Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
23243 | 298 | 25.0 | 67% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
2321 | 4046 | VELOCARDIOFACIAL SYNDROME//DIGEORGE SYNDROME//PSEUDOHYPOPARATHYROIDISM |
Terms with highest relevance score |
Rank | Term | Type of term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|---|
1 | HDR SYNDROME | Author keyword | 56 | 85% | 10% | 29 |
2 | KENNY CAFFEY SYNDROME | Author keyword | 17 | 100% | 3% | 8 |
3 | HYPOPARATHYROIDISM | Author keyword | 14 | 16% | 27% | 81 |
4 | GATA3 GENE | Author keyword | 9 | 83% | 2% | 5 |
5 | SANJAD SAKATI SYNDROME | Author keyword | 6 | 80% | 1% | 4 |
6 | PARATHYROID RELATED DISORDERS | Author keyword | 3 | 100% | 1% | 3 |
7 | DIHYDROTACHYSTEROL | Author keyword | 3 | 60% | 1% | 3 |
8 | RHPTH1 84 | Author keyword | 3 | 60% | 1% | 3 |
9 | FAMILIAL ISOLATED HYPOPARATHYROIDISM | Author keyword | 2 | 67% | 1% | 2 |
10 | KENNY CAFFEY | Author keyword | 1 | 100% | 1% | 2 |
Web of Science journal categories |
Author Key Words |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | HDR SYNDROME | 56 | 85% | 10% | 29 | Search HDR+SYNDROME | Search HDR+SYNDROME |
2 | KENNY CAFFEY SYNDROME | 17 | 100% | 3% | 8 | Search KENNY+CAFFEY+SYNDROME | Search KENNY+CAFFEY+SYNDROME |
3 | HYPOPARATHYROIDISM | 14 | 16% | 27% | 81 | Search HYPOPARATHYROIDISM | Search HYPOPARATHYROIDISM |
4 | GATA3 GENE | 9 | 83% | 2% | 5 | Search GATA3+GENE | Search GATA3+GENE |
5 | SANJAD SAKATI SYNDROME | 6 | 80% | 1% | 4 | Search SANJAD+SAKATI+SYNDROME | Search SANJAD+SAKATI+SYNDROME |
6 | PARATHYROID RELATED DISORDERS | 3 | 100% | 1% | 3 | Search PARATHYROID+RELATED+DISORDERS | Search PARATHYROID+RELATED+DISORDERS |
7 | DIHYDROTACHYSTEROL | 3 | 60% | 1% | 3 | Search DIHYDROTACHYSTEROL | Search DIHYDROTACHYSTEROL |
8 | RHPTH1 84 | 3 | 60% | 1% | 3 | Search RHPTH1+84 | Search RHPTH1+84 |
9 | FAMILIAL ISOLATED HYPOPARATHYROIDISM | 2 | 67% | 1% | 2 | Search FAMILIAL+ISOLATED+HYPOPARATHYROIDISM | Search FAMILIAL+ISOLATED+HYPOPARATHYROIDISM |
10 | KENNY CAFFEY | 1 | 100% | 1% | 2 | Search KENNY+CAFFEY | Search KENNY+CAFFEY |
Key Words Plus |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | CONGENITAL HYPOPARATHYROIDISM | 27 | 78% | 6% | 18 |
2 | RENAL DYSPLASIA SYNDROME | 19 | 76% | 4% | 13 |
3 | PTH1 84 | 19 | 74% | 5% | 14 |
4 | FAMILIAL HYPOPARATHYROIDISM | 14 | 100% | 2% | 7 |
5 | KENNY CAFFEY SYNDROME | 9 | 64% | 3% | 9 |
6 | GATA3 TRANSCRIPTION FACTOR | 8 | 100% | 2% | 5 |
7 | SEVERE GROWTH FAILURE | 7 | 67% | 2% | 6 |
