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 |
21615 | 1 | CORNELIA DE LANGE SYNDROME//BRACHMANN DE LANGE SYNDROME//NIPBL | 436 |
Terms with highest relevance score |
rank | Category | termType | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass |
---|---|---|---|---|---|---|
1 | CORNELIA DE LANGE SYNDROME | authKW | 7459452 | 31% | 77% | 134 |
2 | BRACHMANN DE LANGE SYNDROME | authKW | 3130939 | 11% | 92% | 47 |
3 | NIPBL | authKW | 1705323 | 8% | 69% | 34 |
4 | KBG SYNDROME | authKW | 1593287 | 5% | 96% | 23 |
5 | CDLS | authKW | 1206407 | 5% | 76% | 22 |
6 | DE LANGE SYNDROME | authKW | 867424 | 3% | 100% | 12 |
7 | SMC1A | authKW | 807588 | 4% | 62% | 18 |
8 | CORNELIA DE LANGE | authKW | 743503 | 3% | 86% | 12 |
9 | ANKRD11 | authKW | 612292 | 3% | 71% | 12 |
10 | HARVEY HUMAN GENET | address | 452558 | 3% | 52% | 12 |
Web of Science journal categories |
chi_square_rank | Category | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass |
---|---|---|---|---|---|
1 | Genetics & Heredity | 9795 | 61% | 0% | 268 |
2 | Education, Special | 856 | 5% | 0% | 20 |
3 | Medical Ethics | 479 | 2% | 0% | 9 |
4 | Pediatrics | 347 | 11% | 0% | 46 |
5 | Rehabilitation | 242 | 5% | 0% | 23 |
6 | Obstetrics & Gynecology | 87 | 5% | 0% | 22 |
7 | Otorhinolaryngology | 78 | 3% | 0% | 14 |
8 | Anesthesiology | 46 | 2% | 0% | 10 |
9 | Medicine, Research & Experimental | 18 | 4% | 0% | 16 |
10 | Clinical Neurology | 17 | 4% | 0% | 19 |
Address terms |
chi_square_rank | term | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass |
---|---|---|---|---|---|
1 | HARVEY HUMAN GENET | 452558 | 3% | 52% | 12 |
2 | UNIT CLIN GENET FUNCT GENOM | 437316 | 3% | 55% | 11 |
3 | MED CHILD REHABIL | 216856 | 1% | 100% | 3 |
4 | NEONATAL CHILD NEUROL | 216856 | 1% | 100% | 3 |
5 | SEKT FUNKT GENET | 208344 | 2% | 41% | 7 |
6 | CEREBRA NEURODEV DISORDERS | 179448 | 3% | 21% | 12 |
7 | SECT FUNCT GENET | 165220 | 1% | 57% | 4 |
8 | MED CYTOGENET MOL GENET | 164269 | 2% | 23% | 10 |
9 | GEN NURSERY | 162634 | 1% | 38% | 6 |
10 | CIBERER GCV | 144571 | 0% | 100% | 2 |
Journals |
chi_square_rank | term | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass |
---|---|---|---|---|---|
1 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 33816 | 12% | 1% | 53 |
2 | AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS | 24165 | 3% | 3% | 13 |
3 | AMERICAN JOURNAL OF MEDICAL GENETICS | 23220 | 12% | 1% | 53 |
4 | CLINICAL DYSMORPHOLOGY | 9067 | 3% | 1% | 12 |
5 | CLINICAL GENETICS | 7309 | 5% | 0% | 23 |
6 | GENETIC COUNSELING | 6031 | 2% | 1% | 9 |
7 | AJIDD-AMERICAN JOURNAL ON INTELLECTUAL AND DEVELOPMENTAL DISABILITIES | 3899 | 1% | 1% | 4 |
8 | EUROPEAN JOURNAL OF MEDICAL GENETICS | 3776 | 2% | 1% | 8 |
9 | JOURNAL OF INTELLECTUAL DISABILITY RESEARCH | 2924 | 2% | 0% | 9 |
10 | JOURNAL OF MEDICAL GENETICS | 2401 | 3% | 0% | 14 |
Author Key Words |
chi_square_rank | term | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass | LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | CORNELIA DE LANGE SYNDROME | 7459452 | 31% | 77% | 134 | Search CORNELIA+DE+LANGE+SYNDROME | Search CORNELIA+DE+LANGE+SYNDROME |
2 | BRACHMANN DE LANGE SYNDROME | 3130939 | 11% | 92% | 47 | Search BRACHMANN+DE+LANGE+SYNDROME | Search BRACHMANN+DE+LANGE+SYNDROME |
3 | NIPBL | 1705323 | 8% | 69% | 34 | Search NIPBL | Search NIPBL |
4 | KBG SYNDROME | 1593287 | 5% | 96% | 23 | Search KBG+SYNDROME | Search KBG+SYNDROME |
5 | CDLS | 1206407 | 5% | 76% | 22 | Search CDLS | Search CDLS |
6 | DE LANGE SYNDROME | 867424 | 3% | 100% | 12 | Search DE+LANGE+SYNDROME | Search DE+LANGE+SYNDROME |
7 | SMC1A | 807588 | 4% | 62% | 18 | Search SMC1A | Search SMC1A |
8 | CORNELIA DE LANGE | 743503 | 3% | 86% | 12 | Search CORNELIA+DE+LANGE | Search CORNELIA+DE+LANGE |
9 | ANKRD11 | 612292 | 3% | 71% | 12 | Search ANKRD11 | Search ANKRD11 |
10 | MACRODONTIA | 380440 | 2% | 53% | 10 | Search MACRODONTIA | Search MACRODONTIA |
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 |
rank | cluster_id2 | link |
---|---|---|
1 | 4090 | COHESIN//CONDENSIN//SISTER CHROMATID COHESION |
2 | 18675 | CRI DU CHAT SYNDROME//CRI DU CHAT//5P DELETION |
3 | 24985 | TRISOMY 1Q//PARTIAL TRISOMY 1Q//ZNF238 |
4 | 37710 | TBL1XR1//TBLR1//PLANTAR LIPOMATOSIS |
5 | 37742 | PEG10//AGK114//FAD104 |
6 | 25592 | JACOBSEN SYNDROME//11Q SYNDROME//C SYNDROME |
7 | 28901 | TRISOMY 10Q//MONOSOMY 10Q//10P DUPLICATION |
8 | 35963 | AARSKOG SCOTT SYNDROME//FGD1//FACIOGENITAL DYSPLASIA |
9 | 8049 | SUBTELOMERIC REARRANGEMENTS//ARRAY CGH//MBD5 |
10 | 14571 | TRISOMY 9//TETRASOMY 9P//TRISOMY 9P |