Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
16795 | 635 | 32.9 | 68% |
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 |
551 | 3 | FABRY DISEASE//GAUCHER DISEASE//LYSOSOMAL STORAGE DISEASE | 18099 |
491 | 2 | GAUCHER DISEASE//LYSOSOMAL STORAGE DISEASE//MUCOPOLYSACCHARIDOSIS | 15457 |
16795 | 1 | KRABBE DISEASE//GLOBOID CELL LEUKODYSTROPHY//PSYCHOSINE | 635 |
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 | KRABBE DISEASE | authKW | 6948364 | 27% | 85% | 170 |
2 | GLOBOID CELL LEUKODYSTROPHY | authKW | 4719670 | 16% | 96% | 102 |
3 | PSYCHOSINE | authKW | 2567236 | 10% | 86% | 62 |
4 | GALACTOCEREBROSIDASE | authKW | 1649628 | 6% | 84% | 41 |
5 | TWITCHER MOUSE | authKW | 1400316 | 5% | 94% | 31 |
6 | TWITCHER | authKW | 1017494 | 4% | 92% | 23 |
7 | TWITCHER MICE | authKW | 625117 | 2% | 100% | 13 |
8 | GALC | authKW | 569432 | 2% | 79% | 15 |
9 | GALACTOSYLCERAMIDASE | authKW | 494595 | 2% | 86% | 12 |
10 | GALC GENE | authKW | 288515 | 1% | 100% | 6 |
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 | 1968 | 25% | 0% | 159 |
2 | Neurosciences | 1928 | 33% | 0% | 210 |
3 | Pathology | 583 | 9% | 0% | 58 |
4 | Genetics & Heredity | 580 | 14% | 0% | 87 |
5 | Pediatrics | 574 | 11% | 0% | 71 |
6 | Neuroimaging | 415 | 3% | 0% | 21 |
7 | Medicine, Research & Experimental | 402 | 10% | 0% | 66 |
8 | Biochemistry & Molecular Biology | 226 | 20% | 0% | 124 |
9 | Cell & Tissue Engineering | 164 | 2% | 0% | 10 |
10 | Medical Laboratory Technology | 119 | 3% | 0% | 16 |
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 | HUNTER JAMES KELLY | 204117 | 2% | 28% | 15 |
2 | POPULAT HLTH OBSERV | 173104 | 1% | 60% | 6 |
3 | LYSOSOMAL DIS TESTING | 171733 | 1% | 71% | 5 |
4 | FDN GILLET MERIEUX | 116351 | 2% | 22% | 11 |
5 | NEUROL 2E311 | 96172 | 0% | 100% | 2 |
6 | U189 | 77884 | 1% | 18% | 9 |
7 | UNIT HUMAN ANAT HISTOL | 54093 | 0% | 38% | 3 |
8 | AXOGLIA INTERACT UNIT INSPE | 48086 | 0% | 100% | 1 |
9 | CHILD HEALTHCARE GENET SCI | 48086 | 0% | 100% | 1 |
10 | CHILD NEUROL PATHOL | 48086 | 0% | 100% | 1 |
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 | JOURNAL OF NEUROSCIENCE RESEARCH | 13160 | 8% | 1% | 49 |
2 | PEDIATRIC NEUROLOGY | 5475 | 3% | 1% | 22 |
3 | NEUROPEDIATRICS | 2850 | 2% | 1% | 11 |
4 | MOLECULAR GENETICS AND METABOLISM | 2585 | 2% | 0% | 13 |
5 | JOURNAL OF INHERITED METABOLIC DISEASE | 1775 | 2% | 0% | 13 |
6 | JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY | 1515 | 2% | 0% | 10 |
7 | ACTA NEUROPATHOLOGICA | 1376 | 2% | 0% | 13 |
8 | BRAIN & DEVELOPMENT | 835 | 1% | 0% | 8 |
9 | NEUROBIOLOGY OF DISEASE | 827 | 1% | 0% | 8 |
10 | BIOCHEMICAL AND MOLECULAR MEDICINE | 804 | 0% | 1% | 2 |
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 | KRABBE DISEASE | 6948364 | 27% | 85% | 170 | Search KRABBE+DISEASE | Search KRABBE+DISEASE |
2 | GLOBOID CELL LEUKODYSTROPHY | 4719670 | 16% | 96% | 102 | Search GLOBOID+CELL+LEUKODYSTROPHY | Search GLOBOID+CELL+LEUKODYSTROPHY |
