A citation-based method for searching scientific literature

Gary J Bassell, Stephen T Warren. Neuron 2008
Times Cited: 717







List of co-cited articles
1390 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
41

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
940
25

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.
A J Verkerk, M Pieretti, J S Sutcliffe, Y H Fu, D P Kuhl, A Pizzuti, O Reiner, S Richards, M F Victoria, F P Zhang. Cell 1991
24

The mGluR theory of fragile X mental retardation.
Mark F Bear, Kimberly M Huber, Stephen T Warren. Trends Neurosci 2004
22

FMRP targets distinct mRNA sequence elements to regulate protein expression.
Manuel Ascano, Neelanjan Mukherjee, Pradeep Bandaru, Jason B Miller, Jeffrey D Nusbaum, David L Corcoran, Christine Langlois, Mathias Munschauer, Scott Dewell, Markus Hafner,[...]. Nature 2012
410
15

Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome.
V Brown, P Jin, S Ceman, J C Darnell, W T O'Donnell, S A Tenenbaum, X Jin, Y Feng, K D Wilkinson, J D Keene,[...]. Cell 2001
841
15

FMRP regulates neurotransmitter release and synaptic information transmission by modulating action potential duration via BK channels.
Pan-Yue Deng, Ziv Rotman, Jay A Blundon, Yongcheol Cho, Jianmin Cui, Valeria Cavalli, Stanislav S Zakharenko, Vitaly A Klyachko. Neuron 2013
199
14

Fragile X mental retardation protein controls gating of the sodium-activated potassium channel Slack.
Maile R Brown, Jack Kronengold, Valeswara-Rao Gazula, Yi Chen, John G Strumbos, Fred J Sigworth, Dhasakumar Navaratnam, Leonard K Kaczmarek. Nat Neurosci 2010
147
13


Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function.
J C Darnell, K B Jensen, P Jin, V Brown, S T Warren, R B Darnell. Cell 2001
717
12

Reversible inhibition of PSD-95 mRNA translation by miR-125a, FMRP phosphorylation, and mGluR signaling.
Ravi S Muddashetty, Vijayalaxmi C Nalavadi, Christina Gross, Xiaodi Yao, Lei Xing, Oskar Laur, Stephen T Warren, Gary J Bassell. Mol Cell 2011
256
12

Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits.
T A Comery, J B Harris, P J Willems, B A Oostra, S A Irwin, I J Weiler, W T Greenough. Proc Natl Acad Sci U S A 1997
751
12

Molecular mechanisms of fragile X syndrome: a twenty-year perspective.
Michael R Santoro, Steven M Bray, Stephen T Warren. Annu Rev Pathol 2012
334
12

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
332
11

Altered Neuronal and Circuit Excitability in Fragile X Syndrome.
Anis Contractor, Vitaly A Klyachko, Carlos Portera-Cailliau. Neuron 2015
182
11

The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP.
Ilaria Napoli, Valentina Mercaldo, Pietro Pilo Boyl, Boris Eleuteri, Francesca Zalfa, Silvia De Rubeis, Daniele Di Marino, Evita Mohr, Marzia Massimi, Mattia Falconi,[...]. Cell 2008
383
11

Phosphorylation influences the translation state of FMRP-associated polyribosomes.
Stephanie Ceman, William T O'Donnell, Matt Reed, Stephana Patton, Jan Pohl, Stephen T Warren. Hum Mol Genet 2003
235
10

Dysregulation and restoration of translational homeostasis in fragile X syndrome.
Joel D Richter, Gary J Bassell, Eric Klann. Nat Rev Neurosci 2015
140
10

Local functions for FMRP in axon growth cone motility and activity-dependent regulation of filopodia and spine synapses.
Laura N Antar, Chanxia Li, Honglai Zhang, Reed C Carroll, Gary J Bassell. Mol Cell Neurosci 2006
187
10

The FXG: a presynaptic fragile X granule expressed in a subset of developing brain circuits.
Sean B Christie, Michael R Akins, James E Schwob, Justin R Fallon. J Neurosci 2009
148
10

Fragile X syndrome.
Randi J Hagerman, Elizabeth Berry-Kravis, Heather Cody Hazlett, Donald B Bailey, Herve Moine, R Frank Kooy, Flora Tassone, Ilse Gantois, Nahum Sonenberg, Jean Louis Mandel,[...]. Nat Rev Dis Primers 2017
172
10


Correction of fragile X syndrome in mice.
Gül Dölen, Emily Osterweil, B S Shankaranarayana Rao, Gordon B Smith, Benjamin D Auerbach, Sumantra Chattarji, Mark F Bear. Neuron 2007
674
10

FMR1 protein: conserved RNP family domains and selective RNA binding.
C T Ashley, K D Wilkinson, D Reines, S T Warren. Science 1993
574
9

A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability.
Francesca Zalfa, Boris Eleuteri, Kirsten S Dickson, Valentina Mercaldo, Silvia De Rubeis, Alessandra di Penta, Elisabetta Tabolacci, Pietro Chiurazzi, Giovanni Neri, Seth G N Grant,[...]. Nat Neurosci 2007
265
9

Delayed stabilization of dendritic spines in fragile X mice.
Alberto Cruz-Martín, Michelle Crespo, Carlos Portera-Cailliau. J Neurosci 2010
197
9

