Class information for:
Level 1: AXENFELD RIEGER SYNDROME//PETERS ANOMALY//FOXC1

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
14464 702 30.9 69%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
1995 5043 HIRSCHSPRUNG DISEASE//INTESTINAL NEURONAL DYSPLASIA//AGANGLIONOSIS

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 AXENFELD RIEGER SYNDROME Author keyword 45 80% 4% 28
2 PETERS ANOMALY Author keyword 45 64% 6% 44
3 FOXC1 Author keyword 36 61% 5% 38
4 AXENFELD RIEGER ANOMALY Author keyword 31 92% 2% 12
5 PETERS PLUS SYNDROME Author keyword 30 84% 2% 16
6 RIEGER SYNDROME Author keyword 23 70% 3% 19
7 RING CHROMOSOME 6 Author keyword 21 90% 1% 9
8 PEDIATRIC KERATOPLASTY Author keyword 15 88% 1% 7
9 PITX2 Author keyword 13 27% 6% 42
10 ANTERIOR SEGMENT DYSGENESIS Author keyword 7 40% 2% 14

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 AXENFELD RIEGER SYNDROME 45 80% 4% 28 Search AXENFELD+RIEGER+SYNDROME Search AXENFELD+RIEGER+SYNDROME
2 PETERS ANOMALY 45 64% 6% 44 Search PETERS+ANOMALY Search PETERS+ANOMALY
3 FOXC1 36 61% 5% 38 Search FOXC1 Search FOXC1
4 AXENFELD RIEGER ANOMALY 31 92% 2% 12 Search AXENFELD+RIEGER+ANOMALY Search AXENFELD+RIEGER+ANOMALY
5 PETERS PLUS SYNDROME 30 84% 2% 16 Search PETERS+PLUS+SYNDROME Search PETERS+PLUS+SYNDROME
6 RIEGER SYNDROME 23 70% 3% 19 Search RIEGER+SYNDROME Search RIEGER+SYNDROME
7 RING CHROMOSOME 6 21 90% 1% 9 Search RING+CHROMOSOME+6 Search RING+CHROMOSOME+6
8 PEDIATRIC KERATOPLASTY 15 88% 1% 7 Search PEDIATRIC+KERATOPLASTY Search PEDIATRIC+KERATOPLASTY
9 PITX2 13 27% 6% 42 Search PITX2 Search PITX2
10 ANTERIOR SEGMENT DYSGENESIS 7 40% 2% 14 Search ANTERIOR+SEGMENT+DYSGENESIS Search ANTERIOR+SEGMENT+DYSGENESIS

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 AXENFELD RIEGER SYNDROME 57 60% 9% 61
2 FORKHEAD WINGED HELIX GENE 49 66% 6% 45
3 6P25 42 83% 3% 24
4 FKHL7 37 75% 4% 27
5 MF1 35 86% 3% 18
6 RIEGER SYNDROME 34 36% 11% 75
7 FKHL7 GENE 26 100% 2% 11
8 FOXC1 25 57% 4% 30
9 AUTOSOMAL DOMINANT IRIDOGONIODYSGENESIS 23 79% 2% 15
10 TRANSCRIPTION FACTOR GENE 23 28% 10% 70

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Axenfeld-Rieger syndrome: new perspectives 2012 8 29 90%
Peters Anomaly: Review of the Literature 2011 13 19 79%
Genomics and anterior segment dysgenesis: a review 2014 8 59 39%
A review of anterior segment dysgeneses 2006 46 95 53%
Molecular genetics of Axenfeld-Rieger malformations 2002 89 88 57%
Chromosome 6p25 Deletion Syndrome: Report of a case with optic disc coloboma and review of published ophthalmic findings 2012 1 39 87%
Pediatric Keratoplasty 2009 26 105 35%
Anterior segment development relevant to glaucoma 2004 70 152 19%
The Peters' plus syndrome: a review 2002 27 31 65%
PARTIAL DELETION OF CHROMOSOME 6P - AUTOPSY FINDINGS IN A PREMATURE-INFANT AND REVIEW OF THE LITERATURE 1995 10 11 73%

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 OCULAR GENET 2 25% 1.0% 7
2 KELLOGG EYE 305 1 100% 0.3% 2
3 ASSOC COLUMBUS CLIN 1 50% 0.1% 1
4 EQUIPE ACCUEIL MENRT 2502 1 50% 0.1% 1
5 IST DERMOPAT IMMACULATA 1 50% 0.1% 1
6 KELLOGG EYE 350 1 50% 0.1% 1
7 MARSEILLE NEUROBIOL NEUROPHYSIOL 1 50% 0.1% 1
8 MED PHARMACOLSECT MOL NEUROSCI 1 50% 0.1% 1
9 NEUROBEHAV DEV PEDIAT 1 50% 0.1% 1
10 OCULAR GENET SERV 1 50% 0.1% 1

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000166467 ANIRIDIA//PAX6//PAIRED BOX
2 0.0000119351 MYOCILIN//OPTINEURIN//OLFACTOMEDIN
3 0.0000116927 CHROMOSOME 6Q DELETION//SIM1 GENE//6Q DELETION
4 0.0000097315 DACRYOCYSTORHINOGRAPHY//ORBITAL FAT PROLAPSE//LIMBAL DERMOID
5 0.0000091076 NANOPHTHALMOS//ANOPHTHALMIA//MICROPHTHALMIA
6 0.0000088404 NANCE HORAN SYNDROME//AUTOSOMAL DOMINANT CONGENITAL CATARACT//GJA8
7 0.0000086506 LEFT RIGHT ASYMMETRY//LEFT RIGHT PATTERNING//NODAL FLOW
8 0.0000086188 NEUHAUSER SYNDROME//MEGALOCORNEA//ANTERIOR MEGALOPHTHALMOS
9 0.0000080512 FOXM1//FORKHEAD BOX M1//WINGED HELIX DNA BINDING DOMAIN
10 0.0000070657 WIEDEMANN RAUTENSTRAUCH SYNDROME//NEONATAL PROGEROID SYNDROME//HALLERMANN STREIFF SYNDROME