A citation-based method for searching scientific literature

Atif A Ahmed, Divya S Vundamati, Midhat S Farooqi, Erin Guest. High Throughput 2018
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


Precision medicine in pediatric oncology.
Suzanne J Forrest, Birgit Geoerger, Katherine A Janeway. Curr Opin Pediatr 2018
53
45

Ushering in the next generation of precision trials for pediatric cancer.
Steven G DuBois, Laura B Corson, Kimberly Stegmaier, Katherine A Janeway. Science 2019
27
36

Integrative Clinical Sequencing in the Management of Refractory or Relapsed Cancer in Youth.
Rajen J Mody, Yi-Mi Wu, Robert J Lonigro, Xuhong Cao, Sameek Roychowdhury, Pankaj Vats, Kevin M Frank, John R Prensner, Irfan Asangani, Nallasivam Palanisamy,[...]. JAMA 2015
239
27

Germline Mutations in Predisposition Genes in Pediatric Cancer.
Jinghui Zhang, Michael F Walsh, Gang Wu, Michael N Edmonson, Tanja A Gruber, John Easton, Dale Hedges, Xiaotu Ma, Xin Zhou, Donald A Yergeau,[...]. N Engl J Med 2015
573
27

Precision medicine in pediatric oncology: Lessons learned and next steps.
Rajen J Mody, John R Prensner, Jessica Everett, D Williams Parsons, Arul M Chinnaiyan. Pediatr Blood Cancer 2017
42
27

Next-generation personalised medicine for high-risk paediatric cancer patients - The INFORM pilot study.
Barbara C Worst, Cornelis M van Tilburg, Gnana Prakash Balasubramanian, Petra Fiesel, Ruth Witt, Angelika Freitag, Miream Boudalil, Christopher Previti, Stephan Wolf, Sabine Schmidt,[...]. Eur J Cancer 2016
170
27

Targeting ALK With Crizotinib in Pediatric Anaplastic Large Cell Lymphoma and Inflammatory Myofibroblastic Tumor: A Children's Oncology Group Study.
Yael P Mossé, Stephan D Voss, Megan S Lim, Delphine Rolland, Charles G Minard, Elizabeth Fox, Peter Adamson, Keith Wilner, Susan M Blaney, Brenda J Weigel. J Clin Oncol 2017
182
18

Implementation of next generation sequencing into pediatric hematology-oncology practice: moving beyond actionable alterations.
Jennifer A Oberg, Julia L Glade Bender, Maria Luisa Sulis, Danielle Pendrick, Anthony N Sireci, Susan J Hsiao, Andrew T Turk, Filemon S Dela Cruz, Hanina Hibshoosh, Helen Remotti,[...]. Genome Med 2016
87
18

Precision Medicine in Pediatric Oncology: Translating Genomic Discoveries into Optimized Therapies.
Thai Hoa Tran, Avanthi Tayi Shah, Mignon L Loh. Clin Cancer Res 2017
12
18

Recognition of genetic predisposition in pediatric cancer patients: An easy-to-use selection tool.
Marjolijn C J Jongmans, Jan L C M Loeffen, Esmé Waanders, Peter M Hoogerbrugge, Marjolijn J L Ligtenberg, Roland P Kuiper, Nicoline Hoogerbrugge. Eur J Med Genet 2016
64
18

Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse Intrinsic Pontine Glioma.
Alan Mackay, Anna Burford, Diana Carvalho, Elisa Izquierdo, Janat Fazal-Salom, Kathryn R Taylor, Lynn Bjerke, Matthew Clarke, Mara Vinci, Meera Nandhabalan,[...]. Cancer Cell 2017
392
18

DNA methylation-based classification of central nervous system tumours.
David Capper, David T W Jones, Martin Sill, Volker Hovestadt, Daniel Schrimpf, Dominik Sturm, Christian Koelsche, Felix Sahm, Lukas Chavez, David E Reuss,[...]. Nature 2018
945
18

Molecular characteristics and therapeutic vulnerabilities across paediatric solid tumours.
David T W Jones, Ana Banito, Thomas G P Grünewald, Michelle Haber, Natalie Jäger, Marcel Kool, Till Milde, Jan J Molenaar, Arash Nabbi, Trevor J Pugh,[...]. Nat Rev Cancer 2019
54
18

CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2012-2016.
Quinn T Ostrom, Gino Cioffi, Haley Gittleman, Nirav Patil, Kristin Waite, Carol Kruchko, Jill S Barnholtz-Sloan. Neuro Oncol 2019
839
18


Alterations in ALK/ROS1/NTRK/MET drive a group of infantile hemispheric gliomas.
Ana S Guerreiro Stucklin, Scott Ryall, Kohei Fukuoka, Michal Zapotocky, Alvaro Lassaletta, Christopher Li, Taylor Bridge, Byungjin Kim, Anthony Arnoldo, Paul E Kowalski,[...]. Nat Commun 2019
86
18

