Sun H - Search Results

1

Genetics and Clinical Features of Noncompaction Cardiomyopathy in the Fetal Population.

Sun H, Hao X, Wang X, Zhou X, Zhang Y, Liu X, Han J, Gu X, Sun L, Zhao Y, Yi T, Zhang H, He Y. Sun H, et al. Among authors: sun l. Front Cardiovasc Med. 2021 Jan 20;7:617561. doi: 10.3389/fcvm.2020.617561. eCollection 2020. Front Cardiovasc Med. 2021. PMID: 33553264 Free PMC article.

2

Increased frequency of FBN1 frameshift and nonsense mutations in Marfan syndrome patients with aortic dissection.

Xu S, Li L, Fu Y, Wang X, Sun H, Wang J, Han L, Wu Z, Liu Y, Zhu J, Sun L, Lan F, He Y, Zhang H. Xu S, et al. Among authors: sun l, sun h. Mol Genet Genomic Med. 2020 Jan;8(1):e1041. doi: 10.1002/mgg3.1041. Epub 2019 Dec 12. Mol Genet Genomic Med. 2020. PMID: 31830381 Free PMC article.

3

Characteristics of Cardiac Phenotype in Prenatal Familial Cases With NONO Mutations.

Sun H, Zhou X, Hao X, Zhang Y, Zhang H, He Y. Sun H, et al. Circ Genom Precis Med. 2020 Jun;13(3):e002847. doi: 10.1161/CIRCGEN.119.002847. Epub 2020 May 12. Circ Genom Precis Med. 2020. PMID: 32397791 Clinical Trial. No abstract available.

4

Unique dual indexing PCR reduces chimeric contamination and improves mutation detection in cell-free DNA of pregnant women.

Du M, He Y, Chen J, Sun H, Fu Y, Wang J. Du M, et al. Among authors: sun h. Talanta. 2020 Sep 1;217:121035. doi: 10.1016/j.talanta.2020.121035. Epub 2020 Apr 14. Talanta. 2020. PMID: 32498851

5

Expanding the phenotype of STRA6-related disorder to include left ventricular non-compaction.

Sun H, Yu S, Zhou X, Han L, Zhang H, He Y. Sun H, et al. Mol Genet Genomic Med. 2020 Sep;8(9):e1377. doi: 10.1002/mgg3.1377. Epub 2020 Jun 29. Mol Genet Genomic Med. 2020. PMID: 32597569 Free PMC article.

6

Generation of a NONO homozygous knockout human induced pluripotent stem cell line by CRISPR/Cas9 editing.

Yi T, Bai R, Sun H, Lan F, Zhang H, He Y. Yi T, et al. Among authors: sun h. Stem Cell Res. 2020 Jul 8;47:101893. doi: 10.1016/j.scr.2020.101893. Online ahead of print. Stem Cell Res. 2020. PMID: 32717574 Free article.

7

Marfan syndrome: whole-exome sequencing reveals de novo mutations, second gene and genotype-phenotype correlations in the Chinese population.

Wu Y, Sun H, Wang J, Wang X, Gong M, Han L, He Y, Zhang H. Wu Y, et al. Among authors: sun h. Biosci Rep. 2020 Dec 23;40(12):BSR20203356. doi: 10.1042/BSR20203356. Biosci Rep. 2020. PMID: 33200202 Free PMC article.

8

Case Report: Characterization of a Novel NONO Intronic Mutation in a Fetus With X-Linked Syndromic Mental Retardation-34.

Sun H, Han L, Zhang X, Hao X, Zhou X, Pan R, Zhang H, He Y. Sun H, et al. Front Genet. 2020 Nov 16;11:593688. doi: 10.3389/fgene.2020.593688. eCollection 2020. Front Genet. 2020. PMID: 33304389 Free PMC article.

9

A novel intron mutation in FBN-1 gene identified in a pregnant woman with Marfan syndrome.

Wu Y, Sun H, He Y, Zhang H. Wu Y, et al. Among authors: sun h. Hereditas. 2021 Jan 6;158(1):6. doi: 10.1186/s41065-020-00170-w. Hereditas. 2021. PMID: 33407909 Free PMC article.

10

Detection of TSC1/TSC2 mosaic variants in patients with cardiac rhabdomyoma and tuberous sclerosis complex by hybrid-capture next-generation sequencing.

Wang S, Sun H, Wang J, Gu X, Han L, Wu Y, Yan H, Han L, Zhang H, He Y. Wang S, et al. Among authors: sun h. Mol Genet Genomic Med. 2021 Oct;9(10):e1802. doi: 10.1002/mgg3.1802. Epub 2021 Sep 4. Mol Genet Genomic Med. 2021. PMID: 34480426 Free PMC article.

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