A citation-based method for searching scientific literature

A D Beggs, A R Latchford, H F A Vasen, G Moslein, A Alonso, S Aretz, L Bertario, I Blanco, S Bülow, J Burn, G Capella, C Colas, W Friedl, P Møller, F J Hes, H Järvinen, J-P Mecklin, F M Nagengast, Y Parc, R K S Phillips, W Hyer, M Ponz de Leon, L Renkonen-Sinisalo, J R Sampson, A Stormorken, S Tejpar, H J W Thomas, J T Wijnen, S K Clark, S V Hodgson. Gut 2010
Times Cited: 333







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



Times Cited
  Times     Co-cited
Similarity


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
419
33

High cancer risk in Peutz-Jeghers syndrome: a systematic review and surveillance recommendations.
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
259
27

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
68
30

Peutz-Jeghers syndrome and management recommendations.
Francis M Giardiello, Jill D Trimbath. Clin Gastroenterol Hepatol 2006
218
20

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
18

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
783
18

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
153
18

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
624
18

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
791
15

Complications of childhood Peutz-Jeghers syndrome: implications for pediatric screening.
R Hinds, C Philp, W Hyer, J M Fell. J Pediatr Gastroenterol Nutr 2004
68
20

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
94
13


Peutz-Jeghers syndrome: its natural course and management.
J Utsunomiya, H Gocho, T Miyanaga, E Hamaguchi, A Kashimure. Johns Hopkins Med J 1975
244
11

Nonsurgical management of small-bowel polyps in Peutz-Jeghers syndrome with extensive polypectomy by using double-balloon endoscopy.
Hirotsugu Sakamoto, Hironori Yamamoto, Yoshikazu Hayashi, Tomonori Yano, Tomohiko Miyata, Naoyuki Nishimura, Hakuei Shinhata, Hiroyuki Sato, Keijiro Sunada, Kentaro Sugano. Gastrointest Endosc 2011
42
26

Increased risk for cancer in patients with the Peutz-Jeghers syndrome.
L A Boardman, S N Thibodeau, D J Schaid, N M Lindor, S K McDonnell, L J Burgart, D A Ahlquist, K C Podratz, M Pittelkow, L C Hartmann. Ann Intern Med 1998
274
10

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
62
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
421
10


Effectiveness of Double-balloon Enteroscopy-facilitated Polypectomy in Pediatric Patients With Peutz-Jeghers Syndrome.
Dalia Belsha, Arun Urs, Thomas Attard, Mike Thomson. J Pediatr Gastroenterol Nutr 2017
16
62

Management of small-bowel polyps in Peutz-Jeghers syndrome by using enteroclysis, double-balloon enteroscopy, and videocapsule endoscopy.
Naoki Ohmiya, Masanao Nakamura, Hiroyuki Takenaka, Kenji Morishima, Takeshi Yamamura, Makoto Ishihara, Ryoji Miyahara, Hiroki Kawashima, Akihiro Itoh, Yoshiki Hirooka,[...]. Gastrointest Endosc 2010
48
20

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
116
9

A prospective study of MR enterography versus capsule endoscopy for the surveillance of adult patients with Peutz-Jeghers syndrome.
Arun Gupta, Aymer J Postgate, David Burling, Rajapandian Ilangovan, Michele Marshall, Robin K S Phillips, Susan K Clark, Chris H Fraser. AJR Am J Roentgenol 2010
71
12

Endoscopic therapy of small-bowel polyps by double-balloon enteroscopy in patients with Peutz-Jeghers syndrome.
Hong Gao, Margot G van Lier, Jan Werner Poley, Ernst J Kuipers, Monique E van Leerdam, Peter B Mensink. Gastrointest Endosc 2010
46
19

Peutz-Jeghers syndrome: diagnostic and therapeutic approach.
Marcela Kopacova, Ilja Tacheci, Stanislav Rejchrt, Jan Bures. World J Gastroenterol 2009
86
10

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
98
8

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
59
13

Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis.
A Hemminki, I Tomlinson, D Markie, H Järvinen, P Sistonen, A M Björkqvist, S Knuutila, R Salovaara, W Bodmer, D Shibata,[...]. Nat Genet 1997
338
8

