Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
15263 | 722 | 24.7 | 68% |
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 |
442 | 3 | DERMATOLOGY//VITILIGO//DERMATOL | 26460 |
2116 | 2 | VITILIGO//INCONTINENTIA PIGMENTI//DERMATOLOGY | 5103 |
15263 | 1 | INCONTINENTIA PIGMENTI//HYPOMELANOSIS OF ITO//BLOCH SULZBERGER SYNDROME | 722 |
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 | INCONTINENTIA PIGMENTI | authKW | 4781393 | 17% | 91% | 124 |
2 | HYPOMELANOSIS OF ITO | authKW | 1286218 | 6% | 72% | 42 |
3 | BLOCH SULZBERGER SYNDROME | authKW | 465205 | 2% | 100% | 11 |
4 | NEMO | authKW | 320628 | 6% | 19% | 40 |
5 | IKBKG | authKW | 263502 | 1% | 69% | 9 |
6 | IKBKG GENE | authKW | 253748 | 1% | 100% | 6 |
7 | LINEAR AND WHORLED NEVOID HYPERMELANOSIS | authKW | 253748 | 1% | 100% | 6 |
8 | INCONTINENTIA PIGMENTI ACHROMIANS | authKW | 176212 | 1% | 83% | 5 |
9 | NEMO GENE | authKW | 176212 | 1% | 83% | 5 |
10 | ANHIDROTIC ECTODERMAL DYSPLASIA WITH IMMUNODEFICIENCY | authKW | 169166 | 1% | 100% | 4 |
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 | 10191 | 29% | 0% | 207 |
2 | Pediatrics | 2928 | 22% | 0% | 162 |
3 | Genetics & Heredity | 2063 | 23% | 0% | 166 |
4 | Ophthalmology | 535 | 8% | 0% | 57 |
5 | Clinical Neurology | 328 | 11% | 0% | 77 |
6 | Allergy | 84 | 2% | 0% | 13 |
7 | Immunology | 59 | 6% | 0% | 45 |
8 | Medical Ethics | 51 | 1% | 0% | 4 |
9 | Neuroimaging | 32 | 1% | 0% | 7 |
10 | Medicine, General & Internal | 18 | 4% | 0% | 30 |
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 | MED NECKER ENFANTS MALADESU550 | 84583 | 0% | 100% | 2 |
2 | MOL SIGNALING CELLULAR ACTIVAT UNIT | 84583 | 0% | 100% | 2 |
3 | ABRAMSON PEDIAT IMMUNOL | 42291 | 0% | 100% | 1 |
4 | ALERGIA DERMATOL | 42291 | 0% | 100% | 1 |
5 | DERMATOL REFERENCE GENODERMATOSES | 42291 | 0% | 100% | 1 |
6 | DERMPATHOL | 42291 | 0% | 100% | 1 |
7 | DISCIPLINE ORTHODONT PL SPEECH THER Y | 42291 | 0% | 100% | 1 |
8 | GEN MED NEUROSCI SENSORY ORGANS | 42291 | 0% | 100% | 1 |
9 | GENET HUMAINE MALAD INFECT U980 | 42291 | 0% | 100% | 1 |
10 | GENETUFR | 42291 | 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 | PEDIATRIC DERMATOLOGY | 19232 | 6% | 1% | 41 |
2 | ANNALES DE GENETIQUE | 5300 | 2% | 1% | 12 |
3 | AMERICAN JOURNAL OF MEDICAL GENETICS | 3488 | 4% | 0% | 27 |
4 | JOURNAL OF MEDICAL GENETICS | 2896 | 3% | 0% | 20 |
5 | CLINICAL GENETICS | 2667 | 2% | 0% | 18 |
6 | PEDIATRIC NEUROLOGY | 2536 | 2% | 0% | 16 |
7 | GIORNALE DI NEUROPSICHIATRIA DELL ETA EVOLUTIVA | 2313 | 0% | 3% | 2 |
8 | JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY | 2311 | 4% | 0% | 26 |
9 | CLINICAL DYSMORPHOLOGY | 1846 | 1% | 1% | 7 |
10 | INTERNATIONAL JOURNAL OF DERMATOLOGY | 1653 | 2% | 0% | 17 |
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 | INCONTINENTIA PIGMENTI | 4781393 | 17% | 91% | 124 | Search INCONTINENTIA+PIGMENTI | Search INCONTINENTIA+PIGMENTI |
2 | HYPOMELANOSIS OF ITO | 1286218 | 6% | 72% | 42 | Search HYPOMELANOSIS+OF+ITO | Search HYPOMELANOSIS+OF+ITO |
3 | BLOCH SULZBERGER SYNDROME | 465205 | 2% | 100% | 11 | Search BLOCH+SULZBERGER+SYNDROME | Search BLOCH+SULZBERGER+SYNDROME |
4 | NEMO | 320628 | 6% | 19% | 40 | Search NEMO | Search NEMO |
