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HỒ SƠ TÀI LIỆU · #18.998
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Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

Năm xuất bản2019
Nguồn học thuậtThe Lancet Neurology
Định danhDOI 10.1016/s1474-4422(19)30320-5
TRÍCH DẪN ĐỀ XUẤTAPA 7

Mike A. Nalls; Cornelis Blauwendraat; Costanza L. Vallerga; Karl Heilbron; Sara Bandrés‐Ciga; Diana Chang; Manuela Tan; Demis A. Kia; Alastair J. Noyce; Angli Xue; José Brás; Emily Young; Rainer von Coelln; Javier Simón-Sánchez; Claudia Schulte; Manu Sharma; Lynne Krohn; Lasse Pihlstrøm; Ari Siitonen; Hirotaka Iwaki; Hampton L. Leonard; Faraz Faghri; J Raphael Gibbs; Dena Hernández; Sonja W. Scholz; Juan A. Botía; María Martínez; Jean‐Christophe Corvol; Suzanne Lesage; Joseph Jankovic; Lisa M. Shulman; Margaret Sutherland; Pentti J. Tienari; Kari Majamaa; Mathias Toft; Ole A. Andreassen; Tushar Bangale; Alexis Brice; Jian Yang; Ziv Gan‐Or; Thomas Gasser; Peter Heutink; Joshua Shulman; Nicholas Wood; David A. Hinds; John Hardy; Huw R Morris; Jacob Gratten; Peter M. Visscher; Robert Graham; Andrew B Singleton; Astrid Adarmes‐Gómez; Miquel Aguilar; Akbota Aitkulova; Vadim Akhmetzhanov; Roy N. Alcalay; Ignacio Álvarez; Victoria Álvarez; Sara Bandrés‐Ciga; Francisco Javier Barrero; Jesús Alberto Bergareche Yarza; Inmaculada Bernal‐Bernal; Kimberley J. Billingsley; Cornelis Blauwendraat; Marta Blazquez; Marta Bonilla‐Toribio; Juan A. Botía; María Teresa Boungiorno; José Brás; Alexis Brice; Kathrin Brockmann; Vivien J. Bubb; Dolores Buiza‐Rueda; Anna Maria Novella Càmara; Fátima Carrillo; Mario Carrión‐Claro; Debora Cerdan; Viorica Chelban; Jordi Clarimón; Carl E Clarke; Yaroslau Compta; Mark Cookson; Jean‐Christophe Corvol; David W. Craig; Fabrice Danjou; Mónica Díez-Fairén; Oriol (2019). Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies. The Lancet Neurology, 18(12), 1091-1102. https://doi.org/10.1016/s1474-4422(19)30320-5

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Thông tin thư mục

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Từ khóa

Genome-wide association study; Disease; LRRK2; Genetic association; Single-nucleotide polymorphism; Mendelian randomization; Genetics; Biology; Meta-analysis; Mendelian inheritance; Heritability; Missing heritability problem; Parkinson's disease; Bioinformatics; Medicine; Genotype; Gene; Genetic variants; Internal medicine