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
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
Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus.
Molecular Psychiatry
Desikan, R S RS; Schork, A J AJ; Wang, Y Y; Witoelar, A A; Sharma, M M; McEvoy, L K LK; Holland, D D; Brewer, J B JB; Chen, C-H CH; Thompson, W K WK; Harold, D D; Williams, J J; Owen, M J MJ; O'Donovan, M C MC; Pericak-Vance, M A MA; Mayeux, R R; Haines, J L JL; Farrer, L A LA; Schellenberg, G D GD; Heutink, P P; Singleton, A B AB; Brice, A A; Wood, N W NW; Hardy, J J; Martinez, M M; Choi, S H SH; DeStefano, A A; Ikram, M A MA; Bis, J C JC; Smith, A A; Fitzpatrick, A L AL; Launer, L L; van Duijn, C C; Seshadri, S S; Ulstein, I D ID; Aarsland, D D; Fladby, T T; Djurovic, S S; Hyman, B T BT; Snaedal, J J; Stefansson, H H; Stefansson, K K; Gasser, T T; Andreassen, O A OA; Dale, A M AM; ,
The genetic contributions of SNCA and LRRK2 genes to Lewy Body pathology in Alzheimer's disease.
Human Molecular Genetics
Linnertz, Colton C; Lutz, Michael W MW; Ervin, John F JF; Allen, Jawara J; Miller, Natalie R NR; Welsh-Bohmer, Kathleen A KA; Roses, Allen D AD; Chiba-Falek, Ornit O
An exploratory analysis on gene-environment interactions for Parkinson disease.
Neurobiology Of Aging
Gao, Jianjun J; Nalls, Michael A MA; Shi, Min M; Joubert, Bonnie R BR; Hernandez, Dena G DG; Huang, Xuemei X; Hollenbeck, Albert A; Singleton, Andrew B AB; Chen, Honglei H
No association between Parkinson disease alleles and the risk of melanoma.
Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Meng, Shasha S; Song, Fengju F; Chen, Honglei H; Gao, Xiang X; Amos, Christopher I CI; Lee, Jeffrey E JE; Wei, Qingyi Q; Qureshi, Abrar A AA; Han, Jiali J
Genome-wide association study confirms extant PD risk loci among the Dutch.
European Journal Of Human Genetics : Ejhg
Simón-Sánchez, Javier J; van Hilten, Jacobus J JJ; van de Warrenburg, Bart B; Post, Bart B; Berendse, Henk W HW; Arepalli, Sampath S; Hernandez, Dena G DG; de Bie, Rob M A RM; Velseboer, Daan D; Scheffer, Hans H; Bloem, Bas B; van Dijk, Karin D KD; Rivadeneira, Fernando F; Hofman, Albert A; Uitterlinden, André G AG; Rizzu, Patrizia P; Bochdanovits, Zoltan Z; Singleton, Andrew B AB; Heutink, Peter P
SNCA variant associated with Parkinson disease and plasma alpha-synuclein level.
Archives Of Neurology
Mata, Ignacio F IF; Shi, Min M; Agarwal, Pinky P; Chung, Kathryn A KA; Edwards, Karen L KL; Factor, Stewart A SA; Galasko, Douglas R DR; Ginghina, Carmen C; Griffith, Alida A; Higgins, Donald S DS; Kay, Denise M DM; Kim, Hojoong H; Leverenz, James B JB; Quinn, Joseph F JF; Roberts, John W JW; Samii, Ali A; Snapinn, Katherine W KW; Tsuang, Debby W DW; Yearout, Dora D; Zhang, Jing J; Payami, Haydeh H; Zabetian, Cyrus P CP
The effect of SNCA 3' region on the levels of SNCA-112 splicing variant.
Neurogenetics
McCarthy, Jeanette J JJ; Linnertz, Colton C; Saucier, Laura L; Burke, James R JR; Hulette, Christine M CM; Welsh-Bohmer, Kathleen A KA; Chiba-Falek, Ornit O
Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
Annals Of Human Genetics
Edwards, Todd L TL; Scott, William K WK; Almonte, Cherylyn C; Burt, Amber A; Powell, Eric H EH; Beecham, Gary W GW; Wang, Liyong L; Züchner, Stephan S; Konidari, Ioanna I; Wang, Gaofeng G; Singer, Carlos C; Nahab, Fatta F; Scott, Burton B; Stajich, Jeffrey M JM; Pericak-Vance, Margaret M; Haines, Jonathan J; Vance, Jeffery M JM; Martin, Eden R ER
Genome-wide association study reveals genetic risk underlying Parkinson's disease.
Nature Genetics
Simón-Sánchez, Javier J; Schulte, Claudia C; Bras, Jose M JM; Sharma, Manu M; Gibbs, J Raphael JR; Berg, Daniela D; Paisan-Ruiz, Coro C; Lichtner, Peter P; Scholz, Sonja W SW; Hernandez, Dena G DG; Krüger, Rejko R; Federoff, Monica M; Klein, Christine C; Goate, Alison A; Perlmutter, Joel J; Bonin, Michael M; Nalls, Michael A MA; Illig, Thomas T; Gieger, Christian C; Houlden, Henry H; Steffens, Michael M; Okun, Michael S MS; Racette, Brad A BA; Cookson, Mark R MR; Foote, Kelly D KD; Fernandez, Hubert H HH; Traynor, Bryan J BJ; Schreiber, Stefan S; Arepalli, Sampath S; Zonozi, Ryan R; Gwinn, Katrina K; van der Brug, Marcel M; Lopez, Grisel G; Chanock, Stephen J SJ; Schatzkin, Arthur A; Park, Yikyung Y; Hollenbeck, Albert A; Gao, Jianjun J; Huang, Xuemei X; Wood, Nick W NW; Lorenz, Delia D; Deuschl, Günther G; Chen, Honglei H; Riess, Olaf O; Hardy, John A JA; Singleton, Andrew B AB; Gasser, Thomas T
SNCA variants are associated with increased risk for multiple system atrophy.
Annals Of Neurology
Scholz, Sonja W SW; Houlden, Henry H; Schulte, Claudia C; Sharma, Manu M; Li, Abi A; Berg, Daniela D; Melchers, Anna A; Paudel, Reema R; Gibbs, J Raphael JR; Simon-Sanchez, Javier J; Paisan-Ruiz, Coro C; Bras, Jose J; Ding, Jinhui J; Chen, Honglei H; Traynor, Bryan J BJ; Arepalli, Sampath S; Zonozi, Ryan R RR; Revesz, Tamas T; Holton, Janice J; Wood, Nick N; Lees, Andrew A; Oertel, Wolfgang W; Wüllner, Ullrich U; Goldwurm, Stefano S; Pellecchia, Maria Teresa MT; Illig, Thomas T; Riess, Olaf O; Fernandez, Hubert H HH; Rodriguez, Ramon L RL; Okun, Michael S MS; Poewe, Werner W; Wenning, Gregor K GK; Hardy, John A JA; Singleton, Andrew B AB; Del Sorbo, Francesca F; Schneider, Susanne S; Bhatia, Kailash P KP; Gasser, Thomas T