Grommisch B - 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: grommisch b. Front Genet. 2019 Nov 20;10:1162. doi: 10.3389/fgene.2019.01162. eCollection 2019. Front Genet. 2019. PMID: 31850057 Free PMC article.

2

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: grommisch b. Case Rep Genet. 2020 Dec 2;2020:8897541. doi: 10.1155/2020/8897541. eCollection 2020. Case Rep Genet. 2020. PMID: 33343950 Free PMC article.

3

Cytogenomic Characterization of Giant Ring or Rod Marker Chromosome in Four Cases of Well-Differentiated and Dedifferentiated Liposarcoma.

Chai H, Xu F, DiAdamo A, Grommisch B, Mao H, Li P. Chai H, et al. Among authors: grommisch b. Case Rep Genet. 2022 Apr 12;2022:6341207. doi: 10.1155/2022/6341207. eCollection 2022. Case Rep Genet. 2022. PMID: 35450197 Free PMC article.

4

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: grommisch b. Med Sci (Basel). 2019 Jan 23;7(2):16. doi: 10.3390/medsci7020016. Med Sci (Basel). 2019. PMID: 30678103 Free PMC article.

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: grommisch b. 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

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: grommisch b. 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.

7

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: grommisch b. 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.

8

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: grommisch b. 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

9

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: grommisch b. Mol Cytogenet. 2021 Apr 2;14(1):21. doi: 10.1186/s13039-021-00542-5. Mol Cytogenet. 2021. PMID: 33810806 Free PMC article.

10

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: grommisch b. 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

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