Class information for:
Level 2: GJB2//USHER SYNDROME//CONNEXIN 26

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
2453 4040 34.0 81%


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
2508 1                   GJB2//CONNEXIN 26//SLC26A4 2223
10225 1                   USHER SYNDROME//USH2A//MYO7A 1080
20771 1                   WOLFRAM SYNDROME//WFS1//DIDMOAD 446
25093 1                   CHOROIDEREMIA//POU3F4//CHM GENE 291

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 GJB2 authKW 1543809 6% 87% 234
2 USHER SYNDROME authKW 990290 4% 75% 174
3 CONNEXIN 26 authKW 913005 5% 60% 203
4 WOLFRAM SYNDROME authKW 834619 3% 85% 130
5 SLC26A4 authKW 695914 3% 84% 109
6 NON SYNDROMIC HEARING LOSS authKW 633223 2% 91% 92
7 DEAFNESS authKW 617501 10% 20% 419
8 PENDRED SYNDROME authKW 606955 2% 85% 94
9 WFS1 authKW 342337 1% 85% 53
10 GJB6 authKW 340527 1% 87% 52

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 Otorhinolaryngology 43843 22% 1% 895
2 Genetics & Heredity 30610 36% 0% 1472
3 Audiology & Speech-Language Pathology 4077 4% 0% 173
4 Ophthalmology 2465 7% 0% 292
5 Pediatrics 1115 7% 0% 270
6 Medicine, Research & Experimental 896 7% 0% 270
7 Biochemistry & Molecular Biology 850 16% 0% 658
8 Neurosciences 649 10% 0% 400
9 Cell Biology 406 7% 0% 291
10 Endocrinology & Metabolism 219 4% 0% 167

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 MOL OTOLARYNGOL S 288794 1% 67% 57
2 UNITE GENET DEFICITS SENSORIELS 223502 1% 53% 56
3 UNITE GENET PHYSIOL AUDIT 135722 1% 56% 32
4 HEARING IMPLANT SCI 113492 1% 58% 26
5 SECT HUMAN GENET 106831 1% 43% 33
6 OTOLARYNGOL BRANCH 102242 1% 44% 31
7 SECT GENE STRUCT FUNCT 102002 0% 75% 18
8 INTER PHD PROGRAM GENET 97995 1% 62% 21
9 CHINESE PEOPLES LIBERAT ARMY OTOLARYNGOL 90676 0% 100% 12
10 HEARING SECT 77366 0% 64% 16

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 INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY 30872 4% 2% 166
2 AUDIOLOGY AND NEURO-OTOLOGY 15226 1% 5% 41
3 HUMAN MOLECULAR GENETICS 13735 3% 1% 134
4 JOURNAL OF MEDICAL GENETICS 12659 2% 2% 99
5 CLINICAL GENETICS 12164 2% 2% 91
6 EUROPEAN JOURNAL OF HUMAN GENETICS 11223 2% 2% 74
7 GENETIC TESTING AND MOLECULAR BIOMARKERS 10595 1% 3% 41
8 HUMAN MUTATION 8957 2% 2% 69
9 AMERICAN JOURNAL OF HUMAN GENETICS 7823 2% 1% 92
10 JOURNAL OF HUMAN GENETICS 7782 1% 2% 49

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 GJB2 1543809 6% 87% 234 Search GJB2 Search GJB2
2 USHER SYNDROME 990290 4% 75% 174 Search USHER+SYNDROME Search USHER+SYNDROME
3 CONNEXIN 26 913005 5% 60% 203 Search CONNEXIN+26 Search CONNEXIN+26
4 WOLFRAM SYNDROME 834619 3% 85% 130 Search WOLFRAM+SYNDROME Search WOLFRAM+SYNDROME
5 SLC26A4 695914 3% 84% 109 Search SLC26A4 Search SLC26A4
6 NON SYNDROMIC HEARING LOSS 633223 2% 91% 92 Search NON+SYNDROMIC+HEARING+LOSS Search NON+SYNDROMIC+HEARING+LOSS
7 DEAFNESS 617501 10% 20% 419 Search DEAFNESS Search DEAFNESS
8 PENDRED SYNDROME 606955 2% 85% 94 Search PENDRED+SYNDROME Search PENDRED+SYNDROME
9 WFS1 342337 1% 85% 53 Search WFS1 Search WFS1
10 GJB6 340527 1% 87% 52 Search GJB6 Search GJB6

