Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
603 | 14359 | 42.5 | 81% |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
0 | 4 | BIOCHEMISTRY & MOLECULAR BIOLOGY//CELL BIOLOGY//ONCOLOGY | 4064930 |
603 | 3 | HUNTINGTONS DISEASE//SPINOCEREBELLAR ATAXIA//POLYGLUTAMINE | 14359 |
1645 | 2 | HUNTINGTONS DISEASE//HUNTINGTIN//POLYGLUTAMINE | 6932 |
1711 | 2 | SPINOCEREBELLAR ATAXIA//HEREDITARY SPASTIC PARAPLEGIA//FRIEDREICHS ATAXIA | 6674 |
3956 | 2 | RKIP//RAF KINASE INHIBITOR PROTEIN//HIPPOCAMPAL CHOLINERGIC NEUROSTIMULATING PEPTIDE | 753 |
Terms with highest relevance score |
rank | Term | termType | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|---|
1 | HUNTINGTONS DISEASE | authKW | 2792091 | 16% | 58% | 2267 |
2 | SPINOCEREBELLAR ATAXIA | authKW | 615606 | 3% | 72% | 400 |
3 | POLYGLUTAMINE | authKW | 533393 | 3% | 66% | 383 |
4 | HUNTINGTIN | authKW | 478738 | 2% | 74% | 304 |
5 | HEREDITARY SPASTIC PARAPLEGIA | authKW | 454237 | 2% | 82% | 262 |
6 | FRIEDREICHS ATAXIA | authKW | 401488 | 2% | 76% | 249 |
7 | FRIEDREICH ATAXIA | authKW | 354626 | 1% | 83% | 201 |
8 | MACHADO JOSEPH DISEASE | authKW | 351163 | 1% | 86% | 192 |
9 | FRATAXIN | authKW | 322061 | 1% | 87% | 175 |
10 | 3 NITROPROPIONIC ACID | authKW | 305805 | 2% | 61% | 237 |
Web of Science journal categories |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | Clinical Neurology | 60274 | 29% | 1% | 4143 |
2 | Neurosciences | 34378 | 30% | 0% | 4265 |
3 | Genetics & Heredity | 23266 | 18% | 1% | 2543 |
4 | Biochemistry & Molecular Biology | 7720 | 23% | 0% | 3264 |
5 | Cell Biology | 1918 | 8% | 0% | 1141 |
6 | Neuroimaging | 1421 | 1% | 0% | 198 |
7 | Psychiatry | 1206 | 4% | 0% | 636 |
8 | Pathology | 823 | 3% | 0% | 410 |
9 | Biophysics | 309 | 3% | 0% | 410 |
10 | Pediatrics | 261 | 3% | 0% | 366 |
Address terms |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | NEUROL | 103135 | 25% | 1% | 3521 |
2 | MOL MED THER EUT | 90056 | 1% | 23% | 189 |
3 | ZYTOBIOL ZYTOPATHOL | 82448 | 0% | 63% | 62 |
4 | GENET CYTOGENET | 61826 | 1% | 32% | 91 |
5 | UNIGENE | 57399 | 0% | 52% | 52 |
6 | HUNTINGTON NRW | 37071 | 0% | 73% | 24 |
7 | BRUCE LEFROY GENET HLTH | 35409 | 0% | 35% | 48 |
8 | GENET CYTOGENET EMBRYOL | 34168 | 0% | 34% | 48 |
9 | ZYTOBIOL | 32380 | 0% | 51% | 30 |
10 | NEUROGENET RARE DIS | 32313 | 0% | 89% | 17 |
Journals |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | HUMAN MOLECULAR GENETICS | 64080 | 4% | 6% | 545 |
2 | CEREBELLUM | 55483 | 1% | 17% | 154 |
3 | MOVEMENT DISORDERS | 36548 | 2% | 5% | 337 |
4 | NEUROBIOLOGY OF DISEASE | 27769 | 2% | 6% | 220 |
5 | NEUROGENETICS | 21265 | 1% | 13% | 78 |
6 | NEUROLOGY | 14133 | 3% | 2% | 383 |
7 | JOURNAL OF NEUROLOGY | 13818 | 1% | 3% | 201 |
8 | JOURNAL OF THE NEUROLOGICAL SCIENCES | 12663 | 2% | 2% | 249 |
9 | ARCHIVES OF NEUROLOGY | 10733 | 1% | 3% | 185 |
10 | BRAIN | 10020 | 1% | 3% | 175 |
Author Key Words |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | HUNTINGTONS DISEASE | 2792091 | 16% | 58% | 2267 | Search HUNTINGTONS+DISEASE | Search HUNTINGTONS+DISEASE |
2 | SPINOCEREBELLAR ATAXIA | 615606 | 3% | 72% | 400 | Search SPINOCEREBELLAR+ATAXIA | Search SPINOCEREBELLAR+ATAXIA |
