Farooqi MS - Search Results

1

Reinterpretation of Chromosomal Microarrays with Detailed Medical History.

Farooqi MS, Figueroa S, Gotway G, Wang J, Luu HS, Park JY. Farooqi MS, et al. J Pediatr. 2020 Jul;222:180-185.e1. doi: 10.1016/j.jpeds.2020.03.020. Epub 2020 May 13. J Pediatr. 2020. PMID: 32417076

2

Multi-Institutional FASTQ File Exchange as a Means of Proficiency Testing for Next-Generation Sequencing Bioinformatics and Variant Interpretation.

Davies KD, Farooqi MS, Gruidl M, Hill CE, Woolworth-Hirschhorn J, Jones H, Jones KL, Magliocco A, Mitui M, O'Neill PH, O'Rourke R, Patel NM, Qin D, Ramos E, Rossi MR, Schneider TM, Smith GH, Zhang L, Park JY, Aisner DL. Davies KD, et al. Among authors: farooqi ms. J Mol Diagn. 2016 Jul;18(4):572-9. doi: 10.1016/j.jmoldx.2016.03.002. Epub 2016 May 4. J Mol Diagn. 2016. PMID: 27155050 Free article.

3

High Concentration Capture Probes Enhance Massively Parallel Sequencing Assays.

Farooqi MS, Mitui M, Londin ER, Park JY. Farooqi MS, et al. Clin Chem. 2016 Jul;62(7):1032-4. doi: 10.1373/clinchem.2016.255026. Epub 2016 May 23. Clin Chem. 2016. PMID: 27217445 No abstract available.

4

Chromosomal Microarray Reinterpretation: Applications to Pediatric Practice.

Shi G, Xu J, Barnes SF, Farooqi MS, Luu HS, Gotway G, Park JY. Shi G, et al. Among authors: farooqi ms. J Pediatr. 2022 Apr;243:219-223. doi: 10.1016/j.jpeds.2021.12.036. Epub 2021 Dec 23. J Pediatr. 2022. PMID: 34953820

5

Occurrence and characterization of medulloblastoma in a patient with Curry-Jones syndrome.

Porath B, Farooki S, Gener M, Amudhavalli SM, Grote L, Cooley LD, Ginn K, Farooqi MS. Porath B, et al. Among authors: farooqi ms. Clin Genet. 2020 Apr;97(4):670-671. doi: 10.1111/cge.13681. Epub 2019 Dec 11. Clin Genet. 2020. PMID: 31825089

6

Clinical Validation of Somatic Mutation Detection by the OncoScan CNV Plus Assay.

Smith SC, Farooqi MS, Gener MA, Ginn K, Joyce JM, Bendorf TM, Cooley LD. Smith SC, et al. Among authors: farooqi ms. J Mol Diagn. 2021 Jan;23(1):29-37. doi: 10.1016/j.jmoldx.2020.10.001. Epub 2020 Oct 17. J Mol Diagn. 2021. PMID: 33080408 Free article.

7

Factors Affecting Migration to GRCh38 in Laboratories Performing Clinical Next-Generation Sequencing.

Lansdon LA, Cadieux-Dion M, Yoo B, Miller N, Cohen ASA, Zellmer L, Zhang L, Farrow EG, Thiffault I, Repnikova EA, Cooley LD, Alaimo JT, Porath B, Herriges JC, Saunders CJ, Farooqi MS. Lansdon LA, et al. Among authors: farooqi ms. J Mol Diagn. 2021 May;23(5):651-657. doi: 10.1016/j.jmoldx.2021.02.003. Epub 2021 Feb 22. J Mol Diagn. 2021. PMID: 33631350 Free article.

8

A woman with primary biliary cirrhosis and hyponatremia.

Farooqi MS, Hashim IA. Farooqi MS, et al. Clin Chem. 2015 Aug;61(8):1028-31. doi: 10.1373/clinchem.2014.229773. Clin Chem. 2015. PMID: 26220582 No abstract available.

9

Role of high-throughput sequencing in the diagnosis of cutaneous T-cell lymphoma.

Rea B, Haun P, Emerson R, Vignali M, Farooqi M, Samimi S, Elenitsas R, Kirsch I, Bagg A. Rea B, et al. J Clin Pathol. 2018 Sep;71(9):814-820. doi: 10.1136/jclinpath-2018-205004. Epub 2018 Apr 10. J Clin Pathol. 2018. PMID: 29636372

10

Validation of a next-generation sequencing oncology panel optimized for low input DNA.

Sussman RT, Shaffer S, Azzato EM, DeSloover D, Farooqi MS, Meyer A, Lieberman DB, Bigdeli A, Paolillo C, Ganapathy K, Sukhadia S, Rosenbaum JN, Daber RD, Morrissette JJD. Sussman RT, et al. Among authors: farooqi ms. Cancer Genet. 2018 Dec;228-229:55-63. doi: 10.1016/j.cancergen.2018.08.004. Epub 2018 Sep 19. Cancer Genet. 2018. PMID: 30553474

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