Wang Y - Search Results

1

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: wang h, wang 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

2

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. Among authors: wang y. 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.

3

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: wang 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

4

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: wang 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.

5

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: wang 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.

6

Mosaic duplication of 8q24.1q24.3 detected by chromosomal microarray but not karyotyping in two unrelated fetuses with cardiac defects.

Lin S, Huang S, Ou X, Gu H, Wang Y, Li P, Zhou Y. Lin S, et al. Among authors: wang y. Mol Cytogenet. 2021 May 18;14(1):26. doi: 10.1186/s13039-021-00544-3. Mol Cytogenet. 2021. PMID: 34006293 Free PMC article.

7

Prenatal diagnosis of Treacher Collins syndrome: A case report and literature review.

Wang Y, Wang Y, Yao M, Chen L, Wu S, Liu Y. Wang Y, et al. Int J Gynaecol Obstet. 2023 Dec;163(3):778-781. doi: 10.1002/ijgo.14881. Epub 2023 May 25. Int J Gynaecol Obstet. 2023. PMID: 37231986 Review.

8

Pathogenicity analysis of novel variations in Chinese Han patients with polycystic kidney disease.

Fang Z, Xu S, Wang Y, Sun L, Feng Y, Guo Y, Li H, Jiang W. Fang Z, et al. Among authors: wang y. Gene. 2017 Aug 30;626:433-441. doi: 10.1016/j.gene.2017.05.046. Epub 2017 Jun 1. Gene. 2017. PMID: 28578020

9

Integral Reinforcement-Learning-Based Optimal Containment Control for Partially Unknown Nonlinear Multiagent Systems.

Wu Q, Wu Y, Wang Y. Wu Q, et al. Among authors: wang y. Entropy (Basel). 2023 Jan 23;25(2):221. doi: 10.3390/e25020221. Entropy (Basel). 2023. PMID: 36832588 Free PMC article.

10

Spectrum Sensing Method Based on Information Geometry and Deep Neural Network.

Du K, Wan P, Wang Y, Ai X, Chen H. Du K, et al. Among authors: wang y. Entropy (Basel). 2020 Jan 12;22(1):94. doi: 10.3390/e22010094. Entropy (Basel). 2020. PMID: 33285869 Free PMC article.

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