A citation-based method for searching scientific literature

Roula A Farah, Farid Maalouf, Nassim Abi Chahine, Hussein Farhat, Brittany Campbell, Nataliya Zhukova, Carol Durno, Melyssa Aronson, Cynthia Hawkins, Eric Bouffet, Uri Tabori. Eur J Med Genet 2019
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


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

Biallelic germline mutations of mismatch-repair genes: a possible cause for multiple pediatric malignancies.
Jan-Werner Poley, Anja Wagner, Monique M C P Hoogmans, Fred H Menko, Carli Tops, Johan M Kros, Roel E Reddingius, Hanne Meijers-Heijboer, Ernst J Kuipers, Winand N M Dinjens. Cancer 2007
67
100

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
100

Type A microsatellite instability in pediatric gliomas as an indicator of Turcot syndrome.
Laura Giunti, Valentina Cetica, Ugo Ricci, Sabrina Giglio, Iacopo Sardi, Milena Paglierani, Elena Andreucci, Massimiliano Sanzo, Marco Forni, Anna Maria Buccoliero,[...]. Eur J Hum Genet 2009
21
66

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
66

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
66

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
66

Constitutional mismatch repair deficiency-associated brain tumors: report from the European C4CMMRD consortium.
Léa Guerrini-Rousseau, Pascale Varlet, Chrystelle Colas, Felipe Andreiuolo, Franck Bourdeaut, Karin Dahan, Christine Devalck, Cécile Faure-Conter, Maurizio Genuardi, Yael Goldberg,[...]. Neurooncol Adv 2019
16
66

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
66

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
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
73
66

Glioblastomas, astrocytomas and oligodendrogliomas linked to Lynch syndrome.
C Therkildsen, S Ladelund, E Rambech, A Persson, A Petersen, M Nilbert. Eur J Neurol 2015
39
66

Lynch syndrome-associated ultra-hypermutated pediatric glioblastoma mimicking a constitutional mismatch repair deficiency syndrome.
Chen Yang, Frances Austin, Hope Richard, Michael Idowu, Vernell Williamson, Fernanda Sabato, Andrea Ferreira-Gonzalez, Scott A Turner. Cold Spring Harb Mol Case Stud 2019
12
66

Optic pathway glioma as part of a constitutional mismatch-repair deficiency syndrome in a patient meeting the criteria for neurofibromatosis type 1.
Jacky T Yeung, Ian F Pollack, Sapana Shah, Ronald Jaffe, Marina Nikiforova, Regina I Jakacki. Pediatr Blood Cancer 2013
11
33

DNA Polymerase and Mismatch Repair Exert Distinct Microsatellite Instability Signatures in Normal and Malignant Human Cells.
Jiil Chung, Yosef E Maruvka, Sumedha Sudhaman, Jacalyn Kelly, Nicholas J Haradhvala, Vanessa Bianchi, Melissa Edwards, Victoria J Forster, Nuno M Nunes, Melissa A Galati,[...]. Cancer Discov 2021
21
33

Extensive somatic microsatellite mutations in normal human tissue.
S Vilkki, J L Tsao, A Loukola, M Pöyhönen, O Vierimaa, R Herva, L A Aaltonen, D Shibata. Cancer Res 2001
74
33

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
33

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
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
420
33

Development of a fluorescent multiplex assay for detection of MSI-High tumors.
Jeffery W Bacher, Laura A Flanagan, Regenia L Smalley, Nadine A Nassif, Lawrence J Burgart, Richard B Halberg, Wael M Abdel Megid, Stephen N Thibodeau. Dis Markers 2004
177
33

Universal Screening for Mismatch-Repair Deficiency in Endometrial Cancers to Identify Patients With Lynch Syndrome and Lynch-like Syndrome.
Jaclyn C Watkins, Eric J Yang, Michael G Muto, Colleen M Feltmate, Ross S Berkowitz, Neil S Horowitz, Sapna Syngal, Matthew B Yurgelun, Anu Chittenden, Jason L Hornick,[...]. Int J Gynecol Pathol 2017
57
33

Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: case series, review and follow-up guidelines.
Johanna C Herkert, Renée C Niessen, Maria J W Olderode-Berends, Hermine E Veenstra-Knol, Yvonne J Vos, Heleen M van der Klift, Rene Scheenstra, Carli M J Tops, Arend Karrenbeld, Frans T M Peters,[...]. Eur J Cancer 2011
45
33

A phase II randomized, multicenter, open-label trial of continuing adjuvant temozolomide beyond 6 cycles in patients with glioblastoma (GEINO 14-01).
Carmen Balana, Maria Angeles Vaz, Juan Manuel Sepúlveda, Carlos Mesia, Sonia Del Barco, Estela Pineda, Jose Muñoz-Langa, Anna Estival, Ramón de Las Peñas, Jose Fuster,[...]. Neuro Oncol 2020
32
33

A homozygote splice site PMS2 mutation as cause of Turcot syndrome gives rise to two different abnormal transcripts.
Wenche Sjursen, Inga Bjørnevoll, Lars F Engebretsen, Kristine Fjelland, Tore Halvorsen, Helge E Myrvold. Fam Cancer 2009
25
33



Two PMS2 mutations in a Turcot syndrome family with small bowel cancers.
Marco Agostini, Maria Grazia Tibiletti, Emanuela Lucci-Cordisco, Annamaria Chiaravalli, Hans Morreau, Daniela Furlan, Luigi Boccuto, Salvatore Pucciarelli, Carlo Capella, Mauro Boiocchi,[...]. Am J Gastroenterol 2005
48
33

