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

Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia

CPT1C功能缺失变异:不支持其在遗传性痉挛性截瘫中起因果作用

Zhu, Rui; Liu, Lang; Estiar, Mehrdad A; Asayesh, Farnaz; Ahmad, Jamil; Teferra, Meron; Yoon, Grace; Tarnopolsky, Mark; Boycott, Kym M; Dupre, Nicolas; Dion, Patrick A; Suchowersky, Oksana; Jordanova, Albena; Lee, Yi-Chung; Stevanin, Giovanni; Zuchner, Stephan; Rouleau, Guy A; Gan-Or, Ziv

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

Investigating the Relationship between Stress and Emotional Intelligence with Academic Progress of Dental Students by Measuring Salivary Cortisol Levels

通过测量唾液皮质醇水平,探究压力和情商与牙科学生学业进步之间的关系

Barakian, Yasamin; Kazemimoeen, Fatemeh; Asayesh, Hamid; Hajisadeghi, Samira; Keykha, Elham

Lack of genetic evidence for a role of SLC25A46 in alpha-synucleinopathies

缺乏遗传学证据表明SLC25A46在α-突触核蛋白病中发挥作用

Yu, Han; Parlar, Sitki Cem; Senkevich, Konstantin; Somerville, Emma N; Zhang, Zhao; Liu, Lang; Teferra, Meron; Ahmad, Jamil; Asayesh, Farnaz; Rouleau, Guy A; Gan-Or, Ziv

Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric Disorders

快速眼动睡眠行为障碍与神经退行性疾病和精神疾病的共同致病通路

Zhang, Zhao; Somerville, Emma N; Fang, Zih-Hua; Liu, Lang; Asayesh, Farnaz; Ahmad, Jamil; Amiri, Saeid; Teferra, Meron; Dodet, Pauline; Arnulf, Isabelle; Hu, Michele T M; Desautels, Alex; Dauvilliers, Yves; Aktan-Süzgün, Merve; Ibrahim, Abubaker; Stefani, Ambra; Högl, Birgit; Gaig, Carles; Montini, Angelica; Maya, Gerard; Iranzo, Alex; Serradell, Monica; Gigli, Gian Luigi; Valente, Mariarosaria; Janes, Francesco; Bernardini, Andrea; Sonka, Karel; Kemlink, David; Dusek, Petr; Sommerauer, Michael; Röttgen, Sinah; Figorilli, Michela; Puligheddu, Monica; Mollenhauer, Brit; Trenkwalder, Claudia; Sixel-Doring, Friederike; Plazzi, Giuseppe; Biscarini, Francesco; Antelmi, Elena; De Cock, Valerie Cochen; Terzaghi, Michele; Fiamingo, Giuseppe; Heidbreder, Anna; Ferini-Strambi, Luigi; Ostrozovicova, Miriam; Skorvanek, Matej; Kulcsarova, Kristina; Buskova, Jitka; Abril, Beatriz; Orso, Beatrice; Mattioli, Pietro; Arnaldi, Dario; Boeve, Bradley F; Ju, Yo-El; Ross, Owen A; Wu, Shih-Ying; Lee, Jonghun; Prilutsky, Daria; Blauwendraat, Cornelis; Leonard, Hampton; Postuma, Ronald B; Rouleau, Guy A; Gan-Or, Ziv

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

In memoriam: Sasan Aliniaeifard (1981 – 2025)

悼念:Sasan Aliniaeifard (1981 – 2025)

Vogel, H J; Javadi Asayesh, Elahe; Sobhani, Mohammadhadi; Malcolm Matamoros, Priscilla; Li, Tao; Marcelis, Leo F M; Woltering, Ernst; Kaiser, Elias

LRRK2 rare-variant per-domain genetic burden in Parkinson's Disease: association confined to the kinase domain

LRRK2罕见变异体在帕金森病中的遗传负担:关联仅限于激酶结构域

Parlar, Sitki Cem; Senkevich, Konstantin; Yu, Eric; Ruskey, Jennifer A; Ahmad, Jamil; 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; Fon, Edward A; Trempe, Jean-François; Gan-Or, Ziv

Genome-wide association study of REM sleep behavior disorder in Parkinson's disease

帕金森病快速眼动睡眠行为障碍的全基因组关联研究

Sosero, Yuri L; Heilbron, Karl; Fontanillas, Pierre; Norcliffe-Kaufmann, Lucy; Yu, Eric; Rudakou, Uladzislau; Ruskey, Jennifer A; Freeman, Kathryn; Asayesh, Farnaz; Brolin, Kajsa A; Swanberg, Maria; Morris, Huw R; Wu, Lesley; Real, Raquel; Pihlstrøm, Lasse; Tan, Manuela; Gasser, Thomas; Brockmann, Kathrin; Liu, Hui; Hu, Michele T M; Grosset, Donald G; Lewis, Simon J G; Kwok, John B; Pastor, Pau; Alvarez, Ignacio; Skorvanek, Matej; Lackova, Alexandra; Ostrozovicova, Miriam; Rizig, Mie; Krohn, Lynne; Gan-Or, Ziv