Chen WJ - Search Results

1

Biallelic variants in the COQ7 gene cause distal hereditary motor neuropathy in two Chinese families.

Liu XX, Wang N, Chen YK, Lv WQ, Hong JM, Xu GR, Zhou LY, Chen WJ, Fan DS, He J. Liu XX, et al. Among authors: chen yk, chen wj. Brain. 2023 May 2;146(5):e27-e30. doi: 10.1093/brain/awad040. Brain. 2023. PMID: 36758993 No abstract available.

2

Rapid diagnosis of spinal muscular atrophy using denaturing high-performance liquid chromatography.

Chen WJ, Wu ZY, Wang N, Lin MT, Mu-Rong SX. Chen WJ, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Jun;22(3):291-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15952118

3

Quantitative studies on SMN1 gene and carrier testing of spinal muscular atrophy.

Chen WJ, Wu ZY, Wang N, Lin MT, Mu-rong SX. Chen WJ, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Dec;22(6):559-602. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16331551

4

Mutation analysis of 218 Chinese patients with Wilson disease revealed no correlation between the canine copper toxicosis gene MURR1 and Wilson disease.

Wu ZY, Zhao GX, Chen WJ, Wang N, Wan B, Lin MT, Murong SX, Yu L. Wu ZY, et al. Among authors: chen wj. J Mol Med (Berl). 2006 May;84(5):438-42. doi: 10.1007/s00109-005-0036-y. Epub 2006 Jan 28. J Mol Med (Berl). 2006. PMID: 16649058

5

Molecular analysis and prenatal prediction of spinal muscular atrophy in Chinese patients by the combination of restriction fragment length polymorphism analysis, denaturing high-performance liquid chromatography, and linkage analysis.

Chen WJ, Wu ZY, Lin MT, Su JF, Lin Y, Murong SX, Wang N. Chen WJ, et al. Arch Neurol. 2007 Feb;64(2):225-31. doi: 10.1001/archneur.64.2.225. Arch Neurol. 2007. PMID: 17296838

6

A novel mutation in the senataxin gene identified in a Chinese patient with sporadic amyotrophic lateral sclerosis.

Zhao ZH, Chen WZ, Wu ZY, Wang N, Zhao GX, Chen WJ, Murong SX. Zhao ZH, et al. Among authors: chen wz, chen wj. Amyotroph Lateral Scler. 2009 Apr;10(2):118-22. doi: 10.1080/17482960802572673. Amyotroph Lateral Scler. 2009. PMID: 19058054

7

Rapid diagnosis of spinal muscular atrophy using high-resolution melting analysis.

Chen WJ, Dong WJ, Lin XZ, Lin MT, Murong SX, Wu ZY, Wang N. Chen WJ, et al. BMC Med Genet. 2009 May 29;10:45. doi: 10.1186/1471-2350-10-45. BMC Med Genet. 2009. PMID: 19480685 Free PMC article.

8

Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia.

Chen WJ, Lin Y, Xiong ZQ, Wei W, Ni W, Tan GH, Guo SL, He J, Chen YF, Zhang QJ, Li HF, Lin Y, Murong SX, Xu J, Wang N, Wu ZY. Chen WJ, et al. Among authors: chen yf. Nat Genet. 2011 Nov 20;43(12):1252-5. doi: 10.1038/ng.1008. Nat Genet. 2011. PMID: 22101681

9

Screening for FMR1 expanded alleles in patients with parkinsonism in mainland China.

Zhang X, Zhuang X, Gan S, Wu Z, Chen W, Hu Y, Wang N. Zhang X, et al. Neurosci Lett. 2012 Apr 11;514(1):16-21. doi: 10.1016/j.neulet.2012.02.036. Epub 2012 Feb 22. Neurosci Lett. 2012. PMID: 22387066

10

Modification of phenotype by SMN2 copy numbers in two Chinese families with SMN1 deletion in two continuous generations.

Chen WJ, He J, Zhang QJ, Lin QF, Chen YF, Lin XZ, Lin MT, Murong SX, Wang N. Chen WJ, et al. Among authors: chen yf. Clin Chim Acta. 2012 Nov 20;413(23-24):1855-60. doi: 10.1016/j.cca.2012.07.020. Epub 2012 Aug 4. Clin Chim Acta. 2012. PMID: 22884440

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