A citation-based method for searching scientific literature

Aglaia Vignoli, Rosa Angela Fabio, Francesca La Briola, Samantha Giannatiempo, Alessandro Antonietti, Silvia Maggiolini, Maria Paola Canevini. Epilepsy Behav 2010
Times Cited: 21







List of co-cited articles
109 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

The role of stereotypies in overselectivity process in Rett syndrome.
Rosa Angela Fabio, Samantha Giannatiempo, Alessandro Antonietti, Sarojini Budden. Res Dev Disabil 2009
23
38

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
38

Cognitive performance in Rett syndrome girls: a pilot study using eyetracking technology.
P M Baptista, M T Mercadante, E C Macedo, J S Schwartzman. J Intellect Disabil Res 2006
32
33

Training communication abilities in Rett Syndrome through reading and writing.
Rosa Angela Fabio, Ilaria Castelli, Antonella Marchetti, Alessandro Antonietti. Front Psychol 2013
18
33

Rett syndrome: an eye-tracking study of attention and recognition memory.
Susan A Rose, Aleksandra Djukic, Jeffery J Jankowski, Judith F Feldman, Iris Fishman, Maria Valicenti-McDermott. Dev Med Child Neurol 2013
34
23

Rett syndrome: basic features of visual processing-a pilot study of eye-tracking.
Aleksandra Djukic, Maria Valicenti McDermott, Kathleen Mavrommatis, Cristina L Martins. Pediatr Neurol 2012
22
23

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
23

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
23

Recent insights into genotype-phenotype relationships in patients with Rett syndrome using a fine grain scale.
Rosa Angela Fabio, Barbara Colombo, Silvia Russo, Francesca Cogliati, Maura Masciadri, Silvia Foglia, Alessandro Antonietti, Daniela Tavian. Res Dev Disabil 2014
21
23

Social impairments in Rett syndrome: characteristics and relationship with clinical severity.
W E Kaufmann, E Tierney, C A Rohde, M C Suarez-Pedraza, M A Clarke, C F Salorio, G Bibat, I Bukelis, D Naram, D C Lanham,[...]. J Intellect Disabil Res 2012
65
19

Storybook-based communication intervention for girls with Rett syndrome and their mothers.
D A Koppenhaver, K A Erickson, B Harris, J McLellan, B G Skotko, R A Newton. Disabil Rehabil 2001
19
21



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
19

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
557
19

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
19

Epilepsy in Rett syndrome: clinical and genetic features.
Maria Pintaudi, Maria Grazia Calevo, Aglaia Vignoli, Elena Parodi, Francesca Aiello, Maria Giuseppina Baglietto, Yussef Hayek, Sabrina Buoni, Alessandra Renieri, Silvia Russo,[...]. Epilepsy Behav 2010
54
19

Communication in Individuals with Rett Syndrome: an Assessment of Forms and Functions.
Robert Didden, Hubert Korzilius, Eric Smeets, Vanessa A Green, Russell Lang, Giulio E Lancioni, Leopold M Curfs. J Dev Phys Disabil 2010
33
19

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
19

Concepts of color, shape, size and position in ten children with Rett syndrome.
Renata de Lima Velloso, Ceres Alves de Araújo, José Salomão Schwartzman. Arq Neuropsiquiatr 2009
16
25

FOXG1 is responsible for the congenital variant of Rett syndrome.
Francesca Ariani, Giuseppe Hayek, Dalila Rondinella, Rosangela Artuso, Maria Antonietta Mencarelli, Ariele Spanhol-Rosseto, Marzia Pollazzon, Sabrina Buoni, Ottavia Spiga, Sara Ricciardi,[...]. Am J Hum Genet 2008
260
19

Rett Syndrome.
E E J Smeets, K Pelc, B Dan. Mol Syndromol 2012
46
19

Loss of MeCP2 from forebrain excitatory neurons leads to cortical hyperexcitation and seizures.
Wen Zhang, Matthew Peterson, Barbara Beyer, Wayne N Frankel, Zhong-wei Zhang. J Neurosci 2014
71
19

Cognitive training modifies frequency EEG bands and neuropsychological measures in Rett syndrome.
Rosa Angela Fabio, Lucia Billeci, Giulia Crifaci, Emilia Troise, Gaetano Tortorella, Giovanni Pioggia. Res Dev Disabil 2016
23
19

