Yang Y - Search Results

1

Identification of a Novel Mutation in the Titin Gene in a Chinese Family with Limb-Girdle Muscular Dystrophy 2J.

Zheng W, Chen H, Deng X, Yuan L, Yang Y, Song Z, Yang Z, Wu Y, Deng H. Zheng W, et al. Among authors: yang y, yang z. Mol Neurobiol. 2016 Oct;53(8):5097-102. doi: 10.1007/s12035-015-9439-0. Epub 2015 Sep 21. Mol Neurobiol. 2016. PMID: 26392295

2

Genetic Analysis of FBXO2, FBXO6, FBXO12, and FBXO41 Variants in Han Chinese Patients with Sporadic Parkinson's Disease.

Yuan L, Song Z, Deng X, Yang Z, Yang Y, Guo Y, Lu H, Deng H. Yuan L, et al. Among authors: yang y, yang z. Neurosci Bull. 2017 Oct;33(5):510-514. doi: 10.1007/s12264-017-0122-5. Epub 2017 Mar 24. Neurosci Bull. 2017. PMID: 28341977 Free PMC article.

3

Novel and Recurring Disease-Causing NF1 Variants in Two Chinese Families with Neurofibromatosis Type 1.

Xiao H, Yuan L, Xu H, Yang Z, Huang F, Song Z, Yang Y, Zeng C, Deng H. Xiao H, et al. Among authors: yang y, yang z. J Mol Neurosci. 2018 Aug;65(4):557-563. doi: 10.1007/s12031-018-1128-9. Epub 2018 Jul 25. J Mol Neurosci. 2018. PMID: 30046999

4

Identification of a GNE homozygous mutation in a Han-Chinese family with GNE myopathy.

Wu Y, Yuan L, Guo Y, Lu A, Zheng W, Xu H, Yang Y, Hu P, Gu S, Wang B, Deng H. Wu Y, et al. Among authors: yang y. J Cell Mol Med. 2018 Nov;22(11):5533-5538. doi: 10.1111/jcmm.13827. Epub 2018 Aug 29. J Cell Mol Med. 2018. PMID: 30160005 Free PMC article.

5

Digenic Variants in the TTN and TRAPPC11 Genes Co-segregating With a Limb-Girdle Muscular Dystrophy in a Han Chinese Family.

Chen Q, Zheng W, Xu H, Yang Y, Song Z, Yuan L, Deng H. Chen Q, et al. Among authors: yang y. Front Neurosci. 2021 Mar 4;15:601757. doi: 10.3389/fnins.2021.601757. eCollection 2021. Front Neurosci. 2021. PMID: 33746696 Free PMC article.

6

Genetic analysis of the fused in sarcoma gene in Chinese Han patients with essential tremor.

Zheng W, Deng X, Liang H, Song Z, Gao K, Yang Y, Deng H. Zheng W, et al. Among authors: yang y. Neurobiol Aging. 2013 Aug;34(8):2078.e3-4. doi: 10.1016/j.neurobiolaging.2013.03.001. Epub 2013 Apr 9. Neurobiol Aging. 2013. PMID: 23582660

7

Genetic analysis of the fused in sarcoma gene in Chinese Han patients with Parkinson's disease.

Gao K, Zheng W, Deng X, Xiong W, Song Z, Yang Y, Deng H. Gao K, et al. Among authors: yang y. Parkinsonism Relat Disord. 2014 Jan;20(1):119-21. doi: 10.1016/j.parkreldis.2013.09.010. Epub 2013 Sep 19. Parkinsonism Relat Disord. 2014. PMID: 24080306

8

Identification of a Premature Termination Mutation in the Proline-Rich Transmembrane Protein 2 Gene in a Chinese Family with Febrile Seizures.

Zheng W, Zhang J, Deng X, Xiao J, Yuan L, Yang Y, Guan L, Song Z, Yang Z, Deng H. Zheng W, et al. Among authors: yang y, yang z. Mol Neurobiol. 2016 Mar;53(2):835-841. doi: 10.1007/s12035-014-9047-4. Epub 2014 Dec 15. Mol Neurobiol. 2016. PMID: 25502464

9

Identification of a Novel Mutation in the COL2A1 Gene in a Chinese Family with Spondyloepiphyseal Dysplasia Congenita.

Huang X, Deng X, Xu H, Wu S, Yuan L, Yang Z, Yang Y, Deng H. Huang X, et al. Among authors: yang y, yang z. PLoS One. 2015 Jun 1;10(6):e0127529. doi: 10.1371/journal.pone.0127529. eCollection 2015. PLoS One. 2015. PMID: 26030151 Free PMC article.

10

TCEANC2 rs10788972 and rs12046178 variants in the PARK10 region in Chinese Han patients with sporadic Parkinson's disease.

Guo Y, Tan T, Deng X, Song Z, Yang Z, Yang Y, Deng H. Guo Y, et al. Among authors: yang y, yang z. Neurobiol Aging. 2015 Dec;36(12):3335.e1-3335.e2. doi: 10.1016/j.neurobiolaging.2015.09.002. Epub 2015 Sep 8. Neurobiol Aging. 2015. PMID: 26432391

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