A citation-based method for searching scientific literature

Katrina V Good, John B Vincent, Juan Ausió. Front Genet 2021
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.
R E Amir, I B Van den Veyver, M Wan, C Q Tran, U Francke, H Y Zoghbi. Nat Genet 1999
62

Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA.
J D Lewis, R R Meehan, W J Henzel, I Maurer-Fogy, P Jeppesen, F Klein, A Bird. Cell 1992
31

MeCP2-E1 isoform is a dynamically expressed, weakly DNA-bound protein with different protein and DNA interactions compared to MeCP2-E2.
Alexia Martínez de Paz, Leila Khajavi, Hélène Martin, Rafael Claveria-Gimeno, Susanne Tom Dieck, Manjinder S Cheema, Jose V Sanchez-Mut, Malgorzata M Moksa, Annaick Carles, Nick I Brodie,[...]. Epigenetics Chromatin 2019
25
31

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
745
25

Rett syndrome and MeCP2.
Vichithra R B Liyanage, Mojgan Rastegar. Neuromolecular Med 2014
73
25

Brain region-specific expression of MeCP2 isoforms correlates with DNA methylation within Mecp2 regulatory elements.
Carl O Olson, Robby M Zachariah, Chinelo D Ezeonwuka, Vichithra R B Liyanage, Mojgan Rastegar. PLoS One 2014
59
25

A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome.
Gevork N Mnatzakanian, Hannes Lohi, Iulia Munteanu, Simon E Alfred, Takahiro Yamada, Patrick J M MacLeod, Julie R Jones, Stephen W Scherer, N Carolyn Schanen, Michael J Friez,[...]. Nat Genet 2004
237
25

MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndrome.
Lin Chen, Kaifu Chen, Laura A Lavery, Steven Andrew Baker, Chad A Shaw, Wei Li, Huda Y Zoghbi. Proc Natl Acad Sci U S A 2015
161
25

Wild-type microglia arrest pathology in a mouse model of Rett syndrome.
Noël C Derecki, James C Cronk, Zhenjie Lu, Eric Xu, Stephen B G Abbott, Patrice G Guyenet, Jonathan Kipnis. Nature 2012
435
18

Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation.
Mona D Shahbazian, Barbara Antalffy, Dawna L Armstrong, Huda Y Zoghbi. Hum Mol Genet 2002
377
18

Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
J L Neul, P Fang, J Barrish, J Lane, E B Caeg, E O Smith, H Zoghbi, A Percy, D G Glaze. Neurology 2008
289
18



Restoring Wnt6 signaling ameliorates behavioral deficits in MeCP2 T158A mouse model of Rett syndrome.
Wei-Lun Hsu, Yun-Li Ma, Yen-Chen Liu, Derek J C Tai, Eminy H Y Lee. Sci Rep 2020
14
21

Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome.
Dag H Yasui, Michael L Gonzales, Justin O Aflatooni, Florence K Crary, Daniel J Hu, Bryant J Gavino, Mari S Golub, John B Vincent, N Carolyn Schanen, Carl O Olson,[...]. Hum Mol Genet 2014
48
18

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
18

The Molecular Basis of MeCP2 Function in the Brain.
Rebekah Tillotson, Adrian Bird. J Mol Biol 2019
44
18



Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor.
Matthew J Lyst, Robert Ekiert, Daniel H Ebert, Cara Merusi, Jakub Nowak, Jim Selfridge, Jacky Guy, Nathaniel R Kastan, Nathaniel D Robinson, Flavia de Lima Alves,[...]. Nat Neurosci 2013
226
18

Homeostatic regulation of MeCP2 expression by a CREB-induced microRNA.
Matthew E Klein, Daniel T Lioy, Lin Ma, Soren Impey, Gail Mandel, Richard H Goodman. Nat Neurosci 2007
349
18

