日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Does COMT Play a Role in Parkinson's Disease Susceptibility across Diverse Ancestral Populations?

COMT 在不同祖先人群的帕金森病易感性中是否发挥作用?

Martín-Bórnez, Miguel; Shar, Nisar; Nour, Mohamed Ahmed; Murphy, David; Elsayed, Inas; Nanjundaswamy, Megha Shri; Nwaokorie, Francisca; Olusanya, Adedunni; Kuznetsov, Nicole; Bandres-Ciga, Sara; Noyce, Alastair J; Iwaki, Hirotaka; Jones, Lietsel; Gómez-Garre, Pilar; Mir, Pablo; Periñán, María Teresa

Evaluation of a Mitochondrial Polygenic Score for Parkinson's Disease Across Ancestries

跨种族帕金森病线粒体多基因评分的评估

Ooi, Joshua Chin Ern; Tay, Yi Wen; Tan, Ai Huey; Lin, Chin-Hsien; Brolin, Kajsa Atterling; Laabs, Björn-Hergen; Sendel, Sebastian; König, Inke R; Caliebe, Amke; Gabbert, Carolin; Andersh, Katherine M; Jones, Lietsel; Lange, Lara M; Fiske, Brian; Sue, Carolyn; Klein, Christine; Trinh, Joanne; Lüth, Theresa

Does COMT Play a Role in Parkinson's Disease Susceptibility Across Diverse Ancestral Populations?

COMT 是否在不同祖先人群的帕金森病易感性中发挥作用?

Martín-Bórnez, Miguel; Shar, Nisar; Nour, Mohamed Ahmed; Murphy, David; Elsayed, Inas; Megha, Shri N; Nwaokorie, Francisca; Olusanya, Adedunni; Kuznetsov, Nicole; Bandres-Ciga, Sara; Noyce, Alastair J; Iwaki, Hirotaka; Jones, Lietsel; Gómez-Garre, Pilar; Mir, Pablo; Periñan, Maria Teresa

Assessment of common genetic variation in Alzheimer's and Parkinson's diseases reveals global distinction in population attributable risk

对阿尔茨海默病和帕金森病常见遗传变异的评估揭示了人群归因风险的全球差异

Jones, Lietsel; Cerquera-Cleves, Catalina; Schuh, Artur Fs; Makarious, Mary B; Iwaki, Hirotaka; Nalls, Mike A; Noyce, Alastair J; Blauwendraat, Cornelis; Singleton, Andrew; Mata, Ignacio; Cookson, Mark R; Bandres-Ciga, Sara

Validation of a Mitochondrial Polygenic Score for Parkinson's Disease

帕金森病线粒体多基因评分的验证

Ern Ooi, Joshua Chin; Tay, Yi Wen; Tan, Ai Huey; Lin, Chin-Hsien; Brolin, Kajsa Atterling; Laabs, Björn-Hergen; Sendel, Sebastian; König, Inke R; Caliebe, Amke; Gabbert, Carolin; Andersh, Katherine M; Jones, Lietsel; Lange, Lara Mariah; Fiske, Brian; Sue, Carolyn; Klein, Christine; Trinh, Joanne; Lüth, Theresa

The Global Landscape of Genetic Variation in Parkinson's disease: Multi-Ancestry Insights into Established Disease Genes and their Translational Relevance

帕金森病遗传变异的全球图谱:多种族背景对已确立的疾病基因及其转化意义的启示

Lange, Lara M; Fang, Zih-Hua; Makarious, Mary B; Kuznetsov, Nicole; Brolin, Kajsa Atterling; Ballard, Shannon; Bardien, Soraya; Doquenia, Maria Leila; Heutink, Peter; Houlden, Henry; Iwaki, Hirotaka; Jasaityte, Simona; Jones, Lietsel; Junker, Johanna; Kaiyrzhanov, Rauan; Koretsky, Mathew J; Kumar, Kishore R; Leonard, Hampton L; Levine, Kristin S; Lim, Shen-Yang; Mencacci, Niccoló E; Mohamed, Wael M Y; Nalls, Mike A; Noyce, Alastair J; Ojha, Rajeev; Okubadejo, Njideka U; Rehman, Shoaib Ur; Screven, Laurel; Shashkin, Chingiz; Sopromadze, Sophia; Stafford, Eleanor J; Tan, Ai Huey; Tan, Manuela; Tavadyan, Zaruhi; Trinh, Joanne; Tserensodnom, Bayasgalan; Valente, Enza Maria; Vitale, Dan; Zharkinbekova, Nazira; Lohmann, Katja; Bandres-Ciga, Sara; Blauwendraat, Cornelis; Singleton, Andrew; Morris, Huw R; Klein, Christine

Assessing the lack of diversity in genetics research across neurodegenerative diseases: A systematic review of the GWAS Catalog and literature

评估神经退行性疾病遗传学研究中多样性的缺乏:对 GWAS 目录和文献的系统性回顾

Jonson, Caroline; Levine, Kristin S; Lake, Julie; Hertslet, Linnea; Jones, Lietsel; Patel, Dhairya; Kim, Jeff; Bandres-Ciga, Sara; Terry, Nancy; Mata, Ignacio F; Blauwendraat, Cornelis; Singleton, Andrew B; Nalls, Mike A; Yokoyama, Jennifer S; Leonard, Hampton L

Whose Signals Are Being Amplified? Toward a More Equitable Clinical Psychophysiology

谁的信号被放大了?迈向更公平的临床心理生理学

Bradford, Daniel E; DeFalco, Angelica; Perkins, Emily R; Carbajal, Iván; Kwasa, Jasmine; Goodman, Fallon R; Jackson, Felicia; Richardson, Lietsel N S; Woodley, Nina; Neuberger, Lindsay; Sandoval, Jennifer A; Huang, Helen J; Joyner, Keanan J

A new AI-assisted data standard accelerates interoperability in biomedical research

一种新的人工智能辅助数据标准加速了生物医学研究的互操作性

Long, Rodney Alan; Ballard, Shannon; Shah, Syed; Bianchi, Owen; Jones, Lietsel; Koretsky, Mathew J; Kuznetsov, Nicole; Marsan, Elise; Jen, Bryant; Chiang, Philip; Mukherjee, Abhradeep; Blauwendraat, Cornelis; Leonard, Hampton; Vitale, Dan; Levine, Kristin; Bandres-Ciga, Sara; Jarreau, Paige; Brannelly, Patrick; Pantazis, Caroline; Screven, Laurel; Andersh, Kate; Kapasi, Alifiya; Crary, John F; Gutman, David; Dugger, Brittany N; Biber, Sarah; Hohman, Timothy; Faghri, Faraz; Griswold, Michael; Sargent, Lana; van Keuren-Jensen, Kendall; Singleton, Andrew B; Fann, Yang; Nalls, Mike A; Iwaki, Hirotaka

Assessing the lack of diversity in genetics research across neurodegenerative diseases: a systematic review of the GWAS Catalog and literature

评估神经退行性疾病遗传学研究中多样性的缺乏:对 GWAS 目录和文献的系统性回顾

Jonson, Caroline; Levine, Kristin S; Lake, Julie; Hertslet, Linnea; Jones, Lietsel; Patel, Dhairya; Kim, Jeff; Bandres-Ciga, Sara; Terry, Nancy; Mata, Ignacio F; Blauwendraat, Cornelis; Singleton, Andrew B; Nalls, Mike A; Yokoyama, Jennifer S; Leonard, Hampton L