Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
11213 | 999 | 28.6 | 56% |
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 |
11213 | 1 | METACHROMATIC LEUKODYSTROPHY//ARYLSULFATASE A//MULTIPLE SULFATASE DEFICIENCY | 999 |
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 | METACHROMATIC LEUKODYSTROPHY | authKW | 4877536 | 19% | 83% | 192 |
2 | ARYLSULFATASE A | authKW | 2768958 | 11% | 82% | 111 |
3 | MULTIPLE SULFATASE DEFICIENCY | authKW | 702981 | 2% | 100% | 23 |
4 | PSEUDODEFICIENCY | authKW | 547887 | 2% | 81% | 22 |
5 | ARYLSULFATASE A PSEUDODEFICIENCY | authKW | 303840 | 1% | 76% | 13 |
6 | ARYLSULPHATASE A | authKW | 254700 | 1% | 83% | 10 |
7 | SUMF1 | authKW | 254700 | 1% | 83% | 10 |
8 | ARYLSULFATASE | authKW | 233636 | 3% | 26% | 29 |
9 | ARYLSULFATASE A DEFICIENCY | authKW | 213951 | 1% | 100% | 7 |
10 | ARYLSULFATASE B | authKW | 176640 | 2% | 34% | 17 |
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 | Genetics & Heredity | 2652 | 22% | 0% | 222 |
2 | Clinical Neurology | 1195 | 16% | 0% | 162 |
3 | Biochemistry & Molecular Biology | 1045 | 30% | 0% | 295 |
4 | Medicine, Research & Experimental | 621 | 10% | 0% | 103 |
5 | Pediatrics | 461 | 8% | 0% | 83 |
6 | Medical Laboratory Technology | 363 | 3% | 0% | 34 |
7 | Neurosciences | 161 | 10% | 0% | 99 |
8 | Biophysics | 135 | 5% | 0% | 53 |
9 | Biotechnology & Applied Microbiology | 85 | 5% | 0% | 54 |
10 | Endocrinology & Metabolism | 70 | 5% | 0% | 45 |
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 | BIOCHEM ABT 2 | 106278 | 2% | 17% | 20 |
2 | CHILD NEUROL DIS UNIT | 40751 | 0% | 67% | 2 |
3 | BIOCHEM MOL ZELLBIOL | 31861 | 1% | 8% | 13 |
4 | ADDENBROOKES CAMBRIDGE UNIV HOSP | 30564 | 0% | 100% | 1 |
5 | ASSOC RECH NEUROCHIM | 30564 | 0% | 100% | 1 |
6 | BIOL FUNCTAREA FISIOL | 30564 | 0% | 100% | 1 |
7 | BIOPROMOENSAIA | 30564 | 0% | 100% | 1 |
8 | BIOSCI BIOTECHNOL BIOSCI | 30564 | 0% | 100% | 1 |
9 | CHILDHOOD WHITE MATTER DISORDERS NEUROSCI C | 30564 | 0% | 100% | 1 |
10 | CHILDREN WHITE MATTER DISORDERS | 30564 | 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 INHERITED METABOLIC DISEASE | 4184 | 3% | 1% | 25 |
2 | HUMAN GENETICS | 3187 | 3% | 0% | 29 |
3 | REVUE ROUMAINE DE BIOCHIMIE | 2504 | 1% | 2% | 5 |
4 | HUMAN MUTATION | 1946 | 2% | 0% | 16 |
5 | MOLECULAR GENETICS AND METABOLISM | 1897 | 1% | 0% | 14 |
6 | NEUROPEDIATRICS | 1804 | 1% | 1% | 11 |
7 | DEVELOPMENTAL NEUROSCIENCE | 1576 | 1% | 1% | 9 |
8 | CLINICAL GENETICS | 1512 | 2% | 0% | 16 |
9 | HUMAN GENE THERAPY CLINICAL DEVELOPMENT | 1505 | 0% | 2% | 2 |
10 | MOLECULAR AND CHEMICAL NEUROPATHOLOGY | 1446 | 1% | 1% | 5 |
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 | METACHROMATIC LEUKODYSTROPHY | 4877536 | 19% | 83% | 192 | Search METACHROMATIC+LEUKODYSTROPHY | Search METACHROMATIC+LEUKODYSTROPHY |
2 | ARYLSULFATASE A | 2768958 | 11% | 82% | 111 | Search ARYLSULFATASE+A | Search ARYLSULFATASE+A |
3 | MULTIPLE SULFATASE DEFICIENCY | 702981 | 2% | 100% | 23 | Search MULTIPLE+SULFATASE+DEFICIENCY | Search MULTIPLE+SULFATASE+DEFICIENCY |
4 | PSEUDODEFICIENCY | 547887 | 2% | 81% | 22 | Search PSEUDODEFICIENCY | Search PSEUDODEFICIENCY |