MeCP2-regulated miRNAs control early human neurogenesis through differential effects on ERK and AKT signaling.
N Mellios, D A Feldman, S D Sheridan, J P K Ip, S Kwok, S K Amoah, B Rosen, B A Rodriguez, B Crawford, R Swaminathan,[...]. Mol Psychiatry 2018
131
18

Excitation/inhibition imbalance and impaired synaptic inhibition in hippocampal area CA3 of Mecp2 knockout mice.
Gaston Calfa, Wei Li, John M Rutherford, Lucas Pozzo-Miller. Hippocampus 2015
85
18

MECP2 Is Post-transcriptionally Regulated during Human Neurodevelopment by Combinatorial Action of RNA-Binding Proteins and miRNAs.
Deivid C Rodrigues, Dae-Sung Kim, Guang Yang, Kirill Zaslavsky, Kevin C H Ha, Rebecca S F Mok, P Joel Ross, Melody Zhao, Alina Piekna, Wei Wei,[...]. Cell Rep 2016
37
18

Human-specific regulation of MeCP2 levels in fetal brains by microRNA miR-483-5p.
Kihoon Han, Vincenzo Alessandro Gennarino, Yoontae Lee, Kaifang Pang, Kazue Hashimoto-Torii, Sanaa Choufani, Chandrasekhar S Raju, Michael C Oldham, Rosanna Weksberg, Pasko Rakic,[...]. Genes Dev 2013
75
18

KCC2 rescues functional deficits in human neurons derived from patients with Rett syndrome.
Xin Tang, Julie Kim, Li Zhou, Eric Wengert, Lei Zhang, Zheng Wu, Cassiano Carromeu, Alysson R Muotri, Maria C N Marchetto, Fred H Gage,[...]. Proc Natl Acad Sci U S A 2016
121
18

Selective dendritic alterations in the cortex of Rett syndrome.
D Armstrong, J K Dunn, B Antalffy, R Trivedi. J Neuropathol Exp Neurol 1995
269
18

Methyl CpG binding protein 2 deficiency enhances expression of inflammatory cytokines by sustaining NF-κB signaling in myeloid derived cells.
Cliona M O'Driscoll, Marina Palma Lima, Walter E Kaufmann, Joseph P Bressler. J Neuroimmunol 2015
35
12

Rett syndrome: a neurological disorder with metabolic components.
Stephanie M Kyle, Neeti Vashi, Monica J Justice. Open Biol 2018
57
12

Mitochondrial dysfunction in the skeletal muscle of a mouse model of Rett syndrome (RTT): implications for the disease phenotype.
W A Gold, S L Williamson, S Kaur, I P Hargreaves, J M Land, G J Pelka, P P L Tam, J Christodoulou. Mitochondrion 2014
44
12

Methyl-CpG Binding Protein 2 Regulates Microglia and Macrophage Gene Expression in Response to Inflammatory Stimuli.
James C Cronk, Noël C Derecki, Emily Ji, Yang Xu, Aaron E Lampano, Igor Smirnov, Wendy Baker, Geoffrey T Norris, Ioana Marin, Nathan Coddington,[...]. Immunity 2015
113
12

Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology.
Nurit Ballas, Daniel T Lioy, Christopher Grunseich, Gail Mandel. Nat Neurosci 2009
323
12

The story of Rett syndrome: from clinic to neurobiology.
Maria Chahrour, Huda Y Zoghbi. Neuron 2007
830
12

Exclusive expression of MeCP2 in the nervous system distinguishes between brain and peripheral Rett syndrome-like phenotypes.
Paul D Ross, Jacky Guy, Jim Selfridge, Bushra Kamal, Noha Bahey, K Elizabeth Tanner, Thomas H Gillingwater, Ross A Jones, Christopher M Loughrey, Charlotte S McCarroll,[...]. Hum Mol Genet 2016
36
12

