A citation-based method for searching scientific literature

Stephen E P Smith, Yu-Dong Zhou, Guangping Zhang, Zhe Jin, David C Stoppel, Matthew P Anderson. Sci Transl Med 2011
Times Cited: 153







List of co-cited articles
1558 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


The Angelman Syndrome protein Ube3A regulates synapse development by ubiquitinating arc.
Paul L Greer, Rikinari Hanayama, Brenda L Bloodgood, Alan R Mardinly, David M Lipton, Steven W Flavell, Tae-Kyung Kim, Eric C Griffith, Zachary Waldon, Rene Maehr,[...]. Cell 2010
384
35

Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.
Y H Jiang, D Armstrong, U Albrecht, C M Atkins, J L Noebels, G Eichele, J D Sweatt, A L Beaudet. Neuron 1998
544
34


UBE3A/E6-AP mutations cause Angelman syndrome.
T Kishino, M Lalande, J Wagstaff. Nat Genet 1997
748
28

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Joseph T Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W Brune, Jonathan P Bradfield,[...]. Nature 2009
889
28

Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism.
Jin Nakatani, Kota Tamada, Fumiyuki Hatanaka, Satoko Ise, Hisashi Ohta, Kiyoshi Inoue, Shozo Tomonaga, Yasuhito Watanabe, Yeun Jun Chung, Ruby Banerjee,[...]. Cell 2009
286
25

An Autism-Linked Mutation Disables Phosphorylation Control of UBE3A.
Jason J Yi, Janet Berrios, Jason M Newbern, William D Snider, Benjamin D Philpot, Klaus M Hahn, Mark J Zylka. Cell 2015
84
29

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.
T Matsuura, J S Sutcliffe, P Fang, R J Galjaard, Y H Jiang, C S Benton, J M Rommens, A L Beaudet. Nat Genet 1997
522
22

Ube3a is required for experience-dependent maturation of the neocortex.
Koji Yashiro, Thorfinn T Riday, Kathryn H Condon, Adam C Roberts, Danilo R Bernardo, Rohit Prakash, Richard J Weinberg, Michael D Ehlers, Benjamin D Philpot. Nat Neurosci 2009
219
21

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13.
Amber Hogart, David Wu, Janine M LaSalle, N Carolyn Schanen. Neurobiol Dis 2010
171
20

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication.
E H Cook, V Lindgren, B L Leventhal, R Courchesne, A Lincoln, C Shulman, C Lord, E Courchesne. Am J Hum Genet 1997
422
20

Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons.
U Albrecht, J S Sutcliffe, B M Cattanach, C V Beechey, D Armstrong, G Eichele, A L Beaudet. Nat Genet 1997
319
20

Maternal loss of Ube3a produces an excitatory/inhibitory imbalance through neuron type-specific synaptic defects.
Michael L Wallace, Alain C Burette, Richard J Weinberg, Benjamin D Philpot. Neuron 2012
109
20

Autism gene Ube3a and seizures impair sociability by repressing VTA Cbln1.
Vaishnav Krishnan, David C Stoppel, Yi Nong, Mark A Johnson, Monica J S Nadler, Ekim Ozkaynak, Brian L Teng, Ikue Nagakura, Fahim Mohammad, Michael A Silva,[...]. Nature 2017
57
33

Topoisomerase inhibitors unsilence the dormant allele of Ube3a in neurons.
Hsien-Sung Huang, John A Allen, Angela M Mabb, Ian F King, Jayalakshmi Miriyala, Bonnie Taylor-Blake, Noah Sciaky, J Walter Dutton, Hyeong-Min Lee, Xin Chen,[...]. Nature 2011
218
18

EphB-mediated degradation of the RhoA GEF Ephexin5 relieves a developmental brake on excitatory synapse formation.
Seth S Margolis, John Salogiannis, David M Lipton, Caleigh Mandel-Brehm, Zachary P Wills, Alan R Mardinly, Linda Hu, Paul L Greer, Jay B Bikoff, Hsin-Yi Henry Ho,[...]. Cell 2010
155
18

Role of the ubiquitin ligase E6AP/UBE3A in controlling levels of the synaptic protein Arc.
Simone Kühnle, Benedikt Mothes, Konstantin Matentzoglu, Martin Scheffner. Proc Natl Acad Sci U S A 2013
82
21

