A citation-based method for searching scientific literature

Mijke Visser, Nienke van der Stoep, Nelleke Gruis. Fam Cancer 2019
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents.
Alisa M Goldstein, May Chan, Mark Harland, Nicholas K Hayward, Florence Demenais, D Timothy Bishop, Esther Azizi, Wilma Bergman, Giovanna Bianchi-Scarra, William Bruno,[...]. J Med Genet 2007
257
66

A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma.
Satoru Yokoyama, Susan L Woods, Glen M Boyle, Lauren G Aoude, Stuart MacGregor, Victoria Zismann, Michael Gartside, Anne E Cust, Rizwan Haq, Mark Harland,[...]. Nature 2011
271
66

Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma.
Lauren G Aoude, Antonia L Pritchard, Carla Daniela Robles-Espinoza, Karin Wadt, Mark Harland, Jiyeon Choi, Michael Gartside, Víctor Quesada, Peter Johansson, Jane M Palmer,[...]. J Natl Cancer Inst 2014
100
66

Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus.
A Kamb, D Shattuck-Eidens, R Eeles, Q Liu, N A Gruis, W Ding, C Hussey, T Tran, Y Miki, J Weaver-Feldhaus. Nat Genet 1994
517
66

Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma.
L Zuo, J Weger, Q Yang, A M Goldstein, M A Tucker, G J Walker, N Hayward, N C Dracopoli. Nat Genet 1996
609
66

Germline p16 mutations in familial melanoma.
C J Hussussian, J P Struewing, A M Goldstein, P A Higgins, D S Ally, M D Sheahan, W H Clark, M A Tucker, N C Dracopoli. Nat Genet 1994
66

Update in genetic susceptibility in melanoma.
Miriam Potrony, Celia Badenas, Paula Aguilera, Joan Anton Puig-Butille, Cristina Carrera, Josep Malvehy, Susana Puig. Ann Transl Med 2015
89
66

Multigene panel sequencing of established and candidate melanoma susceptibility genes in a large cohort of Dutch non-CDKN2A/CDK4 melanoma families.
Thomas P Potjer, Sander Bollen, Anneliese J E M Grimbergen, Remco van Doorn, Nelleke A Gruis, Christi J van Asperen, Frederik J Hes, Nienke van der Stoep. Int J Cancer 2019
24
66

Genetics of familial melanoma: 20 years after CDKN2A.
Lauren G Aoude, Karin A W Wadt, Antonia L Pritchard, Nicholas K Hayward. Pigment Cell Melanoma Res 2015
80
66

Melanoma.
Dirk Schadendorf, Alexander C J van Akkooi, Carola Berking, Klaus G Griewank, Ralf Gutzmer, Axel Hauschild, Andreas Stang, Alexander Roesch, Selma Ugurel. Lancet 2018
387
66

Melanoma genetics.
Jazlyn Read, Karin A W Wadt, Nicholas K Hayward. J Med Genet 2016
110
66

POT1 loss-of-function variants predispose to familial melanoma.
Carla Daniela Robles-Espinoza, Mark Harland, Andrew J Ramsay, Lauren G Aoude, Víctor Quesada, Zhihao Ding, Karen A Pooley, Antonia L Pritchard, Jessamy C Tiffen, Mia Petljak,[...]. Nat Genet 2014
217
66

A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant Melanoma.
Craig C Teerlink, Chad Huff, Jeff Stevens, Yao Yu, Sheri L Holmen, Mark R Silvis, Kirby Trombetti, Hua Zhao, Douglas Grossman, James M Farnham,[...]. J Natl Cancer Inst 2018
19
66

TERT promoter mutations in familial and sporadic melanoma.
Susanne Horn, Adina Figl, P Sivaramakrishna Rachakonda, Christine Fischer, Antje Sucker, Andreas Gast, Stephanie Kadel, Iris Moll, Eduardo Nagore, Kari Hemminki,[...]. Science 2013
66

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.
Corine Bertolotto, Fabienne Lesueur, Sandy Giuliano, Thomas Strub, Mahaut de Lichy, Karine Bille, Philippe Dessen, Benoit d'Hayer, Hamida Mohamdi, Audrey Remenieras,[...]. Nature 2011
324
66

POLE mutations in families predisposed to cutaneous melanoma.
Lauren G Aoude, Ellen Heitzer, Peter Johansson, Michael Gartside, Karin Wadt, Antonia L Pritchard, Jane M Palmer, Judith Symmons, Anne-Marie Gerdes, Grant W Montgomery,[...]. Fam Cancer 2015
29
66

Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds.
N A Gruis, P A van der Velden, L A Sandkuijl, D E Prins, J Weaver-Feldhaus, A Kamb, W Bergman, R R Frants. Nat Genet 1995
275
33

Germline BAP1 mutations predispose to malignant mesothelioma.
Joseph R Testa, Mitchell Cheung, Jianming Pei, Jennifer E Below, Yinfei Tan, Eleonora Sementino, Nancy J Cox, A Umran Dogan, Harvey I Pass, Sandra Trusa,[...]. Nat Genet 2011
608
33

Digital PCR validates 8q dosage as prognostic tool in uveal melanoma.
Mieke Versluis, Mark J de Lange, Sake I van Pelt, Claudia A L Ruivenkamp, Wilma G M Kroes, Jinfeng Cao, Martine J Jager, Gre P M Luyten, Pieter A van der Velden. PLoS One 2015
64
33


"Stop Ne(c)king around": How interactomics contributes to functionally characterize Nek family kinases.
Gabriela Vaz Meirelles, Arina Marina Perez, Edmárcia Elisa de Souza, Fernanda Luisa Basei, Priscila Ferreira Papa, Talita Diniz Melo Hanchuk, Vanessa Bomfim Cardoso, Jörg Kobarg. World J Biol Chem 2014
39
33

BAP1: a novel ubiquitin hydrolase which binds to the BRCA1 RING finger and enhances BRCA1-mediated cell growth suppression.
D E Jensen, M Proctor, S T Marquis, H P Gardner, S I Ha, L A Chodosh, A M Ishov, N Tommerup, H Vissing, Y Sekido,[...]. Oncogene 1998
496
33

Nucleolar Nek11 is a novel target of Nek2A in G1/S-arrested cells.
Kohji Noguchi, Hidesuke Fukazawa, Yuko Murakami, Yoshimasa Uehara. J Biol Chem 2004
32
33

Absolute quantification by droplet digital PCR versus analog real-time PCR.
Christopher M Hindson, John R Chevillet, Hilary A Briggs, Emily N Gallichotte, Ingrid K Ruf, Benjamin J Hindson, Robert L Vessella, Muneesh Tewari. Nat Methods 2013
708
33

The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data.
Ethan Cerami, Jianjiong Gao, Ugur Dogrusoz, Benjamin E Gross, Selcuk Onur Sumer, Bülent Arman Aksoy, Anders Jacobsen, Caitlin J Byrne, Michael L Heuer, Erik Larsson,[...]. Cancer Discov 2012
33

dbSNP: the NCBI database of genetic variation.
S T Sherry, M H Ward, M Kholodov, J Baker, L Phan, E M Smigielski, K Sirotkin. Nucleic Acids Res 2001
33

COSMIC: the Catalogue Of Somatic Mutations In Cancer.
John G Tate, Sally Bamford, Harry C Jubb, Zbyslaw Sondka, David M Beare, Nidhi Bindal, Harry Boutselakis, Charlotte G Cole, Celestino Creatore, Elisabeth Dawson,[...]. Nucleic Acids Res 2019
33

The Genome of the Netherlands: design, and project goals.
Dorret I Boomsma, Cisca Wijmenga, Eline P Slagboom, Morris A Swertz, Lennart C Karssen, Abdel Abdellaoui, Kai Ye, Victor Guryev, Martijn Vermaat, Freerk van Dijk,[...]. Eur J Hum Genet 2014
148
33

Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal.
Jianjiong Gao, Bülent Arman Aksoy, Ugur Dogrusoz, Gideon Dresdner, Benjamin Gross, S Onur Sumer, Yichao Sun, Anders Jacobsen, Rileen Sinha, Erik Larsson,[...]. Sci Signal 2013
33

NEK11: linking CHK1 and CDC25A in DNA damage checkpoint signaling.
Claus Storgaard Sørensen, Marina Melixetian, Ditte Kjaersgaard Klein, Kristian Helin. Cell Cycle 2010
23
33


Downregulation of NEK11 is associated with drug resistance in ovarian cancer.
Xia Liu, Yutao Gao, Yi Lu, Jian Zhang, Li Li, Fuqiang Yin. Int J Oncol 2014
13
33

Ensembl 2018.
Daniel R Zerbino, Premanand Achuthan, Wasiu Akanni, M Ridwan Amode, Daniel Barrell, Jyothish Bhai, Konstantinos Billis, Carla Cummins, Astrid Gall, Carlos García Girón,[...]. Nucleic Acids Res 2018
33