5 | ARYLSULFATASE A PSEUDODEFICIENCY | 303840 | 1% | 76% | 13 | Search ARYLSULFATASE+A+PSEUDODEFICIENCY | Search ARYLSULFATASE+A+PSEUDODEFICIENCY |
6 | ARYLSULPHATASE A | 254700 | 1% | 83% | 10 | Search ARYLSULPHATASE+A | Search ARYLSULPHATASE+A |
7 | SUMF1 | 254700 | 1% | 83% | 10 | Search SUMF1 | Search SUMF1 |
8 | ARYLSULFATASE | 233636 | 3% | 26% | 29 | Search ARYLSULFATASE | Search ARYLSULFATASE |
9 | ARYLSULFATASE A DEFICIENCY | 213951 | 1% | 100% | 7 | Search ARYLSULFATASE+A+DEFICIENCY | Search ARYLSULFATASE+A+DEFICIENCY |
10 | ARYLSULFATASE B | 176640 | 2% | 34% | 17 | Search ARYLSULFATASE+B | Search ARYLSULFATASE+B |
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 | CESANI, M , LORIOLI, L , GROSSI, S , AMICO, G , FUMAGALLI, F , SPIGA, I , FILOCAMO, M , BIFFI, A , (2016) MUTATION UPDATE OF ARSA AND PSAP GENES CAUSING METACHROMATIC LEUKODYSTROPHY.HUMAN MUTATION. VOL. 37. ISSUE 1. P. 16 -27 | 92 | 81% | 1 |
2 | MAHMOOD, A , BERRY, J , WENGER, DA , ESCOLAR, M , SOBEIH, M , RAYMOND, G , EICHLER, FS , (2010) METACHROMATIC LEUKODYSTROPHY: A CASE OF TRIPLETS WITH THE LATE INFANTILE VARIANT AND A SYSTEMATIC REVIEW OF THE LITERATURE.JOURNAL OF CHILD NEUROLOGY. VOL. 25. ISSUE 5. P. 572-580 | 66 | 97% | 6 |
3 | VIRGENS, MYF , SIEBERT, M , BOCK, H , BURIN, M , GIUGLIANI, R , SARAIVA-PEREIRA, ML , (2015) GENOTYPIC CHARACTERIZATION OF BRAZILIAN PATIENTS WITH INFANTILE AND JUVENILE FORMS OF METACHROMATIC LEUKODYSTROPHY.GENE. VOL. 568. ISSUE 1. P. 69 -75 | 43 | 91% | 1 |
4 | SCHLOTAWA, L , ENNEMANN, EC , RADHAKRISHNAN, K , SCHMIDT, B , CHAKRAPANI, A , CHRISTEN, HJ , MOSER, H , STEINMANN, B , DIERKS, T , GARTNER, J , (2011) SUMF1 MUTATIONS AFFECTING STABILITY AND ACTIVITY OF FORMYLGLYCINE GENERATING ENZYME PREDICT CLINICAL OUTCOME IN MULTIPLE SULFATASE DEFICIENCY.EUROPEAN JOURNAL OF HUMAN GENETICS. VOL. 19. ISSUE 3. P. 253 -261 | 33 | 83% | 16 |
5 | BATZIOS, SP , ZAFEIRIOU, DI , (2012) DEVELOPING TREATMENT OPTIONS FOR METACHROMATIC LEUKODYSTROPHY.MOLECULAR GENETICS AND METABOLISM. VOL. 105. ISSUE 1. P. 56 -63 | 52 | 50% | 18 |
6 | VAN RAPPARD, DF , BOELENS, JJ , WOLF, NI , (2015) METACHROMATIC LEUKODYSTROPHY: DISEASE SPECTRUM AND APPROACHES FOR TREATMENT.BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM. VOL. 29. ISSUE 2. P. 261 -273 | 29 | 81% | 6 |
7 | GIESELMANN, V , KRAGELOH-MANN, I , (2010) METACHROMATIC LEUKODYSTROPHY - AN UPDATE.NEUROPEDIATRICS. VOL. 41. ISSUE 1. P. 1 -6 | 28 | 85% | 46 |
8 | APPEL, MJ , BERTOZZI, CR , (2015) FORMYLGLYCINE, A POST-TRANSLATIONALLY GENERATED RESIDUE WITH UNIQUE CATALYTIC CAPABILITIES AND BIOTECHNOLOGY APPLICATIONS.ACS CHEMICAL BIOLOGY. VOL. 10. ISSUE 1. P. 72 -84 | 41 | 46% | 15 |
9 | PATIL, SA , MAEGAWA, GHB , (2013) DEVELOPING THERAPEUTIC APPROACHES FOR METACHROMATIC LEUKODYSTROPHY.DRUG DESIGN DEVELOPMENT AND THERAPY. VOL. 7. ISSUE . P. 729-745 | 53 | 42% | 14 |
10 | GIESELMANN, V , MATZNER, U , HESS, B , LULLMANN-RAUCH, R , COENEN, R , HARTMANN, D , D'HOOGE, R , DEDEYN, P , NAGELS, G , (1998) METACHROMATIC LEUKODYSTROPHY: MOLECULAR GENETICS AND AN ANIMAL MODEL.JOURNAL OF INHERITED METABOLIC DISEASE. VOL. 21. ISSUE 5. P. 564 -574 | 39 | 89% | 27 |
Classes with closest relation at Level 1 |