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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 14, 2015
No evidence of association between polymorphisms in four genes and sporadic amyotrophic lateral sclerosis in Han ChineseRan An, Jing Xi, Xinglong Yang, et al.
Frontiers in Endocrinology|February 28, 2019
Rare Co-occurrence of Ocular Myasthenia Gravis and Thyroid-Associated Orbitopathy (Ophthalmopathy) in an Individual With HypothyroidismRan An, Yan Li, Baiyuan Yang, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 22, 2022
Oculopharyngodistal myopathy with CGG repeat expansions in GIPC1: the first report from southwestern ChinaRan An, Huijiao Chen, Weiyue Gu, et al.
Channels (Austin, Tex.)|July 15, 2016
Sequence CLCN1 and SCN4A in patients with Nondystrophic myotonias in Chinese populations: Genetic and pedigree analysis of 10 families and review of the literatureXinglong Yang, Hua Jia, Ran An, et al.
Frontiers in Neurology|October 3, 2022
Abnormal decrement on high-frequency repetitive nerve stimulation in congenital myasthenic syndrome with GFPT1 mutations and review of literatureRan An, Huijiao Chen, Song Lei, et al.
Genetic Testing and Molecular Biomarkers|September 10, 2016
SNP rs1805874 of the Calbindin1 Gene Is Associated with Parkinson's Disease in Han ChineseXinglong Yang, Quanzhen Zhao, Ran An, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 23, 2015
Association of the COQ2 V393A variant with risk of multiple system atrophy in East Asians: a case-control study and meta-analysis of the literatureQuanZhen Zhao, Xinglong Yang, SiJia Tian, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|August 28, 2015
Association of the functional SNP rs2275294 in ZNF512B with risk of amyotrophic lateral sclerosis and Parkinson's disease in Han ChineseXinglong Yang, Quanzhen Zhao, Ran An, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 24, 2015
Lack of evidence for an association between the V393A variant of COQ2 and amyotrophic lateral sclerosis in a Han Chinese populationXinglong Yang, Jing Xi, Ran An, et al.
Parkinsonism & Related Disorders|June 9, 2016
Mutational scanning of the CHCHD2 gene in Han Chinese patients with Parkinson's disease and meta-analysis of the literatureXinglong Yang, Quanzhen Zhao, Ran An, et al.
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