Class information for: |
Basic class information |
| ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
|---|---|---|---|
| 921 | 2877 | 34.1 | 71% |
Classes in level above (level 2) |
| ID, lev. above |
Publications | Label for level above |
|---|---|---|
| 844 | 11080 | PRION PROTEIN//SCRAPIE//CREUTZFELDT JAKOB DISEASE |
Terms with highest relevance score |
| Rank | Term | Type of term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
|---|---|---|---|---|---|---|
| 1 | CREUTZFELDT JAKOB DISEASE | Author keyword | 561 | 59% | 22% | 636 |
| 2 | CJD SURVEILLANCE UNIT | Address | 60 | 47% | 3% | 94 |
| 3 | GERSTMANN STRAUSSLER SCHEINKER DISEASE | Author keyword | 58 | 74% | 1% | 43 |
| 4 | FATAL FAMILIAL INSOMNIA | Author keyword | 45 | 65% | 1% | 43 |
| 5 | CJD SCI TECHNOL | Address | 40 | 82% | 1% | 23 |
| 6 | SPORADIC CREUTZFELDT JAKOB DISEASE | Author keyword | 40 | 67% | 1% | 36 |
| 7 | PRION DISEASE | Author keyword | 39 | 26% | 5% | 131 |
| 8 | PRION DISEASES | Author keyword | 39 | 28% | 4% | 117 |
| 9 | CJD | Author keyword | 31 | 38% | 2% | 65 |
| 10 | PRION PROTEIN GENE | Author keyword | 30 | 52% | 1% | 41 |
Web of Science journal categories |
Author Key Words |
| Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
LCSH search | Wikipedia search |
|---|---|---|---|---|---|---|---|
| 1 | CREUTZFELDT JAKOB DISEASE | 561 | 59% | 22% | 636 | Search CREUTZFELDT+JAKOB+DISEASE | Search CREUTZFELDT+JAKOB+DISEASE |
| 2 | GERSTMANN STRAUSSLER SCHEINKER DISEASE | 58 | 74% | 1% | 43 | Search GERSTMANN+STRAUSSLER+SCHEINKER+DISEASE | Search GERSTMANN+STRAUSSLER+SCHEINKER+DISEASE |
| 3 | FATAL FAMILIAL INSOMNIA | 45 | 65% | 1% | 43 | Search FATAL+FAMILIAL+INSOMNIA | Search FATAL+FAMILIAL+INSOMNIA |
| 4 | SPORADIC CREUTZFELDT JAKOB DISEASE | 40 | 67% | 1% | 36 | Search SPORADIC+CREUTZFELDT+JAKOB+DISEASE | Search SPORADIC+CREUTZFELDT+JAKOB+DISEASE |
| 5 | PRION DISEASE | 39 | 26% | 5% | 131 | Search PRION+DISEASE | Search PRION+DISEASE |
| 6 | PRION DISEASES | 39 | 28% | 4% | 117 | Search PRION+DISEASES | Search PRION+DISEASES |
| 7 | CJD | 31 | 38% | 2% | 65 | Search CJD | Search CJD |
| 8 | PRION PROTEIN GENE | 30 | 52% | 1% | 41 | Search PRION+PROTEIN+GENE | Search PRION+PROTEIN+GENE |
| 9 | PANENCEPHALOPATHIC TYPE | 30 | 100% | 0% | 12 | Search PANENCEPHALOPATHIC+TYPE | Search PANENCEPHALOPATHIC+TYPE |
| 10 | PERIODIC SHARP WAVE COMPLEXES | 26 | 100% | 0% | 11 | Search PERIODIC+SHARP+WAVE+COMPLEXES | Search PERIODIC+SHARP+WAVE+COMPLEXES |
Key Words Plus |
| Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
|---|---|---|---|---|---|
| 1 | CREUTZFELDT JAKOB DISEASE | 153 | 17% | 29% | 824 |
| 2 | GERSTMANN STRAUSSLER SYNDROME | 147 | 60% | 6% | 160 |
| 3 | AMYLOID PRECURSOR GENE | 131 | 87% | 2% | 65 |
| 4 | FATAL FAMILIAL INSOMNIA | 125 | 44% | 7% | 213 |
