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Cited by in CrossRef
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]
URL: https://www.wjgnet.com/2307-8960/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 immunotherapyCancer Letters 2014; 352(1): 113 doi: 10.1016/j.canlet.2013.09.016
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 TextbookUNIPA Springer Series 2021; : 43 doi: 10.1007/978-3-030-56051-5_4
3
I. Gobernado, A. Sanchez-Herranz, A. Jimenez-Escrig. Fundamentals of Advanced Omics Technologies: From Genes to MetabolitesComprehensive Analytical Chemistry 2014; 63: 47 doi: 10.1016/B978-0-444-62651-6.00003-9
4
Kenneth G. Frey, Kimberly A. Bishop-Lilly. Current and Emerging Technologies for the Diagnosis of Microbial InfectionsMethods in Microbiology 2015; 42: 525 doi: 10.1016/bs.mim.2015.06.004
5
Ashwag Albukhari, Fawzi F. Bokhari, Hani Choudhry. Next Generation Sequencing in Cancer Research, Volume 22015; : 39 doi: 10.1007/978-3-319-15811-2_3
6
Seema Sethi, Shadan Ali, Philip Philip, Fazlul Sarkar. Clinical Advances in Molecular Biomarkers for Cancer Diagnosis and TherapyInternational Journal of Molecular Sciences 2013; 14(7): 14771 doi: 10.3390/ijms140714771
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 speechJournal of Neurodevelopmental Disorders 2013; 5(1) doi: 10.1186/1866-1955-5-29
8
Flavia M. Facio, Kristy Lee, Julianne M. O'Daniel. A Genetic Counselor's Guide to Using Next‐Generation Sequencing in Clinical PracticeJournal of Genetic Counseling 2014; 23(4): 455 doi: 10.1007/s10897-013-9662-7
9
Christof Hottenrott. Laparoscopic resections and ENCODE-guided genomics to advance surgery and oncologySurgical Endoscopy 2014; 28(7): 2244 doi: 10.1007/s00464-014-3456-3
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 laboratoryPLOS ONE 2017; 12(8): e0181968 doi: 10.1371/journal.pone.0181968
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 ResearchLife 2022; 12(11): 1939 doi: 10.3390/life12111939
12
Giuseppe Matullo, Cornelia Di Gaetano, Simonetta Guarrera. Next generation sequencing and rare genetic variants: From human population studies to medical geneticsEnvironmental and Molecular Mutagenesis 2013; 54(7): 518 doi: 10.1002/em.21799