Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
12781 | 881 | 29.0 | 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 |
551 | 3 | FABRY DISEASE//GAUCHER DISEASE//LYSOSOMAL STORAGE DISEASE | 18099 |
491 | 2 | GAUCHER DISEASE//LYSOSOMAL STORAGE DISEASE//MUCOPOLYSACCHARIDOSIS | 15457 |
12781 | 1 | ALEXANDER DISEASE//LEUKODYSTROPHY//ROSENTHAL FIBERS | 881 |
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 | ALEXANDER DISEASE | authKW | 3375195 | 12% | 89% | 109 |
2 | LEUKODYSTROPHY | authKW | 1486458 | 14% | 35% | 122 |
3 | ROSENTHAL FIBERS | authKW | 645250 | 4% | 58% | 32 |
4 | MLC1 | authKW | 645173 | 2% | 85% | 22 |
5 | LEUKOENCEPHALOPATHY | authKW | 519794 | 10% | 17% | 89 |
6 | HEPACAM | authKW | 500809 | 2% | 85% | 17 |
7 | VANISHING WHITE MATTER DISEASE | authKW | 458711 | 2% | 88% | 15 |
8 | VANISHING WHITE MATTER | authKW | 399586 | 2% | 82% | 14 |
9 | SUBCORTICAL CYSTS | authKW | 390481 | 1% | 87% | 13 |
10 | HEREDITARY DIFFUSE LEUKOENCEPHALOPATHY WITH SPHEROIDS | authKW | 381243 | 1% | 100% | 11 |
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 | 17175 | 60% | 0% | 530 |
2 | Neurosciences | 1804 | 28% | 0% | 244 |
3 | Pediatrics | 1689 | 16% | 0% | 139 |
4 | Neuroimaging | 1295 | 5% | 0% | 43 |
5 | Pathology | 1031 | 10% | 0% | 90 |
6 | Genetics & Heredity | 679 | 13% | 0% | 112 |
7 | Radiology, Nuclear Medicine & Medical Imaging | 338 | 9% | 0% | 77 |
8 | Psychiatry | 69 | 4% | 0% | 38 |
9 | Medical Ethics | 8 | 0% | 0% | 2 |
10 | Medicine, Research & Experimental | 5 | 2% | 0% | 19 |
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 | REFERENCE LEUCODYSTROPHIES | 154382 | 1% | 64% | 7 |
2 | CHILD NEUROL | 151924 | 14% | 4% | 123 |
3 | UMR 384 | 123767 | 1% | 36% | 10 |
4 | PEDIAT CHILD NEUROL | 115737 | 2% | 19% | 18 |
5 | REFERENCE MALAD RA LEUCODYSTROPHIES | 110905 | 0% | 80% | 4 |
6 | NEUROGENET MOT | 84904 | 1% | 35% | 7 |
7 | INVEST RED ENFERMEDADES RARAS CIBERER | 83173 | 1% | 40% | 6 |
8 | CNRS 6247 | 77980 | 0% | 75% | 3 |
9 | PEROXISOMAL DISORDERS PROGRAM | 77980 | 0% | 75% | 3 |
10 | SECC FISIOL | 70169 | 1% | 23% | 9 |
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 | NEUROPEDIATRICS | 18564 | 4% | 2% | 33 |
2 | JOURNAL OF CHILD NEUROLOGY | 10286 | 4% | 1% | 38 |
3 | BRAIN & DEVELOPMENT | 9746 | 4% | 1% | 32 |
4 | ACTA NEUROPATHOLOGICA | 4631 | 3% | 0% | 28 |
5 | NEUROLOGY | 3875 | 6% | 0% | 49 |
6 | EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY | 3125 | 1% | 1% | 10 |
7 | NEUROGENETICS | 2798 | 1% | 1% | 7 |
8 | ANNALS OF NEUROLOGY | 2532 | 3% | 0% | 24 |
9 | JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY | 2460 | 2% | 0% | 15 |
10 | CLINICAL NEUROPATHOLOGY | 2399 | 1% | 1% | 10 |
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 | ALEXANDER DISEASE | 3375195 | 12% | 89% | 109 | Search ALEXANDER+DISEASE | Search ALEXANDER+DISEASE |
2 | LEUKODYSTROPHY | 1486458 | 14% | 35% | 122 | Search LEUKODYSTROPHY | Search LEUKODYSTROPHY |
3 | ROSENTHAL FIBERS | 645250 | 4% | 58% | 32 | Search ROSENTHAL+FIBERS | Search ROSENTHAL+FIBERS |
4 | MLC1 | 645173 | 2% | 85% | 22 | Search MLC1 | Search MLC1 |
5 | LEUKOENCEPHALOPATHY | 519794 | 10% | 17% | 89 | Search LEUKOENCEPHALOPATHY | Search LEUKOENCEPHALOPATHY |
6 | HEPACAM | 500809 | 2% | 85% | 17 | Search HEPACAM | Search HEPACAM |