Ewing sarcoma.
Thomas G P Grünewald, Florencia Cidre-Aranaz, Didier Surdez, Eleni M Tomazou, Enrique de Álava, Heinrich Kovar, Poul H Sorensen, Olivier Delattre, Uta Dirksen. Nat Rev Dis Primers 2018
226
18


Larotrectinib in patients with TRK fusion-positive solid tumours: a pooled analysis of three phase 1/2 clinical trials.
David S Hong, Steven G DuBois, Shivaani Kummar, Anna F Farago, Catherine M Albert, Kristoffer S Rohrberg, Cornelis M van Tilburg, Ramamoorthy Nagasubramanian, Jordan D Berlin, Noah Federman,[...]. Lancet Oncol 2020
240
18

BRCAness revisited.
Christopher J Lord, Alan Ashworth. Nat Rev Cancer 2016
638
18


Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome.
Michael Rusch, Joy Nakitandwe, Sheila Shurtleff, Scott Newman, Zhaojie Zhang, Michael N Edmonson, Matthew Parker, Yuannian Jiao, Xiaotu Ma, Yanling Liu,[...]. Nat Commun 2018
76
18

Inhibiting TRK Proteins in Clinical Cancer Therapy.
Allison M Lange, Hui-Wen Lo. Cancers (Basel) 2018
84
18

Mutations in chromatin machinery and pediatric high-grade glioma.
Rishi R Lulla, Amanda Muhs Saratsis, Rintaro Hashizume. Sci Adv 2016
42
18

Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups.
Kristian W Pajtler, Hendrik Witt, Martin Sill, David T W Jones, Volker Hovestadt, Fabian Kratochwil, Khalida Wani, Ruth Tatevossian, Chandanamali Punchihewa, Pascal Johann,[...]. Cancer Cell 2015
567
18

Tandem duplication producing a novel oncogenic BRAF fusion gene defines the majority of pilocytic astrocytomas.
David T W Jones, Sylvia Kocialkowski, Lu Liu, Danita M Pearson, L Magnus Bäcklund, Koichi Ichimura, V Peter Collins. Cancer Res 2008
568
18

Molecular Screening for Cancer Treatment Optimization (MOSCATO-01) in Pediatric Patients: A Single-Institutional Prospective Molecular Stratification Trial.
Anne C Harttrampf, Ludovic Lacroix, Marc Deloger, Frederic Deschamps, Stephanie Puget, Nathalie Auger, Philippe Vielh, Pascale Varlet, Zsofia Balogh, Samuel Abbou,[...]. Clin Cancer Res 2017
55
18

Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors.
D Williams Parsons, Angshumoy Roy, Yaping Yang, Tao Wang, Sarah Scollon, Katie Bergstrom, Robin A Kerstein, Stephanie Gutierrez, Andrea K Petersen, Abhishek Bavle,[...]. JAMA Oncol 2016
246
18

Feasibility and clinical integration of molecular profiling for target identification in pediatric solid tumors.
Thomas Pincez, Nathalie Clément, Eve Lapouble, Gaëlle Pierron, Maud Kamal, Ivan Bieche, Virginie Bernard, Paul Fréneaux, Jean Michon, Daniel Orbach,[...]. Pediatr Blood Cancer 2017
28
18

Hotspot mutations in H3F3A and IDH1 define distinct epigenetic and biological subgroups of glioblastoma.
Dominik Sturm, Hendrik Witt, Volker Hovestadt, Dong-Anh Khuong-Quang, David T W Jones, Carolin Konermann, Elke Pfaff, Martje Tönjes, Martin Sill, Sebastian Bender,[...]. Cancer Cell 2012
18

New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs.
Dominik Sturm, Brent A Orr, Umut H Toprak, Volker Hovestadt, David T W Jones, David Capper, Martin Sill, Ivo Buchhalter, Paul A Northcott, Irina Leis,[...]. Cell 2016
425
18

Target and Agent Prioritization for the Children's Oncology Group-National Cancer Institute Pediatric MATCH Trial.
Carl E Allen, Theodore W Laetsch, Rajen Mody, Meredith S Irwin, Megan S Lim, Peter C Adamson, Nita L Seibel, D Williams Parsons, Y Jae Cho, Katherine Janeway. J Natl Cancer Inst 2017
54
18

OncoKids: A Comprehensive Next-Generation Sequencing Panel for Pediatric Malignancies.
Matthew C Hiemenz, Dejerianne G Ostrow, Tracy M Busse, Jonathan Buckley, Dennis T Maglinte, Moiz Bootwalla, James Done, Jianling Ji, Gordana Raca, Alex Ryutov,[...]. J Mol Diagn 2018
36
18

