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: rs2583959

PubMed Link: 34210990

Variant Present in the following documents:

• 41531_2021_196_MOESM1_ESM.pdf

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The cis-Regulatory Element of SNCA Intron 4 Modulates Susceptibility to Parkinson's Disease in Han Chinese.

Frontiers In Genetics

Zhu, Shi-Guo SG; Lu, Hui H; Mao, Miao M; Li, Zhao-Feng ZF; Cui, Lei L; Ovlyakulov, Begench B; Zhang, Xiong X; Zhu, Jian-Hong JH

Publication Date: 2020

Variant appearance in text: rs2583959

PubMed Link: 33193729

Variant Present in the following documents:

• Main text
• fgene-11-590365.pdf

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Genetic Risk Factors for Essential Tremor: A Review.

Tremor And Other Hyperkinetic Movements (New York, N.Y.)

Siokas, Vasileios V; Aloizou, Athina-Maria AM; Tsouris, Zisis Z; Liampas, Ioannis I; Aslanidou, Paraskevi P; Dastamani, Metaxia M; Brotis, Alexandros G AG; Bogdanos, Dimitrios P DP; Hadjigeorgiou, Georgios M GM; Dardiotis, Efthimios E

Publication Date: 2020-06-11

Variant appearance in text: rs2583959

PubMed Link: 32775018

Variant Present in the following documents:

• tohm-10-1-67-s2.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: rs2583959

PubMed Link: 31804560

Variant Present in the following documents:

• 41598_2019_Article_54865.pdf

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Parkinson-Associated SNCA Enhancer Variants Revealed by Open Chromatin in Mouse Dopamine Neurons.

American Journal Of Human Genetics

McClymont, Sarah A SA; Hook, Paul W PW; Soto, Alexandra I AI; Reed, Xylena X; Law, William D WD; Kerans, Samuel J SJ; Waite, Eric L EL; Briceno, Nicole J NJ; Thole, Joey F JF; Heckman, Michael G MG; Diehl, Nancy N NN; Wszolek, Zbigniew K ZK; Moore, Cedric D CD; Zhu, Heng H; Akiyama, Jennifer A JA; Dickel, Diane E DE; Visel, Axel A; Pennacchio, Len A LA; Ross, Owen A OA; Beer, Michael A MA; McCallion, Andrew S AS

Publication Date: 2018-12-06

Variant appearance in text: rs2583959

PubMed Link: 30503521

Variant Present in the following documents:

• Main text

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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: rs2583959

PubMed Link: 28781905

Variant Present in the following documents:

• Main text
• PD2017-4318416.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: rs2583959

PubMed Link: 23507417

Variant Present in the following documents:

• Main text

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Evaluation of the role of SNCA variants in survival without neurological disease.

Plos One

Heckman, Michael G MG; Soto-Ortolaza, Alexandra I AI; Diehl, Nancy N NN; Carrasquillo, Minerva M MM; Uitti, Ryan J RJ; Wszolek, Zbigniew K ZK; Graff-Radford, Neill R NR; Ross, Owen A OA

Publication Date: 2012

Variant appearance in text: rs2583959

PubMed Link: 22912757

Variant Present in the following documents:

• Main text
• pone.0042877.pdf

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Genetic variants of α-synuclein are not associated with essential tremor.

Movement Disorders : Official Journal Of The Movement Disorder Society

Ross, Owen A OA; Conneely, Karen N KN; Wang, Tao T; Vilarino-Guell, Carles C; Soto-Ortolaza, Alexandra I AI; Rajput, Alex A; Wszolek, Zbigniew K ZK; Uitti, Ryan J RJ; Louis, Elan D ED; Clark, Lorraine N LN; Farrer, Matthew J MJ; Testa, Claudia M CM

Publication Date: 2011-12

Variant appearance in text: rs2583959

PubMed Link: 22025277

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: rs2583959

PubMed Link: 21816655

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: rs2583959

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: rs2583959

PubMed Link: 19771175

Variant Present in the following documents:

• Main text
• pone.0007114.pdf

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The alpha-synuclein gene in multiple system atrophy.

Journal Of Neurology, Neurosurgery, And Psychiatry

Ozawa, T T; Healy, D G DG; Abou-Sleiman, P M PM; Ahmadi, K R KR; Quinn, N N; Lees, A J AJ; Shaw, K K; Wullner, U U; Berciano, J J; Moller, J C JC; Kamm, C C; Burk, K K; Josephs, K A KA; Barone, P P; Tolosa, E E; Goldstein, D B DB; Wenning, G G; Geser, F F; Holton, J L JL; Gasser, T T; Revesz, T T; Wood, N W NW; ,

Publication Date: 2006-04

Variant appearance in text: rs2583959

PubMed Link: 16543523

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: rs2583959

PubMed Link: 15637659

Variant Present in the following documents:

• Main text

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