A citation-based method for searching scientific literature

Francesco Longo, Eric Klann. EMBO Rep 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Phosphatase and tensin homologue (PTEN) regulates synaptic plasticity independently of its effect on neuronal morphology and migration.
Margaret Sperow, Raymond B Berry, Ildar T Bayazitov, Guo Zhu, Suzanne J Baker, Stanislav S Zakharenko. J Physiol 2012
71
100

Epilepsy and Tsc2 haploinsufficiency lead to autistic-like social deficit behaviors in rats.
Robert Waltereit, Birte Japs, Miriam Schneider, Petrus J de Vries, Dusan Bartsch. Behav Genet 2011
49
100

Deletion of Pten in mouse brain causes seizures, ataxia and defects in soma size resembling Lhermitte-Duclos disease.
S A Backman, V Stambolic, A Suzuki, J Haight, A Elia, J Pretorius, M S Tsao, P Shannon, B Bolon, G O Ivy,[...]. Nat Genet 2001
357
100

Rett syndrome: a complex disorder with simple roots.
Matthew J Lyst, Adrian Bird. Nat Rev Genet 2015
178
100

Impaired language pathways in tuberous sclerosis complex patients with autism spectrum disorders.
William W Lewis, Mustafa Sahin, Benoit Scherrer, Jurriaan M Peters, Ralph O Suarez, Vanessa K Vogel-Farley, Shafali S Jeste, Matthew C Gregas, Sanjay P Prabhu, Charles A Nelson,[...]. Cereb Cortex 2013
44
100

Global transcriptional and translational repression in human-embryonic-stem-cell-derived Rett syndrome neurons.
Yun Li, Haoyi Wang, Julien Muffat, Albert W Cheng, David A Orlando, Jakob Lovén, Show-Ming Kwok, Danielle A Feldman, Helen S Bateup, Qing Gao,[...]. Cell Stem Cell 2013
186
100

mTOR: from growth signal integration to cancer, diabetes and ageing.
Roberto Zoncu, Alejo Efeyan, David M Sabatini. Nat Rev Mol Cell Biol 2011
100

Dopamine release in the basal ganglia.
M E Rice, J C Patel, S J Cragg. Neuroscience 2011
165
100

Rett syndrome: revised diagnostic criteria and nomenclature.
Jeffrey L Neul, Walter E Kaufmann, Daniel G Glaze, John Christodoulou, Angus J Clarke, Nadia Bahi-Buisson, Helen Leonard, Mark E S Bailey, N Carolyn Schanen, Michele Zappella,[...]. Ann Neurol 2010
681
100

Cell-Type-Specific Translation Profiling Reveals a Novel Strategy for Treating Fragile X Syndrome.
Sophie R Thomson, Sang S Seo, Stephanie A Barnes, Susana R Louros, Melania Muscas, Owen Dando, Caoimhe Kirby, David J A Wyllie, Giles E Hardingham, Peter C Kind,[...]. Neuron 2017
43
100

The Brd4 extraterminal domain confers transcription activation independent of pTEFb by recruiting multiple proteins, including NSD3.
Shaila Rahman, Mathew E Sowa, Matthias Ottinger, Jennifer A Smith, Yang Shi, J Wade Harper, Peter M Howley. Mol Cell Biol 2011
293
100

Potential for treatment of severe autism in tuberous sclerosis complex.
Tanjala T Gipson, Gwendolyn Gerner, Mary Ann Wilson, Mary E Blue, Michael V Johnston. World J Clin Pediatr 2013
10
100

Lessons learned from studying syndromic autism spectrum disorders.
Yehezkel Sztainberg, Huda Y Zoghbi. Nat Neurosci 2016
95
100


ADNP Regulates Cognition: A Multitasking Protein.
Illana Gozes. Front Neurosci 2018
6
100

TOR signaling in growth and metabolism.
Stephan Wullschleger, Robbie Loewith, Michael N Hall. Cell 2006
100

Sexual dimorphism of activity-dependent neuroprotective protein in the mouse arcuate nucleus.
Sharon Furman, Joanna M Hill, Inna Vulih, Roy Zaltzman, Janet M Hauser, Douglas E Brenneman, Illana Gozes. Neurosci Lett 2005
39
100

A case report of Chinese brothers with inherited MECP2-containing duplication: autism and intellectual disability, but not seizures or respiratory infections.
Xiu Xu, Qiong Xu, Ying Zhang, Xiaodi Zhang, Tianlin Cheng, Bingbing Wu, Yanhua Ding, Ping Lu, Jingjing Zheng, Min Zhang,[...]. BMC Med Genet 2012
12
100

Helsmoortel-Van der Aa Syndrome as emerging clinical diagnosis in intellectually disabled children with autistic traits and ocular involvement.
Giulia Pascolini, Emanuele Agolini, Silvia Majore, Antonio Novelli, Paola Grammatico, Maria Cristina Digilio. Eur J Paediatr Neurol 2018
6
100

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
899
100

Ribosomal protein S6 phosphorylation: from protein synthesis to cell size.
Igor Ruvinsky, Oded Meyuhas. Trends Biochem Sci 2006
529
100



Pten regulates neuronal soma size: a mouse model of Lhermitte-Duclos disease.
C H Kwon, X Zhu, J Zhang, L L Knoop, R Tharp, R J Smeyne, C G Eberhart, P C Burger, S J Baker. Nat Genet 2001
334
100

