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