A citation-based method for searching scientific literature

Manon Suerink, Mar Rodríguez-Girondo, Heleen M van der Klift, Chrystelle Colas, Laurence Brugieres, Noémie Lavoine, Marjolijn Jongmans, Gabriel Capellá Munar, D Gareth Evans, Michael P Farrell, Maurizio Genuardi, Yael Goldberg, Encarna Gomez-Garcia, Karl Heinimann, Jessica I Hoell, Stefan Aretz, Kory W Jasperson, Inbal Kedar, Mitul B Modi, Sergey Nikolaev, Theo A M van Os, Tim Ripperger, Daniel Rueda, Leigha Senter, Wenche Sjursen, Lone Sunde, Christina Therkildsen, Maria G Tibiletti, Alison H Trainer, Yvonne J Vos, Anja Wagner, Ingrid Winship, Katharina Wimmer, Stefanie Y Zimmermann, Hans F Vasen, Christi J van Asperen, Jeanine J Houwing-Duistermaat, Sanne W Ten Broeke, Maartje Nielsen. Genet Med 2019
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database.
Pål Møller, Toni Seppälä, Inge Bernstein, Elke Holinski-Feder, Paola Sala, D Gareth Evans, Annika Lindblom, Finlay Macrae, Ignacio Blanco, Rolf Sijmons,[...]. Gut 2017
237
100

CTNNB1-mutant colorectal carcinomas with immediate invasive growth: a model of interval cancers in Lynch syndrome.
Aysel Ahadova, Magnus von Knebel Doeberitz, Hendrik Bläker, Matthias Kloor. Fam Cancer 2016
44
100

Cancer Risks for PMS2-Associated Lynch Syndrome.
Sanne W Ten Broeke, Heleen M van der Klift, Carli M J Tops, Stefan Aretz, Inge Bernstein, Daniel D Buchanan, Albert de la Chapelle, Gabriel Capella, Mark Clendenning, Christoph Engel,[...]. J Clin Oncol 2018
80
100

Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database.
Pål Møller, Toni T Seppälä, Inge Bernstein, Elke Holinski-Feder, Paulo Sala, D Gareth Evans, Annika Lindblom, Finlay Macrae, Ignacio Blanco, Rolf H Sijmons,[...]. Gut 2018
215
100

Three molecular pathways model colorectal carcinogenesis in Lynch syndrome.
Aysel Ahadova, Richard Gallon, Johannes Gebert, Alexej Ballhausen, Volker Endris, Martina Kirchner, Albrecht Stenzinger, John Burn, Magnus von Knebel Doeberitz, Hendrik Bläker,[...]. Int J Cancer 2018
62
66


Prevalence of mismatch repair-deficient crypt foci in Lynch syndrome: a pathological study.
Matthias Kloor, Cathrin Huth, Anita Y Voigt, Axel Benner, Peter Schirmacher, Magnus von Knebel Doeberitz, Hendrik Bläker. Lancet Oncol 2012
85
66

Mismatch repair deficiency commonly precedes adenoma formation in Lynch Syndrome-Associated colorectal tumorigenesis.
Shigeki Sekine, Taisuke Mori, Reiko Ogawa, Masahiro Tanaka, Hiroshi Yoshida, Hirokazu Taniguchi, Takeshi Nakajima, Kokichi Sugano, Teruhiko Yoshida, Mamoru Kato,[...]. Mod Pathol 2017
35
66

Update on Lynch syndrome genomics.
Päivi Peltomäki. Fam Cancer 2016
85
66

RNF43 is mutated less frequently in Lynch Syndrome compared with sporadic microsatellite unstable colorectal cancers.
Lochlan J Fennell, Mark Clendenning, Diane M McKeone, Saara H Jamieson, Samanthy Balachandran, Jennifer Borowsky, John Liu, Futoshi Kawamata, Catherine E Bond, Christophe Rosty,[...]. Fam Cancer 2018
9
66

Milestones of Lynch syndrome: 1895-2015.
Henry T Lynch, Carrie L Snyder, Trudy G Shaw, Christopher D Heinen, Megan P Hitchins. Nat Rev Cancer 2015
345
66

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability.
Asad Umar, C Richard Boland, Jonathan P Terdiman, Sapna Syngal, Albert de la Chapelle, Josef Rüschoff, Richard Fishel, Noralane M Lindor, Lawrence J Burgart, Richard Hamelin,[...]. J Natl Cancer Inst 2004
66

Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2.
Sanne W Ten Broeke, Tom C van Bavel, Anne M L Jansen, Encarnca Gómez-García, Frederik J Hes, Liselot P van Hest, Tom G W Letteboer, Maran J W Olderode-Berends, Dina Ruano, Liesbeth Spruijt,[...]. Gastroenterology 2018
16
66

Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome.
Christoph Engel, Aysel Ahadova, Toni T Seppälä, Stefan Aretz, Marloes Bigirwamungu-Bargeman, Hendrik Bläker, Karolin Bucksch, Reinhard Büttner, Wouter T de Vos Tot Nederveen Cappel, Volker Endris,[...]. Gastroenterology 2020
22
66

