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: 419

List of co-cited articles
859 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

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

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

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

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

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

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

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

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

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

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

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 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

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

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

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

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

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

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

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

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

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

LKB1-dependent signaling pathways.
Dario R Alessi, Kei Sakamoto, Jose R Bayascas. Annu Rev Biochem 2006

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

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

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

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

Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer.
Fergus J Couch, Hermela Shimelis, Chunling Hu, Steven N Hart, Eric C Polley, Jie Na, Emily Hallberg, Raymond Moore, Abigail Thomas, Jenna Lilyquist,[...]. JAMA Oncol 2017

Inactivation of LKB1/STK11 is a common event in adenocarcinomas of the lung.
Montserrat Sanchez-Cespedes, Paola Parrella, Manel Esteller, Shuji Nomoto, Barry Trink, James M Engles, William H Westra, James G Herman, David Sidransky. Cancer Res 2002

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

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

American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography.
Debbie Saslow, Carla Boetes, Wylie Burke, Steven Harms, Martin O Leach, Constance D Lehman, Elizabeth Morris, Etta Pisano, Mitchell Schnall, Stephen Sener,[...]. CA Cancer J Clin 2007

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium.
D Ford, D F Easton, M Stratton, S Narod, D Goldgar, P Devilee, D T Bishop, B Weber, G Lenoir, J Chang-Claude,[...]. Am J Hum Genet 1998

Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer.
Pardeep Kaurah, Andrée MacMillan, Niki Boyd, Janine Senz, Alessandro De Luca, Nicki Chun, Gianpaolo Suriano, Sonya Zaor, Lori Van Manen, Cathy Gilpin,[...]. JAMA 2007

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

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

MO25alpha/beta interact with STRADalpha/beta enhancing their ability to bind, activate and localize LKB1 in the cytoplasm.
Jérôme Boudeau, Annette F Baas, Maria Deak, Nick A Morrice, Agnieszka Kieloch, Mike Schutkowski, Alan R Prescott, Hans C Clevers, Dario R Alessi. EMBO J 2003

STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome.
Zhiqing Wang, Baoping Wu, Rebecca A Mosig, Yulan Chen, Fei Ye, Yali Zhang, Wei Gong, Lanbo Gong, Fei Huang, Xinying Wang,[...]. Hum Mutat 2014

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

The Peutz-Jegher gene product LKB1 is a mediator of p53-dependent cell death.
P Karuman, O Gozani, R D Odze, X C Zhou, H Zhu, R Shaw, T P Brien, C D Bozzuto, D Ooi, L C Cantley,[...]. Mol Cell 2001

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

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

Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer.
Susan J Ramus, Honglin Song, Ed Dicks, Jonathan P Tyrer, Adam N Rosenthal, Maria P Intermaggio, Lindsay Fraser, Aleksandra Gentry-Maharaj, Jane Hayward, Susan Philpott,[...]. J Natl Cancer Inst 2015

Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer.
Silvia Casadei, Barbara M Norquist, Tom Walsh, Sunday Stray, Jessica B Mandell, Ming K Lee, John A Stamatoyannopoulos, Mary-Claire King. Cancer Res 2011

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

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.