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

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
10225 1080 38.4 79%


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
11 4 NEUROSCIENCES//CLINICAL NEUROLOGY//NEUROL 1112395
97 3       OTORHINOLARYNGOLOGY//AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY//HEARING RESEARCH 75796
2453 2             GJB2//USHER SYNDROME//CONNEXIN 26 4040
10225 1                   USHER SYNDROME//USH2A//MYO7A 1080

Terms with highest relevance score


rank Term termType Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 USHER SYNDROME authKW 3413221 15% 72% 167
2 USH2A authKW 603129 2% 89% 24
3 MYO7A authKW 418833 2% 74% 20
4 MYOSIN VIIA authKW 387709 2% 57% 24
5 CADHERIN 23 authKW 353394 1% 83% 15
6 PROTOCADHERIN 15 authKW 318527 1% 87% 13
7 STEREOCILIA authKW 310109 4% 23% 48
8 CDH23 authKW 289135 1% 68% 15
9 USHER SYNDROME TYPE II authKW 285073 1% 92% 11
10 PCDH15 authKW 235596 1% 83% 10

Web of Science journal categories


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 Genetics & Heredity 6594 33% 0% 355
2 Otorhinolaryngology 4749 14% 0% 154
3 Ophthalmology 2652 14% 0% 149
4 Audiology & Speech-Language Pathology 982 4% 0% 44
5 Neurosciences 697 17% 0% 182
6 Biochemistry & Molecular Biology 401 20% 0% 214
7 Cell Biology 376 11% 0% 123
8 Rehabilitation 323 4% 0% 43
9 Education, Special 293 2% 0% 19
10 Developmental Biology 193 3% 0% 33

Address terms


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 USHER SYNDROME 281050 1% 76% 13
2 CELL STRUCT DYNAM 209483 2% 44% 17
3 STUDY TREATMENT USHER SYNDROME 201043 1% 89% 8
4 UNITE GENET PHYSIOL AUDIT 198373 2% 35% 20
5 REFERENCE MALAD RA AFFECT SENSORIELLE 197903 1% 100% 7
6 GRP INVEST ENFERMEDADES NEUROSENSORIALES 163567 1% 64% 9
7 SECT HUMAN GENET 161890 2% 27% 21
8 UNIDAD GENET DIAGNOST PRENATAL 125676 2% 26% 17
9 SECT GENE STRUCT FUNCT 117788 1% 42% 10
10 UNITE GENET DEFICITS SENSORIELS 117588 2% 20% 21

Journals


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 MOLECULAR VISION 9324 3% 1% 33
2 HUMAN MOLECULAR GENETICS 6906 5% 1% 49
3 JOURNAL OF VISUAL IMPAIRMENT & BLINDNESS 4131 2% 1% 17
4 AMERICAN ANNALS OF THE DEAF 3917 1% 1% 13
5 JOURNAL OF MEDICAL GENETICS 2779 2% 0% 24
6 AUDIOLOGY AND NEURO-OTOLOGY 2741 1% 1% 9
7 GENOMICS 2639 3% 0% 28
8 HEARING RESEARCH 2426 2% 0% 23
9 JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY 2343 1% 1% 8
10 HUMAN MUTATION 2279 2% 0% 18

Author Key Words


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class		 LCSH search Wikipedia search
1 USHER SYNDROME 3413221 15% 72% 167 Search USHER+SYNDROME Search USHER+SYNDROME
2 USH2A 603129 2% 89% 24 Search USH2A Search USH2A
3 MYO7A 418833 2% 74% 20 Search MYO7A Search MYO7A
4 MYOSIN VIIA 387709 2% 57% 24 Search MYOSIN+VIIA Search MYOSIN+VIIA
5 CADHERIN 23 353394 1% 83% 15 Search CADHERIN+23 Search CADHERIN+23
6 PROTOCADHERIN 15 318527 1% 87% 13 Search PROTOCADHERIN+15 Search PROTOCADHERIN+15
7 STEREOCILIA 310109 4% 23% 48 Search STEREOCILIA Search STEREOCILIA
8 CDH23 289135 1% 68% 15 Search CDH23 Search CDH23
9 USHER SYNDROME TYPE II 285073 1% 92% 11 Search USHER+SYNDROME+TYPE+II Search USHER+SYNDROME+TYPE+II
10 PCDH15 235596 1% 83% 10 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.


