A citation-based method for searching scientific literature

Silvia De Rubeis, Emanuela Pasciuto, Ka Wan Li, Esperanza Fernández, Daniele Di Marino, Andrea Buzzi, Linnaea E Ostroff, Eric Klann, Fried J T Zwartkruis, Noboru H Komiyama, Seth G N Grant, Christel Poujol, Daniel Choquet, Tilmann Achsel, Danielle Posthuma, August B Smit, Claudia Bagni. Neuron 2013
Times Cited: 158







List of co-cited articles
1349 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
391
50

The autism and schizophrenia associated gene CYFIP1 is critical for the maintenance of dendritic complexity and the stabilization of mature spines.
M Pathania, E C Davenport, J Muir, D F Sheehan, G López-Doménech, J T Kittler. Transl Psychiatry 2014
120
37

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
26

Haploinsufficiency of Cyfip1 produces fragile X-like phenotypes in mice.
Ozlem Bozdagi, Takeshi Sakurai, Nathan Dorr, Marion Pilorge, Nagahide Takahashi, Joseph D Buxbaum. PLoS One 2012
72
30

Increased CYFIP1 dosage alters cellular and dendritic morphology and dysregulates mTOR.
A Oguro-Ando, C Rosensweig, E Herman, Y Nishimura, D Werling, B R Bill, J M Berg, F Gao, G Coppola, B S Abrahams,[...]. Mol Psychiatry 2015
70
30

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
20

Structure and control of the actin regulatory WAVE complex.
Zhucheng Chen, Dominika Borek, Shae B Padrick, Timothy S Gomez, Zoltan Metlagel, Ayman M Ismail, Junko Umetani, Daniel D Billadeau, Zbyszek Otwinowski, Michael K Rosen. Nature 2010
295
20


CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein.
Annette Schenck, Barbara Bardoni, Caillin Langmann, Nicholas Harden, Jean Louis Mandel, Angela Giangrande. Neuron 2003
243
19

Autism and Schizophrenia-Associated CYFIP1 Regulates the Balance of Synaptic Excitation and Inhibition.
Elizabeth C Davenport, Blanka R Szulc, James Drew, James Taylor, Toby Morgan, Nathalie F Higgs, Guillermo López-Doménech, Josef T Kittler. Cell Rep 2019
44
40


New insights into the regulatory function of CYFIP1 in the context of WAVE- and FMRP-containing complexes.
Sabiha Abekhoukh, H Bahar Sahin, Mauro Grossi, Samantha Zongaro, Thomas Maurin, Irene Madrigal, Daniele Kazue-Sugioka, Annick Raas-Rothschild, Mohamed Doulazmi, Pilar Carrera,[...]. Dis Model Mech 2017
36
47

The 15q11.2 BP1-BP2 microdeletion syndrome: a review.
Devin M Cox, Merlin G Butler. Int J Mol Sci 2015
101
16

Cyfip1 Regulates Presynaptic Activity during Development.
Kuangfu Hsiao, Hala Harony-Nicolas, Joseph D Buxbaum, Ozlem Bozdagi-Gunal, Deanna L Benson. J Neurosci 2016
30
53

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
845
15

Modeling a genetic risk for schizophrenia in iPSCs and mice reveals neural stem cell deficits associated with adherens junctions and polarity.
Ki-Jun Yoon, Ha Nam Nguyen, Gianluca Ursini, Fengyu Zhang, Nam-Shik Kim, Zhexing Wen, Georgia Makri, David Nauen, Joo Heon Shin, Youngbin Park,[...]. Cell Stem Cell 2014
163
14

A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder.
Bert van der Zwaag, Wouter G Staal, Ron Hochstenbach, Martin Poot, Henk A Spierenburg, Maretha V de Jonge, Nienke E Verbeek, Ruben van 't Slot, Michael A van Es, Frank J Staal,[...]. Am J Med Genet B Neuropsychiatr Genet 2010
72
19

Large recurrent microdeletions associated with schizophrenia.
Hreinn Stefansson, Dan Rujescu, Sven Cichon, Olli P H Pietiläinen, Andres Ingason, Stacy Steinberg, Ragnheidur Fossdal, Engilbert Sigurdsson, Thordur Sigmundsson, Jacobine E Buizer-Voskamp,[...]. Nature 2008
14

Two-stage translational control of dentate gyrus LTP consolidation is mediated by sustained BDNF-TrkB signaling to MNK.
Debabrata Panja, Justin W Kenney, Laura D'Andrea, Francesca Zalfa, Anni Vedeler, Karin Wibrand, Rikiro Fukunaga, Claudia Bagni, Christopher G Proud, Clive R Bramham. Cell Rep 2014
87
14

