A citation-based method for searching scientific literature

Karolina Malińska, Jakub Deptuła, Emilia Rogoża-Janiszewska, Bohdan Górski, Rodney Scott, Helena Rudnicka, Aniruddh Kashyap, Paweł Domagała, Jolanta Hybiak, Bartłomiej Masojć, Cezary Cybulski, Andrzej Kram, Magdalena Boer, Magdalena Kiedrowicz, Jan Lubiński, Tadeusz Dębniak. Eur J Cancer Prev 2020
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


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
100

A Truncating Germline Mutation of TINF2 in Individuals with Thyroid Cancer or Melanoma Results in Longer Telomeres.
Huiling He, Wei Li, Daniel F Comiskey, Sandya Liyanarachchi, Taina T Nieminen, Yanqiang Wang, Katherine E DeLap, Pamela Brock, Albert de la Chapelle. Thyroid 2020
13
100

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
100

Cutaneous melanoma in Birt-Hogg-Dubé syndrome: part of the clinical spectrum?
E C Sattler, B Ertl-Wagner, C Pellegrini, K Peris, M Reithmair, N Schädle, T Ruzicka, O K Steinlein. Br J Dermatol 2018
8
50


ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
50

Families with BAP1-Tumor Predisposition Syndrome in The Netherlands: Path to Identification and a Proposal for Genetic Screening Guidelines.
Cindy Chau, Remco van Doorn, Natasha M van Poppelen, Nienke van der Stoep, Arjen R Mensenkamp, Rolf H Sijmons, Barbara W van Paassen, Ans M W van den Ouweland, Nicole C Naus, Annemieke H van der Hout,[...]. Cancers (Basel) 2019
20
50

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
50

Variants of SCARB1 and VDR Involved in Complex Genetic Interactions May Be Implicated in the Genetic Susceptibility to Clear Cell Renal Cell Carcinoma.
Ewelina Pośpiech, Janusz Ligęza, Wacław Wilk, Aniela Gołas, Janusz Jaszczyński, Andrzej Stelmach, Janusz Ryś, Aleksandra Blecharczyk, Anna Wojas-Pelc, Jolanta Jura,[...]. Biomed Res Int 2015
10
50

Multi-Omics Analysis Reveals a HIF Network and Hub Gene EPAS1 Associated with Lung Adenocarcinoma.
Zhaoxi Wang, Yongyue Wei, Ruyang Zhang, Li Su, Stephanie M Gogarten, Geoffrey Liu, Paul Brennan, John K Field, James D McKay, Jolanta Lissowska,[...]. EBioMedicine 2018
20
50

New approach for understanding genome variations in KEGG.
Minoru Kanehisa, Yoko Sato, Miho Furumichi, Kanae Morishima, Mao Tanabe. Nucleic Acids Res 2019
828
50

Prevalence of the E318K and V320I MITF germline mutations in Polish cancer patients and multiorgan cancer risk-a population-based study.
Tomasz Gromowski, Bartłomiej Masojć, Rodney J Scott, Cezary Cybulski, Bohdan Górski, Wojciech Kluźniak, Katarzyna Paszkowska-Szczur, Andrzej Rozmiarek, Bogusław Dębniak, Romuald Maleszka,[...]. Cancer Genet 2014
13
50

Pathogenic Germline Variants in 10,389 Adult Cancers.
Kuan-Lin Huang, R Jay Mashl, Yige Wu, Deborah I Ritter, Jiayin Wang, Clara Oh, Marta Paczkowska, Sheila Reynolds, Matthew A Wyczalkowski, Ninad Oak,[...]. Cell 2018
278
50

Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability.
Michael D Morgan, Erola Pairo-Castineira, Konrad Rawlik, Oriol Canela-Xandri, Jonathan Rees, David Sims, Albert Tenesa, Ian J Jackson. Nat Commun 2018
41
50

Most common 'sporadic' cancers have a significant germline genetic component.
Yi Lu, Weronica E Ek, David Whiteman, Thomas L Vaughan, Amanda B Spurdle, Douglas F Easton, Paul D Pharoah, Deborah J Thompson, Alison M Dunning, Nicholas K Hayward,[...]. Hum Mol Genet 2014
60
50

