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Sleep Medicine|September 4, 2025
Prevalence and correlated factors of REM sleep behavior disorder in patients with progressive supranuclear palsyHaitao Lu, Jiafeng Ren, Hua Liu, et al.
Genetic Testing and Molecular Biomarkers|August 16, 2013
Association between two functional fibrinogen-related polymorphisms and ischemic stroke: a case-control studyJingjing Zhang, Lihua Yu, Yanying Yin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 13, 2009
LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland ChinaZijuan Zhang, Jean-Marc Burgunder, Xingkai An, et al.
DNA and Cell Biology|December 10, 2020
Genetic Polymorphisms of Delta-Like 1 Homolog Influence the Susceptibility to Antituberculosis Drug-Induced HepatotoxicityYang Fu, Tangyuheng Liu, Jiajia Song, et al.
Parkinsonism & Related Disorders|June 5, 2012
Penetrance of LRRK2 G2385R and R1628P is modified by common PD-associated genetic variantsChaodong Wang, Yanning Cai, Zheng Zheng, et al.
Neurobiology of Aging|October 8, 2013
Clinical profiles of Parkinson's disease associated with common leucine-rich repeat kinase 2 and glucocerebrosidase genetic variants in Chinese individualsChaodong Wang, Yanning Cai, Zhuqin Gu, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|December 14, 2019
Clinical features of multiple system atrophy with or without rapid eye movement behavior disorder: a cross-sectional study in southwest ChinaHui Wang, Ran An, Yalan Chen, et al.
Life (Basel, Switzerland)|August 29, 2024
Cataloging the Genetic Response: Unveiling Drought-Responsive Gene Expression in Oil Tea Camellia (<i>Camellia oleifera</i> Abel.) through TranscriptomicsZhen Zhang, Yanming Xu, Caixia Liu, et al.
European Journal of Neurology|September 10, 2022
Clinical features and reclassification of essential tremor with NOTCH2NLC GGC repeat expansions based on a long-term follow-upXun Zhou, Hongyan Huang, Runcheng He, et al.
BMC Medical Genomics|August 5, 2022
Identification of TARDBP Gly298Ser as a founder mutation for amyotrophic lateral sclerosis in Southern ChinaFanxi Xu, Sen Huang, Xu-Ying Li, et al.
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