A citation-based method for searching scientific literature

M G F van Lier, A Wagner, E M H Mathus-Vliegen, E J Kuipers, E W Steyerberg, M E van Leerdam. Am J Gastroenterol 2010
Times Cited: 286







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



Times Cited
  Times     Co-cited
Similarity


Very high risk of cancer in familial Peutz-Jeghers syndrome.
F M Giardiello, J D Brensinger, A C Tersmette, S N Goodman, G M Petersen, S V Booker, M Cruz-Correa, J A Offerhaus. Gastroenterology 2000
824
38

Peutz-Jeghers syndrome: a systematic review and recommendations for management.
A D Beggs, A R Latchford, H F A Vasen, G Moslein, A Alonso, S Aretz, L Bertario, I Blanco, S Bülow, J Burn,[...]. Gut 2010
369
38

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
771
37

Frequency and spectrum of cancers in the Peutz-Jeghers syndrome.
Nicholas Hearle, Valérie Schumacher, Fred H Menko, Sylviane Olschwang, Lisa A Boardman, Johan J P Gille, Josbert J Keller, Anne Marie Westerman, Rodney J Scott, Wendy Lim,[...]. Clin Cancer Res 2006
457
35

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.
A Hemminki, D Markie, I Tomlinson, E Avizienyte, S Roth, A Loukola, G Bignell, W Warren, M Aminoff, P Höglund,[...]. Nature 1998
23

International Cancer of the Pancreas Screening (CAPS) Consortium summit on the management of patients with increased risk for familial pancreatic cancer.
Marcia Irene Canto, Femme Harinck, Ralph H Hruban, George Johan Offerhaus, Jan-Werner Poley, Ihab Kamel, Yung Nio, Richard S Schulick, Claudio Bassi, Irma Kluijt,[...]. Gut 2013
472
20

Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase.
D E Jenne, H Reimann, J Nezu, W Friedel, S Loff, R Jeschke, O Müller, W Back, M Zimmer. Nat Genet 1998
814
20

Peutz-Jeghers syndrome and management recommendations.
Francis M Giardiello, Jill D Trimbath. Clin Gastroenterol Hepatol 2006
234
20

High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
Stefan Aretz, Dietlinde Stienen, Siegfried Uhlhaas, Steffan Loff, Walter Back, Constanze Pagenstecher, D Ross McLeod, Gail E Graham, Elisabeth Mangold, René Santer,[...]. Hum Mutat 2005
165
18

Relative frequency and morphology of cancers in STK11 mutation carriers.
Wendy Lim, Sylviane Olschwang, Josbert J Keller, Anne Marie Westerman, Fred H Menko, Lisa A Boardman, Rodney J Scott, Jill Trimbath, Francis M Giardiello, Stephen B Gruber,[...]. Gastroenterology 2004
149
16

Peutz-Jeghers syndrome: its natural course and management.
J Utsunomiya, H Gocho, T Miyanaga, E Hamaguchi, A Kashimure. Johns Hopkins Med J 1975
255
16

Lifetime cancer risks in individuals with germline PTEN mutations.
Min-Han Tan, Jessica L Mester, Joanne Ngeow, Lisa A Rybicki, Mohammed S Orloff, Charis Eng. Clin Cancer Res 2012
473
15

Genotype-phenotype correlations in Peutz-Jeghers syndrome.
C I Amos, M B Keitheri-Cheteri, M Sabripour, C Wei, T J McGarrity, M F Seldin, L Nations, P M Lynch, H H Fidder, E Friedman,[...]. J Med Genet 2004
123
15

Risk of pancreatic cancer in families with Lynch syndrome.
Fay Kastrinos, Bhramar Mukherjee, Nabihah Tayob, Fei Wang, Jennifer Sparr, Victoria M Raymond, Prathap Bandipalliam, Elena M Stoffel, Stephen B Gruber, Sapna Syngal. JAMA 2009
308
15

Management of patients with increased risk for familial pancreatic cancer: updated recommendations from the International Cancer of the Pancreas Screening (CAPS) Consortium.
Michael Goggins, Kasper Alexander Overbeek, Randall Brand, Sapna Syngal, Marco Del Chiaro, Detlef K Bartsch, Claudio Bassi, Alfredo Carrato, James Farrell, Elliot K Fishman,[...]. Gut 2020
176
15

