Yang Y - Search Results

1

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.

Yang Y, Hentati A, Deng HX, Dabbagh O, Sasaki T, Hirano M, Hung WY, Ouahchi K, Yan J, Azim AC, Cole N, Gascon G, Yagmour A, Ben-Hamida M, Pericak-Vance M, Hentati F, Siddique T. Yang Y, et al. Nat Genet. 2001 Oct;29(2):160-5. doi: 10.1038/ng1001-160. Nat Genet. 2001. PMID: 11586297

2

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers.

Hentati A, Ouahchi K, Pericak-Vance MA, Nijhawan D, Ahmad A, Yang Y, Rimmler J, Hung W, Schlotter B, Ahmed A, Ben Hamida M, Hentati F, Siddique T. Hentati A, et al. Among authors: yang y. Neurogenetics. 1998 Dec;2(1):55-60. doi: 10.1007/s100480050052. Neurogenetics. 1998. PMID: 9933301

3

Age and founder effect of SOD1 A4V mutation causing ALS.

Saeed M, Yang Y, Deng HX, Hung WY, Siddique N, Dellefave L, Gellera C, Andersen PM, Siddique T. Saeed M, et al. Among authors: yang y. Neurology. 2009 May 12;72(19):1634-9. doi: 10.1212/01.wnl.0000343509.76828.2a. Epub 2009 Jan 28. Neurology. 2009. PMID: 19176896 Free PMC article.

4

Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia.

Yan J, Deng HX, Siddique N, Fecto F, Chen W, Yang Y, Liu E, Donkervoort S, Zheng JG, Shi Y, Ahmeti KB, Brooks B, Engel WK, Siddique T. Yan J, et al. Among authors: yang y. Neurology. 2010 Aug 31;75(9):807-14. doi: 10.1212/WNL.0b013e3181f07e0c. Epub 2010 Jul 28. Neurology. 2010. PMID: 20668259 Free PMC article.

5

Novel mutations in spastin gene and absence of correlation with age at onset of symptoms.

Hentati A, Deng HX, Zhai H, Chen W, Yang Y, Hung WY, Azim AC, Bohlega S, Tandan R, Warner C, Laing NG, Cambi F, Mitsumoto H, Roos RP, Boustany RM, Ben Hamida M, Hentati F, Siddique T. Hentati A, et al. Among authors: yang y. Neurology. 2000 Nov 14;55(9):1388-90. doi: 10.1212/wnl.55.9.1388. Neurology. 2000. PMID: 11087788

6

Assignment of mitotic arrest deficient protein 2 (MAD2L1) to human chromosome band 5q23.3 by in situ hybridization.

Xu L, Deng HX, Yang Y, Xia JH, Hung WY, Siddque T. Xu L, et al. Among authors: yang y. Cytogenet Cell Genet. 1997;78(1):63-4. doi: 10.1159/000134631. Cytogenet Cell Genet. 1997. PMID: 9345911 No abstract available.

7

Assignment of SATB1 to human chromosome band 3p23 by in situ hybridization.

Xu L, Deng HX, Xia JH, Yang Y, Fan CH, Hung WY, Siddque T. Xu L, et al. Among authors: yang y. Cytogenet Cell Genet. 1997;77(3-4):205-6. doi: 10.1159/000134577. Cytogenet Cell Genet. 1997. PMID: 9284917 No abstract available.

8

A novel de novo MFN2 mutation causing CMT2A with upper motor neuron signs.

Ajroud-Driss S, Fecto F, Ajroud K, Yang Y, Donkervoort S, Siddique N, Siddique T. Ajroud-Driss S, et al. Among authors: yang y. Neurogenetics. 2009 Oct;10(4):359-61. doi: 10.1007/s10048-009-0188-y. Epub 2009 Apr 7. Neurogenetics. 2009. PMID: 19350291 No abstract available.

9

An association analysis of the rs1572931 polymorphism of the RAB7L1 gene in Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy in China.

Guo XY, Chen YP, Song W, Zhao B, Cao B, Wei QQ, Ou RW, Yang Y, Yuan LX, Shang HF. Guo XY, et al. Among authors: yang y. Eur J Neurol. 2014 Oct;21(10):1337-43. doi: 10.1111/ene.12490. Epub 2014 Jul 12. Eur J Neurol. 2014. PMID: 25040112

10

Three novel TBX5 mutations in Chinese patients with Holt-Oram syndrome.

Yang J, Hu D, Xia J, Yang Y, Ying B, Hu J, Zhou X. Yang J, et al. Among authors: yang y. Am J Med Genet. 2000 Jun 5;92(4):237-40. doi: 10.1002/(sici)1096-8628(20000605)92:4<237::aid-ajmg2>3.0.co;2-g. Am J Med Genet. 2000. PMID: 10842287

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