A citation-based method for searching scientific literature

R E Amir, I B Van den Veyver, M Wan, C Q Tran, U Francke, H Y Zoghbi. Nat Genet 1999
Times Cited: 3125







List of co-cited articles
1036 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
23

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
20

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
19

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
19

Reversal of neurological defects in a mouse model of Rett syndrome.
Jacky Guy, Jian Gan, Jim Selfridge, Stuart Cobb, Adrian Bird. Science 2007
733
18



The story of Rett syndrome: from clinic to neurobiology.
Maria Chahrour, Huda Y Zoghbi. Neuron 2007
803
15

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
269
14

Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome.
Vishnu Anand Cuddapah, Rajesh B Pillai, Kiran V Shekar, Jane B Lane, Kathleen J Motil, Steven A Skinner, Daniel Charles Tarquinio, Daniel G Glaze, Gerald McGwin, Walter E Kaufmann,[...]. J Med Genet 2014
155
13

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
208
13

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
996
12

Rett syndrome: a complex disorder with simple roots.
Matthew J Lyst, Adrian Bird. Nat Rev Genet 2015
178
12


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
293
11

Systemic delivery of MeCP2 rescues behavioral and cellular deficits in female mouse models of Rett syndrome.
Saurabh K Garg, Daniel T Lioy, Hélène Cheval, James C McGann, John M Bissonnette, Matthew J Murtha, Kevin D Foust, Brian K Kaspar, Adrian Bird, Gail Mandel. J Neurosci 2013
127
10

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
434
10

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
10

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
733
10

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
606
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
856
9

Preclinical research in Rett syndrome: setting the foundation for translational success.
David M Katz, Joanne E Berger-Sweeney, James H Eubanks, Monica J Justice, Jeffrey L Neul, Lucas Pozzo-Miller, Mary E Blue, Diana Christian, Jacqueline N Crawley, Maurizio Giustetto,[...]. Dis Model Mech 2012
132
9

MECP2 disorders: from the clinic to mice and back.
Laura Marie Lombardi, Steven Andrew Baker, Huda Yahya Zoghbi. J Clin Invest 2015
122
9


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
422
9

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
147
8

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
8

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
60
13

Clinical and biological progress over 50 years in Rett syndrome.
Helen Leonard, Stuart Cobb, Jenny Downs. Nat Rev Neurol 2017
97
8

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
397
8

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
307
8

Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology.
Nurit Ballas, Daniel T Lioy, Christopher Grunseich, Gail Mandel. Nat Neurosci 2009
305
8

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
391
8

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
418
8

The Molecular Basis of MeCP2 Function in the Brain.
Rebekah Tillotson, Adrian Bird. J Mol Biol 2019
29
27

Conversion of 5-methylcytosine to 5-hydroxymethylcytosine in mammalian DNA by MLL partner TET1.
Mamta Tahiliani, Kian Peng Koh, Yinghua Shen, William A Pastor, Hozefa Bandukwala, Yevgeny Brudno, Suneet Agarwal, Lakshminarayan M Iyer, David R Liu, L Aravind,[...]. Science 2009
7

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
413
7

MeCP2 binding to DNA depends upon hydration at methyl-CpG.
Kok Lian Ho, Iain W McNae, Lars Schmiedeberg, Robert J Klose, Adrian P Bird, Malcolm D Walkinshaw. Mol Cell 2008
183
7

Investigating genotype-phenotype relationships in Rett syndrome using an international data set.
A Bebbington, A Anderson, D Ravine, S Fyfe, M Pineda, N de Klerk, B Ben-Zeev, N Yatawara, A Percy, W E Kaufmann,[...]. Neurology 2008
163
7

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
7

Cerebral organoids model human brain development and microcephaly.
Madeline A Lancaster, Magdalena Renner, Carol-Anne Martin, Daniel Wenzel, Louise S Bicknell, Matthew E Hurles, Tessa Homfray, Josef M Penninger, Andrew P Jackson, Juergen A Knoblich. Nature 2013
7

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
14
50

MeCP2 co-ordinates liver lipid metabolism with the NCoR1/HDAC3 corepressor complex.
Stephanie M Kyle, Pradip K Saha, Hannah M Brown, Lawrence C Chan, Monica J Justice. Hum Mol Genet 2016
41
17

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
371
7

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
7

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
140
7

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
891
6

Conserved cell types with divergent features in human versus mouse cortex.
Rebecca D Hodge, Trygve E Bakken, Jeremy A Miller, Kimberly A Smith, Eliza R Barkan, Lucas T Graybuck, Jennie L Close, Brian Long, Nelson Johansen, Osnat Penn,[...]. Nature 2019
286
6

RettBASE: Rett syndrome database update.
Rahul Krishnaraj, Gladys Ho, John Christodoulou. Hum Mutat 2017
42
14

Unique physical properties and interactions of the domains of methylated DNA binding protein 2.
Rajarshi P Ghosh, Tatiana Nikitina, Rachel A Horowitz-Scherer, Lila M Gierasch, Vladimir N Uversky, Kristopher Hite, Jeffrey C Hansen, Christopher L Woodcock. Biochemistry 2010
71
8


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.