Class information for: |
Basic class information |
| ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
|---|---|---|---|
| 33972 | 81 | 24.9 | 64% |
Classes in level above (level 2) |
| ID, lev. above |
Publications | Label for level above |
|---|---|---|
| 2144 | 4561 | MODY//MATURITY ONSET DIABETES OF THE YOUNG//NEONATAL DIABETES |
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 | FANCONI BICKEL SYNDROME | Author keyword | 27 | 72% | 26% | 21 |
| 2 | GLYCOGEN STORAGE DISEASE TYPE XI | Author keyword | 3 | 100% | 4% | 3 |
| 3 | GLUT2 GENE | Author keyword | 2 | 67% | 2% | 2 |
| 4 | FANCONI BICKEL | Author keyword | 1 | 100% | 2% | 2 |
| 5 | SLC2A2 GENE | Author keyword | 1 | 100% | 2% | 2 |
| 6 | FAMILY LINKAGE | Author keyword | 1 | 50% | 1% | 1 |
| 7 | FDN MARIANI MALATTIE METAB INFANZIA | Address | 1 | 50% | 1% | 1 |
| 8 | GLUCOSE TRANSPORTER PROTEIN 2 | Author keyword | 1 | 50% | 1% | 1 |
| 9 | PROXIMAL TUBULAR NEPHROPATHY | Author keyword | 1 | 50% | 1% | 1 |
| 10 | UNITE FONCT GENET | Address | 1 | 50% | 1% | 1 |
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 | FANCONI BICKEL SYNDROME | 27 | 72% | 26% | 21 | Search FANCONI+BICKEL+SYNDROME | Search FANCONI+BICKEL+SYNDROME |
| 2 | GLYCOGEN STORAGE DISEASE TYPE XI | 3 | 100% | 4% | 3 | Search GLYCOGEN+STORAGE+DISEASE+TYPE+XI | Search GLYCOGEN+STORAGE+DISEASE+TYPE+XI |
| 3 | GLUT2 GENE | 2 | 67% | 2% | 2 | Search GLUT2+GENE | Search GLUT2+GENE |
| 4 | FANCONI BICKEL | 1 | 100% | 2% | 2 | Search FANCONI+BICKEL | Search FANCONI+BICKEL |
| 5 | SLC2A2 GENE | 1 | 100% | 2% | 2 | Search SLC2A2+GENE | Search SLC2A2+GENE |
| 6 | FAMILY LINKAGE | 1 | 50% | 1% | 1 | Search FAMILY+LINKAGE | Search FAMILY+LINKAGE |
| 7 | GLUCOSE TRANSPORTER PROTEIN 2 | 1 | 50% | 1% | 1 | Search GLUCOSE+TRANSPORTER+PROTEIN+2 | Search GLUCOSE+TRANSPORTER+PROTEIN+2 |
| 8 | PROXIMAL TUBULAR NEPHROPATHY | 1 | 50% | 1% | 1 | Search PROXIMAL+TUBULAR+NEPHROPATHY | Search PROXIMAL+TUBULAR+NEPHROPATHY |
| 9 | 3 DEOXYFRUCTOSE | 0 | 33% | 1% | 1 | Search 3+DEOXYFRUCTOSE | Search 3+DEOXYFRUCTOSE |
| 10 | FACILITATIVE GLUCOSE TRANSPORT | 0 | 33% | 1% | 1 | Search FACILITATIVE+GLUCOSE+TRANSPORT | Search FACILITATIVE+GLUCOSE+TRANSPORT |
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 | SLC2A2 GLUT2 | 9 | 83% | 6% | 5 |
| 2 | HEPATORENAL GLYCOGENOSIS | 1 | 100% | 2% | 2 |
| 3 | FANCONI BICKEL SYNDROME | 1 | 13% | 7% | 6 |
| 4 | GLUT2 GENE | 1 | 15% | 5% | 4 |
| 5 | TRYPTOPHAN 388 | 0 | 20% | 2% | 2 |
| 6 | BICKEL SYNDROME | 0 | 33% | 1% | 1 |
