; Hammer, Tracy T; Kathol, Iris I; Maarouf, Nadia N; Sarna, Justyna J; Martino, Davide D; Pfeffer, Gerald G; Gan-Or, Ziv Z; Forkert, Nils D ND; Monchi, Oury O

Publication Date: 2021-03-01

Variant appearance in text: rs7689942

PubMed Link: 33649398

Variant Present in the following documents:

• Main text
• 41598_2021_Article_84316.pdf

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Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies.

Annals Of Neurology

Krohn, Lynne L; Wu, Richard Y J RYJ; Heilbron, Karl K; Ruskey, Jennifer A JA; Laurent, Sandra B SB; Blauwendraat, Cornelis C; Alam, Armaghan A; Arnulf, Isabelle I; Hu, Michele T M MTM; Dauvilliers, Yves Y; Högl, Birgit B; Toft, Mathias M; Bjørnarå, Kari Anne KA; Stefani, Ambra A; Holzknecht, Evi E; Monaca, Christelle Charley CC; Abril, Beatriz B; Plazzi, Giuseppe G; Antelmi, Elena E; Ferini-Strambi, Luigi L; Young, Peter P; Heidbreder, Anna A; Cochen De Cock, Valérie V; Mollenhauer, Brit B; Sixel-Döring, Friederike F; Trenkwalder, Claudia C; Sonka, Karel K; Kemlink, David D; Figorilli, Michela M; Puligheddu, Monica M; Dijkstra, Femke F; Viaene, Mineke M; Oertel, Wolfang W; Toffoli, Marco M; Gigli, Gian Luigi GL; Valente, Mariarosaria M; Gagnon, Jean-François JF; Nalls, Mike A MA; Singleton, Andrew B AB; , ; Desautels, Alex A; Montplaisir, Jacques Y JY; Cannon, Paul P; Ross, Owen A OA; Boeve, Bradley F BF; Dupré, Nicolas N; Fon, Edward A EA; Postuma, Ronald B RB; Pihlstrøm, Lasse L; Rouleau, Guy A GA; Gan-Or, Ziv Z

Publication Date: 2020-04

Variant appearance in text: rs7689942

PubMed Link: 31976583

Variant Present in the following documents:

• Main text

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Common genetic variants associated with Parkinson's disease display widespread signature of epigenetic plasticity.

Scientific Reports

Sharma, Amit A; Osato, Naoki N; Liu, Hongde H; Asthana, Shailendra S; Dakal, Tikam Chand TC; Ambrosini, Giovanna G; Bucher, Philipp P; Schmitt, Ina I; Wüllner, Ullrich U

Publication Date: 2019-12-05

Variant appearance in text: rs7689942

PubMed Link: 31804560

Variant Present in the following documents:

• 41598_2019_Article_54865.pdf

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Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases.

Molecular Neurobiology

Zucchelli, Silvia S; Fedele, Stefania S; Vatta, Paolo P; Calligaris, Raffaella R; Heutink, Peter P; Rizzu, Patrizia P; Itoh, Masayoshi M; Persichetti, Francesca F; Santoro, Claudio C; Kawaji, Hideya H; Lassmann, Timo T; Hayashizaki, Yoshihide Y; Carninci, Piero P; Forrest, Alistair R R ARR; , ; Gustincich, Stefano S

Publication Date: 2019-08

Variant appearance in text: rs7689942

PubMed Link: 30610612

Variant Present in the following documents:

• 12035_2018_Article_1465.pdf

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Genetic Variants in SNCA and the Risk of Sporadic Parkinson's Disease and Clinical Outcomes: A Review.

Parkinson'S Disease

Campêlo, Clarissa Loureiro das Chagas CLDC; Silva, Regina Helena RH

Publication Date: 2017

Variant appearance in text: rs7689942

PubMed Link: 28781905

Variant Present in the following documents:

• Main text
• PD2017-4318416.pdf

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