A citation-based method for searching scientific literature

Marco M Bühler, José I Martin-Subero, Qiang Pan-Hammarström, Elias Campo, Richard Rosenquist. J Intern Med 2022
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Genome-wide discovery of somatic coding and noncoding mutations in pediatric endemic and sporadic Burkitt lymphoma.
Bruno M Grande, Daniela S Gerhard, Aixiang Jiang, Nicholas B Griner, Jeremy S Abramson, Thomas B Alexander, Hilary Allen, Leona W Ayers, Jeffrey M Bethony, Kishor Bhatia,[...]. Blood 2019
99
100

Mutations in early follicular lymphoma progenitors are associated with suppressed antigen presentation.
Michael R Green, Shingo Kihira, Chih Long Liu, Ramesh V Nair, Raheleh Salari, Andrew J Gentles, Jonathan Irish, Henning Stehr, Carolina Vicente-Dueñas, Isabel Romero-Camarero,[...]. Proc Natl Acad Sci U S A 2015
231
100

Circulating tumor DNA reveals genetics, clonal evolution, and residual disease in classical Hodgkin lymphoma.
Valeria Spina, Alessio Bruscaggin, Annarosa Cuccaro, Maurizio Martini, Martina Di Trani, Gabriela Forestieri, Martina Manzoni, Adalgisa Condoluci, Alberto Arribas, Lodovico Terzi-Di-Bergamo,[...]. Blood 2018
138
100

The genetics of nodal marginal zone lymphoma.
Valeria Spina, Hossein Khiabanian, Monica Messina, Sara Monti, Luciano Cascione, Alessio Bruscaggin, Elisa Spaccarotella, Antony B Holmes, Luca Arcaini, Marco Lucioni,[...]. Blood 2016
96
100

Epstein-Barr virus status of sporadic Burkitt lymphoma is associated with patient age and mutational features.
Julia Richter, Katharina John, Annette M Staiger, Andreas Rosenwald, Katrin Kurz, Ulf Michgehl, German Ott, Sören Franzenburg, Christian Kohler, Jasmin Finger,[...]. Br J Haematol 2022
6
100

Genomic analyses of flow-sorted Hodgkin Reed-Sternberg cells reveal complementary mechanisms of immune evasion.
Kirsty Wienand, Bjoern Chapuy, Chip Stewart, Andrew J Dunford, David Wu, Jaegil Kim, Atanas Kamburov, Timothy R Wood, Fathima Zumla Cader, Matthew D Ducar,[...]. Blood Adv 2019
57
100

High-throughput sequencing of nodal marginal zone lymphomas identifies recurrent BRAF mutations.
V Pillonel, D Juskevicius, C K Y Ng, A Bodmer, A Zettl, D Jucker, S Dirnhofer, A Tzankov. Leukemia 2018
32
100

Pervasive mutations of JAK-STAT pathway genes in classical Hodgkin lymphoma.
Enrico Tiacci, Erik Ladewig, Gianluca Schiavoni, Alex Penson, Elisabetta Fortini, Valentina Pettirossi, Yuchun Wang, Ariele Rosseto, Alessandra Venanzi, Sofija Vlasevska,[...]. Blood 2018
107
100

Distinct molecular profile of IRF4-rearranged large B-cell lymphoma.
Joan Enric Ramis-Zaldivar, Blanca Gonzalez-Farré, Olga Balagué, Verónica Celis, Ferran Nadeu, Julia Salmerón-Villalobos, Mara Andrés, Idoia Martin-Guerrero, Marta Garrido-Pontnou, Ayman Gaafar,[...]. Blood 2020
26
100

Mutational mechanisms shaping the coding and noncoding genome of germinal center derived B-cell lymphomas.
Daniel Hübschmann, Kortine Kleinheinz, Rabea Wagener, Stephan H Bernhart, Cristina López, Umut H Toprak, Stephanie Sungalee, Naveed Ishaque, Helene Kretzmer, Markus Kreuz,[...]. Leukemia 2021
10
100

Non-Hodgkin lymphoma and pre-existing conditions: spectrum, clinical characteristics and outcome in 213 children and adolescents.
Andishe Attarbaschi, Elisa Carraro, Oussama Abla, Shlomit Barzilai-Birenboim, Simon Bomken, Laurence Brugieres, Eva Bubanska, Birgit Burkhardt, Alan K S Chiang, Monika Csoka,[...]. Haematologica 2016
37
50

