A citation-based method for searching scientific literature

Min-Han Tan, Jessica L Mester, Joanne Ngeow, Lisa A Rybicki, Mohammed S Orloff, Charis Eng. Clin Cancer Res 2012
Times Cited: 415

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

Times Cited
  Times     Co-cited

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

A clinical scoring system for selection of patients for PTEN mutation testing is proposed on the basis of a prospective study of 3042 probands.
Min-Han Tan, Jessica Mester, Charissa Peterson, Yiran Yang, Jin-Lian Chen, Lisa A Rybicki, Kresimira Milas, Holly Pederson, Berna Remzi, Mohammed S Orloff,[...]. Am J Hum Genet 2011

Cancer risk and genotype-phenotype correlations in PTEN hamartoma tumor syndrome.
Marry H Nieuwenhuis, C Marleen Kets, Maureen Murphy-Ryan, Helger G Yntema, D Gareth Evans, Chrystelle Colas, Pal Møller, Frederik J Hes, Shirley V Hodgson, Maran J W Olderode-Berends,[...]. Fam Cancer 2014

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome.
D Liaw, D J Marsh, J Li, P L Dahia, S I Wang, Z Zheng, S Bose, K M Call, H C Tsou, M Peacocke,[...]. Nat Genet 1997

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

Localization of the gene for Cowden disease to chromosome 10q22-23.
M R Nelen, G W Padberg, E A Peeters, A Y Lin, B van den Helm, R R Frants, V Coulon, A M Goldstein, M M van Reen, D F Easton,[...]. Nat Genet 1996

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

PTEN-opathies: from biological insights to evidence-based precision medicine.
Lamis Yehia, Joanne Ngeow, Charis Eng. J Clin Invest 2019

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

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

Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.
M G Butler, M J Dasouki, X-P Zhou, Z Talebizadeh, M Brown, T N Takahashi, J H Miles, C H Wang, R Stratton, R Pilarski,[...]. J Med Genet 2005

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

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

Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations.
M R Nelen, H Kremer, I B Konings, F Schoute, A J van Essen, R Koch, C G Woods, J P Fryns, B Hamel, L H Hoefsloot,[...]. Eur J Hum Genet 1999

PTEN: one gene, many syndromes.
Charis Eng. Hum Mutat 2003

Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation.
D J Marsh, V Coulon, K L Lunetta, P Rocca-Serra, P L Dahia, Z Zheng, D Liaw, S Caron, B Duboué, A Y Lin,[...]. Hum Mol Genet 1998

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

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

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

Second malignant neoplasms in patients with Cowden syndrome with underlying germline PTEN mutations.
Joanne Ngeow, Kim Stanuch, Jessica L Mester, Jill S Barnholtz-Sloan, Charis Eng. J Clin Oncol 2014

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.
D J Marsh, J B Kum, K L Lunetta, M J Bennett, R J Gorlin, S F Ahmed, J Bodurtha, C Crowe, M A Curtis, M Dasouki,[...]. Hum Mol Genet 1999

Cancer and Lhermitte-Duclos disease are common in Cowden syndrome patients.
Douglas L Riegert-Johnson, Ferga C Gleeson, Maegan Roberts, Krysta Tholen, Lauren Youngborg, Melvin Bullock, Lisa A Boardman. Hered Cancer Clin Pract 2010

The Cowden syndrome: a clinical and genetic study in 21 patients.
T M Starink, J P van der Veen, F Arwert, L P de Waal, G G de Lange, J J Gille, A W Eriksson. Clin Genet 1986

The functions and regulation of the PTEN tumour suppressor: new modes and prospects.
Yu-Ru Lee, Ming Chen, Pier Paolo Pandolfi. Nat Rev Mol Cell Biol 2018

PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer.
J Li, C Yen, D Liaw, K Podsypanina, S Bose, S I Wang, J Puc, C Miliaresis, L Rodgers, R McCombie,[...]. Science 1997

Papillary renal cell carcinoma is associated with PTEN hamartoma tumor syndrome.
Jessica L Mester, Ming Zhou, Nichole Prescott, Charis Eng. Urology 2012

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

PTEN hamartoma tumor syndrome: an overview.
Judith A Hobert, Charis Eng. Genet Med 2009

A retrospective chart review of the features of PTEN hamartoma tumour syndrome in children.
Emily Hansen-Kiss, Sarah Beinkampen, Brent Adler, Thomas Frazier, Thomas Prior, Steven Erdman, Charis Eng, Gail Herman. J Med Genet 2017

PTEN hamartoma tumour syndrome: early tumour development in children.
Patroula Smpokou, Victor L Fox, Wen-Hann Tan. Arch Dis Child 2015

Germline mutations in PTEN are present in Bannayan-Zonana syndrome.
D J Marsh, P L Dahia, Z Zheng, D Liaw, R Parsons, R J Gorlin, C Eng. Nat Genet 1997

Beyond Li Fraumeni Syndrome: clinical characteristics of families with p53 germline mutations.
Kelly D Gonzalez, Katie A Noltner, Carolyn H Buzin, Dongqing Gu, Cindy Y Wen-Fong, Vu Q Nguyen, Jennifer H Han, Katrina Lowstuter, Jeffrey Longmate, Steve S Sommer,[...]. J Clin Oncol 2009

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

Lynch syndrome caused by MLH1 mutations is associated with an increased risk of breast cancer: a cohort study.
Elaine F Harkness, Emma Barrow, Katy Newton, Kate Green, Tara Clancy, Fiona Lalloo, James Hill, D Gareth Evans. J Med Genet 2015

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

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies.
A Antoniou, P D P Pharoah, S Narod, H A Risch, J E Eyfjord, J L Hopper, N Loman, H Olsson, O Johannsson, A Borg,[...]. Am J Hum Genet 2003

Germline PIK3CA and AKT1 mutations in Cowden and Cowden-like syndromes.
Mohammed S Orloff, Xin He, Charissa Peterson, Fusong Chen, Jin-Lian Chen, Jessica L Mester, Charis Eng. Am J Hum Genet 2013

Molecular and phenotypic abnormalities in individuals with germline heterozygous PTEN mutations and autism.
T W Frazier, R Embacher, A K Tilot, K Koenig, J Mester, C Eng. Mol Psychiatry 2015

Negative regulation of PKB/Akt-dependent cell survival by the tumor suppressor PTEN.
V Stambolic, A Suzuki, J L de la Pompa, G M Brothers, C Mirtsos, T Sasaki, J Ruland, J M Penninger, D P Siderovski, T W Mak. Cell 1998

Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathway.
Xiao-Ping Zhou, Kristin A Waite, Robert Pilarski, Heather Hampel, Magali J Fernandez, Cindy Bos, Majed Dasouki, Gerald L Feldman, Lois A Greenberg, Jennifer Ivanovich,[...]. Am J Hum Genet 2003

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: 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

Meta-analysis of BRCA1 and BRCA2 penetrance.
Sining Chen, Giovanni Parmigiani. J Clin Oncol 2007

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.