Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
402 | 3530 | 53.3 | 89% |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
11 | 4 | NEUROSCIENCES//CLINICAL NEUROLOGY//NEUROL | 1112395 |
49 | 3 | ALZHEIMERS DISEASE//AMYOTROPHIC LATERAL SCLEROSIS//DEMENTIA | 92146 |
699 | 2 | AMYOTROPHIC LATERAL SCLEROSIS//FRONTOTEMPORAL DEMENTIA//ALS | 13006 |
402 | 1 | AMYOTROPHIC LATERAL SCLEROSIS//SOD1//ALS | 3530 |
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 | AMYOTROPHIC LATERAL SCLEROSIS | authKW | 2378709 | 35% | 22% | 1247 |
2 | SOD1 | authKW | 1221992 | 8% | 51% | 276 |
3 | ALS | authKW | 911034 | 12% | 24% | 435 |
4 | FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS | authKW | 527201 | 2% | 73% | 83 |
5 | MOTOR NEURON | authKW | 403767 | 8% | 17% | 275 |
6 | SUPEROXIDE DISMUTASE 1 | authKW | 346387 | 2% | 52% | 77 |
7 | MOTOR NEURON DISEASE | authKW | 261947 | 6% | 14% | 210 |
8 | AMYOTROPHIC LATERAL SCLEROSIS ALS | authKW | 234692 | 3% | 26% | 105 |
9 | G93A | authKW | 228921 | 1% | 88% | 30 |
10 | SOD1G93A | authKW | 176880 | 1% | 68% | 30 |
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 | 32012 | 55% | 0% | 1941 |
2 | Clinical Neurology | 17082 | 31% | 0% | 1089 |
3 | Biochemistry & Molecular Biology | 2295 | 24% | 0% | 863 |
4 | Pathology | 1112 | 6% | 0% | 200 |
5 | Genetics & Heredity | 301 | 5% | 0% | 187 |
6 | Cell Biology | 189 | 6% | 0% | 208 |
7 | Biophysics | 118 | 3% | 0% | 115 |
8 | Medicine, Research & Experimental | 44 | 3% | 0% | 91 |
9 | Geriatrics & Gerontology | 44 | 1% | 0% | 31 |
10 | Pharmacology & Pharmacy | 24 | 4% | 0% | 156 |
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 | SIGNALISAT MOL NEURODEGENE CENCE | 58105 | 0% | 40% | 17 |
2 | XRAY CRYSTALLOG CORE | 56750 | 0% | 41% | 16 |
3 | NEUROL CLIN TRIALS UNIT | 53863 | 1% | 35% | 18 |
4 | MOTOR NEURON DIS | 52956 | 0% | 44% | 14 |
5 | DAY NEUROMUSCULAR | 51866 | 1% | 33% | 18 |
6 | NEUROL | 49040 | 34% | 0% | 1193 |
7 | GENET BIOCHEM LAGENBIO I3A | 44476 | 0% | 86% | 6 |
8 | YAMANAKA UNIT | 44476 | 0% | 86% | 6 |
9 | METHODIST NEUROL | 42971 | 0% | 38% | 13 |
10 | NEUROSCI PATHOBIOL | 42373 | 0% | 70% | 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 | AMYOTROPHIC LATERAL SCLEROSIS | 292575 | 4% | 22% | 157 |
2 | AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION | 34526 | 1% | 11% | 38 |
3 | AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS | 29894 | 0% | 22% | 16 |
4 | NEUROBIOLOGY OF DISEASE | 24460 | 3% | 3% | 102 |
5 | FRONTIERS IN CELLULAR NEUROSCIENCE | 11797 | 1% | 3% | 47 |
6 | JOURNAL OF THE NEUROLOGICAL SCIENCES | 11784 | 3% | 1% | 118 |
7 | NEURODEGENERATIVE DISEASES | 9801 | 1% | 4% | 28 |
8 | ANNALS OF NEUROLOGY | 6994 | 2% | 1% | 80 |
9 | JOURNAL OF NEUROCHEMISTRY | 5325 | 3% | 1% | 115 |
10 | HUMAN MOLECULAR GENETICS | 5275 | 2% | 1% | 78 |
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 | AMYOTROPHIC LATERAL SCLEROSIS | 2378709 | 35% | 22% | 1247 | Search AMYOTROPHIC+LATERAL+SCLEROSIS | Search AMYOTROPHIC+LATERAL+SCLEROSIS |
2 | SOD1 | 1221992 | 8% | 51% | 276 | Search SOD1 | Search SOD1 |
