A citation-based method for searching scientific literature

Qing Wang, Julie Leclerc, Gaëlle Bougeard, Sylviane Olschwang, Stéphanie Vasseur, Kévin Cassinari, Denis Boidin, Cédrick Lefol, Pierre Naïbo, Thierry Frébourg, Marie Pierre Buisine, Stéphanie Baert-Desurmont. J Med Genet 2020
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


A cryptic paracentric inversion of MSH2 exons 2-6 causes Lynch syndrome.
Qing Liu, Luke B Hesson, Andrea C Nunez, Deborah Packham, Rachel Williams, Robyn L Ward, Mathew A Sloane. Carcinogenesis 2016
22
66

Tumours with loss of MSH6 expression are MSI-H when screened with a pentaplex of five mononucleotide repeats.
J-F You, O Buhard, M J L Ligtenberg, C M Kets, R C Niessen, R M W Hofstra, A Wagner, W N M Dinjens, C Colas, O Lascols,[...]. Br J Cancer 2010
41
66


Neoadjuvant therapy induces loss of MSH6 expression in colorectal carcinoma.
Fei Bao, Nicole C Panarelli, Hanna Rennert, David L Sherr, Rhonda K Yantiss. Am J Surg Pathol 2010
82
66


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
56
66

Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort.
N Lavoine, C Colas, M Muleris, S Bodo, A Duval, N Entz-Werle, F Coulet, O Cabaret, F Andreiuolo, C Charpy,[...]. J Med Genet 2015
70
66

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
955
66

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
403
66

Heterogenous mismatch-repair status in colorectal cancer.
Patrick Joost, Nynke Veurink, Susanne Holck, Louise Klarskov, Anders Bojesen, Maria Harbo, Bo Baldetorp, Eva Rambech, Mef Nilbert. Diagn Pathol 2014
52
66

Retained mismatch repair protein expression occurs in approximately 6% of microsatellite instability-high cancers and is associated with missense mutations in mismatch repair genes.
Jaclyn F Hechtman, Satshil Rana, Sumit Middha, Zsofia K Stadler, Alicia Latham, Ryma Benayed, Robert Soslow, Marc Ladanyi, Rona Yaeger, Ahmet Zehir,[...]. Mod Pathol 2020
24
66

Practical guidance for mismatch repair-deficiency testing in endometrial cancer.
E Stelloo, A M L Jansen, E M Osse, R A Nout, C L Creutzberg, D Ruano, D N Church, H Morreau, V T H B M Smit, T van Wezel,[...]. Ann Oncol 2017
107
66

Microsatellite Instability Is Associated With the Presence of Lynch Syndrome Pan-Cancer.
Alicia Latham, Preethi Srinivasan, Yelena Kemel, Jinru Shia, Chaitanya Bandlamudi, Diana Mandelker, Sumit Middha, Jaclyn Hechtman, Ahmet Zehir, Marianne Dubard-Gault,[...]. J Clin Oncol 2019
219
66


Immunohistochemical testing of conventional adenomas for loss of expression of mismatch repair proteins in Lynch syndrome mutation carriers: a case series from the Australasian site of the colon cancer family registry.
Michael D Walsh, Daniel D Buchanan, Sally-Ann Pearson, Mark Clendenning, Mark A Jenkins, Aung Ko Win, Rhiannon J Walters, Kevin J Spring, Belinda Nagler, Erika Pavluk,[...]. Mod Pathol 2012
52
66


Evaluation of a new panel of six mononucleotide repeat markers for the detection of DNA mismatch repair-deficient tumours.
A Pagin, F Zerimech, J Leclerc, A Wacrenier, S Lejeune, C Descarpentries, F Escande, N Porchet, M-P Buisine. Br J Cancer 2013
30
66

Heterogeneous staining for mismatch repair proteins during population-based prescreening for hereditary nonpolyposis colorectal cancer.
Natasha Watson, Fabienne Grieu, Melinda Morris, Jennet Harvey, Colin Stewart, Lyn Schofield, Jack Goldblatt, Barry Iacopetta. J Mol Diagn 2007
60
66

