A citation-based method for searching scientific literature

Maria Chahrour, Sung Yun Jung, Chad Shaw, Xiaobo Zhou, Stephen T C Wong, Jun Qin, Huda Y Zoghbi. Science 2008
Times Cited: 1159







List of co-cited articles
1122 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
52

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex.
X Nan, H H Ng, C A Johnson, C D Laherty, B M Turner, R N Eisenman, A Bird. Nature 1998
25

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome.
J Guy, B Hendrich, M Holmes, J E Martin, A Bird. Nat Genet 2001
24

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
999
24

The story of Rett syndrome: from clinic to neurobiology.
Maria Chahrour, Huda Y Zoghbi. Neuron 2007
807
21

Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.
Juan I Young, Eugene P Hong, John C Castle, Juan Crespo-Barreto, Aaron B Bowman, Matthew F Rose, Dongcheul Kang, Ron Richman, Jason M Johnson, Susan Berget,[...]. Proc Natl Acad Sci U S A 2005
309
19

Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state.
Peter J Skene, Robert S Illingworth, Shaun Webb, Alastair R W Kerr, Keith D James, Daniel J Turner, Rob Andrews, Adrian P Bird. Mol Cell 2010
435
19

Disruption of DNA-methylation-dependent long gene repression in Rett syndrome.
Harrison W Gabel, Benyam Kinde, Hume Stroud, Caitlin S Gilbert, David A Harmin, Nathaniel R Kastan, Martin Hemberg, Daniel H Ebert, Michael E Greenberg. Nature 2015
296
18


Rett syndrome: a complex disorder with simple roots.
Matthew J Lyst, Adrian Bird. Nat Rev Genet 2015
179
16


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
211
16

Global epigenomic reconfiguration during mammalian brain development.
Ryan Lister, Eran A Mukamel, Joseph R Nery, Mark Urich, Clare A Puddifoot, Nicholas D Johnson, Jacinta Lucero, Yun Huang, Andrew J Dwork, Matthew D Schultz,[...]. Science 2013
15

MeCP2 binds to 5hmC enriched within active genes and accessible chromatin in the nervous system.
Marian Mellén, Pinar Ayata, Scott Dewell, Skirmantas Kriaucionis, Nathaniel Heintz. Cell 2012
608
15

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
188
14

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription.
P L Jones, G J Veenstra, P A Wade, D Vermaak, S U Kass, N Landsberger, J Strouboulis, A P Wolffe. Nat Genet 1998
14

Derepression of BDNF transcription involves calcium-dependent phosphorylation of MeCP2.
Wen G Chen, Qiang Chang, Yingxi Lin, Alexander Meissner, Anne E West, Eric C Griffith, Rudolf Jaenisch, Michael E Greenberg. Science 2003
893
14

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
149
14

Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.
Hsiao-Tuan Chao, Hongmei Chen, Rodney C Samaco, Mingshan Xue, Maria Chahrour, Jong Yoo, Jeffrey L Neul, Shiaoching Gong, Hui-Chen Lu, Nathaniel Heintz,[...]. Nature 2010
738
13

Distribution, recognition and regulation of non-CpG methylation in the adult mammalian brain.
Junjie U Guo, Yijing Su, Joo Heon Shin, Jaehoon Shin, Hongda Li, Bin Xie, Chun Zhong, Shaohui Hu, Thuc Le, Guoping Fan,[...]. Nat Neurosci 2014
419
13

An AT-hook domain in MeCP2 determines the clinical course of Rett syndrome and related disorders.
Steven Andrew Baker, Lin Chen, Angela Dawn Wilkins, Peng Yu, Olivier Lichtarge, Huda Yahya Zoghbi. Cell 2013
141
13

MeCP2 recognizes cytosine methylated tri-nucleotide and di-nucleotide sequences to tune transcription in the mammalian brain.
Sabine Lagger, John C Connelly, Gabriele Schweikert, Shaun Webb, Jim Selfridge, Bernard H Ramsahoye, Miao Yu, Chuan He, Guido Sanguinetti, Lawrence C Sowers,[...]. PLoS Genet 2017
65
20

Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males.
Hilde Van Esch, Marijke Bauters, Jaakko Ignatius, Mieke Jansen, Martine Raynaud, Karen Hollanders, Dorien Lugtenberg, Thierry Bienvenu, Lars Riff Jensen, Jozef Gecz,[...]. Am J Hum Genet 2005
427
13

Reversal of neurological defects in a mouse model of Rett syndrome.
Jacky Guy, Jian Gan, Jim Selfridge, Stuart Cobb, Adrian Bird. Science 2007
737
13

Genome-wide activity-dependent MeCP2 phosphorylation regulates nervous system development and function.
Sonia Cohen, Harrison W Gabel, Martin Hemberg, Ashley N Hutchinson, L Amanda Sadacca, Daniel H Ebert, David A Harmin, Rachel S Greenberg, Vanessa K Verdine, Zhaolan Zhou,[...]. Neuron 2011
200
12

Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation.
Zhaolan Zhou, Elizabeth J Hong, Sonia Cohen, Wen-Ning Zhao, Hsin-Yi Henry Ho, Lauren Schmidt, Wen G Chen, Yingxi Lin, Erin Savner, Eric C Griffith,[...]. Neuron 2006
590
12

Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.
Ann L Collins, Jonathan M Levenson, Alexander P Vilaythong, Ronald Richman, Dawna L Armstrong, Jeffrey L Noebels, J David Sweatt, Huda Y Zoghbi. Hum Mol Genet 2004
401
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
164
11


The MECP2 duplication syndrome.
Melissa B Ramocki, Y Jane Tavyev, Sarika U Peters. Am J Med Genet A 2010
183
11

The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression.
Qiang Chang, Gargi Khare, Vardhan Dani, Sacha Nelson, Rudolf Jaenisch. Neuron 2006
392
11


Rett syndrome and MeCP2.
Vichithra R B Liyanage, Mojgan Rastegar. Neuromolecular Med 2014
64
15

Cell-type-specific repression by methyl-CpG-binding protein 2 is biased toward long genes.
Ken Sugino, Chris M Hempel, Benjamin W Okaty, Hannah A Arnson, Saori Kato, Vardhan S Dani, Sacha B Nelson. J Neurosci 2014
84
11

Characterization of human mosaic Rett syndrome brain tissue by single-nucleus RNA sequencing.
William Renthal, Lisa D Boxer, Sinisa Hrvatin, Emmy Li, Andrew Silberfeld, M Aurel Nagy, Eric C Griffith, Thomas Vierbuchen, Michael E Greenberg. Nat Neurosci 2018
45
22

Reading the unique DNA methylation landscape of the brain: Non-CpG methylation, hydroxymethylation, and MeCP2.
Benyam Kinde, Harrison W Gabel, Caitlin S Gilbert, Eric C Griffith, Michael E Greenberg. Proc Natl Acad Sci U S A 2015
128
10

DNA methylation in the gene body influences MeCP2-mediated gene repression.
Benyam Kinde, Dennis Y Wu, Michael E Greenberg, Harrison W Gabel. Proc Natl Acad Sci U S A 2016
53
18

Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome.
Brian S Johnson, Ying-Tao Zhao, Maria Fasolino, Janine M Lamonica, Yoon Jung Kim, George Georgakilas, Kathleen H Wood, Daniel Bu, Yue Cui, Darren Goffin,[...]. Nat Med 2017
50
20

The Molecular Basis of MeCP2 Function in the Brain.
Rebekah Tillotson, Adrian Bird. J Mol Biol 2019
32
31

L1 retrotransposition in neurons is modulated by MeCP2.
Alysson R Muotri, Maria C N Marchetto, Nicole G Coufal, Ruth Oefner, Gene Yeo, Kinichi Nakashima, Fred H Gage. Nature 2010
402
9

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
420
9

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
9

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
271
9

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
59
15

Radically truncated MeCP2 rescues Rett syndrome-like neurological defects.
Rebekah Tillotson, Jim Selfridge, Martha V Koerner, Kamal K E Gadalla, Jacky Guy, Dina De Sousa, Ralph D Hector, Stuart R Cobb, Adrian Bird. Nature 2017
63
14

Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome.
Paolo Moretti, Jonathan M Levenson, Fortunato Battaglia, Richard Atkinson, Ryan Teague, Barbara Antalffy, Dawna Armstrong, Ottavio Arancio, J David Sweatt, Huda Y Zoghbi. J Neurosci 2006
368
9

A model for neural development and treatment of Rett syndrome using human induced pluripotent stem cells.
Maria C N Marchetto, Cassiano Carromeu, Allan Acab, Diana Yu, Gene W Yeo, Yangling Mu, Gong Chen, Fred H Gage, Alysson R Muotri. Cell 2010
860
9

Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes.
Dag H Yasui, Sailaja Peddada, Mark C Bieda, Roxanne O Vallero, Amber Hogart, Raman P Nagarajan, Karen N Thatcher, Peggy J Farnham, Janine M Lasalle. Proc Natl Acad Sci U S A 2007
278
9

Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome.
Shin-ichi Horike, Shutao Cai, Masaru Miyano, Jan-Fang Cheng, Terumi Kohwi-Shigematsu. Nat Genet 2005
421
9

Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations.
Christopher A Chapleau, Gaston D Calfa, Meredith C Lane, Asher J Albertson, Jennifer L Larimore, Shinichi Kudo, Dawna L Armstrong, Alan K Percy, Lucas Pozzo-Miller. Neurobiol Dis 2009
159
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.