A citation-based method for searching scientific literature

Virginie Bubien, Françoise Bonnet, Veronique Brouste, Stéphanie Hoppe, Emmanuelle Barouk-Simonet, Albert David, Patrick Edery, Armand Bottani, Valérie Layet, Olivier Caron, Brigitte Gilbert-Dussardier, Capucine Delnatte, Catherine Dugast, Jean-Pierre Fricker, Dominique Bonneau, Nicolas Sevenet, Michel Longy, Frédéric Caux. J Med Genet 2013
Times Cited: 143

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

Times Cited
  Times     Co-cited

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Predicting PTEN mutations: an evaluation of Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome clinical features.
Robert Pilarski, Julie A Stephens, Ryan Noss, James L Fisher, Thomas W Prior. J Med Genet 2011

Should patients with Cowden syndrome undergo prophylactic thyroidectomy?
Mira Milas, Jessica Mester, Rosemarie Metzger, Joyce Shin, Jamie Mitchell, Eren Berber, Allan E Siperstein, Charis Eng. Surgery 2012

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

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

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

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

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

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

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

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

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

Bannayan-Riley-Ruvalcaba syndrome.
R J Gorlin, M M Cohen, L M Condon, B A Burke. Am J Med Genet 1992

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

Analysis of prevalence and degree of macrocephaly in patients with germline PTEN mutations and of brain weight in Pten knock-in murine model.
Jessica L Mester, Amanda K Tilot, Lisa A Rybicki, Thomas W Frazier, Charis Eng. Eur J Hum Genet 2011

Cancer risks for BRCA1 and BRCA2 mutation carriers: results from prospective analysis of EMBRACE.
Nasim Mavaddat, Susan Peock, Debra Frost, Steve Ellis, Radka Platte, Elena Fineberg, D Gareth Evans, Louise Izatt, Rosalind A Eeles, Julian Adlard,[...]. J Natl Cancer Inst 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

Germline mutations and variants in the succinate dehydrogenase genes in Cowden and Cowden-like syndromes.
Ying Ni, Kevin M Zbuk, Tammy Sadler, Attila Patocs, Glenn Lobo, Emily Edelman, Petra Platzer, Mohammed S Orloff, Kristin A Waite, Charis Eng. Am J Hum Genet 2008

The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly.
Elizabeth A Varga, Matthew Pastore, Thomas Prior, Gail E Herman, Kim L McBride. Genet Med 2009

When overgrowth bumps into cancer: the PTEN-opathies.
Jessica Mester, Charis Eng. Am J Med Genet C Semin Med Genet 2013

Thyroid nodules and cancer in children with PTEN hamartoma tumor syndrome.
Jessica R Smith, Ellen Marqusee, Susan Webb, Vania Nose, Steven J Fishman, Robert C Shamberger, Mary C Frates, Stephen A Huang. J Clin Endocrinol Metab 2011

Germline epigenetic regulation of KILLIN in Cowden and Cowden-like syndrome.
Kristi L Bennett, Jessica Mester, Charis Eng. JAMA 2010

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1.
Y Miki, J Swensen, D Shattuck-Eidens, P A Futreal, K Harshman, S Tavtigian, Q Liu, C Cochran, L M Bennett, W Ding. Science 1994

Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly.
Kim L McBride, Elizabeth A Varga, Matthew T Pastore, Thomas W Prior, Kandamurugu Manickam, Joan F Atkin, Gail E Herman. Autism Res 2010

Functionally distinct groups of inherited PTEN mutations in autism and tumour syndromes.
Laura Spinelli, Fiona M Black, Jonathan N Berg, Britta J Eickholt, Nicholas R Leslie. J Med Genet 2015

A comprehensive functional analysis of PTEN mutations: implications in tumor- and autism-related syndromes.
Isabel Rodríguez-Escudero, María D Oliver, Amparo Andrés-Pons, María Molina, Víctor J Cid, Rafael Pulido. Hum Mol Genet 2011

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.