Class information for:
Level 1: WOLFRAM SYNDROME//WFS1//DIDMOAD

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
20771 446 31.8 78%


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
20771 1                   WOLFRAM SYNDROME//WFS1//DIDMOAD 446

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 WOLFRAM SYNDROME authKW 7446424 29% 84% 129
2 WFS1 authKW 2872156 11% 82% 51
3 DIDMOAD authKW 2003055 7% 91% 32
4 WFS1 GENE authKW 1574671 5% 100% 23
5 WOLFRAMIN authKW 1516737 5% 92% 24
6 MITONEET authKW 503050 3% 57% 13
7 DIDMOAD SYNDROME authKW 479248 2% 100% 7
8 DFNA6 14 38 authKW 410784 1% 100% 6
9 CISD2 authKW 398332 2% 73% 8
10 CISD1 authKW 308085 1% 75% 6

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 1313 23% 0% 104
2 Endocrinology & Metabolism 1189 21% 0% 92
3 Ophthalmology 326 8% 0% 35
4 Pediatrics 231 9% 0% 39
5 Biochemistry & Molecular Biology 202 21% 0% 95
6 Neurosciences 80 10% 0% 46
7 Medicine, Research & Experimental 77 6% 0% 27
8 Otorhinolaryngology 63 3% 0% 13
9 Medicine, General & Internal 48 7% 0% 29
10 Cell Biology 26 6% 0% 27

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 METAB DIABET LIPID 136928 0% 100% 2
2 ENDOCRINOL METAB HEMATOL SCI THER EUT 117358 1% 29% 6
3 NUTR METAB DIS ENDOCRINOL 100675 1% 29% 5
4 SOCIAL GENET DEV PSYCHIAT PO82 91284 0% 67% 2
5 MOL METAB DIABET 78223 3% 10% 12
6 WOLFSON PL STRUCT BIOL 77112 3% 9% 13
7 ATAXIA UNITCOGNIT BEHAV NEUROL UNIT MED 68464 0% 100% 1
8 ATENC INTEGRAL PACIENTE CON DIABET 68464 0% 100% 1
9 AUDIOL DISABIL SIDR 68464 0% 100% 1
10 CLIN MED CLIN GENET 68464 0% 100% 1

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 HUMAN MOLECULAR GENETICS 2007 4% 0% 17
2 OPHTHALMIC PAEDIATRICS AND GENETICS 1616 1% 1% 3
3 INTERNATIONAL JOURNAL OF DIABETES IN DEVELOPING COUNTRIES 1424 1% 1% 3
4 JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM 1216 2% 0% 8
5 ENDOKRYNOLOGIA POLSKA 1069 1% 1% 3
6 OPHTHALMIC GENETICS 1026 1% 1% 3
7 ORPHANET JOURNAL OF RARE DISEASES 979 1% 0% 4
8 BMC MEDICAL GENETICS 750 1% 0% 4
9 ACTA DIABETOLOGICA LATINA 621 0% 0% 2
10 DIABETES CARE 585 2% 0% 10

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 WOLFRAM SYNDROME 7446424 29% 84% 129 Search WOLFRAM+SYNDROME Search WOLFRAM+SYNDROME
2 WFS1 2872156 11% 82% 51 Search WFS1 Search WFS1
3 DIDMOAD 2003055 7% 91% 32 Search DIDMOAD Search DIDMOAD
4 WFS1 GENE 1574671 5% 100% 23 Search WFS1+GENE Search WFS1+GENE
5 WOLFRAMIN 1516737 5% 92% 24 Search WOLFRAMIN Search WOLFRAMIN
6 MITONEET 503050 3% 57% 13 Search MITONEET Search MITONEET
7 DIDMOAD SYNDROME 479248 2% 100% 7 Search DIDMOAD+SYNDROME Search DIDMOAD+SYNDROME
8 DFNA6 14 38 410784 1% 100% 6 Search DFNA6+14+38 Search DFNA6+14+38
9 CISD2 398332 2% 73% 8 Search CISD2 Search CISD2
10 CISD1 308085 1% 75% 6 Search CISD1 Search CISD1

