A citation-based method for searching scientific literature

Tiantian Wang, Geeske M van Woerden, Ype Elgersma, J Gerard G Borst. Front Cell Neurosci 2018
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


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
121
50

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
609
50

UBE3A/E6-AP mutations cause Angelman syndrome.
T Kishino, M Lalande, J Wagstaff. Nat Genet 1997
888
38

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
203
33

The Angelman syndrome ubiquitin ligase localizes to the synapse and nucleus, and maternal deficiency results in abnormal dendritic spine morphology.
Scott V Dindot, Barbara A Antalffy, Meenakshi B Bhattacharjee, Arthur L Beaudet. Hum Mol Genet 2008
261
33

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
176
33

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
349
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
237
27

Dissociation of locomotor and cerebellar deficits in a murine Angelman syndrome model.
Caroline F Bruinsma, Martijn Schonewille, Zhenyu Gao, Eleonora M A Aronica, Matthew C Judson, Benjamin D Philpot, Freek E Hoebeek, Geeske M van Woerden, Chris I De Zeeuw, Ype Elgersma. J Clin Invest 2015
28
27

GABAergic Neuron-Specific Loss of Ube3a Causes Angelman Syndrome-Like EEG Abnormalities and Enhances Seizure Susceptibility.
Matthew C Judson, Michael L Wallace, Michael S Sidorov, Alain C Burette, Bin Gu, Geeske M van Woerden, Ian F King, Ji Eun Han, Mark J Zylka, Ype Elgersma,[...]. Neuron 2016
96
27

Alterations in intrinsic membrane properties and the axon initial segment in a mouse model of Angelman syndrome.
Hanoch Kaphzan, Shelly A Buffington, Joo In Jung, Matthew N Rasband, Eric Klann. J Neurosci 2011
89
27

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
94
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
71
27

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
127
27

Genetic reduction of the α1 subunit of Na/K-ATPase corrects multiple hippocampal phenotypes in Angelman syndrome.
Hanoch Kaphzan, Shelly A Buffington, Akila B Ramaraj, Jerry B Lingrel, Matthew N Rasband, Emanuela Santini, Eric Klann. Cell Rep 2013
46
27

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
612
27



Loss of nuclear UBE3A causes electrophysiological and behavioral deficits in mice and is associated with Angelman syndrome.
Rossella Avagliano Trezza, Monica Sonzogni, Stijn N V Bossuyt, F Isabella Zampeta, A Mattijs Punt, Marlene van den Berg, Diana C Rotaru, Linda M C Koene, Shashini T Munshi, Jeffrey Stedehouder,[...]. Nat Neurosci 2019
42
27

Angelman syndrome - insights into a rare neurogenetic disorder.
Karin Buiting, Charles Williams, Bernhard Horsthemke. Nat Rev Neurol 2016
160
27

Ube3a reinstatement mitigates epileptogenesis in Angelman syndrome model mice.
Bin Gu, Kelly E Carstens, Matthew C Judson, Katherine A Dalton, Marie Rougié, Ellen P Clark, Serena M Dudek, Benjamin D Philpot. J Clin Invest 2019
30
27

Towards a therapy for Angelman syndrome by targeting a long non-coding RNA.
Linyan Meng, Amanda J Ward, Seung Chun, C Frank Bennett, Arthur L Beaudet, Frank Rigo. Nature 2015
298
27

The autism-linked UBE3A T485A mutant E3 ubiquitin ligase activates the Wnt/β-catenin pathway by inhibiting the proteasome.
Jason J Yi, Smita R Paranjape, Matthew P Walker, Rajarshi Choudhury, Justin M Wolter, Giulia Fragola, Michael J Emanuele, Michael B Major, Mark J Zylka. J Biol Chem 2017
41
22

Decreased tonic inhibition in cerebellar granule cells causes motor dysfunction in a mouse model of Angelman syndrome.
Kiyoshi Egawa, Kyoko Kitagawa, Koichi Inoue, Masakazu Takayama, Chitoshi Takayama, Shinji Saitoh, Tatsuya Kishino, Masatoshi Kitagawa, Atsuo Fukuda. Sci Transl Med 2012
81
22

Subcellular organization of UBE3A in neurons.
Alain C Burette, Matthew C Judson, Susan Burette, Kristen D Phend, Benjamin D Philpot, Richard J Weinberg. J Comp Neurol 2017
30
22

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
72
22

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
419
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
234
22

Behavioral deficits in an Angelman syndrome model: effects of genetic background and age.
Hsien-Sung Huang, Andrew J Burns, Randal J Nonneman, Lorinda K Baker, Natallia V Riddick, Viktoriya D Nikolova, Thorfinn T Riday, Koji Yashiro, Benjamin D Philpot, Sheryl S Moy. Behav Brain Res 2013
87
22

