A citation-based method for searching scientific literature

Qing Liu, Luke B Hesson, Andrea C Nunez, Deborah Packham, Rachel Williams, Robyn L Ward, Mathew A Sloane. Carcinogenesis 2016
Times Cited: 22







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



Times Cited
  Times     Co-cited
Similarity



Colon and endometrial cancers with mismatch repair deficiency can arise from somatic, rather than germline, mutations.
Sigurdis Haraldsdottir, Heather Hampel, Jerneja Tomsic, Wendy L Frankel, Rachel Pearlman, Albert de la Chapelle, Colin C Pritchard. Gastroenterology 2014
243
50

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.
Marjolijn J L Ligtenberg, Roland P Kuiper, Tsun Leung Chan, Monique Goossens, Konnie M Hebeda, Marsha Voorendt, Tracy Y H Lee, Danielle Bodmer, Eveline Hoenselaar, Sandra J B Hendriks-Cornelissen,[...]. Nat Genet 2009
490
50

Somatic mutations in MLH1 and MSH2 are a frequent cause of mismatch-repair deficiency in Lynch syndrome-like tumors.
Arjen R Mensenkamp, Ingrid P Vogelaar, Wendy A G van Zelst-Stams, Monique Goossens, Hicham Ouchene, Sandra J B Hendriks-Cornelissen, Michael P Kwint, Nicoline Hoogerbrugge, Iris D Nagtegaal, Marjolijn J L Ligtenberg. Gastroenterology 2014
227
50

Biallelic MLH1 SNP cDNA expression or constitutional promoter methylation can hide genomic rearrangements causing Lynch syndrome.
Monika Morak, Udo Koehler, Hans Konrad Schackert, Verena Steinke, Brigitte Royer-Pokora, Karsten Schulmann, Matthias Kloor, Wilhelm Höchter, Josef Weingart, Cortina Keiling,[...]. J Med Genet 2011
55
40

Risk of cancer in cases of suspected lynch syndrome without germline mutation.
María Rodríguez-Soler, Lucía Pérez-Carbonell, Carla Guarinos, Pedro Zapater, Adela Castillejo, Victor M Barberá, Miriam Juárez, Xavier Bessa, Rosa M Xicola, Juan Clofent,[...]. Gastroenterology 2013
143
36

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
36

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.
Bryony A Thompson, Amanda B Spurdle, John-Paul Plazzer, Marc S Greenblatt, Kiwamu Akagi, Fahd Al-Mulla, Bharati Bapat, Inge Bernstein, Gabriel Capellá, Johan T den Dunnen,[...]. Nat Genet 2014
311
31

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).
Heather Hampel, Wendy L Frankel, Edward Martin, Mark Arnold, Karamjit Khanduja, Philip Kuebler, Hidewaki Nakagawa, Kaisa Sotamaa, Thomas W Prior, Judith Westman,[...]. N Engl J Med 2005
944
31

Combined mismatch repair and POLE/POLD1 defects explain unresolved suspected Lynch syndrome cancers.
Anne Ml Jansen, Tom van Wezel, Brendy Ewm van den Akker, Marina Ventayol Garcia, Dina Ruano, Carli Mj Tops, Anja Wagner, Tom Gw Letteboer, Encarna B Gómez-García, Peter Devilee,[...]. Eur J Hum Genet 2016
84
31

A 10-Mb paracentric inversion of chromosome arm 2p inactivates MSH2 and is responsible for hereditary nonpolyposis colorectal cancer in a North-American kindred.
Anja Wagner, Heleen van der Klift, Patrick Franken, Juul Wijnen, Cor Breukel, Vladimir Bezrookove, Ron Smits, Yulia Kinarsky, Alicia Barrows, Barbara Franklin,[...]. Genes Chromosomes Cancer 2002
47
31

Somatic aberrations of mismatch repair genes as a cause of microsatellite-unstable cancers.
Willemina R R Geurts-Giele, Celine H M Leenen, Hendrikus J Dubbink, Isabelle C Meijssen, Edward Post, Hein F B M Sleddens, Ernst J Kuipers, Anne Goverde, Ans M W van den Ouweland, Margot G F van Lier,[...]. J Pathol 2014
105
27


Somatic mosaicism and double somatic hits can lead to MSI colorectal tumors.
Isabelle Sourrouille, Florence Coulet, Jeremie H Lefevre, Chrystelle Colas, Mélanie Eyries, Magali Svrcek, Armelle Bardier-Dupas, Yann Parc, Florent Soubrier. Fam Cancer 2013
93
27

