Class information for:
Level 1: RETT SYNDROME//MECP2//MECP2 GENE

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
3223 1959 38.3 82%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
2539 3300 RETT SYNDROME//MECP2//MECP2 GENE

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 1179 80% 38% 739
2 MECP2 Author keyword 296 65% 15% 285
3 MECP2 GENE Author keyword 120 100% 2% 34
4 CDKL5 Author keyword 73 80% 2% 45
5 MECP2 MUTATION Author keyword 44 100% 1% 16
6 METHYL CPG BINDING PROTEIN 2 Author keyword 43 69% 2% 37
7 RETT Address 41 100% 1% 15
8 PRESERVED SPEECH VARIANT Author keyword 33 100% 1% 13
9 WESTERN SYDNEY GENET PROGRAM Address 29 40% 3% 57
10 MECP2 MUTATIONS Author keyword 27 92% 1% 11

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 1179 80% 38% 739 Search RETT+SYNDROME Search RETT+SYNDROME
2 MECP2 296 65% 15% 285 Search MECP2 Search MECP2
3 MECP2 GENE 120 100% 2% 34 Search MECP2+GENE Search MECP2+GENE
4 CDKL5 73 80% 2% 45 Search CDKL5 Search CDKL5
5 MECP2 MUTATION 44 100% 1% 16 Search MECP2+MUTATION Search MECP2+MUTATION
6 METHYL CPG BINDING PROTEIN 2 43 69% 2% 37 Search METHYL+CPG+BINDING+PROTEIN+2 Search METHYL+CPG+BINDING+PROTEIN+2
7 PRESERVED SPEECH VARIANT 33 100% 1% 13 Search PRESERVED+SPEECH+VARIANT Search PRESERVED+SPEECH+VARIANT
8 MECP2 MUTATIONS 27 92% 1% 11 Search MECP2+MUTATIONS Search MECP2+MUTATIONS
9 RETT 17 63% 1% 17 Search RETT Search RETT
10 FOXG1 16 42% 2% 30 Search FOXG1 Search FOXG1

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 2 439 68% 19% 382
2 MECP2 147 43% 13% 260
3 MECP2 MUTATIONS 146 80% 5% 90
4 RETT SYNDROME 143 29% 21% 410
5 METHYL CPG 75 73% 3% 58
6 RETT SYNDROME PATIENTS 59 90% 1% 26
7 PRESERVED SPEECH VARIANT 53 95% 1% 18
8 EXCLUSION MAP 51 91% 1% 21
9 BDNF TRANSCRIPTION 46 53% 3% 62
10 PRESERVED SPEECH 45 94% 1% 16

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 92%
The Role of MeCP2 in the Brain 2011 130 127 81%
The Impact of MeCP2 Loss- or Gain-of-Function on Synaptic Plasticity 2013 31 52 90%
Rett syndrome: a complex disorder with simple roots 2015 2 138 77%
BDNF deregulation in Rett syndrome 2014 18 133 51%
MeCP2 dysfunction in Rett syndrome and related disorders 2006 130 44 98%
Preclinical research in Rett syndrome: setting the foundation for translational success 2012 31 131 85%
Rett Syndrome Exploring the Autism Link 2011 39 20 90%
Rett syndrome in Australia: A review of the epidemiology 2006 108 30 97%
Rett Syndrome and Epilepsy: An Update for Child Neurologists 2013 15 49 90%

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 41 100% 0.8% 15
2 RETT SYNDROME 29 88% 0.7% 14
3 WESTERN SYDNEY GENET PROGRAM 29 40% 2.9% 57
4 GENET EPIGENET CONTROL GENE EXP S 21 90% 0.5% 9
5 NSW RETT SYNDROME 12 86% 0.3% 6
6 BLUE BIRD CIRCLE RETT 11 100% 0.3% 6
7 SAN RAFFAELE RETT 11 78% 0.4% 7
8 ISRAELI RETT 8 75% 0.3% 6
9 P PATHOPHYSIOL REHABIL UNIT 6 71% 0.3% 5
10 CIVITAN INT 6 17% 1.7% 34

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000082554 X LINKED MENTAL RETARDATION//XLMR//PQBP1
2 0.0000056627 SACKLER PROGRAM EPIGENET DEV PSYCHOBIOL//AGING COGNIT DIS//BONNEY 106
3 0.0000056441 DNMT3B//DNA METHYLTRANSFERASE//DNMT1
4 0.0000038488 NEUROLIGIN//SHANK3//NEUREXIN
5 0.0000032350 BRITISH PAEDIAT SURVEILLANCE UNIT//EISENIA SPP//COPPER SULFATE POISONING
6 0.0000031400 WS HALL PSYCHIAT//BROAD AUTISM PHENOTYPE//HYPERSEROTONEMIA
7 0.0000029910 BTBR//BTBR T PLUS TF J//BTBR MICE
8 0.0000023827 PHARMACOEPIGENETICS//ALFRED MED EDUC PROJECT//BANDUNG HOSP
9 0.0000023570 PRADER WILLI SYNDROME//ANGELMAN SYNDROME//UBE3A
10 0.0000023216 5 HYDROXYMETHYLCYTOSINE//5HMC//5 CARBOXYLCYTOSINE