Class information for: |
Basic class information |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
16 | 4 | DENTISTRY, ORAL SURGERY & MEDICINE//ORTHOPEDICS//DENT | 796976 |
201 | 3 | CLEFT PALATE-CRANIOFACIAL JOURNAL//CLEFT PALATE//CRANIOSYNOSTOSIS | 52632 |
387 | 2 | ARRAY CGH//GENETICS & HEREDITY//HOLOPROSENCEPHALY | 17402 |
19155 | 1 | 18Q SYNDROME//PITT HOPKINS SYNDROME//CHROMOSOME 18 | 541 |
Terms with highest relevance score |
rank | Category | termType | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass |
---|---|---|---|---|---|---|
1 | 18Q SYNDROME | authKW | 1464418 | 5% | 93% | 27 |
2 | PITT HOPKINS SYNDROME | authKW | 1327123 | 5% | 84% | 27 |
3 | CHROMOSOME 18 | authKW | 1032065 | 10% | 32% | 56 |
4 | TETRASOMY 18P | authKW | 819215 | 3% | 94% | 15 |
5 | 18Q DELETION SYNDROME | authKW | 761203 | 3% | 93% | 14 |
6 | RING CHROMOSOME 18 | authKW | 745663 | 3% | 80% | 16 |
7 | ISOCHROMOSOME 18P | authKW | 615318 | 2% | 81% | 13 |
8 | 18P DELETION SYNDROME | authKW | 582554 | 2% | 100% | 10 |
9 | MONOSOMY 18P | authKW | 579121 | 2% | 76% | 13 |
10 | 18Q DELETION | authKW | 466036 | 2% | 67% | 12 |
Web of Science journal categories |
chi_square_rank | Category | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass |
---|---|---|---|---|---|
1 | Genetics & Heredity | 15211 | 69% | 0% | 371 |
2 | Medical Ethics | 942 | 3% | 0% | 14 |
3 | Pediatrics | 430 | 11% | 0% | 57 |
4 | Obstetrics & Gynecology | 136 | 6% | 0% | 30 |
5 | Clinical Neurology | 112 | 8% | 0% | 42 |
6 | Medicine, Research & Experimental | 45 | 5% | 0% | 25 |
7 | Biotechnology & Applied Microbiology | 25 | 4% | 0% | 24 |
8 | Neuroimaging | 21 | 1% | 0% | 5 |
9 | Rheumatology | 16 | 1% | 0% | 7 |
10 | Ophthalmology | 14 | 2% | 0% | 11 |
Address terms |
chi_square_rank | term | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass |
---|---|---|---|---|---|
1 | CHROMOSOME CLIN 18 | 242729 | 1% | 83% | 5 |
2 | ASSISTANCE PUBL HOP PARISCLIN NEUROPHYSIOL UNIT | 58255 | 0% | 100% | 1 |
3 | ASSISTANCE PUBL HOP PARISINSERMU663 | 58255 | 0% | 100% | 1 |
4 | ASSISTANCE PUBL HOP PARISINSERMU797 | 58255 | 0% | 100% | 1 |
5 | AUDIOFON | 58255 | 0% | 100% | 1 |
6 | BIOL ORO IALEU714 | 58255 | 0% | 100% | 1 |
7 | BIRTH HLTH GENET | 58255 | 0% | 100% | 1 |
8 | CITOGENOMICA | 58255 | 0% | 100% | 1 |
9 | CLIN IMMUNOL TRANSPLANTOL UNIT | 58255 | 0% | 100% | 1 |
10 | CONGENITAL IMMUNODEFICIENCIES | 58255 | 0% | 100% | 1 |
Journals |
chi_square_rank | term | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass |
---|---|---|---|---|---|
1 | ANNALES DE GENETIQUE | 39869 | 5% | 2% | 28 |
2 | AMERICAN JOURNAL OF MEDICAL GENETICS | 23178 | 11% | 1% | 59 |
3 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 22327 | 9% | 1% | 48 |
4 | GENETIC COUNSELING | 11768 | 3% | 1% | 14 |
5 | EUROPEAN JOURNAL OF MEDICAL GENETICS | 10714 | 3% | 1% | 15 |
6 | CLINICAL GENETICS | 9366 | 5% | 1% | 29 |
7 | MOLECULAR CYTOGENETICS | 9199 | 2% | 2% | 9 |
8 | JOURNAL OF MEDICAL GENETICS | 7776 | 5% | 0% | 28 |
9 | JAPANESE JOURNAL OF HUMAN GENETICS | 2829 | 1% | 1% | 5 |
10 | HUMAN GENETICS | 2599 | 4% | 0% | 19 |
Author Key Words |
chi_square_rank | term | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass | LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | 18Q SYNDROME | 1464418 | 5% | 93% | 27 | Search 18Q+SYNDROME | Search 18Q+SYNDROME |
2 | PITT HOPKINS SYNDROME | 1327123 | 5% | 84% | 27 | Search PITT+HOPKINS+SYNDROME | Search PITT+HOPKINS+SYNDROME |
3 | CHROMOSOME 18 | 1032065 | 10% | 32% | 56 | Search CHROMOSOME+18 | Search CHROMOSOME+18 |
4 | TETRASOMY 18P | 819215 | 3% | 94% | 15 | Search TETRASOMY+18P | Search TETRASOMY+18P |
5 | 18Q DELETION SYNDROME | 761203 | 3% | 93% | 14 | Search 18Q+DELETION+SYNDROME | Search 18Q+DELETION+SYNDROME |
6 | RING CHROMOSOME 18 | 745663 | 3% | 80% | 16 | Search RING+CHROMOSOME+18 | Search RING+CHROMOSOME+18 |
7 | ISOCHROMOSOME 18P | 615318 | 2% | 81% | 13 | Search ISOCHROMOSOME+18P | Search ISOCHROMOSOME+18P |
8 | 18P DELETION SYNDROME | 582554 | 2% | 100% | 10 | Search 18P+DELETION+SYNDROME | Search 18P+DELETION+SYNDROME |
9 | MONOSOMY 18P | 579121 | 2% | 76% | 13 | Search MONOSOMY+18P | Search MONOSOMY+18P |
10 | 18Q DELETION | 466036 | 2% | 67% | 12 | Search 18Q+DELETION | Search 18Q+DELETION |
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. |
Classes with closest relation at Level 1 |