A citation-based method for searching scientific literature

M Pathania, E C Davenport, J Muir, D F Sheehan, G López-Doménech, J T Kittler. Transl Psychiatry 2014
Times Cited: 115







List of co-cited articles
1070 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
149
43

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
380
36

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
40

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
64
39


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
286
22

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
19

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
19

The 15q11.2 BP1-BP2 microdeletion syndrome: a review.
Devin M Cox, Merlin G Butler. Int J Mol Sci 2015
93
20

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
68
26

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
158
18

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
17

Cyfip1 Regulates Presynaptic Activity during Development.
Kuangfu Hsiao, Hala Harony-Nicolas, Joseph D Buxbaum, Ozlem Bozdagi-Gunal, Deanna L Benson. J Neurosci 2016
28
60

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
15

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
370
15


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
32
43

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
38
36

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
154
13

Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioural disturbances.
Marianne Doornbos, Birgit Sikkema-Raddatz, Claudia A L Ruijvenkamp, Trijnie Dijkhuizen, Emilia K Bijlsma, Antoinet C J Gijsbers, Yvonne Hilhorst-Hofstee, Roel Hordijk, Krijn T Verbruggen, W S Mieke Kerstjens-Frederikse,[...]. Eur J Med Genet 2009
114
12

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Joseph T Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W Brune, Jonathan P Bradfield,[...]. Nature 2009
919
11

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
27


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
23
47


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
262
10

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
174
10

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
82
12

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang,[...]. Am J Hum Genet 2014
513
10

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
10

Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Benjamin M Neale, Yan Kou, Li Liu, Avi Ma'ayan, Kaitlin E Samocha, Aniko Sabo, Chiao-Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov,[...]. Nature 2012
9

Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams,[...]. Nature 2010
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
158
9

Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Kai Wang, Haitao Zhang, Deqiong Ma, Maja Bucan, Joseph T Glessner, Brett S Abrahams, Daria Salyakina, Marcin Imielinski, Jonathan P Bradfield, Patrick M A Sleiman,[...]. Nature 2009
660
9

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
48
18

C57BL/6N mutation in cytoplasmic FMRP interacting protein 2 regulates cocaine response.
Vivek Kumar, Kyungin Kim, Chryshanthi Joseph, Saïd Kourrich, Seung-Hee Yoo, Hung Chung Huang, Martha H Vitaterna, Fernando Pardo-Manuel de Villena, Gary Churchill, Antonello Bonci,[...]. Science 2013
106
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
894
9

Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations.
C Toma, B Torrico, A Hervás, R Valdés-Mas, A Tristán-Noguero, V Padillo, M Maristany, M Salgado, C Arenas, X S Puente,[...]. Mol Psychiatry 2014
67
13

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
64

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
81

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
22
40

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
504
8


De novo mutations in schizophrenia implicate synaptic networks.
Menachem Fromer, Andrew J Pocklington, David H Kavanagh, Hywel J Williams, Sarah Dwyer, Padhraig Gormley, Lyudmila Georgieva, Elliott Rees, Priit Palta, Douglas M Ruderfer,[...]. Nature 2014
948
8

Actin in dendritic spines: connecting dynamics to function.
Pirta Hotulainen, Casper C Hoogenraad. J Cell Biol 2010
491
8

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
870
8


Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
Stéphane Jamain, Hélène Quach, Catalina Betancur, Maria Råstam, Catherine Colineaux, I Carina Gillberg, Henrik Soderstrom, Bruno Giros, Marion Leboyer, Christopher Gillberg,[...]. Nat Genet 2003
8

Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways.
Yuhei Nishimura, Christa L Martin, Araceli Vazquez-Lopez, Sarah J Spence, Ana Isabel Alvarez-Retuerto, Marian Sigman, Corinna Steindler, Sandra Pellegrini, N Carolyn Schanen, Stephen T Warren,[...]. Hum Mol Genet 2007
206
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.