| 5 | CODON 178 | 114 | 93% | 1% | 42 |
| 6 | PRION PROTEIN GENE | 111 | 46% | 6% | 182 |
| 7 | CJD | 73 | 49% | 4% | 109 |
| 8 | SCHEINKER DISEASE | 67 | 85% | 1% | 35 |
| 9 | CODON 200 | 64 | 88% | 1% | 30 |
| 10 | PULVINAR SIGN | 58 | 83% | 1% | 33 |
Journals |
Reviews |
| Title | Publ. year | Cit. | Active references | % act. ref. to same field |
|---|---|---|---|---|
| Prion disease genetics | 2006 | 140 | 84 | 85% |
| Sporadic and familial CJD: classification and characterisation | 2003 | 204 | 83 | 84% |
| Mutations of the prion protein gene - Phenotypic spectrum | 2002 | 127 | 129 | 97% |
| Iatrogenic Creutzfeldt-Jakob disease at the millennium | 2000 | 283 | 14 | 71% |
| Iatrogenic Creutzfeldt-Jakob disease - The waning of an era | 2006 | 85 | 64 | 91% |
| The role of cerebrospinal fluid 14-3-3 and other proteins in the diagnosis of sporadic Creutzfeldt-Jakob disease in the UK: a 10-year review | 2010 | 29 | 13 | 92% |
| Sporadic human prion diseases: molecular insights and diagnosis | 2012 | 34 | 70 | 50% |
| The genetics of prion diseases | 2010 | 24 | 47 | 87% |
| EEG in Creutzfeldt-Jakob disease | 2006 | 57 | 101 | 79% |
| Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis | 2011 | 34 | 140 | 58% |
Address terms |
| Rank | Address term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
|---|---|---|---|---|---|
| 1 | CJD SURVEILLANCE UNIT | 60 | 47% | 3.3% | 94 |
| 2 | CJD SCI TECHNOL | 40 | 82% | 0.8% | 23 |
| 3 | AUSTRALIAN CREUTZFELDT JAKOB DIS REGISTRY | 26 | 80% | 0.6% | 16 |
| 4 | CENT NERVOUS SYST STUDIES | 18 | 47% | 1.0% | 29 |
| 5 | CREUTZFELDT JAKOB DIS SURVEILLANCE UNIT | 14 | 39% | 1.0% | 29 |
| 6 | PRION CLIN | 12 | 52% | 0.6% | 16 |
| 7 | MRC PRION UNIT | 11 | 27% | 1.2% | 34 |
| 8 | AUSTRIAN REFERENCE HUMAN PRION DIS | 10 | 73% | 0.3% | 8 |
| 9 | REFERENCE TSE SURVEILLANCE | 10 | 73% | 0.3% | 8 |
| 10 | PRION PROT | 10 | 63% | 0.3% | 10 |
Related classes at same level (level 1) |
| Rank | Relatedness score | Related classes |
|---|---|---|
| 1 | 0.0000201957 | PRION PROTEIN//PRION//CELLULAR PRION PROTEIN |
| 2 | 0.0000197388 | SCRAPIE//CHRONIC WASTING DISEASE//BSE |
| 3 | 0.0000093493 | CELLULAR NEUROL//PROTEOPATHY//PRION LIKE AGGREGATION |
| 4 | 0.0000043903 | HASHIMOTOS ENCEPHALOPATHY//HASHIMOTO ENCEPHALOPATHY//STEROID RESPONSIVE ENCEPHALOPATHY |
| 5 | 0.0000037572 | INFECT OBES//AD 36//ADENOVIRUS 36 |
| 6 | 0.0000034048 | BETA A4 DEPOSITS//SENILE PLAQUES//NEUROFIBRILLARY TANGLES |
| 7 | 0.0000024723 | BXSB MOUSE//LASHLEY MAZE//BIOBEHAV SCI DEGREE PROGRAM |
| 8 | 0.0000023732 | DORSAL VAGUS NUCLEUS//FETUS BRAIN//MARK COWLEY LIDWILL PROGRAM CARDIAC ELE OPHYSIO |
| 9 | 0.0000022212 | DISPOSABLE PRISMS//TONOMETER TIPS//TONOSAFE |
| 10 | 0.0000021474 | PSYCHIAT NEUROCHEM//CLIN MEMORY UNIT//UNIT NEUROCHEM |