Target gene mutational pattern in Lynch syndrome colorectal carcinomas according to tumour location and germline mutation.
Manuela Pinheiro, Carla Pinto, Ana Peixoto, Isabel Veiga, Paula Lopes, Rui Henrique, Helena Baldaia, Fátima Carneiro, Raquel Seruca, Ian Tomlinson,[...]. Br J Cancer 2015
22
66

The "unnatural" history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillance.
Aysel Ahadova, Toni T Seppälä, Christoph Engel, Richard Gallon, John Burn, Elke Holinski-Feder, Verena Steinke-Lange, Gabriela Möslein, Maartje Nielsen, Sanne W Ten Broeke,[...]. Int J Cancer 2021
8
66

Association of Mismatch Repair Mutation With Age at Cancer Onset in Lynch Syndrome: Implications for Stratified Surveillance Strategies.
Neil A J Ryan, Julie Morris, Kate Green, Fiona Lalloo, Emma R Woodward, James Hill, Emma J Crosbie, D Gareth Evans. JAMA Oncol 2017
63
66


Frequent mutation of beta-catenin and APC genes in primary colorectal tumors from patients with hereditary nonpolyposis colorectal cancer.
M Miyaki, T Iijima, J Kimura, M Yasuno, T Mori, Y Hayashi, M Koike, N Shitara, T Iwama, T Kuroki. Cancer Res 1999
156
33

The SWI/SNF complex and cancer.
D Reisman, S Glaros, E A Thompson. Oncogene 2009
410
33

Toward a Molecular Classification of Colorectal Cancer: The Role of BRAF.
Alexandra Thiel, Ari Ristimäki. Front Oncol 2013
34
33

Frequent frameshift mutations in 2 mononucleotide repeats of RNF43 gene and its regional heterogeneity in gastric and colorectal cancers.
Yun Sol Jo, Min Sung Kim, Ju Hwa Lee, Sug Hyung Lee, Chang Hyeok An, Nam Jin Yoo. Hum Pathol 2015
17
33

RNF43 is frequently mutated in colorectal and endometrial cancers.
Marios Giannakis, Eran Hodis, Xinmeng Jasmine Mu, Mai Yamauchi, Joseph Rosenbluh, Kristian Cibulskis, Gordon Saksena, Michael S Lawrence, Zhi Rong Qian, Reiko Nishihara,[...]. Nat Genet 2014
267
33

Loss of ARID1A expression and its relationship with PI3K-Akt pathway alterations, TP53 and microsatellite instability in endometrial cancer.
Tjalling Bosse, Natalja T ter Haar, Laura M Seeber, Paul J v Diest, Frederik J Hes, Hans F A Vasen, Remi A Nout, Carien L Creutzberg, Hans Morreau, Vincent T H B M Smit. Mod Pathol 2013
118
33


Lynch syndrome in the 21st century: clinical perspectives.
A K Tiwari, H K Roy, H T Lynch. QJM 2016
61
33

FBXW7 missense mutation: a novel negative prognostic factor in metastatic colorectal adenocarcinoma.
Krittiya Korphaisarn, Van Karlyle Morris, Michael J Overman, David R Fogelman, Bryan K Kee, Kanwal Pratap Singh Raghav, Shanequa Manuel, Imad Shureiqi, Robert A Wolff, Cathy Eng,[...]. Oncotarget 2017
38
33

Genetic and genomic basis of the mismatch repair system involved in Lynch syndrome.
Kazuo Tamura, Motohide Kaneda, Mashu Futagawa, Miho Takeshita, Sanghyuk Kim, Mina Nakama, Norihito Kawashita, Junko Tatsumi-Miyajima. Int J Clin Oncol 2019
19
33

Molecular genetics of colorectal cancer.
Eric R Fearon. Annu Rev Pathol 2011
33

Alternate-day, low-dose aspirin and cancer risk: long-term observational follow-up of a randomized trial.
Nancy R Cook, I-Min Lee, Shumin M Zhang, M Vinayaga Moorthy, Julie E Buring. Ann Intern Med 2013
198
33

Mechanistic aspects of COX-2 expression in colorectal neoplasia.
Dan A Dixon, Fernando F Blanco, Annalisa Bruno, Paola Patrignani. Recent Results Cancer Res 2013
62
33

Mismatch repair and DNA damage signalling.
Lovorka Stojic, Richard Brun, Josef Jiricny. DNA Repair (Amst) 2004
291
33

Loss of ARID1A/BAF250a expression in ovarian endometriosis and clear cell carcinoma.
Wenbin Xiao, Amad Awadallah, Wei Xin. Int J Clin Exp Pathol 2012
50
33

Mismatch repair deficient-crypts in non-neoplastic colonic mucosa in Lynch syndrome: insights from an illustrative case.
Jinru Shia, Zsofia K Stadler, Martin R Weiser, Efsevia Vakiani, Robin Mendelsohn, Arnold J Markowitz, Moshe Shike, C Richard Boland, David S Klimstra. Fam Cancer 2015
16
33

