A citation-based method for searching scientific literature

V Bourdon, C Philippe, T Bienvenu, B Koenig, M Tardieu, J Chelly, P Jonveaux. J Med Genet 2001
Times Cited: 15







List of co-cited articles
118 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
53

Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots.
M Wan, S S Lee, X Zhang, I Houwink-Manville, H R Song, R E Amir, S Budden, S Naidu, J L Pereira, I F Lo,[...]. Am J Hum Genet 1999
371
46


Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males.
J Clayton-Smith, P Watson, S Ramsden, G C Black. Lancet 2000
117
33

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
33


Classic Rett syndrome in a boy as a result of somatic mosaicism for a MECP2 mutation.
J Armstrong, M Pineda, E Aibar, E Geán, E Monrós. Ann Neurol 2001
42
26

MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin.
R Trappe, F Laccone, J Cobilanschi, M Meins, P Huppke, F Hanefeld, W Engel. Am J Hum Genet 2001
157
26

Somatic mosaicism for a MECP2 mutation associated with classic Rett syndrome in a boy.
Meral Topçu, Cemaliye Akyerli, Ayça Sayi, Gökçe A Törüner, Süha R Koçoğlu, Mine Cimbiş, Tayfun Ozçelik. Eur J Hum Genet 2002
64
26


Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes.
R E Amir, I B Van den Veyver, R Schultz, D M Malicki, C Q Tran, E J Dahle, A Philippi, L Timar, A K Percy, K J Motil,[...]. Ann Neurol 2000
251
26

Two affected boys in a Rett syndrome family: clinical and molecular findings.
L Villard, A Kpebe, C Cardoso, P J Chelly, P M Tardieu, M Fontes. Neurology 2000
158
26

Preserved speech variants of the Rett syndrome: molecular and clinical analysis.
M Zappella, I Meloni, I Longo, G Hayek, A Renieri. Am J Med Genet 2001
93
26

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
373
26

MeCP2 mutations in children with and without the phenotype of Rett syndrome.
K Hoffbuhr, J M Devaney, B LaFleur, N Sirianni, C Scacheri, J Giron, J Schuette, J Innis, M Marino, M Philippart,[...]. Neurology 2001
180
20

Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein.
P Watson, G Black, S Ramsden, M Barrow, M Super, B Kerr, J Clayton-Smith. J Med Genet 2001
149
20

Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.
J P Cheadle, H Gill, N Fleming, J Maynard, A Kerr, H Leonard, M Krawczak, D N Cooper, S Lynch, N Thomas,[...]. Hum Mol Genet 2000
210
20

Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype.
K C Hoffbuhr, L M Moses, M A Jerdonek, S Naidu, E P Hoffman. Ment Retard Dev Disabil Res Rev 2002
77
20

A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome.
Sabine M Klauck, Susan Lindsay, Kim S Beyer, Miranda Splitt, John Burn, Annemarie Poustka. Am J Hum Genet 2002
94
20

Parental origin of de novo MECP2 mutations in Rett syndrome.
M Girard, P Couvert, A Carrié, M Tardieu, J Chelly, C Beldjord, T Bienvenu. Eur J Hum Genet 2001
82
20

MECP2 mutations account for most cases of typical forms of Rett syndrome.
T Bienvenu, A Carrié, N de Roux, M C Vinet, P Jonveaux, P Couvert, L Villard, A Arzimanoglou, C Beldjord, M Fontes,[...]. Hum Mol Genet 2000
214
20

De novo MECP2 frameshift mutation in a boy with moderate mental retardation, obesity and gynaecomastia.
T Kleefstra, H G Yntema, A R Oudakker, T Romein, E Sistermans, W Nillessen, H van Bokhoven, B B A de Vries, B C J Hamel. Clin Genet 2002
52
20

MECP2 is highly mutated in X-linked mental retardation.
P Couvert, T Bienvenu, C Aquaviva, K Poirier, C Moraine, C Gendrot, A Verloes, C Andrès, A C Le Fevre, I Souville,[...]. Hum Mol Genet 2001
212
20


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
20

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
20

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
20

Mutation and cancer: statistical study of retinoblastoma.
A G Knudson. Proc Natl Acad Sci U S A 1971
20

Rett syndrome in females with CTS hot spot deletions: a disorder profile.
E Smeets, P Terhal, P Casaer, A Peters, A Midro, E Schollen, K van Roozendaal, U Moog, G Matthijs, J Herbergs,[...]. Am J Med Genet A 2005
55
20

