Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
1645 | 6932 | 48.6 | 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 |
377 | 1 | HUNTINGTONS DISEASE//HUNTINGTIN//POLYGLUTAMINE | 3565 |
1749 | 1 | HUNTINGTONS DISEASE//PREDICTIVE TESTING//JUVENILE HUNTINGTON DISEASE | 2504 |
19391 | 1 | 3 NITROPROPIONIC ACID//3 NP//MITOCHONDRIAL TOXIN | 507 |
23161 | 1 | 2 NITROPROPANE//INDOSPICINE//INDIGOFERA SUFFRUTICOSA | 356 |
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 | 5676569 | 32% | 57% | 2245 |
2 | HUNTINGTIN | authKW | 972818 | 4% | 73% | 301 |
3 | POLYGLUTAMINE | authKW | 800977 | 5% | 56% | 326 |
4 | 3 NITROPROPIONIC ACID | authKW | 628615 | 3% | 61% | 236 |
5 | POLYGLUTAMINE DISEASE | authKW | 219199 | 1% | 48% | 103 |
6 | ATAXIN 3 | authKW | 217563 | 1% | 70% | 71 |
7 | HUNTINGTON | authKW | 193851 | 1% | 48% | 91 |
8 | MOL MED THER EUT | address | 184972 | 3% | 22% | 188 |
9 | PREDICTIVE TESTING | authKW | 136964 | 1% | 38% | 82 |
10 | MUTANT HUNTINGTIN | authKW | 97258 | 0% | 82% | 27 |
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 | Neurosciences | 28336 | 38% | 0% | 2627 |
2 | Clinical Neurology | 13373 | 20% | 0% | 1395 |
3 | Genetics & Heredity | 9912 | 17% | 0% | 1160 |
4 | Biochemistry & Molecular Biology | 4613 | 25% | 0% | 1710 |
5 | Psychiatry | 1231 | 6% | 0% | 408 |
6 | Cell Biology | 834 | 8% | 0% | 531 |
7 | Neuroimaging | 370 | 1% | 0% | 73 |
8 | Psychology | 229 | 2% | 0% | 120 |
9 | Behavioral Sciences | 225 | 2% | 0% | 122 |
10 | Biophysics | 195 | 3% | 0% | 214 |
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 | MOL MED THER EUT | 184972 | 3% | 22% | 188 |
2 | HUNTINGTON NRW | 76840 | 0% | 73% | 24 |
3 | NEUROGENET RARE DIS | 66969 | 0% | 89% | 17 |
4 | TRANSLAT NEUROENDOCRINE UNIT | 53920 | 0% | 58% | 21 |
5 | STRUCT NEUROPATHOL | 45686 | 1% | 27% | 38 |
6 | NEUROL | 42579 | 23% | 1% | 1576 |
7 | TAUBE KORET HUNTINGTONS DIS | 41086 | 0% | 67% | 14 |
8 | HUNTINGTONS DIS CLIN | 40979 | 0% | 85% | 11 |
9 | NEUROIMAGING AGING NEURODEGENERAT DIS | 32419 | 0% | 82% | 9 |
10 | HUNTINGTONS DIS FORUM | 30821 | 0% | 100% | 7 |
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 | 54658 | 5% | 4% | 349 |
2 | NEUROBIOLOGY OF DISEASE | 47889 | 3% | 5% | 200 |
3 | MOVEMENT DISORDERS | 21636 | 3% | 3% | 180 |
4 | MOLECULAR NEURODEGENERATION | 6133 | 0% | 5% | 28 |
5 | JOURNAL OF MEDICAL GENETICS | 4978 | 1% | 1% | 82 |
6 | CLINICAL GENETICS | 4485 | 1% | 1% | 73 |
7 | EXPERIMENTAL NEUROLOGY | 4028 | 1% | 1% | 94 |
8 | BRAIN | 3297 | 1% | 1% | 70 |
9 | JOURNAL OF GENETIC COUNSELING | 3172 | 0% | 3% | 22 |
10 | JOURNAL OF NEUROCHEMISTRY | 3147 | 2% | 1% | 126 |
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 | 5676569 | 32% | 57% | 2245 | Search HUNTINGTONS+DISEASE | Search HUNTINGTONS+DISEASE |
2 | HUNTINGTIN | 972818 | 4% | 73% | 301 | Search HUNTINGTIN | Search HUNTINGTIN |
3 | POLYGLUTAMINE | 800977 | 5% | 56% | 326 | Search POLYGLUTAMINE | Search POLYGLUTAMINE |
4 | 3 NITROPROPIONIC ACID | 628615 | 3% | 61% | 236 | Search 3+NITROPROPIONIC+ACID | Search 3+NITROPROPIONIC+ACID |
5 | POLYGLUTAMINE DISEASE | 219199 | 1% | 48% | 103 | Search POLYGLUTAMINE+DISEASE | Search POLYGLUTAMINE+DISEASE |
6 | ATAXIN 3 | 217563 | 1% | 70% | 71 | Search ATAXIN+3 | Search ATAXIN+3 |
7 | HUNTINGTON | 193851 | 1% | 48% | 91 | Search HUNTINGTON | Search HUNTINGTON |
8 | PREDICTIVE TESTING | 136964 | 1% | 38% | 82 | Search PREDICTIVE+TESTING | Search PREDICTIVE+TESTING |
9 | MUTANT HUNTINGTIN | 97258 | 0% | 82% | 27 | Search MUTANT+HUNTINGTIN | Search MUTANT+HUNTINGTIN |
10 | R6 2 MICE | 90185 | 0% | 79% | 26 | Search R6+2+MICE | Search R6+2+MICE |
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 | 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 |
3 | 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 | 260 | 74% | 94 |
4 | 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 | 275 | 76% | 12 |
5 | 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 |
6 | 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 |
7 | POULADI, MA , MORTON, AJ , HAYDEN, MR , (2013) CHOOSING AN ANIMAL MODEL FOR THE STUDY OF HUNTINGTON'S DISEASE.NATURE REVIEWS NEUROSCIENCE. VOL. 14. ISSUE 10. P. 708-721 | 162 | 88% | 73 |
8 | ROZE, E , BONNET, C , BETUING, S , CABOCHE, J , (2010) HUNTINGTON'S DISEASE.DISEASES OF DNA REPAIR. VOL. 685. ISSUE . P. 45 -63 | 234 | 85% | 23 |
9 | BATES, GP , DORSEY, R , GUSELLA, JF , HAYDEN, MR , KAY, C , LEAVITT, BR , NANCE, M , ROSS, CA , SCAHILL, RI , WETZEL, R , ET AL (2015) HUNTINGTON DISEASE.NATURE REVIEWS DISEASE PRIMERS. VOL. 1. ISSUE . P. - | 179 | 83% | 16 |
10 | SAUDOU, F , HUMBERT, S , (2016) THE BIOLOGY OF HUNTINGTIN.NEURON. VOL. 89. ISSUE 5. P. 910 -926 | 126 | 87% | 10 |
Classes with closest relation at Level 2 |