Neurophysiological and cognitive effects of Transcranial Direct Current Stimulation in three girls with Rett Syndrome with chronic language impairments.
Rosa Angela Fabio, Antonio Gangemi, Tindara Capri, Sarojini Budden, Alessandra Falzone. Res Dev Disabil 2018
13
30



Facilitating communication in children with multiple disabilities: three case studies of girls with Rett syndrome.
D Ryan, F McGregor, M Akermanis, K Southwell, M Ramke, G Woodyatt. Disabil Rehabil 2004
10
30



Vision, cognition and developmental characteristics of girls and women with Rett syndrome.
S von Tetzchner, K H Jacobsen, L Smith, O H Skjeldal, A Heiberg, J F Fagan. Dev Med Child Neurol 1996
44
14

Improving functional skills and physical fitness in children with Rett syndrome.
M Lotan, E Isakov, J Merrick. J Intellect Disabil Res 2004
47
14

Communication abilities and Rett syndrome.
G Woodyatt, A Ozanne. J Autism Dev Disord 1992
27
14

Epilepsy in Rett syndrome---the experience of a National Rett Center.
Andreea Nissenkorn, Eva Gak, Manuela Vecsler, Haia Reznik, Shay Menascu, Bruria Ben Zeev. Epilepsia 2010
61
14

Seizures in Rett syndrome: an overview from a one-year calendar study.
Le Jian, Lakshmi Nagarajan, Nicholas de Klerk, David Ravine, John Christodoulou, Helen Leonard. Eur J Paediatr Neurol 2007
60
14

The story of Rett syndrome: from clinic to neurobiology.
Maria Chahrour, Huda Y Zoghbi. Neuron 2007
803
14

MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number.
Hsiao-Tuan Chao, Huda Y Zoghbi, Christian Rosenmund. Neuron 2007
332
14

Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett syndrome.
Vardhan S Dani, Qiang Chang, Arianna Maffei, Gina G Turrigiano, Rudolf Jaenisch, Sacha B Nelson. Proc Natl Acad Sci U S A 2005
430
14

Alterations of cortical and hippocampal EEG activity in MeCP2-deficient mice.
Jennifer Anne D'Cruz, Chiping Wu, Tariq Zahid, Youssef El-Hayek, Liang Zhang, James H Eubanks. Neurobiol Dis 2010
59
14

Social preferences in Rett syndrome.
Aleksandra Djukic, Maria Valicenti McDermott. Pediatr Neurol 2012
30
14

Refining the phenotype of common mutations in Rett syndrome.
L Colvin, H Leonard, N de Klerk, M Davis, L Weaving, S Williamson, J Christodoulou. J Med Genet 2004
65
14

Genotype-phenotype relationships as prognosticators in Rett syndrome should be handled with care in clinical practice.
Nicky S J Halbach, Eric E J Smeets, Noortje van den Braak, Kees E P van Roozendaal, Rien M J Blok, Constance T R M Schrander-Stumpel, Jean-Pierre Frijns, Marian A Maaskant, Leopold M G Curfs. Am J Med Genet A 2012
21
14

Cerebrolysin therapy in Rett syndrome: clinical and EEG mapping study.
N Gorbachevskaya, V Bashina, V Gratchev, A Iznak. Brain Dev 2001
14
21

Variant of Rett syndrome and CDKL5 gene: clinical and autonomic description of 10 cases.
Giorgio Pini, Stefania Bigoni, Ingegerd Witt Engerström, Olga Calabrese, Beatrice Felloni, Maria Flora Scusa, Pietro Di Marco, Paolo Borelli, Ubaldo Bonuccelli, Peter O O Julu,[...]. Neuropediatrics 2012
19
15

Clinical manifestations and stages of Rett syndrome.
Bengt Hagberg. Ment Retard Dev Disabil Res Rev 2002
234
14

The role of MeCP2 in the brain.
Jacky Guy, Hélène Cheval, Jim Selfridge, Adrian Bird. Annu Rev Cell Dev Biol 2011
294
9

Behavioral treatment of Rett's disorder: ineffectiveness in three cases.
T Smith, M Klevstrand, O I Lovaas. Am J Ment Retard 1995
20
10


MeCP2 and Rett syndrome: reversibility and potential avenues for therapy.
Kamal K E Gadalla, Mark E S Bailey, Stuart R Cobb. Biochem J 2011
61
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.