Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
13024 | 802 | 32.3 | 85% |
Classes in level above (level 2) |
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 | CADASIL | Author keyword | 643 | 83% | 46% | 367 |
2 | NOTCH3 | Author keyword | 88 | 56% | 13% | 108 |
3 | NOTCH3 GENE | Author keyword | 86 | 96% | 3% | 26 |
4 | CARASIL | Author keyword | 31 | 92% | 1% | 12 |
5 | U740 | Address | 26 | 67% | 3% | 24 |
6 | COL4A1 | Author keyword | 22 | 68% | 2% | 19 |
7 | CEREBRAL AUTOSOMAL DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY | Author keyword | 19 | 80% | 1% | 12 |
8 | CEREBRAL AUTOSOMAL DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY CADASIL | Author keyword | 15 | 88% | 1% | 7 |
9 | GRANULAR OSMIOPHILIC MATERIAL | Author keyword | 14 | 100% | 1% | 7 |
10 | NOTCH 3 GENE | Author keyword | 14 | 100% | 1% | 7 |
Web of Science journal categories |
Author Key Words |
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 | SUBCORTICAL INFARCTS | 469 | 78% | 38% | 307 |
2 | AUTOSOMAL DOMINANT ARTERIOPATHY | 367 | 69% | 39% | 311 |
3 | LEUKOENCEPHALOPATHY CADASIL | 285 | 93% | 13% | 107 |
4 | NOTCH3 MUTATIONS | 202 | 82% | 15% | 118 |
5 | CADASIL | 66 | 45% | 14% | 112 |
6 | LEUKOENCEPHALOPATHY | 43 | 20% | 24% | 195 |
7 | CADASIL PATIENTS | 33 | 67% | 4% | 29 |
8 | CONDITION CAUSING STROKE | 25 | 73% | 2% | 19 |
9 | NOTCH3 GENE | 24 | 82% | 2% | 14 |
10 | COLLAGEN IV A1 | 22 | 81% | 2% | 13 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
CADASIL | 2009 | 195 | 114 | 91% |
COL4A1 Mutations as a Monogenic Cause of Cerebral Small Vessel Disease A Systematic Review | 2010 | 43 | 21 | 90% |
Diagnostic strategies in CADASIL | 2002 | 134 | 19 | 95% |
Interpretation of NOTCH3 mutations in the diagnosis of CADASIL | 2014 | 5 | 81 | 96% |
Cerebral hemorrhages in CADASIL: Report of four cases and a brief review | 2013 | 12 | 20 | 85% |
Molecular genetics and pathology of hereditary small vessel diseases of the brain | 2011 | 28 | 151 | 71% |
Notch and disease: A growing field | 2012 | 44 | 109 | 30% |
Hereditary cerebral small vessel diseases: A review | 2012 | 16 | 31 | 65% |
Pathogenesis of CADASIL Transgenic and knock-out mice to probe function and dysfunction of the mutated gene, Notch3, in the cerebrovasculature | 2011 | 23 | 55 | 65% |
Lacunar Infarction and Small Vessel Disease: Pathology and Pathophysiology | 2015 | 2 | 12 | 25% |
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 | U740 | 26 | 67% | 3.0% | 24 |
2 | UMR S 1161 | 4 | 75% | 0.4% | 3 |
3 | STROKE DEMENTIA | 3 | 12% | 3.2% | 26 |
4 | GRP HOSP LARIBOISIERE FERNAND WIDAL | 3 | 35% | 0.9% | 7 |
5 | E365 | 3 | 50% | 0.5% | 4 |
6 | UMR740 | 3 | 60% | 0.4% | 3 |
7 | IMSEB | 2 | 67% | 0.2% | 2 |
8 | NEUROVASC TREATMENT UNIT | 2 | 67% | 0.2% | 2 |
9 | SITE LARIBOISIERE | 2 | 67% | 0.2% | 2 |
10 | UMR S740 | 2 | 36% | 0.5% | 4 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000120199 | CHROMOSOME 12P13//PRKCH//PDE4D |
2 | 0.0000115945 | LEUKOARAIOSIS//WHITE MATTER LESIONS//WHITE MATTER HYPERINTENSITIES |
3 | 0.0000088841 | VASCULAR DEMENTIA//POSTSTROKE DEMENTIA//VASCULAR COGNITIVE IMPAIRMENT |
4 | 0.0000072614 | CEREBRAL AMYLOID ANGIOPATHY//CEREBRAL MICROBLEEDS//MICROBLEEDS |
5 | 0.0000065734 | FAMILIAL HEMIPLEGIC MIGRAINE//HEMIPLEGIC MIGRAINE//ALTERNATING HEMIPLEGIA OF CHILDHOOD |
6 | 0.0000064444 | MIGRAINE WITH AURA//SERV CLIN GOVERNANCE//MIGRAINOUS INFARCT |
7 | 0.0000059981 | NOTCH//NOTCH SIGNALING//NOTCH1 |
8 | 0.0000054810 | ALEXANDER DISEASE//LEUKODYSTROPHY//VANISHING WHITE MATTER DISEASE |
9 | 0.0000051265 | SUSAC SYNDROME//SUSACS SYNDROME//ENDOTHELIOPATHY |
10 | 0.0000045395 | AICARDI GOUTIERES SYNDROME//TREX1//RIBONUCLEASE H |