Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
22503 | 379 | 20.7 | 62% |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
23 | 4 | OPHTHALMOLOGY//OPHTHALMOL//JOURNAL OF CATARACT AND REFRACTIVE SURGERY | 148248 |
242 | 3 | OPHTHALMOLOGY//OPHTHALMOL//AGE RELATED MACULAR DEGENERATION | 47399 |
2848 | 2 | CHARGE SYNDROME//CHOANAL ATRESIA//AICARDI SYNDROME | 2948 |
22503 | 1 | AICARDI SYNDROME//FOCAL DERMAL HYPOPLASIA//GOLTZ SYNDROME | 379 |
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 | AICARDI SYNDROME | authKW | 4361975 | 16% | 87% | 62 |
2 | FOCAL DERMAL HYPOPLASIA | authKW | 3040178 | 11% | 88% | 43 |
3 | GOLTZ SYNDROME | authKW | 2419540 | 8% | 97% | 31 |
4 | CHORIORETINAL LACUNAE | authKW | 725107 | 2% | 100% | 9 |
5 | PORCN | authKW | 725101 | 3% | 75% | 12 |
6 | GOLTZ GORLIN SYNDROME | authKW | 501992 | 2% | 69% | 9 |
7 | PORCN GENE | authKW | 483405 | 2% | 100% | 6 |
8 | ASTROCYTIC INCLUSIONS | authKW | 414345 | 2% | 86% | 6 |
9 | MLS SYNDROME | authKW | 251770 | 1% | 63% | 5 |
10 | HYALINE PROTOPLASMIC ASTROCYTOPATHY | authKW | 241702 | 1% | 100% | 3 |
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 | 2932 | 21% | 0% | 81 |
2 | Pediatrics | 2114 | 26% | 0% | 99 |
3 | Genetics & Heredity | 1362 | 26% | 0% | 97 |
4 | Clinical Neurology | 586 | 18% | 0% | 69 |
5 | Ophthalmology | 555 | 11% | 0% | 41 |
6 | Pathology | 218 | 7% | 0% | 28 |
7 | Neuroimaging | 51 | 2% | 0% | 6 |
8 | Medical Ethics | 24 | 1% | 0% | 2 |
9 | Dentistry, Oral Surgery & Medicine | 20 | 2% | 0% | 9 |
10 | Radiology, Nuclear Medicine & Medical Imaging | 11 | 3% | 0% | 13 |
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 | AGCP | 80567 | 0% | 100% | 1 |
2 | AMBULANZZENTRUM DERMATOONKOL | 80567 | 0% | 100% | 1 |
3 | ARNOT OGDEN MED | 80567 | 0% | 100% | 1 |
4 | COMPETENZZENTRUM DERMAT FOR | 80567 | 0% | 100% | 1 |
5 | DERMATOVENEROL DERMATOONCOL CLIN | 80567 | 0% | 100% | 1 |
6 | DEV BIOL OPHTHALMOL | 80567 | 0% | 100% | 1 |
7 | ELECT MICROSCOPY UNIT GENET | 80567 | 0% | 100% | 1 |
8 | EMAM REZA EDUC HOSP | 80567 | 0% | 100% | 1 |
9 | GENET GENOM MEDPEDIAT | 80567 | 0% | 100% | 1 |
10 | GENET IFR111 | 80567 | 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 | AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS | 13494 | 2% | 2% | 9 |
2 | PEDIATRIC DERMATOLOGY | 7056 | 5% | 0% | 18 |
3 | DERMATOLOGISCHE MONATSSCHRIFT | 5034 | 0% | 6% | 1 |
4 | CLINICAL DYSMORPHOLOGY | 4613 | 2% | 1% | 8 |
5 | BRAIN & DEVELOPMENT | 3183 | 3% | 0% | 12 |
6 | AMERICAN JOURNAL OF MEDICAL GENETICS | 2338 | 4% | 0% | 16 |
7 | PEDIATRIC NEUROLOGY | 1891 | 3% | 0% | 10 |
8 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 1675 | 3% | 0% | 11 |
9 | METABOLIC AND PEDIATRIC OPHTHALMOLOGY | 1364 | 0% | 2% | 1 |
10 | METABOLIC PEDIATRIC AND SYSTEMIC OPHTHALMOLOGY | 1364 | 0% | 2% | 1 |
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 | AICARDI SYNDROME | 4361975 | 16% | 87% | 62 | Search AICARDI+SYNDROME | Search AICARDI+SYNDROME |
2 | FOCAL DERMAL HYPOPLASIA | 3040178 | 11% | 88% | 43 | Search FOCAL+DERMAL+HYPOPLASIA | Search FOCAL+DERMAL+HYPOPLASIA |
3 | GOLTZ SYNDROME | 2419540 | 8% | 97% | 31 | Search GOLTZ+SYNDROME | Search GOLTZ+SYNDROME |
