Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
26478 | 254 | 17.0 | 57% |
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 |
1503 | 2 | ALOPECIA AREATA//ALOPECIA//HAIR FOLLICLE | 7543 |
26478 | 1 | GAPO SYNDROME//ICHTHYOSIS FOLLICULARIS//IFAP SYNDROME | 254 |
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 | GAPO SYNDROME | authKW | 1472664 | 6% | 88% | 14 |
2 | ICHTHYOSIS FOLLICULARIS | authKW | 961742 | 3% | 100% | 8 |
3 | IFAP SYNDROME | authKW | 961742 | 3% | 100% | 8 |
4 | PSEUDOANODONTIA | authKW | 841525 | 3% | 100% | 7 |
5 | WOODHOUSE SAKATI SYNDROME | authKW | 769391 | 3% | 80% | 8 |
6 | MBTPS2 | authKW | 736332 | 3% | 88% | 7 |
7 | KERATOSIS FOLLICULARIS SPINULOSA DECALVANS | authKW | 618261 | 2% | 86% | 6 |
8 | KERATOSIS PILARIS | authKW | 538741 | 4% | 41% | 11 |
9 | JOHNSON MCMILLIN SYNDROME | authKW | 480871 | 2% | 100% | 4 |
10 | IFAP | authKW | 320578 | 2% | 67% | 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 | 12548 | 53% | 0% | 135 |
2 | Genetics & Heredity | 1344 | 31% | 0% | 78 |
3 | Pediatrics | 278 | 12% | 0% | 31 |
4 | Ophthalmology | 114 | 6% | 0% | 16 |
5 | Medical Ethics | 38 | 1% | 0% | 2 |
6 | Developmental Biology | 1 | 1% | 0% | 2 |
7 | Planning & Development | 1 | 0% | 0% | 1 |
8 | Emergency Medicine | 1 | 0% | 0% | 1 |
9 | Anatomy & Morphology | 1 | 0% | 0% | 1 |
10 | Pathology | 1 | 1% | 0% | 3 |
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 | BURNS ALLEN AHMANSON PEDIATMED G | 120218 | 0% | 100% | 1 |
2 | FDN MALAD SYST NERVEUX | 120218 | 0% | 100% | 1 |
3 | HOSP PEDIAT NICE | 120218 | 0% | 100% | 1 |
4 | KLINHAUTKRANKHEITEN | 120218 | 0% | 100% | 1 |
5 | OPHTHALMOL OTORRHINOLARYNGOL | 120218 | 0% | 100% | 1 |
6 | PEDIAT DERMATOLFDN IRCCS CA GRANDA | 120218 | 0% | 100% | 1 |
7 | SOBELL MOTOR NEROSCI MOVEMENT DISORDERS | 120218 | 0% | 100% | 1 |
8 | U346EA 3732 | 120218 | 0% | 100% | 1 |
9 | UPGEM GENET MOL BIOL UNIT | 120218 | 0% | 100% | 1 |
10 | ADDICT ME HLTH | 60108 | 0% | 50% | 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 | 13024 | 8% | 1% | 20 |
2 | AMERICAN JOURNAL OF MEDICAL GENETICS | 8582 | 10% | 0% | 25 |
3 | CLINICAL AND EXPERIMENTAL DERMATOLOGY | 4746 | 6% | 0% | 14 |
4 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 4074 | 6% | 0% | 14 |
5 | CUTIS | 3461 | 4% | 0% | 11 |
6 | JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY | 2512 | 6% | 0% | 16 |
7 | JOURNAL OF COSMETIC AND LASER THERAPY | 2087 | 1% | 1% | 3 |
8 | CLINICAL DYSMORPHOLOGY | 1719 | 2% | 0% | 4 |
9 | ARCHIVES OF DERMATOLOGY | 1569 | 4% | 0% | 9 |
10 | INDIAN JOURNAL OF DERMATOLOGY VENEREOLOGY & LEPROLOGY | 1348 | 1% | 0% | 3 |
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 | GAPO SYNDROME | 1472664 | 6% | 88% | 14 | Search GAPO+SYNDROME | Search GAPO+SYNDROME |
2 | ICHTHYOSIS FOLLICULARIS | 961742 | 3% | 100% | 8 | Search ICHTHYOSIS+FOLLICULARIS | Search ICHTHYOSIS+FOLLICULARIS |
3 | IFAP SYNDROME | 961742 | 3% | 100% | 8 | Search IFAP+SYNDROME | Search IFAP+SYNDROME |
4 | PSEUDOANODONTIA | 841525 | 3% | 100% | 7 | Search PSEUDOANODONTIA | Search PSEUDOANODONTIA |
5 | WOODHOUSE SAKATI SYNDROME | 769391 | 3% | 80% | 8 | Search WOODHOUSE+SAKATI+SYNDROME | Search WOODHOUSE+SAKATI+SYNDROME |
6 | MBTPS2 | 736332 | 3% | 88% | 7 | Search MBTPS2 | Search MBTPS2 |
