A citation-based method for searching scientific literature

Lucia Parisi, Teresa Di Filippo, Michele Roccella. Ment Illn 2016
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


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
66

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
50

Rett Syndrome.
E E J Smeets, K Pelc, B Dan. Mol Syndromol 2012
46
50

Clinical severity and quality of life in children and adolescents with Rett syndrome.
J B Lane, H-S Lee, L W Smith, P Cheng, A K Percy, D G Glaze, J L Neul, K J Motil, J O Barrish, S A Skinner,[...]. Neurology 2011
42
50

Caretaker Quality of Life in Rett Syndrome: Disorder Features and Psychological Predictors.
John T Killian, Jane B Lane, Hye-Seung Lee, James H Pelham, Steve A Skinner, Walter E Kaufmann, Daniel G Glaze, Jeffrey L Neul, Alan K Percy. Pediatr Neurol 2016
14
50

Anxiety-like behavior in Rett syndrome: characteristics and assessment by anxiety scales.
Katherine V Barnes, Francesca R Coughlin, Heather M O'Leary, Natalie Bruck, Grace A Bazin, Emily B Beinecke, Alexandra C Walco, Nicole G Cantwell, Walter E Kaufmann. J Neurodev Disord 2015
35
33

Conceptualizing a quality of life framework for girls with Rett syndrome using qualitative methods.
Amy Epstein, Helen Leonard, Elise Davis, Katrina Williams, Dinah Reddihough, Nada Murphy, Andrew Whitehouse, Jenny Downs. Am J Med Genet A 2016
33
33


Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy.
Cyril Mignot, Celina von Stülpnagel, Caroline Nava, Dorothée Ville, Damien Sanlaville, Gaetan Lesca, Agnès Rastetter, Benoit Gachet, Yannick Marie, G Christoph Korenke,[...]. J Med Genet 2016
66
33

Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.
Latha Soorya, Alexander Kolevzon, Jessica Zweifach, Teresa Lim, Yuriy Dobry, Lily Schwartz, Yitzchak Frank, A Ting Wang, Guiqing Cai, Elena Parkhomenko,[...]. Mol Autism 2013
143
33

Parental perspectives on the communication abilities of their daughters with Rett syndrome.
Anna Urbanowicz, Helen Leonard, Sonya Girdler, Natalie Ciccone, Jenny Downs. Dev Neurorehabil 2016
15
16

Eye Gaze Technology as a Form of Augmentative and Alternative Communication for Individuals with Rett Syndrome: Experiences of Families in The Netherlands.
Gillian S Townend, Peter B Marschik, Eric Smeets, Raymond van de Berg, Mariёlle van den Berg, Leopold M G Curfs. J Dev Phys Disabil 2016
22
16


Perspectives on hand function in girls and women with Rett syndrome.
Jenny Downs, Stephanie Parkinson, Sonia Ranelli, Helen Leonard, Pamela Diener, Meir Lotan. Dev Neurorehabil 2014
10
16

Rett syndrome: a preliminary analysis of stereotypy, stress, and negative affect.
Kelsey M Quest, Breanne J Byiers, Ameante Payen, Frank J Symons. Res Dev Disabil 2014
8
16

Rett syndrome: a complex disorder with simple roots.
Matthew J Lyst, Adrian Bird. Nat Rev Genet 2015
178
16


Prevalence of inherited ichthyosis in France: a study using capture-recapture method.
Isabelle Dreyfus, Cécile Chouquet, Khaled Ezzedine, Sophie Henner, Christine Chiavérini, Aude Maza, Sandrine Pascal, Lauriane Rodriguez, Pierre Vabres, Ludovic Martin,[...]. Orphanet J Rare Dis 2014
35
16



Technological aids to support choice strategies by three girls with Rett syndrome.
Fabrizio Stasolla, Viviana Perilli, Antonia Di Leone, Rita Damiani, Vincenza Albano, Anna Stella, Concetta Damato. Res Dev Disabil 2015
23
16

Cardiorespiratory challenges in Rett's syndrome.
Peter Oo Julu, Ingegerd Witt Engerström, Stig Hansen, Flora Apartopoulos, Bengt Engerström, Giorgio Pini, Robert S Delamont, Eric E j Smeets. Lancet 2008
40
16

