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Journal of the National Cancer Institute|February 6, 2023
Comprehensive analysis of germline drivers in endometrial cancerSushmita Gordhandas, Eric Rios-Doria, Karen A Cadoo, et al.Haematologica|March 7, 2024
Cell-free DNA from nail clippings as source of normal control for genomic studies in hematologic malignanciesMelissa Krystel-Whittemore, Kseniya Petrova-Drus, Ryan N Ptashkin, et al.Cancer Discovery|August 26, 2024
Chromothripsis-Mediated Small Cell Lung CarcinomaNatasha Rekhtman, Sam E Tischfield, Christopher A Febres-Aldana, et al.Nature Communications|October 29, 2023
Enhanced clinical assessment of hematologic malignancies through routine paired tumor and normal sequencingRyan N Ptashkin, Mark D Ewalt, Gowtham Jayakumaran, et al.Blood Advances|March 26, 2020
RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AMLAnna L Brown, Peer Arts, Catherine L Carmichael, et al.Plos One|March 6, 2015
Comparative genomics of Cluster O mycobacteriophagesSteven G Cresawn, Welkin H Pope, Deborah Jacobs-Sera, et al.Science (New York, N.Y.)|March 26, 2016
Reproducibility in density functional theory calculations of solidsKurt Lejaeghere, Gustav Bihlmayer, Torbjörn Björkman, et al.Nature Communications|June 19, 2021
Enhanced specificity of clinical high-sensitivity tumor mutation profiling in cell-free DNA via paired normal sequencing using MSK-ACCESSA Rose Brannon, Gowtham Jayakumaran, Monica Diosdado, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 21, 2024
The Australian Genomics Mitochondrial Flagship: A national program delivering mitochondrial diagnosesRocio Rius, Alison G Compton, Naomi L Baker, et al.Blood Advances|July 5, 2023
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41Claire C Homan, Michael W Drazer, Kai Yu, et al.Pageof 48