A citation-based method for searching scientific literature

Arne V Pladsen, Gro Nilsen, Oscar M Rueda, Miriam R Aure, Ørnulf Borgan, Knut Liestøl, Valeria Vitelli, Arnoldo Frigessi, Anita Langerød, Anthony Mathelier, Olav Engebråten, Vessela Kristensen, David C Wedge, Peter Van Loo, Carlos Caldas, Anne-Lise Børresen-Dale, Hege G Russnes, Ole Christian Lingjærde. Commun Biol 2020
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Ultra-Mutation in IDH Wild-Type Glioblastomas of Patients Younger than 55 Years is Associated with Defective Mismatch Repair, Microsatellite Instability, and Giant Cell Enrichment.
Valeria Barresi, Michele Simbolo, Andrea Mafficini, Maria Liliana Piredda, Maria Caffo, Salvatore Massimiliano Cardali, Antonino Germanò, Sara Cingarlini, Claudio Ghimenton, Aldo Scarpa. Cancers (Basel) 2019
10
50

Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors.
Jeanette E Eckel-Passow, Daniel H Lachance, Annette M Molinaro, Kyle M Walsh, Paul A Decker, Hugues Sicotte, Melike Pekmezci, Terri Rice, Matt L Kosel, Ivan V Smirnov,[...]. N Engl J Med 2015
938
50

Evolution of DNA repair defects during malignant progression of low-grade gliomas after temozolomide treatment.
Hinke F van Thuijl, Tali Mazor, Brett E Johnson, Shaun D Fouse, Koki Aihara, Chibo Hong, Annika Malmström, Martin Hallbeck, Jan J Heimans, Jenneke J Kloezeman,[...]. Acta Neuropathol 2015
95
50

DELLY: structural variant discovery by integrated paired-end and split-read analysis.
Tobias Rausch, Thomas Zichner, Andreas Schlattl, Adrian M Stütz, Vladimir Benes, Jan O Korbel. Bioinformatics 2012
803
50

Histopathological spectrum of paediatric diffuse intrinsic pontine glioma: diagnostic and therapeutic implications.
Pawel Buczkowicz, Ute Bartels, Eric Bouffet, Oren Becher, Cynthia Hawkins. Acta Neuropathol 2014
153
50

Mechanisms and therapeutic implications of hypermutation in gliomas.
Mehdi Touat, Yvonne Y Li, Adam N Boynton, Liam F Spurr, J Bryan Iorgulescu, Craig L Bohrson, Isidro Cortes-Ciriano, Cristina Birzu, Jack E Geduldig, Kristine Pelton,[...]. Nature 2020
101
50



The evolutionary history of 2,658 cancers.
Moritz Gerstung, Clemency Jolly, Ignaty Leshchiner, Stefan C Dentro, Santiago Gonzalez, Daniel Rosebrock, Thomas J Mitchell, Yulia Rubanova, Pavana Anur, Kaixian Yu,[...]. Nature 2020
181
50

Mutational landscape and clonal architecture in grade II and III gliomas.
Hiromichi Suzuki, Kosuke Aoki, Kenichi Chiba, Yusuke Sato, Yusuke Shiozawa, Yuichi Shiraishi, Teppei Shimamura, Atsushi Niida, Kazuya Motomura, Fumiharu Ohka,[...]. Nat Genet 2015
433
50

A practical framework and online tool for mutational signature analyses show inter-tissue variation and driver dependencies.
Andrea Degasperi, Tauanne Dias Amarante, Jan Czarnecki, Scott Shooter, Xueqing Zou, Dominik Glodzik, Sandro Morganella, Arjun S Nanda, Cherif Badja, Gene Koh,[...]. Nat Cancer 2020
27
50

Novel MSH6 mutations in treatment-naïve glioblastoma and anaplastic oligodendroglioma contribute to temozolomide resistance independently of MGMT promoter methylation.
Stephanie A Nguyen, Owen D M Stechishin, H Artee Luchman, Xueqing Q Lun, Donna L Senger, Stephen M Robbins, J Gregory Cairncross, Samuel Weiss. Clin Cancer Res 2014
43
50

Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.
Daniel J Brat, Roel G W Verhaak, Kenneth D Aldape, W K Alfred Yung, Sofie R Salama, Lee A D Cooper, Esther Rheinbay, C Ryan Miller, Mark Vitucci, Olena Morozova,[...]. N Engl J Med 2015
50

Whole exome sequencing-based analysis to identify DNA damage repair deficiency as a major contributor to gliomagenesis in adult diffuse gliomas.
Ege Ülgen, Özge Can, Kaya Bilguvar, Yavuz Oktay, Cemaliye B Akyerli, Ayça Erşen Danyeli, M Cengiz Yakıcıer, O Uğur Sezerman, M Necmettin Pamir, Koray Özduman. J Neurosurg 2019
7
50

