Publications:

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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: rs356186

PubMed Link: 34210990

Variant Present in the following documents:

• 41531_2021_196_MOESM1_ESM.pdf

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Replication-Based Rearrangements Are a Common Mechanism for SNCA Duplication in Parkinson's Disease.

Movement Disorders : Official Journal Of The Movement Disorder Society

Seo, Soo Hyun SH; Bacolla, Albino A; Yoo, Dallah D; Koo, Yoon Jung YJ; Cho, Sung Im SI; Kim, Man Jin MJ; Seong, Moon-Woo MW; Kim, Han-Joon HJ; Kim, Jong-Min JM; Tainer, John A JA; Park, Sung Sup SS; Kim, Ji Yeon JY; Jeon, Beomseok B

Publication Date: 2020-05

Variant appearance in text: rs356186

PubMed Link: 32039503

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: rs356186

PubMed Link: 31804560

Variant Present in the following documents:

• Main text
• 41598_2019_Article_54865.pdf

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Variants in the SNCA Locus Are Associated With the Progression of Parkinson's Disease.

Frontiers In Aging Neuroscience

Luo, Ningdi N; Li, Yuanyuan Y; Niu, Mengyue M; Zhou, Liche L; Yao, Mengsha M; Zhu, Lin L; Ye, Guanyu G; Kang, Wenyan W; Liu, Jun J

Publication Date: 2019

Variant appearance in text: rs356186

PubMed Link: 31244647

Variant Present in the following documents:

• Main text
• fnagi-11-00110.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: rs356186

PubMed Link: 30410434

Variant Present in the following documents:

• Main text
• fnmol-11-00391.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: rs356186

PubMed Link: 28781905

Variant Present in the following documents:

• Main text
• PD2017-4318416.pdf

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Human genetic variation and Parkinson's disease.

Journal Of Movement Disorders

Chung, Sun Ju SJ

Publication Date: 2010-05

Variant appearance in text: rs356186

PubMed Link: 24868370

Variant Present in the following documents:

• Main text
• jmd-3-1-1-1.pdf

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Genetic susceptibility loci, environmental exposures, and Parkinson's disease: a case-control study of gene-environment interactions.

Parkinsonism & Related Disorders

Chung, Sun Ju SJ; Armasu, Sebastian M SM; Anderson, Kari J KJ; Biernacka, Joanna M JM; Lesnick, Timothy G TG; Rider, David N DN; Cunningham, Julie M JM; Ahlskog, J Eric JE; Frigerio, Roberta R; Maraganore, Demetrius M DM

Publication Date: 2013-06

Variant appearance in text: rs356186

PubMed Link: 23507417

Variant Present in the following documents:

• Main text

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Evidence for a genetic component for substance dependence in Native Americans.

The American Journal Of Psychiatry

Ehlers, Cindy L CL; Gizer, Ian R IR

Publication Date: 2013-02

Variant appearance in text: rs356186

PubMed Link: 23377636

Variant Present in the following documents:

• Main text

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SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population.

Parkinsonism & Related Disorders

Trotta, Luca L; Guella, Ilaria I; Soldà, Giulia G; Sironi, Francesca F; Tesei, Silvana S; Canesi, Margherita M; Pezzoli, Gianni G; Goldwurm, Stefano S; Duga, Stefano S; Asselta, Rosanna R

Publication Date: 2012-03

Variant appearance in text: rs356186

PubMed Link: 22104010

Variant Present in the following documents:

• Main text

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Do interactions between SNCA, MAPT, and LRRK2 genes contribute to Parkinson's disease susceptibility?

Parkinsonism & Related Disorders

Biernacka, Joanna M JM; Armasu, Sebastian M SM; Cunningham, Julie M JM; Ahlskog, J Eric JE; Chung, Sun Ju SJ; Maraganore, Demetrius M DM

Publication Date: 2011-12

Variant appearance in text: rs356186

PubMed Link: 21816655

Variant Present in the following documents:

• Main text

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Common variants in PARK loci and related genes and Parkinson's disease.

Movement Disorders : Official Journal Of The Movement Disorder Society

Chung, Sun Ju SJ; Armasu, Sebastian M SM; Biernacka, Joanna M JM; Lesnick, Timothy G TG; Rider, David N DN; Lincoln, Sarah J SJ; Ortolaza, Alexandra I AI; Farrer, Matthew J MJ; Cunningham, Julie M JM; Rocca, Walter A WA; Maraganore, Demetrius M DM

Publication Date: 2011-02-01

Variant appearance in text: rs356186

PubMed Link: 21412835

Variant Present in the following documents:

• Main text

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Association of alpha-, beta-, and gamma-Synuclein with diffuse lewy body disease.

Archives Of Neurology

Nishioka, Kenya K; Wider, Christian C; Vilariño-Güell, Carles C; Soto-Ortolaza, Alexandra I AI; Lincoln, Sarah J SJ; Kachergus, Jennifer M JM; Jasinska-Myga, Barbara B; Ross, Owen A OA; Rajput, Alex A; Robinson, Christopher A CA; Ferman, Tanis J TJ; Wszolek, Zbigniew K ZK; Dickson, Dennis W DW; Farrer, Matthew J MJ

Publication Date: 2010-08

Variant appearance in text: rs356186

PubMed Link: 20697047

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: rs356186

PubMed Link: 19771175

Variant Present in the following documents:

• Main text
• pone.0007114.pdf

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Familial genes in sporadic disease: common variants of alpha-synuclein gene associate with Parkinson's disease.

Mechanisms Of Ageing And Development

Ross, Owen A OA; Gosal, David D; Stone, Jeremy T JT; Lincoln, Sarah J SJ; Heckman, Michael G MG; Irvine, G Brent GB; Johnston, Janet A JA; Gibson, J Mark JM; Farrer, Matthew J MJ; Lynch, Timothy T

Publication Date: 2007

Variant appearance in text: rs356186

PubMed Link: 17531291

Variant Present in the following documents:

• Main text

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Linkage disequilibrium patterns and tagSNP transferability among European populations.

American Journal Of Human Genetics

Mueller, Jakob C JC; Lõhmussaar, Elin E; Mägi, Reedik R; Remm, Maido M; Bettecken, Thomas T; Lichtner, Peter P; Biskup, Saskia S; Illig, Thomas T; Pfeufer, Arne A; Luedemann, Jan J; Schreiber, Stefan S; Pramstaller, Peter P; Pichler, Irene I; Romeo, Giovanni G; Gaddi, Anthony A; Testa, Alessandra A; Wichmann, Heinz-Erich HE; Metspalu, Andres A; Meitinger, Thomas T

Publication Date: 2005-03

Variant appearance in text: rs356186

PubMed Link: 15637659

Variant Present in the following documents:

• Main text

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