A citation-based method for searching scientific literature

Young Jae Woo, Alexandros K Kanellopoulos, Parisa Hemati, Jill Kirschen, Rebecca A Nebel, Tao Wang, Claudia Bagni, Brett S Abrahams. Biol Psychiatry 2019
Times Cited: 6







List of co-cited articles
43 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
381
83

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
39
83

Rare CNVs and tag SNPs at 15q11.2 are associated with schizophrenia in the Han Chinese population.
Qian Zhao, Tao Li, XinZhi Zhao, Ke Huang, Ti Wang, ZhiQiang Li, Jue Ji, Zhen Zeng, Zhao Zhang, Kan Li,[...]. Schizophr Bull 2013
38
83

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
371
83


15q11.2 microdeletion (BP1-BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: a series of 52 patients.
Clémence Vanlerberghe, Florence Petit, Valérie Malan, Catherine Vincent-Delorme, Sonia Bouquillon, Odile Boute, Muriel Holder-Espinasse, Bruno Delobel, Bénédicte Duban, Louis Vallee,[...]. Eur J Med Genet 2015
49
66

CYFIP1 coordinates mRNA translation and cytoskeleton remodeling to ensure proper dendritic spine formation.
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,[...]. Neuron 2013
152
66

The 15q11.2 BP1-BP2 microdeletion syndrome: a review.
Devin M Cox, Merlin G Butler. Int J Mol Sci 2015
94
50

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
50

Behavioral training rescues motor deficits in Cyfip1 haploinsufficiency mouse model of autism spectrum disorders.
Sven O Bachmann, Monika Sledziowska, Ellen Cross, Shireene Kalbassi, Sophie Waldron, Fangli Chen, Adam Ranson, Stéphane J Baudouin. Transl Psychiatry 2019
11
50

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
66
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
116
50

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
50

Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders.
Regina Waltes, Eftichia Duketis, Michael Knapp, Richard J L Anney, Guillaume Huguet, Sabine Schlitt, Tomasz A Jarczok, Michael Sachse, Laura M Kämpfer, Tina Kleinböck,[...]. Hum Genet 2014
39
50

Confirmed rare copy number variants implicate novel genes in schizophrenia.
Gloria W C Tam, Louie N van de Lagemaat, Richard Redon, Karen E Strathdee, Mike D R Croning, Mary P Malloy, Walter J Muir, Ben S Pickard, Ian J Deary, Douglas H R Blackwood,[...]. Biochem Soc Trans 2010
102
50

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
69
50

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
24
50

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
50

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
24
50

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
35
50

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
241
50


Parental origin impairment of synaptic functions and behaviors in cytoplasmic FMRP interacting protein 1 (Cyfip1) deficient mice.
Leeyup Chung, Xiaoming Wang, Li Zhu, Aaron J Towers, Xinyu Cao, Il Hwan Kim, Yong-hui Jiang. Brain Res 2015
14
33

Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study.
Ana I Silva, Magnus O Ulfarsson, Hreinn Stefansson, Omar Gustafsson, G Bragi Walters, David E J Linden, Lawrence S Wilkinson, Mark Drakesmith, Michael J Owen, Jeremy Hall,[...]. Biol Psychiatry 2019
18
33

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
289
33

Cyfip1 Regulates Presynaptic Activity during Development.
Kuangfu Hsiao, Hala Harony-Nicolas, Joseph D Buxbaum, Ozlem Bozdagi-Gunal, Deanna L Benson. J Neurosci 2016
29
33

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
175
33

Peripheral Mechanosensory Neuron Dysfunction Underlies Tactile and Behavioral Deficits in Mouse Models of ASDs.
Lauren L Orefice, Amanda L Zimmerman, Anda M Chirila, Steven J Sleboda, Joshua P Head, David D Ginty. Cell 2016
129
33

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
875
33

MD and Docking Studies Reveal That the Functional Switch of CYFIP1 is Mediated by a Butterfly-like Motion.
Daniele Di Marino, Giovanni Chillemi, Silvia De Rubeis, Anna Tramontano, Tilmann Achsel, Claudia Bagni. J Chem Theory Comput 2015
13
33



Drosophila: genetics meets behaviour.
M B Sokolowski. Nat Rev Genet 2001
250
33

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
83
33

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
Claire S Leblond, Jutta Heinrich, Richard Delorme, Christian Proepper, Catalina Betancur, Guillaume Huguet, Marina Konyukh, Pauline Chaste, Elodie Ey, Maria Rastam,[...]. PLoS Genet 2012
263
33

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
159
33

Phenotypic features in patients with 15q11.2(BP1-BP2) deletion: further delineation of an emerging syndrome.
Michiala Cafferkey, Joo Wook Ahn, Frances Flinter, Caroline Ogilvie. Am J Med Genet A 2014
35
33


Conditioned responses in courtship behavior of normal and mutant Drosophila.
R W Siegel, J C Hall. Proc Natl Acad Sci U S A 1979
299
33


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
325
33

CYFIP1 overexpression increases fear response in mice but does not affect social or repetitive behavioral phenotypes.
Catherine Fricano-Kugler, Aaron Gordon, Grace Shin, Kun Gao, Jade Nguyen, Jamee Berg, Mary Starks, Daniel H Geschwind. Mol Autism 2019
9
33

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
231
33

Cognitive flexibility in ASD; task switching with emotional faces.
Marieke de Vries, Hilde M Geurts. J Autism Dev Disord 2012
37
16


Corpus callosal atrophy and associations with cognitive impairment in Parkinson disease.
Jennifer G Goldman, Ian O Bledsoe, Doug Merkitch, Vy Dinh, Bryan Bernard, Glenn T Stebbins. Neurology 2017
31
16

Corpus callosum abnormalities and their association with psychotic symptoms in patients with schizophrenia.
Thomas J Whitford, Marek Kubicki, Jason S Schneiderman, Lauren J O'Donnell, Rebecca King, Jorge L Alvarado, Usman Khan, Douglas Markant, Paul G Nestor, Margaret Niznikiewicz,[...]. Biol Psychiatry 2010
121
16

Balanced interhemispheric cortical activity is required for correct targeting of the corpus callosum.
Rodrigo Suárez, Laura R Fenlon, Roger Marek, Lilach Avitan, Pankaj Sah, Geoffrey J Goodhill, Linda J Richards. Neuron 2014
46
16

Adult restoration of Shank3 expression rescues selective autistic-like phenotypes.
Yuan Mei, Patricia Monteiro, Yang Zhou, Jin-Ah Kim, Xian Gao, Zhanyan Fu, Guoping Feng. Nature 2016
174
16

Array-based comparative genomic hybridization analysis of recurrent chromosome 15q rearrangements.
Trilochan Sahoo, Chad A Shaw, Andrew S Young, Nathan L Whitehouse, Richard J Schroer, Roger E Stevenson, Arthur L Beaudet. Am J Med Genet A 2005
38
16


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.