Signatures of mutational processes in human cancer.
Ludmil B Alexandrov, Serena Nik-Zainal, David C Wedge, Samuel A J R Aparicio, Sam Behjati, Andrew V Biankin, Graham R Bignell, Niccolò Bolli, Ake Borg, Anne-Lise Børresen-Dale,[...]. Nature 2013
50

Use of telomerase promoter mutations to mark specific molecular subsets with reciprocal clinical behavior in IDH mutant and IDH wild-type diffuse gliomas.
Cemaliye B Akyerli, Şirin Yüksel, Özge Can, E Zeynep Erson-Omay, Yavuz Oktay, Erdal Coşgun, Ege Ülgen, Yiğit Erdemgil, Aydın Sav, Andreas von Deimling,[...]. J Neurosurg 2018
10
50

Origin of Gliomas.
Daniel Cahill, Sevin Turcan. Semin Neurol 2018
15
50

Double minute chromosomes in glioblastoma multiforme are revealed by precise reconstruction of oncogenic amplicons.
J Zachary Sanborn, Sofie R Salama, Mia Grifford, Cameron W Brennan, Tom Mikkelsen, Suresh Jhanwar, Sol Katzman, Lynda Chin, David Haussler. Cancer Res 2013
57
50

cIMPACT-NOW update 3: recommended diagnostic criteria for "Diffuse astrocytic glioma, IDH-wildtype, with molecular features of glioblastoma, WHO grade IV".
Daniel J Brat, Kenneth Aldape, Howard Colman, Eric C Holland, David N Louis, Robert B Jenkins, B K Kleinschmidt-DeMasters, Arie Perry, Guido Reifenberger, Roger Stupp,[...]. Acta Neuropathol 2018
248
50

The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary.
David N Louis, Arie Perry, Guido Reifenberger, Andreas von Deimling, Dominique Figarella-Branger, Webster K Cavenee, Hiroko Ohgaki, Otmar D Wiestler, Paul Kleihues, David W Ellison. Acta Neuropathol 2016
50

Replication stress links structural and numerical cancer chromosomal instability.
Rebecca A Burrell, Sarah E McClelland, David Endesfelder, Petra Groth, Marie-Christine Weller, Nadeem Shaikh, Enric Domingo, Nnennaya Kanu, Sally M Dewhurst, Eva Gronroos,[...]. Nature 2013
460
50

Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV.
Jarupon Fah Sathirapongsasuti, Hane Lee, Basil A J Horst, Georg Brunner, Alistair J Cochran, Scott Binder, John Quackenbush, Stanley F Nelson. Bioinformatics 2011
266
50

CTLPScanner: a web server for chromothripsis-like pattern detection.
Jian Yang, Jixiang Liu, Liang Ouyang, Yi Chen, Bo Liu, Haoyang Cai. Nucleic Acids Res 2016
28
50

K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas.
Dong-Anh Khuong-Quang, Pawel Buczkowicz, Patricia Rakopoulos, Xiao-Yang Liu, Adam M Fontebasso, Eric Bouffet, Ute Bartels, Steffen Albrecht, Jeremy Schwartzentruber, Louis Letourneau,[...]. Acta Neuropathol 2012
515
50

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
720
50

Mutational burden, immune checkpoint expression, and mismatch repair in glioma: implications for immune checkpoint immunotherapy.
Tiffany R Hodges, Martina Ott, Joanne Xiu, Zoran Gatalica, Jeff Swensen, Shouhao Zhou, Jason T Huse, John de Groot, Shulin Li, Willem W Overwijk,[...]. Neuro Oncol 2017
168
50

Longitudinal analysis of treatment-induced genomic alterations in gliomas.
E Zeynep Erson-Omay, Octavian Henegariu, S Bülent Omay, Akdes Serin Harmancı, Mark W Youngblood, Ketu Mishra-Gorur, Jie Li, Koray Özduman, Geneive Carrión-Grant, Victoria E Clark,[...]. Genome Med 2017
12
50

Cytogenetics of human brain tumors.
S H Bigner, J Mark, D D Bigner. Cancer Genet Cytogenet 1990
208
50

The causes and consequences of genetic heterogeneity in cancer evolution.
Rebecca A Burrell, Nicholas McGranahan, Jiri Bartek, Charles Swanton. Nature 2013
50

Incidence and clinicopathologic features of H3 K27M mutations in adults with radiographically-determined midline gliomas.
Karisa C Schreck, Surabhi Ranjan, Nebojša Skorupan, Chetan Bettegowda, Charles G Eberhart, Heather M Ames, Matthias Holdhoff. J Neurooncol 2019
27
50


Criteria for inference of chromothripsis in cancer genomes.
Jan O Korbel, Peter J Campbell. Cell 2013
286
50

Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors.
Beatrice S Melin, Jill S Barnholtz-Sloan, Margaret R Wrensch, Christoffer Johansen, Dora Il'yasova, Ben Kinnersley, Quinn T Ostrom, Karim Labreche, Yanwen Chen, Georgina Armstrong,[...]. Nat Genet 2017
124
50