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 CHAN, DK , CHANG, KW , (2014) GJB2-ASSOCIATED HEARING LOSS: SYSTEMATIC REVIEW OF WORLDWIDE PREVALENCE, GENOTYPE, AND AUDITORY PHENOTYPE.LARYNGOSCOPE. VOL. 124. ISSUE 2. P. E34-E53 193 98% 29
2 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
3 PETERSEN, MB , WILLEMS, PJ , (2006) NON-SYNDROMIC, AUTOSOMAL-RECESSIVE DEAFNESS.CLINICAL GENETICS. VOL. 69. ISSUE 5. P. 371-392 190 81% 103
4 DUMAN, D , TEKIN, M , (2012) AUTOSOMAL RECESSIVE NONSYNDROMIC DEAFNESS GENES: A REVIEW.FRONTIERS IN BIOSCIENCE-LANDMARK. VOL. 17. ISSUE . P. 2213-2236 153 76% 31
5 FINSTERER, J , FELLINGER, J , (2005) NUCLEAR AND MITOCHONDRIAL GENES MUTATED IN NONSYNDROMIC IMPAIRED HEARING.INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY. VOL. 69. ISSUE 5. P. 621 -647 176 82% 28
6 DEL CASTILLO, FJ , DEL CASTILLO, I , (2011) THE DFNB1 SUBTYPE OF AUTOSOMAL RECESSIVE NON-SYNDROMIC HEARING IMPAIRMENT.FRONTIERS IN BIOSCIENCE-LANDMARK. VOL. 16. ISSUE . P. 3252 -3274 132 83% 15
7 OUYANG, XM , YAN, D , YUAN, HJ , PU, D , DU, LL , HAN, DY , LIU, XZ , (2009) THE GENETIC BASES FOR NON-SYNDROMIC HEARING LOSS AMONG CHINESE.JOURNAL OF HUMAN GENETICS. VOL. 54. ISSUE 3. P. 131-140 118 98% 18
8 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
9 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 95 90% 15
10 TSUKADA, K , NISHIO, S , HATTORI, M , USAMI, S , (2015) ETHNIC-SPECIFIC SPECTRUM OF GJB2 AND SLC26A4 MUTATIONS: THEIR ORIGIN AND A LITERATURE REVIEW.ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY. VOL. 124. ISSUE . P. 61S -76S 85 97% 5

Classes with closest relation at Level 2


Rank Class id link
1 132 HEARING RESEARCH//COCHLEA//TINNITUS
2 1822 GAP JUNCTION//CONNEXIN//CONNEXIN43
3 593 OTORHINOLARYNGOLOGY//OTOACOUSTIC EMISSIONS//AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY
4 266 RETINITIS PIGMENTOSA//OPHTHALMOLOGY//RETINA
5 381 MITOCHONDRIA//MELAS//MITOCHONDRIAL DISEASE
6 626 COCHLEAR IMPLANT//VESTIBULAR SCHWANNOMA//OTORHINOLARYNGOLOGY
7 1866 AMERICAN ANNALS OF THE DEAF//JOURNAL OF DEAF STUDIES AND DEAF EDUCATION//SIGN LANGUAGE
8 2417 HIRSCHSPRUNGS DISEASE//HIRSCHSPRUNG DISEASE//AGANGLIONOSIS
9 861 EPIDERMOLYSIS BULLOSA//INTERMEDIATE FILAMENTS//KERATIN
10 1456 Y CHROMOSOME//Y STR//HAPLOGROUP

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