Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
15734 | 625 | 20.3 | 60% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
1680 | 6226 | MARFAN SYNDROME//FIBRILLIN//LYSYL OXIDASE |
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 | CUTIS LAXA | Author keyword | 39 | 54% | 8% | 50 |
2 | MID DERMAL ELASTOLYSIS | Author keyword | 32 | 88% | 2% | 15 |
3 | ANNULAR ELASTOLYTIC GIANT CELL GRANULOMA | Author keyword | 21 | 78% | 2% | 14 |
4 | ANETODERMA | Author keyword | 21 | 57% | 4% | 25 |
5 | ACTINIC GRANULOMA | Author keyword | 19 | 80% | 2% | 12 |
6 | ELASTOPHAGOCYTOSIS | Author keyword | 19 | 80% | 2% | 12 |
7 | ELASTOLYSIS | Author keyword | 17 | 51% | 4% | 24 |
8 | DE BARSY SYNDROME | Author keyword | 15 | 88% | 1% | 7 |
9 | ARTERIAL TORTUOSITY SYNDROME | Author keyword | 15 | 73% | 2% | 11 |
10 | AUTOSOMAL RECESSIVE CUTIS LAXA | Author keyword | 14 | 100% | 1% | 7 |
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 | CUTIS LAXA | 39 | 54% | 8% | 50 | Search CUTIS+LAXA | Search CUTIS+LAXA |
2 | MID DERMAL ELASTOLYSIS | 32 | 88% | 2% | 15 | Search MID+DERMAL+ELASTOLYSIS | Search MID+DERMAL+ELASTOLYSIS |
3 | ANNULAR ELASTOLYTIC GIANT CELL GRANULOMA | 21 | 78% | 2% | 14 | Search ANNULAR+ELASTOLYTIC+GIANT+CELL+GRANULOMA | Search ANNULAR+ELASTOLYTIC+GIANT+CELL+GRANULOMA |
4 | ANETODERMA | 21 | 57% | 4% | 25 | Search ANETODERMA | Search ANETODERMA |
5 | ACTINIC GRANULOMA | 19 | 80% | 2% | 12 | Search ACTINIC+GRANULOMA | Search ACTINIC+GRANULOMA |
6 | ELASTOPHAGOCYTOSIS | 19 | 80% | 2% | 12 | Search ELASTOPHAGOCYTOSIS | Search ELASTOPHAGOCYTOSIS |
7 | ELASTOLYSIS | 17 | 51% | 4% | 24 | Search ELASTOLYSIS | Search ELASTOLYSIS |
8 | DE BARSY SYNDROME | 15 | 88% | 1% | 7 | Search DE+BARSY+SYNDROME | Search DE+BARSY+SYNDROME |
9 | ARTERIAL TORTUOSITY SYNDROME | 15 | 73% | 2% | 11 | Search ARTERIAL+TORTUOSITY+SYNDROME | Search ARTERIAL+TORTUOSITY+SYNDROME |
10 | AUTOSOMAL RECESSIVE CUTIS LAXA | 14 | 100% | 1% | 7 | Search AUTOSOMAL+RECESSIVE+CUTIS+LAXA | Search AUTOSOMAL+RECESSIVE+CUTIS+LAXA |
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 | MIDDERMAL ELASTOLYSIS | 57 | 95% | 3% | 19 |
2 | GENERALIZED ELASTOLYSIS | 41 | 90% | 3% | 18 |
3 | WHITE FIBROUS PAPULOSIS | 38 | 93% | 2% | 14 |
4 | ACTINIC GRANULOMA | 20 | 58% | 4% | 23 |
5 | MID DERMAL ELASTOLYSIS | 19 | 74% | 2% | 14 |
6 | WRINKLY SKIN SYNDROME | 17 | 68% | 2% | 15 |
7 | POSTINFLAMMATORY ELASTOLYSIS | 17 | 100% | 1% | 8 |
8 | REDUCED ORNITHINE | 13 | 69% | 2% | 11 |
9 | ENCODING DELTA1 PYRROLINE 5 CARBOXYLATE SYNTHASE | 12 | 63% | 2% | 12 |
