Works matching DE "GENOME-wide association studies"


Results: 5000
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    Rare SV2C coding variants in Parkinson's disease risk.

    Published in:
    Journal of Parkinson's Disease, 2025, v. 15, n. 1, p. 66, doi. 10.1177/1877718X241300298
    By:
    • Chang, Chu Hua;
    • Chew, Elaine Guo Yan;
    • Lian, Michelle Mulan;
    • Tandiono, Moses;
    • Li, Zheng;
    • Chung, Sun Ju;
    • Tan, Louis CS;
    • Au, Wing-Lok;
    • Prakash, Kumar M;
    • Ahmad-Annuar, Azlina;
    • Tan, Ai Huey;
    • Mok, Vincent;
    • Chan, Anne YY;
    • Lin, Juei-Jueng;
    • Jeon, Beom S;
    • Khor, Chiea Chuen;
    • Lim, Shen-Yang;
    • Tan, Eng-King;
    • Foo, Jia Nee
    Publication type:
    Article
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    Cohort profile: the CORDELIA study (Collaborative cOhorts Reassembled Data to study mEchanisms and Longterm Incidence of chronic diseAses).

    Published in:
    European Journal of Epidemiology, 2025, v. 40, n. 5, p. 581, doi. 10.1007/s10654-025-01229-6
    By:
    • Hernáez, Álvaro;
    • Camps-Vilaró, Anna;
    • Polo-Alonso, Sara;
    • Subirana, Isaac;
    • Ramos, Rafel;
    • de Cid, Rafael;
    • Rodríguez-Artalejo, Fernando;
    • Elosua, Roberto;
    • Chirlaque, M. Dolores;
    • Amiano, Pilar;
    • Bermúdez-López, Marcelino;
    • Guevara, Marcela;
    • Cinza-Sanjurjo, Sergio;
    • Sánchez, María-José;
    • de León, Antonio Cabrera;
    • Laclaustra, Martín;
    • Rojo-Martínez, Gemma;
    • Guembe-Suescun, María J.;
    • Pérez-Gómez, Beatriz;
    • Vega-Alonso, Tomás
    Publication type:
    Article
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