A citation-based method for searching scientific literature

Roland P Kuiper, Nicoline Hoogerbrugge. Oncotarget 2015
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer.
Robbert D A Weren, Marjolijn J L Ligtenberg, C Marleen Kets, Richarda M de Voer, Eugène T P Verwiel, Liesbeth Spruijt, Wendy A G van Zelst-Stams, Marjolijn C Jongmans, Christian Gilissen, Jayne Y Hehir-Kwa,[...]. Nat Genet 2015
229
81

Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas.
Claire Palles, Jean-Baptiste Cazier, Kimberley M Howarth, Enric Domingo, Angela M Jones, Peter Broderick, Zoe Kemp, Sarah L Spain, Estrella Guarino, Israel Salguero,[...]. Nat Genet 2013
642
56

Biallelic NTHL1 Mutations in a Woman with Multiple Primary Tumors.
Barbara Rivera, Ester Castellsagué, Ismaël Bah, Léon C van Kempen, William D Foulkes. N Engl J Med 2015
65
50


Hereditary and familial colon cancer.
Kory W Jasperson, Thérèse M Tuohy, Deborah W Neklason, Randall W Burt. Gastroenterology 2010
683
37

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
31

dbSNP: a database of single nucleotide polymorphisms.
E M Smigielski, K Sirotkin, M Ward, S T Sherry. Nucleic Acids Res 2000
336
25


Genic intolerance to functional variation and the interpretation of personal genomes.
Slavé Petrovski, Quanli Wang, Erin L Heinzen, Andrew S Allen, David B Goldstein. PLoS Genet 2013
607
25

A general framework for estimating the relative pathogenicity of human genetic variants.
Martin Kircher, Daniela M Witten, Preti Jain, Brian J O'Roak, Gregory M Cooper, Jay Shendure. Nat Genet 2014
25

Whole genome sequencing reveals DICER1 as a candidate predisposing gene in familial Hodgkin lymphoma.
Obul Reddy Bandapalli, Nagarajan Paramasivam, Sara Giangiobbe, Abhishek Kumar, Wolfgang Benisch, Andreas Engert, Mathias Witzens-Harig, Mathias Schlesner, Kari Hemminki, Asta Försti. Int J Cancer 2018
10
40


The GeneCards Suite: From Gene Data Mining to Disease Genome Sequence Analyses.
Gil Stelzer, Naomi Rosen, Inbar Plaschkes, Shahar Zimmerman, Michal Twik, Simon Fishilevich, Tsippi Iny Stein, Ron Nudel, Iris Lieder, Yaron Mazor,[...]. Curr Protoc Bioinformatics 2016
25

Distribution and intensity of constraint in mammalian genomic sequence.
Gregory M Cooper, Eric A Stone, George Asimenos, Eric D Green, Serafim Batzoglou, Arend Sidow. Genome Res 2005
939
25

Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family.
Abhishek Kumar, Obul Reddy Bandapalli, Nagarajan Paramasivam, Sara Giangiobbe, Chiara Diquigiovanni, Elena Bonora, Roland Eils, Matthias Schlesner, Kari Hemminki, Asta Försti. Sci Rep 2018
18
25

A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
25


Update on Hereditary Colorectal Cancer: Improving the Clinical Utility of Multigene Panel Testing.
Marie Lorans, Eryn Dow, Finlay A Macrae, Ingrid M Winship, Daniel D Buchanan. Clin Colorectal Cancer 2018
40
25


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
600
25

Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes.
Adam Siepel, Gill Bejerano, Jakob S Pedersen, Angie S Hinrichs, Minmei Hou, Kate Rosenbloom, Hiram Clawson, John Spieth, Ladeana W Hillier, Stephen Richards,[...]. Genome Res 2005
25

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
25

RNF43 germline and somatic mutation in serrated neoplasia pathway and its association with BRAF mutation.
Helen H N Yan, Jeffrey C W Lai, Siu Lun Ho, Wai Keung Leung, Wai Lun Law, Janet F Y Lee, Anthony K W Chan, Wai Yin Tsui, Annie S Y Chan, Bernard C H Lee,[...]. Gut 2017
119
25

Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.
M L Bisgaard, K Fenger, S Bülow, E Niebuhr, J Mohr. Hum Mutat 1994
297
18

The growing complexity of the intestinal polyposis syndromes.
Emanuela Lucci-Cordisco, Mauro Risio, Tiziana Venesio, Maurizio Genuardi. Am J Med Genet A 2013
25
18


8-oxoguanine causes spontaneous de novo germline mutations in mice.
Mizuki Ohno, Kunihiko Sakumi, Ryutaro Fukumura, Masato Furuichi, Yuki Iwasaki, Masaaki Hokama, Toshimichi Ikemura, Teruhisa Tsuzuki, Yoichi Gondo, Yusaku Nakabeppu. Sci Rep 2014
105
18

Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas.
Isabel Spier, Stefanie Holzapfel, Janine Altmüller, Bixiao Zhao, Sukanya Horpaopan, Stefanie Vogt, Sophia Chen, Monika Morak, Susanne Raeder, Katrin Kayser,[...]. Int J Cancer 2015
100
18

Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis.
Ronja Adam, Isabel Spier, Bixiao Zhao, Michael Kloth, Jonathan Marquez, Inga Hinrichsen, Jutta Kirfel, Aylar Tafazzoli, Sukanya Horpaopan, Siegfried Uhlhaas,[...]. Am J Hum Genet 2016
129
18