7 | KERATOSIS FOLLICULARIS SPINULOSA DECALVANS | 618261 | 2% | 86% | 6 | Search KERATOSIS+FOLLICULARIS+SPINULOSA+DECALVANS | Search KERATOSIS+FOLLICULARIS+SPINULOSA+DECALVANS |
8 | KERATOSIS PILARIS | 538741 | 4% | 41% | 11 | Search KERATOSIS+PILARIS | Search KERATOSIS+PILARIS |
9 | JOHNSON MCMILLIN SYNDROME | 480871 | 2% | 100% | 4 | Search JOHNSON+MCMILLIN+SYNDROME | Search JOHNSON+MCMILLIN+SYNDROME |
10 | IFAP | 320578 | 2% | 67% | 4 | Search IFAP | Search IFAP |
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 | PIETRZAK, A , KANITAKIS, J , STASKIEWICZ, G , SOBCZYNSKA-TOMASZEWSKA, A , DYBIEC, E , SZUMILO, J , KANDZIERSKI, G , WAWRZYCKI, B , CHODOROWSKA, G , (2012) IFAP SYNDROME WITH SEVERE CUTANEOUS, NEUROLOGIC AND SKELETAL MANIFESTATIONS DUE TO A NOVEL MBTPS2 MUTATION IN A POLISH PATIENT.EUROPEAN JOURNAL OF DERMATOLOGY. VOL. 22. ISSUE 4. P. 467 -472 | 22 | 96% | 4 |
2 | CASTORI, M , COVACIU, C , PARADISI, M , ZAMBRUNO, G , (2009) CLINICAL AND GENETIC HETEROGENEITY IN KERATOSIS FOLLICULARIS SPINULOSA DECALVANS.EUROPEAN JOURNAL OF MEDICAL GENETICS. VOL. 52. ISSUE 1. P. 53-58 | 25 | 89% | 3 |
3 | MEGARBANE, H , MEGARBANE, A , (2011) ICHTHYOSIS FOLLICULARIS, ALOPECIA, AND PHOTOPHOBIA (IFAP) SYNDROME.ORPHANET JOURNAL OF RARE DISEASES. VOL. 6. ISSUE . P. - | 18 | 90% | 17 |
4 | CORUJEIRA, S , AGUEDA, S , MONTEIRO, G , CANELHAS, A , SAMPAIO, M , ROCHA, R , LEAO, M , (2013) EXPANDING THE PHENOTYPE OF IFAP/BRESECK SYNDROME: A NEW CASE WITH SEVERE HYPOGAMMAGLOBULINEMIA.EUROPEAN JOURNAL OF MEDICAL GENETICS. VOL. 56. ISSUE 11. P. 603-605 | 16 | 100% | 2 |
5 | TANG, L , LIANG, JY , WANG, WZ , YU, L , YAO, ZR , (2011) A NOVEL MUTATION IN MBTPS2 CAUSES A BROAD PHENOTYPIC SPECTRUM OF ICHTHYOSIS FOLLICULARIS, ATRICHIA, AND PHOTOPHOBIA SYNDROME IN A LARGE CHINESE FAMILY.JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY. VOL. 64. ISSUE 4. P. 716-722 | 18 | 90% | 11 |
6 | ANIM, JT , ALSALEH, QA , AL-KHAWARI, MA , AL-ATEEQI, WA , NANDA, A , (2010) GAPO SYNDROME: A REPORT OF TWO SIBLINGS AND A REVIEW OF LITERATURE.PEDIATRIC DERMATOLOGY. VOL. 27. ISSUE 2. P. 156 -161 | 15 | 100% | 6 |
7 | BORNHOLDT, D , ATKINSON, TP , BOUADJAR, B , CATTEAU, B , COX, H , DE SILVA, D , FISCHER, J , GUNASEKERA, CN , HADJ-RABIA, S , HAPPLE, R , ET AL (2013) GENOTYPE-PHENOTYPE CORRELATIONS EMERGING FROM THE IDENTIFICATION OF MISSENSE MUTATIONS IN MBTPS2.HUMAN MUTATION. VOL. 34. ISSUE 4. P. 587-594 | 18 | 75% | 8 |
8 | BOZKURT, B , YILDIRIM, MS , OKKA, M , BITIRGEN, G , (2013) GAPO SYNDROME: FOUR NEW PATIENTS WITH CONGENITAL GLAUCOMA AND MYELINATED RETINAL NERVE FIBER LAYER.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 161A. ISSUE 4. P. 829-834 | 14 | 100% | 1 |
9 | RATHER, S , YASEEN, A , MUKHIJA, M , (2016) ERYTHROMELANOSIS FOLLICULARIS FACIEI ET COLLI - A CROSS-SECTIONAL, DESCRIPTIVE STUDY.INDIAN JOURNAL OF DERMATOLOGY. VOL. 61. ISSUE 3. P. 308 -313 | 13 | 100% | 0 |
10 | GOLONI-BERTOLLO, EM , RUIZ, MT , GOLONI, CBV , MUNIZ, MP , VALERIO, NI , PAVARINO-BERTELLI, EC , (2008) GAPO SYNDROME: THREE NEW BRAZILIAN CASES, ADDITIONAL OSSEOUS MANIFESTATIONS, AND REVIEW OF THE LITERATURE.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 146A. ISSUE 12. P. 1523-1529 | 15 | 100% | 11 |
Classes with closest relation at Level 1 |