Reversal of neurological defects in a mouse model of Rett syndrome.
Jacky Guy, Jian Gan, Jim Selfridge, Stuart Cobb, Adrian Bird. Science 2007
775
12

Rett syndrome: a complex disorder with simple roots.
Matthew J Lyst, Adrian Bird. Nat Rev Genet 2015
194
12

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
200
12


Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine.
Shinsuke Ito, Li Shen, Qing Dai, Susan C Wu, Leonard B Collins, James A Swenberg, Chuan He, Yi Zhang. Science 2011
12

Misregulation of Alternative Splicing in a Mouse Model of Rett Syndrome.
Ronghui Li, Qiping Dong, Xinni Yuan, Xin Zeng, Yu Gao, Cassandra Chiao, Hongda Li, Xinyu Zhao, Sunduz Keles, Zefeng Wang,[...]. PLoS Genet 2016
30
12

MeCP2-dependent repression of an imprinted miR-184 released by depolarization.
Tasuku Nomura, Mika Kimura, Takuro Horii, Sumiyo Morita, Hidenobu Soejima, Shinichi Kudo, Izuho Hatada. Hum Mol Genet 2008
93
12

Whole brain delivery of an instability-prone Mecp2 transgene improves behavioral and molecular pathological defects in mouse models of Rett syndrome.
Mirko Luoni, Serena Giannelli, Marzia Tina Indrigo, Antonio Niro, Luca Massimino, Angelo Iannielli, Laura Passeri, Fabio Russo, Giuseppe Morabito, Piera Calamita,[...]. Elife 2020
17
12

Genome-wide analysis reveals methyl-CpG-binding protein 2-dependent regulation of microRNAs in a mouse model of Rett syndrome.
Hao Wu, Jifang Tao, Pauline J Chen, Atif Shahab, Weihong Ge, Ronald P Hart, Xiaoan Ruan, Yijun Ruan, Yi E Sun. Proc Natl Acad Sci U S A 2010
121
12

Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action.
Francesco Bedogni, Riccardo L Rossi, Francesco Galli, Clementina Cobolli Gigli, Anna Gandaglia, Charlotte Kilstrup-Nielsen, Nicoletta Landsberger. Neurosci Biobehav Rev 2014
36
12

Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus.
Shay Ben-Shachar, Maria Chahrour, Christina Thaller, Chad A Shaw, Huda Y Zoghbi. Hum Mol Genet 2009
174
12

Exploring the possible link between MeCP2 and oxidative stress in Rett syndrome.
Stefania Filosa, Alessandra Pecorelli, Maurizio D'Esposito, Giuseppe Valacchi, Joussef Hajek. Free Radic Biol Med 2015
39
12

Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks.
Pavel V Belichenko, Elena E Wright, Nadia P Belichenko, Eliezer Masliah, Hong Hua Li, William C Mobley, Uta Francke. J Comp Neurol 2009
174
12

Dysregulation of BRD4 Function Underlies the Functional Abnormalities of MeCP2 Mutant Neurons.
Yangfei Xiang, Yoshiaki Tanaka, Benjamin Patterson, Sung-Min Hwang, Eriona Hysolli, Bilal Cakir, Kun-Yong Kim, Wanshan Wang, Young-Jin Kang, Ethan M Clement,[...]. Mol Cell 2020
23
12

Histone deacetylase 3 associates with MeCP2 to regulate FOXO and social behavior.
Alexi Nott, Jemmie Cheng, Fan Gao, Yuan-Ta Lin, Elizabeta Gjoneska, Tak Ko, Paras Minhas, Alicia Viridiana Zamudio, Jia Meng, Feiran Zhang,[...]. Nat Neurosci 2016
63
12

Heterogeneity in residual function of MeCP2 carrying missense mutations in the methyl CpG binding domain.
S Kudo, Y Nomura, M Segawa, N Fujita, M Nakao, C Schanen, M Tamura. J Med Genet 2003
62
12


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.