Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
14769 | 751 | 24.5 | 60% |
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 |
336 | 3 | DERMATOLOGY//BEHCETS DISEASE//DERMATOL | 37504 |
861 | 2 | EPIDERMOLYSIS BULLOSA//INTERMEDIATE FILAMENTS//KERATIN | 11606 |
14769 | 1 | KID SYNDROME//MAL DE MELEDA//PALMOPLANTAR KERATODERMA | 751 |
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 | KID SYNDROME | authKW | 896173 | 3% | 96% | 23 |
2 | MAL DE MELEDA | authKW | 853823 | 3% | 100% | 21 |
3 | PALMOPLANTAR KERATODERMA | authKW | 553824 | 5% | 36% | 38 |
4 | ERYTHROKERATODERMIA VARIABILIS | authKW | 458079 | 2% | 87% | 13 |
5 | KERATITIS ICHTHYOSIS DEAFNESS SYNDROME | authKW | 406582 | 1% | 100% | 10 |
6 | CLOUSTON SYNDROME | authKW | 365918 | 2% | 75% | 12 |
7 | VOHWINKEL SYNDROME | authKW | 329330 | 1% | 90% | 9 |
8 | ERYTHROKERATODERMA | authKW | 312751 | 1% | 77% | 10 |
9 | AINHUM | authKW | 299389 | 1% | 82% | 9 |
10 | HIDROTIC ECTODERMAL DYSPLASIA | authKW | 274438 | 1% | 75% | 9 |
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 | Dermatology | 50284 | 62% | 0% | 464 |
2 | Genetics & Heredity | 750 | 14% | 0% | 107 |
3 | Pediatrics | 142 | 6% | 0% | 43 |
4 | Otorhinolaryngology | 29 | 2% | 0% | 13 |
5 | Mycology | 28 | 1% | 0% | 7 |
6 | MEDICINE, MISCELLANEOUS | 24 | 0% | 0% | 1 |
7 | Ophthalmology | 18 | 2% | 0% | 15 |
8 | Pathology | 12 | 2% | 0% | 14 |
9 | Medicine, General & Internal | 6 | 3% | 0% | 24 |
10 | Dentistry, Oral Surgery & Medicine | 4 | 1% | 0% | 9 |
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 | RARE GENET SKIN DIS | 81316 | 0% | 100% | 2 |
2 | DERMATOGENET UNIT | 73182 | 0% | 60% | 3 |
3 | CUTANEOUS | 70708 | 3% | 7% | 24 |
4 | GENET STUDIES SECT | 54206 | 1% | 33% | 4 |
5 | AF HP | 40658 | 0% | 100% | 1 |
6 | BERNSTEIN COMPUTAT NEUROSCI MED | 40658 | 0% | 100% | 1 |
7 | BIOCHEM DRUG DISCOVERY | 40658 | 0% | 100% | 1 |
8 | BIOCHIM INSERM U587SERV GENET MED | 40658 | 0% | 100% | 1 |
9 | BIOCHIM INSERM U587SERV ORL | 40658 | 0% | 100% | 1 |
10 | BT 437 | 40658 | 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 | DERMATOLOGICA | 13698 | 3% | 1% | 23 |
2 | PEDIATRIC DERMATOLOGY | 9232 | 4% | 1% | 29 |
3 | BRITISH JOURNAL OF DERMATOLOGY | 9189 | 7% | 0% | 50 |
4 | ACTA DERMATO-VENEREOLOGICA | 7689 | 4% | 1% | 29 |
5 | INTERNATIONAL JOURNAL OF DERMATOLOGY | 6045 | 4% | 0% | 33 |
6 | HAUTARZT | 5719 | 3% | 1% | 26 |
7 | JOURNAL OF INVESTIGATIVE DERMATOLOGY | 4423 | 5% | 0% | 34 |
8 | CLINICAL AND EXPERIMENTAL DERMATOLOGY | 3943 | 3% | 0% | 22 |
9 | MYKOSEN | 3682 | 1% | 1% | 7 |
10 | JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY | 3594 | 4% | 0% | 33 |
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 | KID SYNDROME | 896173 | 3% | 96% | 23 | Search KID+SYNDROME | Search KID+SYNDROME |
2 | MAL DE MELEDA | 853823 | 3% | 100% | 21 | Search MAL+DE+MELEDA | Search MAL+DE+MELEDA |
3 | PALMOPLANTAR KERATODERMA | 553824 | 5% | 36% | 38 | Search PALMOPLANTAR+KERATODERMA | Search PALMOPLANTAR+KERATODERMA |
4 | ERYTHROKERATODERMIA VARIABILIS | 458079 | 2% | 87% | 13 | Search ERYTHROKERATODERMIA+VARIABILIS | Search ERYTHROKERATODERMIA+VARIABILIS |
