DiAdamo A - 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. Among authors: diadamo a. Front Genet. 2019 Nov 20;10:1162. doi: 10.3389/fgene.2019.01162. eCollection 2019. Front Genet. 2019. PMID: 31850057 Free PMC article.

2

Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia.

Bajaj R, Xu F, Xiang B, Wilcox K, Diadamo AJ, Kumar R, Pietraszkiewicz A, Halene S, Li P. Bajaj R, et al. Among authors: diadamo aj. Mol Cytogenet. 2011 Jan 20;4:3. doi: 10.1186/1755-8166-4-3. Mol Cytogenet. 2011. PMID: 21251322 Free PMC article.

3

Changes in and Efficacies of Indications for Invasive Prenatal Diagnosis of Cytogenomic Abnormalities: 13 Years of Experience in a Single Center.

Meng J, Matarese C, Crivello J, Wilcox K, Wang D, DiAdamo A, Xu F, Li P. Meng J, et al. Among authors: diadamo a. Med Sci Monit. 2015 Jul 5;21:1942-8. doi: 10.12659/MSM.893870. Med Sci Monit. 2015. PMID: 26143093 Free PMC article.

4

Spectrum of Cytogenomic Abnormalities Revealed by Array Comparative Genomic Hybridization on Products of Conception Culture Failure and Normal Karyotype Samples.

Zhou Q, Wu SY, Amato K, DiAdamo A, Li P. Zhou Q, et al. Among authors: diadamo a. J Genet Genomics. 2016 Mar 20;43(3):121-31. doi: 10.1016/j.jgg.2016.02.002. Epub 2016 Feb 13. J Genet Genomics. 2016. PMID: 27020032

5

Jumping Translocations of 1q in Myelodysplastic Syndrome and Acute Myeloid Leukemia: Report of Three Cases and Review of Literature.

Couture T, Amato K, DiAdamo A, Li P. Couture T, et al. Among authors: diadamo a. Case Rep Genet. 2018 Sep 9;2018:8296478. doi: 10.1155/2018/8296478. eCollection 2018. Case Rep Genet. 2018. PMID: 30271640 Free PMC article.

6

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. Among authors: diadamo a. Med Sci (Basel). 2019 Jan 23;7(2):16. doi: 10.3390/medsci7020016. Med Sci (Basel). 2019. PMID: 30678103 Free PMC article.

7

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: diadamo a. Mol Cytogenet. 2019 Mar 6;12:12. doi: 10.1186/s13039-019-0424-6. eCollection 2019. Mol Cytogenet. 2019. PMID: 30886647 Free PMC article.

8

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. Among authors: diadamo a. 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.

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: diadamo a. 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. Among authors: diadamo a. 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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