A citation-based method for searching scientific literature

Minho Cho, Soomin Ahn, Mineui Hong, Heejin Bang, Michael Van Vrancken, Seungtae Kim, Jeeyun Lee, Se Hoon Park, Joon Oh Park, Young Suk Park, Ho Yeong Lim, Won Ki Kang, Jong-Mu Sun, Se Hoon Lee, Myung-Ju Ahn, Keunchil Park, Duk Hwan Kim, Seunggwan Lee, Woongyang Park, Kyoung-Mee Kim. Oncotarget 2017
Times Cited: 13







List of co-cited articles
20 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing.
Garrett M Frampton, Alex Fichtenholtz, Geoff A Otto, Kai Wang, Sean R Downing, Jie He, Michael Schnall-Levin, Jared White, Eric M Sanford, Peter An,[...]. Nat Biotechnol 2013
23

Guidelines for Validation of Next-Generation Sequencing-Based Oncology Panels: A Joint Consensus Recommendation of the Association for Molecular Pathology and College of American Pathologists.
Lawrence J Jennings, Maria E Arcila, Christopher Corless, Suzanne Kamel-Reid, Ira M Lubin, John Pfeifer, Robyn L Temple-Smolkin, Karl V Voelkerding, Marina N Nikiforova. J Mol Diagn 2017
210
23


Genome sequencing in microfabricated high-density picolitre reactors.
Marcel Margulies, Michael Egholm, William E Altman, Said Attiya, Joel S Bader, Lisa A Bemben, Jan Berka, Michael S Braverman, Yi-Ju Chen, Zhoutao Chen,[...]. Nature 2005
15

Advances in understanding cancer genomes through second-generation sequencing.
Matthew Meyerson, Stacey Gabriel, Gad Getz. Nat Rev Genet 2010
695
15

Next-generation sequencing: advances and applications in cancer diagnosis.
Simona Serratì, Simona De Summa, Brunella Pilato, Daniela Petriella, Rosanna Lacalamita, Stefania Tommasi, Rosamaria Pinto. Onco Targets Ther 2016
64
15

Feasibility of image-guided transthoracic core-needle biopsy in the BATTLE lung trial.
Alda L Tam, Edward S Kim, J Jack Lee, Joe E Ensor, Marshall E Hicks, Ximing Tang, George R Blumenschein, Christine M Alden, Jeremy J Erasmus, Anne Tsao,[...]. J Thorac Oncol 2013
53
15

Adequacy of core needle biopsy specimens and fine-needle aspirates for molecular testing of lung adenocarcinomas.
Frank Schneider, Matthew A Smith, Molly C Lane, Liron Pantanowitz, Sanja Dacic, N Paul Ohori. Am J Clin Pathol 2015
43
15

DNA Yield From Tissue Samples in Surgical Pathology and Minimum Tissue Requirements for Molecular Testing.
Melissa C Austin, Christina Smith, Colin C Pritchard, Jonathan F Tait. Arch Pathol Lab Med 2016
9
22

Image-Guided Biopsy in the Era of Personalized Cancer Care: Proceedings from the Society of Interventional Radiology Research Consensus Panel.
Alda L Tam, Howard J Lim, Ignacio I Wistuba, Anobel Tamrazi, Michael D Kuo, Etay Ziv, Stephen Wong, Albert J Shih, Robert J Webster, Gregory S Fischer,[...]. J Vasc Interv Radiol 2016
32
15

Factors affecting the success of next-generation sequencing in cytology specimens.
Sinchita Roy-Chowdhuri, Rashmi S Goswami, Hui Chen, Keyur P Patel, Mark J Routbort, Rajesh R Singh, Russell R Broaddus, Bedia A Barkoh, Jawad Manekia, Hui Yao,[...]. Cancer Cytopathol 2015
80
15

Next-Generation Sequencing in Cancer Diagnostics.
Christopher L Corless. J Mol Diagn 2016
7
28

Core needle lung biopsy specimens: adequacy for EGFR and KRAS mutational analysis.
Stephen B Solomon, Maureen F Zakowski, William Pao, Raymond H Thornton, Marc Ladanyi, Mark G Kris, Valerie W Rusch, Naiyer A Rizvi. AJR Am J Roentgenol 2010
82
15

Mutational landscape of metastatic cancer revealed from prospective clinical sequencing of 10,000 patients.
Ahmet Zehir, Ryma Benayed, Ronak H Shah, Aijazuddin Syed, Sumit Middha, Hyunjae R Kim, Preethi Srinivasan, Jianjiong Gao, Debyani Chakravarty, Sean M Devlin,[...]. Nat Med 2017
15