Randomized controlled trial transfusing convalescent plasma as post-exposure prophylaxis against SARS-CoV-2 infection.
Shmuel Shoham, Evan M Bloch, Arturo Casadevall, Daniel Hanley, Bryan Lau, Kelly Gebo, Edward Cachay, Seble G Kassaye, James H Paxton, Jonathan Gerber,[...]. medRxiv 2021
5
50

Comprehensive Characterization of Cancer Driver Genes and Mutations.
Matthew H Bailey, Collin Tokheim, Eduard Porta-Pardo, Sohini Sengupta, Denis Bertrand, Amila Weerasinghe, Antonio Colaprico, Michael C Wendl, Jaegil Kim, Brendan Reardon,[...]. Cell 2018
915
50

Clonal Relatedness and Mutational Differences between Upper Tract and Bladder Urothelial Carcinoma.
François Audenet, Sumit Isharwal, Eugene K Cha, Mark T A Donoghue, Esther N Drill, Irina Ostrovnaya, Eugene J Pietzak, John P Sfakianos, Aditya Bagrodia, Paari Murugan,[...]. Clin Cancer Res 2019
112
50

KMT2D Deficiency Impairs Super-Enhancers to Confer a Glycolytic Vulnerability in Lung Cancer.
Hunain Alam, Ming Tang, Mayinuer Maitituoheti, Shilpa S Dhar, Manish Kumar, Chae Young Han, Chandrashekar R Ambati, Samir B Amin, Bingnan Gu, Tsai-Yu Chen,[...]. Cancer Cell 2020
66
50

Cancer Management in Kabuki Syndrome: The First Case of Wilms Tumor and a Literature Review.
Hideto Teranishi, Yuhki Koga, Kentaro Nakashima, Eiji Morihana, Kanako Ishii, Yasunari Sakai, Tomoaki Taguchi, Yoshinao Oda, Noriko Miyake, Naomichi Matsumoto,[...]. J Pediatr Hematol Oncol 2018
10
50

Epidemiology of childhood cancer.
Peter Kaatsch. Cancer Treat Rev 2010
563
50

Patient with Kabuki syndrome and acute leukemia.
Sabine Scherer, Ursel Theile, Vera Beyer, Rudolf Ferrari, Christiane Kreck, Manfred Rister. Am J Med Genet A 2003
24
50

Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology.
Tim Ripperger, Stefan S Bielack, Arndt Borkhardt, Ines B Brecht, Birgit Burkhardt, Gabriele Calaminus, Klaus-Michael Debatin, Hedwig Deubzer, Uta Dirksen, Cornelia Eckert,[...]. Am J Med Genet A 2017
121
50

Flow sorting and exome sequencing reveal the oncogenome of primary Hodgkin and Reed-Sternberg cells.
Jonathan Reichel, Amy Chadburn, Paul G Rubinstein, Lisa Giulino-Roth, Wayne Tam, Yifang Liu, Rafael Gaiolla, Kenneth Eng, Joshua Brody, Giorgio Inghirami,[...]. Blood 2015
201
50

Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma.
Masafumi Seki, Riki Nishimura, Kenichi Yoshida, Teppei Shimamura, Yuichi Shiraishi, Yusuke Sato, Motohiro Kato, Kenichi Chiba, Hiroko Tanaka, Noriko Hoshino,[...]. Nat Commun 2015
114
50

Genomic landscape of pediatric B-other acute lymphoblastic leukemia in a consecutive European cohort.
Marketa Zaliova, Jan Stuchly, Lucie Winkowska, Alena Musilova, Karel Fiser, Martina Slamova, Julia Starkova, Martina Vaskova, Ondrej Hrusak, Lucie Sramkova,[...]. Haematologica 2019
54
50

SWI/SNF complex in disorder: SWItching from malignancies to intellectual disability.
Gijs W E Santen, Marjolein Kriek, Haico van Attikum. Epigenetics 2012
59
50

Comprehensive Genomic Characterization of Upper Tract Urothelial Carcinoma.
Tyler J Moss, Yuan Qi, Liu Xi, Bo Peng, Tae-Beom Kim, Nader E Ezzedine, Maribel E Mosqueda, Charles C Guo, Bogdan A Czerniak, Michael Ittmann,[...]. Eur Urol 2017
121
50

Pediatric Cancer Predisposition and Surveillance: An Overview, and a Tribute to Alfred G. Knudson Jr.
Garrett M Brodeur, Kim E Nichols, Sharon E Plon, Joshua D Schiffman, David Malkin. Clin Cancer Res 2017
84
50