Biallelic MUTYH mutations can mimic Lynch syndrome.
Monika Morak, Barbara Heidenreich, Gisela Keller, Heather Hampel, Andreas Laner, Albert de la Chapelle, Elke Holinski-Feder. Eur J Hum Genet 2014
63
27

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
616
27

Prevalence of germline MUTYH mutations among Lynch-like syndrome patients.
Adela Castillejo, Gardenia Vargas, María Isabel Castillejo, Matilde Navarro, Víctor Manuel Barberá, Sara González, Eva Hernández-Illán, Joan Brunet, Teresa Ramón y Cajal, Judith Balmaña,[...]. Eur J Cancer 2014
47
27

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
73
27

Assessment of Tumor Sequencing as a Replacement for Lynch Syndrome Screening and Current Molecular Tests for Patients With Colorectal Cancer.
Heather Hampel, Rachel Pearlman, Mallory Beightol, Weiqiang Zhao, Daniel Jones, Wendy L Frankel, Paul J Goodfellow, Ahmet Yilmaz, Kristin Miller, Jason Bacher,[...]. JAMA Oncol 2018
87
27

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
376
22

Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.
Valérie Bonadona, Bernard Bonaïti, Sylviane Olschwang, Sophie Grandjouan, Laetitia Huiart, Michel Longy, Rosine Guimbaud, Bruno Buecher, Yves-Jean Bignon, Olivier Caron,[...]. JAMA 2011
614
22

Identification of Lynch syndrome among patients with colorectal cancer.
Leticia Moreira, Francesc Balaguer, Noralane Lindor, Albert de la Chapelle, Heather Hampel, Lauri A Aaltonen, John L Hopper, Loic Le Marchand, Steven Gallinger, Polly A Newcomb,[...]. JAMA 2012
312
22

Mutation deep within an intron of MSH2 causes Lynch syndrome.
Mark Clendenning, Daniel D Buchanan, Michael D Walsh, Belinda Nagler, Christophe Rosty, Bryony Thompson, Amanda B Spurdle, John L Hopper, Mark A Jenkins, Joanne P Young. Fam Cancer 2011
34
22

Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases.
Kandelaria Rumilla, Karen V Schowalter, Noralane M Lindor, Brittany C Thomas, Kara A Mensink, Steven Gallinger, Spring Holter, Polly A Newcomb, John D Potter, Mark A Jenkins,[...]. J Mol Diagn 2011
62
22

Elucidating the molecular basis of MSH2-deficient tumors by combined germline and somatic analysis.
Gardenia M Vargas-Parra, Maribel González-Acosta, Bryony A Thompson, Carolina Gómez, Anna Fernández, Estela Dámaso, Tirso Pons, Monika Morak, Jesús Del Valle, Silvia Iglesias,[...]. Int J Cancer 2017
17
29

Insertion of an SVA element, a nonautonomous retrotransposon, in PMS2 intron 7 as a novel cause of Lynch syndrome.
Heleen M van der Klift, Carli M Tops, Frederik J Hes, Peter Devilee, Juul T Wijnen. Hum Mutat 2012
31
22

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
256
18

Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.
Heather Hampel, Wendy Frankel, Jenny Panescu, Janet Lockman, Kaisa Sotamaa, Daniel Fix, Ilene Comeras, Jennifer La Jeunesse, Hidewaki Nakagawa, Judith A Westman,[...]. Cancer Res 2006
400
18

Clinicopathological comparison of colorectal and endometrial carcinomas in patients with Lynch-like syndrome versus patients with Lynch syndrome.
Jenny Mas-Moya, Beth Dudley, Randall E Brand, Darcy Thull, Nathan Bahary, Marina N Nikiforova, Reetesh K Pai. Hum Pathol 2015
46
18

Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing.
Daniel D Buchanan, Yen Y Tan, Michael D Walsh, Mark Clendenning, Alexander M Metcalf, Kaltin Ferguson, Sven T Arnold, Bryony A Thompson, Felicity A Lose, Michael T Parsons,[...]. J Clin Oncol 2014
135
18

Clinical problems of colorectal cancer and endometrial cancer cases with unknown cause of tumor mismatch repair deficiency (suspected Lynch syndrome).
Daniel D Buchanan, Christophe Rosty, Mark Clendenning, Amanda B Spurdle, Aung Ko Win. Appl Clin Genet 2014
64
18

Recurrence and variability of germline EPCAM deletions in Lynch syndrome.
Roland P Kuiper, Lisenka E L M Vissers, Ramprasath Venkatachalam, Danielle Bodmer, Eveline Hoenselaar, Monique Goossens, Aline Haufe, Eveline Kamping, Renée C Niessen, Frans B L Hogervorst,[...]. Hum Mutat 2011
101
18


Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts.
Hans F A Vasen, Ignacio Blanco, Katja Aktan-Collan, Jessica P Gopie, Angel Alonso, Stefan Aretz, Inge Bernstein, Lucio Bertario, John Burn, Gabriel Capella,[...]. Gut 2013
444
18

Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome.
Alexandre Xavier, Maren Fridtjofsen Olsen, Liss A Lavik, Jostein Johansen, Ashish Kumar Singh, Wenche Sjursen, Rodney J Scott, Bente A Talseth-Palmer. Mol Genet Genomic Med 2019
14
28

Histology of colorectal adenocarcinoma with double somatic mismatch-repair mutations is indistinguishable from those caused by Lynch syndrome.
Jessica A Hemminger, Rachel Pearlman, Sigurdis Haraldsdottir, Deborah Knight, Jon Gunnlaugur Jonasson, Colin C Pritchard, Heather Hampel, Wendy L Frankel. Hum Pathol 2018
19
21

Prevalence of CNV-neutral structural genomic rearrangements in MLH1, MSH2, and PMS2 not detectable in routine NGS diagnostics.
Monika Morak, Verena Steinke-Lange, Trisari Massdorf, Anna Benet-Pages, Melanie Locher, Andreas Laner, Katrin Kayser, Stefan Aretz, Elke Holinski-Feder. Fam Cancer 2020
9
44

Somatic mosaicism in a patient with Lynch syndrome.
Chiara Pastrello, Mara Fornasarig, Elisa Pin, Eleonora Berto, Barbara Pivetta, Alessandra Viel. Am J Med Genet A 2009
14
28

Somatic mosaicism by a de novo MLH1 mutation as a cause of Lynch syndrome.
Willemina R Geurts-Giele, Efraim H Rosenberg, Anja van Rens, Monique E van Leerdam, Winand N Dinjens, Fonnet E Bleeker. Mol Genet Genomic Med 2019
11
36

Using Somatic Mutations from Tumors to Classify Variants in Mismatch Repair Genes.
Brian H Shirts, Eric Q Konnick, Sarah Upham, Tom Walsh, John Michael O Ranola, Angela L Jacobson, Mary-Claire King, Rachel Pearlman, Heather Hampel, Colin C Pritchard. Am J Hum Genet 2018
17
23

Mismatch repair deficiency predicts response of solid tumors to PD-1 blockade.
Dung T Le, Jennifer N Durham, Kellie N Smith, Hao Wang, Bjarne R Bartlett, Laveet K Aulakh, Steve Lu, Holly Kemberling, Cara Wilt, Brandon S Luber,[...]. Science 2017
18

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
18

Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines.
Elena M Stoffel, Pamela B Mangu, Stephen B Gruber, Stanley R Hamilton, Matthew F Kalady, Michelle Wan Yee Lau, Karen H Lu, Nancy Roach, Paul J Limburg. J Clin Oncol 2015
191
13

Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome.
Marietta E Kovacs, Janos Papp, Zoltan Szentirmay, Szabolcs Otto, Edith Olah. Hum Mutat 2009
116
13

A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: meeting highlights and Bethesda guidelines.
M A Rodriguez-Bigas, C R Boland, S R Hamilton, D E Henson, J R Jass, P M Khan, H Lynch, M Perucho, T Smyrk, L Sobin,[...]. J Natl Cancer Inst 1997
795
13

Microsatellite instability in colorectal cancer.
C Richard Boland, Ajay Goel. Gastroenterology 2010
13

Mutated MCM9 is associated with predisposition to hereditary mixed polyposis and colorectal cancer in addition to primary ovarian failure.
Yael Goldberg, Naama Halpern, Ayala Hubert, Samuel N Adler, Sherri Cohen, Morasha Plesser-Duvdevani, Orit Pappo, Avraham Shaag, Vardiella Meiner. Cancer Genet 2015
41
13

Hereditary colorectal cancer.
Henry T Lynch, Albert de la Chapelle. N Engl J Med 2003
13

Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are risk factors for colorectal cancer.
Richarda M de Voer, Ad Geurts van Kessel, Robbert D A Weren, Marjolijn J L Ligtenberg, Dominique Smeets, Lei Fu, Lilian Vreede, Eveline J Kamping, Eugène T P Verwiel, Marc-Manuel Hahn,[...]. Gastroenterology 2013
62
13

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
72
13


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.