The 2021 WHO Classification of Tumors of the Central Nervous System: a summary.
David N Louis, Arie Perry, Pieter Wesseling, Daniel J Brat, Ian A Cree, Dominique Figarella-Branger, Cynthia Hawkins, H K Ng, Stefan M Pfister, Guido Reifenberger,[...]. Neuro Oncol 2021
473
18


Mutations in exon 3 of the CTNNB1 gene (beta-catenin gene) in cutaneous adnexal tumors.
Dmitry V Kazakov, Radek Sima, Tomas Vanecek, Heinz Kutzner, Gabriele Palmedo, Denisa Kacerovska, Petr Grossmann, Michal Michal. Am J Dermatopathol 2009
36
9

Ethmoidal desmoid tumor in a pediatric patient.
Hiram Alvarez Neri, Eric J Villagra, Alicia C Alvarez, Pedro Valencia, Elsa Jiménez, Carlos de la Torre, Marcos A Rodríguez, Rafael Espinosa. Otolaryngol Head Neck Surg 2007
3
33

Pediatric aggressive fibromatosis of the head and neck: a 20-year retrospective review.
Alok Sharma, Bo-Yee Ngan, George K B Sándor, Paolo Campisi, Vito Forte. J Pediatr Surg 2008
40
9


Is immunohistochemical staining for β-catenin the definitive pathological diagnostic tool for desmoid-type fibromatosis? A multi-institutional study.
Hiroshi Koike, Yoshihiro Nishida, Kei Kohno, Yoshie Shimoyama, Toru Motoi, Shunsuke Hamada, Akira Kawai, Akira Ogose, Toshifumi Ozaki, Toshiyuki Kunisada,[...]. Hum Pathol 2019
9
11

Identification of Medically Actionable Secondary Findings in the 1000 Genomes.
Emily Olfson, Catherine E Cottrell, Nicholas O Davidson, Christina A Gurnett, Jonathan W Heusel, Nathan O Stitziel, Li-Shiun Chen, Sarah Hartz, Rakesh Nagarajan, Nancy L Saccone,[...]. PLoS One 2015
53
9

Oral and maxillofacial tumours in children: a review.
M Sato, N Tanaka, T Sato, T Amagasa. Br J Oral Maxillofac Surg 1997
97
9

Pediatric sinonasal desmoid tumor.
Jonathan Choi, Evan Walgama, John McClay, Pete S Batra, Ron B Mitchell. Ear Nose Throat J 2017
2
50

Fibro-Osseous Lesions of the Skull Base in the Pediatric Population.
Meghan Wilson, Carl Snyderman. J Neurol Surg B Skull Base 2018
5
20

CTNNB1 mutation analysis is a useful tool for the diagnosis of desmoid tumors: a study of 260 desmoid tumors and 191 potential morphologic mimics.
Sophie Le Guellec, Isabelle Soubeyran, Philippe Rochaix, Thomas Filleron, Agnès Neuville, Isabelle Hostein, Jean-Michel Coindre. Mod Pathol 2012
84
9

Desmoid tumor of the head and neck.
Cheng-Ping Wang, Yih-Leong Chang, Jenq-Yuh Ko, Chia-Hsien Cheng, Chun-Fong Yeh, Pei-Jen Lou. Head Neck 2006
41
9

Nuclear β-catenin localization and mutation of the CTNNB1 gene: a context-dependent association.
Grace Kim, Katherine C Kurnit, Bojana Djordjevic, Charanjeet Singh, Mark F Munsell, Wei-Lien Wang, Alexander J Lazar, Wei Zhang, Russell Broaddus. Mod Pathol 2018
50
9

Analysis of β-catenin expression and exon 3 mutations in pediatric sporadic aggressive fibromatosis.
Ning Bo, Dahui Wang, Bingbing Wu, Lian Chen, Ruixue Ma. Pediatr Dev Pathol 2012
22
9

Psammomatoid juvenile ossifying fibroma: case study and a review.
Leonardo Morais Godoy Figueiredo, Thaís Feitosa Leitão de Oliveira, Gardênia Matos Paraguassú, Rômulo Oliveira de Hollanda Valente, Wilson Rodrigo Muniz da Costa, Viviane Almeida Sarmento. Oral Maxillofac Surg 2014
6
16

β-catenin (CTNNB1) mutations and clinicopathological features of mesenteric desmoid-type fibromatosis.
Sebastian Huss, Julia Nehles, Elke Binot, Eva Wardelmann, Jens Mittler, Michaela Angelika Kleine, Helen Künstlinger, Wolfgang Hartmann, Peter Hohenberger, Sabine Merkelbach-Bruse,[...]. Histopathology 2013
72
9


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.