Publications:

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Association between the LRP1B and APOE loci in the development of Parkinson's disease dementia.

Brain : A Journal Of Neurology

Real, Raquel R; Martinez-Carrasco, Alejandro A; Reynolds, Regina H RH; Lawton, Michael A MA; Tan, Manuela M X MMX; Shoai, Maryam M; Corvol, Jean-Christophe JC; Ryten, Mina M; Bresner, Catherine C; Hubbard, Leon L; Brice, Alexis A; Lesage, Suzanne S; Faouzi, Johann J; Elbaz, Alexis A; Artaud, Fanny F; Williams, Nigel N; Hu, Michele T M MTM; Ben-Shlomo, Yoav Y; Grosset, Donald G DG; Hardy, John J; Morris, Huw R HR

Publication Date: 2022-11-09

Variant appearance in text: rs7684318

PubMed Link: 36348503

Variant Present in the following documents:

• Main text
• awac414.pdf

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Alpha-Synuclein Aggregation in Parkinson's Disease.

Frontiers In Medicine

Srinivasan, E E; Chandrasekhar, G G; Chandrasekar, P P; Anbarasu, K K; Vickram, A S AS; Karunakaran, Rohini R; Rajasekaran, R R; Srikumar, P S PS

Publication Date: 2021

Variant appearance in text: rs7684318

PubMed Link: 34733860

Variant Present in the following documents:

• Main text
• fmed-08-736978.pdf

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Differences in MTHFR and LRRK2 variant's association with sporadic Parkinson's disease in Mexican Mestizos correlated to Native American ancestry.

Npj Parkinson'S Disease

Romero-Gutiérrez, Elizabeth E; Vázquez-Cárdenas, Paola P; Moreno-Macías, Hortensia H; Salas-Pacheco, José J; Tusié-Luna, Teresa T; Arias-Carrión, Oscar O

Publication Date: 2021-02-11

Variant appearance in text: rs7684318

PubMed Link: 33574311

Variant Present in the following documents:

• Main text
• 41531_2021_Article_157.pdf

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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: rs7684318

PubMed Link: 31804560

Variant Present in the following documents:

• Main text
• 41598_2019_Article_54865.pdf

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A Comprehensive Analysis of the Association Between SNCA Polymorphisms and the Risk of Parkinson's Disease.

Frontiers In Molecular Neuroscience

Zhang, Yuan Y; Shu, Li L; Sun, Qiying Q; Pan, Hongxu H; Guo, Jifeng J; Tang, Beisha B

Publication Date: 2018

Variant appearance in text: rs7684318

PubMed Link: 30410434

Variant Present in the following documents:

• Main text
• fnmol-11-00391.pdf

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Alpha-synuclein mRNA isoform formation and translation affected by polymorphism in the human SNCA 3'UTR.

Molecular Genetics & Genomic Medicine

Barrie, Elizabeth S ES; Lee, Sung-Ha SH; Frater, John T JT; Kataki, Maria M; Scharre, Douglas W DW; Sadee, Wolfgang W

Publication Date: 2018-05-06

Variant appearance in text: rs7684318

PubMed Link: 29730891

Variant Present in the following documents:

• Main text
• MGG3-6-565.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: rs7684318

PubMed Link: 28781905

Variant Present in the following documents:

• Main text

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Variants in SNCA Gene Are Associated with Parkinson's Disease Risk and Cognitive Symptoms in a Brazilian Sample.

Frontiers In Aging Neuroscience

Campêlo, Clarissa L C CLC; Cagni, Fernanda C FC; de Siqueira Figueredo, Diego D; Oliveira, Luiz G LG; Silva-Neto, Antônio B AB; Macêdo, Priscila T PT; Santos, José R JR; Izídio, Geison S GS; Ribeiro, Alessandra M AM; de Andrade, Tiago G TG; de Oliveira Godeiro, Clécio C; Silva, Regina H RH

Publication Date: 2017

Variant appearance in text: rs7684318

PubMed Link: 28676755

Variant Present in the following documents:

• Main text

View BVdb publication page

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Dissecting the Molecular Mechanisms of Neurodegenerative Diseases through Network Biology.

Frontiers In Aging Neuroscience

Santiago, Jose A JA; Bottero, Virginie V; Potashkin, Judith A JA

Publication Date: 2017

Variant appearance in text: rs7684318

PubMed Link: 28611656

Variant Present in the following documents:

• Main text
• fnagi-09-00166.pdf

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Alpha-synuclein (SNCA) polymorphisms exert protective effects on memory after mild traumatic brain injury.

Neuroscience Letters

Shee, Kevin K; Lucas, Alexandra A; Flashman, Laura A LA; Nho, Kwangsik K; Tsongalis, Gregory J GJ; McDonald, Brenna C BC; Saykin, Andrew J AJ; McAllister, Thomas W TW; Rhodes, C Harker CH

Publication Date: 2016-09-06

Variant appearance in text: rs7684318

PubMed Link: 27478013

Variant Present in the following documents:

• Main text

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Computational Modelling Approaches on Epigenetic Factors in Neurodegenerative and Autoimmune Diseases and Their Mechanistic Analysis.

Journal Of Immunology Research

Khanam Irin, Afroza A; Kodamullil, Alpha Tom AT; Gündel, Michaela M; Hofmann-Apitius, Martin M

Publication Date: 2015

Variant appearance in text: rs7684318

PubMed Link: 26636108

Variant Present in the following documents:

• Main text
• JIR2015-737168.pdf

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UCHL1 S18Y variant is a risk factor for Parkinson's disease in Japan.

Bmc Neurology

Miyake, Yoshihiro Y; Tanaka, Keiko K; Fukushima, Wakaba W; Kiyohara, Chikako C; Sasaki, Satoshi S; Tsuboi, Yoshio Y; Yamada, Tatsuo T; Oeda, Tomoko T; Shimada, Hiroyuki H; Kawamura, Nobutoshi N; Sakae, Nobutaka N; Fukuyama, Hidenao H; Hirota, Yoshio Y; Nagai, Masaki M; ,

Publication Date: 2012-07-28

Variant appearance in text: rs7684318

PubMed Link: 22839974

Variant Present in the following documents:

• Main text
• 1471-2377-12-62.pdf

View BVdb publication page

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