Chai H - Search Results

1

Patterns of Cytogenomic Findings from a Case Series of Recurrent Pregnancy Loss Provide Insight into the Extent of Genetic Defects Causing Miscarriages.

DiAdamo A, Chai H, Chong ML, Wang G, Wen J, Jiang YH, Li P. DiAdamo A, et al. Among authors: chai h. Glob Med Genet. 2024 Mar 29;11(1):123-131. doi: 10.1055/s-0044-1785227. eCollection 2024 Jan. Glob Med Genet. 2024. PMID: 38560483 Free PMC article.

2

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.

3

Integrated FISH, Karyotyping and aCGH Analyses for Effective Prenatal Diagnosis of Common Aneuploidies and Other Cytogenomic Abnormalities.

Chai H, DiAdamo A, Grommisch B, Boyle J, Amato K, Wang D, Wen J, Li P. Chai H, et al. Med Sci (Basel). 2019 Jan 23;7(2):16. doi: 10.3390/medsci7020016. Med Sci (Basel). 2019. PMID: 30678103 Free PMC article.

4

Inverted duplication, triplication and quintuplication through sequential breakage-fusion-bridge events induced by a terminal deletion at 5p in a case of spontaneous abortion.

Chai H, Grommisch B, DiAdamo A, Wen J, Hui P, Li P. Chai H, et al. Mol Genet Genomic Med. 2019 Oct;7(10):e00965. doi: 10.1002/mgg3.965. Epub 2019 Sep 2. Mol Genet Genomic Med. 2019. PMID: 31478360 Free PMC article.

5

A Retrospective Analysis of 10-Year Data Assessed the Diagnostic Accuracy and Efficacy of Cytogenomic Abnormalities in Current Prenatal and Pediatric Settings.

Chai H, DiAdamo A, Grommisch B, Xu F, Zhou Q, Wen J, Mahoney M, Bale A, McGrath J, Spencer-Manzon M, Li P, Zhang H. Chai H, et al. Front Genet. 2019 Nov 20;10:1162. doi: 10.3389/fgene.2019.01162. eCollection 2019. Front Genet. 2019. PMID: 31850057 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

Ring chromosome formation by intra-strand repairing of subtelomeric double stand breaks and clinico-cytogenomic correlations for ring chromosome 9.

Chai H, Ji W, Wen J, DiAdamo A, Grommisch B, Hu Q, Szekely AM, Li P. Chai H, et al. Am J Med Genet A. 2020 Dec;182(12):3023-3028. doi: 10.1002/ajmg.a.61890. Epub 2020 Sep 26. Am J Med Genet A. 2020. PMID: 32978894

8

Exome sequencing analysis on products of conception: a cohort study to evaluate clinical utility and genetic etiology for pregnancy loss.

Zhao C, Chai H, Zhou Q, Wen J, Reddy UM, Kastury R, Jiang Y, Mak W, Bale AE, Zhang H, Li P. Zhao C, et al. Among authors: chai h. Genet Med. 2021 Mar;23(3):435-442. doi: 10.1038/s41436-020-01008-6. Epub 2020 Oct 26. Genet Med. 2021. PMID: 33100332 Free article.

9

Cytogenomic Abnormalities in 19 Cases of Salivary Gland Tumors of Parotid Gland Origin.

Zerjav M, DiAdamo A, Grommisch B, Katherine A, Chai H, Peng G, Li P. Zerjav M, et al. Among authors: chai h. Case Rep Genet. 2020 Dec 2;2020:8897541. doi: 10.1155/2020/8897541. eCollection 2020. Case Rep Genet. 2020. PMID: 33343950 Free PMC article.

10

Detection of cytogenomic abnormalities by OncoScan microarray assay for products of conception from formalin-fixed paraffin-embedded and fresh fetal tissues.

Wen J, Grommisch B, DiAdamo A, Chai H, Ng SME, Hui P, Bale A, Mak W, Wang G, Li P. Wen J, et al. Among authors: chai h. Mol Cytogenet. 2021 Apr 2;14(1):21. doi: 10.1186/s13039-021-00542-5. Mol Cytogenet. 2021. PMID: 33810806 Free PMC article.

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