4 | CHORIORETINAL LACUNAE | 725107 | 2% | 100% | 9 | Search CHORIORETINAL+LACUNAE | Search CHORIORETINAL+LACUNAE |
5 | PORCN | 725101 | 3% | 75% | 12 | Search PORCN | Search PORCN |
6 | GOLTZ GORLIN SYNDROME | 501992 | 2% | 69% | 9 | Search GOLTZ+GORLIN+SYNDROME | Search GOLTZ+GORLIN+SYNDROME |
7 | PORCN GENE | 483405 | 2% | 100% | 6 | Search PORCN+GENE | Search PORCN+GENE |
8 | ASTROCYTIC INCLUSIONS | 414345 | 2% | 86% | 6 | Search ASTROCYTIC+INCLUSIONS | Search ASTROCYTIC+INCLUSIONS |
9 | MLS SYNDROME | 251770 | 1% | 63% | 5 | Search MLS+SYNDROME | Search MLS+SYNDROME |
10 | HYALINE PROTOPLASMIC ASTROCYTOPATHY | 241702 | 1% | 100% | 3 | Search HYALINE+PROTOPLASMIC+ASTROCYTOPATHY | Search HYALINE+PROTOPLASMIC+ASTROCYTOPATHY |
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 | WANG, L , JIN, X , ZHAO, X , LIU, D , HU, T , LI, W , JIANG, L , DAN, H , ZENG, X , CHEN, Q , (2014) FOCAL DERMAL HYPOPLASIA: UPDATES.ORAL DISEASES. VOL. 20. ISSUE 1. P. 17 -24 | 37 | 90% | 7 |
2 | VERGULT, S , LEROY, B , CLAERHOUT, I , MENTEN, B , (2013) FAMILIAL CASES OF A SUBMICROSCOPIC XP22.2 DELETION: GENOTYPE-PHENOTYPE CORRELATION IN MICROPHTHALMIA WITH LINEAR SKIN DEFECTS SYNDROME.MOLECULAR VISION. VOL. 19. ISSUE . P. 311-318 | 35 | 78% | 6 |
3 | VAN DEN VEYVER, IB , (2002) MICROPHTHALMIA WITH LINEAR SKIN DEFECTS (MLS), AICARDI, AND GOLTZ SYNDROMES: ARE THEY RELATED X-LINKED DOMINANT MALE-LETHAL DISORDERS?.CYTOGENETIC AND GENOME RESEARCH. VOL. 99. ISSUE 1-4. P. 289-296 | 52 | 60% | 22 |
4 | FERNANDEZ-RAMOS, JA , LOPEZ-LASO, E , HERAS, RSD , CAMINO-LEON, R , GUERRA-GARCIA, P , CAMACHO-SALAS, A , AGUILAR-QUINTERO, M , NUNEZ-ENAMORADO, N , (2013) AICARDI SYNDROME: RETROSPECTIVE STUDY OF A SERIES OF SEVEN CASE REPORTS.REVISTA DE NEUROLOGIA. VOL. 57. ISSUE 11. P. 481-488 | 22 | 100% | 2 |
5 | SUTTON, VR , HOPKINS, BJ , EBLE, TN , GAMBHIR, N , LEWIS, RA , VAN DEN VEYVER, IB , (2005) FACIAL AND PHYSICAL FEATURES OF AICARDI SYNDROME: INFANTS TO TEENAGERS.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 138A. ISSUE 3. P. 254-258 | 26 | 87% | 26 |
6 | SMITH, CD , RYAN, SJ , HOOVER, SL , BAUMANN, RJ , (1996) MAGNETIC RESONANCE IMAGING OF THE BRAIN IN AICARDI'S SYNDROME - REPORT OF 20 PATIENTS.JOURNAL OF NEUROIMAGING. VOL. 6. ISSUE 4. P. 214-221 | 36 | 82% | 15 |
7 | WANG, XL , SUTTON, VR , EBLE, TN , LEWIS, RA , GUNARATNE, P , PATEL, A , VAN DEN VEYVER, IB , (2009) A GENOME-WIDE SCREEN FOR COPY NUMBER ALTERATIONS IN AICARDI SYNDROME.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 149A. ISSUE 10. P. 2113-2121 | 26 | 74% | 0 |
8 | LAGUADO-HERRERA, YV , MANRIQUE-HERNANDEZ, EF , PENALOZA-MANTILLA, CA , QUINTERO-GOMEZ, DA , CONTRERAS-GARCIA, GA , SANDOVAL-MARTINEZ, DK , (2015) AICARDI SYNDROME WITH DANDY-WALKER TYPE MALFORMATION.REVISTA DE NEUROLOGIA. VOL. 61. ISSUE 2. P. 71 -74 | 17 | 94% | 0 |
9 | STEVENSON, DA , CHIRPICH, M , CONTRERAS, Y , HANSON, H , DENT, K , (2014) GOLTZ SYNDROME AND PORCN MOSAICISM.INTERNATIONAL JOURNAL OF DERMATOLOGY. VOL. 53. ISSUE 12. P. 1481 -1484 | 16 | 100% | 2 |
10 | HAPPLE, R , (2016) GOLTZ SYNDROME AND PORCN: A VIEW FROM EUROPE.AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. VOL. 172. ISSUE 1. P. 21 -23 | 18 | 86% | 0 |
Classes with closest relation at Level 1 |