Class information for:
Level 1: KBG SYNDROME//AARSKOG SCOTT SYNDROME//FACIOGENITAL DYSPLASIA

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
30243 140 23.5 66%


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 KBG SYNDROME Author keyword 53 95% 13% 18
2 AARSKOG SCOTT SYNDROME Author keyword 44 100% 11% 16
3 FACIOGENITAL DYSPLASIA Author keyword 14 100% 5% 7
4 FGD1 GENE Author keyword 14 100% 5% 7
5 ANKRD11 Author keyword 12 75% 6% 9
6 FGD1 Author keyword 12 75% 6% 9
7 AARSKOG SYNDROME Author keyword 11 65% 8% 11
8 MACRODONTIA Author keyword 6 50% 6% 8
9 UOC MOL MED Address 6 100% 3% 4
10 FRABIN Author keyword 3 57% 3% 4

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 KBG SYNDROME 53 95% 13% 18 Search KBG+SYNDROME Search KBG+SYNDROME
2 AARSKOG SCOTT SYNDROME 44 100% 11% 16 Search AARSKOG+SCOTT+SYNDROME Search AARSKOG+SCOTT+SYNDROME
3 FACIOGENITAL DYSPLASIA 14 100% 5% 7 Search FACIOGENITAL+DYSPLASIA Search FACIOGENITAL+DYSPLASIA
4 FGD1 GENE 14 100% 5% 7 Search FGD1+GENE Search FGD1+GENE
5 ANKRD11 12 75% 6% 9 Search ANKRD11 Search ANKRD11
6 FGD1 12 75% 6% 9 Search FGD1 Search FGD1
7 AARSKOG SYNDROME 11 65% 8% 11 Search AARSKOG+SYNDROME Search AARSKOG+SYNDROME
8 MACRODONTIA 6 50% 6% 8 Search MACRODONTIA Search MACRODONTIA
9 FRABIN 3 57% 3% 4 Search FRABIN Search FRABIN
10 16Q243 MICRODELETION 2 67% 1% 2 Search 16Q243+MICRODELETION Search 16Q243+MICRODELETION

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 FACIOGENITAL DYSPLASIA FGD1 13 80% 6% 8
2 FACIOGENITAL DYSPLASIA 11 54% 10% 14
3 DIGITAL GENITAL SYNDROME 8 100% 4% 5
4 AARSKOG SCOTT SYNDROME 4 42% 6% 8
5 FGD1 GENE 4 56% 4% 5
6 AARSKOG SYNDROME 4 44% 5% 7
7 FGD1 3 57% 3% 4
8 KBG SYNDROME 3 50% 3% 4
9 FRABIN 2 40% 3% 4
10 CRANIOFACIAL DYSMORPHISM 2 27% 4% 6

Journals

Reviews


Title Publ. year Cit. Active
references		 % act. ref.
to same field
KBG syndrome: Report of twins, neurological characteristics, and delineation of diagnostic criteria 2007 20 9 100%
KBG syndrome 2006 12 9 100%
KBG syndrome: review of the literature and findings of 5 affected patients 2009 2 8 88%
Frabin and other related Cdc42-specific guanine nucleotide exchange factors couple the actin cytoskeleton with the plasma membrane 2008 17 43 35%
A CASE OF AARSKOG SYNDROME WITH A REVIEW OF JAPANESE LITERATURE 1982 1 5 100%

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 UOC MOL MED 6 100% 2.9% 4
2 JCR PHARMACEUT CO LTDNISHI KU 1 50% 1.4% 2
3 DISCIPLINES GENET MED 0 20% 1.4% 2
4 PEDIAT NEUROL PSYCHIAT UNIT 0 33% 0.7% 1
5 RADIOL BIOMOL IMAGING 0 33% 0.7% 1
6 HUMAN GENET CYTOGENET 0 25% 0.7% 1
7 SEZ CARDIOCHIRURG 0 25% 0.7% 1
8 CRC ONCOGENE SIGNAL TRANSDUCT GRP 0 20% 0.7% 1
9 MOTHERCARE UNIT CLIN GENET 0 20% 0.7% 1
10 RIC DISABIL MENTALE MOTORIA 0 20% 0.7% 1

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000139377 X LINKED MENTAL RETARDATION//XLMR//PQBP1
2 0.0000113822 TIAM1//RHOB//RHOGDI2
3 0.0000099342 PODOSOMES//INVADOPODIA//CORTACTIN
4 0.0000087406 DOOR SYNDROME//KIRNERS DEFORMITY//COFFIN SIRIS SYNDROME
5 0.0000077985 KABUKI SYNDROME//KABUKI MAKE UP SYNDROME//NIIKAWA KUROKI SYNDROME
6 0.0000077661 VAV//VAV1//VAV3
7 0.0000068966 FRONTONASAL DYSPLASIA//PROBOSCIS LATERALIS//CRANIOFRONTONASAL DYSPLASIA
8 0.0000067767 REVISED AMSTERDAM CRITERIA//POPULATION MEDICAL GENETICS//BOOLEAN SEARCH
9 0.0000067275 BREATHLESS//TRACHEALESS//TRACHEAL SYSTEM
10 0.0000064979 NECTIN//TSLC1//AFADIN