A citation-based method for searching scientific literature

B Rivera, J Perea, E Sánchez, M Villapún, E Sánchez-Tomé, F Mercadillo, M Robledo, J Benítez, M Urioste. Eur J Hum Genet 2014
Times Cited: 33







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



Times Cited
  Times     Co-cited
Similarity


Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer.
Laura Lammi, Sirpa Arte, Mirja Somer, Heikki Jarvinen, Paivi Lahermo, Irma Thesleff, Sinikka Pirinen, Pekka Nieminen. Am J Hum Genet 2004
431
72

AXIN2-associated autosomal dominant ectodermal dysplasia and neoplastic syndrome.
Monica L Marvin, Serina M Mazzoni, Casey M Herron, Sean Edwards, Stephen B Gruber, Elizabeth M Petty. Am J Med Genet A 2011
58
66

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
54

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
51

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
48

ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
Sapna Syngal, Randall E Brand, James M Church, Francis M Giardiello, Heather L Hampel, Randall W Burt. Am J Gastroenterol 2015
800
36

POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillance.
Fernando Bellido, Marta Pineda, Gemma Aiza, Rafael Valdés-Mas, Matilde Navarro, Diana A Puente, Tirso Pons, Sara González, Silvia Iglesias, Esther Darder,[...]. Genet Med 2016
154
36

Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1.
Emma Jaeger, Simon Leedham, Annabelle Lewis, Stefania Segditsas, Martin Becker, Pedro Rodenas Cuadrado, Hayley Davis, Kulvinder Kaur, Karl Heinimann, Kimberley Howarth,[...]. Nat Genet 2012
151
33

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
33


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
30

Validation of Recently Proposed Colorectal Cancer Susceptibility Gene Variants in an Analysis of Families and Patients-a Systematic Review.
Peter Broderick, Sara E Dobbins, Daniel Chubb, Ben Kinnersley, Malcolm G Dunlop, Ian Tomlinson, Richard S Houlston. Gastroenterology 2017
60
30

Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer.
Aung Ko Win, James G Dowty, Sean P Cleary, Hyeja Kim, Daniel D Buchanan, Joanne P Young, Mark Clendenning, Christophe Rosty, Robert J MacInnis, Graham G Giles,[...]. Gastroenterology 2014
114
27

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
27

Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors.
Nada Al-Tassan, Nikolas H Chmiel, Julie Maynard, Nick Fleming, Alison L Livingston, Geraint T Williams, Angela K Hodges, D Rhodri Davies, Sheila S David, Julian R Sampson,[...]. Nat Genet 2002
934
24

GREM1 and POLE variants in hereditary colorectal cancer syndromes.
Anna Rohlin, Frida Eiengård, Ulf Lundstam, Theofanis Zagoras, Staffan Nilsson, Anders Edsjö, Jan Pedersen, Janhenry Svensson, Stefan Skullman, B Göran Karlsson,[...]. Genes Chromosomes Cancer 2016
31
25

Germline mutation of RPS20, encoding a ribosomal protein, causes predisposition to hereditary nonpolyposis colorectal carcinoma without DNA mismatch repair deficiency.
Taina T Nieminen, Marie-Françoise O'Donohue, Yunpeng Wu, Hannes Lohi, Stephen W Scherer, Andrew D Paterson, Pekka Ellonen, Wael M Abdel-Rahman, Satu Valo, Jukka-Pekka Mecklin,[...]. Gastroenterology 2014
113
24

New insights into POLE and POLD1 germline mutations in familial colorectal cancer and polyposis.
Laura Valle, Eva Hernández-Illán, Fernando Bellido, Gemma Aiza, Adela Castillejo, María-Isabel Castillejo, Matilde Navarro, Nuria Seguí, Gardenia Vargas, Carla Guarinos,[...]. Hum Mol Genet 2014
102
24

Germline variants in POLE are associated with early onset mismatch repair deficient colorectal cancer.
Fadwa A Elsayed, C Marleen Kets, Dina Ruano, Brendy van den Akker, Arjen R Mensenkamp, Melanie Schrumpf, Maartje Nielsen, Juul T Wijnen, Carli M Tops, Marjolijn J Ligtenberg,[...]. Eur J Hum Genet 2015
77
24

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
24

Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1.
Daniel D Buchanan, Jenna R Stewart, Mark Clendenning, Christophe Rosty, Khalid Mahmood, Bernard J Pope, Mark A Jenkins, John L Hopper, Melissa C Southey, Finlay A Macrae,[...]. Genet Med 2018
30
26

NTHL1 and MUTYH polyposis syndromes: two sides of the same coin?
Robbert DA Weren, Marjolijn Jl Ligtenberg, Ad Geurts van Kessel, Richarda M De Voer, Nicoline Hoogerbrugge, Roland P Kuiper. J Pathol 2018
41
24

Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
Matthew B Yurgelun, Brian Allen, Rajesh R Kaldate, Karla R Bowles, Thaddeus Judkins, Praveen Kaushik, Benjamin B Roa, Richard J Wenstrup, Anne-Renee Hartman, Sapna Syngal. Gastroenterology 2015
167
21

Inactivating germ-line and somatic mutations in polypeptide N-acetylgalactosaminyltransferase 12 in human colon cancers.
Kishore Guda, Helen Moinova, Jian He, Oliver Jamison, Lakshmeswari Ravi, Leanna Natale, James Lutterbaugh, Earl Lawrence, Susan Lewis, James K V Willson,[...]. Proc Natl Acad Sci U S A 2009
107
21

Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and Surveillance.
Sari Lieberman, Tom Walsh, Menachem Schechter, Tomer Adar, Eran Goldin, Rachel Beeri, Nitzan Sharon, Hagit Baris, Liat Ben Avi, Elizabeth Half,[...]. Gastroenterology 2017
24
29

Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.
Matthew B Yurgelun, Matthew H Kulke, Charles S Fuchs, Brian A Allen, Hajime Uno, Jason L Hornick, Chinedu I Ukaegbu, Lauren K Brais, Philip G McNamara, Robert J Mayer,[...]. J Clin Oncol 2017
240
21

Inherited deleterious variants in GALNT12 are associated with CRC susceptibility.
Erica Clarke, Roger C Green, Jane S Green, Krista Mahoney, Patrick S Parfrey, H Banfield Younghusband, Michael O Woods. Hum Mutat 2012
37
21

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
24

Hereditary and familial colon cancer.
Kory W Jasperson, Thérèse M Tuohy, Deborah W Neklason, Randall W Burt. Gastroenterology 2010
683
21

Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene.
Catherine Beard, Rebecca Purvis, Ingrid M Winship, Finlay A Macrae, Daniel D Buchanan. Fam Cancer 2019
13
53

Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating beta-catenin/TCF signalling.
W Liu, X Dong, M Mai, R S Seelan, K Taniguchi, K K Krishnadath, K C Halling, J M Cunningham, L A Boardman, C Qian,[...]. Nat Genet 2000
404
18

Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair.
Nuria Seguí, Leonardo B Mina, Conxi Lázaro, Rebeca Sanz-Pamplona, Tirso Pons, Matilde Navarro, Fernando Bellido, Adriana López-Doriga, Rafael Valdés-Mas, Marta Pineda,[...]. Gastroenterology 2015
75
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

A deleterious RNF43 germline mutation in a severely affected serrated polyposis kindred.
Douglas Taupin, Wesley Lam, David Rangiah, Larissa McCallum, Belinda Whittle, Yafei Zhang, Daniel Andrews, Matthew Field, Christopher C Goodnow, Matthew C Cook. Hum Genome Var 2015
36
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

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
18

Clinical and molecular features of the hereditary mixed polyposis syndrome.
S C Whitelaw, V A Murday, I P Tomlinson, H J Thomas, S Cottrell, A Ginsberg, S Bukofzer, S V Hodgson, R B Skudowitz, J R Jass,[...]. Gastroenterology 1997
93
18

A mutation in POLE predisposing to a multi-tumour phenotype.
Anna Rohlin, Theofanis Zagoras, Staffan Nilsson, Ulf Lundstam, Jan Wahlström, Leif Hultén, Tommy Martinsson, Göran B Karlsson, Margareta Nordling. Int J Oncol 2014
45
18

Germline TP53 Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family Registry.
Matthew B Yurgelun, Serena Masciari, Victoria A Joshi, Rowena C Mercado, Noralane M Lindor, Steven Gallinger, John L Hopper, Mark A Jenkins, Daniel D Buchanan, Polly A Newcomb,[...]. JAMA Oncol 2015
61
18

POLE and POLD1 screening in 155 patients with multiple polyps and early-onset colorectal cancer.
Clara Esteban-Jurado, David Giménez-Zaragoza, Jenifer Muñoz, Sebastià Franch-Expósito, Miriam Álvarez-Barona, Teresa Ocaña, Miriam Cuatrecasas, Sabela Carballal, María López-Cerón, Maria Marti-Solano,[...]. Oncotarget 2017
30
20

Lack of evidence for germline RNF43 mutations in patients with serrated polyposis syndrome from a large multinational study.
Daniel D Buchanan, Mark Clendenning, Li Zhuoer, Jenna R Stewart, Sharelle Joseland, Sonja Woodall, Julie Arnold, Kara Semotiuk, Melyssa Aronson, Spring Holter,[...]. Gut 2017
32
18

Mutations in the SMAD4/DPC4 gene in juvenile polyposis.
J R Howe, S Roth, J C Ringold, R W Summers, H J Järvinen, P Sistonen, I P Tomlinson, R S Houlston, S Bevan, F A Mitros,[...]. Science 1998
670
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

Extending the clinical phenotype associated with biallelic NTHL1 germline mutations.
Florentia Fostira, Emmanouil Kontopodis, Paraskevi Apostolou, Maria Fragkaki, Nikolaos Androulakis, Drakoulis Yannoukakos, Irene Konstantopoulou, Emmanouil Saloustros. Clin Genet 2018
18
33

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
15

Identification and characterization of the familial adenomatous polyposis coli gene.
J Groden, A Thliveris, W Samowitz, M Carlson, L Gelbert, H Albertsen, G Joslyn, J Stevens, L Spirio, M Robertson. Cell 1991
15

Familial adenomatous polyposis.
Polymnia Galiatsatos, William D Foulkes. Am J Gastroenterol 2006
343
15

Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD).
Katharina Wimmer, Christian P Kratz, Hans F A Vasen, Olivier Caron, Chrystelle Colas, Natacha Entz-Werle, Anne-Marie Gerdes, Yael Goldberg, Denisa Ilencikova, Martine Muleris,[...]. J Med Genet 2014
253
15

Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22.
Courtney Gray-McGuire, Kishore Guda, Indra Adrianto, Chee Paul Lin, Leanna Natale, John D Potter, Polly Newcomb, Elizabeth M Poole, Cornelia M Ulrich, Noralane Lindor,[...]. Cancer Res 2010
37
15

Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer.
Daniel Chubb, Peter Broderick, Sara E Dobbins, Matthew Frampton, Ben Kinnersley, Steven Penegar, Amy Price, Yussanne P Ma, Amy L Sherborne, Claire Palles,[...]. Nat Commun 2016
93
15


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.