Yang X - Search Results

1

Spectrum Analysis of Albinism Genes in a Large Cohort of Chinese Index Patients.

Wei A, Zhang T, Yuan Y, Qi Z, Bai D, Zhang Y, Zhang Y, Liu T, Huang Q, Yang X, Li W. Wei A, et al. Among authors: yang x. J Invest Dermatol. 2022 Jun;142(6):1752-1755.e3. doi: 10.1016/j.jid.2021.11.014. Epub 2021 Nov 24. J Invest Dermatol. 2022. PMID: 34838614 Free article. No abstract available.

2

Implementation of an optimized strategy for genetic testing of the Chinese patients with oculocutaneous albinism.

Wei A, Yang X, Lian S, Li W. Wei A, et al. Among authors: yang x. J Dermatol Sci. 2011 May;62(2):124-7. doi: 10.1016/j.jdermsci.2011.02.009. Epub 2011 Mar 5. J Dermatol Sci. 2011. PMID: 21458243

3

Genetic analyses of Chinese patients with digenic oculocutaneous albinism.

Wei AH, Yang XM, Lian S, Li W. Wei AH, et al. Chin Med J (Engl). 2013 Jan;126(2):226-30. Chin Med J (Engl). 2013. PMID: 23324268

4

Exome sequencing identifies SLC24A5 as a candidate gene for nonsyndromic oculocutaneous albinism.

Wei AH, Zang DJ, Zhang Z, Liu XZ, He X, Yang L, Wang Y, Zhou ZY, Zhang MR, Dai LL, Yang XM, Li W. Wei AH, et al. Among authors: yang xm, yang l. J Invest Dermatol. 2013 Jul;133(7):1834-40. doi: 10.1038/jid.2013.49. Epub 2013 Jan 30. J Invest Dermatol. 2013. PMID: 23364476 Free article.

5

Prenatal genotyping of four common oculocutaneous albinism genes in 51 Chinese families.

Wei AH, Zang DJ, Zhang Z, Yang XM, Li W. Wei AH, et al. J Genet Genomics. 2015 Jun 20;42(6):279-86. doi: 10.1016/j.jgg.2015.05.001. Epub 2015 May 29. J Genet Genomics. 2015. PMID: 26165494

6

NGS-based 100-gene panel of hypopigmentation identifies mutations in Chinese Hermansky-Pudlak syndrome patients.

Wei A, Yuan Y, Bai D, Ma J, Hao Z, Zhang Y, Yu J, Zhou Z, Yang L, Yang X, Li L, Li W. Wei A, et al. Among authors: yang l, yang x. Pigment Cell Melanoma Res. 2016 Nov;29(6):702-706. doi: 10.1111/pcmr.12534. Epub 2016 Oct 19. Pigment Cell Melanoma Res. 2016. PMID: 27593200

7

Eccrine porocarcinoma of the nose: A case report and literature review.

Liu T, Wei A, Wang T, Zhong Q, Wang Y, Wang Y, Liu Y, Liu H, Yang X. Liu T, et al. Among authors: yang x. Australas J Dermatol. 2019 May;60(2):e162-e164. doi: 10.1111/ajd.12939. Epub 2018 Sep 30. Australas J Dermatol. 2019. PMID: 30270434 Review. No abstract available.

8

Instability of BLOC-2 and BLOC-3 in Chinese patients with Hermansky-Pudlak syndrome.

Wei A, Yuan Y, Qi Z, Liu T, Bai D, Zhang Y, Yu J, Yang L, Yang X, Li W. Wei A, et al. Among authors: yang l, yang x. Pigment Cell Melanoma Res. 2019 May;32(3):373-380. doi: 10.1111/pcmr.12748. Epub 2018 Nov 22. Pigment Cell Melanoma Res. 2019. PMID: 30387913

9

Application of multiplex ligation-dependent probe amplification in the genetic testing of oculocutaneous albinism.

Zhang YZ, Bai DY, Qi Z, Zhao SZ, Yang XM, Li W, Wei AH. Zhang YZ, et al. Chin Med J (Engl). 2019 Aug 20;132(16):2011-2012. doi: 10.1097/CM9.0000000000000356. Chin Med J (Engl). 2019. PMID: 31356463 Free PMC article. No abstract available.

10

Identification of two Chinese oculocutaneous albinism type 6 patients and mutation updates of the SLC24A5 gene.

Zhang Y, Zhang Y, Liu T, Bai D, Yang X, Li W, Wei A. Zhang Y, et al. Among authors: yang x. J Dermatol. 2019 Nov;46(11):1027-1030. doi: 10.1111/1346-8138.15065. Epub 2019 Sep 4. J Dermatol. 2019. PMID: 31486119

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