Unexplained autism is frequently associated with low-level mosaic aneuploidy.
Y B Yurov, S G Vorsanova, I Y Iourov, I A Demidova, A K Beresheva, V S Kravetz, V V Monakhov, A D Kolotii, V Y Voinova-Ulas, N L Gorbachevskaya. J Med Genet 2007
80
20

Influence of mutation type and location on phenotype in 123 patients with Rett syndrome.
P Huppke, M Held, F Hanefeld, W Engel, F Laccone. Neuropediatrics 2002
68
13

Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome.
K Amano, Y Nomura, M Segawa, K Yamakawa. J Hum Genet 2000
58
13

Preserved speech variant is allelic of classic Rett syndrome.
C De Bona, M Zappella, G Hayek, I Meloni, F Vitelli, M Bruttini, R Cusano, P Loffredo, I Longo, A Renieri. Eur J Hum Genet 2000
89
13

Cytogenetic and molecular-cytogenetic studies of Rett syndrome (RTT): a retrospective analysis of a Russian cohort of RTT patients (the investigation of 57 girls and three boys).
S G Vorsanova, Y B Yurov, V Y Ulas, I A Demidova, V O Sharonin, A D Kolotii, N L Gorbatchevskaia, A K Beresheva, I V Soloviev. Brain Dev 2001
23
13

A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males.
I Meloni, M Bruttini, I Longo, F Mari, F Rizzolio, P D'Adamo, K Denvriendt, J P Fryns, D Toniolo, A Renieri. Am J Hum Genet 2000
173
13

A Rett syndrome MECP2 mutation that causes mental retardation in men.
M T Dotti, A Orrico, N De Stefano, C Battisti, F Sicurelli, S Severi, C W Lam, L Galli, V Sorrentino, A Federico. Neurology 2002
56
13



Low frequency of MECP2 mutations in mentally retarded males.
Helger G Yntema, Tjitske Kleefstra, Astrid R Oudakker, Tom Romein, Bert B A de Vries, Willy Nillesen, Erik A Sistermans, Han G Brunner, Ben C J Hamel, Hans van Bokhoven. Eur J Hum Genet 2002
41
13

MECP2 mutation in male patients with non-specific X-linked mental retardation.
A Orrico, C Lam, L Galli, M T Dotti, G Hayek, S F Tong, P M Poon, M Zappella, A Federico, V Sorrentino. FEBS Lett 2000
189
13

De novo MECP2 mutation in a 46,XX male patient with Rett syndrome.
Robert Maiwald, Anselm Bönte, Helena Jung, Pavel Bitter, Zoe Storm, Franco Laccone, Peter Herkenrath. Neurogenetics 2002
16
13

RettBASE: The IRSA MECP2 variation database-a new mutation database in evolution.
John Christodoulou, Andrew Grimm, Tony Maher, Bruce Bennetts. Hum Mutat 2003
117
13

MECP2 mutation in non-fatal, non-progressive encephalopathy in a male.
B Imessaoudene, J P Bonnefont, G Royer, V Cormier-Daire, S Lyonnet, G Lyon, A Munnich, J Amiel. J Med Genet 2001
77
13

MECP2 mutation in a boy with language disorder and schizophrenia.
David Cohen, Gabriela Lazar, Philippe Couvert, Vincent Desportes, Didier Lippe, Philippe Mazet, Delphine Héron. Am J Psychiatry 2002
79
13

Rett syndrome: epidemiology and geographical variability.
B Hagberg, G Hagberg. Eur Child Adolesc Psychiatry 1997
56
13


Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome.
C W Lam, W L Yeung, C H Ko, P M Poon, S F Tong, K Y Chan, I F Lo, L Y Chan, J Hui, V Wong,[...]. J Med Genet 2000
114
13

Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the disease.
L Villard, N Lévy, F Xiang, A Kpebe, V Labelle, C Chevillard, Z Zhang, C E Schwartz, M Tardieu, J Chelly,[...]. J Med Genet 2001
42
13

Characterisation of breathing and associated central autonomic dysfunction in the Rett disorder.
P O Julu, A M Kerr, F Apartopoulos, S Al-Rawas, I W Engerström, L Engerström, G A Jamal, S Hansen. Arch Dis Child 2001
185
13

Early clinical signs in the Rett disorder.
A M Kerr. Neuropediatrics 1995
58
13


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.