Kadri S - Search Results

1

Genomic Autopsy of Sudden Deaths in Young Individuals.

Webster G, Puckelwartz MJ, Pesce LL, Dellefave-Castillo LM, Vanoye CG, Potet F, Page P, Kearns SD, Pottinger T, White S, Arunkumar P, Olson R, Kofman A, Ibrahim N, Ing A, Brew C, Yap KL, Kadri S, George AL Jr, McNally EM. Webster G, et al. Among authors: kadri s. JAMA Cardiol. 2021 Nov 1;6(11):1247-1256. doi: 10.1001/jamacardio.2021.2789. JAMA Cardiol. 2021. PMID: 34379075 Free PMC article.

2

A performance evaluation study: Variant annotation tools - the enigma of clinical next generation sequencing (NGS) based genetic testing.

Tuteja S, Kadri S, Yap KL. Tuteja S, et al. Among authors: kadri s. J Pathol Inform. 2022 Jul 28;13:100130. doi: 10.1016/j.jpi.2022.100130. eCollection 2022. J Pathol Inform. 2022. PMID: 36268089 Free PMC article.

3

Transcript analysis for variant classification resolution in a child with primary ciliary dyskinesia.

Ing A, Wlodaver A, Kirschmann D, Toledo E, McCabe C, Kadri S, McIntyre MK, Salazar J, Firestein K, Charrow J, Sanders V, Laguna T, Yap KL. Ing A, et al. Among authors: kadri s. Cold Spring Harb Mol Case Stud. 2021 Feb 19;7(1):a005363. doi: 10.1101/mcs.a005363. Print 2021 Feb. Cold Spring Harb Mol Case Stud. 2021. PMID: 33608380 Free PMC article.

4

Diagnostic evaluation of RNA sequencing for the detection of genetic abnormalities associated with Ph-like acute lymphoblastic leukemia (ALL).

Yap KL, Furtado LV, Kiyotani K, Curran E, Stock W, McNeer JL, Kadri S, Segal JP, Nakamura Y, Le Beau MM, Gurbuxani S, Raca G. Yap KL, et al. Among authors: kadri s. Leuk Lymphoma. 2017 Apr;58(4):950-958. doi: 10.1080/10428194.2016.1219902. Epub 2016 Nov 17. Leuk Lymphoma. 2017. PMID: 27855558 Free PMC article.

5

Detailed Phenotypic and Functional Characterization of a Rare, Antibody-Dependent SLAM-Associated Protein Expression Pattern.

Khanolkar A, Wilks JD, Liu G, Caparelli EA, De Moura M, Yap KL, Mustafa A, Kadri S, Huang W, Zheng XT. Khanolkar A, et al. Among authors: kadri s. Immunohorizons. 2020 Apr 10;4(4):153-164. doi: 10.4049/immunohorizons.1900060. Immunohorizons. 2020. PMID: 32276922 Free article.

6

Are Sporadic Eosinophilic Solid and Cystic Renal Cell Carcinomas Characterized by Somatic Tuberous Sclerosis Gene Mutations?

Parilla M, Kadri S, Patil SA, Ritterhouse L, Segal J, Henriksen KJ, Antic T. Parilla M, et al. Among authors: kadri s. Am J Surg Pathol. 2018 Jul;42(7):911-917. doi: 10.1097/PAS.0000000000001067. Am J Surg Pathol. 2018. PMID: 29668487

7

Integrating a Large Next-Generation Sequencing Panel into the Clinical Diagnosis of Gliomas Provides a Comprehensive Platform for Classification from FFPE Tissue or Smear Preparations.

Parilla M, Kadri S, Patil SA, Fitzpatrick C, Ritterhouse L, Segal J, Collins J, Pytel P. Parilla M, et al. Among authors: kadri s. J Neuropathol Exp Neurol. 2019 Mar 1;78(3):257-267. doi: 10.1093/jnen/nly130. J Neuropathol Exp Neurol. 2019. PMID: 30698790

8

Correlation Between Surrogate End Points and Overall Survival in a Multi-institutional Clinicogenomic Cohort of Patients With Non-Small Cell Lung or Colorectal Cancer.

Kehl KL, Riely GJ, Lepisto EM, Lavery JA, Warner JL, LeNoue-Newton ML, Sweeney SM, Rudolph JE, Brown S, Yu C, Bedard PL, Schrag D, Panageas KS; American Association of Cancer Research (AACR) Project Genomics Evidence Neoplasia Information Exchange (GENIE) Consortium. Kehl KL, et al. JAMA Netw Open. 2021 Jul 1;4(7):e2117547. doi: 10.1001/jamanetworkopen.2021.17547. JAMA Netw Open. 2021. PMID: 34309669 Free PMC article.

9

Fewer actionable mutations but higher tumor mutational burden characterizes NSCLC in black patients at an urban academic medical center.

Choudhury NJ, Eghtesad M, Kadri S, Cursio J, Ritterhouse L, Segal J, Husain A, Patel JD. Choudhury NJ, et al. Among authors: kadri s. Oncotarget. 2019 Oct 8;10(56):5817-5823. doi: 10.18632/oncotarget.27212. eCollection 2019 Oct 8. Oncotarget. 2019. PMID: 31645901 Free PMC article.

10

Measurable residual disease monitoring for patients with acute myeloid leukemia following hematopoietic cell transplantation using error corrected hybrid capture next generation sequencing.

Balagopal V, Hantel A, Kadri S, Steinhardt G, Zhen CJ, Kang W, Wanjari P, Ritterhouse LL, Stock W, Segal JP. Balagopal V, et al. Among authors: kadri s. PLoS One. 2019 Oct 28;14(10):e0224097. doi: 10.1371/journal.pone.0224097. eCollection 2019. PLoS One. 2019. PMID: 31658273 Free PMC article.

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