3 | PSYCHOSINE | 2567236 | 10% | 86% | 62 | Search PSYCHOSINE | Search PSYCHOSINE |
4 | GALACTOCEREBROSIDASE | 1649628 | 6% | 84% | 41 | Search GALACTOCEREBROSIDASE | Search GALACTOCEREBROSIDASE |
5 | TWITCHER MOUSE | 1400316 | 5% | 94% | 31 | Search TWITCHER+MOUSE | Search TWITCHER+MOUSE |
6 | TWITCHER | 1017494 | 4% | 92% | 23 | Search TWITCHER | Search TWITCHER |
7 | TWITCHER MICE | 625117 | 2% | 100% | 13 | Search TWITCHER+MICE | Search TWITCHER+MICE |
8 | GALC | 569432 | 2% | 79% | 15 | Search GALC | Search GALC |
9 | GALACTOSYLCERAMIDASE | 494595 | 2% | 86% | 12 | Search GALACTOSYLCERAMIDASE | Search GALACTOSYLCERAMIDASE |
10 | GALC GENE | 288515 | 1% | 100% | 6 | Search GALC+GENE | Search GALC+GENE |
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 | GRAZIANO, ACE , CARDILE, V , (2015) HISTORY, GENETIC, AND RECENT ADVANCES ON KRABBE DISEASE.GENE. VOL. 555. ISSUE 1. P. 2 -13 | 111 | 93% | 13 |
2 | WON, JS , SINGH, AK , SINGH, I , (2016) BIOCHEMICAL, CELL BIOLOGICAL, PATHOLOGICAL, AND THERAPEUTIC ASPECTS OF KRABBE'S DISEASE.JOURNAL OF NEUROSCIENCE RESEARCH. VOL. 94. ISSUE 11. P. 990 -1006 | 110 | 55% | 1 |
3 | BONGARZONE, ER , ESCOLAR, ML , GRAY, SJ , KAFRI, T , VITE, CH , SANDS, MS , (2016) INSIGHTS INTO THE PATHOGENESIS AND TREATMENT OF KRABBE DISEASE.PEDIATRIC ENDOCRINOLOGY REVIEWS PER. VOL. 13. ISSUE . P. 689 -696 | 58 | 89% | 1 |
4 | WENGER, DA , RAFI, MA , LUZI, P , (2016) KRABBE DISEASE: ONE HUNDRED YEARS FROM THE BEDSIDE TO THE BENCH TO THE BEDSIDE.JOURNAL OF NEUROSCIENCE RESEARCH. VOL. 94. ISSUE 11. P. 982 -989 | 55 | 98% | 0 |
5 | MIKULKA, CR , SANDS, MS , (2016) TREATMENT FOR KRABBE'S DISEASE: FINDING THE COMBINATION.JOURNAL OF NEUROSCIENCE RESEARCH. VOL. 94. ISSUE 11. P. 1126 -1137 | 63 | 82% | 0 |
6 | POTTER, GB , SANTOS, M , DAVISSON, MT , ROWITCH, DH , MARKS, DL , BONGARZONE, ER , PETRYNIAK, MA , (2013) MISSENSE MUTATION IN MOUSE GALC MIMICS HUMAN GENE DEFECT AND OFFERS NEW INSIGHTS INTO KRABBE DISEASE.HUMAN MOLECULAR GENETICS. VOL. 22. ISSUE 17. P. 3397-3414 | 56 | 88% | 12 |
7 | RICCA, A , GRITTI, A , (2016) PERSPECTIVE ON INNOVATIVE THERAPIES FOR GLOBOID CELL LEUKODYSTROPHY.JOURNAL OF NEUROSCIENCE RESEARCH. VOL. 94. ISSUE 11. P. 1304 -1317 | 82 | 59% | 0 |
8 | LI, YD , SANDS, MS , (2014) EXPERIMENTAL THERAPIES IN THE MURINE MODEL OF GLOBOID CELL LEUKODYSTROPHY.PEDIATRIC NEUROLOGY. VOL. 51. ISSUE 5. P. 600 -606 | 49 | 82% | 12 |
9 | KARUMUTHIL-MELETHIL, S , GRAY, SJ , (2016) IMMUNOLOGICAL CONSIDERATIONS FOR TREATING GLOBOID CELL LEUKODYSTROPHY.JOURNAL OF NEUROSCIENCE RESEARCH. VOL. 94. ISSUE 11. P. 1349 -1358 | 54 | 78% | 0 |
10 | LIAO, P , GELINAS, J , SIRRS, S , (2014) PHENOTYPIC VARIABILITY OF KRABBE DISEASE ACROSS THE LIFESPAN.CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES. VOL. 41. ISSUE 1. P. 5 -12 | 48 | 89% | 1 |
Classes with closest relation at Level 1 |