Class information for:
Level 1: ANIRIDIA//PAX6//PAIRED BOX

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
10442 997 45.7 85%


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 ANIRIDIA Author keyword 78 59% 9% 88
2 PAX6 Author keyword 74 34% 18% 179
3 PAIRED BOX Author keyword 18 52% 3% 25
4 SMALL EYE Author keyword 17 57% 2% 20
5 PAX6 GENE Author keyword 15 68% 1% 13
6 PAIRED DOMAIN Author keyword 13 48% 2% 20
7 PAX GENES Author keyword 12 36% 3% 27
8 GILLESPIE SYNDROME Author keyword 11 100% 1% 6
9 PAX 6 Author keyword 11 34% 3% 26
10 PAIRED BOX HOMEOBOX GENES Author keyword 6 100% 0% 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 ANIRIDIA 78 59% 9% 88 Search ANIRIDIA Search ANIRIDIA
2 PAX6 74 34% 18% 179 Search PAX6 Search PAX6
3 PAIRED BOX 18 52% 3% 25 Search PAIRED+BOX Search PAIRED+BOX
4 SMALL EYE 17 57% 2% 20 Search SMALL+EYE Search SMALL+EYE
5 PAX6 GENE 15 68% 1% 13 Search PAX6+GENE Search PAX6+GENE
6 PAIRED DOMAIN 13 48% 2% 20 Search PAIRED+DOMAIN Search PAIRED+DOMAIN
7 PAX GENES 12 36% 3% 27 Search PAX+GENES Search PAX+GENES
8 GILLESPIE SYNDROME 11 100% 1% 6 Search GILLESPIE+SYNDROME Search GILLESPIE+SYNDROME
9 PAX 6 11 34% 3% 26 Search PAX+6 Search PAX+6
10 PAIRED BOX HOMEOBOX GENES 6 100% 0% 4 Search PAIRED+BOX+HOMEOBOX+GENES Search PAIRED+BOX+HOMEOBOX+GENES

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 PAIRED DOMAIN 81 42% 15% 147
2 SMALL EYE 79 73% 6% 61
3 HOMEOBOX CONTAINING GENE 68 34% 16% 164
4 ANIRIDIA 50 35% 12% 115
5 DNA BINDING SUBDOMAINS 49 94% 2% 17
6 AUTOSOMAL DOMINANT ANIRIDIA 38 89% 2% 17
7 NASAL DEVELOPMENT 30 57% 4% 35
8 CONGENITAL ANIRIDIA 24 68% 2% 21
9 SMALL EYE SEY 22 81% 1% 13
10 PAIRED BOX GENE 21 27% 6% 64

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Concise review: Pax6 transcription factor contributes to both embryonic and adult neurogenesis as a multifunctional regulator 2008 130 134 43%
Clinical and molecular aspects of aniridia 2010 38 98 82%
Regulation of cerebral cortical neurogenesis by the Pax6 transcription factor 2015 1 220 41%
The Role of Pax6 in Forebrain Development 2011 43 146 30%
Anterior eye development and ocular mesenchyme: new insights from mouse models and human diseases 2004 113 79 56%
Aniridia: current pathology and management 2008 53 70 56%
Developmental malformations of the eye: the role of PAX6, SOX2 and OTX2 2006 77 116 47%
Pax-6 in development and evolution 1997 277 130 54%
Pax6; a pleiotropic player in development 2002 168 93 56%
PAX6 in sensory development 2002 119 78 64%

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 INHERITED EYE DIS 2 32% 0.6% 6
2 MOL MED OPHTHALMOL 2 67% 0.2% 2
3 DEV NEUROSCIAOBA KU 2 26% 0.5% 5
4 CFB 1 100% 0.2% 2
5 CNRS EP 560 1 50% 0.2% 2
6 LIFE SCI MAXILLO IAL SYST 1 100% 0.2% 2
7 NEURAL TUBE 1 100% 0.2% 2
8 OPHTHALMOL VISUAL SCI GENET 1 50% 0.2% 2
9 MOL PATHOL MOL GENET 1 25% 0.4% 4
10 INT MAX PLANCK IMPRS ORGANISMAL BIOL 1 40% 0.2% 2

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000261921 WAARDENBURG SYNDROME//WAARDENBURGS SYNDROME//KLEIN WAARDENBURG SYNDROME
2 0.0000217624 SIX1//EYA1//SINE OCULIS
3 0.0000166467 AXENFELD RIEGER SYNDROME//PETERS ANOMALY//FOXC1
4 0.0000112256 ISTHMIC ORGANIZER//GBX2//RHOMBOMERE 1
5 0.0000110935 MULLER GLIA//RETINAL REGENERATION//RETINOGENESIS
6 0.0000103084 NANCE HORAN SYNDROME//AUTOSOMAL DOMINANT CONGENITAL CATARACT//GJA8
7 0.0000095715 NANOPHTHALMOS//ANOPHTHALMIA//MICROPHTHALMIA
8 0.0000080327 NINA IRELAND DEV NEUROBIOL//PROTOMAP//AREALIZATION
9 0.0000071985 INSULIN GENE//PDX 1//ISLET CELL TRANSPLANT PROGRAM
10 0.0000064940 WT1//DENYS DRASH SYNDROME//WILMS TUMOR GENE