A citation-based method for searching scientific literature

Andrew Y Shuen, Stella Lanni, Gagan B Panigrahi, Melissa Edwards, Lisa Yu, Brittany B Campbell, Ariane Mandel, Cindy Zhang, Nataliya Zhukova, Musa Alharbi, Mark Bernstein, Daniel C Bowers, Sara Carroll, Kristina A Cole, Shlomi Constantini, Bruce Crooks, Rina Dvir, Roula Farah, Nobuko Hijiya, Ben George, Theodore W Laetsch, Valerie Larouche, Scott Lindhorst, Rebecca C Luiten, Vanan Magimairajan, Gary Mason, Warren Mason, Oz Mordechai, Naureen Mushtaq, Garth Nicholas, Michael Oren, Laura Palma, Luis Alberto Pedroza, Jagadeesh Ramdas, David Samuel, Kami Wolfe Schneider, Andrea Seeley, Kara Semotiuk, Ashraf Shamvil, David Sumerauer, Helen Toledano, Patrick Tomboc, Margaret Wierman, An Van Damme, Yi-Yen Lee, Michal Zapotocky, Eric Bouffet, Carol Durno, Melyssa Aronson, Steve Gallinger, William D Foulkes, David Malkin, Uri Tabori, Christopher E Pearson. J Clin Oncol 2019
Times Cited: 19







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



Times Cited
  Times     Co-cited
Similarity


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
57

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
52

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
52

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
47

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
47

Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: report from the constitutional mismatch repair deficiency consortium.
Doua Bakry, Melyssa Aronson, Carol Durno, Hala Rimawi, Roula Farah, Qasim Kholaif Alharbi, Musa Alharbi, Ashraf Shamvil, Shay Ben-Shachar, Matthew Mistry,[...]. Eur J Cancer 2014
130
42

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
36

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
36

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
36

Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers.
Adam Shlien, Brittany B Campbell, Richard de Borja, Ludmil B Alexandrov, Daniele Merico, David Wedge, Peter Van Loo, Patrick S Tarpey, Paul Coupland, Sam Behjati,[...]. Nat Genet 2015
218
36

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
420
31

High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers.
Maribel González-Acosta, Fátima Marín, Benjamin Puliafito, Nuria Bonifaci, Anna Fernández, Matilde Navarro, Hector Salvador, Francesc Balaguer, Silvia Iglesias, Angela Velasco,[...]. J Med Genet 2020
10
60

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
391
26


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
22


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
21

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
21

Germline deletions in the EPCAM gene as a cause of Lynch syndrome - literature review.
Katarzyna Tutlewska, Jan Lubinski, Grzegorz Kurzawski. Hered Cancer Clin Pract 2013
66
21

A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiency.
Katharina Wimmer, Andreas Beilken, Rainer Nustede, Tim Ripperger, Britta Lamottke, Benno Ure, Diana Steinmann, Tanja Reineke-Plaass, Ulrich Lehmann, Johannes Zschocke,[...]. Fam Cancer 2017
35
21

High frequency of mismatch repair deficiency among pediatric high grade gliomas in Jordan.
Nisreen Amayiri, Uri Tabori, Brittany Campbell, Doua Bakry, Melyssa Aronson, Carol Durno, Patricia Rakopoulos, David Malkin, Ibrahim Qaddoumi, Awni Musharbash,[...]. Int J Cancer 2016
43
21

Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study.
Marlies J E Kempers, Roland P Kuiper, Charlotte W Ockeloen, Pierre O Chappuis, Pierre Hutter, Nils Rahner, Hans K Schackert, Verena Steinke, Elke Holinski-Feder, Monika Morak,[...]. Lancet Oncol 2011
178
21

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
73
21

Phenotypic and genotypic characterisation of biallelic mismatch repair deficiency (BMMR-D) syndrome.
Carol A Durno, Philip M Sherman, Melyssa Aronson, David Malkin, Cynthia Hawkins, Doua Bakry, Eric Bouffet, Steven Gallinger, Aaron Pollett, Brittany Campbell,[...]. Eur J Cancer 2015
66
21

PD-1 Blockade in Tumors with Mismatch-Repair Deficiency.
Dung T Le, Jennifer N Uram, Hao Wang, Bjarne R Bartlett, Holly Kemberling, Aleksandra D Eyring, Andrew D Skora, Brandon S Luber, Nilofer S Azad, Dan Laheru,[...]. N Engl J Med 2015
21

Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity.
Hagit N Baris, Inbal Barnes-Kedar, Helen Toledano, Marisa Halpern, Dov Hershkovitz, Alexander Lossos, Israela Lerer, Tamar Peretz, Revital Kariv, Shlomi Cohen,[...]. Pediatr Blood Cancer 2016
21
21