Rescue of neurological deficits in a mouse model for Angelman syndrome by reduction of alphaCaMKII inhibitory phosphorylation.
Geeske M van Woerden, Karen D Harris, Mohammad Reza Hojjati, Richard M Gustin, Shenfeng Qiu, Rogerio de Avila Freire, Yong-hui Jiang, Ype Elgersma, Edwin J Weeber. Nat Neurosci 2007
189
17

The Angelman syndrome protein Ube3a is required for polarized dendrite morphogenesis in pyramidal neurons.
Sheng Miao, Renchao Chen, Jiahao Ye, Guo-He Tan, Shuai Li, Jing Zhang, Yong-hui Jiang, Zhi-Qi Xiong. J Neurosci 2013
62
27

UBE3A Regulates Synaptic Plasticity and Learning and Memory by Controlling SK2 Channel Endocytosis.
Jiandong Sun, Guoqi Zhu, Yan Liu, Steve Standley, Angela Ji, Rashmi Tunuguntla, Yubin Wang, Chad Claus, Yun Luo, Michel Baudry,[...]. Cell Rep 2015
64
26

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction.
João Peça, Cátia Feliciano, Jonathan T Ting, Wenting Wang, Michael F Wells, Talaignair N Venkatraman, Christopher D Lascola, Zhanyan Fu, Guoping Feng. Nature 2011
751
16

Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a.
K Yamasaki, K Joh, T Ohta, H Masuzaki, T Ishimaru, T Mukai, N Niikawa, M Ogawa, J Wagstaff, T Kishino. Hum Mol Genet 2003
178
16

The interstitial duplication 15q11.2-q13 syndrome includes autism, mild facial anomalies and a characteristic EEG signature.
Nora Urraca, Julie Cleary, Victoria Brewer, Eniko K Pivnick, Kathryn McVicar, Ronald L Thibert, N Carolyn Schanen, Carmen Esmer, Dustin Lamport, Lawrence T Reiter. Autism Res 2013
83
18

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.
Olga Peñagarikano, Brett S Abrahams, Edward I Herman, Kellen D Winden, Amos Gdalyahu, Hongmei Dong, Lisa I Sonnenblick, Robin Gruver, Joel Almajano, Anatol Bragin,[...]. Cell 2011
519
15

Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function.
Hyejung Won, Hye-Ryeon Lee, Heon Yung Gee, Won Mah, Jae-Ick Kim, Jiseok Lee, Seungmin Ha, Changuk Chung, Eun Suk Jung, Yi Sul Cho,[...]. Nature 2012
385
15


Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
14

Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.
Peter T Tsai, Court Hull, YunXiang Chu, Emily Greene-Colozzi, Abbey R Sadowski, Jarrett M Leech, Jason Steinberg, Jacqueline N Crawley, Wade G Regehr, Mustafa Sahin. Nature 2012
435
14

Allelic specificity of Ube3a expression in the mouse brain during postnatal development.
Matthew C Judson, Jason O Sosa-Pagan, Wilmer A Del Cid, Ji Eun Han, Benjamin D Philpot. J Comp Neurol 2014
61
22


The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
13

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
Stéphane Jamain, Hélène Quach, Catalina Betancur, Maria Råstam, Catherine Colineaux, I Carina Gillberg, Henrik Soderstrom, Bruno Giros, Marion Leboyer, Christopher Gillberg,[...]. Nat Genet 2003
13

Derangements of hippocampal calcium/calmodulin-dependent protein kinase II in a mouse model for Angelman mental retardation syndrome.
Edwin J Weeber, Yong-Hui Jiang, Ype Elgersma, Andrew W Varga, Yarimar Carrasquillo, Sarah E Brown, Jill M Christian, Banefsheh Mirnikjoo, Alcino Silva, Arthur L Beaudet,[...]. J Neurosci 2003
167
13

Angelman syndrome 2005: updated consensus for diagnostic criteria.
Charles A Williams, Arthur L Beaudet, Jill Clayton-Smith, Joan H Knoll, Martin Kyllerman, Laura A Laan, R Ellen Magenis, Ann Moncla, Albert A Schinzel, Jane A Summers,[...]. Am J Med Genet A 2006
298
13

