Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
2837 | 2060 | 34.2 | 82% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
1789 | 5796 | HEREDITARY SPASTIC PARAPLEGIA//FRIEDREICHS ATAXIA//FRIEDREICH ATAXIA |
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 | MACHADO JOSEPH DISEASE | Author keyword | 198 | 72% | 7% | 154 |
2 | SPINOCEREBELLAR ATAXIA | Author keyword | 183 | 54% | 11% | 233 |
3 | SCA2 | Author keyword | 125 | 83% | 3% | 70 |
4 | AUTOSOMAL DOMINANT CEREBELLAR ATAXIA | Author keyword | 100 | 85% | 3% | 52 |
5 | SPINOCEREBELLAR ATAXIA TYPE 2 | Author keyword | 90 | 83% | 2% | 50 |
6 | SPINOCEREBELLAR ATAXIAS | Author keyword | 85 | 73% | 3% | 65 |
7 | SCA6 | Author keyword | 50 | 76% | 2% | 35 |
8 | SCA3 | Author keyword | 48 | 65% | 2% | 45 |
9 | DENTATORUBRAL PALLIDOLUYSIAN ATROPHY | Author keyword | 43 | 69% | 2% | 37 |
10 | SPINOCEREBELLAR ATAXIA TYPE 3 | Author keyword | 34 | 56% | 2% | 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 | MACHADO JOSEPH DISEASE | 198 | 72% | 7% | 154 | Search MACHADO+JOSEPH+DISEASE | Search MACHADO+JOSEPH+DISEASE |
2 | SPINOCEREBELLAR ATAXIA | 183 | 54% | 11% | 233 | Search SPINOCEREBELLAR+ATAXIA | Search SPINOCEREBELLAR+ATAXIA |
3 | SCA2 | 125 | 83% | 3% | 70 | Search SCA2 | Search SCA2 |
4 | AUTOSOMAL DOMINANT CEREBELLAR ATAXIA | 100 | 85% | 3% | 52 | Search AUTOSOMAL+DOMINANT+CEREBELLAR+ATAXIA | Search AUTOSOMAL+DOMINANT+CEREBELLAR+ATAXIA |
5 | SPINOCEREBELLAR ATAXIA TYPE 2 | 90 | 83% | 2% | 50 | Search SPINOCEREBELLAR+ATAXIA+TYPE+2 | Search SPINOCEREBELLAR+ATAXIA+TYPE+2 |
6 | SPINOCEREBELLAR ATAXIAS | 85 | 73% | 3% | 65 | Search SPINOCEREBELLAR+ATAXIAS | Search SPINOCEREBELLAR+ATAXIAS |
7 | SCA6 | 50 | 76% | 2% | 35 | Search SCA6 | Search SCA6 |
8 | SCA3 | 48 | 65% | 2% | 45 | Search SCA3 | Search SCA3 |
9 | DENTATORUBRAL PALLIDOLUYSIAN ATROPHY | 43 | 69% | 2% | 37 | Search DENTATORUBRAL+PALLIDOLUYSIAN+ATROPHY | Search DENTATORUBRAL+PALLIDOLUYSIAN+ATROPHY |
10 | SPINOCEREBELLAR ATAXIA TYPE 3 | 34 | 56% | 2% | 41 | Search SPINOCEREBELLAR+ATAXIA+TYPE+3 | Search SPINOCEREBELLAR+ATAXIA+TYPE+3 |
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 | DOMINANT CEREBELLAR ATAXIA | 411 | 72% | 16% | 325 |
2 | MACHADO JOSEPH DISEASE | 326 | 52% | 22% | 449 |
3 | SCA2 | 192 | 84% | 5% | 105 |
4 | DRPLA | 125 | 83% | 3% | 70 |
5 | HEREDITARY ATAXIA | 98 | 82% | 3% | 58 |
6 | SPINOCEREBELLAR ATAXIA | 95 | 33% | 11% | 232 |
7 | CHROMOSOME 3P12 P211 | 94 | 97% | 1% | 28 |
8 | DOMINANT CEREBELLAR ATAXIAS | 89 | 69% | 4% | 76 |
