Wang H - Search Results

1

High-risk phenotypes of genetic disease in a Neonatal Intensive Care Unit population.

Xiao T, Ni Q, Chen H, Wang H, Yang L, Wu B, Cao Y, Cheng G, Wang L, Hu L, Mei H, Lu Y, Gong M, Dong X, Zhou W. Xiao T, et al. Among authors: wang h, wang l. Chin Med J (Engl). 2022 Jan 13;135(5):625-627. doi: 10.1097/CM9.0000000000001959. Chin Med J (Engl). 2022. PMID: 35026772 Free PMC article. No abstract available.

2

Tissue factor pathway inhibitor-2: a novel gene involved in zebrafish central nervous system development.

Zhang Y, Wang L, Zhou W, Wang H, Zhang J, Deng S, Li W, Li H, Mao Z, Ma D. Zhang Y, et al. Among authors: wang h, wang l. Dev Biol. 2013 Sep 1;381(1):38-49. doi: 10.1016/j.ydbio.2013.06.018. Epub 2013 Jun 22. Dev Biol. 2013. PMID: 23796905 Free article.

3

Paternal ethanol exposure and behavioral abnormities in offspring: associated alterations in imprinted gene methylation.

Liang F, Diao L, Liu J, Jiang N, Zhang J, Wang H, Zhou W, Huang G, Ma D. Liang F, et al. Among authors: wang h. Neuropharmacology. 2014 Jun;81:126-33. doi: 10.1016/j.neuropharm.2014.01.025. Epub 2014 Jan 30. Neuropharmacology. 2014. PMID: 24486713

4

microRNA expression profiling of heart tissue during fetal development.

Zhou J, Dong X, Zhou Q, Wang H, Qian Y, Tian W, Ma D, Li X. Zhou J, et al. Among authors: wang h. Int J Mol Med. 2014 May;33(5):1250-60. doi: 10.3892/ijmm.2014.1691. Epub 2014 Mar 7. Int J Mol Med. 2014. PMID: 24604530

5

De novo GLI3 mutation in esophageal atresia: reproducing the phenotypic spectrum of Gli3 defects in murine models.

Yang L, Shen C, Mei M, Zhan G, Zhao Y, Wang H, Huang G, Qiu Z, Lu W, Zhou W. Yang L, et al. Among authors: wang h. Biochim Biophys Acta. 2014 Sep;1842(9):1755-61. doi: 10.1016/j.bbadis.2014.05.001. Epub 2014 May 9. Biochim Biophys Acta. 2014. PMID: 24819706 Free article.

6

[Analysis of genomic copy number variations in two unrelated neonates with 8p deletion and duplication associated with congenital heart disease].

Mei M, Yang L, Zhan G, Wang H, Ma D, Zhou W, Huang G. Mei M, et al. Among authors: wang h. Zhonghua Er Ke Za Zhi. 2014 Jun;52(6):460-3. Zhonghua Er Ke Za Zhi. 2014. PMID: 25190168 Chinese.

7

KRAS G12D mosaic mutation in a Chinese linear nevus sebaceous syndrome infant.

Wang H, Qian Y, Wu B, Zhang P, Zhou W. Wang H, et al. BMC Med Genet. 2015 Oct 31;16:101. doi: 10.1186/s12881-015-0247-1. BMC Med Genet. 2015. PMID: 26521233 Free PMC article.

8

EDN1 Gene Variant is Associated with Neonatal Persistent Pulmonary Hypertension.

Mei M, Cheng G, Sun B, Yang L, Wang H, Sun J, Zhou W. Mei M, et al. Among authors: wang h. Sci Rep. 2016 Jul 18;6:29877. doi: 10.1038/srep29877. Sci Rep. 2016. PMID: 27425626 Free PMC article.

9

Mutations in Interleukin-10 Receptor and Clinical Phenotypes in Patients with Very Early Onset Inflammatory Bowel Disease: A Chinese VEO-IBD Collaboration Group Survey.

Huang Z, Peng K, Li X, Zhao R, You J, Cheng X, Wang Z, Wang Y, Wu B, Wang H, Zeng H, Yu Z, Zheng C, Wang Y, Huang Y. Huang Z, et al. Among authors: wang h, wang z, wang y. Inflamm Bowel Dis. 2017 Apr;23(4):578-590. doi: 10.1097/MIB.0000000000001058. Inflamm Bowel Dis. 2017. PMID: 28267044

10

Novel compound heterozygous mutations in the PEX1 gene in two Chinese newborns with Zellweger syndrome based on whole exome sequencing.

Ge MM, Hu L, Li Z, Cheng G, Yan K, Kong Y, Wang H, Yang L, Zhou W. Ge MM, et al. Among authors: wang h. Clin Chim Acta. 2017 Jul;470:24-28. doi: 10.1016/j.cca.2017.04.016. Epub 2017 Apr 19. Clin Chim Acta. 2017. PMID: 28432012

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