3 | POLYGLUTAMINE | 533393 | 3% | 66% | 383 | Search POLYGLUTAMINE | Search POLYGLUTAMINE |
4 | HUNTINGTIN | 478738 | 2% | 74% | 304 | Search HUNTINGTIN | Search HUNTINGTIN |
5 | HEREDITARY SPASTIC PARAPLEGIA | 454237 | 2% | 82% | 262 | Search HEREDITARY+SPASTIC+PARAPLEGIA | Search HEREDITARY+SPASTIC+PARAPLEGIA |
6 | FRIEDREICHS ATAXIA | 401488 | 2% | 76% | 249 | Search FRIEDREICHS+ATAXIA | Search FRIEDREICHS+ATAXIA |
7 | FRIEDREICH ATAXIA | 354626 | 1% | 83% | 201 | Search FRIEDREICH+ATAXIA | Search FRIEDREICH+ATAXIA |
8 | MACHADO JOSEPH DISEASE | 351163 | 1% | 86% | 192 | Search MACHADO+JOSEPH+DISEASE | Search MACHADO+JOSEPH+DISEASE |
9 | FRATAXIN | 322061 | 1% | 87% | 175 | Search FRATAXIN | Search FRATAXIN |
10 | 3 NITROPROPIONIC ACID | 305805 | 2% | 61% | 237 | Search 3+NITROPROPIONIC+ACID | Search 3+NITROPROPIONIC+ACID |
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. |
Rank | Reference | # ref. in cl. |
Shr. of ref. in cl. |
Citations |
---|---|---|---|---|
1 | ZUCCATO, C , VALENZA, M , CATTANEO, E , (2010) MOLECULAR MECHANISMS AND POTENTIAL THERAPEUTICAL TARGETS IN HUNTINGTON'S DISEASE.PHYSIOLOGICAL REVIEWS. VOL. 90. ISSUE 3. P. 905-981 | 461 | 72% | 309 |
2 | FIGIEL, M , SZLACHCIC, WJ , SWITONSKI, PM , GABKA, A , KRZYZOSIAK, WJ , (2012) MOUSE MODELS OF POLYGLUTAMINE DISEASES: REVIEW AND DATA TABLE. PART I.MOLECULAR NEUROBIOLOGY. VOL. 46. ISSUE 2. P. 393-429 | 299 | 82% | 12 |
3 | SANTOS, R , LEFEVRE, S , SLIWA, D , SEGUIN, A , CAMADRO, JM , LESUISSE, E , (2010) FRIEDREICH ATAXIA: MOLECULAR MECHANISMS, REDOX CONSIDERATIONS, AND THERAPEUTIC OPPORTUNITIES.ANTIOXIDANTS & REDOX SIGNALING. VOL. 13. ISSUE 5. P. 651 -690 | 264 | 87% | 59 |
4 | BAUER, PO , NUKINA, N , (2009) THE PATHOGENIC MECHANISMS OF POLYGLUTAMINE DISEASES AND CURRENT THERAPEUTIC STRATEGIES.JOURNAL OF NEUROCHEMISTRY. VOL. 110. ISSUE 6. P. 1737 -1765 | 278 | 80% | 94 |
5 | GIL, JM , REGO, AC , (2008) MECHANISMS OF NEURODEGENERATION IN HUNTINGTON'S DISEASE.EUROPEAN JOURNAL OF NEUROSCIENCE. VOL. 27. ISSUE 11. P. 2803 -2820 | 215 | 82% | 200 |
6 | JONES, L , HUGHES, A , (2011) PATHOGENIC MECHANISMS IN HUNTINGTON'S DISEASE.PATHOPHYSIOLOGY, PHARMACOLOGY, AND BIOCHEMISTRY OF DYSKINESIA. VOL. 98. ISSUE . P. 373 -418 | 263 | 82% | 10 |
7 | ROSS, CA , TABRIZI, SJ , (2011) HUNTINGTON'S DISEASE: FROM MOLECULAR PATHOGENESIS TO CLINICAL TREATMENT.LANCET NEUROLOGY. VOL. 10. ISSUE 1. P. 83-98 | 127 | 84% | 395 |
8 | SCHOLS, L , PAULSON, H , AUBURGER, G , KERMER, P , JEN, JC , SEIDEL, K , KORF, HW , DELLER, T , RUB, U , (2013) CLINICAL FEATURES, NEUROGENETICS AND NEUROPATHOLOGY OF THE POLYGLUTAMINE SPINOCEREBELLAR ATAXIAS TYPE 1, 2, 3, 6 AND 7.PROGRESS IN NEUROBIOLOGY. VOL. 104. ISSUE . P. 38 -66 | 221 | 72% | 48 |
9 | COSTA, MD , PAULSON, HL , (2012) TOWARD UNDERSTANDING MACHADO-JOSEPH DISEASE.PROGRESS IN NEUROBIOLOGY. VOL. 97. ISSUE 2. P. 239 -257 | 193 | 89% | 44 |
10 | SEIDEL, K , SISWANTO, S , BRUNT, ERP , DEN DUNNEN, W , KORF, HW , RUB, U , (2012) BRAIN PATHOLOGY OF SPINOCEREBELLAR ATAXIAS.ACTA NEUROPATHOLOGICA. VOL. 124. ISSUE 1. P. 1 -21 | 168 | 92% | 75 |
Classes with closest relation at Level 3 |