A citation-based method for searching scientific literature

Robert Pilarski, Randall Burt, Wendy Kohlman, Lana Pho, Kristen M Shannon, Elizabeth Swisher. J Natl Cancer Inst 2013
Times Cited: 214







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



Times Cited
  Times     Co-cited
Similarity


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
411
24

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
143
15

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
206
15

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
78
16

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
404
13

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
601
12


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
456
11

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
11

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
187
10

Brain magnetic resonance imaging in patients with Cowden syndrome.
Catherine Lok, Valérie Viseux, Marie Françoise Avril, Marie Aleth Richard, Catherine Gondry-Jouet, Hervé Deramond, Caroline Desfossez-Tribout, Sandrine Courtade, Michèle Delaunay, Fréderic Piette,[...]. Medicine (Baltimore) 2005
62
16


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
379
10

The spectrum of vascular anomalies in patients with PTEN mutations: implications for diagnosis and management.
Wen-Hann Tan, Hagit N Baris, Patricia E Burrows, Caroline D Robson, Ahmad I Alomari, John B Mulliken, Steven J Fishman, Mira B Irons. J Med Genet 2007
146
10


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
59
15

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
147
9

Germline inactivation of PTEN and dysregulation of the phosphoinositol-3-kinase/Akt pathway cause human Lhermitte-Duclos disease in adults.
Xiao-Ping Zhou, Deborah J Marsh, Carl D Morrison, Abhik R Chaudhury, Marius Maxwell, Guido Reifenberger, Charis Eng. Am J Hum Genet 2003
110
9


Thyroid pathology in PTEN-hamartoma tumor syndrome: characteristic findings of a distinct entity.
Anna Ray Laury, Massimo Bongiovanni, Jean-Christophe Tille, Harry Kozakewich, Vânia Nosé. Thyroid 2011
39
20

Colonic polyposis and neoplasia in Cowden syndrome.
Peter P Stanich, Victoria L Owens, Seth Sweetser, Sherezade Khambatta, Thomas C Smyrk, Ronald L Richardson, Matthew P Goetz, Mrinal M Patnaik. Mayo Clin Proc 2011
42
19

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
488
8

PTEN hamartoma tumor syndrome: an overview.
Judith A Hobert, Charis Eng. Genet Med 2009
190
8

Upper and Lower Gastrointestinal Findings in PTEN Mutation-Positive Cowden Syndrome Patients Participating in an Active Surveillance Program.
Zohar Levi, Hagit N Baris, Inbal Kedar, Yaron Niv, Alex Geller, Eyal Gal, Rachel Gingold, Sara Morgenstern, Yacov Baruch, Brandie Heald Leach,[...]. Clin Transl Gastroenterol 2011
28
25

A mosaic activating mutation in AKT1 associated with the Proteus syndrome.
Marjorie J Lindhurst, Julie C Sapp, Jamie K Teer, Jennifer J Johnston, Erin M Finn, Kathryn Peters, Joyce Turner, Jennifer L Cannons, David Bick, Laurel Blakemore,[...]. N Engl J Med 2011
499
7

Colonic manifestations of PTEN hamartoma tumor syndrome: case series and systematic review.
Peter P Stanich, Robert Pilarski, Jonathan Rock, Wendy L Frankel, Samer El-Dika, Marty M Meyer. World J Gastroenterol 2014
24
29

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
330
7

Morphologic characterization of hamartomatous gastrointestinal polyps in Cowden syndrome, Peutz-Jeghers syndrome, and juvenile polyposis syndrome.
Ruthy Shaco-Levy, Kory W Jasperson, Katie Martin, N Jewel Samadder, Randall W Burt, Jian Ying, Mary P Bronner. Hum Pathol 2016
18
38

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
486
7

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
174
6

Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) syndrome is related to mosaic PTEN nullizygosity.
Frédéric Caux, Henri Plauchu, Frédéric Chibon, Laurence Faivre, Olivier Fain, Pierre Vabres, Françoise Bonnet, Zied Ben Selma, Liliane Laroche, Marion Gérard,[...]. Eur J Hum Genet 2007
74
8

PTEN: one gene, many syndromes.
Charis Eng. Hum Mutat 2003
560
6


PTEN, DICER1, FH, and Their Associated Tumor Susceptibility Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood.
Kris Ann P Schultz, Surya P Rednam, Junne Kamihara, Leslie Doros, Maria Isabel Achatz, Jonathan D Wasserman, Lisa R Diller, Laurence Brugières, Harriet Druker, Katherine A Schneider,[...]. Clin Cancer Res 2017
69
8

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
416
6


Magnetic resonance characteristics of adult-onset Lhermitte-Duclos disease: An indicator for active cancer surveillance?
Guangquan Wei, Wei Zhang, Qinlong Li, Xiaowei Kang, Haitao Zhao, Xianping Liu, Xing Tang, Yuanming Wu, Juntao Han, Hong Yin. Mol Clin Oncol 2014
11
54

Clinical presentation of PTEN mutations in childhood in the absence of family history of Cowden syndrome.
T Busa, M Milh, N Degardin, N Girard, S Sigaudy, M Longy, S Olshchwang, H Sobol, B Chabrol, N Philip. Eur J Paediatr Neurol 2015
18
33

Lhermitte-Duclos disease: a report of 31 cases with immunohistochemical analysis of the PTEN/AKT/mTOR pathway.
Ty W Abel, Suzanne J Baker, Melissa M Fraser, Tarik Tihan, James S Nelson, Anthony T Yachnis, John-Paul Bouffard, Hernando Mena, Peter C Burger, Charles G Eberhart. J Neuropathol Exp Neurol 2005
53
11

Hidden association of Cowden syndrome, PTEN mutation and meningioma frequency.
Eduard Yakubov, Ali Ghoochani, Rolf Buslei, Michael Buchfelder, Ilker Y Eyüpoglu, Nicolai Savaskan. Oncoscience 2016
19
31

Lhermitte-Duclos Disease (Dysplastic Gangliocytoma of the Cerebellum) and Cowden Syndrome: Clinical Experience From a Single Institution with Long-Term Follow-Up.
Tao Jiang, Junmei Wang, Jiang Du, Shiqi Luo, Raynald Liu, Jian Xie, Ying Wang, Chunde Li. World Neurosurg 2017
10
60

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
34
17


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
32
15

The functions and regulation of the PTEN tumour suppressor.
Min Sup Song, Leonardo Salmena, Pier Paolo Pandolfi. Nat Rev Mol Cell Biol 2012
5

Pten regulates neuronal arborization and social interaction in mice.
Chang-Hyuk Kwon, Bryan W Luikart, Craig M Powell, Jing Zhou, Sharon A Matheny, Wei Zhang, Yanjiao Li, Suzanne J Baker, Luis F Parada. Neuron 2006
645
5


PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes.
Kyle C Kurek, Emily Howard, L B Tennant, Joseph Upton, Ahmad I Alomari, Patricia E Burrows, Kim Chalache, David J Harris, Cameron C Trenor, Charis Eng,[...]. Am J Surg Pathol 2012
57
8

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
102
5

Sirolimus treatment of severe PTEN hamartoma tumor syndrome: case report and in vitro studies.
Gordian L Schmid, Franziska Kässner, Holm H Uhlig, Antje Körner, Jürgen Kratzsch, Norman Händel, Fred-P Zepp, Frank Kowalzik, Andreas Laner, Sven Starke,[...]. Pediatr Res 2014
29
17


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.