Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
2184 | 2255 | 33.0 | 72% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
330 | 17366 | FABRY DISEASE//GAUCHER DISEASE//MUCOPOLYSACCHARIDOSES |
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 | GAUCHER DISEASE | Author keyword | 917 | 77% | 27% | 619 |
2 | GLUCOCEREBROSIDASE | Author keyword | 372 | 82% | 10% | 216 |
3 | GAUCHERS DISEASE | Author keyword | 202 | 72% | 7% | 157 |
4 | GAUCHER CLIN | Address | 195 | 80% | 5% | 122 |
5 | IMIGLUCERASE | Author keyword | 109 | 92% | 2% | 44 |
6 | ALGLUCERASE | Author keyword | 68 | 100% | 1% | 22 |
7 | TYPE 1 GAUCHER DISEASE | Author keyword | 45 | 94% | 1% | 16 |
8 | ENZYME REPLACEMENT THERAPY | Author keyword | 35 | 20% | 7% | 160 |
9 | SECT MOL NEUROGENET | Address | 35 | 52% | 2% | 48 |
10 | VELAGLUCERASE ALFA | Author keyword | 27 | 92% | 0% | 11 |
Web of Science journal categories |
Author Key Words |
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 |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | GAUCHER DISEASE | 917 | 77% | 27% | 619 | Search GAUCHER+DISEASE | Search GAUCHER+DISEASE |
2 | GLUCOCEREBROSIDASE | 372 | 82% | 10% | 216 | Search GLUCOCEREBROSIDASE | Search GLUCOCEREBROSIDASE |
3 | GAUCHERS DISEASE | 202 | 72% | 7% | 157 | Search GAUCHERS+DISEASE | Search GAUCHERS+DISEASE |
4 | IMIGLUCERASE | 109 | 92% | 2% | 44 | Search IMIGLUCERASE | Search IMIGLUCERASE |
5 | ALGLUCERASE | 68 | 100% | 1% | 22 | Search ALGLUCERASE | Search ALGLUCERASE |
6 | TYPE 1 GAUCHER DISEASE | 45 | 94% | 1% | 16 | Search TYPE+1+GAUCHER+DISEASE | Search TYPE+1+GAUCHER+DISEASE |
7 | ENZYME REPLACEMENT THERAPY | 35 | 20% | 7% | 160 | Search ENZYME+REPLACEMENT+THERAPY | Search ENZYME+REPLACEMENT+THERAPY |
8 | VELAGLUCERASE ALFA | 27 | 92% | 0% | 11 | Search VELAGLUCERASE+ALFA | Search VELAGLUCERASE+ALFA |
9 | GBA GENE | 26 | 100% | 0% | 11 | Search GBA+GENE | Search GBA+GENE |
10 | BETA GLUCOCEREBROSIDASE | 26 | 68% | 1% | 23 | Search BETA+GLUCOCEREBROSIDASE | Search BETA+GLUCOCEREBROSIDASE |
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 | MACROPHAGE TARGETED GLUCOCEREBROSIDASE | 261 | 85% | 6% | 137 |
2 | ACID BETA GLUCOSIDASE | 237 | 68% | 9% | 208 |
3 | GLUCOCEREBROSIDASE | 204 | 59% | 10% | 229 |
4 | GLUCOCEREBROSIDASE GENE | 125 | 69% | 5% | 106 |
5 | NORRBOTTNIAN TYPE | 116 | 97% | 1% | 33 |
6 | HUMAN GLUCOCEREBROSIDASE GENE | 91 | 67% | 4% | 82 |
7 | ALGLUCERASE | 83 | 90% | 2% | 36 |
8 | IMIGLUCERASE | 81 | 81% | 2% | 48 |
9 | GAUCHER DISEASE | 67 | 25% | 11% | 238 |
10 | ENZYME REPLACEMENT THERAPY | 60 | 16% | 15% | 337 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
The link between the GBA gene and parkinsonism | 2012 | 55 | 89 | 80% |
Gaucher disease: Mutation and polymorphism spectrum in the glucocerebrosidase gene (GBA) | 2008 | 127 | 155 | 94% |
Taliglucerase alfa: An enzyme replacement therapy using plant cell expression technology | 2014 | 18 | 36 | 53% |
Lysosomal storage disease 1 - Phenotype, diagnosis, and treatment of Gaucher's disease | 2008 | 129 | 82 | 79% |
Enzyme therapy for Gaucher disease: the first 5 years | 1998 | 116 | 64 | 73% |
Gaucher disease: pathological mechanisms and modern management | 2005 | 114 | 91 | 79% |
How I treat Gaucher disease | 2011 | 27 | 81 | 96% |
Emerging therapeutic targets for Gaucher disease | 2015 | 1 | 103 | 54% |
Gaucher disease: complexity in a "simple" disorder | 2004 | 159 | 63 | 75% |
The Role of Glucocerebrosidase Mutations in Parkinson Disease and Lewy Body Disorders | 2010 | 44 | 68 | 68% |
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 | GAUCHER CLIN | 195 | 80% | 5.4% | 122 |
2 | SECT MOL NEUROGENET | 35 | 52% | 2.1% | 48 |
3 | DEV METAB NEUROL BRANCH | 8 | 18% | 1.7% | 39 |
4 | MED GENET BRANCH | 7 | 11% | 2.9% | 65 |
5 | LYSOSOMAL STORAGE DISORDERS UNIT | 6 | 38% | 0.6% | 13 |
6 | GAUCHER DIS TREATMENT | 6 | 100% | 0.2% | 4 |
7 | ENZYMOL CELLULAR FUNCT | 5 | 31% | 0.6% | 13 |
8 | REFERENCE MALAD LYSOSOMALES | 4 | 44% | 0.3% | 7 |
9 | CLIN NEUROSCI BRANCH | 3 | 14% | 1.0% | 23 |
10 | DIAGNOST GENET BIOCHIM MALATTIE METAB | 3 | 43% | 0.3% | 6 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000153401 | PROSAPOSIN//SPHINGOLIPID ACTIVATOR PROTEIN//SAPOSIN B |
2 | 0.0000070480 | GM2 GANGLIOSIDOSIS//SANDHOFF DISEASE//TAY SACHS DISEASE |
3 | 0.0000069393 | YKL 40//CHITOTRIOSIDASE//CHI3L1 |
4 | 0.0000068137 | GLOBOID CELL LEUKODYSTROPHY//KRABBE DISEASE//PSYCHOSINE |
5 | 0.0000066675 | FARBER DISEASE//ASAH1//FARBER LIPOGRANULOMATOSIS |
6 | 0.0000059536 | MUCOPOLYSACCHARIDOSES//HUNTER SYNDROME//MAROTEAUX LAMY SYNDROME |
7 | 0.0000057545 | CONGENITAL OCULAR MOTOR APRAXIA//JAMES PARKINSON//OCULAR MOTOR APRAXIA |
8 | 0.0000051695 | NIEMANN PICK DISEASE TYPE C//NIEMANN PICK TYPE C//NIEMANN PICK DISEASE |
9 | 0.0000050192 | FABRY DISEASE//ALPHA GALACTOSIDASE A//FABRYS DISEASE |
10 | 0.0000039172 | POMPE DISEASE//GLYCOGEN STORAGE DISEASE TYPE II//ACID ALPHA GLUCOSIDASE |