A citation-based method for searching scientific literature

Carol Durno, C Richard Boland, Shlomi Cohen, Jason A Dominitz, Frank M Giardiello, David A Johnson, Tonya Kaltenbach, T R Levin, David Lieberman, Douglas J Robertson, Douglas K Rex. Gastrointest Endosc 2017
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Mutations in the DNA mismatch repair gene MLH1 associated with early-onset colon cancer.
Irene Marcos, Salud Borrego, Miguel Urioste, Carmen García-Vallés, Guillermo Antiñolo. J Pediatr 2006
11
100

Cancer prevention by aspirin in children with Constitutional Mismatch Repair Deficiency (CMMRD).
Erika K S M Leenders, Harm Westdorp, Roger J Brüggemann, Jan Loeffen, Christian Kratz, John Burn, Nicoline Hoogerbrugge, Marjolijn C J Jongmans. Eur J Hum Genet 2018
18
100

Immune Checkpoint Inhibition for Hypermutant Glioblastoma Multiforme Resulting From Germline Biallelic Mismatch Repair Deficiency.
Eric Bouffet, Valérie Larouche, Brittany B Campbell, Daniele Merico, Richard de Borja, Melyssa Aronson, Carol Durno, Joerg Krueger, Vanja Cabric, Vijay Ramaswamy,[...]. J Clin Oncol 2016
511
100

RNA-based mutation analysis identifies an unusual MSH6 splicing defect and circumvents PMS2 pseudogene interference.
J Etzler, A Peyrl, A Zatkova, H-U Schildhaus, A Ficek, S Merkelbach-Bruse, C P Kratz, A Attarbaschi, J A Hainfellner, S Yao,[...]. Hum Mutat 2008
57
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
250
100

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
268
100

Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer.
Aung Ko Win, Mark A Jenkins, James G Dowty, Antonis C Antoniou, Andrew Lee, Graham G Giles, Daniel D Buchanan, Mark Clendenning, Christophe Rosty, Dennis J Ahnen,[...]. Cancer Epidemiol Biomarkers Prev 2017
178
100

Microsatellite instability in the peripheral blood leukocytes of HNPCC patients.
Mary I Coolbaugh-Murphy, Jing-Ping Xu, Louis S Ramagli, Brian C Ramagli, Barry W Brown, Patrick M Lynch, Stanley R Hamilton, Marsha L Frazier, Michael J Siciliano. Hum Mutat 2010
22
100

Navigating highly homologous genes in a molecular diagnostic setting: a resource for clinical next-generation sequencing.
Diana Mandelker, Ryan J Schmidt, Arunkanth Ankala, Kristin McDonald Gibson, Mark Bowser, Himanshu Sharma, Elizabeth Duffy, Madhuri Hegde, Avni Santani, Matthew Lebo,[...]. Genet Med 2016
90
100

Functional Repair Assay for the Diagnosis of Constitutional Mismatch Repair Deficiency From Non-Neoplastic Tissue.
Andrew Y Shuen, Stella Lanni, Gagan B Panigrahi, Melissa Edwards, Lisa Yu, Brittany B Campbell, Ariane Mandel, Cindy Zhang, Nataliya Zhukova, Musa Alharbi,[...]. J Clin Oncol 2019
19
100



Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome.
Michel De Vos, Bruce E Hayward, Susan Picton, Eamonn Sheridan, David T Bonthron. Am J Hum Genet 2004
140
100

Clinical Management and Tumor Surveillance Recommendations of Inherited Mismatch Repair Deficiency in Childhood.
Uri Tabori, Jordan R Hansford, Maria Isabel Achatz, Christian P Kratz, Sharon E Plon, Thierry Frebourg, Laurence Brugières. Clin Cancer Res 2017
102
100

Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium "Care for CMMR-D" (C4CMMR-D).
H F A Vasen, Z Ghorbanoghli, F Bourdeaut, O Cabaret, O Caron, A Duval, N Entz-Werle, Y Goldberg, D Ilencikova, C P Kratz,[...]. J Med Genet 2014
132
100

