A citation-based method for searching scientific literature

Nien-Pei Tsai, Julia R Wilkerson, Weirui Guo, Marina A Maksimova, George N DeMartino, Christopher W Cowan, Kimberly M Huber. Cell 2012
Times Cited: 189







List of co-cited articles
1526 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Fragile X mental retardation protein is required for synapse elimination by the activity-dependent transcription factor MEF2.
Brad E Pfeiffer, Tong Zang, Julia R Wilkerson, Makoto Taniguchi, Marina A Maksimova, Laura N Smith, Christopher W Cowan, Kimberly M Huber. Neuron 2010
110
24

Identifying autism loci and genes by tracing recent shared ancestry.
Eric M Morrow, Seung-Yun Yoo, Steven W Flavell, Tae-Kyung Kim, Yingxi Lin, Robert Sean Hill, Nahit M Mukaddes, Soher Balkhy, Generoso Gascon, Asif Hashmi,[...]. Science 2008
504
18

FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism.
Jennifer C Darnell, Sarah J Van Driesche, Chaolin Zhang, Ka Ying Sharon Hung, Aldo Mele, Claire E Fraser, Elizabeth F Stone, Cynthia Chen, John J Fak, Sung Wook Chi,[...]. Cell 2011
15

Activity-dependent regulation of MEF2 transcription factors suppresses excitatory synapse number.
Steven W Flavell, Christopher W Cowan, Tae-Kyung Kim, Paul L Greer, Yingxi Lin, Suzanne Paradis, Eric C Griffith, Linda S Hu, Chinfei Chen, Michael E Greenberg. Science 2006
406
14

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

Ubiquitination regulates PSD-95 degradation and AMPA receptor surface expression.
Marcie Colledge, Eric M Snyder, Robert A Crozier, Jacquelyn A Soderling, Yetao Jin, Lorene K Langeberg, Hua Lu, Mark F Bear, John D Scott. Neuron 2003
413
13

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
856
13

FMRP-dependent Mdm2 dephosphorylation is required for MEF2-induced synapse elimination.
Nien-Pei Tsai, Julia R Wilkerson, Weirui Guo, Kimberly M Huber. Hum Mol Genet 2017
18
66

Genome-wide analysis of MEF2 transcriptional program reveals synaptic target genes and neuronal activity-dependent polyadenylation site selection.
Steven W Flavell, Tae-Kyung Kim, Jesse M Gray, David A Harmin, Martin Hemberg, Elizabeth J Hong, Eirene Markenscoff-Papadimitriou, Daniel M Bear, Michael E Greenberg. Neuron 2008
330
11

MEF2C, a transcription factor that facilitates learning and memory by negative regulation of synapse numbers and function.
Ana C Barbosa, Mi-Sung Kim, Mert Ertunc, Megumi Adachi, Erika D Nelson, John McAnally, James A Richardson, Ege T Kavalali, Lisa M Monteggia, Rhonda Bassel-Duby,[...]. Proc Natl Acad Sci U S A 2008
191
11

Association of mouse Dlg4 (PSD-95) gene deletion and human DLG4 gene variation with phenotypes relevant to autism spectrum disorders and Williams' syndrome.
Michael Feyder, Rose-Marie Karlsson, Poonam Mathur, Matthew Lyman, Roland Bock, Reza Momenan, Jeeva Munasinghe, Maria Luisa Scattoni, Jessica Ihne, Marguerite Camp,[...]. Am J Psychiatry 2010
144
10



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
437
10

Rapid translation of Arc/Arg3.1 selectively mediates mGluR-dependent LTD through persistent increases in AMPAR endocytosis rate.
Maggie W Waung, Brad E Pfeiffer, Elena D Nosyreva, Jennifer A Ronesi, Kimberly M Huber. Neuron 2008
347
10


De novo mutations in schizophrenia implicate synaptic networks.
Menachem Fromer, Andrew J Pocklington, David H Kavanagh, Hywel J Williams, Sarah Dwyer, Padhraig Gormley, Lyudmila Georgieva, Elliott Rees, Priit Palta, Douglas M Ruderfer,[...]. Nature 2014
10

Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3.
Xiaoming Wang, Portia A McCoy, Ramona M Rodriguiz, Yanzhen Pan, H Shawn Je, Adam C Roberts, Caroline J Kim, Janet Berrios, Jennifer S Colvin, Danielle Bousquet-Moore,[...]. Hum Mol Genet 2011
350
10

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
411
10

PSD-95 involvement in maturation of excitatory synapses.
A E El-Husseini, E Schnell, D M Chetkovich, R A Nicoll, D S Bredt. Science 2000
867
9

Enhanced long-term potentiation and impaired learning in mice with mutant postsynaptic density-95 protein.
M Migaud, P Charlesworth, M Dempster, L C Webster, A M Watabe, M Makhinson, Y He, M F Ramsay, R G Morris, J H Morrison,[...]. Nature 1998
895
9

Contact-dependent promotion of cell migration by the OL-protocadherin-Nap1 interaction.
Shinsuke Nakao, Anna Platek, Shinji Hirano, Masatoshi Takeichi. J Cell Biol 2008
87
10


Activity-induced protocadherin arcadlin regulates dendritic spine number by triggering N-cadherin endocytosis via TAO2beta and p38 MAP kinases.
Shin Yasuda, Hidekazu Tanaka, Hiroko Sugiura, Ko Okamura, Taiki Sakaguchi, Uyen Tran, Takako Takemiya, Akira Mizoguchi, Yoshiki Yagita, Takeshi Sakurai,[...]. Neuron 2007
135
9

Sociability Deficits and Altered Amygdala Circuits in Mice Lacking Pcdh10, an Autism Associated Gene.
Hannah Schoch, Arati S Kreibich, Sarah L Ferri, Rachel S White, Dominique Bohorquez, Anamika Banerjee, Russell G Port, Holly C Dow, Lucero Cordero, Ashley A Pallathra,[...]. Biol Psychiatry 2017
36
25

A role for dendritic mGluR5-mediated local translation of Arc/Arg3.1 in MEF2-dependent synapse elimination.
Julia R Wilkerson, Nien-Pei Tsai, Marina A Maksimova, Hao Wu, Nicole P Cabalo, Kristofer W Loerwald, Jason B Dictenberg, Jay R Gibson, Kimberly M Huber. Cell Rep 2014
44
20

Dendritic spine pathology in neuropsychiatric disorders.
Peter Penzes, Michael E Cahill, Kelly A Jones, Jon-Eric VanLeeuwen, Kevin M Woolfrey. Nat Neurosci 2011
930
9

A direct role for FMRP in activity-dependent dendritic mRNA transport links filopodial-spine morphogenesis to fragile X syndrome.
Jason B Dictenberg, Sharon A Swanger, Laura N Antar, Robert H Singer, Gary J Bassell. Dev Cell 2008
340
8

Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses.
Sarah R Gilman, Ivan Iossifov, Dan Levy, Michael Ronemus, Michael Wigler, Dennis Vitkup. Neuron 2011
448
8

Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination.
S A Irwin, B Patel, M Idupulapati, J B Harris, R A Crisostomo, B P Larsen, F Kooy, P J Willems, P Cras, P B Kozlowski,[...]. Am J Med Genet 2001
516
8

OL-Protocadherin is essential for growth of striatal axons and thalamocortical projections.
Masato Uemura, Shinsuke Nakao, Shintaro T Suzuki, Masatoshi Takeichi, Shinji Hirano. Nat Neurosci 2007
116
8


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
397
8

Disrupted Homer scaffolds mediate abnormal mGluR5 function in a mouse model of fragile X syndrome.
Jennifer A Ronesi, Katie A Collins, Seth A Hays, Nien-Pei Tsai, Weirui Guo, Shari G Birnbaum, Jia-Hua Hu, Paul F Worley, Jay R Gibson, Kimberly M Huber. Nat Neurosci 2012
178
8

Protocadherin-17 mediates collective axon extension by recruiting actin regulator complexes to interaxonal contacts.
Shuichi Hayashi, Yoko Inoue, Hiroshi Kiyonari, Takaya Abe, Kazuyo Misaki, Hiroyuki Moriguchi, Yo Tanaka, Masatoshi Takeichi. Dev Cell 2014
54
14