Somatic MMR gene mutations as a cause for MSI-H sebaceous neoplasms in Muir-Torre syndrome-like patients.
Marie-Odile Joly, Valéry Attignon, Jean-Christophe Saurin, Françoise Desseigne, Dominique Leroux, Tanguy Martin-Denavit, Sophie Giraud, Marie-Noëlle Bonnet-Dupeyron, Laurence Faivre, Jessie Auclair,[...]. Hum Mutat 2015
15
66

An optimized pentaplex PCR for detecting DNA mismatch repair-deficient colorectal cancers.
Ajay Goel, Takeshi Nagasaka, Richard Hamelin, C Richard Boland. PLoS One 2010
106
66

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
66

Evaluation of tumor microsatellite instability using five quasimonomorphic mononucleotide repeats and pentaplex PCR.
Nirosha Suraweera, Alex Duval, Maryline Reperant, Christelle Vaury, Daniela Furlan, Karen Leroy, Raquel Seruca, Barry Iacopetta, Richard Hamelin. Gastroenterology 2002
434
66

Tumour MLH1 promoter region methylation testing is an effective prescreen for Lynch Syndrome (HNPCC).
K Newton, N M Jorgensen, A J Wallace, D D Buchanan, F Lalloo, R F T McMahon, J Hill, D G Evans. J Med Genet 2014
40
33

Value of immunohistochemical detection of DNA mismatch repair proteins in predicting germline mutation in hereditary colorectal neoplasms.
Jinru Shia, David S Klimstra, Khedoudja Nafa, Kenneth Offit, Jose G Guillem, Arnold J Markowitz, William L Gerald, Nathan A Ellis. Am J Surg Pathol 2005
112
33

Comprehensive Analysis of Hypermutation in Human Cancer.
Brittany B Campbell, Nicholas Light, David Fabrizio, Matthew Zatzman, Fabio Fuligni, Richard de Borja, Scott Davidson, Melissa Edwards, Julia A Elvin, Karl P Hodel,[...]. Cell 2017
412
33


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
247
33

MLH1 promoter hypermethylation in the analytical algorithm of Lynch syndrome: a cost-effectiveness study.
Mireia Gausachs, Pilar Mur, Julieta Corral, Marta Pineda, Sara González, Llúcia Benito, Mireia Menéndez, Josep Alfons Espinàs, Joan Brunet, María Dolores Iniesta,[...]. Eur J Hum Genet 2012
62
33

Universal Lynch Syndrome Screening Should be Performed in All Upper Tract Urothelial Carcinomas.
Jennifer Y Ju, Anne M Mills, Mani S Mahadevan, Jinbo Fan, Stephen H Culp, Martha H Thomas, Helen P Cathro. Am J Surg Pathol 2018
29
33

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
265
33

Mechanisms and therapeutic implications of hypermutation in gliomas.
Mehdi Touat, Yvonne Y Li, Adam N Boynton, Liam F Spurr, J Bryan Iorgulescu, Craig L Bohrson, Isidro Cortes-Ciriano, Cristina Birzu, Jack E Geduldig, Kristine Pelton,[...]. Nature 2020
182
33

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
90
33

Evaluation of yield and experiences of age-related molecular investigation for heritable and nonheritable causes of mismatch repair deficient colorectal cancer to identify Lynch syndrome.
Janet R Vos, Ingrid E Fakkert, Liesbeth Spruijt, Riki W Willems, Sera Langenveld, Arjen R Mensenkamp, Edward M Leter, Iris D Nagtegaal, Marjolijn J L Ligtenberg, Nicoline Hoogerbrugge. Int J Cancer 2020
8
33

Characteristics of Lynch syndrome associated ovarian cancer.
J M Woolderink, G H De Bock, J A de Hullu, H Hollema, R P Zweemer, B F M Slangen, K N Gaarenstroom, M van Beurden, H C van Doorn, R H Sijmons,[...]. Gynecol Oncol 2018
18
33