Role of PI3K/AKT pathway in cancer: the framework of malignant behavior.
Ningni Jiang, Qijie Dai, Xiaorui Su, Jianjiang Fu, Xuancheng Feng, Juan Peng. Mol Biol Rep 2020
89
50

FLCN: The causative gene for Birt-Hogg-Dubé syndrome.
Laura S Schmidt, W Marston Linehan. Gene 2018
49
50

WikiPathways: connecting communities.
Marvin Martens, Ammar Ammar, Anders Riutta, Andra Waagmeester, Denise N Slenter, Kristina Hanspers, Ryan A Miller, Daniela Digles, Elisson N Lopes, Friederike Ehrhart,[...]. Nucleic Acids Res 2021
61
50

Cutaneous melanoma: From pathogenesis to therapy (Review).
Giulia C Leonardi, Luca Falzone, Rossella Salemi, Antonino Zanghì, Demetrios A Spandidos, James A Mccubrey, Saverio Candido, Massimo Libra. Int J Oncol 2018
155
50

BRCA Genes: The Role in Genome Stability, Cancer Stemness and Therapy Resistance.
Ielizaveta Gorodetska, Iryna Kozeretska, Anna Dubrovska. J Cancer 2019
50
50

MITF-the first 25 years.
Colin R Goding, Heinz Arnheiter. Genes Dev 2019
94
50

A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3.
Pablo Cingolani, Adrian Platts, Le Lily Wang, Melissa Coon, Tung Nguyen, Luan Wang, Susan J Land, Xiangyi Lu, Douglas M Ruden. Fly (Austin) 2012
50

Second-generation PLINK: rising to the challenge of larger and richer datasets.
Christopher C Chang, Carson C Chow, Laurent Cam Tellier, Shashaank Vattikuti, Shaun M Purcell, James J Lee. Gigascience 2015
50

Characteristics of the coexistence of melanoma and renal cell carcinoma.
Eve Maubec, Valérie Chaudru, Hamida Mohamdi, Florent Grange, Jean-Jacques Patard, Stéphane Dalle, Béatrice Crickx, Brigitte Bressac-de Paillerets, Florence Demenais, Marie-Françoise Avril. Cancer 2010
19
50

Clinical and Molecular Characterization of Microphthalmia-associated Transcription Factor (MITF)-related Renal Cell Carcinoma.
Martin Lang, Cathy D Vocke, Christopher J Ricketts, Adam R Metwalli, Mark W Ball, Laura S Schmidt, William M Linehan. Urology 2021
7
50

A framework for variation discovery and genotyping using next-generation DNA sequencing data.
Mark A DePristo, Eric Banks, Ryan Poplin, Kiran V Garimella, Jared R Maguire, Christopher Hartl, Anthony A Philippakis, Guillermo del Angel, Manuel A Rivas, Matt Hanna,[...]. Nat Genet 2011
50

The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma.
F Lesueur, M de Lichy, M Barrois, G Durand, J Bombled, M-F Avril, A Chompret, F Boitier, G M Lenoir, B Bressac-de Paillerets,[...]. Br J Cancer 2008
23
50

A Systematic Literature Review of Whole Exome and Genome Sequencing Population Studies of Genetic Susceptibility to Cancer.
Melissa Rotunno, Rolando Barajas, Mindy Clyne, Elise Hoover, Naoko I Simonds, Tram Kim Lam, Leah E Mechanic, Alisa M Goldstein, Elizabeth M Gillanders. Cancer Epidemiol Biomarkers Prev 2020
5
50

The mTOR signalling pathway in human cancer.
Helena Pópulo, José Manuel Lopes, Paula Soares. Int J Mol Sci 2012
445
50

Genome-wide association study identifies multiple risk loci for renal cell carcinoma.
Ghislaine Scelo, Mark P Purdue, Kevin M Brown, Mattias Johansson, Zhaoming Wang, Jeanette E Eckel-Passow, Yuanqing Ye, Jonathan N Hofmann, Jiyeon Choi, Matthieu Foll,[...]. Nat Commun 2017
41
50

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
50

MC1R is a potent regulator of PTEN after UV exposure in melanocytes.
Juxiang Cao, Lixin Wan, Elke Hacker, Xiangpeng Dai, Stefania Lenna, Celia Jimenez-Cervantes, Yongjun Wang, Nick R Leslie, George X Xu, Hans R Widlund,[...]. Mol Cell 2013
93
50

