Hongyan Chai - Search Results

Year	Number of Results
2005	1
2010	1
2012	2
2013	1
2014	3
2015	4
2016	3
2017	2
2018	5
2019	8
2020	5
2021	4
2022	3
2023	3
2024	1

1

Estimation on risk of spontaneous abortions by genomic disorders from a meta-analysis of microarray results on large case series of pregnancy losses.

Peng G, Zhou Q, Chai H, Wen J, Zhao H, Taylor HS, Jiang YH, Li P. Peng G, et al. Among authors: chai h. Mol Genet Genomic Med. 2023 Aug;11(8):e2181. doi: 10.1002/mgg3.2181. Epub 2023 Apr 4. Mol Genet Genomic Med. 2023. PMID: 37013615 Free PMC article.

2

Molecular and clinicopathologic characterization of intravenous leiomyomatosis.

Ordulu Z, Chai H, Peng G, McDonald AG, De Nictolis M, Garcia-Fernandez E, Hardisson D, Prat J, Li P, Hui P, Oliva E, Buza N. Ordulu Z, et al. Among authors: chai h. Mod Pathol. 2020 Sep;33(9):1844-1860. doi: 10.1038/s41379-020-0546-8. Epub 2020 Apr 27. Mod Pathol. 2020. PMID: 32341498 Free PMC article.

3

Human ring chromosome registry for cases in the Chinese population: re-emphasizing Cytogenomic and clinical heterogeneity and reviewing diagnostic and treatment strategies.

Hu Q, Chai H, Shu W, Li P. Hu Q, et al. Among authors: chai h. Mol Cytogenet. 2018 Feb 27;11:19. doi: 10.1186/s13039-018-0367-3. eCollection 2018. Mol Cytogenet. 2018. PMID: 29492108 Free PMC article. Review.

4

Integrated exome sequencing and microarray analyses detected genetic defects and underlying pathways of hepatocellular carcinoma.

Chong ML, Knight J, Peng G, Ji W, Chai H, Lu Y, Wu S, Li P, Hu Q. Chong ML, et al. Among authors: chai h. Cancer Genet. 2023 Aug;276-277:30-35. doi: 10.1016/j.cancergen.2023.06.002. Epub 2023 Jun 28. Cancer Genet. 2023. PMID: 37418972

5

[Retracted] MicroRNA‑744 suppresses cell proliferation and invasion of papillary thyroid cancer by directly targeting NOB1.

Liu H, Guo J, Chai H, Meng X. Liu H, et al. Among authors: chai h. Mol Med Rep. 2023 Oct;28(4):179. doi: 10.3892/mmr.2023.13066. Epub 2023 Aug 18. Mol Med Rep. 2023. PMID: 37594052 Free PMC article.

6

Diagnostic cytogenetic testing following positive noninvasive prenatal screening results of sex chromosome abnormalities: Report of five cases and systematic review of evidence.

Xie X, Tan W, Li F, Carrano E, Ramirez P, DiAdamo A, Grommisch B, Amato K, Chai H, Wen J, Li P. Xie X, et al. Among authors: chai h. Mol Genet Genomic Med. 2020 Jul;8(7):e1297. doi: 10.1002/mgg3.1297. Epub 2020 May 8. Mol Genet Genomic Med. 2020. PMID: 32383339 Free PMC article. Review.

7

Efficient genome-wide first-generation phenotypic screening system in mice using the piggyBac transposon.

Chang H, Pan Y, Landrette S, Ding S, Yang D, Liu L, Tian L, Chai H, Li P, Li DM, Xu T. Chang H, et al. Among authors: chai h. Proc Natl Acad Sci U S A. 2019 Sep 10;116(37):18507-18516. doi: 10.1073/pnas.1906354116. Epub 2019 Aug 26. Proc Natl Acad Sci U S A. 2019. PMID: 31451639 Free PMC article.

8

Detecting regions of homozygosity improves the diagnosis of pathogenic variants and uniparental disomy in pediatric patients.

Wen J, Chai H, Grommisch B, DiAdamo A, Dykas D, Ma D, Popa A, Zhao C, Spencer-Manzon M, Jiang YH, McGrath J, Li P, Bale A, Zhang H. Wen J, et al. Among authors: chai h. Am J Med Genet A. 2022 Jun;188(6):1728-1738. doi: 10.1002/ajmg.a.62693. Epub 2022 Feb 23. Am J Med Genet A. 2022. PMID: 35199448

9

Correlating genomic copy number alterations with clinicopathologic findings in 75 cases of hepatocellular carcinoma.

Peng G, Chai H, Ji W, Lu Y, Wu S, Zhao H, Li P, Hu Q. Peng G, et al. Among authors: chai h. BMC Med Genomics. 2021 Jun 8;14(1):150. doi: 10.1186/s12920-021-00998-9. BMC Med Genomics. 2021. PMID: 34103027 Free PMC article.

10

Genotype-Phenotype Correlations for Putative Haploinsufficient Genes in Deletions of 6q26-q27: Report of Eight Patients and Review of Literature.

Xie X, Chai H, DiAdamo A, Grommisch B, Wen J, Zhang H, Li P. Xie X, et al. Among authors: chai h. Glob Med Genet. 2022 Mar 11;9(2):166-174. doi: 10.1055/s-0042-1743568. eCollection 2022 Jun. Glob Med Genet. 2022. PMID: 35707784 Free PMC article.

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