Molecular Profiling Reveals Biologically Discrete Subsets and Pathways of Progression in Diffuse Glioma.
Michele Ceccarelli, Floris P Barthel, Tathiane M Malta, Thais S Sabedot, Sofie R Salama, Bradley A Murray, Olena Morozova, Yulia Newton, Amie Radenbaugh, Stefano M Pagnotta,[...]. Cell 2016
913
50

Distribution of EGFR amplification, combined chromosome 7 gain and chromosome 10 loss, and TERT promoter mutation in brain tumors and their potential for the reclassification of IDHwt astrocytoma to glioblastoma.
Damian Stichel, Azadeh Ebrahimi, David Reuss, Daniel Schrimpf, Takahiro Ono, Mitsuaki Shirahata, Guido Reifenberger, Michael Weller, Daniel Hänggi, Wolfgang Wick,[...]. Acta Neuropathol 2018
72
50

IDH mutation in glioma: molecular mechanisms and potential therapeutic targets.
Sue Han, Yang Liu, Sabrina J Cai, Mingyu Qian, Jianyi Ding, Mioara Larion, Mark R Gilbert, Chunzhang Yang. Br J Cancer 2020
43
50

cIMPACT-NOW update 6: new entity and diagnostic principle recommendations of the cIMPACT-Utrecht meeting on future CNS tumor classification and grading.
David N Louis, Pieter Wesseling, Kenneth Aldape, Daniel J Brat, David Capper, Ian A Cree, Charles Eberhart, Dominique Figarella-Branger, Maryam Fouladi, Gregory N Fuller,[...]. Brain Pathol 2020
104
50

H3 K27M-mutant gliomas in adults vs. children share similar histological features and adverse prognosis.
Bette K Kleinschmidt-DeMasters, Jean M Mulcahy Levy. Clin Neuropathol 2018
46
50

The integrated landscape of driver genomic alterations in glioblastoma.
Veronique Frattini, Vladimir Trifonov, Joseph Minhow Chan, Angelica Castano, Marie Lia, Francesco Abate, Stephen T Keir, Alan X Ji, Pietro Zoppoli, Francesco Niola,[...]. Nat Genet 2013
308
50

Double minutes in human tumor cells.
P E Barker. Cancer Genet Cytogenet 1982
186
50

IDH-mutant glioma specific association of rs55705857 located at 8q24.21 involves MYC deregulation.
Yavuz Oktay, Ege Ülgen, Özge Can, Cemaliye B Akyerli, Şirin Yüksel, Yiğit Erdemgil, I Melis Durası, Octavian Ioan Henegariu, E Paolo Nanni, Nathalie Selevsek,[...]. Sci Rep 2016
13
50

Somatic POLE mutations cause an ultramutated giant cell high-grade glioma subtype with better prognosis.
E Zeynep Erson-Omay, Ahmet Okay Çağlayan, Nikolaus Schultz, Nils Weinhold, S Bülent Omay, Koray Özduman, Yavuz Köksal, Jie Li, Akdes Serin Harmancı, Victoria Clark,[...]. Neuro Oncol 2015
66
50

Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing.
Isidro Cortés-Ciriano, Jake June-Koo Lee, Ruibin Xi, Dhawal Jain, Youngsook L Jung, Lixing Yang, Dmitry Gordenin, Leszek J Klimczak, Cheng-Zhong Zhang, David S Pellman,[...]. Nat Genet 2020
103
50

Non-BRCA familial breast cancer: review of reported pathology and molecular findings.
Michael G Keeney, Fergus J Couch, Daniel W Visscher, Noralane M Lindor. Pathology 2017
13
50

Decoding cancer heterogeneity: studying patient-specific signaling signatures towards personalized cancer therapy.
Efrat Flashner-Abramson, Swetha Vasudevan, Ibukun Adesoji Adejumobi, Amir Sonnenblick, Nataly Kravchenko-Balasha. Theranostics 2019
8
50

SpidermiR: An R/Bioconductor Package for Integrative Analysis with miRNA Data.
Claudia Cava, Antonio Colaprico, Gloria Bertoli, Alex Graudenzi, Tiago C Silva, Catharina Olsen, Houtan Noushmehr, Gianluca Bontempi, Giancarlo Mauri, Isabella Castiglioni. Int J Mol Sci 2017
33
50

p53 overexpression is a prognosticator of poor outcome in esophageal cancer.
Nathaniel Melling, Sonja Norrenbrock, Martina Kluth, Ronald Simon, Claudia Hube-Magg, Stefan Steurer, Andrea Hinsch, Eike Burandt, Frank Jacobsen, Waldemar Wilczak,[...]. Oncol Lett 2019
9
50

ELP-dependent expression of MCL1 promotes resistance to EGFR inhibition in triple-negative breast cancer cells.
Peter Cruz-Gordillo, Megan E Honeywell, Nicholas W Harper, Thomas Leete, Michael J Lee. Sci Signal 2020
3
50



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.