9 | CAG REPEAT | 85 | 25% | 14% | 292 |
10 | CAG REPEAT EXPANSION | 84 | 68% | 4% | 75 |
Journals |
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 | CEREBELLUM | 10 | 11% | 4% | 86 |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond | 2010 | 151 | 99 | 80% |
Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis | 2004 | 425 | 135 | 68% |
Brain pathology of spinocerebellar ataxias | 2012 | 51 | 182 | 82% |
The Global Epidemiology of Hereditary Ataxia and Spastic Paraplegia: A Systematic Review of Prevalence Studies | 2014 | 9 | 48 | 65% |
The preclinical stage of spinocerebellar ataxias | 2015 | 1 | 57 | 81% |
Clinical features, neurogenetics and neuropathology of the polyglutamine spinocerebellar ataxias type 1, 2, 3, 6 and 7 | 2013 | 27 | 305 | 55% |
Spinocerebellar ataxia 2 (SCA2) | 2008 | 72 | 97 | 80% |
Movement Disorders in Spinocerebellar Ataxias | 2011 | 30 | 100 | 85% |
The autosomal dominant spinocerebellar ataxias: emerging mechanistic themes suggest pervasive Purkinje cell vulnerability | 2015 | 1 | 100 | 66% |
SCA3: Neurological features, pathogenesis and animal models | 2008 | 60 | 113 | 52% |
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 | ENFERMEDADES NEUROL | 11 | 100% | 0.3% | 6 |
2 | ROSE MOSS PARKINSON NEURODEGENERAT DIS | 11 | 100% | 0.3% | 6 |
3 | UNIGENE | 11 | 31% | 1.4% | 29 |
4 | IBMC UNIGENE | 8 | 100% | 0.2% | 5 |
5 | HLTH SCI GERMANS TRIAS PUJOL IGTP | 7 | 67% | 0.3% | 6 |
6 | ROSE MOSS PARKINSONS NEURODEGENERAT DIS | 5 | 55% | 0.3% | 6 |
7 | CLIN NEUROANAT | 4 | 13% | 1.6% | 32 |
8 | HOP BEN AKNOUM | 4 | 75% | 0.1% | 3 |
9 | MONTREAL GEN HOSP NEUROSCI | 4 | 75% | 0.1% | 3 |
10 | NAT OURCES CIRN | 4 | 33% | 0.5% | 10 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000138912 | FRIEDREICH ATAXIA//FRIEDREICHS ATAXIA//FRATAXIN |
2 | 0.0000132438 | HUNTINGTIN//POLYGLUTAMINE//HUNTINGTONS DISEASE |
3 | 0.0000125921 | NEUROBEHAV NEUROBIOL NEUROPSYCHOL UNIT//TANDOSPIRONE CITRATE//3 MT |
4 | 0.0000108272 | SPINAL AND BULBAR MUSCULAR ATROPHY//KENNEDYS DISEASE//KENNEDY DISEASE |
5 | 0.0000097888 | MULTIPLE SYSTEM ATROPHY//STRIATONIGRAL DEGENERATION//OLIVOPONTOCEREBELLAR ATROPHY |
6 | 0.0000077273 | AOA2//ARSACS//APRATAXIN |
7 | 0.0000067789 | FEN1//BRAUN S//CREAT INITIAT CELL CYCLE CONTROL |
8 | 0.0000054931 | CEREBELLAR MUTISM//POSTERIOR FOSSA SYNDROME//MUTISM |
9 | 0.0000052964 | HEREDITARY SPASTIC PARAPLEGIA//SPG4//SPASTIN |
10 | 0.0000051617 | HUNTINGTONS DISEASE//HUNTINGTON DISEASE//NEUROGENET RARE DIS |