8 | IDIOPATHIC HYPOPARATHYROIDISM | 5 | 24% | 7% | 20 |
9 | AUTOSOMAL RECESSIVE HYPOPARATHYROIDISM | 4 | 75% | 1% | 3 |
10 | TUBULAR STENOSIS | 4 | 75% | 1% | 3 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references |
% act. ref. to same field |
---|---|---|---|---|
Mini-review: new therapeutic options in hypoparathyroidism | 2012 | 6 | 18 | 83% |
Oral manifestations of patients with Kenny-Caffey Syndrome | 2012 | 2 | 18 | 94% |
THE SYNDROME OF HYPOPARATHYROIDISM, DEAFNESS, AND RENAL ANOMALIES | 2013 | 2 | 38 | 76% |
Use of parathyroid hormone in hypoparathyroidism | 2013 | 1 | 33 | 70% |
Recombinant Human Parathyroid Hormone (1-84): A Review in Hypoparathyroidism | 2015 | 0 | 23 | 83% |
Hypoparathyroidism: from diagnosis to treatment | 2012 | 6 | 26 | 42% |
Hypocalcemia Updates in diagnosis and management for primary care | 2012 | 10 | 40 | 30% |
Bone disease in hypoparathyroidism | 2014 | 0 | 23 | 61% |
PTH replacement therapy of hypoparathyroidism | 2013 | 3 | 46 | 35% |
Hypoparathyroidism-retardation-dysmorphism (HRD) syndrome - A review | 2004 | 7 | 34 | 56% |
Address terms |
Rank | Address term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | NUFFIELD MED ENDOCRINE UNIT | 1 | 50% | 0.7% | 2 |
2 | CHILDRENS MED NEPHROL SECT | 1 | 50% | 0.3% | 1 |
3 | DIAG THER Y PREVENT NEUROHANDIC | 1 | 50% | 0.3% | 1 |
4 | PEDIAT ENDOCRINOL METABOL UNIT | 1 | 50% | 0.3% | 1 |
5 | VISCERAL THORAC GEN SURG | 1 | 50% | 0.3% | 1 |
6 | VITAL IT HIGH PERFORMANCE COMP | 1 | 50% | 0.3% | 1 |
7 | ENDOCRINOLMETAB BONE DIS UNIT | 1 | 22% | 0.7% | 2 |
8 | THG | 0 | 11% | 1.3% | 4 |
9 | AIMS PONEKKARA | 0 | 33% | 0.3% | 1 |
10 | BOOALI GEN HOSP | 0 | 33% | 0.3% | 1 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000201614 | FAHRS DISEASE//BASAL GANGLIA CALCIFICATION//FAHRS SYNDROME |
2 | 0.0000160621 | PSEUDOHYPOPARATHYROIDISM//ALBRIGHT HEREDITARY OSTEODYSTROPHY//ALBRIGHTS HEREDITARY OSTEODYSTROPHY |
3 | 0.0000150391 | CALCIUM SENSING RECEPTOR//FAMILIAL HYPOCALCIURIC HYPERCALCEMIA//CASR |
4 | 0.0000114375 | MAMMAGLOBIN//MAMMAGLOBIN A//HUMAN MAMMAGLOBIN |
5 | 0.0000114075 | TERIPARATIDE//PTH//REG BONE |
6 | 0.0000107978 | VELOCARDIOFACIAL SYNDROME//DIGEORGE SYNDROME//VELO CARDIO FACIAL SYNDROME |
7 | 0.0000085610 | THYROID SURGERY//THYROIDECTOMY//RECURRENT LARYNGEAL NERVE |
8 | 0.0000085609 | FENOVERINE//IDIOPATHIC HYPER CK EMIA//HYPERCKEMIA |
9 | 0.0000085045 | IONIZED CALCIUM//ELECTROLYTE BALANCED HEPARIN//CORRECTION FORMULAE |
10 | 0.0000084606 | GLIAL CELLS MISSING//GLIDE GCM//NEURODEV GRP |