10 | BARSY SYNDROME | 11 | 100% | 1% | 6 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Mid-dermal elastolysis revisited | 2010 | 17 | 60 | 82% |
Elastophagocytosis: Underlying mechanisms and associated cutaneous entities | 2014 | 4 | 56 | 48% |
Acquired disorders of elastic tissue: Part II. Decreased elastic tissue | 2004 | 63 | 113 | 65% |
Anetoderma associated with antiphospholipid antibodies: case report and review of the literature | 2001 | 15 | 14 | 100% |
Cutis laxa: Intersection of elastic fiber biogenesis, TGF beta signaling, the secretory pathway and metabolism | 2014 | 4 | 89 | 34% |
Cutis laxa, fat pads and retinopathy due to ALDH18A1 mutation and review of the literature | 2014 | 2 | 16 | 50% |
Cardiovascular findings in a boy with arterial tortuosity syndrome: case report and review of the literature | 2011 | 3 | 6 | 100% |
De Barsy syndrome: a review of the phenotype | 2008 | 17 | 16 | 81% |
Primary anetoderma and antiphospholipid antibodies - Review of the literature | 2007 | 13 | 20 | 80% |
The utility of elastic Verhoeff-Van Gieson staining in dermatopathology | 2013 | 4 | 55 | 40% |
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 | SECT CLIN GENET DYSMORPHOL | 2 | 43% | 0.5% | 3 |
2 | EM CORE IL | 1 | 40% | 0.3% | 2 |
3 | FG DEV DIS | 1 | 20% | 0.6% | 4 |
4 | DERMATOL OUT PATIENT CLIN | 1 | 33% | 0.3% | 2 |
5 | CLIN GENET OBSTET GYNECOL | 1 | 50% | 0.2% | 1 |
6 | DALMIA OPHTHALM PATHOL SERV | 1 | 50% | 0.2% | 1 |
7 | HEMATOLSERV HEMATOL | 1 | 50% | 0.2% | 1 |
8 | HOP NECKER ENFANTS MALADINSERMU781 | 1 | 50% | 0.2% | 1 |
9 | HOSP CRIANCAS MARIA PIA | 1 | 50% | 0.2% | 1 |
10 | MED GENET CHARITE | 1 | 50% | 0.2% | 1 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000216019 | FIBULIN 1//EFEMP1//FIBULIN 3 |
2 | 0.0000111964 | REACTIVE PERFORATING COLLAGENOSIS//ELASTOSIS PERFORANS SERPIGINOSA//ACQUIRED PERFORATING DERMATOSIS |
3 | 0.0000086797 | GRANULOMA ANNULARE//NECROBIOSIS LIPOIDICA//SUBCUTANEOUS GRANULOMA ANNULARE |
4 | 0.0000084515 | PSEUDOXANTHOMA ELASTICUM//ANGIOID STREAKS//ABCC6 |
5 | 0.0000069912 | ISODESMOSINE//ELASTIN LAMININ RECEPTOR//DESMOSINE |
6 | 0.0000069340 | MELORHEOSTOSIS//OSTEOPOIKILOSIS//CRANIAL SCLEROSIS |
7 | 0.0000065862 | HYPERKERATOSIS LENTICULARIS PERSTANS//AQUAGENIC PALMOPLANTAR KERATODERMA//FLEGELS DISEASE |
8 | 0.0000061540 | ALLERGIC CONTACT CHEILITIS//ASCHER SYNDROME//CHEILITIS GLANDULARIS |
9 | 0.0000061463 | EHLERS DANLOS SYNDROME//EHLERS DANLOS SYNDROME TYPE IV//JOINT HYPERMOBILITY |
10 | 0.0000061096 | CONGENITAL DISORDERS OF GLYCOSYLATION//CARBOHYDRATE DEFICIENT GLYCOPROTEIN SYNDROME//CDG |