Class information for:
Level 2: RETT SYNDROME//MECP2//MECP2 GENE

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
2539 3300 35.1 81%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 3)


ID, lev.
above		 Publications Label for level above
96 73697 DNA METHYLATION//FRAGILE X SYNDROME//RETT SYNDROME

Classes in level below (level 1)


ID, lev. below Publications Label for level below
3223 1959 RETT SYNDROME//MECP2//MECP2 GENE
8258 1201 X LINKED MENTAL RETARDATION//XLMR//PQBP1
30243 140 KBG SYNDROME//AARSKOG SCOTT SYNDROME//FACIOGENITAL DYSPLASIA

Terms with highest relevance score


Rank Term Type of term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 RETT SYNDROME Author keyword 1196 80% 22% 742
2 MECP2 Author keyword 349 68% 9% 302
3 MECP2 GENE Author keyword 120 100% 1% 34
4 X LINKED MENTAL RETARDATION Author keyword 85 50% 4% 124
5 CDKL5 Author keyword 73 80% 1% 45
6 XLMR Author keyword 62 73% 1% 48
7 KBG SYNDROME Author keyword 53 95% 1% 18
8 AARSKOG SCOTT SYNDROME Author keyword 44 100% 0% 16
9 MECP2 MUTATION Author keyword 44 100% 0% 16
10 METHYL CPG BINDING PROTEIN 2 Author keyword 43 69% 1% 37

Web of Science journal categories

Author Key Words


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class		 LCSH search Wikipedia search
1 RETT SYNDROME 1196 80% 22% 742 Search RETT+SYNDROME Search RETT+SYNDROME
2 MECP2 349 68% 9% 302 Search MECP2 Search MECP2
3 MECP2 GENE 120 100% 1% 34 Search MECP2+GENE Search MECP2+GENE
4 X LINKED MENTAL RETARDATION 85 50% 4% 124 Search X+LINKED+MENTAL+RETARDATION Search X+LINKED+MENTAL+RETARDATION
5 CDKL5 73 80% 1% 45 Search CDKL5 Search CDKL5
6 XLMR 62 73% 1% 48 Search XLMR Search XLMR
7 KBG SYNDROME 53 95% 1% 18 Search KBG+SYNDROME Search KBG+SYNDROME
8 AARSKOG SCOTT SYNDROME 44 100% 0% 16 Search AARSKOG+SCOTT+SYNDROME Search AARSKOG+SCOTT+SYNDROME
9 MECP2 MUTATION 44 100% 0% 16 Search MECP2+MUTATION Search MECP2+MUTATION
10 METHYL CPG BINDING PROTEIN 2 43 69% 1% 37 Search METHYL+CPG+BINDING+PROTEIN+2 Search METHYL+CPG+BINDING+PROTEIN+2

Key Words Plus


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 CPG BINDING PROTEIN 2 456 69% 12% 387
2 RETT SYNDROME 195 34% 14% 472
3 MECP2 165 45% 8% 273
4 MECP2 MUTATIONS 158 82% 3% 92
5 LINKED MENTAL RETARDATION 119 31% 10% 328
6 MECP2 GENE 86 80% 2% 53
7 METHYL CPG 75 73% 2% 58
8 RETT SYNDROME PATIENTS 59 90% 1% 26
9 RENPENNING SYNDROME 58 92% 1% 23
10 PRESERVED SPEECH VARIANT 53 95% 1% 18

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
The story of Rett syndrome: From clinic to neurobiology 2007 448 119 94%
The Role of MeCP2 in the Brain 2011 130 127 83%
The Impact of MeCP2 Loss- or Gain-of-Function on Synaptic Plasticity 2013 31 52 96%
Rett syndrome: a complex disorder with simple roots 2015 2 138 78%
BDNF deregulation in Rett syndrome 2014 18 133 51%
Fragile X and X-Linked Intellectual Disability: Four Decades of Discovery 2012 49 81 69%
MeCP2 dysfunction in Rett syndrome and related disorders 2006 130 44 100%
Preclinical research in Rett syndrome: setting the foundation for translational success 2012 31 131 85%
Rett Syndrome Exploring the Autism Link 2011 39 20 95%
Rett syndrome in Australia: A review of the epidemiology 2006 108 30 97%

Address terms


Rank Address term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 RETT SYNDROME 42 94% 0.5% 15
2 RETT 41 100% 0.5% 15
3 WESTERN SYDNEY GENET PROGRAM 30 40% 1.8% 58
4 GENET EPIGENET CONTROL GENE EXP S 21 90% 0.3% 9
5 NSW RETT SYNDROME 12 86% 0.2% 6
6 BLUE BIRD CIRCLE RETT 11 100% 0.2% 6
7 SAN RAFFAELE RETT 11 78% 0.2% 7
8 ISRAELI RETT 8 75% 0.2% 6
9 P PATHOPHYSIOL REHABIL UNIT 6 71% 0.2% 5
10 JC SELF HUMAN GENET 6 23% 0.7% 24

Related classes at same level (level 2)


Rank Relatedness score Related classes
1 0.0000026267 XIST//X CHROMOSOME INACTIVATION//TSIX
2 0.0000021208 FRAGILE X SYNDROME//FRAGILE X//FMR1
3 0.0000017059 PRADER WILLI SYNDROME//ANGELMAN SYNDROME//PAR 4
4 0.0000013553 COMMUNITY BASED REHABILITATION//DISABIL STUDIES PROGRAMME//ANGANWADI
5 0.0000010595 DNA METHYLATION//EPIGENETICS//HISTONE DEACETYLASE INHIBITOR
6 0.0000010503 SMITH LEMLI OPITZ SYNDROME//INCONTINENTIA PIGMENTI//CHONDRODYSPLASIA PUNCTATA
7 0.0000010313 AUTISM//JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS//AUTISM SPECTRUM DISORDERS
8 0.0000008783 SOTOS SYNDROME//WEAVER SYNDROME//CEREBRAL GIGANTISM
9 0.0000008478 WOLF HIRSCHHORN SYNDROME//HOLOPROSENCEPHALY//ANNALES DE GENETIQUE
10 0.0000008312 TURNER SYNDROME//SRY//TURNERS SYNDROME