The Gastrointestinal Tract Is an Alternative Route for SARS-CoV-2 Infection in a Nonhuman Primate Model.
Li Jiao, Haiyan Li, Jingwen Xu, Mengli Yang, Chunxia Ma, Jingmei Li, Siwen Zhao, Haixuan Wang, Yun Yang, Wenhai Yu,[...]. Gastroenterology 2021
54
50

A Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor.
Samantha Gadd, Vicki Huff, Amy L Walz, Ariadne H A G Ooms, Amy E Armstrong, Daniela S Gerhard, Malcolm A Smith, Jaime M Guidry Auvil, Daoud Meerzaman, Qing-Rong Chen,[...]. Nat Genet 2017
165
50

Genetic and Functional Drivers of Diffuse Large B Cell Lymphoma.
Anupama Reddy, Jenny Zhang, Nicholas S Davis, Andrea B Moffitt, Cassandra L Love, Alexander Waldrop, Sirpa Leppa, Annika Pasanen, Leo Meriranta, Marja-Liisa Karjalainen-Lindsberg,[...]. Cell 2017
569
50

CHARGE and Kabuki Syndromes: Gene-Specific DNA Methylation Signatures Identify Epigenetic Mechanisms Linking These Clinically Overlapping Conditions.
Darci T Butcher, Cheryl Cytrynbaum, Andrei L Turinsky, Michelle T Siu, Michal Inbar-Feigenberg, Roberto Mendoza-Londono, David Chitayat, Susan Walker, Jerry Machado, Oana Caluseriu,[...]. Am J Hum Genet 2017
106
50

Epstein-Barr Virus in Inborn Immunodeficiency-More Than Infection.
Ciro Novaes Rosa Lino, Sujal Ghosh. Cancers (Basel) 2021
7
50

Kabuki syndrome: international consensus diagnostic criteria.
Margaret P Adam, Siddharth Banka, Hans T Bjornsson, Olaf Bodamer, Albert E Chudley, Jaqueline Harris, Hiroshi Kawame, Brendan C Lanpher, Andrew W Lindsley, Giuseppe Merla,[...]. J Med Genet 2019
77
50

Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes.
Erfan Aref-Eshghi, David I Rodenhiser, Laila C Schenkel, Hanxin Lin, Cindy Skinner, Peter Ainsworth, Guillaume Paré, Rebecca L Hood, Dennis E Bulman, Kristin D Kernohan,[...]. Am J Hum Genet 2018
84
50

The whole-genome landscape of medulloblastoma subtypes.
Paul A Northcott, Ivo Buchhalter, A Sorana Morrissy, Volker Hovestadt, Joachim Weischenfeldt, Tobias Ehrenberger, Susanne Gröbner, Maia Segura-Wang, Thomas Zichner, Vasilisa A Rudneva,[...]. Nature 2017
532
50

The landscape of genomic alterations across childhood cancers.
Susanne N Gröbner, Barbara C Worst, Joachim Weischenfeldt, Ivo Buchhalter, Kortine Kleinheinz, Vasilisa A Rudneva, Pascal D Johann, Gnana Prakash Balasubramanian, Maia Segura-Wang, Sebastian Brabetz,[...]. Nature 2018
657
50

Cancer gene mutation frequencies for the U.S. population.
Gaurav Mendiratta, Eugene Ke, Meraj Aziz, David Liarakos, Melinda Tong, Edward C Stites. Nat Commun 2021
28
50

Identification of KMT2D and KDM6A mutations by exome sequencing in Korean patients with Kabuki syndrome.
Chong Kun Cheon, Young Bae Sohn, Jung Min Ko, Yeoun Joo Lee, Ji Sun Song, Jea Woo Moon, Bo Kyoung Yang, Il Soo Ha, Eun Jung Bae, Hyun-Seok Jin,[...]. J Hum Genet 2014
34
50

Whole-exome sequencing reveals critical genes underlying metastasis in oesophageal squamous cell carcinoma.
Wei Dai, Josephine Mun Yee Ko, Sheyne Sta Ana Choi, Zhouyou Yu, Luwen Ning, Hong Zheng, Vinod Gopalan, Kin Tak Chan, Nikki Pui-Yue Lee, Kwok Wah Chan,[...]. J Pathol 2017
41
50