3 | ALS | 911034 | 12% | 24% | 435 | Search ALS | Search ALS |
4 | FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS | 527201 | 2% | 73% | 83 | Search FAMILIAL+AMYOTROPHIC+LATERAL+SCLEROSIS | Search FAMILIAL+AMYOTROPHIC+LATERAL+SCLEROSIS |
5 | MOTOR NEURON | 403767 | 8% | 17% | 275 | Search MOTOR+NEURON | Search MOTOR+NEURON |
6 | SUPEROXIDE DISMUTASE 1 | 346387 | 2% | 52% | 77 | Search SUPEROXIDE+DISMUTASE+1 | Search SUPEROXIDE+DISMUTASE+1 |
7 | MOTOR NEURON DISEASE | 261947 | 6% | 14% | 210 | Search MOTOR+NEURON+DISEASE | Search MOTOR+NEURON+DISEASE |
8 | AMYOTROPHIC LATERAL SCLEROSIS ALS | 234692 | 3% | 26% | 105 | Search AMYOTROPHIC+LATERAL+SCLEROSIS+ALS | Search AMYOTROPHIC+LATERAL+SCLEROSIS+ALS |
9 | G93A | 228921 | 1% | 88% | 30 | Search G93A | Search G93A |
10 | SOD1G93A | 176880 | 1% | 68% | 30 | Search SOD1G93A | Search SOD1G93A |
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 | TURNER, BJ , TALBOT, K , (2008) TRANSGENICS, TOXICITY AND THERAPEUTICS IN RODENT MODELS OF MUTANT SOD1-MEDIATED FAMILIAL ALS.PROGRESS IN NEUROBIOLOGY. VOL. 85. ISSUE 1. P. 94 -134 | 278 | 70% | 255 |
2 | BOILLEE, S , VANDE VELDE, C , CLEVELAND, DW , (2006) ALS: A DISEASE OF MOTOR NEURONS AND THEIR NONNEURONAL NEIGHBORS.NEURON. VOL. 52. ISSUE 1. P. 39 -59 | 164 | 67% | 722 |
3 | COZZOLINO, M , FERRI, A , CARRI, MT , (2008) AMYOTROPHIC LATERAL SCLEROSIS: FROM CURRENT DEVELOPMENTS IN THE LABORATORY TO CLINICAL IMPLICATIONS.ANTIOXIDANTS & REDOX SIGNALING. VOL. 10. ISSUE 3. P. 405 -443 | 247 | 60% | 70 |
4 | BARBER, SC , SHAW, PJ , (2010) OXIDATIVE STRESS IN ALS: KEY ROLE IN MOTOR NEURON INJURY AND THERAPEUTIC TARGET.FREE RADICAL BIOLOGY AND MEDICINE. VOL. 48. ISSUE 5. P. 629-641 | 153 | 67% | 199 |
5 | COZZOLINO, M , PESARESI, MG , GERBINO, V , GROSSKREUTZ, J , CARRI, MT , (2012) AMYOTROPHIC LATERAL SCLEROSIS: NEW INSIGHTS INTO UNDERLYING MOLECULAR MECHANISMS AND OPPORTUNITIES FOR THERAPEUTIC INTERVENTION.ANTIOXIDANTS & REDOX SIGNALING. VOL. 17. ISSUE 9. P. 1277 -1330 | 267 | 46% | 18 |
6 | REDLER, RL , DOKHOLYAN, NV , (2012) THE COMPLEX MOLECULAR BIOLOGY OF AMYOTROPHIC LATERAL SCLEROSIS (ALS).MOLECULAR BIOLOGY OF NEURODEGENERATIVE DISEASES. VOL. 107. ISSUE . P. 215 -262 | 195 | 56% | 44 |
7 | ROTUNNO, MS , BOSCO, DA , (2013) AN EMERGING ROLE FOR MISFOLDED WILD-TYPE SOD1 IN SPORADIC ALS PATHOGENESIS.FRONTIERS IN CELLULAR NEUROSCIENCE. VOL. 7. ISSUE . P. - | 123 | 77% | 46 |
8 | COZZOLINO, M , CARRI, MT , (2012) MITOCHONDRIAL DYSFUNCTION IN ALS.PROGRESS IN NEUROBIOLOGY. VOL. 97. ISSUE 2. P. 54 -66 | 131 | 72% | 63 |
9 | WANG, Q , JOHNSON, JL , AGAR, NYR , AGAR, JN , (2008) PROTEIN AGGREGATION AND PROTEIN INSTABILITY GOVERN FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS PATIENT SURVIVAL.PLOS BIOLOGY. VOL. 6. ISSUE 7. P. 1508 -1526 | 152 | 70% | 79 |
10 | SEETHARAMAN, SV , PRUDENCIO, M , KARCH, C , HOLLOWAY, SP , BORCHELT, DR , HART, PJ , (2009) IMMATURE COPPER-ZINC SUPEROXIDE DISMUTASE AND FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS.EXPERIMENTAL BIOLOGY AND MEDICINE. VOL. 234. ISSUE 10. P. 1140-1154 | 112 | 87% | 39 |
Classes with closest relation at Level 1 |