A citation-based method for searching scientific literature

Elisabeth F P Peterse, Steffie K Naber, Corinne Daly, Aaron Pollett, Lawrence F Paszat, Manon C W Spaander, Melyssa Aronson, Robert Gryfe, Linda Rabeneck, Iris Lansdorp-Vogelaar, Nancy N Baxter. Clin Gastroenterol Hepatol 2020
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies.
Christoph Engel, Hans F Vasen, Toni Seppälä, Stefan Aretz, Marloes Bigirwamungu-Bargeman, Sybrand Y de Boer, Karolin Bucksch, Reinhard Büttner, Elke Holinski-Feder, Stefanie Holzapfel,[...]. Gastroenterology 2018
62
50

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
633
33

Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-Society Task Force on colorectal cancer.
Francis M Giardiello, John I Allen, Jennifer E Axilbund, C Richard Boland, Carol A Burke, Randall W Burt, James M Church, Jason A Dominitz, David A Johnson, Tonya Kaltenbach,[...]. Gastroenterology 2014
274
33

Comparison of Prediction Models for Lynch Syndrome Among Individuals With Colorectal Cancer.
Fay Kastrinos, Rohit P Ojha, Celine Leenen, Carmelita Alvero, Rowena C Mercado, Judith Balmaña, Irene Valenzuela, Francesc Balaguer, Roger Green, Noralane M Lindor,[...]. J Natl Cancer Inst 2015
23
33


Uptake of genetic testing by relatives of lynch syndrome probands: a systematic review.
Ravi N Sharaf, Parvathi Myer, Christopher D Stave, Lisa C Diamond, Uri Ladabaum. Clin Gastroenterol Hepatol 2013
90
33

Factors determining dissemination of results and uptake of genetic testing in families with known BRCA1/2 mutations.
Esme Finlay, Jill E Stopfer, Eric Burlingame, Katherine Goldfeder Evans, Katherine L Nathanson, Barbara L Weber, Katrina Armstrong, Timothy R Rebbeck, Susan M Domchek. Genet Test 2008
109
33

Uptake and predictors of colonoscopy use in family members not participating in cascade genetic testing for Lynch syndrome.
Donald W Hadley, Dina Eliezer, Yonit Addissie, Andrea Goergen, Sato Ashida, Laura Koehly. Sci Rep 2020
5
40


The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice.
Fred H Menko, Jacqueline A Ter Stege, Lizet E van der Kolk, Kiki N Jeanson, Winnie Schats, Daoud Ait Moha, Eveline M A Bleiker. Fam Cancer 2019
52
33

Hereditary and familial colon cancer.
Kory W Jasperson, Thérèse M Tuohy, Deborah W Neklason, Randall W Burt. Gastroenterology 2010
663
33



EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.
Joanne Traeger-Synodinos, Cornelis L Harteveld, John M Old, Mary Petrou, Renzo Galanello, Piero Giordano, Michael Angastioniotis, Barbara De la Salle, Shirley Henderson, Alison May. Eur J Hum Genet 2015
49
16


Mismatch repair.
Richard Fishel. J Biol Chem 2015
111
16

Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications.
Henry T Lynch, C Richard Boland, Gordon Gong, Trudy G Shaw, Patrick M Lynch, Riccardo Fodde, Jane F Lynch, Albert de la Chapelle. Eur J Hum Genet 2006
102
16

A comprehensive custom panel design for routine hereditary cancer testing: preserving control, improving diagnostics and revealing a complex variation landscape.
Elisabeth Castellanos, Bernat Gel, Inma Rosas, Eva Tornero, Sheila Santín, Raquel Pluvinet, Juan Velasco, Lauro Sumoy, Jesús Del Valle, Manuel Perucho,[...]. Sci Rep 2017
31
16

First FDA Approval Agnostic of Cancer Site - When a Biomarker Defines the Indication.
Steven Lemery, Patricia Keegan, Richard Pazdur. N Engl J Med 2017
331
16


The practice of universal screening for Lynch syndrome in newly diagnosed endometrial carcinoma.
Aifen Wang, Jenna McCracken, Yanjing Li, Lingfan Xu. Health Sci Rep 2018
6
16

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
16

MutS/MutL crystal structure reveals that the MutS sliding clamp loads MutL onto DNA.
Flora S Groothuizen, Ines Winkler, Michele Cristóvão, Alexander Fish, Herrie H K Winterwerp, Annet Reumer, Andreas D Marx, Nicolaas Hermans, Robert A Nicholls, Garib N Murshudov,[...]. Elife 2015
58
16


Extracolonic manifestations of lynch syndrome.
Brian J Bansidhar. Clin Colon Rectal Surg 2012
29
16

