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

In memoriam: Professor Dan J. Stein (1962-2025) — a global pioneer with an African heart

缅怀:丹·J·斯坦教授(1962-2025)——一位拥有非洲情怀的全球先驱

Nalls, Mike A; Pankratz, Nathan; Lill, Christina M; Do, Chuong B; Hernandez, Dena G; Saad, Mohamad; DeStefano, Anita L; Kara, Eleanna; Bras, Jose; Sharma, Manu; Schulte, Claudia; Keller, Margaux F; Arepalli, Sampath; Letson, Christopher; Edsall, Connor; Stefansson, Hreinn; Liu, Xinmin; Pliner, Hannah; Lee, Joseph H; Cheng, Rong; Ikram, M Arfan; Ioannidis, John P A; Hadjigeorgiou, Georgios M; Bis, Joshua C; Martinez, Maria; Perlmutter, Joel S; Goate, Alison; Marder, Karen; Fiske, Brian; Sutherland, Margaret; Xiromerisiou, Georgia; Myers, Richard H; Clark, Lorraine N; Stefansson, Kari; Hardy, John A; Heutink, Peter; Chen, Honglei; Wood, Nicholas W; Houlden, Henry; Payami, Haydeh; Brice, Alexis; Scott, William K; Gasser, Thomas; Bertram, Lars; Eriksson, Nicholas; Foroud, Tatiana; Singleton, Andrew B; Wegener, Gregers; Lerer, Bernard; Frazer, Alan; Grace, Anthony; Ikeda, Kazutaka; Gobbi, Gabriella; Young, Allan; Zohar, Joseph; Blier, Pierre; Kasper, Siegfried; Krystal, John; Yamawaki, Shigeto; Philips, Anthony; Möller, Hans-Jürgen; Belmaker, Robert H; Atwoli, Lukoye; Nutt, David; Harvey, Brian H; Seedat, Soraya; Berk, Michael; Emsley, Robin

The insertion of an ATTTC repeat in an Alu element hyperactivates a neurodevelopmental enhancer in spinocerebellar ataxia type 37

在脊髓小脑性共济失调37型中,Alu元件中插入ATTTC重复序列会过度激活神经发育增强子。

Loureiro, Joana R; Castro, Ana F; Figueiredo, Ana S; Eufrásio, Ana; Dhingra, Ashutosh; Galhardo, Mafalda; Marcelino, Hugo; Rodrigues, Catarina C; Sampaio, Paula; Azevedo, Maria; Sousa, Mafalda; Dória, Sofia; Rizzu, Patrizia; Heutink, Peter; Bessa, José; Silveira, Isabel

Chr:17q21.31 locus risk haplotype H1 susceptibility to ferroptosis is mediated by endolysosomal pathway

17号染色体q21.31位点风险单倍型H1对铁死亡的易感性是由内溶酶体途径介导的。

Sadikoglou, Eldem; Domingo-Fernández, Daniel; Savytska, Natalia; Fernandes, Noemia; Rizzu, Patrizia; Illarionova, Anastasia; Strauß, Tabea; Schwarz, Sigrid C; Kodamullil, Alpha; Höglinger, Günter U; Dhingra, Ashutosh; Gasser, Thomas; Heutink, Peter

A role for astrocytic miR-129-5p in frontotemporal dementia

星形胶质细胞 miR-129-5p 在额颞叶痴呆中的作用

Kaurani, Lalit; Pradhan, Ranjit; Schröder, Sophie; Burkhardt, Susanne; Schuetz, Anna-Lena; Krüger, Dennis M; Pena, Tonatiuh; Heutink, Peter; Sananbenesi, Farahnaz; Fischer, Andre

DNA methylation as a contributor to dysregulation of STX6 and other frontotemporal Lobar degeneration genetic risk-associated loci

DNA甲基化是STX6和其他额颞叶变性遗传风险相关位点失调的促成因素

Rambarack, Naiomi; Fodder, Katherine; Murthy, Megha; Toomey, Christina; de Silva, Rohan; Heutink, Peter; Humphrey, Jack; Raj, Towfique; Lashley, Tammaryn; Bettencourt, Conceição

Effect of image‐processing and statistical harmonization methods on tau PET cognitive group separability for multisite cross‐sectional and longitudinal studies using (18)F‐Flortaucipir PET

图像处理和统计协调方法对使用 (18)F-Flortaucipir PET 的多中心横断面和纵向研究中 tau PET 认知组可分离性的影响

Rambarack, Naiomi; Fodder, Katherine; Murthy, Megha; Toomey, Christina; de Silva, Rohan; Heutink, Peter; Humphrey, Jack; Raj, Towfique; Lashley, Tammaryn; Bettencourt, Conceição; Marcatti, Michela; Fracassi, Anna; Zhang, Wenru; Kayed, Rakez; Taglialatela, Giulio; Cui, Mei; Huang, Yu‐Yuan; Fan, Yiren; Yu, Jin‐Tai; Noel, Anastasia; Brison, Elodie; Griffin, Laura; Bedell, Barry J; Luo, Weiquan; Laymon, Charles M; Baker, Suzanne L; Aizenstein, Howard J; Tudorascu, Dana L; Minhas, Davneet S

Polygenic scores for disease risk are not associated with clinical outcomes in Parkinson's disease

帕金森病疾病风险的多基因评分与临床结果无关

Tan, Manuela Mx; Iwaki, Hirotaka; Bandres-Ciga, Sara; Sosero, Yuri; Shoai, Maryam; Brockmann, Kathrin; Williams, Nigel M; Alcalay, Roy N; Maple-Grødem, Jodi; Alves, Guido; Tysnes, Ole-Bjørn; Auinger, Peggy; Eberly, Shirley; Heutink, Peter; Simon, David K; Kieburtz, Karl; Hardy, John; Williams-Gray, Caroline H; Grosset, Donald G; Corvol, Jean-Christophe; Gan-Or, Ziv; Toft, Mathias; Pihlstrøm, Lasse

The Global Parkinson's Disease Genetics (GP2) Genome Browser

全球帕金森病遗传学(GP2)基因组浏览器

Fang, Zih-Hua; Grant, Riley H; Vitale, Dan; Hernandez, Carlos F; Hong, Samantha; Leonard, Hampton L; Makarious, Mary B; Lange, Lara M; Solomonson, Matthew; Heutink, Peter; Dilliott, Allison A; Galvelis, Kamalini Ghosh; Nalls, Mike A; Singleton, Andrew B; Blauwendraat, Cornelis

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

Open science in precision medicine for neurodegenerative diseases

神经退行性疾病精准医学领域的开放科学

Leonard, Hampton L; Nalls, Mike A; Day-Williams, Aaron; Esmaeeli, Sahar; Jarreau, Paige; Bandres-Ciga, Sara; Heutink, Peter; Sardi, S Pablo; Singleton, Andrew B