Cell cycle regulation by the NEK family of protein kinases.
Andrew M Fry, Laura O'Regan, Sarah R Sabir, Richard Bayliss. J Cell Sci 2012
208
33

ONCOMINE: a cancer microarray database and integrated data-mining platform.
Daniel R Rhodes, Jianjun Yu, K Shanker, Nandan Deshpande, Radhika Varambally, Debashis Ghosh, Terrence Barrette, Akhilesh Pandey, Arul M Chinnaiyan. Neoplasia 2004
33

Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers.
Mohamed H Abdel-Rahman, Robert Pilarski, Colleen M Cebulla, James B Massengill, Benjamin N Christopher, Getachew Boru, Peter Hovland, Frederick H Davidorf. J Med Genet 2011
293
33

Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing.
Mykyta Artomov, Alexander J Stratigos, Ivana Kim, Raj Kumar, Martin Lauss, Bobby Y Reddy, Benchun Miao, Carla Daniela Robles-Espinoza, Aravind Sankar, Ching-Ni Njauw,[...]. J Natl Cancer Inst 2017
14
33

UALCAN: A Portal for Facilitating Tumor Subgroup Gene Expression and Survival Analyses.
Darshan S Chandrashekar, Bhuwan Bashel, Sai Akshaya Hodigere Balasubramanya, Chad J Creighton, Israel Ponce-Rodriguez, Balabhadrapatruni V S K Chakravarthi, Sooryanarayana Varambally. Neoplasia 2017
33

Nek11, a new member of the NIMA family of kinases, involved in DNA replication and genotoxic stress responses.
Kohji Noguchi, Hidesuke Fukazawa, Yuko Murakami, Yoshimasa Uehara. J Biol Chem 2002
54
33

Selection criteria for genetic assessment of patients with familial melanoma.
Sancy A Leachman, John Carucci, Wendy Kohlmann, Kimberly C Banks, Maryam M Asgari, Wilma Bergman, Giovanna Bianchi-Scarrà, Teresa Brentnall, Brigitte Bressac-de Paillerets, William Bruno,[...]. J Am Acad Dermatol 2009
106
33

Kaviar: an accessible system for testing SNV novelty.
Gustavo Glusman, Juan Caballero, Denise E Mauldin, Leroy Hood, Jared C Roach. Bioinformatics 2011
122
33

NEK11 regulates CDC25A degradation and the IR-induced G2/M checkpoint.
Marina Melixetian, Ditte Kjaersgaard Klein, Claus Storgaard Sørensen, Kristian Helin. Nat Cell Biol 2009
93
33

Toward an improved definition of the tumor spectrum associated with BAP1 germline mutations.
Thomas Wiesner, Isabella Fried, Peter Ulz, Elvira Stacher, Helmut Popper, Rajmohan Murali, Heinz Kutzner, Sigurd Lax, Freya Smolle-Jüttner, Jochen B Geigl,[...]. J Clin Oncol 2012
69
33

Germline mutations in candidate predisposition genes in individuals with cutaneous melanoma and at least two independent additional primary cancers.
Antonia L Pritchard, Peter A Johansson, Vaishnavi Nathan, Madeleine Howlie, Judith Symmons, Jane M Palmer, Nicholas K Hayward. PLoS One 2018
9
33

Targeting MDMX and PKCδ to improve current uveal melanoma therapeutic strategies.
R C Heijkants, M Nieveen, K C 't Hart, A F A S Teunisse, A G Jochemsen. Oncogenesis 2018
7
33

Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study.
Christopher DeBoever, Yosuke Tanigawa, Malene E Lindholm, Greg McInnes, Adam Lavertu, Erik Ingelsson, Chris Chang, Euan A Ashley, Carlos D Bustamante, Mark J Daly,[...]. Nat Commun 2018
44
33

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
33

Lentiviral vectors efficiently transduce quiescent mature 3T3-L1 adipocytes.
Françoise Carlotti, Merlijn Bazuine, Tuija Kekarainen, Jurgen Seppen, Philippe Pognonec, J Antonie Maassen, Rob C Hoeben. Mol Ther 2004
123
33

A new role for cortactin in invadopodia: regulation of protease secretion.
Emily S Clark, Alissa M Weaver. Eur J Cell Biol 2008
126
33

Lumican effects in the control of tumour progression and their links with metalloproteinases and integrins.
Stéphane Brézillon, Katarzyna Pietraszek, François-Xavier Maquart, Yanusz Wegrowski. FEBS J 2013
64
33


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.