EpCAM: structure and function in health and disease.
Ulrike Schnell, Vincenzo Cirulli, Ben N G Giepmans. Biochim Biophys Acta 2013
160
16

Microsatellite instability--MSI markers (BAT26, BAT25, D2S123, D5S346, D17S250) in rectal cancer.
Graziele Moraes Losso, Roberto da Silveira Moraes, Arthur C Gentili, Iara Taborda Messias-Reason. Arq Bras Cir Dig 2012
16
16

Exonuclease 1-dependent and independent mismatch repair.
Eva M Goellner, Christopher D Putnam, Richard D Kolodner. DNA Repair (Amst) 2015
73
16

Endonuclease activities of MutLα and its homologs in DNA mismatch repair.
Lyudmila Y Kadyrova, Farid A Kadyrov. DNA Repair (Amst) 2016
37
16

Recent Advances in Lynch Syndrome: Diagnosis, Treatment, and Cancer Prevention.
Matthew B Yurgelun, Heather Hampel. Am Soc Clin Oncol Educ Book 2018
36
16


Lynch Syndrome: Current management In 2019.
B Menahem, A Alves, J M Regimbeau, C Sabbagh. J Visc Surg 2019
6
16

Scoping the family history: assessment of Lynch syndrome (hereditary nonpolyposis colorectal cancer) in primary care settings--a primer for nurse practitioners.
Ann Maradiegue, Kory Jasperson, Quannetta T Edwards, Katrina Lowstuter, Jeffrey Weitzel. J Am Acad Nurse Pract 2008
12
16

Lynch syndrome related endometrial cancer: clinical significance beyond the endometrium.
Yiying Wang, Yue Wang, Jie Li, Janiel Cragun, Kenneth Hatch, Setsuko K Chambers, Wenxin Zheng. J Hematol Oncol 2013
28
16

Update on Lynch syndrome genomics.
Päivi Peltomäki. Fam Cancer 2016
86
16

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
241
16

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
385
16

A new strategy to screen MMR genes in Lynch Syndrome: HA-CAE, MLPA and RT-PCR.
Lucia Perez-Cabornero, Eladio Velasco, Mar Infante, David Sanz, Enrique Lastra, Lara Hernández, Cristina Miner, Mercedes Duran. Eur J Cancer 2009
12
16


Epithelial cell adhesion molecule expression (CD326) in cancer: a short review.
Carlo Patriarca, Roberto Maria Macchi, Anja K Marschner, Hakan Mellstedt. Cancer Treat Rev 2012
283
16

NGS Technologies as a Turning Point in Rare Disease Research , Diagnosis and Treatment.
Ana Fernandez-Marmiesse, Sofia Gouveia, Maria L Couce. Curr Med Chem 2018
69
16

Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families.
Bente A Talseth-Palmer, Denis C Bauer, Wenche Sjursen, Tiffany J Evans, Mary McPhillips, Anthony Proietto, Geoffrey Otton, Allan D Spigelman, Rodney J Scott. Cancer Med 2016
18
16

Methylation-specific MLPA (MS-MLPA): simultaneous detection of CpG methylation and copy number changes of up to 40 sequences.
Anders O H Nygren, Najim Ameziane, Helena M B Duarte, Raymon N C P Vijzelaar, Quinten Waisfisz, Corine J Hess, Jan P Schouten, Abdellatif Errami. Nucleic Acids Res 2005
281
16

Lynch syndrome: an updated review.
Rishabh Sehgal, Kieran Sheahan, Patrick R O'Connell, Ann M Hanly, Sean T Martin, Desmond C Winter. Genes (Basel) 2014
72
16

Antibody Based EpCAM Targeted Therapy of Cancer, Review and Update.
Shirin Eyvazi, Safar Farajnia, Siavoush Dastmalchi, Farzad Kanipour, Habib Zarredar, Mojghan Bandehpour. Curr Cancer Drug Targets 2018
38
16

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
757
16

Review: Clinical aspects of hereditary DNA Mismatch repair gene mutations.
Rolf H Sijmons, Robert M W Hofstra. DNA Repair (Amst) 2016
39
16

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
16

Universal screening of both endometrial and colon cancers increases the detection of Lynch syndrome.
Tomer Adar, Linda H Rodgers, Kristen M Shannon, Makoto Yoshida, Tianle Ma, Anthony Mattia, Gregory Y Lauwers, Anthony J Iafrate, Nicole M Hartford, Esther Oliva,[...]. Cancer 2018
47
16

Molecular testing for Lynch syndrome in people with colorectal cancer: systematic reviews and economic evaluation.
Tristan Snowsill, Helen Coelho, Nicola Huxley, Tracey Jones-Hughes, Simon Briscoe, Ian M Frayling, Chris Hyde. Health Technol Assess 2017
53
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.