Lifetime cancer risks in individuals with germline PTEN mutations.
Min-Han Tan, Jessica L Mester, Joanne Ngeow, Lisa A Rybicki, Mohammed S Orloff, Charis Eng. Clin Cancer Res 2012
437
50

SUMO under stress.
Denis Tempé, Marc Piechaczyk, Guillaume Bossis. Biochem Soc Trans 2008
129
50

Exome sequencing and the genetic basis of complex traits.
Adam Kiezun, Kiran Garimella, Ron Do, Nathan O Stitziel, Benjamin M Neale, Paul J McLaren, Namrata Gupta, Pamela Sklar, Patrick F Sullivan, Jennifer L Moran,[...]. Nat Genet 2012
270
50

Epidemiology and Risk Factors for Kidney Cancer.
Ghislaine Scelo, Tricia L Larose. J Clin Oncol 2018
46
50

Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing.
Thomas Husson, Jean-Baptiste Duboc, Olivier Quenez, Camille Charbonnier, Maud Rotharmel, Macarena Cuenca, Xavier Jegouzo, Anne-Claire Richard, Thierry Frebourg, Jean-François Deleuze,[...]. Transl Psychiatry 2018
5
50

ClinVar: improving access to variant interpretations and supporting evidence.
Melissa J Landrum, Jennifer M Lee, Mark Benson, Garth R Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Wonhee Jang,[...]. Nucleic Acids Res 2018
955
50

Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.
Freddie Bray, Jacques Ferlay, Isabelle Soerjomataram, Rebecca L Siegel, Lindsey A Torre, Ahmedin Jemal. CA Cancer J Clin 2018
50

The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma.
Christopher J Ricketts, Aguirre A De Cubas, Huihui Fan, Christof C Smith, Martin Lang, Ed Reznik, Reanne Bowlby, Ewan A Gibb, Rehan Akbani, Rameen Beroukhim,[...]. Cell Rep 2018
241
50

Multiple desmoplastic melanomas in Birt-Hogg-Dubé syndrome and a proposed signaling link between folliculin, the mTOR pathway, and melanoma susceptibility.
Raymond A Cocciolone, Kerry A Crotty, Lesley Andrews, Nikolas K Haass, Fergal J Moloney. Arch Dermatol 2010
11
50

Hypoxia, angiogenesis, and metabolism in the hereditary kidney cancers.
John C Chappell, Laura Beth Payne, W Kimryn Rathmell. J Clin Invest 2019
37
50

Immune-checkpoint inhibitors in melanoma and kidney cancer: from sequencing to rational selection.
Michael Flynn, Lisa Pickering, James Larkin, Samra Turajlic. Ther Adv Med Oncol 2018
5
50

Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications.
Andy Rimmer, Hang Phan, Iain Mathieson, Zamin Iqbal, Stephen R F Twigg, Andrew O M Wilkie, Gil McVean, Gerton Lunter. Nat Genet 2014
521
50

Prevalence of MITF p.E318K in Patients With Melanoma Independent of the Presence of CDKN2A Causative Mutations.
Miriam Potrony, Joan Anton Puig-Butille, Paula Aguilera, Celia Badenas, Gemma Tell-Marti, Cristina Carrera, Luis Javier Del Pozo, Julian Conejo-Mir, Josep Malvehy, Susana Puig. JAMA Dermatol 2016
28
50

Familial Kidney Cancer: Implications of New Syndromes and Molecular Insights.
Maria I Carlo, A Ari Hakimi, Grant D Stewart, Gennady Bratslavsky, James Brugarolas, Ying-Bei Chen, W Marston Linehan, Eamonn R Maher, Maria J Merino, Kenneth Offit,[...]. Eur Urol 2019
36
50

Sambamba: fast processing of NGS alignment formats.
Artem Tarasov, Albert J Vilella, Edwin Cuppen, Isaac J Nijman, Pjotr Prins. Bioinformatics 2015
482
50


Cancer statistics, 2019.
Rebecca L Siegel, Kimberly D Miller, Ahmedin Jemal. CA Cancer J Clin 2019
50

Comprehensive evaluation of allele frequency differences of MC1R variants across populations.
Meg R Gerstenblith, Alisa M Goldstein, Maria Concetta Fargnoli, Ketty Peris, Maria Teresa Landi. Hum Mutat 2007
116
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.