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 |
---|---|---|---|
0 | 4 | ONCOLOGY//CELL BIOLOGY//BIOCHEMISTRY & MOLECULAR BIOLOGY | 2934640 |
304 | 3 | DNA METHYLATION//FRAGILE X SYNDROME//RETT SYNDROME | 41307 |
2127 | 2 | RETT SYNDROME//MECP2//X CHROMOSOME INACTIVATION | 5430 |
10602 | 1 | X LINKED MENTAL RETARDATION//PQBP1//XLMR | 1078 |
Terms with highest relevance score |
rank | Category | termType | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass |
---|---|---|---|---|---|---|
1 | X LINKED MENTAL RETARDATION | authKW | 1374857 | 10% | 44% | 108 |
2 | PQBP1 | authKW | 584696 | 2% | 100% | 20 |
3 | XLMR | authKW | 519897 | 3% | 52% | 34 |
4 | ARX | authKW | 486931 | 4% | 39% | 43 |
5 | FG SYNDROME | authKW | 442163 | 2% | 69% | 22 |
6 | BORJESON FORSSMAN LEHMANN SYNDROME | authKW | 409287 | 1% | 100% | 14 |
7 | MRX | authKW | 382405 | 2% | 59% | 22 |
8 | ARX GENE | authKW | 380052 | 1% | 100% | 13 |
9 | NONSPECIFIC X LINKED MENTAL RETARDATION | authKW | 321583 | 1% | 100% | 11 |
10 | SLC9A6 | authKW | 321583 | 1% | 100% | 11 |
Web of Science journal categories |
chi_square_rank | Category | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass |
---|---|---|---|---|---|
1 | Genetics & Heredity | 33472 | 72% | 0% | 776 |
2 | Clinical Neurology | 179 | 7% | 0% | 77 |
3 | Biochemistry & Molecular Biology | 129 | 14% | 0% | 146 |
4 | Pediatrics | 120 | 5% | 0% | 50 |
5 | Neurosciences | 116 | 9% | 0% | 93 |
6 | Medical Ethics | 78 | 1% | 0% | 6 |
7 | Developmental Biology | 59 | 2% | 0% | 20 |
8 | Education, Special | 31 | 1% | 0% | 7 |
9 | Cell Biology | 24 | 5% | 0% | 50 |
10 | Biotechnology & Applied Microbiology | 18 | 3% | 0% | 36 |
Address terms |
chi_square_rank | term | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass |
---|---|---|---|---|---|
1 | GOLD SERV HUNTER GENET | 116939 | 0% | 100% | 4 |
2 | JC SELF HUMAN GENET | 116115 | 2% | 19% | 21 |
3 | NEURONS NETWORKS GRP | 93550 | 0% | 80% | 4 |
4 | JC SELF | 68191 | 1% | 17% | 14 |
5 | GRP MOL NEUROBIOLBUNKYO KU | 58470 | 0% | 100% | 2 |
6 | U316 | 50684 | 1% | 12% | 14 |
7 | SERV GENET | 43841 | 4% | 3% | 47 |
8 | HUNTER GENET | 42985 | 0% | 29% | 5 |
9 | GREENWOOD GENET | 42518 | 0% | 36% | 4 |
10 | U129 | 39694 | 1% | 11% | 12 |
Journals |
chi_square_rank | term | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass |
---|---|---|---|---|---|
1 | AMERICAN JOURNAL OF MEDICAL GENETICS | 101338 | 16% | 2% | 174 |
2 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 49622 | 9% | 2% | 101 |
3 | EUROPEAN JOURNAL OF MEDICAL GENETICS | 18732 | 3% | 2% | 28 |
4 | JOURNAL OF MEDICAL GENETICS | 17928 | 6% | 1% | 60 |
5 | CLINICAL GENETICS | 11808 | 4% | 1% | 46 |
6 | EUROPEAN JOURNAL OF HUMAN GENETICS | 11640 | 4% | 1% | 39 |
7 | AMERICAN JOURNAL OF HUMAN GENETICS | 10447 | 5% | 1% | 54 |
8 | HUMAN MOLECULAR GENETICS | 5254 | 4% | 0% | 43 |
9 | HUMAN GENETICS | 2426 | 2% | 0% | 26 |
10 | GENOMICS | 1670 | 2% | 0% | 22 |
Author Key Words |
chi_square_rank | term | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass | LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | X LINKED MENTAL RETARDATION | 1374857 | 10% | 44% | 108 | Search X+LINKED+MENTAL+RETARDATION | Search X+LINKED+MENTAL+RETARDATION |
2 | PQBP1 | 584696 | 2% | 100% | 20 | Search PQBP1 | Search PQBP1 |
3 | XLMR | 519897 | 3% | 52% | 34 | Search XLMR | Search XLMR |
4 | ARX | 486931 | 4% | 39% | 43 | Search ARX | Search ARX |
5 | FG SYNDROME | 442163 | 2% | 69% | 22 | Search FG+SYNDROME | Search FG+SYNDROME |
6 | BORJESON FORSSMAN LEHMANN SYNDROME | 409287 | 1% | 100% | 14 | Search BORJESON+FORSSMAN+LEHMANN+SYNDROME | Search BORJESON+FORSSMAN+LEHMANN+SYNDROME |
7 | MRX | 382405 | 2% | 59% | 22 | Search MRX | Search MRX |
8 | ARX GENE | 380052 | 1% | 100% | 13 | Search ARX+GENE | Search ARX+GENE |
9 | NONSPECIFIC X LINKED MENTAL RETARDATION | 321583 | 1% | 100% | 11 | Search NONSPECIFIC+X+LINKED+MENTAL+RETARDATION | Search NONSPECIFIC+X+LINKED+MENTAL+RETARDATION |
10 | SLC9A6 | 321583 | 1% | 100% | 11 | Search SLC9A6 | Search SLC9A6 |
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 | 28592 | ATR X SYNDROME//ATRX//ATR X |
2 | 35963 | AARSKOG SCOTT SYNDROME//FGD1//FACIOGENITAL DYSPLASIA |
3 | 25520 | CHOROIDEREMIA//POU3F4//RAB ESCORT PROTEIN 1 |
4 | 8049 | SUBTELOMERIC REARRANGEMENTS//ARRAY CGH//MBD5 |
5 | 20421 | GRP HLTH SECUR//KALYANI SPECIAL//SUPPORT EXPERT PERSONS INTELLECTUAL DISABIL |
6 | 23603 | X CHROMOSOME INACTIVATION//HUMARA//CLONALITY |
7 | 34359 | TRAPP//SEDLIN//TRAPP COMPLEX |
8 | 20438 | SHOX//LERI WEILL DYSCHONDROSTEOSIS//SHOX GENE |
9 | 2297 | RETT SYNDROME//MECP2//CDKL5 |
10 | 1146 | FRAGILE X SYNDROME//FRAGILE X//FMR1 |