Double somatic mutations in mismatch repair genes are frequent in colorectal cancer after Hodgkin's lymphoma treatment.
Lisanne S Rigter, Petur Snaebjornsson, Efraim H Rosenberg, Peggy N Atmodimedjo, Berthe M Aleman, Jelle Ten Hoeve, Willemina R Geurts-Giele, Thomas W van Ravesteyn, Johan Hoeksel, Gerrit A Meijer,[...]. Gut 2018
21
33

Differential cancer predisposition in Lynch syndrome: insights from molecular analysis of brain and urinary tract tumors.
A H S Gylling, T T Nieminen, W M Abdel-Rahman, K Nuorva, M Juhola, E I Joensuu, H J Järvinen, J-P Mecklin, M Aarnio, P T Peltomäki. Carcinogenesis 2008
67
33

Hereditary pancreatic cancer.
Shilpa Grover, Sapna Syngal. Gastroenterology 2010
67
33

Mismatch Repair Deficiency in Ovarian Carcinoma: Frequency, Causes, and Consequences.
Susanna Leskela, Ignacio Romero, Eva Cristobal, Belén Pérez-Mies, Juan M Rosa-Rosa, Ana Gutierrez-Pecharroman, Tamara Caniego-Casas, Almudena Santón, Belén Ojeda, Raquel López-Reig,[...]. Am J Surg Pathol 2020
24
33

Low frequency of BRAF and CDKN2A mutations in endometrial cancer.
Helga B Salvesen, Rajiv Kumar, Ingunn Stefansson, Sabrina Angelini, Nicola MacDonald, Johanna Smeds, Ian J Jacobs, Kari Hemminki, Soma Das, Lars A Akslen. Int J Cancer 2005
37
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
255
33

Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors.
Noralane M Lindor, Lawrence J Burgart, Olga Leontovich, Richard M Goldberg, Julie M Cunningham, Daniel J Sargent, Catherine Walsh-Vockley, Gloria M Petersen, Michael D Walsh, Barbara A Leggett,[...]. J Clin Oncol 2002
589
33

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
628
33


Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer.
Rebecca A Barnetson, Albert Tenesa, Susan M Farrington, Iain D Nicholl, Roseanne Cetnarskyj, Mary E Porteous, Harry Campbell, Malcolm G Dunlop. N Engl J Med 2006
317
33

Utility of p16 immunohistochemistry for the identification of Lynch syndrome.
Artemio Payá, Cristina Alenda, Lucía Pérez-Carbonell, Estefanía Rojas, José-Luis Soto, Carmen Guillén, Adela Castillejo, Victor M Barberá, Alfredo Carrato, Antoni Castells,[...]. Clin Cancer Res 2009
17
33

The role of mismatch repair gene defects in the development of adenomas in patients with HNPCC.
Andrea E De Jong, Hans Morreau, Marjo Van Puijenbroek, Paul H c Eilers, Juul Wijnen, Fokko M Nagengast, Gerrit Griffioen, Annemieke Cats, Fred H Menko, Jan H Kleibeuker,[...]. Gastroenterology 2004
133
33

Incidence of Mismatch Repair Protein Deficiency and Associated Clinicopathologic Features in a Cohort of 104 Ovarian Endometrioid Carcinomas.
Jennifer A Bennett, Anna Pesci, Vicente Morales-Oyarvide, Annacarolina Da Silva, Valentina Nardi, Esther Oliva. Am J Surg Pathol 2019
15
33

BRAF V600E-specific immunohistochemistry for the exclusion of Lynch syndrome in MSI-H colorectal cancer.
David Capper, Anita Voigt, Gergana Bozukova, Aysel Ahadova, Philipp Kickingereder, Andreas von Deimling, Magnus von Knebel Doeberitz, Matthias Kloor. Int J Cancer 2013
82
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.