A citation-based method for searching scientific literature

Peter Priestley, Jonathan Baber, Martijn P Lolkema, Neeltje Steeghs, Ewart de Bruijn, Charles Shale, Korneel Duyvesteyn, Susan Haidari, Arne van Hoeck, Wendy Onstenk, Paul Roepman, Mircea Voda, Haiko J Bloemendal, Vivianne C G Tjan-Heijnen, Carla M L van Herpen, Mariette Labots, Petronella O Witteveen, Egbert F Smit, Stefan Sleijfer, Emile E Voest, Edwin Cuppen. Nature 2019
Times Cited: 312



Ludmil B Alexandrov, Jaegil Kim, Nicholas J Haradhvala, Mi Ni Huang, Alvin Wei Tian Ng, Yang Wu, Arnoud Boot, Kyle R Covington, Dmitry A Gordenin, Erik N Bergstrom, S M Ashiqul Islam, Nuria Lopez-Bigas, Leszek J Klimczak, John R McPherson, Sandro Morganella, Radhakrishnan Sabarinathan, David A Wheeler, Ville Mustonen, Gad Getz, Steven G Rozen, Michael R Stratton. Nature 2020
Times Cited: 901




List of shared articles



Times cited

Clinical utility of whole-genome sequencing in precision oncology.
Richard Rosenquist, Edwin Cuppen, Reinhard Buettner, Carlos Caldas, Helene Dreau, Olivier Elemento, Geert Frederix, Sean Grimmond, Torsten Haferlach, Vaidehi Jobanputra,[...]. Semin Cancer Biol 2022
7

Computational analysis of cancer genome sequencing data.
Isidro Cortés-Ciriano, Doga C Gulhan, Jake June-Koo Lee, Giorgio E M Melloni, Peter J Park. Nat Rev Genet 2022
4

Intratumor genetic heterogeneity and clonal evolution to decode endometrial cancer progression.
Alba Mota, Sara S Oltra, Pier Selenica, Cristian P Moiola, Carlos Casas-Arozamena, Carlos López-Gil, Eva Diaz, Sonia Gatius, María Ruiz-Miro, Ana Calvo,[...]. Oncogene 2022
0

Identifying Transcripts with Tandem Duplications from RNA-Sequencing Data to Predict BRCA1-Type Primary Breast Cancer.
Shuoying Qu, John W M Martens, Antoinette Hollestelle, Marcel Smid. Cancers (Basel) 2022
0

MutationalPatterns: the one stop shop for the analysis of mutational processes.
Freek Manders, Arianne M Brandsma, Jurrian de Kanter, Mark Verheul, Rurika Oka, Markus J van Roosmalen, Bastiaan van der Roest, Arne van Hoeck, Edwin Cuppen, Ruben van Boxtel. BMC Genomics 2022
0

Mutational signatures and processes in hepatobiliary cancers.
Ekaterina Zhuravleva, Colm J O'Rourke, Jesper B Andersen. Nat Rev Gastroenterol Hepatol 2022
0


Distinct Genomic Profiles Are Associated with Treatment Response and Survival in Ovarian Cancer.
Chris J de Witte, Joachim Kutzera, Arne van Hoeck, Luan Nguyen, Ingrid A Boere, Mathilde Jalving, Petronella B Ottevanger, Christa van Schaik-van de Mheen, Marion Stevense, Wigard P Kloosterman,[...]. Cancers (Basel) 2022
1


Genome-wide analysis of somatic noncoding mutation patterns in cancer.
Felix Dietlein, Alex B Wang, Christian Fagre, Anran Tang, Nicolle J M Besselink, Edwin Cuppen, Chunliang Li, Shamil R Sunyaev, James T Neal, Eliezer M Van Allen. Science 2022
2

Rearrangement processes and structural variations show evidence of selection in oesophageal adenocarcinomas.
Alvin Wei Tian Ng, Gianmarco Contino, Sarah Killcoyne, Ginny Devonshire, Ray Hsu, Sujath Abbas, Jing Su, Aisling M Redmond, Jamie M J Weaver, Matthew D Eldridge,[...]. Commun Biol 2022
0

The translational challenges of precision oncology.
Oriol Pich, Chris Bailey, Thomas B K Watkins, Simone Zaccaria, Mariam Jamal-Hanjani, Charles Swanton. Cancer Cell 2022
0


Elevated Mutational Age in Blood of Children Treated for Cancer Contributes to Therapy-Related Myeloid Neoplasms.
Eline J M Bertrums, Axel K M Rosendahl Huber, Jurrian K de Kanter, Arianne M Brandsma, Anaïs J C N van Leeuwen, Mark Verheul, Marry M van den Heuvel-Eibrink, Rurika Oka, Markus J van Roosmalen, Hester A de Groot-Kruseman,[...]. Cancer Discov 2022
0

Whole-genome and transcriptome analysis enhances precision cancer treatment options.
E Pleasance, A Bohm, L M Williamson, J M T Nelson, Y Shen, M Bonakdar, E Titmuss, V Csizmok, K Wee, S Hosseinzadeh,[...]. Ann Oncol 2022
0

Genome-wide mapping of somatic mutation rates uncovers drivers of cancer.
Maxwell A Sherman, Adam U Yaari, Oliver Priebe, Felix Dietlein, Po-Ru Loh, Bonnie Berger. Nat Biotechnol 2022
0

A new deep learning technique reveals the exclusive functional contributions of individual cancer mutations.
Prashant Gupta, Aashi Jindal, Gaurav Ahuja, Jayadeva, Debarka Sengupta. J Biol Chem 2022
0

The impact of rare germline variants on human somatic mutation processes.
Mischan Vali-Pour, Ben Lehner, Fran Supek. Nat Commun 2022
0


Discovering the drivers of clonal hematopoiesis.
Oriol Pich, Iker Reyes-Salazar, Abel Gonzalez-Perez, Nuria Lopez-Bigas. Nat Commun 2022
0

Mutation or not, what directly establishes a neoplastic state, namely cellular immortality and autonomy, still remains unknown and should be prioritized in our research.
Shengming Zhu, Jiangang Wang, Lucas Zellmer, Ningzhi Xu, Mei Liu, Yun Hu, Hong Ma, Fei Deng, Wenxiu Yang, Dezhong Joshua Liao. J Cancer 2022
0

Whole genome sequencing reveals the independent clonal origin of multifocal ileal neuroendocrine tumors.
Netta Mäkinen, Meng Zhou, Zhouwei Zhang, Yosuke Kasai, Elizabeth Perez, Grace E Kim, Chrissie Thirlwell, Eric Nakakura, Matthew Meyerson. Genome Med 2022
0

Substitution mutational signatures in whole-genome-sequenced cancers in the UK population.
Andrea Degasperi, Xueqing Zou, Tauanne Dias Amarante, Andrea Martinez-Martinez, Gene Ching Chiek Koh, João M L Dias, Laura Heskin, Lucia Chmelova, Giuseppe Rinaldi, Valerie Ya Wen Wang,[...]. Science 2022
3

Whole genome analysis reveals the genomic complexity in metastatic cutaneous squamous cell carcinoma.
Amarinder Singh Thind, Bruce Ashford, Dario Strbenac, Jenny Mitchell, Jenny Lee, Simon A Mueller, Elahe Minaei, Jay R Perry, Sydney Ch'ng, N Gopalakrishna Iyer,[...]. Front Oncol 2022
0