Frequent detection of pancreatic lesions in asymptomatic high-risk individuals.
Marcia Irene Canto, Ralph H Hruban, Elliot K Fishman, Ihab R Kamel, Richard Schulick, Zhe Zhang, Mark Topazian, Naoki Takahashi, Joel Fletcher, Gloria Petersen,[...]. Gastroenterology 2012
411
14

Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study.
Nicoletta Resta, Daniela Pierannunzio, Gennaro Mariano Lenato, Alessandro Stella, Riccardo Capocaccia, Rosanna Bagnulo, Patrizia Lastella, Francesco Claudio Susca, Cristina Bozzao, Daria Carmela Loconte,[...]. Dig Liver Dis 2013
68
19

Risk of colorectal cancer in juvenile polyposis.
Lodewijk A A Brosens, Arnout van Hattem, Linda M Hylind, Christine Iacobuzio-Donahue, Katharine E Romans, Jennifer Axilbund, Marcia Cruz-Correa, Anne C Tersmette, G Johan A Offerhaus, Francis M Giardiello. Gut 2007
138
13

High cumulative risk of intussusception in patients with Peutz-Jeghers syndrome: time to update surveillance guidelines?
M G F van Lier, E M H Mathus-Vliegen, A Wagner, M E van Leerdam, E J Kuipers. Am J Gastroenterol 2011
80
15

The hamartomatous polyposis syndromes: a clinical and molecular review.
Ian Roy Schreibman, Maria Baker, Christopher Amos, Thomas J McGarrity. Am J Gastroenterol 2005
192
12

Risk of Neoplastic Progression in Individuals at High Risk for Pancreatic Cancer Undergoing Long-term Surveillance.
Marcia Irene Canto, Jose Alejandro Almario, Richard D Schulick, Charles J Yeo, Alison Klein, Amanda Blackford, Eun Ji Shin, Abanti Sanyal, Gayane Yenokyan, Anne Marie Lennon,[...]. Gastroenterology 2018
168
12

Prospective risk of pancreatic cancer in familial pancreatic cancer kindreds.
Alison P Klein, Kieran A Brune, Gloria M Petersen, Michael Goggins, Anne C Tersmette, G Johan A Offerhaus, Constance Griffin, John L Cameron, Charles J Yeo, Scott Kern,[...]. Cancer Res 2004
426
11

High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome.
Margot G F van Lier, Anne Marie Westerman, Anja Wagner, Caspar W N Looman, J H Paul Wilson, Felix W M de Rooij, Valery E P P Lemmens, Ernst J Kuipers, Elisabeth M H Mathus-Vliegen, Monique E van Leerdam. Gut 2011
104
11

Complications of childhood Peutz-Jeghers syndrome: implications for pediatric screening.
R Hinds, C Philp, W Hyer, J M Fell. J Pediatr Gastroenterol Nutr 2004
75
14

Hereditary pancreatitis and the risk of pancreatic cancer. International Hereditary Pancreatitis Study Group.
A B Lowenfels, P Maisonneuve, E P DiMagno, Y Elitsur, L K Gates, J Perrault, D C Whitcomb. J Natl Cancer Inst 1997
675
11


Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas.
Claire Palles, Jean-Baptiste Cazier, Kimberley M Howarth, Enric Domingo, Angela M Jones, Peter Broderick, Zoe Kemp, Sarah L Spain, Estrella Guarino, Israel Salguero,[...]. Nat Genet 2013
634
10

The risk of gastrointestinal carcinoma in familial juvenile polyposis.
J R Howe, F A Mitros, R W Summers. Ann Surg Oncol 1998
177
10

Frequent gastrointestinal polyps and colorectal adenocarcinomas in a prospective series of PTEN mutation carriers.
Brandie Heald, Jessica Mester, Lisa Rybicki, Mohammed S Orloff, Carol A Burke, Charis Eng. Gastroenterology 2010
166
10

ATM mutations in patients with hereditary pancreatic cancer.
Nicholas J Roberts, Yuchen Jiao, Jun Yu, Levy Kopelovich, Gloria M Petersen, Melissa L Bondy, Steven Gallinger, Ann G Schwartz, Sapna Syngal, Michele L Cote,[...]. Cancer Discov 2012
317
10

Association Between Inherited Germline Mutations in Cancer Predisposition Genes and Risk of Pancreatic Cancer.
Chunling Hu, Steven N Hart, Eric C Polley, Rohan Gnanaolivu, Hermela Shimelis, Kun Y Lee, Jenna Lilyquist, Jie Na, Raymond Moore, Samuel O Antwi,[...]. JAMA 2018
241
10

Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond.
Samantha Hansford, Pardeep Kaurah, Hector Li-Chang, Michelle Woo, Janine Senz, Hugo Pinheiro, Kasmintan A Schrader, David F Schaeffer, Karey Shumansky, George Zogopoulos,[...]. JAMA Oncol 2015
352
9

LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome.
E Volikos, J Robinson, K Aittomäki, J-P Mecklin, H Järvinen, A M Westerman, F W M de Rooji, T Vogel, G Moeslein, V Launonen,[...]. J Med Genet 2006
101
9

High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome.
S Aretz, D Stienen, S Uhlhaas, M Stolte, M M Entius, S Loff, W Back, A Kaufmann, K-M Keller, S H Blaas,[...]. J Med Genet 2007
121
9

Morphologic characterization of hamartomatous gastrointestinal polyps in Cowden syndrome, Peutz-Jeghers syndrome, and juvenile polyposis syndrome.
Ruthy Shaco-Levy, Kory W Jasperson, Katie Martin, N Jewel Samadder, Randall W Burt, Jian Ying, Mary P Bronner. Hum Pathol 2016
25
36

Cowden syndrome and the PTEN hamartoma tumor syndrome: systematic review and revised diagnostic criteria.
Robert Pilarski, Randall Burt, Wendy Kohlman, Lana Pho, Kristen M Shannon, Elizabeth Swisher. J Natl Cancer Inst 2013
265
9

Peutz-Jeghers syndrome.
I P Tomlinson, R S Houlston. J Med Genet 1997
188
9

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
637
9


Cancer risks in BRCA2 families: estimates for sites other than breast and ovary.
C J van Asperen, R M Brohet, E J Meijers-Heijboer, N Hoogerbrugge, S Verhoef, H F A Vasen, M G E M Ausems, F H Menko, E B Gomez Garcia, J G M Klijn,[...]. J Med Genet 2005
283
9

Management of Peutz-Jeghers Syndrome in Children and Adolescents: A Position Paper From the ESPGHAN Polyposis Working Group.
Andrew Latchford, Shlomi Cohen, Marcus Auth, Michele Scaillon, Jerome Viala, Richard Daniels, Cecile Talbotec, Thomas Attard, Carol Durno, Warren Hyer. J Pediatr Gastroenterol Nutr 2019
29
31

The LKB1-AMPK pathway: metabolism and growth control in tumour suppression.
David B Shackelford, Reuben J Shaw. Nat Rev Cancer 2009
9

Benefit of Surveillance for Pancreatic Cancer in High-Risk Individuals: Outcome of Long-Term Prospective Follow-Up Studies From Three European Expert Centers.
Hans Vasen, Isaura Ibrahim, Carmen Guillen Ponce, Emily P Slater, Elvira Matthäi, Alfredo Carrato, Julie Earl, Kristin Robbers, Anneke M van Mil, Thomas Potjer,[...]. J Clin Oncol 2016
200
9

Breast-cancer risk in families with mutations in PALB2.
Antonis C Antoniou, Silvia Casadei, Tuomas Heikkinen, Daniel Barrowdale, Katri Pylkäs, Jonathan Roberts, Andrew Lee, Deepak Subramanian, Kim De Leeneer, Florentia Fostira,[...]. N Engl J Med 2014
513
8

High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome.
Virginie Bubien, Françoise Bonnet, Veronique Brouste, Stéphanie Hoppe, Emmanuelle Barouk-Simonet, Albert David, Patrick Edery, Armand Bottani, Valérie Layet, Olivier Caron,[...]. J Med Genet 2013
178
8


Clinical and genetic characteristics of hereditary pancreatitis in Europe.
Nathan Howes, Markus M Lerch, William Greenhalf, Deborah D Stocken, Ian Ellis, Peter Simon, Kaspar Truninger, Rudi Ammann, Giorgio Cavallini, Richard M Charnley,[...]. Clin Gastroenterol Hepatol 2004
385
8

Cancer risks in LKB1 germline mutation carriers.
H Mehenni, N Resta, J-G Park, M Miyaki, G Guanti, M C Costanza. Gut 2006
72
11

Juvenile polyposis syndrome: a study of genotype, phenotype, and long-term outcome.
Andrew R Latchford, Kay Neale, Robin K S Phillips, Susan K Clark. Dis Colon Rectum 2012
72
11



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.