Paediatric systemic lupus erythematosus as a manifestation of constitutional mismatch repair deficiency.
Helen Toledano, Naama Orenstein, Efrat Sofrin, Noa Ruhrman-Shahar, Gil Amarilyo, Lina Basel-Salmon, Alan R Shuldiner, Pola Smirin-Yosef, Melyssa Aronson, Hibs Al-Tarrah,[...]. J Med Genet 2020
7
57

Germline POLE mutation in a child with hypermutated medulloblastoma and features of constitutional mismatch repair deficiency.
Holly Lindsay, Sarah Scollon, Jacquelyn Reuther, Horatiu Voicu, Surya P Rednam, Frank Y Lin, Kevin E Fisher, Murali Chintagumpala, Adekunle M Adesina, D Will Parsons,[...]. Cold Spring Harb Mol Case Stud 2019
15
26

Recommendations on Surveillance and Management of Biallelic Mismatch Repair Deficiency (BMMRD) Syndrome: A Consensus Statement by the US Multi-Society Task Force on Colorectal Cancer.
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,[...]. Gastroenterology 2017
37
21

Multiple Brain Developmental Venous Anomalies as a Marker for Constitutional Mismatch Repair Deficiency Syndrome.
S I Shiran, L Ben-Sira, R Elhasid, J Roth, U Tabori, M Yalon, S Constantini, R Dvir. AJNR Am J Neuroradiol 2018
13
30

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
15

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
15

Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome.
Heleen M van der Klift, Arjen R Mensenkamp, Mark Drost, Elsa C Bik, Yvonne J Vos, Hans J J P Gille, Bert E J W Redeker, Yvonne Tiersma, José B M Zonneveld, Encarna Gómez García,[...]. Hum Mutat 2016
33
15

Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
Matthew B Yurgelun, Brian Allen, Rajesh R Kaldate, Karla R Bowles, Thaddeus Judkins, Praveen Kaushik, Benjamin B Roa, Richard J Wenstrup, Anne-Renee Hartman, Sapna Syngal. Gastroenterology 2015
160
15

Human mismatch repair: reconstitution of a nick-directed bidirectional reaction.
Nicoleta Constantin, Leonid Dzantiev, Farid A Kadyrov, Paul Modrich. J Biol Chem 2005
170
15

Reconstitution of 5'-directed human mismatch repair in a purified system.
Yanbin Zhang, Fenghua Yuan, Steven R Presnell, Keli Tian, Yin Gao, Alan E Tomkinson, Liya Gu, Guo-Min Li. Cell 2005
277
15

Oncologic surveillance for subjects with biallelic mismatch repair gene mutations: 10 year follow-up of a kindred.
Carol A Durno, Melyssa Aronson, Uri Tabori, David Malkin, Steven Gallinger, Helen S L Chan. Pediatr Blood Cancer 2012
56
15

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
15

Durable Response to Nivolumab in a Pediatric Patient with Refractory Glioblastoma and Constitutional Biallelic Mismatch Repair Deficiency.
Musa AlHarbi, Nahla Ali Mobark, Latifa AlMubarak, Rasha Aljelaify, Mariam AlSaeed, Amal Almutairi, Fatmah Alqubaishi, M Emarat Hussain, Ali Abdullah O Balbaid, Amal Said Marie,[...]. Oncologist 2018
40
15

Diagnostic challenges in a child with early onset desmoplastic medulloblastoma and homozygous variants in MSH2 and MSH6.
Julia Taeubner, Katharina Wimmer, Martine Muleris, Olivier Lascols, Chrystelle Colas, Christine Fauth, Triantafyllia Brozou, Joerg Felsberg, Jasmin Riemer, Michael Gombert,[...]. Eur J Hum Genet 2018
12
25

Eukaryotic Mismatch Repair in Relation to DNA Replication.
Thomas A Kunkel, Dorothy A Erie. Annu Rev Genet 2015
216
15


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
18

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
10

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
10

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
10

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,[...]. Am J Gastroenterol 2014
278
10

Microsatellite instability detection by next generation sequencing.
Stephen J Salipante, Sheena M Scroggins, Heather L Hampel, Emily H Turner, Colin C Pritchard. Clin Chem 2014
227
10

Approaches to diagnose DNA mismatch repair gene defects in cancer.
Javier Peña-Diaz, Lene Juel Rasmussen. DNA Repair (Amst) 2016
22
10

A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndrome.
Mark Drost, Yvonne Tiersma, Bryony A Thompson, Jane H Frederiksen, Guido Keijzers, Dylan Glubb, Scott Kathe, Jan Osinga, Helga Westers, Lisa Pappas,[...]. Genet Med 2019
20
10


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.