Angelman syndrome: insights into genomic imprinting and neurodevelopmental phenotypes.
Angela M Mabb, Matthew C Judson, Mark J Zylka, Benjamin D Philpot. Trends Neurosci 2011
153
13

The Angelman syndrome-associated protein, E6-AP, is a coactivator for the nuclear hormone receptor superfamily.
Z Nawaz, D M Lonard, C L Smith, E Lev-Lehman, S Y Tsai, M J Tsai, B W O'Malley. Mol Cell Biol 1999
303
13

Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families.
E L Nurmi, Y Bradford, Y Chen, J Hall, B Arnone, M B Gardiner, H B Hutcheson, J R Gilbert, M A Pericak-Vance, S A Copeland-Yates,[...]. Genomics 2001
102
13

Epigenetic regulation of UBE3A and roles in human neurodevelopmental disorders.
Janine M LaSalle, Lawrence T Reiter, Stormy J Chamberlain. Epigenomics 2015
59
22

Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2.
Michael J Schmeisser, Elodie Ey, Stephanie Wegener, Juergen Bockmann, A Vanessa Stempel, Angelika Kuebler, Anna-Lena Janssen, Patrick T Udvardi, Ehab Shiban, Christina Spilker,[...]. Nature 2012
358
12

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
Christelle M Durand, Catalina Betancur, Tobias M Boeckers, Juergen Bockmann, Pauline Chaste, Fabien Fauchereau, Gudrun Nygren, Maria Rastam, I Carina Gillberg, Henrik Anckarsäter,[...]. Nat Genet 2007
880
12

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
624
12

Tissue-specific variation of Ube3a protein expression in rodents and in a mouse model of Angelman syndrome.
Richard M Gustin, Terry Jo Bichell, Michael Bubser, Jennifer Daily, Irina Filonova, Davit Mrelashvili, Ariel Y Deutch, Roger J Colbran, Edwin J Weeber, Kevin F Haas. Neurobiol Dis 2010
71
16

Truncation of Ube3a-ATS unsilences paternal Ube3a and ameliorates behavioral defects in the Angelman syndrome mouse model.
Linyan Meng, Richard Erwin Person, Wei Huang, Ping Jun Zhu, Mauro Costa-Mattioli, Arthur L Beaudet. PLoS Genet 2013
79
15

Expression of the Rho-GEF Pbl/ECT2 is regulated by the UBE3A E3 ubiquitin ligase.
Lawrence T Reiter, Tiffany N Seagroves, Megan Bowers, Ethan Bier. Hum Mol Genet 2006
68
17

Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice.
Kiyonori Miura, Tatsuya Kishino, En Li, Hayley Webber, Pieter Dikkes, Gregory L Holmes, Joseph Wagstaff. Neurobiol Dis 2002
158
12

Seizure-like activity in a juvenile Angelman syndrome mouse model is attenuated by reducing Arc expression.
Caleigh Mandel-Brehm, John Salogiannis, Sameer C Dhamne, Alexander Rotenberg, Michael E Greenberg. Proc Natl Acad Sci U S A 2015
50
24

15q11.2 Duplication Encompassing Only the UBE3A Gene Is Associated with Developmental Delay and Neuropsychiatric Phenotypes.
Abdul Noor, Lucie Dupuis, Kirti Mittal, Anath C Lionel, Christian R Marshall, Stephen W Scherer, Tracy Stockley, John B Vincent, Roberto Mendoza-Londono, Dimitri J Stavropoulos. Hum Mutat 2015
42
28

Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome model.
Sara Silva-Santos, Geeske M van Woerden, Caroline F Bruinsma, Edwin Mientjes, Mehrnoush Aghadavoud Jolfaei, Ben Distel, Steven A Kushner, Ype Elgersma. J Clin Invest 2015
97
12

Angelman syndrome - insights into a rare neurogenetic disorder.
Karin Buiting, Charles Williams, Bernhard Horsthemke. Nat Rev Neurol 2016
110
12

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Brian J O'Roak, Laura Vives, Santhosh Girirajan, Emre Karakoc, Niklas Krumm, Bradley P Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D Smith,[...]. Nature 2012
11


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.