Transcriptome profiling in engrailed-2 mutant mice reveals common molecular pathways associated with autism spectrum disorders.
Paola Sgadò, Giovanni Provenzano, Erik Dassi, Valentina Adami, Giulia Zunino, Sacha Genovesi, Simona Casarosa, Yuri Bozzi. Mol Autism 2013
22
100

Genetic heritability and shared environmental factors among twin pairs with autism.
Joachim Hallmayer, Sue Cleveland, Andrea Torres, Jennifer Phillips, Brianne Cohen, Tiffany Torigoe, Janet Miller, Angie Fedele, Jack Collins, Karen Smith,[...]. Arch Gen Psychiatry 2011
971
100

Neuroanatomic observations of the brain in autism: a review and future directions.
Margaret L Bauman, Thomas L Kemper. Int J Dev Neurosci 2005
506
100

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
100


Maternal Experience-Dependent Cortical Plasticity in Mice Is Circuit- and Stimulus-Specific and Requires MECP2.
Billy Y B Lau, Keerthi Krishnan, Z Josh Huang, Stephen D Shea. J Neurosci 2020
10
100



The DNA methyltransferases associate with HP1 and the SUV39H1 histone methyltransferase.
François Fuks, Paul J Hurd, Rachel Deplus, Tony Kouzarides. Nucleic Acids Res 2003
507
100

Increased signaling by the autism-related Engrailed-2 protein enhances dendritic branching and spine density, alters synaptic structural matching, and exaggerates protein synthesis.
Asma Soltani, Solène Lebrun, Gilles Carpentier, Giulia Zunino, Sandrine Chantepie, Auriane Maïza, Yuri Bozzi, Claire Desnos, François Darchen, Olivier Stettler. PLoS One 2017
10
100

MeCP2, a key contributor to neurological disease, activates and represses transcription.
Maria Chahrour, Sung Yun Jung, Chad Shaw, Xiaobo Zhou, Stephen T C Wong, Jun Qin, Huda Y Zoghbi. Science 2008
100

The transcription factor Engrailed-2 guides retinal axons.
Isabelle Brunet, Christine Weinl, Michael Piper, Alain Trembleau, Michel Volovitch, William Harris, Alain Prochiantz, Christine Holt. Nature 2005
190
100


Cell Type-Specific mRNA Dysregulation in Hippocampal CA1 Pyramidal Neurons of the Fragile X Syndrome Mouse Model.
Laura Ceolin, Nathalie Bouquier, Jihane Vitre-Boubaker, Stéphanie Rialle, Dany Severac, Emmanuel Valjent, Julie Perroy, Emma Puighermanal. Front Mol Neurosci 2017
13
100


Molecular and phenotypic abnormalities in individuals with germline heterozygous PTEN mutations and autism.
T W Frazier, R Embacher, A K Tilot, K Koenig, J Mester, C Eng. Mol Psychiatry 2015
82
100

Reduced AKT/mTOR signaling and protein synthesis dysregulation in a Rett syndrome animal model.
Sara Ricciardi, Elena M Boggio, Stefano Grosso, Giuseppina Lonetti, Greta Forlani, Gilda Stefanelli, Eleonora Calcagno, Noemi Morello, Nicoletta Landsberger, Stefano Biffo,[...]. Hum Mol Genet 2011
138
100

Engrailed2 modulates cerebellar granule neuron precursor proliferation, differentiation and insulin-like growth factor 1 signaling during postnatal development.
Ian T Rossman, Lulu Lin, Katherine M Morgan, Marissa Digiovine, Elise K Van Buskirk, Silky Kamdar, James H Millonig, Emanuel Dicicco-Bloom. Mol Autism 2014
17
100

Autism-associated haplotype affects the regulation of the homeobox gene, ENGRAILED 2.
Rym Benayed, Jiyeon Choi, Paul G Matteson, Neda Gharani, Silky Kamdar, Linda M Brzustowicz, James H Millonig. Biol Psychiatry 2009
41
100

Autism-linked dopamine transporter mutation alters striatal dopamine neurotransmission and dopamine-dependent behaviors.
Gabriella E DiCarlo, Jenny I Aguilar, Heinrich Jg Matthies, Fiona E Harrison, Kyle E Bundschuh, Alyssa West, Parastoo Hashemi, Freja Herborg, Mattias Rickhag, Hao Chen,[...]. J Clin Invest 2019
25
100

How will DSM-5 affect autism diagnosis? A systematic literature review and meta-analysis.
Kristine M Kulage, Arlene M Smaldone, Elizabeth G Cohn. J Autism Dev Disord 2014
58
100


Surgical treatment of West syndrome.
E Asano, D C Chugani, C Juhász, O Muzik, H T Chugani. Brain Dev 2001
50
100


Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome.
D Liaw, D J Marsh, J Li, P L Dahia, S I Wang, Z Zheng, S Bose, K M Call, H C Tsou, M Peacocke,[...]. Nat Genet 1997
100

Hippocampal dysregulation of neurofibromin-dependent pathways is associated with impaired spatial learning in engrailed 2 knock-out mice.
Giovanni Provenzano, Luca Pangrazzi, Andrea Poli, Mattia Pernigo, Paola Sgadò, Sacha Genovesi, Giulia Zunino, Nicoletta Berardi, Simona Casarosa, Yuri Bozzi. J Neurosci 2014
16
100


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.