Chai H - Search Results

1

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.

2

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.

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

[A practice-based competencies training, certifying and evaluating system for genetic counseling in the United States].

Chai H, Wang W, Shang X, Li P. Chai H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jan 10;36(1):37-43. doi: 10.3760/cma.j.issn.1003-9406.2019.01.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30722091 Chinese. No abstract available.

5

Analytical validation and chromosomal distribution of regions of homozygosity by oligonucleotide array comparative genomic hybridization from normal prenatal and postnatal case series.

Wen J, Comerford K, Xu Z, Wu W, Amato K, Grommisch B, DiAdamo A, Xu F, Chai H, Li P. Wen J, et al. Among authors: chai h. Mol Cytogenet. 2019 Mar 6;12:12. doi: 10.1186/s13039-019-0424-6. eCollection 2019. Mol Cytogenet. 2019. PMID: 30886647 Free PMC article.

6

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.

7

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.

8

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.

9

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.

10

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

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