7 | VANISHING WHITE MATTER DISEASE | 458711 | 2% | 88% | 15 | Search VANISHING+WHITE+MATTER+DISEASE | Search VANISHING+WHITE+MATTER+DISEASE |
8 | VANISHING WHITE MATTER | 399586 | 2% | 82% | 14 | Search VANISHING+WHITE+MATTER | Search VANISHING+WHITE+MATTER |
9 | SUBCORTICAL CYSTS | 390481 | 1% | 87% | 13 | Search SUBCORTICAL+CYSTS | Search SUBCORTICAL+CYSTS |
10 | HEREDITARY DIFFUSE LEUKOENCEPHALOPATHY WITH SPHEROIDS | 381243 | 1% | 100% | 11 | Search HEREDITARY+DIFFUSE+LEUKOENCEPHALOPATHY+WITH+SPHEROIDS | Search HEREDITARY+DIFFUSE+LEUKOENCEPHALOPATHY+WITH+SPHEROIDS |
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 | GOROSPE, JR , MALETKOVIC, J , (2006) ALEXANDER DISEASE AND MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS: LEUKODYSTROPHIES ARISING FROM ASTROCYTE DYSFUNCTION.MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS. VOL. 12. ISSUE 2. P. 113-122 | 80 | 83% | 10 |
2 | BUGIANI, M , BOOR, I , POWERS, JM , SCHEPER, GC , VAN DER KNAAP, MS , (2010) LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER: A REVIEW.JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. VOL. 69. ISSUE 10. P. 987-996 | 65 | 74% | 45 |
3 | VAN DER KNAAP, MS , BOOR, I , ESTEVEZ, R , (2012) MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS: CHRONIC WHITE MATTER OEDEMA DUE TO A DEFECT IN BRAIN ION AND WATER HOMOEOSTASIS.LANCET NEUROLOGY. VOL. 11. ISSUE 11. P. 973 -985 | 58 | 66% | 21 |
4 | KONNO, T , YOSHIDA, K , MIZUNO, T , KAWARAI, T , TADA, M , NOZAKI, H , IKEDA, SI , NISHIZAWA, M , ONODERA, O , WSZOLEK, ZK , ET AL (2017) CLINICAL AND GENETIC CHARACTERIZATION OF ADULT-ONSET LEUKOENCEPHALOPATHY WITH AXONAL SPHEROIDS AND PIGMENTED GLIA ASSOCIATED WITH CSF1R MUTATION.EUROPEAN JOURNAL OF NEUROLOGY. VOL. 24. ISSUE 1. P. 37 -45 | 35 | 97% | 0 |
5 | KLINGELHOEFER, L , MISBAHUDDIN, A , JAWAD, T , MELLERS, J , JAROSZ, J , WEEKS, R , CHAUDHURI, KR , (2014) VANISHING WHITE MATTER DISEASE PRESENTING AS OPSOCLONUS MYOCLONUS SYNDROME IN CHILDHOOD-A CASE REPORT AND REVIEW OF THE LITERATURE.PEDIATRIC NEUROLOGY. VOL. 51. ISSUE 1. P. 157 -164 | 39 | 91% | 1 |
6 | JOHNSON, AB , BRENNER, M , (2003) ALEXANDER'S DISEASE: CLINICAL, PATHOLOGIC, AND GENETIC FEATURES.JOURNAL OF CHILD NEUROLOGY. VOL. 18. ISSUE 9. P. 625-632 | 46 | 94% | 32 |
7 | PRUST, M , WANG, J , MORIZONO, H , MESSING, A , BRENNER, M , GORDON, E , HARTKA, T , SOKOHL, A , SCHIFFMANN, R , GORDISH-DRESSMAN, H , ET AL (2011) GFAP MUTATIONS, AGE AT ONSET, AND CLINICAL SUBTYPES IN ALEXANDER DISEASE.NEUROLOGY. VOL. 77. ISSUE 13. P. 1287-1294 | 30 | 100% | 53 |
8 | YOSHIDA, T , NAKAGAWA, M , (2012) CLINICAL ASPECTS AND PATHOLOGY OF ALEXANDER DISEASE, AND MORPHOLOGICAL AND FUNCTIONAL ALTERATION OF ASTROCYTES INDUCED BY GFAP MUTATION.NEUROPATHOLOGY. VOL. 32. ISSUE 4. P. 440-446 | 35 | 95% | 10 |
9 | FERNANDEZ-VEGA, I , DE HEREDIA-GONI, KP , SANTOS-JUANES, J , IMIZCOZ, MG , ZALDUMBIDE, L , ZARRANZ, JJ , FERRER, I , (2016) SPORADIC ADULT-ONSET LEUCODYSTROPHY WITH AXONAL SPHEROIDS AND PIGMENTED GLIA WITH NO MUTATIONS IN THE KNOWN TARGETED GENES.HISTOPATHOLOGY. VOL. 68. ISSUE 2. P. 308 -312 | 31 | 91% | 1 |
10 | LABAUGE, P , BOESPFLUG-TANGUY, O , (2010) GENETIC DEMYELINATING DISEASES.PRESSE MEDICALE. VOL. 39. ISSUE 3. P. 363-370 | 40 | 85% | 1 |
Classes with closest relation at Level 1 |