Assessment of the latest NGS enrichment capture methods in clinical context.
Gema García-García, David Baux, Valérie Faugère, Mélody Moclyn, Michel Koenig, Mireille Claustres, Anne-Françoise Roux. Sci Rep 2016
46
15

Assessment of the quality of DNA from various formalin-fixed paraffin-embedded (FFPE) tissues and the use of this DNA for next-generation sequencing (NGS) with no artifactual mutation.
Naoki Einaga, Akio Yoshida, Hiroko Noda, Masaaki Suemitsu, Yuki Nakayama, Akihisa Sakurada, Yoshiko Kawaji, Hiromi Yamaguchi, Yasushi Sasaki, Takashi Tokino,[...]. PLoS One 2017
41
15

Pre-Analytical Considerations for Successful Next-Generation Sequencing (NGS): Challenges and Opportunities for Formalin-Fixed and Paraffin-Embedded Tumor Tissue (FFPE) Samples.
Gladys Arreaza, Ping Qiu, Ling Pang, Andrew Albright, Lewis Z Hong, Matthew J Marton, Diane Levitan. Int J Mol Sci 2016
27
15

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
15

Performance of next-generation sequencing on small tumor specimens and/or low tumor content samples using a commercially available platform.
Scott M Morris, Janakiraman Subramanian, Esma S Gel, George C Runger, Eric J Thompson, David W Mallery, Glen J Weiss. PLoS One 2018
12
16


Targeted, high-depth, next-generation sequencing of cancer genes in formalin-fixed, paraffin-embedded and fine-needle aspiration tumor specimens.
Andrew G Hadd, Jeff Houghton, Ashish Choudhary, Sachin Sah, Liangjing Chen, Adam C Marko, Tiffany Sanford, Kalyan Buddavarapu, Julie Krosting, Lana Garmire,[...]. J Mol Diagn 2013
143
7

Whole-exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas.
Lauren Fishbein, Sanika Khare, Bradley Wubbenhorst, Daniel DeSloover, Kurt D'Andrea, Shana Merrill, Nam Woo Cho, Roger A Greenberg, Tobias Else, Kathleen Montone,[...]. Nat Commun 2015
92
7

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur J Hum Genet 2013
194
7

Universal genetic screening uncovers a novel presentation of an SDHAF2 mutation.
Ruth Casey, Aoife Garrahy, Antoinette Tuthill, Domhnall O'Halloran, Caroline Joyce, Mary B Casey, Paula O'Shea, Marcia Bell. J Clin Endocrinol Metab 2014
27
7

Spatiotemporal Heterogeneity Characterizes the Genetic Landscape of Pheochromocytoma and Defines Early Events in Tumorigenesis.
Joakim Crona, Samuel Backman, Rajani Maharjan, Markus Mayrhofer, Peter Stålberg, Anders Isaksson, Per Hellman, Peyman Björklund. Clin Cancer Res 2015
21
7

Next generation sequencing and the future of genetic diagnosis.
Katja Lohmann, Christine Klein. Neurotherapeutics 2014
75
7

A window into third-generation sequencing.
Eric E Schadt, Steve Turner, Andrew Kasarskis. Hum Mol Genet 2010
360
7

Paraganglioma and phaeochromocytoma: from genetics to personalized medicine.
Judith Favier, Laurence Amar, Anne-Paule Gimenez-Roqueplo. Nat Rev Endocrinol 2015
227
7

Advances in clinical next-generation sequencing: target enrichment and sequencing technologies.
Leomar Y Ballester, Rajyalakshmi Luthra, Rashmi Kanagal-Shamanna, Rajesh R Singh. Expert Rev Mol Diagn 2016
35
7

Mosaicism in HIF2A-related polycythemia-paraganglioma syndrome.
Alexandre Buffet, Sarra Smati, Ludovic Mansuy, Mélanie Ménara, Maëlle Lebras, Marie-Françoise Heymann, Christophe Simian, Judith Favier, Arnaud Murat, Bertrand Cariou,[...]. J Clin Endocrinol Metab 2014
53
7


Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma.
Iñaki Comino-Méndez, Francisco J Gracia-Aznárez, Francesca Schiavi, Iñigo Landa, Luis J Leandro-García, Rocío Letón, Emiliano Honrado, Rocío Ramos-Medina, Daniela Caronia, Guillermo Pita,[...]. Nat Genet 2011
332
7

