For: | Ku CS, Cooper DN, Roukos DH. Clinical relevance of cancer genome sequencing. World J Gastroenterol 2013; 19(13): 2011-2018 [PMID: 23599619 DOI: 10.3748/wjg.v19.i13.2011] |
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URL: | https://www.wjgnet.com/1007-9327/full/v19/i13/2011.htm |
Number | Citing Articles |
1 |
Laura Wayteck, Karine Breckpot, Jo Demeester, Stefaan C. De Smedt, Koen Raemdonck. A personalized view on cancer immunotherapy. Cancer Letters 2014; 352(1): 113 doi: 10.1016/j.canlet.2013.09.016
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2 |
Fiorella Guadagni, Sofia Cutaia, Giorgio Madonia, Valerio Gristina, Lorena Incorvaia, Lidia Rita Corsini, Daniele Fanale, Claudio Longhitano, Federica Martorana, Juan Lucio Iovanna, Viviana Bazan, Paolo Vigneri. Practical Medical Oncology Textbook. UNIPA Springer Series 2021; : 43 doi: 10.1007/978-3-030-56051-5_4
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3 |
I. Gobernado, A. Sanchez-Herranz, A. Jimenez-Escrig. Fundamentals of Advanced Omics Technologies: From Genes to Metabolites. Comprehensive Analytical Chemistry 2014; 63: 47 doi: 10.1016/B978-0-444-62651-6.00003-9
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4 |
Kenneth G. Frey, Kimberly A. Bishop-Lilly. Current and Emerging Technologies for the Diagnosis of Microbial Infections. Methods in Microbiology 2015; 42: 525 doi: 10.1016/bs.mim.2015.06.004
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5 |
Ashwag Albukhari, Fawzi F. Bokhari, Hani Choudhry. Next Generation Sequencing in Cancer Research, Volume 2. 2015; : 39 doi: 10.1007/978-3-319-15811-2_3
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6 |
Seema Sethi, Shadan Ali, Philip Philip, Fazlul Sarkar. Clinical Advances in Molecular Biomarkers for Cancer Diagnosis and Therapy. International Journal of Molecular Sciences 2013; 14(7): 14771 doi: 10.3390/ijms140714771
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7 |
Elizabeth A Worthey, Gordana Raca, Jennifer J Laffin, Brandon M Wilk, Jeremy M Harris, Kathy J Jakielski, David P Dimmock, Edythe A Strand, Lawrence D Shriberg. Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech. Journal of Neurodevelopmental Disorders 2013; 5(1) doi: 10.1186/1866-1955-5-29
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8 |
Flavia M. Facio, Kristy Lee, Julianne M. O'Daniel. A Genetic Counselor's Guide to Using Next‐Generation Sequencing in Clinical Practice. Journal of Genetic Counseling 2014; 23(4): 455 doi: 10.1007/s10897-013-9662-7
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9 |
Christof Hottenrott. Laparoscopic resections and ENCODE-guided genomics to advance surgery and oncology. Surgical Endoscopy 2014; 28(7): 2244 doi: 10.1007/s00464-014-3456-3
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10 |
Meenakshi Mehrotra, Dzifa Yawa Duose, Rajesh R. Singh, Bedia A. Barkoh, Jawad Manekia, Michael A. Harmon, Keyur P. Patel, Mark J. Routbort, L. Jeffrey Medeiros, Ignacio I. Wistuba, Rajyalakshmi Luthra, Junwen Wang. Versatile ion S5XL sequencer for targeted next generation sequencing of solid tumors in a clinical laboratory. PLOS ONE 2017; 12(8): e0181968 doi: 10.1371/journal.pone.0181968
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11 |
Adrián Muñoz-Barrera, Luis A. Rubio-Rodríguez, Ana Díaz-de Usera, David Jáspez, José M. Lorenzo-Salazar, Rafaela González-Montelongo, Víctor García-Olivares, Carlos Flores. From Samples to Germline and Somatic Sequence Variation: A Focus on Next-Generation Sequencing in Melanoma Research. Life 2022; 12(11): 1939 doi: 10.3390/life12111939
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12 |
Giuseppe Matullo, Cornelia Di Gaetano, Simonetta Guarrera. Next generation sequencing and rare genetic variants: From human population studies to medical genetics. Environmental and Molecular Mutagenesis 2013; 54(7): 518 doi: 10.1002/em.21799
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