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

Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global Scale

团队科学方法在全球范围内揭示单基因帕金森病的奥秘

Junker, Johanna; Lange, Lara M; Vollstedt, Eva-Juliane; Roopnarain, Karisha; Doquenia, Maria Leila M; Annuar, Azlina Ahmad; Avenali, Micol; Bardien, Soraya; Bahr, Natascha; Ellis, Melina; Galandra, Caterina; Gasser, Thomas; Heutink, Peter; Illarionova, Anastasia; Kanana, Yuliia; Keller Sarmiento, Ignacio J; Kumar, Kishore R; Lim, Shen-Yang; Madoev, Harutyun; Mata, Ignacio F; Mencacci, Niccolò E; Nalls, Mike A; Padmanabhan, Shalini; Shambetova, Cholpon; Solle, J C; Tan, Ai-Huey; Trinh, Joanne; Valente, Enza Maria; Singleton, Andrew; Blauwendraat, Cornelis; Lohmann, Katja; Fang, Zih-Hua; Klein, Christine

Understanding monogenic Parkinson's disease at a global scale

从全球层面了解单基因帕金森病

Junker, Johanna; Lange, Lara M; Vollstedt, Eva-Juliane; Roopnarain, Karisha; Doquenia, Maria Leila M; Annuar, Azlina Ahmad; Avenali, Micol; Bardien, Soraya; Bahr, Natascha; Ellis, Melina; Galandra, Caterina; Gasser, Thomas; Heutink, Peter; Illarionova, Anastasia; Kanana, Yuliia; Keller Sarmiento, Ignacio J; Kumar, Kishore R; Lim, Shen-Yang; Madoev, Harutyun; Mata, Ignacio F; Mencacci, Niccolò E; Nalls, Mike A; Padmanabhan, Shalini; Shambetova, Cholpon; Solle, J; Tan, Ai-Huey; Trinh, Joanne; Valente, Enza Maria; Singleton, Andrew; Blauwendraat, Cornelis; Lohmann, Katja; Fang, Zih-Hua; Klein, Christine

Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)

作者更正:阐明全球帕金森病遗传学计划 (GP2) 中遗传性帕金森病的致病基因变异

Lange, Lara M; Avenali, Micol; Ellis, Melina; Illarionova, Anastasia; Keller Sarmiento, Ignacio J; Tan, Ai-Huey; Madoev, Harutyun; Galandra, Caterina; Junker, Johanna; Roopnarain, Karisha; Solle, Justin; Wegel, Claire; Fang, Zih-Hua; Heutink, Peter; Kumar, Kishore R; Lim, Shen-Yang; Valente, Enza Maria; Nalls, Mike; Blauwendraat, Cornelis; Singleton, Andrew; Mencacci, Niccolo; Lohmann, Katja; Klein, Christine

Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)

全球帕金森病遗传学计划 (GP2) 中遗传性帕金森病致病基因变异的阐明

Lange, Lara M; Avenali, Micol; Ellis, Melina; Illarionova, Anastasia; Keller Sarmiento, Ignacio J; Tan, Ai-Huey; Madoev, Harutyun; Galandra, Caterina; Junker, Johanna; Roopnarain, Karisha; Solle, Justin; Wegel, Claire; Fang, Zih-Hua; Heutink, Peter; Kumar, Kishore R; Lim, Shen-Yang; Valente, Enza Maria; Nalls, Mike; Blauwendraat, Cornelis; Singleton, Andrew; Mencacci, Niccolo; Lohmann, Katja; Klein, Christine

Genetic Testing for GBA and LRRK2 Mutations: Is it Time for Routine Use?

GBA 和 LRRK2 基因突变检测:是时候常规应用了吗?

Roopnarain, Karisha; Klein, Christine

Neural network execution using nicked DNA and microfluidics

利用切口DNA和微流控技术实现神经网络

Solanki, Arnav; Griffin, Zak; Sutradhar, Purab Ranjan; Pradhan, Karisha; Merritt, Caiden; Ganguly, Amlan; Riedel, Marc

Prevalence of COVID-19 vaccine reactogenicity among Bangladeshi physicians

孟加拉国医生中新冠疫苗反应原性的患病率

Majumder, Md Anwarul Azim; Lutfor, Afzalunnessa Binte; Rabbi, Ahbab Mohammad Fazle; Alam, A B M Muksudul; Rahman, Mizanur; Saha, Narayan; Campbell, Michael H; Haque, Mainul; Nessa, Kamrun; Khondoker, Mohib Ullah; Das, Tapas Ranjan; Rahman, Sayeeda; Jahan, Fauzia; Mashreky, Saidur Rahman; Wahab, Abrar; Siddiqui, Md Tosaddeque Hossain; Hinkson-Lacorbiniere, Karisha; Ivy, Roksana; Islam, Rezaul; Haider, Yusuf; Omar, Eliza; Ahmed, S M Moslehuddin; Reza, A M Selim; Daud, A K M; Choudhury, Muiz Uddin Ahmed; Hossain, Md Abed; Pappu, Abdul Matin; Jahan, Nusrat; Razzaque, Mohammed S