Quality control in molecular genetic testing.
E Dequeker, S Ramsden, W W Grody, T T Stenzel, D E Barton. Nat Rev Genet 2001
75
7

Next-generation sequencing platforms.
Elaine R Mardis. Annu Rev Anal Chem (Palo Alto Calif) 2013
275
7

Visualization and analysis of gene expression in tissue sections by spatial transcriptomics.
Patrik L Ståhl, Fredrik Salmén, Sanja Vickovic, Anna Lundmark, José Fernández Navarro, Jens Magnusson, Stefania Giacomello, Michaela Asp, Jakub O Westholm, Mikael Huss,[...]. Science 2016
448
7

A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers.
Michael A Quail, Miriam Smith, Paul Coupland, Thomas D Otto, Simon R Harris, Thomas R Connor, Anna Bertoni, Harold P Swerdlow, Yong Gu. BMC Genomics 2012
971
7

Circulating tumor cells: liquid biopsy of cancer.
Catherine Alix-Panabières, Klaus Pantel. Clin Chem 2013
596
7

In vivo and in vitro oncogenic effects of HIF2A mutations in pheochromocytomas and paragangliomas.
Rodrigo A Toledo, Yuejuan Qin, Subramanya Srikantan, Nicole Paes Morales, Qun Li, Yilun Deng, Sang-Woo Kim, Maria Adelaide A Pereira, Sergio P A Toledo, Xiaoping Su,[...]. Endocr Relat Cancer 2013
83
7

SDH mutations establish a hypermethylator phenotype in paraganglioma.
Eric Letouzé, Cosimo Martinelli, Céline Loriot, Nelly Burnichon, Nasséra Abermil, Chris Ottolenghi, Maxime Janin, Mélanie Menara, An Thach Nguyen, Paule Benit,[...]. Cancer Cell 2013
399
7

Complex MAX Rearrangement in a Family With Malignant Pheochromocytoma, Renal Oncocytoma, and Erythrocytosis.
Esther Korpershoek, Djamailys Koffy, Bert H Eussen, Lindsey Oudijk, Thomas G Papathomas, Francien H van Nederveen, Eric J T Belt, Gaston J H Franssen, David F J Restuccia, Niels M G Krol,[...]. J Clin Endocrinol Metab 2016
23
7

DNA Methylation Profiling in Pheochromocytoma and Paraganglioma Reveals Diagnostic and Prognostic Markers.
Aguirre A de Cubas, Esther Korpershoek, Lucia Inglada-Pérez, Eric Letouzé, Maria Currás-Freixes, Agustin F Fernández, Iñaki Comino-Méndez, Francesca Schiavi, Veronika Mancikova, Graeme Eisenhofer,[...]. Clin Cancer Res 2015
34
7

Fundamentals of pyrosequencing.
Colleen T Harrington, Elaine I Lin, Matthew T Olson, James R Eshleman. Arch Pathol Lab Med 2013
43
7

A new method for sequencing DNA.
A M Maxam, W Gilbert. Proc Natl Acad Sci U S A 1977
7

Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients.
Marc Bennedbæk, Maria Rossing, Åse K Rasmussen, Anne-Marie Gerdes, Anne-Bine Skytte, Uffe B Jensen, Finn C Nielsen, Thomas V O Hansen. Hered Cancer Clin Pract 2016
11
9

Next-generation sequencing for the diagnosis of hereditary pheochromocytoma and paraganglioma syndromes.
Rodrigo A Toledo, Patricia L M Dahia. Curr Opin Endocrinol Diabetes Obes 2015
21
7

Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur J Hum Genet 2013
80
7

The promise of whole-exome sequencing in medical genetics.
Bahareh Rabbani, Mustafa Tekin, Nejat Mahdieh. J Hum Genet 2014
221
7

Liquid biopsy: a step forward towards precision medicine in urologic malignancies.
Ashley Di Meo, Jenni Bartlett, Yufeng Cheng, Maria D Pasic, George M Yousef. Mol Cancer 2017
145
7

Profiling the cancer genome.
Prue A Cowin, Michael Anglesio, Dariush Etemadmoghadam, David D L Bowtell. Annu Rev Genomics Hum Genet 2010
25
7

Comparison of next-generation sequencing systems.
Lin Liu, Yinhu Li, Siliang Li, Ni Hu, Yimin He, Ray Pong, Danni Lin, Lihua Lu, Maggie Law. J Biomed Biotechnol 2012
593
7


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.