Xia Y - Search Results

1

Role of the ADCY9 gene in cardiac abnormalities of the Rubinstein-Taybi syndrome.

Wu Y, Xia Y, Li P, Qu HQ, Liu Y, Yang Y, Lin J, Zheng M, Tian L, Wu Z, Huang S, Qin X, Zhou X, Chen S, Liu Y, Wang Y, Li X, Zeng H, Hakonarson H, Zhuang J. Wu Y, et al. Among authors: xia y. Orphanet J Rare Dis. 2020 Apr 22;15(1):101. doi: 10.1186/s13023-020-01378-9. Orphanet J Rare Dis. 2020. PMID: 32321550 Free PMC article.

2

Clinical application of chromosomal microarray analysis for the prenatal diagnosis of chromosomal abnormalities and copy number variations in fetuses with congenital heart disease.

Xia Y, Yang Y, Huang S, Wu Y, Li P, Zhuang J. Xia Y, et al. Prenat Diagn. 2018 May;38(6):406-413. doi: 10.1002/pd.5249. Epub 2018 Apr 27. Prenat Diagn. 2018. PMID: 29573438 Clinical Trial.

3

Clinical application of chromosomal microarray analysis for the diagnosis of Williams-Beuren syndrome in Chinese Han patients.

Xia Y, Huang S, Wu Y, Yang Y, Chen S, Li P, Zhuang J. Xia Y, et al. Mol Genet Genomic Med. 2019 Feb;7(2):e00517. doi: 10.1002/mgg3.517. Epub 2018 Dec 18. Mol Genet Genomic Med. 2019. PMID: 30565396 Free PMC article.

4

Ankyrin repeat domain 1: A novel gene for cardiac septal defects.

Yang Y, Xia Y, Wu Y, Huang S, Teng Y, Liu X, Li P, Chen J, Zhuang J. Yang Y, et al. Among authors: xia y. J Gene Med. 2019 Apr;21(4):e3070. doi: 10.1002/jgm.3070. Epub 2019 Feb 19. J Gene Med. 2019. PMID: 30659708

5

A Case of a Derivative Chromosome: der(Y)t(Y;18)Pat with Congenital Abnormalities.

Huang S, Xia Y, Ding H, Wang Y, Wu Y, Chen S, Zhuang J, Li P. Huang S, et al. Among authors: xia y. Fetal Pediatr Pathol. 2021 Jun;40(3):256-261. doi: 10.1080/15513815.2019.1695297. Epub 2019 Dec 5. Fetal Pediatr Pathol. 2021. PMID: 31805817

6

FLNC and MYLK2 Gene Mutations in a Chinese Family with Different Phenotypes of Cardiomyopathy.

Qin X, Li P, Qu HQ, Liu Y, Xia Y, Chen S, Yang Y, Huang S, Wen P, Zhou X, Li X, Wang Y, Tian L, Hakonarson H, Wu Y, Zhuang J. Qin X, et al. Among authors: xia y. Int Heart J. 2021 Jan 30;62(1):127-134. doi: 10.1536/ihj.20-351. Epub 2021 Jan 16. Int Heart J. 2021. PMID: 33455984 Free article.

7

Novel insertion mutation (Arg1822_Glu1823dup) in MYH6 coiled-coil domain causing familial atrial septal defect.

Huang S, Wu Y, Chen S, Yang Y, Wang Y, Wang H, Li P, Zhuang J, Xia Y. Huang S, et al. Among authors: xia y. Eur J Med Genet. 2021 Nov;64(11):104314. doi: 10.1016/j.ejmg.2021.104314. Epub 2021 Sep 1. Eur J Med Genet. 2021. PMID: 34481090

8

Novel Mutation in MYH6 in 2 Unrelated Chinese Han Families With Familial Atrial Septal Defect.

Xia Y, Chen S, Yang Y, Wu Y, Huang S, Wang Y, Ding H, He W, Li P, Zhuang J. Xia Y, et al. Circ Genom Precis Med. 2019 Nov;12(11):e002732. doi: 10.1161/CIRCGEN.119.002732. Epub 2019 Oct 22. Circ Genom Precis Med. 2019. PMID: 31638415 No abstract available.

9

Corrigendum for Xia Y, Yang Y, Huang S, et al (2018) https://doi.org/10.1002/pd.5249.

Xia Y, Yang Y, Huang S, Wu Y, Li P, Zhuang J. Xia Y, et al. Prenat Diagn. 2019 Mar;39(4):328. doi: 10.1002/pd.5432. Epub 2019 Feb 20. Prenat Diagn. 2019. PMID: 30916817 No abstract available.

10

Distinguishing Ventricular Arrhythmias Originating from the Posterior Right Ventricular Outflow Tract, or Near the Right Coronary Cusp or Near the His-Bundle.

Yu M, Liu J, Zhang H, Xia Y, Li X, Fang P. Yu M, et al. Among authors: xia y. Am J Cardiol. 2020 Jul 1;126:37-44. doi: 10.1016/j.amjcard.2020.03.046. Epub 2020 Apr 7. Am J Cardiol. 2020. PMID: 32336534

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