Class information for:
Level 1: GJB2//CONNEXIN 26//PENDRED SYNDROME

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
1892 2367 32.4 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
2408 3723 GJB2//CONNEXIN 26//USHER SYNDROME

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 GJB2 Author keyword 593 93% 10% 227
2 CONNEXIN 26 Author keyword 279 75% 9% 202
3 PENDRED SYNDROME Author keyword 195 92% 3% 78
4 SLC26A4 Author keyword 179 85% 4% 95
5 GJB6 Author keyword 144 93% 2% 54
6 DFNB1 Author keyword 130 97% 2% 36
7 35DELG Author keyword 103 97% 1% 30
8 DFNA9 Author keyword 102 100% 1% 30
9 GJB2 GENE Author keyword 82 92% 1% 33
10 NON SYNDROMIC HEARING LOSS Author keyword 76 86% 2% 38

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 GJB2 593 93% 10% 227 Search GJB2 Search GJB2
2 CONNEXIN 26 279 75% 9% 202 Search CONNEXIN+26 Search CONNEXIN+26
3 PENDRED SYNDROME 195 92% 3% 78 Search PENDRED+SYNDROME Search PENDRED+SYNDROME
4 SLC26A4 179 85% 4% 95 Search SLC26A4 Search SLC26A4
5 GJB6 144 93% 2% 54 Search GJB6 Search GJB6
6 DFNB1 130 97% 2% 36 Search DFNB1 Search DFNB1
7 35DELG 103 97% 1% 30 Search 35DELG Search 35DELG
8 DFNA9 102 100% 1% 30 Search DFNA9 Search DFNA9
9 GJB2 GENE 82 92% 1% 33 Search GJB2+GENE Search GJB2+GENE
10 NON SYNDROMIC HEARING LOSS 76 86% 2% 38 Search NON+SYNDROMIC+HEARING+LOSS Search NON+SYNDROMIC+HEARING+LOSS

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 DFNB1 506 94% 8% 178
2 CONNEXIN 26 GENE 412 88% 8% 191
3 SENSORINEURAL DEAFNESS 310 54% 17% 398
4 NON SYNDROMIC DEAFNESS 229 73% 7% 176
5 RECESSIVE DEAFNESS 208 65% 8% 200
6 A1555G MUTATION 172 79% 5% 110
7 GJB2 168 81% 4% 100
8 GJB2 MUTATIONS 166 86% 4% 83
9 ENLARGED VESTIBULAR AQUEDUCT 165 82% 4% 96
10 PRELINGUAL DEAFNESS 147 78% 4% 98

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
GJB2-Associated Hearing Loss: Systematic Review of Worldwide Prevalence, Genotype, and Auditory Phenotype 2014 14 196 98%
Transmembrane channel-like (TMC) genes are required for auditory and vestibular mechanosensation 2015 4 34 41%
The role of connexins in ear and skin physiology - Functional insights from disease-associated mutations 2013 33 116 65%
Forty-six genes causing nonsyndromic hearing impairment: Which ones should be analyzed in DNA diagnostics? 2009 137 43 67%
Current concepts: Newborn hearing screening - A silent revolution 2006 300 32 53%
Connexins and skin disease: insights into the role of beta connexins in skin homeostasis 2015 2 123 41%
Genetic investigations in childhood deafness 2015 1 39 69%
GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: A HuGE review 2002 178 70 93%
Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity 2011 33 96 66%
SLC26A4 Genotypes and Phenotypes Associated with Enlargement of the Vestibular Aqueduct 2011 20 40 83%

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 MOL OTOLARYNGOL S 42 58% 2.1% 49
2 CHINESE PEOPLES LIBERAT ARMY OTOLARYNGOL 24 91% 0.4% 10
3 UNITE GENET DEFICITS SENSORIELS 18 37% 1.6% 39
4 OTOLARYNGOL BRANCH 11 37% 1.0% 24
5 INTER PHD PROGRAM GENET 11 52% 0.6% 15
6 GENET TESTING DEAFNESS 9 83% 0.2% 5
7 UNIDAD GENET MOL 8 23% 1.3% 30
8 HEARING DEAFNESS 7 14% 1.9% 46
9 AUDIOL BALANCE UNIT 6 80% 0.2% 4
10 INTERDEPARTMENTAL PHD PROGRAM GENET 6 80% 0.2% 4

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000179351 USHER SYNDROME//USH2A//MYO7A
2 0.0000131147 AUDITORY NEUROPATHY//AUDITORY NEUROPATHY SPECTRUM DISORDER//OTOF
3 0.0000113259 CHOROIDEREMIA//POU3F4//DFN3
4 0.0000082060 UNIVERSAL NEWBORN HEARING SCREENING//NEWBORN HEARING SCREENING//HEARING ASSESSMENT MANAGEMENT
5 0.0000065702 STRIA VASCULARIS//ENDOLYMPH//ENDOLYMPHATIC SAC
6 0.0000065531 WOLFRAM SYNDROME//WFS1//WOLFRAMIN
7 0.0000062264 AUDITORY BRAINSTEM IMPLANT//LARGE VESTIBULAR AQUEDUCT SYNDROME//INTRALABYRINTHINE SCHWANNOMA
8 0.0000060191 WAARDENBURG SYNDROME//WAARDENBURGS SYNDROME//KLEIN WAARDENBURG SYNDROME
9 0.0000053188 CONNEXIN 43//GAP JUNCTION//CONNEXIN
10 0.0000049033 PRESTIN//STEREOCILIA//OUTER HAIR CELL