A citation-based method for searching scientific literature

Giovanni Stefani, Claire E Fraser, Jennifer C Darnell, Robert B Darnell. J Neurosci 2004
Times Cited: 181







List of co-cited articles
1410 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
68

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
384
39

Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles.
Edouard W Khandjian, Marc-Etienne Huot, Sandra Tremblay, Laetitia Davidovic, Rachid Mazroui, Barbara Bardoni. Proc Natl Acad Sci U S A 2004
133
38

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
37

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
32


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
435
30

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
946
28

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
28

FMR1 protein: conserved RNP family domains and selective RNA binding.
C T Ashley, K D Wilkinson, D Reines, S T Warren. Science 1993
574
26

The mGluR theory of fragile X mental retardation.
Mark F Bear, Kimberly M Huber, Stephen T Warren. Trends Neurosci 2004
24

The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses.
Francesca Zalfa, Marcello Giorgi, Beatrice Primerano, Annamaria Moro, Alessandra Di Penta, Surya Reis, Ben Oostra, Claudia Bagni. Cell 2003
514
24


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
719
24

Molecular mechanisms of fragile X syndrome: a twenty-year perspective.
Michael R Santoro, Steven M Bray, Stephen T Warren. Annu Rev Pathol 2012
335
24

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
414
24


Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes.
Y Feng, C A Gutekunst, D E Eberhart, H Yi, S T Warren, S M Hersch. J Neurosci 1997
377
22

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
333
22

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
339
21

Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function.
Y Q Zhang, A M Bailey, H J Matthies, R B Renden, M A Smith, S D Speese, G M Rubin, K Broadie. Cell 2001
497
21

Dysregulation of mTOR signaling in fragile X syndrome.
Ali Sharma, Charles A Hoeffer, Yukihiro Takayasu, Takahiro Miyawaki, Sean M McBride, Eric Klann, R Suzanne Zukin. J Neurosci 2010
386
21

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
21

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
257
21

The fragile X mental retardation protein is associated with poly(A)+ mRNA in actively translating polyribosomes.
F Corbin, M Bouillon, A Fortin, S Morin, F Rousseau, E W Khandjian. Hum Mol Genet 1997
190
20

The fragile X mental retardation protein inhibits translation via interacting with mRNA.
Z Li, Y Zhang, L Ku, K D Wilkinson, S T Warren, Y Feng. Nucleic Acids Res 2001
349
20

A Drosophila fragile X protein interacts with components of RNAi and ribosomal proteins.
Akira Ishizuka, Mikiko C Siomi, Haruhiko Siomi. Genes Dev 2002
437
20

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
20


RNA cargoes associating with FMRP reveal deficits in cellular functioning in Fmr1 null mice.
Kevin Y Miyashiro, Andrea Beckel-Mitchener, T Patrick Purk, Kevin G Becker, Tanya Barret, Lei Liu, Salvatore Carbonetto, Ivan Jeanne Weiler, William T Greenough, James Eberwine. Neuron 2003
384
19



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
753
18

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
675
18

The fragile X mental retardation protein is associated with ribosomes.
E W Khandjian, F Corbin, S Woerly, F Rousseau. Nat Genet 1996
192
18


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
17

FMRP phosphorylation reveals an immediate-early signaling pathway triggered by group I mGluR and mediated by PP2A.
Usha Narayanan, Vijayalaxmi Nalavadi, Mika Nakamoto, David C Pallas, Stephanie Ceman, Gary J Bassell, Stephen T Warren. J Neurosci 2007
165
17

A point mutation in the FMR-1 gene associated with fragile X mental retardation.
K De Boulle, A J Verkerk, E Reyniers, L Vits, J Hendrickx, B Van Roy, F Van den Bos, E de Graaff, B A Oostra, P J Willems. Nat Genet 1993
489
17


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
16

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
149
16

Genetic removal of p70 S6 kinase 1 corrects molecular, synaptic, and behavioral phenotypes in fragile X syndrome mice.
Aditi Bhattacharya, Hanoch Kaphzan, Amanda C Alvarez-Dieppa, Jaclyn P Murphy, Philippe Pierre, Eric Klann. Neuron 2012
200
16

Genetic and acute CPEB1 depletion ameliorate fragile X pathophysiology.
Tsuyoshi Udagawa, Natalie G Farny, Mira Jakovcevski, Hanoch Kaphzan, Juan Marcos Alarcon, Shobha Anilkumar, Maria Ivshina, Jessica A Hurt, Kentaro Nagaoka, Vijayalaxmi C Nalavadi,[...]. Nat Med 2013
80
20

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
125
16

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
15

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
188
15


Regulation of synaptic structure and function by FMRP-associated microRNAs miR-125b and miR-132.
Dieter Edbauer, Joel R Neilson, Kelly A Foster, Chi-Fong Wang, Daniel P Seeburg, Matthew N Batterton, Tomoko Tada, Bridget M Dolan, Phillip A Sharp, Morgan Sheng. Neuron 2010
521
14

Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repression.
Rachid Mazroui, Marc-Etienne Huot, Sandra Tremblay, Christine Filion, Yves Labelle, Edouard W Khandjian. Hum Mol Genet 2002
255
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.