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 KUMAR, S , (2010) WOLFRAM SYNDROME: IMPORTANT IMPLICATIONS FOR PEDIATRICIANS AND PEDIATRIC ENDOCRINOLOGISTS.PEDIATRIC DIABETES. VOL. 11. ISSUE 1. P. 28 -37 95 92% 25
2 RIGOLI, L , LOMBARDO, F , DI BELLA, C , (2011) WOLFRAM SYNDROME AND WFS1 GENE.CLINICAL GENETICS. VOL. 79. ISSUE 2. P. 103-117 89 89% 33
3 MATHIS, S , PAQUIS, V , MESNAGE, V , BALABOI, I , GIL, R , GILBERT, B , NEAU, JP , (2007) WOLFRAM'S SYNDROME PRESENTING AS A CEREBELLAR ATAXIA..REVUE NEUROLOGIQUE. VOL. 163. ISSUE 2. P. 197-204 51 85% 5
4 URANO, F , (2016) WOLFRAM SYNDROME: DIAGNOSIS, MANAGEMENT, AND TREATMENT.CURRENT DIABETES REPORTS. VOL. 16. ISSUE 1. P. - 31 76% 6
5 CRYNS, K , SIVAKUMARAN, TA , VAN DEN OUWELAND, JMW , PENNINGS, RJE , CREMERS, CWRJ , FLOTHMANN, K , YOUNG, TL , SMITH, RJH , LESPERANCE, MM , VAN CAMP, G , (2003) MUTATIONAL SPECTRUM OF THE WFS1 GENE IN WOLFRAM SYNDROME, NONSYNDROMIC HEARING IMPAIRMENT, DIABETES MELLITUS, AND PSYCHIATRIC DISEASE.HUMAN MUTATION. VOL. 22. ISSUE 4. P. 275-287 42 93% 80
6 ALOI, C , SALINA, A , PASQUALI, L , LUGANI, F , PERRI, K , RUSSO, C , TALLONE, R , GHIGGERI, GM , LORINI, R , D'ANNUNZIO, G , (2012) WOLFRAM SYNDROME: NEW MUTATIONS, DIFFERENT PHENOTYPE.PLOS ONE. VOL. 7. ISSUE 1. P. - 35 92% 13
7 QIAN, XL , QIN, LY , XING, GQ , CAO, X , (2015) PHENOTYPE PREDICTION OF PATHOGENIC NONSYNONYMOUS SINGLE NUCLEOTIDE POLYMORPHISMS IN WFS1.SCIENTIFIC REPORTS. VOL. 5. ISSUE . P. - 39 76% 3
8 RIGOLI, L , DI BELLA, C , (2012) WOLFRAM SYNDROME 1 AND WOLFRAM SYNDROME 2.CURRENT OPINION IN PEDIATRICS. VOL. 24. ISSUE 4. P. 512-517 35 85% 27
9 BOUTZIOS, G , LIVADAS, S , MARINAKIS, E , OPIE, N , ECONOMOU, F , DIAMANTI-KANDARAKIS, E , (2011) ENDOCRINE AND METABOLIC ASPECTS OF THE WOLFRAM SYNDROME.ENDOCRINE. VOL. 40. ISSUE 1. P. 10-13 30 97% 6
10 TAMIR, S , PADDOCK, ML , DARASH-YAHANA-BARAM, M , HOLT, SH , SOHN, YS , AGRANAT, L , MICHAELI, D , STOFLETH, JT , LIPPER, CH , MORCOS, F , ET AL (2015) STRUCTURE-FUNCTION ANALYSIS OF NEET PROTEINS UNCOVERS THEIR ROLE AS KEY REGULATORS OF IRON AND ROS HOMEOSTASIS IN HEALTH AND DISEASE.BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH. VOL. 1853. ISSUE 6. P. 1294 -1315 48 46% 11

Classes with closest relation at Level 1


Rank Class id link
1 32237 ALSTROM SYNDROME//ALMS1//ALMS1 GENE
2 2508 GJB2//CONNEXIN 26//SLC26A4
3 9055 LEBERS HEREDITARY OPTIC NEUROPATHY//LHON//LEBER HEREDITARY OPTIC NEUROPATHY
4 21807 BENFOTIAMINE//SLC19A2//SLC19A3
5 415 UNFOLDED PROTEIN RESPONSE//ENDOPLASMIC RETICULUM STRESS//ER STRESS
6 16491 NEONATAL DIABETES//NEONATAL DIABETES MELLITUS//WOLCOTT RALLISON SYNDROME
7 5860 TCF7L2//SLC30A8//CDKAL1
8 15479 DIABETES INSIPIDUS//CENTRAL DIABETES INSIPIDUS//ADIPSIA
9 3134 FRATAXIN//FRIEDREICHS ATAXIA//FRIEDREICH ATAXIA
10 26631 C10ORF70//INVEST BIOQUIM BUENOS AI BIOL CELULA//MITOCHONDRIAL EXPRESSED GENES

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