Qin H - Search Results

1

De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders.

Jia X, Zhang S, Tan S, Du B, He M, Qin H, Chen J, Duan X, Luo J, Chen F, Ouyang L, Wang J, Chen G, Yu B, Zhang G, Zhang Z, Lyu Y, Huang Y, Jiao J, Chen JYH, Swoboda KJ, Agolini E, Novelli A, Leoni C, Zampino G, Cappuccio G, Brunetti-Pierri N, Gerard B, Ginglinger E, Richer J, McMillan H, White-Brown A, Hoekzema K, Bernier RA, Kurtz-Nelson EC, Earl RK, Meddens C, Alders M, Fuchs M, Caumes R, Brunelle P, Smol T, Kuehl R, Day-Salvatore DL, Monaghan KG, Morrow MM, Eichler EE, Hu Z, Yuan L, Tan J, Xia K, Shen Y, Guo H. Jia X, et al. Among authors: qin h. Sci Adv. 2022 Aug 19;8(33):eabo7112. doi: 10.1126/sciadv.abo7112. Epub 2022 Aug 17. Sci Adv. 2022. PMID: 35977029 Free PMC article.

2

Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability.

Zhang S, Qin H, Wang J, OuYang L, Luo S, Fu C, Fan X, Su J, Chen R, Xie B, Hu X, Chen S, Shen Y. Zhang S, et al. Among authors: qin h. Mol Cytogenet. 2016 Aug 24;9(1):66. doi: 10.1186/s13039-016-0274-4. eCollection 2016. Mol Cytogenet. 2016. PMID: 27559361 Free PMC article.

3

Novel genotypes and phenotypes among Chinese patients with Floating-Harbor syndrome.

Zhang S, Chen S, Qin H, Yuan H, Pi Y, Yang Y, Huang H, Li G, Sun Y, Wang Z, Ma H, Fu X, Zhou T, Wang J, Zhang H, Shen Y. Zhang S, et al. Among authors: qin h. Orphanet J Rare Dis. 2019 Jun 14;14(1):144. doi: 10.1186/s13023-019-1111-8. Orphanet J Rare Dis. 2019. PMID: 31200758 Free PMC article.

4

Mutation screening of DUOX2 in Chinese patients with congenital hypothyroidism.

Fu C, Zhang S, Su J, Luo S, Zheng H, Wang J, Qin H, Chen Y, Shen Y, Hu X, Fan X, Luo J, Xie B, Chen R, Chen S. Fu C, et al. Among authors: qin h. J Endocrinol Invest. 2015 Nov;38(11):1219-24. doi: 10.1007/s40618-015-0382-8. Epub 2015 Sep 9. J Endocrinol Invest. 2015. PMID: 26349762

5

[Application of SNP-array technology in the genetic analysis of pediatric patients with growth retardation].

Luo S, Fu C, Zhang S, Wang J, Fan X, Luo J, Chen R, Hu X, Qin H, Li C, Ou S, Li Q, Chen S. Luo S, et al. Among authors: qin h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Jun 10;34(3):321-326. doi: 10.3760/cma.j.issn.1003-9406.2017.03.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28604947 Chinese.

6

Novel and reported APC germline mutations in Chinese patients with familial adenomatous polyposis.

Zhang S, Qin H, Lv W, Luo S, Wang J, Fu C, Ma R, Shen Y, Chen S, Wu L. Zhang S, et al. Among authors: qin h. Gene. 2016 Feb 15;577(2):187-92. doi: 10.1016/j.gene.2015.11.034. Epub 2015 Nov 25. Gene. 2016. PMID: 26625971

7

The application of expanded noninvasive prenatal screening for genome-wide chromosomal abnormalities and genetic counseling.

Chen Y, Lai Y, Xu F, Qin H, Tang Y, Huang X, Meng L, Su J, Sun W, Shen Y, Wei H. Chen Y, et al. Among authors: qin h. J Matern Fetal Neonatal Med. 2021 Aug;34(16):2710-2716. doi: 10.1080/14767058.2021.1907333. Epub 2021 May 2. J Matern Fetal Neonatal Med. 2021. PMID: 33938369

8

Common genetic polymorphisms at three loci affect HbF levels in β-thalassemia patients from Southern China.

Yi S, Lai Y, Zuo Y, Chen Y, Qin H, Wei Y, Yang Q, Lin L, Luo J, Fan X, Zheng C. Yi S, et al. Among authors: qin h. Blood Cells Mol Dis. 2016 Nov;62:22-23. doi: 10.1016/j.bcmd.2016.10.019. Epub 2016 Oct 26. Blood Cells Mol Dis. 2016. PMID: 27835778 No abstract available.

9

Potential biomarkers in the fibrosis progression of nonalcoholic steatohepatitis (NASH).

Wang Z, Zhao Z, Xia Y, Cai Z, Wang C, Shen Y, Liu R, Qin H, Jia J, Yuan G. Wang Z, et al. Among authors: qin h. J Endocrinol Invest. 2022 Jul;45(7):1379-1392. doi: 10.1007/s40618-022-01773-y. Epub 2022 Feb 28. J Endocrinol Invest. 2022. PMID: 35226336

10

Leveraging ANFIS with Adam and PSO optimizers for Parkinson's disease.

Pasha A, Ahmed ST, Painam RK, Mathivanan SK, P K, Mallik S, Qin H. Pasha A, et al. Among authors: qin h. Heliyon. 2024 Apr 26;10(9):e30241. doi: 10.1016/j.heliyon.2024.e30241. eCollection 2024 May 15. Heliyon. 2024. PMID: 38720763 Free PMC article.

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