A citation-based method for searching scientific literature

Mariona Terradas, Gabriel Capellá, Laura Valle. J Clin Med 2020
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity



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
66

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
66

Update on genetic predisposition to colorectal cancer and polyposis.
Laura Valle, Richarda M de Voer, Yael Goldberg, Wenche Sjursen, Asta Försti, Clara Ruiz-Ponte, Trinidad Caldés, Pilar Garré, Maren F Olsen, Margareta Nordling,[...]. Mol Aspects Med 2019
70
50

Candidate genes for hereditary colorectal cancer: Mutational screening and systematic review.
Sami Belhadj, Mariona Terradas, Pau M Munoz-Torres, Gemma Aiza, Matilde Navarro, Gabriel Capellá, Laura Valle. Hum Mutat 2020
18
50

Cumulative Burden of Colorectal Cancer-Associated Genetic Variants Is More Strongly Associated With Early-Onset vs Late-Onset Cancer.
Alexi N Archambault, Yu-Ru Su, Jihyoun Jeon, Minta Thomas, Yi Lin, David V Conti, Aung Ko Win, Lori C Sakoda, Iris Lansdorp-Vogelaar, Elisabeth F P Peterse,[...]. Gastroenterology 2020
61
50

Contribution to colonic polyposis of recently proposed predisposing genes and assessment of the prevalence of NTHL1- and MSH3-associated polyposes.
Mariona Terradas, Pau M Munoz-Torres, Sami Belhadj, Gemma Aiza, Matilde Navarro, Joan Brunet, Gabriel Capellá, Laura Valle. Hum Mutat 2019
18
50

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
33

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
33

High Prevalence of Hereditary Cancer Syndromes in Adolescents and Young Adults With Colorectal Cancer.
Maureen E Mork, Y Nancy You, Jun Ying, Sarah A Bannon, Patrick M Lynch, Miguel A Rodriguez-Bigas, Eduardo Vilar. J Clin Oncol 2015
114
33

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
33

Germline Genetic Features of Young Individuals With Colorectal Cancer.
Elena M Stoffel, Erika Koeppe, Jessica Everett, Peter Ulintz, Mark Kiel, Jenae Osborne, Linford Williams, Kristen Hanson, Stephen B Gruber, Laura S Rozek. Gastroenterology 2018
135
33

A novel ribosomal protein S20 variant in a family with unexplained colorectal cancer and polyposis.
Bryony A Thompson, Angela K Snow, Cathryn Koptiuch, Wendy K Kohlmann, Ryan Mooney, Sara Johnson, Chad D Huff, Yao Yu, Craig C Teerlink, Bing-Jian Feng,[...]. Clin Genet 2020
12
33

First evidence for digenic inheritance in hereditary colorectal cancer by mutations in the base excision repair genes.
Monika Morak, Trisari Massdorf, Helena Sykora, Martina Kerscher, Elke Holinski-Feder. Eur J Cancer 2011
28
33

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
33

A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patients.
Holly LaDuca, Eric C Polley, Amal Yussuf, Lily Hoang, Stephanie Gutierrez, Steven N Hart, Siddhartha Yadav, Chunling Hu, Jie Na, David E Goldgar,[...]. Genet Med 2020
80
33

Somatic APC mosaicism and oligogenic inheritance in genetically unsolved colorectal adenomatous polyposis patients.
Michele Ciavarella, Sara Miccoli, Anna Prossomariti, Tommaso Pippucci, Elena Bonora, Francesco Buscherini, Flavia Palombo, Roberta Zuntini, Tiziana Balbi, Claudio Ceccarelli,[...]. Eur J Hum Genet 2018
18
33

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
33

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
33

The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
Aaron McKenna, Matthew Hanna, Eric Banks, Andrey Sivachenko, Kristian Cibulskis, Andrew Kernytsky, Kiran Garimella, David Altshuler, Stacey Gabriel, Mark Daly,[...]. Genome Res 2010
33

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
33

Efficacy of immune checkpoint blockade in MUTYH-associated hereditary colorectal cancer.
Nikita M Volkov, Grigoriy A Yanus, Alexandr O Ivantsov, Fedor V Moiseenko, Olga G Matorina, Ilya V Bizin, Vladimir M Moiseyenko, Evgeny N Imyanitov. Invest New Drugs 2020
11
33

Update on the World Health Organization Criteria for Diagnosis of Serrated Polyposis Syndrome.
Evelien Dekker, Arne Bleijenberg, Francesc Balaguer. Gastroenterology 2020
22
33

Pembrolizumab in Microsatellite-Instability-High Advanced Colorectal Cancer.
Thierry André, Kai-Keen Shiu, Tae Won Kim, Benny Vittrup Jensen, Lars Henrik Jensen, Cornelis Punt, Denis Smith, Rocio Garcia-Carbonero, Manuel Benavides, Peter Gibbs,[...]. N Engl J Med 2020
660
33

NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas.
Sami Belhadj, Isabel Quintana, Pilar Mur, Pau M Munoz-Torres, M Henar Alonso, Matilde Navarro, Mariona Terradas, Virginia Piñol, Joan Brunet, Victor Moreno,[...]. Sci Rep 2019
16
33

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

Evidence suggests that germline RNF43 mutations are a rare cause of serrated polyposis.
Isabel Quintana, Raquel Mejías-Luque, Mariona Terradas, Matilde Navarro, Virginia Piñol, Pilar Mur, Sami Belhadj, Elia Grau, Esther Darder, Ares Solanes,[...]. Gut 2018
36
33

Discovery of common and rare genetic risk variants for colorectal cancer.
Jeroen R Huyghe, Stephanie A Bien, Tabitha A Harrison, Hyun Min Kang, Sai Chen, Stephanie L Schmit, David V Conti, Conghui Qu, Jihyoun Jeon, Christopher K Edlund,[...]. Nat Genet 2019
208
33

Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia.
Xose S Puente, Magda Pinyol, Víctor Quesada, Laura Conde, Gonzalo R Ordóñez, Neus Villamor, Georgia Escaramis, Pedro Jares, Sílvia Beà, Marcos González-Díaz,[...]. Nature 2011
33

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
33

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
16

Clinical analysis of PMS2: mutation detection and avoidance of pseudogenes.
Cecily P Vaughn, Jorge Robles, Jeffrey J Swensen, Christine E Miller, Elaine Lyon, Rong Mao, Pinar Bayrak-Toydemir, Wade S Samowitz. Hum Mutat 2010
68
16

Mosdepth: quick coverage calculation for genomes and exomes.
Brent S Pedersen, Aaron R Quinlan. Bioinformatics 2018
227
16

GALNT12 is not a major contributor of familial colorectal cancer type X.
Nuria Seguí, Marta Pineda, Matilde Navarro, Conxi Lázaro, Joan Brunet, Mar Infante, Mercedes Durán, José Luis Soto, Ignacio Blanco, Gabriel Capellá,[...]. Hum Mutat 2014
18
16

Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results.
Sharon E Plon, Diana M Eccles, Douglas Easton, William D Foulkes, Maurizio Genuardi, Marc S Greenblatt, Frans B L Hogervorst, Nicoline Hoogerbrugge, Amanda B Spurdle, Sean V Tavtigian. Hum Mutat 2008
607
16

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
16

A rare missense variant in APC interrupts splicing and causes AFAP in two Danish families.
Malene Djursby, Karin Wadt, Jane Hübertz Frederiksen, Majbritt Busk Madsen, Lukas Adrian Berchtold, Jane Preuss Hasselby, Gro Linno Willemoe, Thomas V O Hansen, Anne-Marie Gerdes. Hered Cancer Clin Pract 2020
1
100

Orexin activation counteracts decreases in nonexercise activity thermogenesis (NEAT) caused by high-fat diet.
P E Bunney, A N Zink, A A Holm, C J Billington, C M Kotz. Physiol Behav 2017
610
16

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
16

Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.
Anna Rohlin, Eva Rambech, Anders Kvist, Therese Törngren, Frida Eiengård, Ulf Lundstam, Theofanis Zagoras, Samuel Gebre-Medhin, Åke Borg, Jan Björk,[...]. Fam Cancer 2017
39
16

Novel genetic mutations detected by multigene panel are associated with hereditary colorectal cancer predisposition.
Lorena Martin-Morales, Paula Rofes, Eduardo Diaz-Rubio, Patricia Llovet, Victor Lorca, Inmaculada Bando, Pedro Perez-Segura, Miguel de la Hoya, Pilar Garre, Vanesa Garcia-Barberan,[...]. PLoS One 2018
13
16

Genetic diagnosis of high-penetrance susceptibility for colorectal cancer (CRC) is achievable for a high proportion of familial CRC by exome sequencing.
Daniel Chubb, Peter Broderick, Matthew Frampton, Ben Kinnersley, Amy Sherborne, Steven Penegar, Amy Lloyd, Yussanne P Ma, Sara E Dobbins, Richard S Houlston. J Clin Oncol 2015
64
16

Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers.
Gaëlle Bougeard, Mariette Renaux-Petel, Jean-Michel Flaman, Camille Charbonnier, Pierre Fermey, Muriel Belotti, Marion Gauthier-Villars, Dominique Stoppa-Lyonnet, Emilie Consolino, Laurence Brugières,[...]. J Clin Oncol 2015
357
16

Germline epigenetic silencing of the tumor suppressor gene PTPRJ in early-onset familial colorectal cancer.
Ramprasath Venkatachalam, Marjolijn J L Ligtenberg, Nicoline Hoogerbrugge, Hans K Schackert, Heike Görgens, Marc-Manuel Hahn, Eveline J Kamping, Lilian Vreede, Eveline Hoenselaar, Erica van der Looij,[...]. Gastroenterology 2010
33
16

Role of GALNT12 in the genetic predisposition to attenuated adenomatous polyposis syndrome.
Víctor Lorca, Daniel Rueda, Lorena Martín-Morales, Carmen Poves, María Jesús Fernández-Aceñero, Clara Ruiz-Ponte, Patricia Llovet, David Marrupe, Vanesa García-Barberán, Beatriz García-Paredes,[...]. PLoS One 2017
8
16

Detection of PMS2 Mutations by Screening Hereditary Nonpolyposis Colon Cancer Families from Denmark and Sweden.
Henrik Okkels, Kristina Lagerstedt-Robinsson, Friedrik P Wikman, Thomas V O Hansen, Ihab Lolas, Lars Joachim Lindberg, Henrik B Krarup. Genet Test Mol Biomarkers 2019
1
100

Interplay between human nucleolar GNL1 and RPS20 is critical to modulate cell proliferation.
Rehna Krishnan, Neelima Boddapati, Sundarasamy Mahalingam. Sci Rep 2018
9
16

Evidence for GALNT12 as a moderate penetrance gene for colorectal cancer.
Daniel R Evans, Srividya Venkitachalam, Leslie Revoredo, Amanda T Dohey, Erica Clarke, Julia J Pennell, Amy E Powell, Erina Quinn, Lakshmeswari Ravi, Thomas A Gerken,[...]. Hum Mutat 2018
11
16

Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposis.
Pilar Mur, Ann-Sofie Jemth, Luka Bevc, Nuno Amaral, Matilde Navarro, Rafael Valdés-Mas, Tirso Pons, Gemma Aiza, Miguel Urioste, Alfonso Valencia,[...]. Hum Mutat 2018
6
16

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
16


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.