Delineating the Phenotypic Spectrum of the NTHL1-Associated Polyposis.
Sami Belhadj, Pilar Mur, Matilde Navarro, Sara González, Victor Moreno, Gabriel Capellá, Laura Valle. Clin Gastroenterol Hepatol 2017
29
18

Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
Rachel Pearlman, Wendy L Frankel, Benjamin Swanson, Weiqiang Zhao, Ahmet Yilmaz, Kristin Miller, Jason Bacher, Christopher Bigley, Lori Nelsen, Paul J Goodfellow,[...]. JAMA Oncol 2017
341
18

Hallmarks of cancer: the next generation.
Douglas Hanahan, Robert A Weinberg. Cell 2011
18

Molecular origins of cancer: Molecular basis of colorectal cancer.
Sanford D Markowitz, Monica M Bertagnolli. N Engl J Med 2009
18

Update on Hereditary Colorectal Cancer.
Felipe Carneiro DA Silva, Patrik Wernhoff, Constantino Dominguez-Barrera, Mev Dominguez-Valentin. Anticancer Res 2016
40
18

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype.
Judith E Grolleman, Richarda M de Voer, Fadwa A Elsayed, Maartje Nielsen, Robbert D A Weren, Claire Palles, Marjolijn J L Ligtenberg, Janet R Vos, Sanne W Ten Broeke, Noel F C C de Miranda,[...]. Cancer Cell 2019
80
18

Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland.
P Lichtenstein, N V Holm, P K Verkasalo, A Iliadou, J Kaprio, M Koskenvuo, E Pukkala, A Skytthe, K Hemminki. N Engl J Med 2000
18

Better prediction of functional effects for sequence variants.
Maximilian Hecht, Yana Bromberg, Burkhard Rost. BMC Genomics 2015
264
18


Whole Genome Sequencing of Familial Non-Medullary Thyroid Cancer Identifies Germline Alterations in MAPK/ERK and PI3K/AKT Signaling Pathways.
Aayushi Srivastava, Abhishek Kumar, Sara Giangiobbe, Elena Bonora, Kari Hemminki, Asta Försti, Obul Reddy Bandapalli. Biomolecules 2019
19
18

Cancer Genome Interpreter annotates the biological and clinical relevance of tumor alterations.
David Tamborero, Carlota Rubio-Perez, Jordi Deu-Pons, Michael P Schroeder, Ana Vivancos, Ana Rovira, Ignasi Tusquets, Joan Albanell, Jordi Rodon, Josep Tabernero,[...]. Genome Med 2018
238
18

Germline mutations in oncogene-induced senescence pathways are associated with multiple sessile serrated adenomas.
Manish K Gala, Yusuke Mizukami, Long P Le, Kentaro Moriichi, Thomas Austin, Masayoshi Yamamoto, Gregory Y Lauwers, Nabeel Bardeesy, Daniel C Chung. Gastroenterology 2014
88
18

Somatic APC mosaicism: an underestimated cause of polyposis coli.
F J Hes, M Nielsen, E C Bik, D Konvalinka, J T Wijnen, E Bakker, H F A Vasen, M H Breuning, C M J Tops. Gut 2008
105
12

Adenoma development in familial adenomatous polyposis and MUTYH-associated polyposis: somatic landscape and driver genes.
Mamunur Rashid, Andrej Fischer, Cathy H Wilson, Jessamy Tiffen, Alistair G Rust, Philip Stevens, Shelley Idziaszczyk, Julie Maynard, Geraint T Williams, Ville Mustonen,[...]. J Pathol 2016
29
12

Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases.
Isabel Spier, Dmitriy Drichel, Martin Kerick, Jutta Kirfel, Sukanya Horpaopan, Andreas Laner, Stefanie Holzapfel, Sophia Peters, Ronja Adam, Bixiao Zhao,[...]. J Med Genet 2016
34
12

A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiency.
Katharina Wimmer, Andreas Beilken, Rainer Nustede, Tim Ripperger, Britta Lamottke, Benno Ure, Diana Steinmann, Tanja Reineke-Plaass, Ulrich Lehmann, Johannes Zschocke,[...]. Fam Cancer 2017
37
12

Familial adenomatous polyposis.
Elizabeth Half, Dani Bercovich, Paul Rozen. Orphanet J Rare Dis 2009
309
12

Identification of FAP locus genes from chromosome 5q21.
K W Kinzler, M C Nilbert, L K Su, B Vogelstein, T M Bryan, D B Levy, K J Smith, A C Preisinger, P Hedge, D McKechnie. Science 1991
12

Somatic APC mosaicism: a frequent cause of familial adenomatous polyposis (FAP).
Stefan Aretz, Dietlinde Stienen, Nicolaus Friedrichs, Susanne Stemmler, Siegfried Uhlhaas, Nils Rahner, Peter Propping, Waltraut Friedl. Hum Mutat 2007
97
12

A novel POLE mutation associated with cancers of colon, pancreas, ovaries and small intestine.
Maren F Hansen, Jostein Johansen, Inga Bjørnevoll, Anna E Sylvander, Kristin S Steinsbekk, Pål Sætrom, Arne K Sandvik, Finn Drabløs, Wenche Sjursen. Fam Cancer 2015
52
12

Familial adenomatous polyposis.
Polymnia Galiatsatos, William D Foulkes. Am J Gastroenterol 2006
343
12


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.