Class information for:
Level 1: TRIPLE A SYNDROME//ALLGROVE SYNDROME//ALACRIMA

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
25883 269 24.0 75%


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
0 4 BIOCHEMISTRY & MOLECULAR BIOLOGY//CELL BIOLOGY//ONCOLOGY 4064930
633 3       TYROSINASE//MELANOGENESIS//PIGMENT CELL RESEARCH 12915
2294 2             MELANOCORTIN//MELANOCORTIN RECEPTOR//MELANOCORTIN 4 RECEPTOR 4561
25883 1                   TRIPLE A SYNDROME//ALLGROVE SYNDROME//ALACRIMA 269

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 TRIPLE A SYNDROME authKW 5457404 19% 96% 50
2 ALLGROVE SYNDROME authKW 3862630 13% 97% 35
3 ALACRIMA authKW 3391569 13% 85% 35
4 AAAS GENE authKW 1589197 5% 100% 14
5 FAMILIAL GLUCOCORTICOID DEFICIENCY authKW 1170980 5% 74% 14
6 ACTH RESISTANCE authKW 945947 4% 83% 10
7 GLUCOCORTICOID DEFICIENCY authKW 871984 5% 59% 13
8 ALACRIMIA authKW 807209 3% 89% 8
9 AAAS GENE MUTATION authKW 681084 2% 100% 6
10 ALADIN authKW 515962 4% 45% 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 Endocrinology & Metabolism 3313 43% 0% 115
2 Pediatrics 1444 26% 0% 69
3 Genetics & Heredity 233 13% 0% 36
4 Medicine, Research & Experimental 97 8% 0% 22
5 Gastroenterology & Hepatology 48 5% 0% 13
6 Clinical Neurology 43 7% 0% 19
7 Medical Ethics 36 1% 0% 2
8 Ophthalmology 9 2% 0% 6
9 Nutrition & Dietetics 6 2% 0% 5
10 Neurosciences 4 5% 0% 14

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 WILLIAM HARVEY ENDOCRINOL 151351 1% 67% 2
2 BARTS LONDON MED DENTJOHN VANE SCI 113514 0% 100% 1
3 BIOL INFORMAT AIST 113514 0% 100% 1
4 CELLULAR MOL SCREENING PROC 113514 0% 100% 1
5 FINE MORPHOL MINATO KU 113514 0% 100% 1
6 HEREDITARY DIS BRANCH 113514 0% 100% 1
7 IFR 162 113514 0% 100% 1
8 INSERM U449INRA UMR 1235 113514 0% 100% 1
9 INSERMUNITE RECH HANDIC S GENET 113514 0% 100% 1
10 LR1 1IPT05 113514 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 JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM 5367 5% 0% 13
2 HORMONE RESEARCH IN PAEDIATRICS 4947 2% 1% 6
3 HORMONE RESEARCH 2633 3% 0% 9
4 EUROPEAN JOURNAL OF PEDIATRICS 2570 5% 0% 13
5 JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM 2096 8% 0% 21
6 CLINICAL ENDOCRINOLOGY 1504 4% 0% 10
7 ENDOCRINE RESEARCH 1328 1% 0% 4
8 ENDOCRINE JOURNAL 977 2% 0% 5
9 ANNALES D ENDOCRINOLOGIE 880 1% 0% 4
10 EUROPEAN JOURNAL OF ENDOCRINOLOGY 781 2% 0% 6

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 TRIPLE A SYNDROME 5457404 19% 96% 50 Search TRIPLE+A+SYNDROME Search TRIPLE+A+SYNDROME
2 ALLGROVE SYNDROME 3862630 13% 97% 35 Search ALLGROVE+SYNDROME Search ALLGROVE+SYNDROME
3 ALACRIMA 3391569 13% 85% 35 Search ALACRIMA Search ALACRIMA
4 AAAS GENE 1589197 5% 100% 14 Search AAAS+GENE Search AAAS+GENE
5 FAMILIAL GLUCOCORTICOID DEFICIENCY 1170980 5% 74% 14 Search FAMILIAL+GLUCOCORTICOID+DEFICIENCY Search FAMILIAL+GLUCOCORTICOID+DEFICIENCY
6 ACTH RESISTANCE 945947 4% 83% 10 Search ACTH+RESISTANCE Search ACTH+RESISTANCE
7 GLUCOCORTICOID DEFICIENCY 871984 5% 59% 13 Search GLUCOCORTICOID+DEFICIENCY Search GLUCOCORTICOID+DEFICIENCY
8 ALACRIMIA 807209 3% 89% 8 Search ALACRIMIA Search ALACRIMIA
9 AAAS GENE MUTATION 681084 2% 100% 6 Search AAAS+GENE+MUTATION Search AAAS+GENE+MUTATION
10 ALADIN 515962 4% 45% 10 Search ALADIN Search ALADIN