Long-term follow-up of functioning after spinal surgery in patients with Rett syndrome.
Eva-Lena Larsson, Stig Aaro, Peter Ahlinder, Helena Normelli, Hans Tropp, Birgitta Oberg. Eur Spine J 2009
13
16


Rett syndrome: establishing a novel outcome measure for walking activity in an era of clinical trials for rare disorders.
Jenny Downs, Helen Leonard, Peter Jacoby, Lauren Brisco, Gordon Baikie, Kylie Hill. Disabil Rehabil 2015
17
16


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
16



Social preferences in Rett syndrome.
Aleksandra Djukic, Maria Valicenti McDermott. Pediatr Neurol 2012
30
16

Development of a genomic DNA reference material panel for Rett syndrome (MECP2-related disorders) genetic testing.
Lisa V Kalman, Jack C Tarleton, Alan K Percy, Swaroop Aradhya, Sherri Bale, Shannon D Barker, Pinar Bayrak-Toydemir, Christina Bridges, Arlene M Buller-Burckle, Soma Das,[...]. J Mol Diagn 2014
5
20

Belonging, occupation, and human well-being: an exploration.
Karen R Whalley Hammell. Can J Occup Ther 2014
36
16

Neurophysiological responses to music and vibroacoustic stimuli in Rett syndrome.
Märith Bergström-Isacsson, Bengt Lagerkvist, Ulla Holck, Christian Gold. Res Dev Disabil 2014
7
16

Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study.
Nicky Halbach, Eric E Smeets, Peter Julu, Ingegerd Witt-Engerström, Giorgio Pini, Stefania Bigoni, Stig Hansen, Flora Apartopoulos, Robert Delamont, Kees van Roozendaal,[...]. Am J Med Genet A 2016
11
16

Learning ability in children with Rett syndrome.
Cochavit Elefant, Tony Wigram. Brain Dev 2005
16
16

The conductive environment enhances gross motor function of girls with Rett syndrome. A pilot study.
Meir Lotan, Rony Schenker, Judy Wine, Jenny Downs. Dev Neurorehabil 2012
21
16

Three different profiles: early socio-communicative capacities in typical Rett syndrome, the preserved speech variant and normal development.
Peter B Marschik, Katrin D Bartl-Pokorny, Helen Tager-Flusberg, Walter E Kaufmann, Florian Pokorny, Tobias Grossmann, Christian Windpassinger, Erwin Petek, Christa Einspieler. Dev Neurorehabil 2014
14
16


Guided eating or feeding: three girls with Rett syndrome.
Inga Qvarfordt, Ingegerd Witt Engerstrom, Ann-Christin Eliasson. Scand J Occup Ther 2009
7
16


Rett syndrome from a family perspective: The Swedish Rett Center survey.
Gunilla Larsson, Britta Lindström, Ingegerd Witt Engerström. Brain Dev 2005
18
16

Rett syndrome in Australia: a review of the epidemiology.
Crystal L Laurvick, Nicholas de Klerk, Carol Bower, John Christodoulou, David Ravine, Carolyn Ellaway, Sarah Williamson, Helen Leonard. J Pediatr 2006
201
16

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
16




Normal reactions to orthostatic stress in Rett syndrome.
Gunilla Larsson, Peter O O Julu, Ingegerd Witt Engerström, Marlene Sandlund, Britta Lindström. Res Dev Disabil 2013
7
16

Pharmacologic Treatment of Rett Syndrome With Glatiramer Acetate.
Aleksandra Djukic, Roee Holtzer, Shlomo Shinnar, Hiren Muzumdar, Susan A Rose, Wenzhu Mowrey, Aristea S Galanopoulou, Ruth Shinnar, Jeffrey J Jankowski, Judith F Feldman,[...]. Pediatr Neurol 2016
18
16

The trajectories of sleep disturbances in Rett syndrome.
Kingsley Wong, Helen Leonard, Peter Jacoby, Carolyn Ellaway, Jenny Downs. J Sleep Res 2015
50
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.