Class information for:
Level 1: GJB2//CONNEXIN 26//SLC26A4

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
2508 2223 33.3 84%


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

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 2782111 10% 87% 233
2 CONNEXIN 26 authKW 1643281 9% 59% 202
3 SLC26A4 authKW 1264907 5% 84% 109
4 PENDRED SYNDROME authKW 1103213 4% 85% 94
5 NON SYNDROMIC HEARING LOSS authKW 914321 4% 81% 82
6 DEAFNESS authKW 650723 14% 15% 319
7 GJB6 authKW 618946 2% 87% 52
8 DFNB1 authKW 494795 2% 97% 37
9 HEREDITARY HEARING LOSS authKW 463900 2% 66% 51
10 DFNA9 authKW 453232 1% 100% 33

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 47481 31% 1% 687
2 Genetics & Heredity 20649 40% 0% 893
3 Audiology & Speech-Language Pathology 3688 5% 0% 121
4 Pediatrics 1134 9% 0% 193
5 Medicine, Research & Experimental 735 8% 0% 175
6 Biochemistry & Molecular Biology 274 14% 0% 306
7 Neurosciences 141 7% 0% 163
8 Cell Biology 107 6% 0% 127
9 Biophysics 87 3% 0% 76
10 Endocrinology & Metabolism 57 3% 0% 73

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 372239 2% 56% 48
2 UNITE GENET DEFICITS SENSORIELS 158675 2% 33% 35
3 INTER PHD PROGRAM GENET 145809 1% 56% 19
4 OTOLARYNGOL BRANCH 140985 1% 38% 27
5 CHINESE PEOPLES LIBERAT ARMY OTOLARYNGOL 138486 0% 92% 11
6 UNIDAD GENET MOL 101481 1% 24% 31
7 MOL OTOLARYNGOL RENAL S 80982 1% 35% 17
8 HEARING DEAFNESS 78709 2% 13% 45
9 HEARING IMPLANT SCI 78112 1% 36% 16
10 OTOLARYNGOL 74916 20% 1% 443

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 44175 7% 2% 147
2 GENETIC TESTING AND MOLECULAR BIOMARKERS 19322 2% 3% 41
3 AUDIOLOGY AND NEURO-OTOLOGY 15842 1% 4% 31
4 GENETIC TESTING 11255 1% 4% 23
5 JOURNAL OF MEDICAL GENETICS 10568 3% 1% 67
6 EUROPEAN JOURNAL OF HUMAN GENETICS 10495 2% 1% 53
7 CLINICAL GENETICS 9314 3% 1% 59
8 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 8488 3% 1% 60
9 JOURNAL OF HUMAN GENETICS 7658 2% 2% 36
10 GENETICS IN MEDICINE 7117 1% 2% 29

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 2782111 10% 87% 233 Search GJB2 Search GJB2
2 CONNEXIN 26 1643281 9% 59% 202 Search CONNEXIN+26 Search CONNEXIN+26
3 SLC26A4 1264907 5% 84% 109 Search SLC26A4 Search SLC26A4
4 PENDRED SYNDROME 1103213 4% 85% 94 Search PENDRED+SYNDROME Search PENDRED+SYNDROME
5 NON SYNDROMIC HEARING LOSS 914321 4% 81% 82 Search NON+SYNDROMIC+HEARING+LOSS Search NON+SYNDROMIC+HEARING+LOSS
6 DEAFNESS 650723 14% 15% 319 Search DEAFNESS Search DEAFNESS
7 GJB6 618946 2% 87% 52 Search GJB6 Search GJB6
8 DFNB1 494795 2% 97% 37 Search DFNB1 Search DFNB1
9 HEREDITARY HEARING LOSS 463900 2% 66% 51 Search HEREDITARY+HEARING+LOSS Search HEREDITARY+HEARING+LOSS
10 DFNA9 453232 1% 100% 33 Search DFNA9 Search DFNA9

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 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
3 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. 131-140 114 94% 18
4 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
5 PETERSEN, MB , WILLEMS, PJ , (2006) NON-SYNDROMIC, AUTOSOMAL-RECESSIVE DEAFNESS.CLINICAL GENETICS. VOL. 69. ISSUE 5. P. 371-392 142 61% 103
6 BARASHKOV, NA , PSHENNIKOVA, VG , POSUKH, OL , TERYUTIN, FM , SOLOVYEV, AV , KLAROV, LA , ROMANOV, GP , GOTOVTSEV, NN , KOZHEVNIKOV, AA , KIRILLINA, EV , ET AL (2016) SPECTRUM AND FREQUENCY OF THE GJB2 GENE PATHOGENIC VARIANTS IN A LARGE COHORT OF PATIENTS WITH HEARING IMPAIRMENT LIVING IN A SUBARCTIC REGION OF RUSSIA (THE SAKHA REPUBLIC).PLOS ONE. VOL. 11. ISSUE 5. P. - 75 96% 0
7 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 -647 139 65% 28
8 BARBARINO, JM , MCGREGOR, TL , ALTMAN, RB , KLEIN, TE , (2016) PHARMGKB SUMMARY: VERY IMPORTANT PHARMACOGENE INFORMATION FOR MT-RNR1.PHARMACOGENETICS AND GENOMICS. VOL. 26. ISSUE 12. P. 558 -567 84 79% 0
9 VONA, B , NANDA, I , HOFRICHTER, MAH , SHEHATA-DIELER, W , HAAF, T , (2015) NON-SYNDROMIC HEARING LOSS GENE IDENTIFICATION: A BRIEF HISTORY AND GLIMPSE INTO THE FUTURE.MOLECULAR AND CELLULAR PROBES. VOL. 29. ISSUE 5. P. 260 -270 102 63% 3
10 MAHDIEH, N , RABBANI, B , WILEY, S , AKBARI, MT , ZEINALI, S , (2010) GENETIC CAUSES OF NONSYNDROMIC HEARING LOSS IN IRAN IN COMPARISON WITH OTHER POPULATIONS.JOURNAL OF HUMAN GENETICS. VOL. 55. ISSUE 10. P. 639 -648 78 82% 9

Classes with closest relation at Level 1


Rank Class id link
1 10225 USHER SYNDROME//USH2A//MYO7A
2 24707 AUDITORY NEUROPATHY//AUDITORY NEUROPATHY SPECTRUM DISORDER//AUDITORY DYS SYNCHRONY
3 14769 KID SYNDROME//MAL DE MELEDA//PALMOPLANTAR KERATODERMA
4 25093 CHOROIDEREMIA//POU3F4//CHM GENE
5 5523 NEWBORN HEARING SCREENING//HEARING SCREENING//UNIVERSAL NEWBORN HEARING SCREENING
6 9146 STRIA VASCULARIS//ENDOLYMPH//MARGINAL CELL
7 14005 PRESBYCUSIS//AGE RELATED HEARING LOSS//PRESBYACUSIS
8 7466 AUDITORY BRAINSTEM IMPLANT//INNER EAR MALFORMATION//LARGE VESTIBULAR AQUEDUCT SYNDROME
9 20771 WOLFRAM SYNDROME//WFS1//DIDMOAD
10 21001 WAARDENBURG SYNDROME//PAX3//KLEIN WAARDENBURG SYNDROME

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