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 ELIAS, LLK , CLARK, AJL , (2009) THE MOLECULAR BASIS OF ADRENOCORTICOTROPHIN RESISTANCE SYNDROME.G PROTEIN-COUPLED RECEPTORS IN HEALTH AND DISEASE, PT A. VOL. 88. ISSUE . P. 155 -171 59 66% 1
2 SARATHI, V , SHAH, NS , (2010) TRIPLE-A SYNDROME.DISEASES OF DNA REPAIR. VOL. 685. ISSUE . P. 1 -8 39 89% 10
3 DUMIC, M , BARISIC, N , ROJNIC-PUTAREK, N , KUSEC, V , STANIMIROVIC, A , KOEHLER, K , HUEBNER, A , (2011) TWO SIBLINGS WITH TRIPLE A SYNDROME AND NOVEL MUTATION PRESENTING AS HEREDITARY POLYNEUROPATHY.EUROPEAN JOURNAL OF PEDIATRICS. VOL. 170. ISSUE 3. P. 393 -396 25 96% 8
4 RUDENSKAYA, GE , ZAKHAROVA, EY , KAREVA, MA , (2013) NEUROLOGICAL PRESENTATIONS OF ALLGROVE (AAA) SYNDROME.ZHURNAL NEVROLOGII I PSIKHIATRII IMENI S S KORSAKOVA. VOL. 113. ISSUE 4. P. 70-74 23 100% 0
5 VALLET, AE , VERSCHUEREN, A , PETIOT, P , VANDENBERGHE, N , NICOLINO, M , ROMAN, S , POUGET, J , VIAL, C , (2012) NEUROLOGICAL FEATURES IN ADULT TRIPLE-A (ALLGROVE) SYNDROME.JOURNAL OF NEUROLOGY. VOL. 259. ISSUE 1. P. 39-46 22 100% 13
6 DUMIC, M , BARISIC, N , KUSEC, V , STINGL, K , SKEGRO, M , STANIMIROVIC, A , KOEHLER, K , HUEBNER, A , (2012) LONG-TERM CLINICAL FOLLOW-UP AND MOLECULAR GENETIC FINDINGS IN EIGHT PATIENTS WITH TRIPLE A SYNDROME.EUROPEAN JOURNAL OF PEDIATRICS. VOL. 171. ISSUE 10. P. 1453 -1459 22 92% 5
7 BROOKS, BP , KLETA, R , STUART, C , TUCHMAN, M , JEONG, A , STERGIOPOULOS, SG , BEI, T , BJORNSON, B , RUSSELL, L , CHANOINE, JP , ET AL (2005) GENOTYPIC HETEROGENEITY AND CLINICAL PHENOTYPE IN TRIPLE A SYNDROME: A REVIEW OF THE NIH EXPERIENCE 2000-2005.CLINICAL GENETICS. VOL. 68. ISSUE 3. P. 215-221 25 89% 36
8 LI, WJ , GONG, CX , QI, Z , WU, D , CAO, BY , (2015) IDENTIFICATION OF AAAS GENE MUTATION IN ALLGROVE SYNDROME: A REPORT OF THREE CASES.EXPERIMENTAL AND THERAPEUTIC MEDICINE. VOL. 10. ISSUE 4. P. 1277 -1282 20 91% 0
9 RAZAVI, Z , TAGHDIRI, MM , EGHBALIAN, F , BAZZAZI, N , (2010) PREMATURE LOSS OF PERMANENT TEETH IN ALLGROVE (4A) SYNDROME IN TWO RELATED FAMILIES.IRANIAN JOURNAL OF PEDIATRICS. VOL. 20. ISSUE 1. P. 101 -106 20 100% 2
10 NAVILLE, D , PENHOAT, A , BEGEOT, M , (2000) ACTH RESISTANCE SYNDROMES.ANNALES D ENDOCRINOLOGIE. VOL. 61. ISSUE 5. P. 428 -439 38 69% 1

Classes with closest relation at Level 1


Rank Class id link
1 2515 MELANOCORTIN//MELANOCORTIN RECEPTOR//MELANOCORTIN 4 RECEPTOR
2 3911 ACHALASIA//HELLER MYOTOMY//ESOPHAGEAL ACHALASIA
3 24145 TRANSHYDROGENASE//NICOTINAMIDE NUCLEOTIDE//NICOTINAMIDE NUCLEOTIDE TRANSHYDROGENASE
4 8257 STEROIDOGENIC FACTOR 1//ADRENAL HYPOPLASIA CONGENITA//SF 1
5 11907 GLOMERULOSA CELLS//ALDOSTERONE SECRETION//ADRENAL GLOMERULOSA
6 11660 ADRENAL INSUFFICIENCY//ADDISONS DISEASE//ADRENAL CRISIS
7 10728 STEROIDOGENIC ACUTE REGULATORY PROTEIN//STAR//STEROIDOGENIC ACUTE REGULATORY PROTEIN STAR
8 17969 SEPTO OPTIC DYSPLASIA//SEPTUM PELLUCIDUM//OPTIC NERVE HYPOPLASIA
9 37008 BARNACLE FIBER//SODIUM ION EFFLUX//5 GUANYLYL IMIDODIPHOSPHATE
10 22205 RACK1//EIF6//RECEPTOR FOR ACTIVATED C KINASE 1 RACK1

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