Rank Reference # ref. in
cl.		 Shr. of ref. in
cl.		 Citations
1 MATHUR, P , YANG, J , (2015) USHER SYNDROME: HEARING LOSS, RETINAL DEGENERATION AND ASSOCIATED ABNORMALITIES.BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. VOL. 1852. ISSUE 3. P. 406 -420 153 77% 17
2 YAN, D , LIU, XZ , (2010) GENETICS AND PATHOLOGICAL MECHANISMS OF USHER SYNDROME.JOURNAL OF HUMAN GENETICS. VOL. 55. ISSUE 6. P. 327 -335 100 95% 58
3 COSGROVE, D , ZALLOCCHI, M , (2014) USHER PROTEIN FUNCTIONS IN HAIR CELLS AND PHOTORECEPTORS.INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY. VOL. 46. ISSUE . P. 80-89 94 89% 15
4 SAIHAN, Z , WEBSTER, AR , LUXON, L , BITNER-GLINDZICZ, M , (2009) UPDATE ON USHER SYNDROME.CURRENT OPINION IN NEUROLOGY. VOL. 22. ISSUE 1. P. 19-27 96 87% 64
5 COHEN, M , BITNER-GLINDZICZ, M , LUXON, L , (2007) THE CHANGING FACE OF USHER SYNDROME: CLINICAL IMPLICATIONS.INTERNATIONAL JOURNAL OF AUDIOLOGY. VOL. 46. ISSUE 2. P. 82-93 85 97% 31
6 EL-AMRAOUI, A , PETIT, C , (2014) THE RETINAL PHENOTYPE OF USHER SYNDROME: PATHOPHYSIOLOGICAL INSIGHTS FROM ANIMAL MODELS.COMPTES RENDUS BIOLOGIES. VOL. 337. ISSUE 3. P. 167 -177 90 77% 4
7 BONNET, C , GRATI, M , MARLIN, S , LEVILLIERS, J , HARDELIN, JP , PARODI, M , NIASME-GRARE, M , ZELENIKA, D , DELEPINE, M , FELDMANN, D , ET AL (2011) COMPLETE EXON SEQUENCING OF ALL KNOWN USHER SYNDROME GENES GREATLY IMPROVES MOLECULAR DIAGNOSIS.ORPHANET JOURNAL OF RARE DISEASES. VOL. 6. ISSUE . P. - 71 92% 31
8 WILLIAMS, DS , (2008) USHER SYNDROME: ANIMAL MODELS, RETINAL FUNCTION OF USHER PROTEINS, AND PROSPECTS FOR GENE THERAPY.VISION RESEARCH. VOL. 48. ISSUE 3. P. 433-441 74 88% 82
9 REINERS, J , NAGEL-WOLFRUM, K , JURGENS, K , MARKER, T , WOLFRUM, U , (2006) MOLECULAR BASIS OF HUMAN USHER SYNDROME: DECIPHERING THE MESHES OF THE USHER PROTEIN NETWORK PROVIDES INSIGHTS INTO THE PATHOMECHANISMS OF THE USHER DISEASE.EXPERIMENTAL EYE RESEARCH. VOL. 83. ISSUE 1. P. 97 -119 101 64% 113
10 PAN, LF , ZHANG, MJ , (2012) STRUCTURES OF USHER SYNDROME 1 PROTEINS AND THEIR COMPLEXES.PHYSIOLOGY. VOL. 27. ISSUE 1. P. 25-42 83 67% 13

Classes with closest relation at Level 1


Rank Class id link
1 2508 GJB2//CONNEXIN 26//SLC26A4
2 6575 UNCONVENTIONAL MYOSIN//MYOSIN VI//MYOSIN I
3 4434 RETINITIS PIGMENTOSA//RPGR//AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA
4 1237 OUTER HAIR CELL//HEARING RESEARCH//ELECTROMOTILITY
5 14005 PRESBYCUSIS//AGE RELATED HEARING LOSS//PRESBYACUSIS
6 2816 HAIR CELL//HAIR CELL REGENERATION//INNER EAR
7 30188 TUBBY//TULP1//ORF PHAGE DISPLAY
8 23614 FASCIN//FASCIN 1//FSCN1
9 25093 CHOROIDEREMIA//POU3F4//CHM GENE
10 21001 WAARDENBURG SYNDROME//PAX3//KLEIN WAARDENBURG SYNDROME

Go to start page