Niroshi Senaratne

Title(s)	HS Assistant Clinical Professor, Pathology and Laboratory Medicine
School	Medicine
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Publications

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.

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The Role of Preprocedure Genetic Counseling in Pregnancies Interrupted for Fetal Abnormalities. Am J Perinatol. 2024 03; 41(4):383-394. Francoeur AA, Kang SL, Senaratne TN, Saitta S, Murali A, Peters K, Hansman E, Chen A, Parvataneni R, Patil R, Rible R, Sridhar A, Stoddard A, Zapata M, Krakow D, Pluym ID. PMID: 38154468.

View in: PubMed Mentions: Fields:
Per Perinatology
Translation:Humans
Current clinical practices and challenges in molecular testing: a GOAL Consortium Hematopathology Working Group report. Blood Adv. 2023 08 22; 7(16):4599-4607. Lee TD, Aisner DL, David MP, Eno CC, Gagan J, Gocke CD, Guseva NV, Haley L, Jajosky AN, Jones D, Mansukhani MM, Mroz P, Murray SS, Newsom KJ, Paulson V, Roy S, Rushton C, Segal JP, Senaratne TN, Siddon AJ, Starostik P, Van Ziffle JAG, Wu D, Xian RR, Yohe S, Kim AS. PMID: 37236162; PMCID: PMC10425685.

View in: PubMed Mentions: Fields:
Hem Hematology
Translation:Humans
Outcomes of two different unbalanced segregations from a maternal t(4;10)(q33;p15.1) translocation. BMC Med Genomics. 2023 03 29; 16(1):65. Fan J, Senaratne TN, Liu JY, Bina M, Martinez-Agosto JA, Quintero-Rivera F, Wang JJ. PMID: 36991446; PMCID: PMC10061865.

View in: PubMed Mentions: Fields:
Gen Genetics
Translation:Humans
Evaluating Genetic Disorders in the Neonate: The Role of Exome Sequencing in the NICU. Neoreviews. 2022 12 01; 23(12):e829-e840. Senaratne TN, Saitta SC. PMID: 36450644.

View in: PubMed Mentions: Fields:
Per Perinatology
Translation:Humans
Plasticity of Extrachromosomal and Intrachromosomal BRAF Amplifications in Overcoming Targeted Therapy Dosage Challenges. Cancer Discov. 2022 04 01; 12(4):1046-1069. Song K, Minami JK, Huang A, Dehkordi SR, Lomeli SH, Luebeck J, Goodman MH, Moriceau G, Krijgsman O, Dharanipragada P, Ridgley T, Crosson WP, Salazar J, Pazol E, Karin G, Jayaraman R, Balanis NG, Alhani S, Sheu K, Ten Hoeve J, Palermo A, Motika SE, Senaratne TN, Paraiso KH, Hergenrother PJ, Rao PN, Multani AS, Peeper DS, Bafna V, Lo RS, Graeber TG. PMID: 34930786; PMCID: PMC9192483.

View in: PubMed Mentions: 32 Fields:
Neo Neoplasms
Translation:Humans Cells
Concordance of Peripheral Blood and Bone Marrow Next-Generation Sequencing in Hematologic Neoplasms. Adv Hematol. 2022; 2022:8091746. Jumniensuk C, Nobori A, Lee T, Senaratne TN, Rao D, Pullarkat S. PMID: 35378848; PMCID: PMC8976630.

View in: PubMed Mentions: 5
Identification of novel PIEZO1 variants using prenatal exome sequencing and correlation to ultrasound and autopsy findings of recurrent hydrops fetalis. Am J Med Genet A. 2018 12; 176(12):2829-2834. Datkhaeva I, Arboleda VA, Senaratne TN, Nikpour G, Meyerson C, Geng Y, Afshar Y, Scibetta E, Goldstein J, Quintero-Rivera F, Crandall BF, Grody WW, Deignan J, Janzen C. PMID: 30244526.

View in: PubMed Mentions: 14 Fields:
Gen Genetics
Translation:Humans
De novo loss-of-function variants in STAG2 are associated with developmental delay, microcephaly, and congenital anomalies. Am J Med Genet A. 2017 May; 173(5):1319-1327. Mullegama SV, Klein SD, Mulatinho MV, Senaratne TN, Singh K, UCLA Clinical Genomics Center, Nguyen DC, Gallant NM, Strom SP, Ghahremani S, Rao NP, Martinez-Agosto JA. PMID: 28296084; PMCID: PMC7033032.

View in: PubMed Mentions: 24 Fields:
Gen Genetics
Translation:Humans