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
19
42

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
137
7

High prevalence of germline STK11 mutations in Hungarian Peutz-Jeghers Syndrome patients.
Janos Papp, Marietta Eva Kovacs, Szilvia Solyom, Miklos Kasler, Anne-Lise Børresen-Dale, Edith Olah. BMC Med Genet 2010
26
26

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
124
7

Peutz-Jegher syndrome in childhood: need for updated recommendations?
Stephanie A Goldstein, Edward J Hoffenberg. J Pediatr Gastroenterol Nutr 2013
21
33

Cancer risk in patients with Peutz-Jeghers syndrome: A retrospective cohort study of 336 cases.
Hong-Yu Chen, Xiao-Wei Jin, Bai-Rong Li, Ming Zhu, Jing Li, Gao-Ping Mao, Ya-Fei Zhang, Shou-Bin Ning. Tumour Biol 2017
13
53

Peutz-Jeghers syndrome: intriguing suggestion of gastrointestinal cancer prevention from surveillance.
A R Latchford, K Neale, R K S Phillips, S K Clark. Dis Colon Rectum 2011
28
25

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
291
7

Truncating mutations in Peutz-Jeghers syndrome are associated with more polyps, surgical interventions and cancers.
Heidi Salloch, Anke Reinacher-Schick, Karsten Schulmann, Christian Pox, Jörg Willert, Andrea Tannapfel, Stefan Heringlake, Timm O Goecke, Stefan Aretz, Susanne Stemmler,[...]. Int J Colorectal Dis 2010
27
22

Disease pattern in Danish patients with Peutz-Jeghers syndrome.
A M Jelsig, N Qvist, L Sunde, K Brusgaard, Tvo Hansen, F P Wikman, C B Nielsen, I K Nielsen, A M Gerdes, A Bojesen,[...]. Int J Colorectal Dis 2016
7
85

Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome.
W Lim, N Hearle, B Shah, V Murday, S V Hodgson, A Lucassen, D Eccles, I Talbot, K Neale, A G Lim,[...]. Br J Cancer 2003
98
6

Cancer risks in LKB1 germline mutation carriers.
H Mehenni, N Resta, J-G Park, M Miyaki, G Guanti, M C Costanza. Gut 2006
68
8

First report of somatic mosaicism for mutations in STK11 in four patients with Peutz-Jeghers syndrome.
Victoria McKay, Diane Cairns, David Gokhale, Roger Mountford, Lynn Greenhalgh. Fam Cancer 2016
8
75

The hamartomatous polyposis syndromes: a clinical and molecular review.
Ian Roy Schreibman, Maria Baker, Christopher Amos, Thomas J McGarrity. Am J Gastroenterol 2005
179
6

Peutz-Jeghers syndrome.
T J McGarrity, H E Kulin, R J Zaino. Am J Gastroenterol 2000
156
6

Cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal Cancer Syndromes in Childhood.
Maria Isabel Achatz, Christopher C Porter, Laurence Brugières, Harriet Druker, Thierry Frebourg, William D Foulkes, Christian P Kratz, Roland P Kuiper, Jordan R Hansford, Hector Salvador Hernandez,[...]. Clin Cancer Res 2017
43
13

Update on imaging of Peutz-Jeghers syndrome.
Catherine Tomas, Philippe Soyer, Anthony Dohan, Xavier Dray, Mourad Boudiaf, Christine Hoeffel. World J Gastroenterol 2014
22
27


Hereditary Colorectal Polyposis and Cancer Syndromes: A Primer on Diagnosis and Management.
Priyanka Kanth, Jade Grimmett, Marjan Champine, Randall Burt, N Jewel Samadder. Am J Gastroenterol 2017
48
12

Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients.
R J Scott, R Crooks, C J Meldrum, L Thomas, C J A Smith, D Mowat, M McPhillips, A D Spigelman. Clin Genet 2002
41
12

STK11 genotyping and cancer risk in Peutz-Jeghers syndrome.
V Schumacher, T Vogel, B Leube, C Driemel, T Goecke, G Möslein, B Royer-Pokora. J Med Genet 2005
57
8

Increased risk of cancer in the Peutz-Jeghers syndrome.
F M Giardiello, S B Welsh, S R Hamilton, G J Offerhaus, A M Gittelsohn, S V Booker, A J Krush, J H Yardley, G D Luk. N Engl J Med 1987
597
5

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
107
5


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.