Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
7164 | 1321 | 29.2 | 64% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
1822 | 5688 | POMPE DISEASE//GLYCOGEN STORAGE DISEASE TYPE II//GLYCOGEN STORAGE DISEASE |
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 | GLYCOGEN STORAGE DISEASE TYPE III | Author keyword | 98 | 94% | 3% | 34 |
2 | SECT CELLULAR DIFFERENTIAT | Address | 96 | 88% | 3% | 45 |
3 | GLUCOSE 6 PHOSPHATASE | Author keyword | 89 | 43% | 12% | 157 |
4 | GLYCOGEN STORAGE DISEASE TYPE IA | Author keyword | 56 | 84% | 2% | 31 |
5 | GLYCOGEN STORAGE DISEASE TYPE I | Author keyword | 50 | 88% | 2% | 23 |
6 | GLYCOGEN STORAGE DISEASE | Author keyword | 49 | 40% | 7% | 94 |
7 | GLYCOGEN STORAGE DISEASE TYPE 1 | Author keyword | 45 | 94% | 1% | 16 |
8 | GLYCOGEN STORAGE DISEASE TYPE IB | Author keyword | 38 | 89% | 1% | 17 |
9 | GLUCOSE 6 PHOSPHATE TRANSPORTER | Author keyword | 35 | 86% | 1% | 18 |
10 | GLYCOGEN STORAGE DIS PROGRAM | Address | 33 | 83% | 1% | 19 |
Web of Science journal categories |
Author Key Words |
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 | MICROSOMAL GLUCOSE 6 PHOSPHATASE | 106 | 79% | 5% | 68 |
2 | HEPATIC MICROSOMAL GLUCOSE 6 PHOSPHATASE | 86 | 96% | 2% | 26 |
3 | DEBRANCHING ENZYME GENE | 72 | 91% | 2% | 30 |
4 | STORAGE DISEASE TYPE 1A | 66 | 83% | 3% | 38 |
5 | PUTATIVE GLUCOSE 6 PHOSPHATE TRANSLOCASE | 51 | 83% | 2% | 29 |
6 | GLUCOSE 6 PHOSPHATASE GENE | 50 | 62% | 4% | 51 |
7 | PHOSPHOHISTIDINE ENZYME INTERMEDIATE | 45 | 94% | 1% | 16 |
8 | ENZYME DEFICIENT | 42 | 83% | 2% | 24 |
9 | MICROSOMAL GLUCOSE 6 PHOSPHATASE SYSTEM | 36 | 77% | 2% | 24 |
10 | DEBRANCHING ENZYME DEFICIENCY | 30 | 100% | 1% | 12 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
The glucose-6-phosphatase system | 2002 | 164 | 215 | 73% |
Glucose-6-phosphatase Catalytic Subunit Gene Family | 2009 | 42 | 50 | 62% |
Glucose-6-phosphatase deficiency | 2011 | 24 | 107 | 89% |
Mutations in the glucose-6-phosphatase-alpha (G6PC) gene that cause type Ia glycogen storage disease | 2008 | 31 | 89 | 94% |
Glycogen storage disease type I and G6Pase-beta deficiency: etiology and therapy | 2010 | 19 | 113 | 90% |
Liver transplantation in glycogen storage disease type I | 2014 | 2 | 51 | 80% |
Regulation of glucose production by the liver | 1999 | 219 | 88 | 52% |
GLYCOGEN-STORAGE-DISEASE IN ADULTS | 1994 | 97 | 23 | 96% |
New lessons in the regulation of glucose metabolism taught by the glucose 6-phosphatase system | 2000 | 75 | 182 | 62% |
The SLC37 family of phosphate-linked sugar phosphate antiporters | 2013 | 3 | 64 | 83% |
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 | SECT CELLULAR DIFFERENTIAT | 96 | 88% | 3.4% | 45 |
2 | GLYCOGEN STORAGE DIS PROGRAM | 33 | 83% | 1.4% | 19 |
3 | U855 | 17 | 51% | 1.8% | 24 |
4 | HERITABLE DISORDERS BRANCH | 9 | 19% | 3.2% | 42 |
5 | MED LYON EST LAENNEC | 3 | 100% | 0.2% | 3 |
6 | U449 | 3 | 15% | 1.3% | 17 |
7 | BIOCHEM ENDOCRINE METAB UNIT | 2 | 44% | 0.3% | 4 |
8 | NUTR ENDOCRINOL METAB | 2 | 44% | 0.3% | 4 |
9 | SECC BIOQUIM MED | 2 | 36% | 0.4% | 5 |
10 | PATOL METAB | 2 | 67% | 0.2% | 2 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000121219 | PHOSPHORYLASE KINASE//PHOSPHORYLASE KINASE DEFICIENCY//GLYCOGEN STORAGE DISEASE TYPE IX |
2 | 0.0000119458 | FANCONI BICKEL SYNDROME//GLYCOGEN STORAGE DISEASE TYPE XI//GLUT2 GENE |
3 | 0.0000083219 | MCARDLES DISEASE//MCARDLE DISEASE//MYOPHOSPHORYLASE |
4 | 0.0000072867 | TURING CHILD FIELD//MODIFIED WACHSTEIN AND MEISEL METHOD//CLESID |
5 | 0.0000061405 | SEVERE CONGENITAL NEUTROPENIA//HAX 1//CYCLIC NEUTROPENIA |
6 | 0.0000057869 | GLUCONEOGENESIS//GLYCOGENOLYSIS//ENDOGENOUS GLUCOSE PRODUCTION |
7 | 0.0000054186 | POMPE DISEASE//GLYCOGEN STORAGE DISEASE TYPE II//ACID ALPHA GLUCOSIDASE |
8 | 0.0000051839 | GLUCOKINASE ACTIVATOR//GLUCOKINASE//GLUCOKINASE REGULATORY PROTEIN |
9 | 0.0000043442 | LAFORA DISEASE//POLYGLUCOSAN BODIES//UNVERRICHT LUNDBORG DISEASE |
10 | 0.0000037839 | PHOSPHOENOLPYRUVATE CARBOXYKINASE//GLYCERONEOGENESIS//PHOSPHOENOLPYRUVATE CARBOXYKINASE GENE |