Mutations causing syndromic autism define an axis of synaptic pathophysiology.
Benjamin D Auerbach, Emily K Osterweil, Mark F Bear. Nature 2011
413
13

Reducing eIF4E-eIF4G interactions restores the balance between protein synthesis and actin dynamics in fragile X syndrome model mice.
Emanuela Santini, Thu N Huynh, Francesco Longo, So Yeon Koo, Edward Mojica, Laura D'Andrea, Claudia Bagni, Eric Klann. Sci Signal 2017
40
32

The autism- and schizophrenia-associated protein CYFIP1 regulates bilateral brain connectivity and behaviour.
Nuria Domínguez-Iturza, Adrian C Lo, Disha Shah, Marcelo Armendáriz, Anna Vannelli, Valentina Mercaldo, Massimo Trusel, Ka Wan Li, Denise Gastaldo, Ana Rita Santos,[...]. Nat Commun 2019
29
44

Cyfip1 haploinsufficient rats show white matter changes, myelin thinning, abnormal oligodendrocytes and behavioural inflexibility.
Ana I Silva, Josephine E Haddon, Yasir Ahmed Syed, Simon Trent, Tzu-Ching E Lin, Yateen Patel, Jenny Carter, Niels Haan, Robert C Honey, Trevor Humby,[...]. Nat Commun 2019
28
46

Fragile X-like behaviors and abnormal cortical dendritic spines in cytoplasmic FMR1-interacting protein 2-mutant mice.
Kihoon Han, Hogmei Chen, Vincenzo A Gennarino, Ronald Richman, Hui-Chen Lu, Huda Y Zoghbi. Hum Mol Genet 2015
40
30

p140Sra-1 (specifically Rac1-associated protein) is a novel specific target for Rac1 small GTPase.
K Kobayashi, S Kuroda, M Fukata, T Nakamura, T Nagase, N Nomura, Y Matsuura, N Yoshida-Kubomura, A Iwamatsu, K Kaibuchi. J Biol Chem 1998
177
12

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
12

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
952
12

Autism-related deficits via dysregulated eIF4E-dependent translational control.
Christos G Gkogkas, Arkady Khoutorsky, Israeli Ran, Emmanouil Rampakakis, Tatiana Nevarko, Daniel B Weatherill, Cristina Vasuta, Stephanie Yee, Morgan Truitt, Paul Dallaire,[...]. Nature 2013
335
12

CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle,[...]. Nature 2014
385
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
759
11

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
159
11


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
422
11

Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics.
Claudia Bagni, Flora Tassone, Giovanni Neri, Randi Hagerman. J Clin Invest 2012
188
11

Dysregulation and restoration of translational homeostasis in fragile X syndrome.
Joel D Richter, Gary J Bassell, Eric Klann. Nat Rev Neurosci 2015
146
11


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
337
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
681
10

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
516
10

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
421
10

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
510
9

Actin in dendritic spines: connecting dynamics to function.
Pirta Hotulainen, Casper C Hoogenraad. J Cell Biol 2010
506
9

De novo gene disruptions in children on the autistic spectrum.
Ivan Iossifov, Michael Ronemus, Dan Levy, Zihua Wang, Inessa Hakker, Julie Rosenbaum, Boris Yamrom, Yoon-Ha Lee, Giuseppe Narzisi, Anthony Leotta,[...]. Neuron 2012
916
9

From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome.
Claudia Bagni, William T Greenough. Nat Rev Neurosci 2005
361
9

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.
Rachel D Burnside, Romela Pasion, Fady M Mikhail, Andrew J Carroll, Nathaniel H Robin, Erin L Youngs, Inder K Gadi, Elizabeth Keitges, Vikram L Jaswaney, Peter R Papenhausen,[...]. Hum Genet 2011
163
9

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
9

Exaggerated translation causes synaptic and behavioural aberrations associated with autism.
Emanuela Santini, Thu N Huynh, Andrew F MacAskill, Adam G Carter, Philippe Pierre, Davide Ruggero, Hanoch Kaphzan, Eric Klann. Nature 2013
239
9

Dendritic spine pathology in neuropsychiatric disorders.
Peter Penzes, Michael E Cahill, Kelly A Jones, Jon-Eric VanLeeuwen, Kevin M Woolfrey. Nat Neurosci 2011
903
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
269
9


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.