Racial Disparities in Epigenetic Aging of the Right vs Left Colon.
Matthew Devall, Xiangqing Sun, Fangcheng Yuan, Gregory S Cooper, Joseph Willis, Daniel J Weisenberger, Graham Casey, Li Li. J Natl Cancer Inst 2021
13
50

Enhancer Reprogramming Confers Dependence on Glycolysis and IGF Signaling in KMT2D Mutant Melanoma.
Mayinuer Maitituoheti, Emily Z Keung, Ming Tang, Liang Yan, Hunain Alam, Guangchun Han, Anand K Singh, Ayush T Raman, Christopher Terranova, Sharmistha Sarkar,[...]. Cell Rep 2020
15
50

Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours.
Xiaotu Ma, Yu Liu, Yanling Liu, Ludmil B Alexandrov, Michael N Edmonson, Charles Gawad, Xin Zhou, Yongjin Li, Michael C Rusch, John Easton,[...]. Nature 2018
402
50

Spinal ependymoma in a patient with Kabuki syndrome: a case report.
Davide Roma, Paolo Palma, Rossella Capolino, Lorenzo Figà-Talamanca, Francesca Diomedi-Camassei, Francesca Romana Lepri, Maria Cristina Digilio, Carlo Efisio Marras, Raffaella Messina, Andrea Carai,[...]. BMC Med Genet 2015
18
50

Spatial intratumoral heterogeneity and temporal clonal evolution in esophageal squamous cell carcinoma.
Jia-Jie Hao, De-Chen Lin, Huy Q Dinh, Anand Mayakonda, Yan-Yi Jiang, Chen Chang, Ye Jiang, Chen-Chen Lu, Zhi-Zhou Shi, Xin Xu,[...]. Nat Genet 2016
150
50

Sarcoma classification by DNA methylation profiling.
Christian Koelsche, Daniel Schrimpf, Damian Stichel, Martin Sill, Felix Sahm, David E Reuss, Mirjam Blattner, Barbara Worst, Christoph E Heilig, Katja Beck,[...]. Nat Commun 2021
118
50

Clinical and mutational profiles of adult medulloblastoma groups.
Gabriel Chun-Hei Wong, Kay Ka-Wai Li, Wei-Wei Wang, Anthony Pak-Yin Liu, Queenie Junqi Huang, Aden Ka-Yin Chan, Manix Fung-Man Poon, Nellie Yuk-Fei Chung, Queenie Hoi-Wing Wong, Hong Chen,[...]. Acta Neuropathol Commun 2020
17
50

Further delineation of Kabuki syndrome in 48 well-defined new individuals.
Linlea Armstrong, Azza Abd El Moneim, Kirk Aleck, David J Aughton, Clarisse Baumann, Stephen R Braddock, Gabriele Gillessen-Kaesbach, John M Graham, Theresa A Grebe, Karen W Gripp,[...]. Am J Med Genet A 2005
68
50

KMT2D Mutation Is Associated With Poor Prognosis in Non-Small-Cell Lung Cancer.
Fatemeh Ardeshir-Larijani, Priyanka Bhateja, Mary Beth Lipka, Neelesh Sharma, Pingfu Fu, Afshin Dowlati. Clin Lung Cancer 2018
24
50

Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement.
Frédéric Brioude, Jennifer M Kalish, Alessandro Mussa, Alison C Foster, Jet Bliek, Giovanni Battista Ferrero, Susanne E Boonen, Trevor Cole, Robert Baker, Monica Bertoletti,[...]. Nat Rev Endocrinol 2018
239
50

Anaplastic rhabdomyosarcoma in TP53 germline mutation carriers.
Simone Hettmer, Natasha M Archer, Gino R Somers, Ana Novokmet, Amy J Wagers, Lisa Diller, Carlos Rodriguez-Galindo, Lisa A Teot, David Malkin. Cancer 2014
66
50

Defects of B-cell terminal differentiation in patients with type-1 Kabuki syndrome.
Andrew W Lindsley, Howard M Saal, Thomas A Burrow, Robert J Hopkin, Oleg Shchelochkov, Pooja Khandelwal, Changchun Xie, Jack Bleesing, Lisa Filipovich, Kimberly Risma,[...]. J Allergy Clin Immunol 2016
48
50

Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances.
Susanne Bens, Julia Kolarova, Jasmin Beygo, Karin Buiting, Almuth Caliebe, Thomas Eggermann, Gabriele Gillessen-Kaesbach, Dirk Prawitt, Susanne Thiele-Schmitz, Matthias Begemann,[...]. Epigenomics 2016
19
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.