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

Alpha-synuclein co-pathology in a real-world early Alzheimer's disease cohort

真实世界中早期阿尔茨海默病队列的α-突触核蛋白共病理学

Shiner, Tamara; Nathan, Talya; Levy, Mori Hai; David, Aya Bar; Omer, Nurit; Awad, Anan Abu; Ash, Elissa; Weisz, Mali Gana; Goldstein, Orly; Alcalay, Yifat; Regev, Keren; Lamoureux, Jennifer; Van Keuren-Jensen, Kendall; Blauwendraat, Cornelis; Alcalay, Roy N; Bregman, Noa

Optimizing Parkinson's disease progression scales using computational methods

利用计算方法优化帕金森病进展量表

Benesh, Assaf; Alcalay, Roy N; Mirelman, Anat; Shamir, Ron

Rare but Relevant? Assessing Variants in Dystonia-Linked Genes in Parkinson's Disease

罕见但重要?评估帕金森病中与肌张力障碍相关的基因变异

Lange, Lara M; Fang, Zih-Hua; Screven, Laurel; Tan, Ai Huey; Alcalay, Roy N; Amouri, Rim; Bovenzi, Roberta; Fenn, Matilda; Frost, Joshua L I; Jankovic, Joseph; Jasaityte, Simona; Jaunmuktane, Zane; Jeon, Beomseok; Sarmiento, Ignacio Juan Keller; Krüger, Rejko; Kuhlenbäumer, Gregor; Lin, Chin-Hsien; Pavelka, Lukas; Periñan, Maria Teresa; Sassi, Samia Ben; Schirinzi, Tommaso; Shin, Jung Hwan; Shulman, Joshua M; Tay, Yi Wen; Uitti, Ryan; Warner, Tom; Wszolek, Zbigniew K; Wu, Lesley; Wu, Ruey-Meei; Zeuner, Kirsten E; Blauwendraat, Cornelis; Singleton, Andrew; Mencacci, Niccolò E; Morris, Huw R; Lim, Shen-Yang; Lohmann, Katja; Klein, Christine

Lack of association between G6PD variants and Parkinson disease

G6PD变异与帕金森病之间缺乏关联

Chifamba, Leah V; Parlar, Sitki Cem; Liu, Lang; Sokol, Leonard L; Yu, Eric; Asayesh, Farnaz; Ahmad, Jamil; Ruskey, Jennifer A; Spiegelman, Dan; Waters, Cheryl; Monchi, Oury; Dauvilliers, Yves; Dupré, Nicolas; Timofeeva, Alla; Emelyanov, Anton; Pchelina, Sofya; Miliukhina, Irina; Greenbaum, Lior; Hassin-Baer, Sharon; Alcalay, Roy N; Espay, Alberto J; Gan-Or, Ziv; Senkevich, Konstantin

Change in movement disorder specialist attitudes to genetic testing after implementation of PD GENEration

PD GENEration实施后,运动障碍专家对基因检测的态度发生了改变。

Wang, Jesse; Ibrahim, Vanessa; Agin-Liebes, Julian; Nance, Martha; Caulfield, Margaret E; Naito, Anna; Galvelis, Kamalini Ghosh; Beck, James C; Alcalay, Roy N; Wills, Anne-Marie

Rare-variant burden across lysosomal genes implicates sialylation and ganglioside metabolism in Parkinson's disease

溶酶体基因中罕见变异负荷表明唾液酸化和神经节苷脂代谢与帕金森病有关

Senkevich, Konstantin; Parlar, Sitki Cem; Chantereault, Cloe; Liu, Lang; Yu, Eric; Rudakou, Uladzislau; Ahmad, Jamil; Ruskey, Jennifer A; Asayesh, Farnaz; Spiegelman, Dan; Waters, Cheryl; Monchi, Oury; Dauvilliers, Yves; Dupré, Nicolas; Greenbaum, Lior; Hassin-Baer, Sharon; Miliukhina, Irina; Timofeeva, Alla; Emelyanov, Anton; Pchelina, Sofya; Alcalay, Roy N; Gan-Or, Ziv

The GBA1 p.E427K (p.E388K) Variant is a Risk Factor for Synucleinopathies: A Meta-Analysis

GBA1 p.E427K (p.E388K) 变异是突触核蛋白病的一个风险因素:一项荟萃分析

Chifamba, Leah V; Parlar, Sitki Cem; Somerville, Emma N; Liu, Lang; Yu, Eric; Asayesh, Farnaz; Ahmad, Jamil; Teferra, Meron; Ruskey, Jennifer A; Waters, Cheryl; Monchi, Oury; Dauvilliers, Yves; Dupré, Nicolas; Timofeeva, Alla; Emelyanov, Anton; Pchelina, Sofya; Miliukhina, Irina; Greenbaum, Lior; Hassin-Baer, Sharon; Goldstein, Orly; Radefeldt, Mandy; Bauer, Peter; Beetz, Christian; Dilliott, Allison A; Beck, James C; Senkevich, Konstantin; Klein, Christine; Alcalay, Roy N; Gan-Or, Ziv

Toward a biological definition of neuronal and glial synucleinopathies

神经元和胶质细胞突触核蛋白病的生物学定义

Soto, Claudio; Mollenhauer, Brit; Hansson, Oskar; Kang, Un Jung; Alcalay, Roy N; Standaert, David; Trenkwalder, Claudia; Marek, Kenneth; Galasko, Douglas; Poston, Kathleen

Engineered depalmitoylases enable selective manipulation of protein localization and function.

工程化的脱棕榈酰化酶能够选择性地操控蛋白质的定位和功能

Jayaraman Srinidhi, Kochiss Audrey, Alcalay Thy-Lan, Del Rivero Morfin Pedro J, Ben-Johny Manu

Quantitative modeling of mRNA degradation reveals tempo-dependent mRNA clearance in early embryos

mRNA降解的定量模型揭示了早期胚胎中mRNA清除的节奏依赖性

Tawil, Mazal; Alcalay, Dina; Greenberg, Pnina; Har-Sheffer, Shirel; Fishman, Lior; Rabani, Michal