Class information for:
Level 1: USHER SYNDROME//USH2A//MYO7A

Basic class information
Bar chart of Publication_year

Last years might be incomplete

Hierarchy of classes
The table includes all classes above and classes immediately below the current class.


Cluster id Level Cluster label #P
5 4 NEUROSCIENCES//CLINICAL NEUROLOGY//PSYCHOLOGY, EXPERIMENTAL 1830502
82 3       AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY//OTORHINOLARYNGOLOGY//HEARING RESEARCH 83168
1636 2             GJB2//CONNEXIN 26//DEAFNESS 7244
10794 1                   USHER SYNDROME//USH2A//MYO7A 1062

Terms with highest relevance score


rank Category termType chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 USHER SYNDROME authKW 3618535 16% 72% 170
2 USH2A authKW 662389 2% 89% 25
3 MYO7A authKW 506382 2% 74% 23
4 MYOSIN VIIA authKW 477611 2% 62% 26
5 CADHERIN 23 authKW 370936 1% 83% 15
6 STEREOCILIA authKW 336011 5% 23% 49
7 PROTOCADHERIN 15 authKW 334338 1% 87% 13
8 USHER SYNDROME TYPE II authKW 299224 1% 92% 11
9 CDH23 authKW 290291 1% 65% 15
10 PCDH15 authKW 276205 1% 85% 11

Web of Science journal categories


chi_square_rank Category chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 Genetics & Heredity 6351 32% 0% 345
2 Otorhinolaryngology 4219 14% 0% 144
3 Ophthalmology 2836 14% 0% 152
4 Audiology & Speech-Language Pathology 739 4% 0% 38
5 Neurosciences 581 16% 0% 167
6 Cell Biology 435 12% 0% 129
7 Rehabilitation 401 4% 0% 47
8 Biochemistry & Molecular Biology 397 20% 0% 210
9 Education, Special 295 2% 0% 19
10 Developmental Biology 244 3% 0% 36

Address terms


chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 USHER SYNDROME 342134 1% 82% 14
2 STUDY TREATMENT USHER SYNDROME 267078 1% 100% 9
3 UNITE GENET PHYSIOL AUDIT 239353 2% 37% 22
4 REFERENCE MALAD RA AFFECT SENSORIELLE 207727 1% 100% 7
5 GRP INVEST ENFERMEDADES NEUROSENSORIALES 171686 1% 64% 9
6 CELL STRUCT DYNAM 171185 1% 38% 15
7 SECT HUMAN GENET 137315 2% 24% 19
8 UNIDAD GENET DIAGNOST PRENATAL 131916 2% 26% 17
9 UNITE GENET DEFICITS SENSORIELS 123427 2% 20% 21
10 SECT GENE STRUCT FUNCT 100143 1% 38% 9

Journals


chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 MOLECULAR VISION 9636 3% 1% 33
2 HUMAN MOLECULAR GENETICS 7523 5% 1% 51
3 JOURNAL OF VISUAL IMPAIRMENT & BLINDNESS 6538 2% 1% 21
4 AMERICAN ANNALS OF THE DEAF 4058 1% 1% 13
5 JOURNAL OF MEDICAL GENETICS 2883 2% 0% 24
6 CLINICAL GENETICS 2476 2% 0% 21
7 JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY 2364 1% 1% 8
8 GENOMICS 2196 2% 0% 25
9 HEARING RESEARCH 2085 2% 0% 21
10 HUMAN MUTATION 2074 2% 0% 17

Author Key Words


chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass LCSH search Wikipedia search
1 USHER SYNDROME 3618535 16% 72% 170 Search USHER+SYNDROME Search USHER+SYNDROME
2 USH2A 662389 2% 89% 25 Search USH2A Search USH2A
3 MYO7A 506382 2% 74% 23 Search MYO7A Search MYO7A
4 MYOSIN VIIA 477611 2% 62% 26 Search MYOSIN+VIIA Search MYOSIN+VIIA
5 CADHERIN 23 370936 1% 83% 15 Search CADHERIN+23 Search CADHERIN+23
6 STEREOCILIA 336011 5% 23% 49 Search STEREOCILIA Search STEREOCILIA
7 PROTOCADHERIN 15 334338 1% 87% 13 Search PROTOCADHERIN+15 Search PROTOCADHERIN+15
8 USHER SYNDROME TYPE II 299224 1% 92% 11 Search USHER+SYNDROME+TYPE+II Search USHER+SYNDROME+TYPE+II
9 CDH23 290291 1% 65% 15 Search CDH23 Search CDH23
10 PCDH15 276205 1% 85% 11 Search PCDH15 Search PCDH15

Core articles
The table includes core articles in the class. The following variables is taken into account for the relevance score of an article in a cluster c:
(1) Number of references referring to publications in the class.
(2) Share of total number of active references referring to publications in the class.
(3) Age of the article. New articles get higher score than old articles.
(4) Citation rate, normalized to year.

Classes with closest relation at Level 1


rank cluster_id2 link
1 2436 GJB2//CONNEXIN 26//NON SYNDROMIC HEARING LOSS
2 7732 UNCONVENTIONAL MYOSIN//MYOSIN VI//MYOSIN I
3 3376 RETINITIS PIGMENTOSA//RPGR//PERIPHERIN RDS
4 1264 OUTER HAIR CELL//HEARING RESEARCH//ELECTROMOTILITY
5 25911 RETINITIS PIGMENTOSA//CRB1 MUTATION//RETINITIS PIGMENTOSA REFERENCE
6 15387 PRESBYCUSIS//AGE RELATED HEARING LOSS//AGE RELATED HEARING IMPAIRMENT
7 34048 TUBBY//TULP1//ORF PHAGE DISPLAY
8 1620 HAIR CELL//INNER EAR//HAIR CELL REGENERATION
9 37572 OCP2//OCP1//CYTOPLASMIC GLYCOSYLATION
10 25520 CHOROIDEREMIA//POU3F4//RAB ESCORT PROTEIN 1

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