Jiang Q - Search Results

1

Genetic Modifiers of Age at Onset for Amyotrophic Lateral Sclerosis: A Genome-Wide Association Study.

Li C, Lin J, Jiang Q, Yang T, Xiao Y, Huang J, Hou Y, Wei Q, Cui Y, Wang S, Zheng X, Ou R, Liu K, Chen X, Song W, Zhao B, Shang H. Li C, et al. Among authors: jiang q. Ann Neurol. 2023 Nov;94(5):933-941. doi: 10.1002/ana.26752. Epub 2023 Aug 14. Ann Neurol. 2023. PMID: 37528491

2

Mutation Screening of TFG in α-Synucleinopathy and Amyotrophic Lateral Sclerosis.

Li C, Lin J, Gu X, Hou Y, Liu K, Jiang Q, Ou R, Wei Q, Chen X, Song W, Zhao B, Wu Y, Chen Y, Shang H. Li C, et al. Among authors: jiang q. Mov Disord. 2022 Aug;37(8):1756-1761. doi: 10.1002/mds.29079. Epub 2022 May 31. Mov Disord. 2022. PMID: 35642252

3

Health-Related Quality of Life in Cervical Dystonia Using EQ-5D-5L: A Large Cross-Sectional Study in China.

Liang Y, Lin J, Hou Y, Zhang L, Ou R, Li C, Wei Q, Cao B, Liu K, Jiang Z, Yang T, Yang J, Zhang M, Kang S, Xiao Y, Jiang Q, Yang J, Song W, Chen X, Zhao B, Wu Y, Shang H. Liang Y, et al. Among authors: jiang q, jiang z. Front Neurol. 2022 Jun 23;13:895272. doi: 10.3389/fneur.2022.895272. eCollection 2022. Front Neurol. 2022. PMID: 35812100 Free PMC article.

4

Rare variant screening and burden analysis of PLXNA1 in Parkinson's disease.

Li C, Lin J, Jiang Q, Shang H. Li C, et al. Among authors: jiang q. Eur J Neurol. 2022 Dec;29(12):3737-3741. doi: 10.1111/ene.15512. Epub 2022 Jul 29. Eur J Neurol. 2022. PMID: 35852441

5

Gray Matter Abnormalities in Myotonic Dystrophy Type 1: A Voxel-Wise Meta-Analysis.

Jiang Q, Lin J, Li C, Hou Y, Shang H. Jiang Q, et al. Front Neurol. 2022 Jul 7;13:891789. doi: 10.3389/fneur.2022.891789. eCollection 2022. Front Neurol. 2022. PMID: 35873771 Free PMC article.

6

Physical activity and risk of multiple sclerosis: A Mendelian randomization study.

Li C, Lin J, Yang T, Xiao Y, Jiang Q, Shang H. Li C, et al. Among authors: jiang q. Front Immunol. 2022 Sep 21;13:872126. doi: 10.3389/fimmu.2022.872126. eCollection 2022. Front Immunol. 2022. PMID: 36211369 Free PMC article.

7

Genetic analysis of and clinical characteristics associated with ANXA11 variants in a Chinese cohort with amyotrophic lateral sclerosis.

Jiang Q, Lin J, Wei Q, Li C, Hou Y, Cao B, Zhang L, Ou R, Liu K, Yang T, Xiao Y, Shang H. Jiang Q, et al. Neurobiol Dis. 2022 Dec;175:105907. doi: 10.1016/j.nbd.2022.105907. Epub 2022 Oct 21. Neurobiol Dis. 2022. PMID: 36280108 Free article. Review.

8

Stability of motor-nonmotor subtype in early-stage Parkinson's disease.

Xiao Y, Wei Q, Ou R, Hou Y, Zhang L, Liu K, Lin J, Yang T, Jiang Q, Shang H. Xiao Y, et al. Among authors: jiang q. Front Aging Neurosci. 2022 Nov 10;14:1040405. doi: 10.3389/fnagi.2022.1040405. eCollection 2022. Front Aging Neurosci. 2022. PMID: 36437989 Free PMC article.

9

Genetic and clinical characteristics of ALS patients with NEK1 gene variants.

Jiang Q, Lin J, Wei Q, Li C, Hou Y, Zhang L, Ou R, Liu K, Yang T, Xiao Y, Hadano S, Shang H. Jiang Q, et al. Neurobiol Aging. 2023 Mar;123:191-199. doi: 10.1016/j.neurobiolaging.2022.11.001. Epub 2022 Nov 6. Neurobiol Aging. 2023. PMID: 36443167 Free article.

10

Lack of association of TP73 rare variants with amyotrophic lateral sclerosis in a Chinese cohort.

Li C, Hou Y, Wei Q, Lin J, Jiang Q, Yang T, Xiao Y, Huang J, Cheng Y, Ou R, Liu K, Chen X, Song W, Zhao B, Wu Y, Cao B, Chen Y, Shang H. Li C, et al. Among authors: jiang q. Hum Genomics. 2022 Nov 30;16(1):63. doi: 10.1186/s40246-022-00437-5. Hum Genomics. 2022. PMID: 36451215 Free PMC article.

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