The WAVE regulatory complex links diverse receptors to the actin cytoskeleton.
Baoyu Chen, Klaus Brinkmann, Zhucheng Chen, Chi W Pak, Yuxing Liao, Shuoyong Shi, Lisa Henry, Nick V Grishin, Sven Bogdan, Michael K Rosen. Cell 2014
165
8

Protocadherin-18b interacts with Nap1 to control motor axon growth and arborization in zebrafish.
Sayantanee Biswas, Michelle R Emond, Phan Q Duy, Le T Hao, Christine E Beattie, James D Jontes. Mol Biol Cell 2014
31
25

Arc/Arg3.1 interacts with the endocytic machinery to regulate AMPA receptor trafficking.
Shoaib Chowdhury, Jason D Shepherd, Hiroyuki Okuno, Gregory Lyford, Ronald S Petralia, Niels Plath, Dietmar Kuhl, Richard L Huganir, Paul F Worley. Neuron 2006
530
8

MDM2 inhibition rescues neurogenic and cognitive deficits in a mouse model of fragile X syndrome.
Yue Li, Michael E Stockton, Ismat Bhuiyan, Brian E Eisinger, Yu Gao, Jessica L Miller, Anita Bhattacharyya, Xinyu Zhao. Sci Transl Med 2016
32
25

Altered synaptic plasticity in a mouse model of fragile X mental retardation.
Kimberly M Huber, Sean M Gallagher, Stephen T Warren, Mark F Bear. Proc Natl Acad Sci U S A 2002
963
8

PDZ domain proteins of synapses.
Eunjoon Kim, Morgan Sheng. Nat Rev Neurosci 2004
7

Non-clustered protocadherin.
Soo-Young Kim, Shin Yasuda, Hidekazu Tanaka, Kanato Yamagata, Hyun Kim. Cell Adh Migr 2011
156
7

Transcription factor MEF2C influences neural stem/progenitor cell differentiation and maturation in vivo.
Hao Li, Jonathan C Radford, Michael J Ragusa, Katherine L Shea, Scott R McKercher, Jeffrey D Zaremba, Walid Soussou, Zhiguo Nie, Yeon-Joo Kang, Nobuki Nakanishi,[...]. Proc Natl Acad Sci U S A 2008
164
7


Experience-dependent structural synaptic plasticity in the mammalian brain.
Anthony Holtmaat, Karel Svoboda. Nat Rev Neurosci 2009
7

Dendritic spine instability and insensitivity to modulation by sensory experience in a mouse model of fragile X syndrome.
Feng Pan, Georgina M Aldridge, William T Greenough, Wen-Biao Gan. Proc Natl Acad Sci U S A 2010
134
7

Feedback modulation of neural network synchrony and seizure susceptibility by Mdm2-p53-Nedd4-2 signaling.
Kathryn A Jewett, Catherine A Christian, Jonathan T Bacos, Kwan Young Lee, Jiuhe Zhu, Nien-Pei Tsai. Mol Brain 2016
19
36

A polygenic burden of rare disruptive mutations in schizophrenia.
Shaun M Purcell, Jennifer L Moran, Menachem Fromer, Douglas Ruderfer, Nadia Solovieff, Panos Roussos, Colm O'Dushlaine, Kimberly Chambert, Sarah E Bergen, Anna Kähler,[...]. Nature 2014
919
7

Smaller dendritic spines, weaker synaptic transmission, but enhanced spatial learning in mice lacking Shank1.
Albert Y Hung, Kensuke Futai, Carlo Sala, Juli G Valtschanoff, Jubin Ryu, Mollie A Woodworth, Fleur L Kidd, Clifford C Sung, Tsuyoshi Miyakawa, Mark F Bear,[...]. J Neurosci 2008
245
7

A complex of Protocadherin-19 and N-cadherin mediates a novel mechanism of cell adhesion.
Michelle R Emond, Sayantanee Biswas, Cheasequah J Blevins, James D Jontes. J Cell Biol 2011
64
10


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.