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
33

Pembrolizumab Activity in Recurrent High-Grade Gliomas with Partial or Complete Loss of Mismatch Repair Protein Expression: A Monocentric, Observational and Prospective Pilot Study.
Giuseppe Lombardi, Valeria Barresi, Stefano Indraccolo, Michele Simbolo, Matteo Fassan, Susanna Mandruzzato, Matteo Simonelli, Mario Caccese, Marco Pizzi, Arianna Fassina,[...]. Cancers (Basel) 2020
28
33

A homozygous MSH6 mutation in a child with café-au-lait spots, oligodendroglioma and rectal cancer.
Fred H Menko, Gertjan L Kaspers, Gerrit A Meijer, Kathleen Claes, Johanna M van Hagen, Johan J P Gille. Fam Cancer 2004
56
33

PMS2 mutations in childhood cancer.
Michel De Vos, Bruce E Hayward, Ruth Charlton, Graham R Taylor, Adam W Glaser, Susan Picton, Trevor R Cole, Eamonn R Maher, Carole M E McKeown, Jill R Mann,[...]. J Natl Cancer Inst 2006
60
33

Early onset brain tumor and lymphoma in MSH2-deficient children.
Gaëlle Bougeard, Françoise Charbonnier, Alexandre Moerman, Cosette Martin, Marie M Ruchoux, Nathalie Drouot, Thierry Frébourg. Am J Hum Genet 2003
66
33

MSI detection and its pitfalls in CMMRD syndrome in a family with a bi-allelic MLH1 mutation.
Aurélia Nguyen, Gaelle Bougeard, Meriam Koob, Marie Pierre Chenard, Anne Schneider, Christine Maugard, Natacha Entz-Werle. Fam Cancer 2016
7
33

Frameshift mutational target gene analysis identifies similarities and differences in constitutional mismatch repair-deficiency and Lynch syndrome.
Claudia Maletzki, Maja Huehns, Ingrid Bauer, Tim Ripperger, Maureen M Mork, Eduardo Vilar, Sabine Klöcking, Heike Zettl, Friedrich Prall, Michael Linnebacher. Mol Carcinog 2017
12
33

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
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,[...]. Am J Gastroenterol 2014
278
33

Delineating a new feature of constitutional mismatch repair deficiency (CMMRD) syndrome: breast cancer.
Lisa Bush, Melyssa Aronson, Uri Tabori, Brittany B Campbell, Raymond B Bedgood, Kory Jasperson. Fam Cancer 2019
5
33

Constitutional mismatch repair deficiency presenting in childhood as three simultaneous malignancies.
Andrew W Walter, Sara Ennis, Hunter Best, Cecily P Vaughn, Jeffrey J Swensen, Amanda Openshaw, Karen W Gripp. Pediatr Blood Cancer 2013
10
33

Neurofibromatosis type 1 gene as a mutational target in a mismatch repair-deficient cell type.
Qing Wang, Gilles Montmain, Eric Ruano, Meena Upadhyaya, Sandra Dudley, R Michael Liskay, Stephen N Thibodeau, Alain Puisieux. Hum Genet 2003
75
33

Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype.
Hilde Brems, Magdalena Chmara, Mourad Sahbatou, Ellen Denayer, Koji Taniguchi, Reiko Kato, Riet Somers, Ludwine Messiaen, Sofie De Schepper, Jean-Pierre Fryns,[...]. Nat Genet 2007
283
33

The gastrointestinal manifestation of constitutional mismatch repair deficiency syndrome: from a single adenoma to polyposis-like phenotype and early onset cancer.
Z Levi, R Kariv, I Barnes-Kedar, Y Goldberg, E Half, S Morgentern, B Eli, H N Baris, A Vilkin, R G Belfer,[...]. Clin Genet 2015
19
33

Biallelic PMS2 mutations and a distinctive childhood cancer syndrome.
Tiong Yang Tan, Lisa M Orme, Elly Lynch, Matthew A Croxford, Christopher Dow, Paddy A Dewan, Lara Lipton. J Pediatr Hematol Oncol 2008
23
33

Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1.
Stefan Krüger, Miriam Kinzel, Constanze Walldorf, Sven Gottschling, Andrea Bier, Sigrid Tinschert, Arend von Stackelberg, Wolfram Henn, Heike Görgens, Stephanie Boue,[...]. Eur J Hum Genet 2008
56
33

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
33

Multipopulation analysis of polymorphisms in five mononucleotide repeats used to determine the microsatellite instability status of human tumors.
Olivier Buhard, Francesca Cattaneo, Yick Fu Wong, So Fan Yim, Eitan Friedman, Jean-François Flejou, Alex Duval, Richard Hamelin. J Clin Oncol 2006
164
33

Hereditary brain tumor with a homozygous germline mutation in PMS2: pedigree analysis and prenatal screening in a family with constitutional mismatch repair deficiency (CMMRD) syndrome.
Shahid Mahmood Baig, Ambrin Fatima, Muhammad Tariq, Tahir Naeem Khan, Zafar Ali, Mohammad Faheem, Humera Mahmood, Patrick Killela, Matthew Waitkus, Yiping He,[...]. Fam Cancer 2019
3
33

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
33

Simultaneous colonic adenocarcinoma and medulloblastoma in a 12-year-old with biallelic deletions in PMS2.
Holly Lindsay, Rima F Jubran, Larry Wang, Benjamin R Kipp, William A May. J Pediatr 2013
9
33

Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations.
P C Johannesma, H M van der Klift, N C T van Grieken, D Troost, H Te Riele, M A J M Jacobs, T J Postma, D A M Heideman, C M J Tops, J T Wijnen,[...]. Clin Genet 2011
23
33

Neurofibromatosis and early onset of cancers in hMLH1-deficient children.
Q Wang, C Lasset, F Desseigne, D Frappaz, C Bergeron, C Navarro, E Ruano, A Puisieux. Cancer Res 1999
185
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.