BRAF mutation is frequently present in sporadic colorectal cancer with methylated hMLH1, but not in hereditary nonpolyposis colorectal cancer.
Guoren Deng, Ian Bell, Suzanne Crawley, James Gum, Jonathan P Terdiman, Brian A Allen, Brindusa Truta, Marvin H Sleisenger, Young S Kim. Clin Cancer Res 2004
302
33

Signatures of mutational processes in human cancer.
Ludmil B Alexandrov, Serena Nik-Zainal, David C Wedge, Samuel A J R Aparicio, Sam Behjati, Andrew V Biankin, Graham R Bignell, Niccolò Bolli, Ake Borg, Anne-Lise Børresen-Dale,[...]. Nature 2013
33

BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing.
E Domingo, P Laiho, M Ollikainen, M Pinto, L Wang, A J French, J Westra, T Frebourg, E Espín, M Armengol,[...]. J Med Genet 2004
252
33

Somatic mutations in the chromatin remodeling gene ARID1A occur in several tumor types.
Siân Jones, Meng Li, D Williams Parsons, Xiaosong Zhang, Jelle Wesseling, Petra Kristel, Marjanka K Schmidt, Sanford Markowitz, Hai Yan, Darell Bigner,[...]. Hum Mutat 2012
198
33

Analysis of PTEN, BRAF, and EGFR status in determining benefit from cetuximab therapy in wild-type KRAS metastatic colon cancer.
Pierre Laurent-Puig, Anne Cayre, Gilles Manceau, Emmanuel Buc, Jean-Baptiste Bachet, Thierry Lecomte, Philippe Rougier, Astrid Lievre, Bruno Landi, Valérie Boige,[...]. J Clin Oncol 2009
539
33

Exome sequencing reveals frequent inactivating mutations in ARID1A, ARID1B, ARID2 and ARID4A in microsatellite unstable colorectal cancer.
Tatiana Cajuso, Ulrika A Hänninen, Johanna Kondelin, Alexandra E Gylfe, Tomas Tanskanen, Riku Katainen, Esa Pitkänen, Heikki Ristolainen, Eevi Kaasinen, Minna Taipale,[...]. Int J Cancer 2014
74
33

DNA mismatch repair and oxidative DNA damage: implications for cancer biology and treatment.
Gemma Bridge, Sukaina Rashid, Sarah A Martin. Cancers (Basel) 2014
62
33

Immunohistochemical detection of ARID1A in colorectal carcinoma: loss of staining is associated with sporadic microsatellite unstable tumors with medullary histology and high TNM stage.
Jiqing Ye, Yi Zhou, Martin R Weiser, Mithat Gönen, Liying Zhang, Tushar Samdani, Ruben Bacares, Deborah DeLair, Sinisa Ivelja, Efsevia Vakiani,[...]. Hum Pathol 2014
29
33

Increased incidence of FBXW7 and POLE proofreading domain mutations in young adult colorectal cancers.
Nishi Kothari, Jamie K Teer, Andrea M Abbott, Thejal Srikumar, Yonghong Zhang, Sean J Yoder, Andrew S Brohl, Richard D Kim, Damon R Reed, David Shibata. Cancer 2016
33
33

Mutational signature analysis identifies MUTYH deficiency in colorectal cancers and adrenocortical carcinomas.
Camilla Pilati, Jayendra Shinde, Ludmil B Alexandrov, Guillaume Assié, Thierry André, Zofia Hélias-Rodzewicz, Romain Ducoudray, Delphine Le Corre, Jessica Zucman-Rossi, Jean-François Emile,[...]. J Pathol 2017
70
33

Distinct mutational signatures characterize concurrent loss of polymerase proofreading and mismatch repair.
N J Haradhvala, J Kim, Y E Maruvka, P Polak, D Rosebrock, D Livitz, J M Hess, I Leshchiner, A Kamburov, K W Mouw,[...]. Nat Commun 2018
72
33

Portrait of a cancer: mutational signature analyses for cancer diagnostics.
Arne Van Hoeck, Niels H Tjoonk, Ruben van Boxtel, Edwin Cuppen. BMC Cancer 2019
37
33

Mutant p53 in colon cancer.
Mizuho Nakayama, Masanobu Oshima. J Mol Cell Biol 2019
65
33


FBXW7 in Cancer: What Has Been Unraveled Thus Far?
Bethsebie Lalduhsaki Sailo, Kishore Banik, Sosmitha Girisa, Devivasha Bordoloi, Lu Fan, Clarissa Esmeralda Halim, Hong Wang, Alan Prem Kumar, Dali Zheng, Xinliang Mao,[...]. Cancers (Basel) 2019
65
33

Frequent PIK3CA Mutations in Colorectal and Endometrial Tumors With 2 or More Somatic Mutations in Mismatch Repair Genes.
Stacey A Cohen, Emily H Turner, Mallory B Beightol, Angela Jacobson, Ted A Gooley, Stephen J Salipante, Sigurdis Haraldsdottir, Christina Smith, Sheena Scroggins, Jonathan F Tait,[...]. Gastroenterology 2016
24
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.