Class information for:
Level 1: X LINKED MENTAL RETARDATION//XLMR//PQBP1

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
8258 1201 31.3 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 X LINKED MENTAL RETARDATION Author keyword 75 47% 10% 118
2 XLMR Author keyword 40 62% 3% 41
3 PQBP1 Author keyword 37 100% 1% 14
4 ARX GENE Author keyword 33 100% 1% 13
5 BORJESON FORSSMAN LEHMANN SYNDROME Author keyword 33 100% 1% 13
6 NONSPECIFIC X LINKED MENTAL RETARDATION Author keyword 26 100% 1% 11
7 FG SYNDROME Author keyword 24 68% 2% 21
8 ATR X SYNDROME Author keyword 19 80% 1% 12
9 MRX Author keyword 18 56% 2% 22
10 XQ28 DUPLICATION Author keyword 18 89% 1% 8

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 X LINKED MENTAL RETARDATION 75 47% 10% 118 Search X+LINKED+MENTAL+RETARDATION Search X+LINKED+MENTAL+RETARDATION
2 XLMR 40 62% 3% 41 Search XLMR Search XLMR
3 PQBP1 37 100% 1% 14 Search PQBP1 Search PQBP1
4 ARX GENE 33 100% 1% 13 Search ARX+GENE Search ARX+GENE
5 BORJESON FORSSMAN LEHMANN SYNDROME 33 100% 1% 13 Search BORJESON+FORSSMAN+LEHMANN+SYNDROME Search BORJESON+FORSSMAN+LEHMANN+SYNDROME
6 NONSPECIFIC X LINKED MENTAL RETARDATION 26 100% 1% 11 Search NONSPECIFIC+X+LINKED+MENTAL+RETARDATION Search NONSPECIFIC+X+LINKED+MENTAL+RETARDATION
7 FG SYNDROME 24 68% 2% 21 Search FG+SYNDROME Search FG+SYNDROME
8 ATR X SYNDROME 19 80% 1% 12 Search ATR+X+SYNDROME Search ATR+X+SYNDROME
9 MRX 18 56% 2% 22 Search MRX Search MRX
10 XQ28 DUPLICATION 18 89% 1% 8 Search XQ28+DUPLICATION Search XQ28+DUPLICATION

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 RENPENNING SYNDROME 58 92% 2% 23
2 LINKED MENTAL RETARDATION 58 22% 20% 235
3 XLMR GENES 52 82% 3% 31
4 HOMEOBOX GENE ARX 38 93% 1% 14
5 ABNORMAL GENITALIA 34 61% 3% 36
6 DISTAL XQ 31 92% 1% 12
7 XLMR 30 84% 1% 16
8 FUNCTIONAL DISOMY 27 78% 1% 18
9 OLIGOPHRENIN 1 GENE 27 92% 1% 11
10 PROTEIN ATRX 26 80% 1% 16

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Fragile X and X-Linked Intellectual Disability: Four Decades of Discovery 2012 49 81 69%
Genetics of recessive cognitive disorders 2014 14 99 28%
Alpha thalassaemia-mental retardation, X linked 2006 50 30 90%
XLMR genes: update 2007 2008 86 52 48%
ARX: a gene for all seasons 2006 66 36 69%
XLMR genes: update 2000 2001 62 46 74%
X-linked mental retardation 2005 224 118 31%
The genetic landscape of intellectual disability arising from chromosome X 2009 75 90 46%
X-linked mental retardation: many genes for a complex disorder 2006 91 64 48%
ARX Spectrum Disorders: Making Inroads into the Molecular Pathology 2010 49 97 52%

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 JC SELF HUMAN GENET 6 22% 1.9% 23
2 JC SELF 4 20% 1.3% 16
3 GOLD SERV HUNTER GENET 3 100% 0.2% 3
4 MED PREVENT SOCIAL PEDIAT 2 67% 0.2% 2
5 NEIDERS CHILDREN MED ISRAEL 2 67% 0.2% 2
6 NEUROPAEDIAT SECT 2 67% 0.2% 2
7 PAEDIAT NEUROL NEUROGENET UNIT S 2 67% 0.2% 2
8 POPULAT HLTHMINIST EDUC 2 67% 0.2% 2
9 U316 2 13% 1.2% 15
10 GREENWOOD GENET 2 40% 0.3% 4

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000139377 KBG SYNDROME//AARSKOG SCOTT SYNDROME//FACIOGENITAL DYSPLASIA
2 0.0000129579 CHOROIDEREMIA//POU3F4//DFN3
3 0.0000097902 SUBTELOMERIC REARRANGEMENTS//IDIOPATHIC MENTAL RETARDATION//MBD5
4 0.0000082554 RETT SYNDROME//MECP2//MECP2 GENE
5 0.0000074626 TUMOR CLONALITY//CLONAL REMISSION//M27 BETA
6 0.0000070515 ANGANWADI//DISABIL STUDIES PROGRAMME//COUNCIL DISABLED CHILDREN
7 0.0000066609 COFFIN LOWRY SYNDROME//RSK2//SL0101
8 0.0000060822 GLYCEROL KINASE DEFICIENCY//COMPLEX GLYCEROL KINASE DEFICIENCY//KOHLSCHUTTER TONZ SYNDROME
9 0.0000054721 XIST//X CHROMOSOME INACTIVATION//TSIX
10 0.0000052272 FRAGILE X SYNDROME//FRAGILE X//FMR1