Class information for: |
Basic class information |
| ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
|---|---|---|---|
| 14195 | 720 | 35.5 | 76% |
Classes in level above (level 2) |
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 | USHER SYNDROME | Author keyword | 212 | 75% | 21% | 152 |
| 2 | USH2A | Author keyword | 41 | 85% | 3% | 22 |
| 3 | MYO7A | Author keyword | 30 | 79% | 3% | 19 |
| 4 | USHER SYNDROME TYPE II | Author keyword | 27 | 92% | 2% | 11 |
| 5 | CDH23 | Author keyword | 23 | 79% | 2% | 15 |
| 6 | PCDH15 | Author keyword | 21 | 90% | 1% | 9 |
| 7 | STUDY TREATMENT USHER SYNDROME | Address | 18 | 89% | 1% | 8 |
| 8 | USH1C | Author keyword | 17 | 100% | 1% | 8 |
| 9 | USHERIN | Author keyword | 15 | 82% | 1% | 9 |
| 10 | MYOSIN VIIA | Author keyword | 15 | 51% | 3% | 21 |
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 | USHER SYNDROME | 212 | 75% | 21% | 152 | Search USHER+SYNDROME | Search USHER+SYNDROME |
| 2 | USH2A | 41 | 85% | 3% | 22 | Search USH2A | Search USH2A |
| 3 | MYO7A | 30 | 79% | 3% | 19 | Search MYO7A | Search MYO7A |
| 4 | USHER SYNDROME TYPE II | 27 | 92% | 2% | 11 | Search USHER+SYNDROME+TYPE+II | Search USHER+SYNDROME+TYPE+II |
| 5 | CDH23 | 23 | 79% | 2% | 15 | Search CDH23 | Search CDH23 |
| 6 | PCDH15 | 21 | 90% | 1% | 9 | Search PCDH15 | Search PCDH15 |
| 7 | USH1C | 17 | 100% | 1% | 8 | Search USH1C | Search USH1C |
| 8 | USHERIN | 15 | 82% | 1% | 9 | Search USHERIN | Search USHERIN |
| 9 | MYOSIN VIIA | 15 | 51% | 3% | 21 | Search MYOSIN+VIIA | Search MYOSIN+VIIA |
| 10 | USH3 | 14 | 100% | 1% | 7 | Search USH3 | Search USH3 |
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 | SYNDROME TYPE 1F | 75 | 71% | 8% | 60 |
| 2 | HARMONIN | 56 | 75% | 6% | 40 |
| 3 | SYNDROME TYPE 1D | 51 | 54% | 9% | 65 |
| 4 | PROTOCADHERIN GENE | 50 | 76% | 5% | 35 |
| 5 | SYNDROME TYPE IIA | 48 | 65% | 6% | 45 |
| 6 | USHER SYNDROME | 42 | 34% | 14% | 99 |
| 7 | MYOSIN VIIA | 42 | 41% | 11% | 80 |
| 8 | MYOSIN VIIA GENE | 30 | 37% | 9% | 64 |
| 9 | EAR SENSORY CELLS | 28 | 81% | 2% | 17 |
| 10 | ANKLE LINK COMPLEX | 26 | 68% | 3% | 23 |
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 | 67% |
| Update on Usher syndrome | 2009 | 60 | 110 | 85% |
| Usher protein functions in hair cells and photoreceptors | 2014 | 7 | 106 | 77% |
| Usher syndrome: Animal models, retinal function of Usher proteins, and prospects for gene therapy | 2008 | 78 | 84 | 85% |
| Genetics and pathological mechanisms of Usher syndrome | 2010 | 47 | 105 | 90% |
| Usher syndrome (sensorineural deafness and retinitis pigmentosa): pathogenesis, molecular diagnosis and therapeutic approaches | 2012 | 31 | 69 | 58% |
| An Update on the Genetics of Usher Syndrome | 2011 | 18 | 63 | 90% |
| Molecular basis of human Usher syndrome: Deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease | 2006 | 105 | 159 | 61% |
| The molecular genetics of Usher syndrome | 2003 | 89 | 92 | 80% |
| The Usher syndromes | 1999 | 79 | 80 | 78% |
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 | USHER SYNDROME | 24 | 82% | 1.9% | 14 |
| 2 | STUDY TREATMENT USHER SYNDROME | 18 | 89% | 1.1% | 8 |
| 3 | GRP INVEST ENFERMEDADES NEUROSENSORIALES | 15 | 77% | 1.4% | 10 |
| 4 | REFERENCE MALAD RA AFFECT SENSORIELLE | 11 | 100% | 0.8% | 6 |
| 5 | UNIDAD GENET DIAGNOST PRENATAL | 6 | 29% | 2.5% | 18 |
| 6 | UNITE GENET DEFICITS SENSORIELS | 4 | 19% | 2.8% | 20 |
| 7 | UNITE GENET PHYSIOL AUDIT | 2 | 20% | 1.3% | 9 |
| 8 | HEREDITARY COMMUN DISORDERS | 2 | 23% | 1.0% | 7 |
| 9 | SECT HUMAN GENET | 2 | 14% | 1.5% | 11 |
| 10 | U827 | 2 | 13% | 1.7% | 12 |
Related classes at same level (level 1) |
| Rank | Relatedness score | Related classes |
|---|---|---|
| 1 | 0.0000179351 | GJB2//CONNEXIN 26//PENDRED SYNDROME |
| 2 | 0.0000155320 | PRESTIN//STEREOCILIA//OUTER HAIR CELL |
| 3 | 0.0000130756 | RETINITIS PIGMENTOSA//PERIPHERIN RDS//AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA |
| 4 | 0.0000121956 | MYOSIN I//UNCONVENTIONAL MYOSIN//MYOSIN VI |
| 5 | 0.0000079990 | RPGR//X LINKED RETINITIS PIGMENTOSA//RP2 |
| 6 | 0.0000067851 | MYOSIN VA//RAB27A//GRISCELLI SYNDROME |
| 7 | 0.0000066824 | WAARDENBURG SYNDROME//WAARDENBURGS SYNDROME//KLEIN WAARDENBURG SYNDROME |
| 8 | 0.0000066340 | CHOROIDEREMIA//POU3F4//DFN3 |
| 9 | 0.0000063721 | ALSTROM SYNDROME//ALMS1//TUBBY |
| 10 | 0.0000055743 | LEBER CONGENITAL AMAUROSIS//RPE65//CNGB3 |