Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
2408 | 3723 | 32.8 | 80% |
Classes in level above (level 3) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
82 | 78668 | OTORHINOLARYNGOLOGY//HEARING RESEARCH//AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY |
Classes in level below (level 1) |
ID, lev. below | Publications | Label for level below |
---|---|---|
1892 | 2367 | GJB2//CONNEXIN 26//PENDRED SYNDROME |
14195 | 720 | USHER SYNDROME//USH2A//MYO7A |
20071 | 413 | WOLFRAM SYNDROME//WFS1//WOLFRAMIN |
25837 | 223 | ALSTROM SYNDROME//ALMS1//TUBBY |
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 | 608 | 93% | 6% | 228 |
2 | CONNEXIN 26 | Author keyword | 283 | 75% | 5% | 203 |
3 | USHER SYNDROME | Author keyword | 241 | 78% | 4% | 158 |
4 | WOLFRAM SYNDROME | Author keyword | 225 | 85% | 3% | 117 |
5 | PENDRED SYNDROME | Author keyword | 195 | 92% | 2% | 78 |
6 | SLC26A4 | Author keyword | 179 | 85% | 3% | 95 |
7 | GJB6 | Author keyword | 144 | 93% | 1% | 54 |
8 | DFNB1 | Author keyword | 134 | 100% | 1% | 37 |
9 | 35DELG | Author keyword | 103 | 97% | 1% | 30 |
10 | DFNA9 | Author keyword | 102 | 100% | 1% | 30 |
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 | 608 | 93% | 6% | 228 | Search GJB2 | Search GJB2 |
2 | CONNEXIN 26 | 283 | 75% | 5% | 203 | Search CONNEXIN+26 | Search CONNEXIN+26 |
3 | USHER SYNDROME | 241 | 78% | 4% | 158 | Search USHER+SYNDROME | Search USHER+SYNDROME |
4 | WOLFRAM SYNDROME | 225 | 85% | 3% | 117 | Search WOLFRAM+SYNDROME | Search WOLFRAM+SYNDROME |
5 | PENDRED SYNDROME | 195 | 92% | 2% | 78 | Search PENDRED+SYNDROME | Search PENDRED+SYNDROME |
6 | SLC26A4 | 179 | 85% | 3% | 95 | Search SLC26A4 | Search SLC26A4 |
7 | GJB6 | 144 | 93% | 1% | 54 | Search GJB6 | Search GJB6 |
8 | DFNB1 | 134 | 100% | 1% | 37 | Search DFNB1 | Search DFNB1 |
9 | 35DELG | 103 | 97% | 1% | 30 | Search 35DELG | Search 35DELG |
10 | DFNA9 | 102 | 100% | 1% | 30 | Search DFNA9 | Search DFNA9 |
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% | 5% | 178 |
2 | CONNEXIN 26 GENE | 412 | 88% | 5% | 191 |
3 | RECESSIVE DEAFNESS | 370 | 78% | 7% | 242 |
4 | SENSORINEURAL DEAFNESS | 322 | 55% | 11% | 404 |
5 | NON SYNDROMIC DEAFNESS | 254 | 75% | 5% | 182 |
6 | DIDMOAD SYNDROME | 249 | 92% | 3% | 100 |
7 | MYOSIN VIIA GENE | 221 | 80% | 4% | 138 |
8 | GJB2 | 210 | 86% | 3% | 106 |
9 | DEAFNESS | 185 | 24% | 18% | 683 |
10 | GJB2 MUTATIONS | 175 | 88% | 2% | 84 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities | 2015 | 3 | 200 | 69% |
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 | 50% |
Forty-six genes causing nonsyndromic hearing impairment: Which ones should be analyzed in DNA diagnostics? | 2009 | 137 | 43 | 86% |
The role of connexins in ear and skin physiology - Functional insights from disease-associated mutations | 2013 | 33 | 116 | 65% |
Current concepts: Newborn hearing screening - A silent revolution | 2006 | 300 | 32 | 53% |
Usher syndrome: Animal models, retinal function of Usher proteins, and prospects for gene therapy | 2008 | 78 | 84 | 87% |
Usher protein functions in hair cells and photoreceptors | 2014 | 7 | 106 | 79% |
Update on Usher syndrome | 2009 | 60 | 110 | 87% |
Genetic investigations in childhood deafness | 2015 | 1 | 39 | 77% |
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 | 60 | 66% | 1.5% | 56 |
2 | UNITE GENET DEFICITS SENSORIELS | 48 | 56% | 1.6% | 59 |
3 | USHER SYNDROME | 24 | 82% | 0.4% | 14 |
4 | CHINESE PEOPLES LIBERAT ARMY OTOLARYNGOL | 24 | 91% | 0.3% | 10 |
5 | STUDY TREATMENT USHER SYNDROME | 20 | 100% | 0.2% | 9 |
6 | HEARING IMPLANT SCI | 16 | 54% | 0.6% | 21 |
7 | INTER PHD PROGRAM GENET | 15 | 59% | 0.5% | 17 |
8 | GRP INVEST ENFERMEDADES NEUROSENSORIALES | 15 | 77% | 0.3% | 10 |
9 | OTOLARYNGOL BRANCH | 13 | 40% | 0.7% | 26 |
10 | URA 1968 | 13 | 47% | 0.6% | 21 |
Related classes at same level (level 2) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000018590 | HEARING RESEARCH//COCHLEA//TINNITUS |
2 | 0.0000017122 | GAP JUNCTION//CONNEXIN//CONNEXIN 43 |
3 | 0.0000014625 | COCHLEAR IMPLANT//AMERICAN ANNALS OF THE DEAF//EAR AND HEARING |
4 | 0.0000009531 | RETINITIS PIGMENTOSA//RETINAL DEGENERATION//RETINA |
5 | 0.0000008136 | ACHONDROPLASIA//HYPOCHONDROPLASIA//THANATOPHORIC DYSPLASIA |
6 | 0.0000007223 | MELAS//MITOCHONDRIAL DNA//LEBERS HEREDITARY OPTIC NEUROPATHY |
7 | 0.0000006426 | AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE//POLYCYSTIC KIDNEY DISEASE//ADPKD |
8 | 0.0000005481 | NEXT GENERATION SEQUENCING//RNA SEQ//COPY NUMBER VARIATION |
9 | 0.0000005037 | HIRSCHSPRUNG DISEASE//INTESTINAL NEURONAL DYSPLASIA//AGANGLIONOSIS |
10 | 0.0000004896 | Y CHROMOSOME//HUMAN BIOLOGY//Y STR |