Three-dimensional reconstruction of a calyx of Held and its postsynaptic principal neuron in the medial nucleus of the trapezoid body.
Kurt Sätzler, Leander F Söhl, Johann H Bollmann, J Gerard G Borst, Michael Frotscher, Bert Sakmann, Joachim H R Lübke. J Neurosci 2002
242
22

Synaptic inputs compete during rapid formation of the calyx of Held: a new model system for neural development.
Paul S Holcomb, Brian K Hoffpauir, Mitchell C Hoyson, Dakota R Jackson, Thomas J Deerinck, Glenn S Marrs, Marlin Dehoff, Jonathan Wu, Mark H Ellisman, George A Spirou. J Neurosci 2013
72
22


Optimizing synaptic architecture and efficiency for high-frequency transmission.
Holger Taschenberger, Ricardo M Leão, Kevin C Rowland, George A Spirou, Henrique von Gersdorff. Neuron 2002
298
22

A behavioral test battery for mouse models of Angelman syndrome: a powerful tool for testing drugs and novel Ube3a mutants.
Monica Sonzogni, Ilse Wallaard, Sara Silva Santos, Jenina Kingma, Dorine du Mee, Geeske M van Woerden, Ype Elgersma. Mol Autism 2018
43
22

Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.
Jana Stanurova, Anika Neureiter, Michaela Hiber, Hannah de Oliveira Kessler, Kristin Stolp, Roman Goetzke, Diana Klein, Agnes Bankfalvi, Hannes Klump, Laura Steenpass. Sci Rep 2016
44
16

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
87
16

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
98
16

Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy.
Frank H Yu, Massimo Mantegazza, Ruth E Westenbroek, Carol A Robbins, Franck Kalume, Kimberly A Burton, William J Spain, G Stanley McKnight, Todd Scheuer, William A Catterall. Nat Neurosci 2006
690
16

Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation.
Ikuo Ogiwara, Hiroyuki Miyamoto, Noriyuki Morita, Nafiseh Atapour, Emi Mazaki, Ikuyo Inoue, Tamaki Takeuchi, Shigeyoshi Itohara, Yuchio Yanagawa, Kunihiko Obata,[...]. J Neurosci 2007
541
16


Region-specific impairments in striatal synaptic transmission and impaired instrumental learning in a mouse model of Angelman syndrome.
Volodya Hayrapetyan, Stephen Castro, Tatyana Sukharnikova, Chunxiu Yu, Xinyu Cao, Yong-Hui Jiang, Henry H Yin. Eur J Neurosci 2014
15
20

Ube3a loss increases excitability and blunts orientation tuning in the visual cortex of Angelman syndrome model mice.
Michael L Wallace, Geeske M van Woerden, Ype Elgersma, Spencer L Smith, Benjamin D Philpot. J Neurophysiol 2017
14
21

Adeno-associated virus-mediated rescue of the cognitive defects in a mouse model for Angelman syndrome.
Jennifer L Daily, Kevin Nash, Umesh Jinwal, Todd Golde, Justin Rogers, Melinda M Peters, Rebecca D Burdine, Chad Dickey, Jessica L Banko, Edwin J Weeber. PLoS One 2011
66
16

Preclinical research in Rett syndrome: setting the foundation for translational success.
David M Katz, Joanne E Berger-Sweeney, James H Eubanks, Monica J Justice, Jeffrey L Neul, Lucas Pozzo-Miller, Mary E Blue, Diana Christian, Jacqueline N Crawley, Maurizio Giustetto,[...]. Dis Model Mech 2012
141
16

Strain-dependence of the Angelman Syndrome phenotypes in Ube3a maternal deficiency mice.
Heather A Born, An T Dao, Amber T Levine, Wai Ling Lee, Natasha M Mehta, Shubhangi Mehra, Edwin J Weeber, Anne E Anderson. Sci Rep 2017
43
16

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.
J H Knoll, R D Nicholls, R E Magenis, J M Graham, M Lalande, S A Latt. Am J Med Genet 1989
454
16



Fiji: an open-source platform for biological-image analysis.
Johannes Schindelin, Ignacio Arganda-Carreras, Erwin Frise, Verena Kaynig, Mark Longair, Tobias Pietzsch, Stephan Preibisch, Curtis Rueden, Stephan Saalfeld, Benjamin Schmid,[...]. Nat Methods 2012
16

Remodelling at the calyx of Held-MNTB synapse in mice developing with unilateral conductive hearing loss.
Giovanbattista Grande, Jaina Negandhi, Robert V Harrison, Lu-Yang Wang. J Physiol 2014
19
16


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.