A citation-based method for searching scientific literature

Jacky Guy, Jian Gan, Jim Selfridge, Stuart Cobb, Adrian Bird. Science 2007
Times Cited: 741







List of co-cited articles
1383 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
56

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
36

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
743
24


The story of Rett syndrome: from clinic to neurobiology.
Maria Chahrour, Huda Y Zoghbi. Neuron 2007
810
21

Adult restoration of Shank3 expression rescues selective autistic-like phenotypes.
Yuan Mei, Patricia Monteiro, Yang Zhou, Jin-Ah Kim, Xian Gao, Zhanyan Fu, Guoping Feng. Nature 2016
183
21

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
691
20

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
64
28

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
394
18


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
129
18

Adult neural function requires MeCP2.
Christopher M McGraw, Rodney C Samaco, Huda Y Zoghbi. Science 2011
171
17

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
17

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
214
17

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
189
16

Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.
Emanuela Giacometti, Sandra Luikenhuis, Caroline Beard, Rudolf Jaenisch. Proc Natl Acad Sci U S A 2007
189
16

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
273
15

Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities.
Rodney C Samaco, Caleigh Mandel-Brehm, Hsiao-Tuan Chao, Christopher S Ward, Sharyl L Fyffe-Maricich, Jun Ren, Keith Hyland, Christina Thaller, Stephen M Maricich, Peter Humphreys,[...]. Proc Natl Acad Sci U S A 2009
170
15

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
14

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
437
14

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
52
26

Morphological and functional reversal of phenotypes in a mouse model of Rett syndrome.
Lianne Robinson, Jacky Guy, Leanne McKay, Emma Brockett, Rosemary C Spike, Jim Selfridge, Dina De Sousa, Cara Merusi, Gernot Riedel, Adrian Bird,[...]. Brain 2012
90
15

The Molecular Basis of MeCP2 Function in the Brain.
Rebekah Tillotson, Adrian Bird. J Mol Biol 2019
34
41

Clinical and biological progress over 50 years in Rett syndrome.
Helen Leonard, Stuart Cobb, Jenny Downs. Nat Rev Neurol 2017
99
13

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
299
13

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
403
13

Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice.
Daniela Tropea, Emanuela Giacometti, Nathan R Wilson, Caroline Beard, Cortina McCurry, Dong Dong Fu, Ruth Flannery, Rudolf Jaenisch, Mriganka Sur. Proc Natl Acad Sci U S A 2009
361
13

Rett syndrome: insights into genetic, molecular and circuit mechanisms.
Jacque P K Ip, Nikolaos Mellios, Mriganka Sur. Nat Rev Neurosci 2018
74
16


Female Mecp2(+/-) mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies.
Rodney C Samaco, Christopher M McGraw, Christopher S Ward, Yaling Sun, Jeffrey L Neul, Huda Y Zoghbi. Hum Mol Genet 2013
104
12

Functional recovery with recombinant human IGF1 treatment in a mouse model of Rett Syndrome.
Jorge Castro, Rodrigo I Garcia, Showming Kwok, Abhishek Banerjee, Jeremy Petravicz, Jonathan Woodson, Nikolaos Mellios, Daniela Tropea, Mriganka Sur. Proc Natl Acad Sci U S A 2014
123
12

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
428
12

Double-blind, randomized, placebo-controlled study of trofinetide in pediatric Rett syndrome.
Daniel G Glaze, Jeffrey L Neul, Walter E Kaufmann, Elizabeth Berry-Kravis, Sean Condon, George Stoms, Sean Oosterholt, Oscar Della Pasqua, Larry Glass, Nancy E Jones,[...]. Neurology 2019
32
37

MECP2 disorders: from the clinic to mice and back.
Laura Marie Lombardi, Steven Andrew Baker, Huda Yahya Zoghbi. J Clin Invest 2015
125
12

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
157
12

Improved MECP2 Gene Therapy Extends the Survival of MeCP2-Null Mice without Apparent Toxicity after Intracisternal Delivery.
Sarah E Sinnett, Ralph D Hector, Kamal K E Gadalla, Clifford Heindel, Daphne Chen, Violeta Zaric, Mark E S Bailey, Stuart R Cobb, Steven J Gray. Mol Ther Methods Clin Dev 2017
31
38

Reversal of phenotypes in MECP2 duplication mice using genetic rescue or antisense oligonucleotides.
Yehezkel Sztainberg, Hong-mei Chen, John W Swann, Shuang Hao, Bin Tang, Zhenyu Wu, Jianrong Tang, Ying-Wooi Wan, Zhandong Liu, Frank Rigo,[...]. Nature 2015
99
12

Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome model.
Sara Silva-Santos, Geeske M van Woerden, Caroline F Bruinsma, Edwin Mientjes, Mehrnoush Aghadavoud Jolfaei, Ben Distel, Steven A Kushner, Ype Elgersma. J Clin Invest 2015
108
12

Rett syndrome: a complex disorder with simple roots.
Matthew J Lyst, Adrian Bird. Nat Rev Genet 2015
180
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
46
23

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
11

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
133
11

Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice.
Sandra Luikenhuis, Emanuela Giacometti, Caroline F Beard, Rudolf Jaenisch. Proc Natl Acad Sci U S A 2004
243
11

Improved survival and reduced phenotypic severity following AAV9/MECP2 gene transfer to neonatal and juvenile male Mecp2 knockout mice.
Kamal K E Gadalla, Mark E S Bailey, Rosemary C Spike, Paul D Ross, Kenton T Woodard, Sahana Nagabhushan Kalburgi, Lavanya Bachaboina, Jie V Deng, Anne E West, R Jude Samulski,[...]. Mol Ther 2013
73
15

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
10

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
10

Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3.
Mona Shahbazian, Juan Young, Lisa Yuva-Paylor, Corinne Spencer, Barbara Antalffy, Jeffrey Noebels, Dawna Armstrong, Richard Paylor, Huda Zoghbi. Neuron 2002
559
10

A role for glia in the progression of Rett's syndrome.
Daniel T Lioy, Saurabh K Garg, Caitlin E Monaghan, Jacob Raber, Kevin D Foust, Brian K Kaspar, Petra G Hirrlinger, Frank Kirchhoff, John M Bissonnette, Nurit Ballas,[...]. Nature 2011
320
10

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
313
10

Postnatal inactivation reveals enhanced requirement for MeCP2 at distinct age windows.
Hélène Cheval, Jacky Guy, Cara Merusi, Dina De Sousa, Jim Selfridge, Adrian Bird. Hum Mol Genet 2012
61
16


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.