A citation-based method for searching scientific literature

Gary J Bassell, Stephen T Warren. Neuron 2008
Times Cited: 736







List of co-cited articles
1399 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
35

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
21

The mGluR theory of fragile X mental retardation.
Mark F Bear, Kimberly M Huber, Stephen T Warren. Trends Neurosci 2004
20

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
18

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
436
13

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
769
13


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
11

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
212
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
153
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
220
10

Molecular mechanisms of fragile X syndrome: a twenty-year perspective.
Michael R Santoro, Steven M Bray, Stephen T Warren. Annu Rev Pathol 2012
352
9

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
161
9

FMR1 and the fragile X syndrome: human genome epidemiology review.
D C Crawford, J M Acuña, S L Sherman. Genet Med 2001
414
9

Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization.
Lisa Cordeiro, Elizabeth Ballinger, Randi Hagerman, David Hessl. J Neurodev Disord 2011
184
9

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
9

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
850
9

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
728
9

Altered Neuronal and Circuit Excitability in Fragile X Syndrome.
Anis Contractor, Vitaly A Klyachko, Carlos Portera-Cailliau. Neuron 2015
202
9


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
192
8

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
36
22

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
233
8

Dysregulation and restoration of translational homeostasis in fragile X syndrome.
Joel D Richter, Gary J Bassell, Eric Klann. Nat Rev Neurosci 2015
157
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


FMR1 protein: conserved RNP family domains and selective RNA binding.
C T Ashley, K D Wilkinson, D Reines, S T Warren. Science 1993
582
8

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
242
8

From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome.
Claudia Bagni, William T Greenough. Nat Rev Neurosci 2005
362
8

Delayed stabilization of dendritic spines in fragile X mice.
Alberto Cruz-Martín, Michelle Crespo, Carlos Portera-Cailliau. J Neurosci 2010
210
8

Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome.
H L Hinds, C T Ashley, J S Sutcliffe, D L Nelson, S T Warren, D E Housman, M Schalling. Nat Genet 1993
300
8

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
689
8

Local translation in neurons: visualization and function.
Christine E Holt, Kelsey C Martin, Erin M Schuman. Nat Struct Mol Biol 2019
155
8

Fmr1 deficiency promotes age-dependent alterations in the cortical synaptic proteome.
Bin Tang, Tingting Wang, Huida Wan, Li Han, Xiaoyan Qin, Yaoyang Zhang, Jian Wang, Chunlei Yu, Fulvia Berton, Walter Francesconi,[...]. Proc Natl Acad Sci U S A 2015
49
14

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
97
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
58
12

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
85
8

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
7

Autism profiles of males with fragile X syndrome.
Susan W Harris, David Hessl, Beth Goodlin-Jones, Jessica Ferranti, Susan Bacalman, Ingrid Barbato, Flora Tassone, Paul J Hagerman, Herman Herman, Randi J Hagerman. Am J Ment Retard 2008
266
7

Phenotypic variation and FMRP levels in fragile X.
Danuta Z Loesch, Richard M Huggins, Randi J Hagerman. Ment Retard Dev Disabil Res Rev 2004
196
7

Autism Spectrum Disorder in Fragile X Syndrome: Cooccurring Conditions and Current Treatment.
Walter E Kaufmann, Sharon A Kidd, Howard F Andrews, Dejan B Budimirovic, Amy Esler, Barbara Haas-Givler, Tracy Stackhouse, Catharine Riley, Georgina Peacock, Stephanie L Sherman,[...]. Pediatrics 2017
94
7

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
7

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
7

In the right place at the right time: visualizing and understanding mRNA localization.
Adina R Buxbaum, Gal Haimovich, Robert H Singer. Nat Rev Mol Cell Biol 2015
316
7

Dynamic translational and proteasomal regulation of fragile X mental retardation protein controls mGluR-dependent long-term depression.
Lingfei Hou, Marcia D Antion, Daoying Hu, Corinne M Spencer, Richard Paylor, Eric Klann. Neuron 2006
348
7

Fragile X mental retardation protein regulates translation by binding directly to the ribosome.
Eileen Chen, Manjuli R Sharma, Xinying Shi, Rajendra K Agrawal, Simpson Joseph. Mol Cell 2014
133
7

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
268
7

Multifarious Functions of the Fragile X Mental Retardation Protein.
Jenna K Davis, Kendal Broadie. Trends Genet 2017
56
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
439
7

Aberrant RNA translation in fragile X syndrome: From FMRP mechanisms to emerging therapeutic strategies.
Anwesha Banerjee, Marius F Ifrim, Arielle N Valdez, Nisha Raj, Gary J Bassell. Brain Res 2018
50
14


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.