A citation-based method for searching scientific literature

Lamis Yehia, Emma Keel, Charis Eng. Annu Rev Med 2020
Times Cited: 21







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



Times Cited
  Times     Co-cited
Similarity


PTEN-opathies: from biological insights to evidence-based precision medicine.
Lamis Yehia, Joanne Ngeow, Charis Eng. J Clin Invest 2019
55
38

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
212
33

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
82
33

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
494
28

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
421
23

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
157
19

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
179
19

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
245
19



Neural transcriptome of constitutional Pten dysfunction in mice and its relevance to human idiopathic autism spectrum disorder.
A K Tilot, G Bebek, F Niazi, J B Altemus, T Romigh, T W Frazier, C Eng. Mol Psychiatry 2016
35
19

Germline disruption of Pten localization causes enhanced sex-dependent social motivation and increased glial production.
Amanda K Tilot, Mary K Gaugler, Qi Yu, Todd Romigh, Wanfeng Yu, Robert H Miller, Thomas W Frazier, Charis Eng. Hum Mol Genet 2014
36
19



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
14

Cognitive characteristics of PTEN hamartoma tumor syndromes.
Robyn M Busch, Jessica S Chapin, Jessica Mester, Lisa Ferguson, Jennifer S Haut, Thomas W Frazier, Charis Eng. Genet Med 2013
22
14

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
14

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
150
14

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
39
14

PTENβ is an alternatively translated isoform of PTEN that regulates rDNA transcription.
Hui Liang, Xi Chen, Qi Yin, Danhui Ruan, Xuyang Zhao, Cong Zhang, Michael A McNutt, Yuxin Yin. Nat Commun 2017
57
14

Cytoplasmic-predominant Pten increases microglial activation and synaptic pruning in a murine model with autism-like phenotype.
Nicholas Sarn, Ritika Jaini, Stetson Thacker, Hyunpil Lee, Ranjan Dutta, Charis Eng. Mol Psychiatry 2021
12
25

PTEN Nuclear Functions.
Jason Ho, Edward S Cruise, Ryan J O Dowling, Vuk Stambolic. Cold Spring Harb Perspect Med 2020
8
37

Cancer-associated PTEN mutants act in a dominant-negative manner to suppress PTEN protein function.
Antonella Papa, Lixin Wan, Massimo Bonora, Leonardo Salmena, Min Sup Song, Robin M Hobbs, Andrea Lunardi, Kaitlyn Webster, Christopher Ng, Ryan H Newton,[...]. Cell 2014
165
14

Pharmacological inhibition of mTORC1 suppresses anatomical, cellular, and behavioral abnormalities in neural-specific Pten knock-out mice.
Jing Zhou, Jacqueline Blundell, Shiori Ogawa, Chang-Hyuk Kwon, Wei Zhang, Christopher Sinton, Craig M Powell, Luis F Parada. J Neurosci 2009
284
14

Crystal structure of the PTEN tumor suppressor: implications for its phosphoinositide phosphatase activity and membrane association.
J O Lee, H Yang, M M Georgescu, A Di Cristofano, T Maehama, Y Shi, J E Dixon, P Pandolfi, N P Pavletich. Cell 1999
787
14

Genetic basis of Cowden syndrome and its implications for clinical practice and risk management.
Amanda Gammon, Kory Jasperson, Marjan Champine. Appl Clin Genet 2016
20
10

PTEN Hamartoma Tumor Syndrome: A Clinical Overview.
Robert Pilarski. Cancers (Basel) 2019
34
9

Essential role for nuclear PTEN in maintaining chromosomal integrity.
Wen Hong Shen, Adayabalam S Balajee, Jianli Wang, Hong Wu, Charis Eng, Pier Paolo Pandolfi, Yuxin Yin. Cell 2007
680
9

WWP1 Gain-of-Function Inactivation of PTEN in Cancer Predisposition.
Yu-Ru Lee, Lamis Yehia, Takahiro Kishikawa, Ying Ni, Brandie Leach, Jinfang Zhang, Nivedita Panch, Jing Liu, Wenyi Wei, Charis Eng,[...]. N Engl J Med 2020
11
18


Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B gene.
Paola Bianchi, Elisa Fermo, Cristina Vercellati, Carla Boschetti, Wilma Barcellini, Alessandra Iurlo, Anna Paola Marcello, Pier Giorgio Righetti, Alberto Zanella. Hum Mutat 2009
114
9

Unexpected cancer-predisposition gene variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients without underlying germline PTEN mutations.
Lamis Yehia, Ying Ni, Kaitlin Sesock, Farshad Niazi, Benjamin Fletcher, Hannah Jin Lian Chen, Thomas LaFramboise, Charis Eng. PLoS Genet 2018
13
15

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
381
9

Identification of nucleolus-localized PTEN and its function in regulating ribosome biogenesis.
Pingdong Li, Danni Wang, Haiyang Li, Zhenkun Yu, Xiaohong Chen, Jugao Fang. Mol Biol Rep 2014
26
9

PTENα, a PTEN isoform translated through alternative initiation, regulates mitochondrial function and energy metabolism.
Hui Liang, Shiming He, Jingyi Yang, Xinying Jia, Pan Wang, Xi Chen, Zhong Zhang, Xiajuan Zou, Michael A McNutt, Wen Hong Shen,[...]. Cell Metab 2014
137
9

PTEN represses RNA Polymerase I transcription by disrupting the SL1 complex.
Cheng Zhang, Lucio Comai, Deborah L Johnson. Mol Cell Biol 2005
77
9

Frequent inactivation of PTEN by promoter hypermethylation in microsatellite instability-high sporadic colorectal cancers.
Ajay Goel, Christian N Arnold, Donna Niedzwiecki, John M Carethers, Jeannette M Dowell, Linda Wasserman, Carolyn Compton, Robert J Mayer, Monica M Bertagnolli, C Richard Boland. Cancer Res 2004
217
9

Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.
Klaus Schwarz, Achille Iolascon, Fatima Verissimo, Nikolaus S Trede, Wyatt Horsley, Wen Chen, Barry H Paw, Karl-Peter Hopfner, Karlheinz Holzmann, Roberta Russo,[...]. Nat Genet 2009
170
9

Nuclear PTEN controls DNA repair and sensitivity to genotoxic stress.
C Bassi, J Ho, T Srikumar, R J O Dowling, C Gorrini, S J Miller, T W Mak, B G Neel, B Raught, V Stambolic. Science 2013
251
9

Non-canonical role of cancer-associated mutant SEC23B in the ribosome biogenesis pathway.
Lamis Yehia, Supriya Jindal, Anton A Komar, Charis Eng. Hum Mol Genet 2018
5
40

Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer.
Lamis Yehia, Farshad Niazi, Ying Ni, Joanne Ngeow, Madhav Sankunny, Zhigang Liu, Wei Wei, Jessica L Mester, Ruth A Keri, Bin Zhang,[...]. Am J Hum Genet 2015
37
9


Targeting the nucleolus for cancer intervention.
Jaclyn E Quin, Jennifer R Devlin, Donald Cameron, Kate M Hannan, Richard B Pearson, Ross D Hannan. Biochim Biophys Acta 2014
136
9

COPII: a membrane coat formed by Sec proteins that drive vesicle budding from the endoplasmic reticulum.
C Barlowe, L Orci, T Yeung, M Hosobuchi, S Hamamoto, N Salama, M F Rexach, M Ravazzola, M Amherdt, R Schekman. Cell 1994
9

Reactivation of PTEN tumor suppressor for cancer treatment through inhibition of a MYC-WWP1 inhibitory pathway.
Yu-Ru Lee, Ming Chen, Jonathan D Lee, Jinfang Zhang, Shu-Yu Lin, Tian-Min Fu, Hao Chen, Tomoki Ishikawa, Shang-Yin Chiang, Jesse Katon,[...]. Science 2019
74
9

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
405
9

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
9



Ubiquitination regulates PTEN nuclear import and tumor suppression.
Lloyd C Trotman, Xinjiang Wang, Andrea Alimonti, Zhenbang Chen, Julie Teruya-Feldstein, Haijuan Yang, Nikola P Pavletich, Brett S Carver, Carlos Cordon-Cardo, Hediye Erdjument-Bromage,[...]. Cell 2007
518
9


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.