5 | KERATITIS ICHTHYOSIS DEAFNESS SYNDROME | 406582 | 1% | 100% | 10 | Search KERATITIS+ICHTHYOSIS+DEAFNESS+SYNDROME | Search KERATITIS+ICHTHYOSIS+DEAFNESS+SYNDROME |
6 | CLOUSTON SYNDROME | 365918 | 2% | 75% | 12 | Search CLOUSTON+SYNDROME | Search CLOUSTON+SYNDROME |
7 | VOHWINKEL SYNDROME | 329330 | 1% | 90% | 9 | Search VOHWINKEL+SYNDROME | Search VOHWINKEL+SYNDROME |
8 | ERYTHROKERATODERMA | 312751 | 1% | 77% | 10 | Search ERYTHROKERATODERMA | Search ERYTHROKERATODERMA |
9 | AINHUM | 299389 | 1% | 82% | 9 | Search AINHUM | Search AINHUM |
10 | HIDROTIC ECTODERMAL DYSPLASIA | 274438 | 1% | 75% | 9 | Search HIDROTIC+ECTODERMAL+DYSPLASIA | Search HIDROTIC+ECTODERMAL+DYSPLASIA |
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 | PEREZ, C , KHACHEMOUNE, A , (2016) MAL DE MELEDA: A FOCUSED REVIEW.AMERICAN JOURNAL OF CLINICAL DERMATOLOGY. VOL. 17. ISSUE 1. P. 63 -70 | 37 | 79% | 2 |
2 | MARKOVA, TG , BRAZHKINA, NB , BLIZNECH, EA , BAKHSHINYAN, VV , POLYAKOV, AV , TAVARTKILADZE, GA , (2016) PHENOTYPE IN A PATIENT WITH P.D50N MUTATION IN GJB2 GENE RESEMBLE BOTH KID AND CLOUSTON SYNDROMES.INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY. VOL. 81. ISSUE 2. P. 10 -14 | 32 | 86% | 0 |
3 | COGGSHALL, K , FARSANI, T , RUBEN, B , MCCALMONT, TH , BERGER, TG , FOX, LP , SHINKAI, K , (2013) KERATITIS, ICHTHYOSIS, AND DEAFNESS (KID) SYNDROME: A REVIEW OF INFECTIOUS AND NEOPLASTIC COMPLICATIONS.JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY. VOL. 69. ISSUE 1. P. 127-+ | 40 | 68% | 11 |
4 | NOFAL, A , ASSAF, M , NASSAR, A , NOFAL, E , SHEHAB, M , EL-KABANY, M , (2010) NONMUTILATING PALMOPLANTAR AND PERIORIFICIAL KERTODERMA: A VARIANT OF OLMSTED SYNDROME OR A DISTINCT ENTITY?.INTERNATIONAL JOURNAL OF DERMATOLOGY. VOL. 49. ISSUE 6. P. 658 -665 | 29 | 100% | 2 |
5 | DUCHATELET, S , HOVNANIAN, A , (2015) OLMSTED SYNDROME: CLINICAL, MOLECULAR AND THERAPEUTIC ASPECTS.ORPHANET JOURNAL OF RARE DISEASES. VOL. 10. ISSUE . P. - | 31 | 76% | 2 |
6 | SCOTT, CA , TATTERSALL, D , O'TOOLE, EA , KELSELL, DP , (2012) CONNEXINS IN EPIDERMAL HOMEOSTASIS AND SKIN DISEASE.BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES. VOL. 1818. ISSUE 8. P. 1952-1961 | 55 | 43% | 23 |
7 | GARCIA, IE , BOSEN, F , MUJICA, P , PUPO, A , FLORES-MUNOZ, C , JARA, O , GONZALEZ, C , WILLECKE, K , MARTINEZ, AD , (2016) FROM HYPERACTIVE CONNEXIN26 HEMICHANNELS TO IMPAIRMENTS IN EPIDERMAL CALCIUM GRADIENT AND PERMEABILITY BARRIER IN THE KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME.JOURNAL OF INVESTIGATIVE DERMATOLOGY. VOL. 136. ISSUE 3. P. 574 -583 | 48 | 48% | 0 |
8 | AVSHALUMOVA, L , FABRIKANT, J , KORIAKOS, A , (2014) OVERVIEW OF SKIN DISEASES LINKED TO CONNEXIN GENE MUTATIONS.INTERNATIONAL JOURNAL OF DERMATOLOGY. VOL. 53. ISSUE 2. P. 192 -205 | 38 | 57% | 11 |
9 | LILLY, E , SELLITTO, C , MILSTONE, LM , WHITE, TW , (2016) CONNEXIN CHANNELS IN CONGENITAL SKIN DISORDERS.SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY. VOL. 50. ISSUE . P. 4 -12 | 41 | 45% | 2 |
10 | MARTIN, PEM , VAN STEENSEL, M , (2015) CONNEXINS AND SKIN DISEASE: INSIGHTS INTO THE ROLE OF BETA CONNEXINS IN SKIN HOMEOSTASIS.CELL AND TISSUE RESEARCH. VOL. 360. ISSUE 3. P. 645 -658 | 48 | 39% | 7 |
Classes with closest relation at Level 1 |