Altered mRNA transport, docking, and protein translation in neurons lacking fragile X mental retardation protein.
Der-I Kao, Georgina M Aldridge, Ivan Jeanne Weiler, William T Greenough. Proc Natl Acad Sci U S A 2010
98
9


From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome.
Claudia Bagni, William T Greenough. Nat Rev Neurosci 2005
357
9

Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway.
Peng Jin, Daniela C Zarnescu, Stephanie Ceman, Mika Nakamoto, Julie Mowrey, Thomas A Jongens, David L Nelson, Kevin Moses, Stephen T Warren. Nat Neurosci 2004
454
8

Fragile X mental retardation protein is required for rapid experience-dependent regulation of the potassium channel Kv3.1b.
John G Strumbos, Maile R Brown, Jack Kronengold, Daniel B Polley, Leonard K Kaczmarek. J Neurosci 2010
88
9

Fragile X mental retardation protein controls synaptic vesicle exocytosis by modulating N-type calcium channel density.
Laurent Ferron, Manuela Nieto-Rostro, John S Cassidy, Annette C Dolphin. Nat Commun 2014
81
9

Axonal ribosomes and mRNAs associate with fragile X granules in adult rodent and human brains.
Michael R Akins, Hanna E Berk-Rauch, Kenneth Y Kwan, Molly E Mitchell, Katherine A Shepard, Lulu I T Korsak, Emily E Stackpole, Jennifer L Warner-Schmidt, Nenad Sestan, Heather A Cameron,[...]. Hum Mol Genet 2017
33
24

Dynamic Axonal Translation in Developing and Mature Visual Circuits.
Toshiaki Shigeoka, Hosung Jung, Jane Jung, Benita Turner-Bridger, Jiyeon Ohk, Julie Qiaojin Lin, Paul S Amieux, Christine E Holt. Cell 2016
210
8

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.
R E Amir, I B Van den Veyver, M Wan, C Q Tran, U Francke, H Y Zoghbi. Nat Genet 1999
8

A novel function for fragile X mental retardation protein in translational activation.
Elias G Bechara, Marie Cecile Didiot, Mireille Melko, Laetitia Davidovic, Mounia Bensaid, Patrick Martin, Marie Castets, Philippe Pognonec, Edouard W Khandjian, Hervé Moine,[...]. PLoS Biol 2009
131
8

Absence of expression of the FMR-1 gene in fragile X syndrome.
M Pieretti, F P Zhang, Y H Fu, S T Warren, B A Oostra, C T Caskey, D L Nelson. Cell 1991
8

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.
Y H Fu, D P Kuhl, A Pizzuti, M Pieretti, J S Sutcliffe, S Richards, A J Verkerk, J J Holden, R G Fenwick, S T Warren. Cell 1991
8

Increased expression of the PI3K enhancer PIKE mediates deficits in synaptic plasticity and behavior in fragile X syndrome.
Christina Gross, Chia-Wei Chang, Seth M Kelly, Aditi Bhattacharya, Sean M J McBride, Scott W Danielson, Michael Q Jiang, Chi Bun Chan, Keqiang Ye, Jay R Gibson,[...]. Cell Rep 2015
63
12

Evidence that fragile X mental retardation protein is a negative regulator of translation.
B Laggerbauer, D Ostareck, E M Keidel, A Ostareck-Lederer, U Fischer. Hum Mol Genet 2001
434
8

Kissing complex RNAs mediate interaction between the Fragile-X mental retardation protein KH2 domain and brain polyribosomes.
Jennifer C Darnell, Claire E Fraser, Olga Mostovetsky, Giovanni Stefani, Thomas A Jones, Sean R Eddy, Robert B Darnell. Genes Dev 2005
195
8

Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures.
Leila K Myrick, Pan-Yue Deng, Hideharu Hashimoto, Young Mi Oh, Yongcheol Cho, Mickael J Poidevin, Joshua A Suhl, Jeannie Visootsak, Valeria Cavalli, Peng Jin,[...]. Proc Natl Acad Sci U S A 2015
69
10

A chromatin-dependent role of the fragile X mental retardation protein FMRP in the DNA damage response.
Roman Alpatov, Bluma J Lesch, Mika Nakamoto-Kinoshita, Andres Blanco, Shuzhen Chen, Alexandra Stützer, Karim J Armache, Matthew D Simon, Chao Xu, Muzaffar Ali,[...]. Cell 2014
88
7

Minocycline promotes dendritic spine maturation and improves behavioural performance in the fragile X mouse model.
T V Bilousova, L Dansie, M Ngo, J Aye, J R Charles, D W Ethell, I M Ethell. J Med Genet 2009
305
7


Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics.
Claudia Bagni, Flora Tassone, Giovanni Neri, Randi Hagerman. J Clin Invest 2012
183
7


FMR1 and the fragile X syndrome: human genome epidemiology review.
D C Crawford, J M Acuña, S L Sherman. Genet Med 2001
397
7

Human FMRP contains an integral tandem Agenet (Tudor) and KH motif in the amino terminal domain.
Leila K Myrick, Hideharu Hashimoto, Xiaodong Cheng, Stephen T Warren. Hum Mol Genet 2015
51
13

The state of synapses in fragile X syndrome.
Brad E Pfeiffer, Kimberly M Huber. Neuroscientist 2009
141
7


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.