| 7 | DIAGNOSTIC MOLECULAR PATHOLOGY | 0 | 25% | 1% | 1 |
| 8 | DEBRE SYNDROME | 0 | 20% | 1% | 1 |
| 9 | GLUT2 GLUCOSE TRANSPORTER | 0 | 20% | 1% | 1 |
| 10 | HEPATIC GLYCOGENOSIS | 0 | 20% | 1% | 1 |
Journals |
Reviews |
| Title | Publ. year | Cit. | Active references | % act. ref. to same field |
|---|---|---|---|---|
| Fanconi-Bickel syndrome - the original patient and his natural history, historical steps leading to the primary defect, and a review of the literature | 1998 | 54 | 40 | 30% |
| GLUT2 mutations, translocation, and receptor function in diet sugar managing | 2009 | 71 | 85 | 4% |
| Carbohydrate Intake | 2012 | 2 | 57 | 5% |
| The molecular pathology laboratory of the 21st century | 1999 | 3 | 106 | 8% |
| Molecular pathology for the general pathologist: Second oration of the Indian College of Pathologists | 2010 | 0 | 16 | 6% |
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 | FDN MARIANI MALATTIE METAB INFANZIA | 1 | 50% | 1.2% | 1 |
| 2 | UNITE FONCT GENET | 1 | 50% | 1.2% | 1 |
| 3 | HUMAN GENET BIRTH DEFECTS | 0 | 25% | 1.2% | 1 |
| 4 | PEDIAT HUMAN GENET MOL BIOL | 0 | 14% | 1.2% | 1 |
| 5 | UMR S 1155 | 0 | 11% | 1.2% | 1 |
| 6 | GROWTH SIGNALLING | 0 | 10% | 1.2% | 1 |
| 7 | ABT STOFFWECHSELKRANKHEITEN MOL PADIAT | 0 | 100% | 1.2% | 1 |
| 8 | ASAN MED SONPA GU | 0 | 100% | 1.2% | 1 |
| 9 | CHU PARIS NORD VAL DE SEINE | 0 | 100% | 1.2% | 1 |
| 10 | RENAL EMERGENCY KIDNEY TRANSPLANTAT | 0 | 100% | 1.2% | 1 |
Related classes at same level (level 1) |
| Rank | Relatedness score | Related classes |
|---|---|---|
| 1 | 0.0000172315 | PHOSPHORYLASE KINASE//PHOSPHORYLASE KINASE DEFICIENCY//GLYCOGEN STORAGE DISEASE TYPE IX |
| 2 | 0.0000149433 | NEONATAL DIABETES MELLITUS//NEONATAL DIABETES//WOLCOTT RALLISON SYNDROME |
| 3 | 0.0000129007 | RENAL TUBULAR ACIDOSIS//DISTAL RENAL TUBULAR ACIDOSIS//RENAL TUBULAR ACIDOSIS RTA |
| 4 | 0.0000123676 | SGLT2 INHIBITOR//DAPAGLIFLOZIN//CANAGLIFLOZIN |
| 5 | 0.0000119458 | GLYCOGEN STORAGE DISEASE TYPE III//SECT CELLULAR DIFFERENTIAT//GLUCOSE 6 PHOSPHATASE |
| 6 | 0.0000111026 | MODY//MATURITY ONSET DIABETES OF THE YOUNG//MATURITY ONSET DIABETES OF THE YOUNG MODY |
| 7 | 0.0000088093 | LOWE SYNDROME//OCULOCEREBRORENAL SYNDROME//OCRL1 |
| 8 | 0.0000087875 | GALACTOSEMIA//GALACTOSE 1 PHOSPHATE URIDYLTRANSFERASE//GALACTOSE 1 PHOSPHATE |
| 9 | 0.0000084112 | ENGLANDER DENT MUSEUM//SURG DEV SCI//SPECIFIC PLAQUE HYPOTHESIS |
| 10 | 0.0000078579 | GLUCOSE TRANSPORTER//GLUT4//GLUT1 |