A citation-based method for searching scientific literature

John A Heath, Jeanette C Reece, Daniel D Buchanan, Graham Casey, Carol A Durno, Steven Gallinger, Robert W Haile, Polly A Newcomb, John D Potter, Stephen N Thibodeau, Loïc Le Marchand, Noralane M Lindor, John L Hopper, Mark A Jenkins, Aung Ko Win. Fam Cancer 2015
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.
Mev Dominguez-Valentin, Julian R Sampson, Toni T Seppälä, Sanne W Ten Broeke, John-Paul Plazzer, Sigve Nakken, Christoph Engel, Stefan Aretz, Mark A Jenkins, Lone Sunde,[...]. Genet Med 2020
130
66

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability.
Asad Umar, C Richard Boland, Jonathan P Terdiman, Sapna Syngal, Albert de la Chapelle, Josef Rüschoff, Richard Fishel, Noralane M Lindor, Lawrence J Burgart, Richard Hamelin,[...]. J Natl Cancer Inst 2004
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
9
66

p53 polymorphism and age of onset of hereditary nonpolyposis colorectal cancer in a Caucasian population.
J Shawn Jones, Xuedong Chi, Xiangjun Gu, Patrick M Lynch, Christopher I Amos, Marsha L Frazier. Clin Cancer Res 2004
78
33

Refractory myeloid sarcoma with a FIP1L1-PDGFRA rearrangement detected by clinical high throughput somatic sequencing.
Diana Mandelker, Paola Dal Cin, Heather A Jacene, Philippe Armand, Richard M Stone, Neal I Lindeman. Exp Hematol Oncol 2015
4
33

Adrenocortical carcinoma.
Tobias Else, Alex C Kim, Aaron Sabolch, Victoria M Raymond, Asha Kandathil, Elaine M Caoili, Shruti Jolly, Barbra S Miller, Thomas J Giordano, Gary D Hammer. Endocr Rev 2014
404
33


Adrenocortical carcinoma in the United States: treatment utilization and prognostic factors.
Karl Y Bilimoria, Wen T Shen, Dina Elaraj, David J Bentrem, David J Winchester, Electron Kebebew, Cord Sturgeon. Cancer 2008
304
33

Exome sequencing of serous endometrial tumors identifies recurrent somatic mutations in chromatin-remodeling and ubiquitin ligase complex genes.
Matthieu Le Gallo, Andrea J O'Hara, Meghan L Rudd, Mary Ellen Urick, Nancy F Hansen, Nigel J O'Neil, Jessica C Price, Suiyuan Zhang, Bryant M England, Andrew K Godwin,[...]. Nat Genet 2012
271
33


Extent of disease at presentation and outcome for adrenocortical carcinoma: have we made progress?
Electron Kebebew, Emily Reiff, Quan-Yang Duh, Orlo H Clark, Alex McMillan. World J Surg 2006
252
33


Heterogenous loss of mismatch repair (MMR) protein expression: a challenge for immunohistochemical interpretation and microsatellite instability (MSI) evaluation.
Aoife J McCarthy, Jose-Mario Capo-Chichi, Tara Spence, Sylvie Grenier, Tracy Stockley, Suzanne Kamel-Reid, Stefano Serra, Peter Sabatini, Runjan Chetty. J Pathol Clin Res 2019
33
33

European Society of Endocrinology Clinical Practice Guidelines on the management of adrenocortical carcinoma in adults, in collaboration with the European Network for the Study of Adrenal Tumors
Martin Fassnacht, Olaf Dekkers, Tobias Else, Eric Baudin, Alfredo Berruti, Ronald de Krijger, Harm Haak, Radu Mihai, Guillaume Assie, Massimo Terzolo. Eur J Endocrinol 2018
152
33

[Endometrial cancers and predisposition].
Olivier Caron. Bull Cancer 2012
2
50

Mismatch repair.
Richard Fishel. J Biol Chem 2015
97
33

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer.
R Fishel, M K Lescoe, M R Rao, N G Copeland, N A Jenkins, J Garber, M Kane, R Kolodner. Cell 1993
33

An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma.
R C Ribeiro, F Sandrini, B Figueiredo, G P Zambetti, E Michalkiewicz, A R Lafferty, L DeLacerda, M Rabin, C Cadwell, G Sampaio,[...]. Proc Natl Acad Sci U S A 2001
344
33

VarSome: the human genomic variant search engine.
Christos Kopanos, Vasilis Tsiolkas, Alexandros Kouris, Charles E Chapple, Monica Albarca Aguilera, Richard Meyer, Andreas Massouras. Bioinformatics 2019
439
33

Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer.
C E Bronner, S M Baker, P T Morrison, G Warren, L G Smith, M K Lescoe, M Kane, C Earabino, J Lipford, A Lindblom. Nature 1994
33

Expression of insulin-like growth factor-II and its receptor in pediatric and adult adrenocortical tumors.
Madson Q Almeida, Maria Candida Barisson Villares Fragoso, Claudimara Ferini Pacicco Lotfi, Mariza Gerdulo Santos, Mirian Yumie Nishi, Marcia Helena Soares Costa, Antonio Marcondes Lerario, Carolina Canton Maciel, Gabriele Ebling Mattos, Alexander Augusto Lima Jorge,[...]. J Clin Endocrinol Metab 2008
116
33

The associated contributions of p53 and the DNA mismatch repair protein Msh6 to spontaneous tumorigenesis.
Leah C Young, Angela M Keuling, Raymond Lai, Patrick N Nation, Victor A Tron, Susan E Andrew. Carcinogenesis 2007
16
33

Adrenal cortical carcinoma.
A P Dackiw, J E Lee, R F Gagel, D B Evans. World J Surg 2001
229
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
253
33

EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome.
Glenn E Palomaki, Monica R McClain, Stephanie Melillo, Heather L Hampel, Stephen N Thibodeau. Genet Med 2009
327
33


Molecular epidemiology of adrenocortical tumors in southern Brazil.
Gislaine Custódio, Heloisa Komechen, Francisco R O Figueiredo, Natasha D Fachin, Mara A D Pianovski, Bonald C Figueiredo. Mol Cell Endocrinol 2012
37
33

An inherited mutation outside the highly conserved DNA-binding domain of the p53 tumor suppressor protein in children and adults with sporadic adrenocortical tumors.
A C Latronico, E M Pinto, S Domenice, M C Fragoso, R M Martin, M C Zerbini, A M Lucon, B B Mendonca. J Clin Endocrinol Metab 2001
142
33

The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC).
H F Vasen, J P Mecklin, P M Khan, H T Lynch. Dis Colon Rectum 1991
33

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.
F S Leach, N C Nicolaides, N Papadopoulos, B Liu, J Jen, R Parsons, P Peltomäki, P Sistonen, L A Aaltonen, M Nyström-Lahti. Cell 1993
33

Mutation of a mutL homolog in hereditary colon cancer.
N Papadopoulos, N C Nicolaides, Y F Wei, S M Ruben, K C Carter, C A Rosen, W A Haseltine, R D Fleischmann, C M Fraser, M D Adams. Science 1994
33

Lynch syndrome: a pediatric perspective.
Sherry C Huang, Carol A Durno, Steven H Erdman. J Pediatr Gastroenterol Nutr 2014
9
33

Adrenocortical carcinoma: clinical and laboratory observations.
B L Wajchenberg, M A Albergaria Pereira, B B Medonca, A C Latronico, P Campos Carneiro, V A Alves, M C Zerbini, B Liberman, G Carlos Gomes, M A Kirschner. Cancer 2000
272
33

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
345
33

Hereditary factors in cancer. Study of two large midwestern kindreds.
H T Lynch, M W Shaw, C W Magnuson, A L Larsen, A J Krush. Arch Intern Med 1966
292
33

Identification of Lynch syndrome among patients with colorectal cancer.
Leticia Moreira, Francesc Balaguer, Noralane Lindor, Albert de la Chapelle, Heather Hampel, Lauri A Aaltonen, John L Hopper, Loic Le Marchand, Steven Gallinger, Polly A Newcomb,[...]. JAMA 2012
303
33

Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome.
Christian P Kratz, Maria Isabel Achatz, Laurence Brugières, Thierry Frebourg, Judy E Garber, Mary-Louise C Greer, Jordan R Hansford, Katherine A Janeway, Wendy K Kohlmann, Rose McGee,[...]. Clin Cancer Res 2017
202
33

Genetic polymorphisms of multiple DNA repair pathways impact age at diagnosis and TP53 mutations in breast cancer.
Tasha R Smith, Wen Liu-Mares, Beth O Van Emburgh, Edward A Levine, Glenn O Allen, Jeff W Hill, Isildinha M Reis, Laura A Kresty, Mark D Pegram, Mark S Miller,[...]. Carcinogenesis 2011
20
33

Childhood adrenocortical tumors.
R Sandrini, R C Ribeiro, L DeLacerda. J Clin Endocrinol Metab 1997
160
33

Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome.
Marietta E Kovacs, Janos Papp, Zoltan Szentirmay, Szabolcs Otto, Edith Olah. Hum Mutat 2009
116
33

[Lynch syndrome: selection of families by microsatellite instability and immunohistochemistry].
Ana María Wielandt, Alejandro J Zárate, Claudia Hurtado, Paulina Orellana, Karin Alvarez, Eliana Pinto, Luis Contreras, Alejandro Corvalán, Udo Kronberg, Francisco López-Köstner. Rev Med Chil 2012
8
33

Microsatellite Instability: A Predictive Biomarker for Cancer Immunotherapy.
Liisa Chang, Minna Chang, Hanna M Chang, Fuju Chang. Appl Immunohistochem Mol Morphol 2018
119
33

A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer.
C R Boland, S N Thibodeau, S R Hamilton, D Sidransky, J R Eshleman, R W Burt, S J Meltzer, M A Rodriguez-Bigas, R Fodde, G N Ranzani,[...]. Cancer Res 1998
33

Founder effect for the highly prevalent R337H mutation of tumor suppressor p53 in Brazilian patients with adrenocortical tumors.
Emilia M Pinto, Ana Elisa C Billerbeck, Maria Candida B F Villares, Sorahia Domenice, Berenice B Mendonça, Ana Claudia Latronico. Arq Bras Endocrinol Metabol 2004
75
33

Adrenocortical carcinoma is a lynch syndrome-associated cancer.
Victoria M Raymond, Jessica N Everett, Larissa V Furtado, Shanna L Gustafson, Chelsy R Jungbluth, Stephen B Gruber, Gary D Hammer, Elena M Stoffel, Joel K Greenson, Thomas J Giordano,[...]. J Clin Oncol 2013
101
33

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.
Bryony A Thompson, Amanda B Spurdle, John-Paul Plazzer, Marc S Greenblatt, Kiwamu Akagi, Fahd Al-Mulla, Bharati Bapat, Inge Bernstein, Gabriel Capellá, Johan T den Dunnen,[...]. Nat Genet 2014
304
33

CONTRA: copy number analysis for targeted resequencing.
Jason Li, Richard Lupat, Kaushalya C Amarasinghe, Ella R Thompson, Maria A Doyle, Georgina L Ryland, Richard W Tothill, Saman K Halgamuge, Ian G Campbell, Kylie L Gorringe. Bioinformatics 2012
206
33

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
30
33

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
453
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
55
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.