A citation-based method for searching scientific literature

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, Jill D Trimbath, Francis M Giardiello, Stephen B Gruber, G Johan A Offerhaus, Felix W M de Rooij, J H Paul Wilson, Anika Hansmann, Gabriela Möslein, Brigitte Royer-Pokora, Tilman Vogel, Robin K S Phillips, Allan D Spigelman, Richard S Houlston. Clin Cancer Res 2006
Times Cited: 457

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

Times Cited
  Times     Co-cited

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Risks of first and subsequent cancers among TP53 mutation carriers in the National Cancer Institute Li-Fraumeni syndrome cohort.
Phuong L Mai, Ana F Best, June A Peters, Rosamma M DeCastro, Payal P Khincha, Jennifer T Loud, Renée C Bremer, Philip S Rosenberg, Sharon A Savage. Cancer 2016

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

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

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

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

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

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

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

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

Cancer risks and mortality in heterozygous ATM mutation carriers.
Deborah Thompson, Silvia Duedal, Jennifer Kirner, Lesley McGuffog, James Last, Anne Reiman, Philip Byrd, Malcolm Taylor, Douglas F Easton. J Natl Cancer Inst 2005

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

Gene-panel sequencing and the prediction of breast-cancer risk.
Douglas F Easton, Paul D P Pharoah, Antonis C Antoniou, Marc Tischkowitz, Sean V Tavtigian, Katherine L Nathanson, Peter Devilee, Alfons Meindl, Fergus J Couch, Melissa Southey,[...]. N Engl J Med 2015

Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene.
Siân Jones, Ralph H Hruban, Mihoko Kamiyama, Michael Borges, Xiaosong Zhang, D Williams Parsons, Jimmy Cheng-Ho Lin, Emily Palmisano, Kieran Brune, Elizabeth M Jaffee,[...]. Science 2009

Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database.
Pål Møller, Toni T Seppälä, Inge Bernstein, Elke Holinski-Feder, Paulo Sala, D Gareth Evans, Annika Lindblom, Finlay Macrae, Ignacio Blanco, Rolf H Sijmons,[...]. Gut 2018

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

Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers.
Karoline B Kuchenbaecker, John L Hopper, Daniel R Barnes, Kelly-Anne Phillips, Thea M Mooij, Marie-José Roos-Blom, Sarah Jervis, Flora E van Leeuwen, Roger L Milne, Nadine Andrieu,[...]. JAMA 2017

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

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

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

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

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

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

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

Management of duodenal-jejunal polyps in children with peutz-jeghers syndrome with single-balloon enteroscopy.
Barbara Bizzarri, Osvaldo Borrelli, Nicola de'Angelis, Alessia Ghiselli, Giorgio Nervi, Marco Manfredi, Gian Luigi de'Angelis. J Pediatr Gastroenterol Nutr 2014

ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles.
Anthony Renwick, Deborah Thompson, Sheila Seal, Patrick Kelly, Tasnim Chagtai, Munaza Ahmed, Bernard North, Hiran Jayatilake, Rita Barfoot, Katarina Spanova,[...]. Nat Genet 2006

Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations.
Hanne Meijers-Heijboer, Ans van den Ouweland, Jan Klijn, Marijke Wasielewski, Anja de Snoo, Rogier Oldenburg, Antoinette Hollestelle, Mark Houben, Ellen Crepin, Monique van Veghel-Plandsoen,[...]. Nat Genet 2002

Rare variants in the ATM gene and risk of breast cancer.
David E Goldgar, Sue Healey, James G Dowty, Leonard Da Silva, Xiaoqing Chen, Amanda B Spurdle, Mary Beth Terry, Mary J Daly, Saundra M Buys, Melissa C Southey,[...]. Breast Cancer Res 2011

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

Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment.
Allison W Kurian, Emily E Hare, Meredith A Mills, Kerry E Kingham, Lisa McPherson, Alice S Whittemore, Valerie McGuire, Uri Ladabaum, Yuya Kobayashi, Stephen E Lincoln,[...]. J Clin Oncol 2014

A study of over 35,000 women with breast cancer tested with a 25-gene panel of hereditary cancer genes.
Saundra S Buys, John F Sandbach, Amanda Gammon, Gayle Patel, John Kidd, Krystal L Brown, Lavania Sharma, Jennifer Saam, Johnathan Lancaster, Mary B Daly. Cancer 2017

Pancreatic cancer risk in Peutz-Jeghers syndrome patients: a large cohort study and implications for surveillance.
Susanne E Korsse, Femme Harinck, Margot G F van Lier, Katharina Biermann, G Johan A Offerhaus, Nanda Krak, Caspar W N Looman, Wendy van Veelen, Ernst J Kuipers, Anja Wagner,[...]. J Med Genet 2013

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.