PMS2 monoallelic mutation carriers: the known unknown.
McKinsey L Goodenberger, Brittany C Thomas, Douglas Riegert-Johnson, C Richard Boland, Sharon E Plon, Mark Clendenning, Aung Ko Win, Leigha Senter, Steven M Lipkin, Zsofia K Stadler,[...]. Genet Med 2016
42
100

A brief review of short tandem repeat mutation.
Hao Fan, Jia-You Chu. Genomics Proteomics Bioinformatics 2007
101
100

Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents.
Sahra Bodo, Chrystelle Colas, Olivier Buhard, Ada Collura, Julie Tinat, Noémie Lavoine, Agathe Guilloux, Alexandra Chalastanis, Philippe Lafitte, Florence Coulet,[...]. Gastroenterology 2015
61
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
93
100

The landscape of genomic alterations across childhood cancers.
Susanne N Gröbner, Barbara C Worst, Joachim Weischenfeldt, Ivo Buchhalter, Kortine Kleinheinz, Vasilisa A Rudneva, Pascal D Johann, Gnana Prakash Balasubramanian, Maia Segura-Wang, Sebastian Brabetz,[...]. Nature 2018
589
100

A novel panel of short mononucleotide repeats linked to informative polymorphisms enabling effective high volume low cost discrimination between mismatch repair deficient and proficient tumours.
Lisa Redford, Ghanim Alhilal, Stephanie Needham, Ottie O'Brien, Julie Coaker, John Tyson, Leonardo Maldaner Amorim, Iona Middleton, Osagi Izuogu, Mark Arends,[...]. PLoS One 2018
9
100

Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy.
Manon Suerink, Tim Ripperger, Ludwine Messiaen, Fred H Menko, Franck Bourdeaut, Chrystelle Colas, Marjolijn Jongmans, Yael Goldberg, Maartje Nielsen, Martine Muleris,[...]. J Med Genet 2019
27
100

Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD).
Katharina Wimmer, Christian P Kratz, Hans F A Vasen, Olivier Caron, Chrystelle Colas, Natacha Entz-Werle, Anne-Marie Gerdes, Yael Goldberg, Denisa Ilencikova, Martine Muleris,[...]. J Med Genet 2014
245
100

Repopulating defect of mismatch repair-deficient hematopoietic stem cells.
Jane S Reese, Lili Liu, Stanton L Gerson. Blood 2003
75
100

A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes.
Richard Gallon, Barbara Mühlegger, Sören-Sebastian Wenzel, Harsh Sheth, Christine Hayes, Stefan Aretz, Karin Dahan, William Foulkes, Christian P Kratz, Tim Ripperger,[...]. Hum Mutat 2019
17
100

Microsatellite instability (MSI) increases with age in normal somatic cells.
Mary I Coolbaugh-Murphy, Jingping Xu, Louis S Ramagli, Barry W Brown, Michael J Siciliano. Mech Ageing Dev 2005
31
100

A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotype.
Lili Li, Nancy Hamel, Kristi Baker, Michael J McGuffin, Martin Couillard, Adrian Gologan, Victoria A Marcus, Bernard Chodirker, Albert Chudley, Camelia Stefanovici,[...]. J Med Genet 2015
24
100

Single molecule molecular inversion probes for targeted, high-accuracy detection of low-frequency variation.
Joseph B Hiatt, Colin C Pritchard, Stephen J Salipante, Brian J O'Roak, Jay Shendure. Genome Res 2013
220
100

Simple detection of germline microsatellite instability for diagnosis of constitutional mismatch repair cancer syndrome.
Danielle Ingham, Christine P Diggle, Ian Berry, Claire A Bristow, Bruce E Hayward, Nazneen Rahman, Alexander F Markham, Eamonn G Sheridan, David T Bonthron, Ian M Carr. Hum Mutat 2013
33
100


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.