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: 331



Serena Nik-Zainal, Helen Davies, Johan Staaf, Manasa Ramakrishna, Dominik Glodzik, Xueqing Zou, Inigo Martincorena, Ludmil B Alexandrov, Sancha Martin, David C Wedge, Peter Van Loo, Young Seok Ju, Marcel Smid, Arie B Brinkman, Sandro Morganella, Miriam R Aure, Ole Christian Lingjærde, Anita Langerød, Markus Ringnér, Sung-Min Ahn, Sandrine Boyault, Jane E Brock, Annegien Broeks, Adam Butler, Christine Desmedt, Luc Dirix, Serge Dronov, Aquila Fatima, John A Foekens, Moritz Gerstung, Gerrit K J Hooijer, Se Jin Jang, David R Jones, Hyung-Yong Kim, Tari A King, Savitri Krishnamurthy, Hee Jin Lee, Jeong-Yeon Lee, Yilong Li, Stuart McLaren, Andrew Menzies, Ville Mustonen, Sarah O'Meara, Iris Pauporté, Xavier Pivot, Colin A Purdie, Keiran Raine, Kamna Ramakrishnan, F Germán Rodríguez-González, Gilles Romieu, Anieta M Sieuwerts, Peter T Simpson, Rebecca Shepherd, Lucy Stebbings, Olafur A Stefansson, Jon Teague, Stefania Tommasi, Isabelle Treilleux, Gert G Van den Eynden, Peter Vermeulen, Anne Vincent-Salomon, Lucy Yates, Carlos Caldas, Laura van't Veer, Andrew Tutt, Stian Knappskog, Benita Kiat Tee Tan, Jos Jonkers, Åke Borg, Naoto T Ueno, Christos Sotiriou, Alain Viari, P Andrew Futreal, Peter J Campbell, Paul N Span, Steven Van Laere, Sunil R Lakhani, Jorunn E Eyfjord, Alastair M Thompson, Ewan Birney, Hendrik G Stunnenberg, Marc J van de Vijver, John W M Martens, Anne-Lise Børresen-Dale, Andrea L Richardson, Gu Kong, Gilles Thomas, Michael R Stratton. Nature 2016
Times Cited: 1162




List of shared articles



Times cited

Analytical demands to use whole-genome sequencing in precision oncology.
Manja Meggendorfer, Vaidehi Jobanputra, Kazimierz O Wrzeszczynski, Paul Roepman, Ewart de Bruijn, Edwin Cuppen, Reinhard Buttner, Carlos Caldas, Sean Grimmond, Charles G Mullighan,[...]. Semin Cancer Biol 2022
3

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
6

Validation of HER2 Status in Whole Genome Sequencing Data of Breast Cancers with the Ploidy-Corrected Copy Number Approach.
Marzena Wojtaszewska, Rafał Stępień, Alicja Woźna, Maciej Piernik, Pawel Sztromwasser, Maciej Dąbrowski, Michał Gniot, Sławomir Szymański, Maciej Socha, Piotr Kasprzak,[...]. Mol Diagn Ther 2022
0

Patient-derived xenograft models capture genomic heterogeneity in endometrial cancer.
Vanessa F Bonazzi, Olga Kondrashova, Deborah Smith, Katia Nones, Asmerom T Sengal, Robert Ju, Leisl M Packer, Lambros T Koufariotis, Stephen H Kazakoff, Aimee L Davidson,[...]. Genome Med 2022
4


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



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

Structural Variation in Cancer: Role, Prevalence, and Mechanisms.
Marco Raffaele Cosenza, Bernardo Rodriguez-Martin, Jan O Korbel. Annu Rev Genomics Hum Genet 2022
0

Functional RECAP (REpair CAPacity) assay identifies homologous recombination deficiency undetected by DNA-based BRCAness tests.
Titia G Meijer, Luan Nguyen, Arne Van Hoeck, Anieta M Sieuwerts, Nicole S Verkaik, Marjolijn M Ladan, Kirsten Ruigrok-Ritstier, Carolien H M van Deurzen, Harmen J G van de Werken, Esther H Lips,[...]. Oncogene 2022
1

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