5 | IKBKG | 263502 | 1% | 69% | 9 | Search IKBKG | Search IKBKG |
6 | IKBKG GENE | 253748 | 1% | 100% | 6 | Search IKBKG+GENE | Search IKBKG+GENE |
7 | LINEAR AND WHORLED NEVOID HYPERMELANOSIS | 253748 | 1% | 100% | 6 | Search LINEAR+AND+WHORLED+NEVOID+HYPERMELANOSIS | Search LINEAR+AND+WHORLED+NEVOID+HYPERMELANOSIS |
8 | INCONTINENTIA PIGMENTI ACHROMIANS | 176212 | 1% | 83% | 5 | Search INCONTINENTIA+PIGMENTI+ACHROMIANS | Search INCONTINENTIA+PIGMENTI+ACHROMIANS |
9 | NEMO GENE | 176212 | 1% | 83% | 5 | Search NEMO+GENE | Search NEMO+GENE |
10 | ANHIDROTIC ECTODERMAL DYSPLASIA WITH IMMUNODEFICIENCY | 169166 | 1% | 100% | 4 | Search ANHIDROTIC+ECTODERMAL+DYSPLASIA+WITH+IMMUNODEFICIENCY | Search ANHIDROTIC+ECTODERMAL+DYSPLASIA+WITH+IMMUNODEFICIENCY |
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 | EHRENREICH, M , TARLOW, MM , GODLEWSKA-JANUSZ, E , SCHWARTZ, RA , (2007) INCONTINENTIA PIGMENTI (BLOCH-SULZBERGER SYNDROME): A SYSTEMIC DISORDER.CUTIS. VOL. 79. ISSUE 5. P. 355-362 | 80 | 93% | 25 |
2 | POZIOMCZYK, CS , RECUERO, JK , BRINGHENTI, L , MARIA, FDS , CAMPOS, CW , TRAVI, GM , FREITAS, AM , MAAHS, MAP , ZEN, PRG , FIEGENBAUM, M , ET AL (2014) INCONTINENTIA PIGMENTI.ANAIS BRASILEIROS DE DERMATOLOGIA. VOL. 89. ISSUE 1. P. 26 -36 | 61 | 98% | 4 |
3 | SWINNEY, CC , HAN, DP , KARTH, PA , (2015) INCONTINENTIA PIGMENTI: A COMPREHENSIVE REVIEW AND UPDATE.OPHTHALMIC SURGERY LASERS & IMAGING RETINA. VOL. 46. ISSUE 6. P. 650 -657 | 43 | 91% | 1 |
4 | RUGGIERI, M , PAVONE, L , (2000) HYPOMELANOSIS OF ITO: CLINICAL SYNDROME OR JUST PHENOTYPE?.JOURNAL OF CHILD NEUROLOGY. VOL. 15. ISSUE 10. P. 635 -644 | 61 | 86% | 38 |
5 | BERLIN, AL , PALLER, AS , CHAN, LS , (2002) INCONTINENTIA PIGMENTI: A REVIEW AND UPDATE ON THE MOLECULAR BASIS OF PATHOPHYSIOLOGY.JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY. VOL. 47. ISSUE 2. P. 169 -187 | 67 | 64% | 105 |
6 | MEUWISSEN, MEC , MANCINI, GMS , (2012) NEUROLOGICAL FINDINGS IN INCONTINENTIA PIGMENTI; A REVIEW.EUROPEAN JOURNAL OF MEDICAL GENETICS. VOL. 55. ISSUE 5. P. 323-331 | 38 | 75% | 26 |
7 | FUSCO, F , PESCATORE, A , CONTE, MI , MIRABELLI, P , PACIOLLA, M , ESPOSITO, E , LIOI, MB , URSINI, MV , (2015) EDA-ID AND IP, TWO FACES OF THE SAME COIN: HOW THE SAME IKBKG/NEMO MUTATION AFFECTING THE NF-KAPPA B PATHWAY CAN CAUSE IMMUNODEFICIENCY AND/OR INFLAMMATION.INTERNATIONAL REVIEWS OF IMMUNOLOGY. VOL. 34. ISSUE 6. P. 445 -459 | 41 | 66% | 2 |
8 | PASCUAL-CASTROVIEJO, I , ROCHE, C , MARTINEZ-BERMEJO, A , ARCAS, J , LOPEZ-MARTIN, V , TENDERO, A , ESQUIROZ, JLH , PASCUAL-PASCUAL, SI , (1998) HYPOMELANOSIS OF ITO. A STUDY OF 76 INFANTILE CASES.BRAIN & DEVELOPMENT. VOL. 20. ISSUE 1. P. 36 -43 | 42 | 95% | 45 |
9 | HADJ-RABIA, S , FROIDEVAUX, D , BODAK, N , HAMEL-TEILLAC, D , SMAHI, A , TOUIL, Y , FRAITAG, S , DE PROST, Y , BODEMER, C , (2003) CLINICAL STUDY OF 40 CASES OF INCONTINENTIA PIGMENTI.ARCHIVES OF DERMATOLOGY. VOL. 139. ISSUE 9. P. 1163-1170 | 36 | 88% | 75 |
10 | BRUCKNER, AL , (2004) INCONTINENTIA PIGMENTI: A WINDOW TO THE ROLE OF NF-KAPPA B FUNCTION.SEMINARS IN CUTANEOUS MEDICINE AND SURGERY. VOL. 23. ISSUE 2. P. 116-124 | 38 | 81% | 6 |
Classes with closest relation at Level 1 |