Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
14512 | 699 | 31.9 | 81% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
1014 | 9854 | CONGENITAL DISORDERS OF GLYCOSYLATION//GLYCOPROTEOMICS//OLIGOSACCHARYLTRANSFERASE |
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 | CONGENITAL DISORDERS OF GLYCOSYLATION | Author keyword | 100 | 69% | 12% | 85 |
2 | CARBOHYDRATE DEFICIENT GLYCOPROTEIN SYNDROME | Author keyword | 91 | 85% | 7% | 47 |
3 | CDG | Author keyword | 79 | 74% | 8% | 59 |
4 | PMM2 | Author keyword | 38 | 93% | 2% | 14 |
5 | CDG IA | Author keyword | 37 | 100% | 2% | 14 |
6 | CONGENITAL DISORDER OF GLYCOSYLATION | Author keyword | 34 | 63% | 5% | 35 |
7 | PHOSPHOMANNOMUTASE DEFICIENCY | Author keyword | 20 | 100% | 1% | 9 |
8 | PHOSPHOMANNOMUTASE | Author keyword | 19 | 51% | 4% | 27 |
9 | GLYCOBIOL CARBOHYDRATE CHEM PROGRAM | Address | 17 | 63% | 2% | 17 |
10 | PMM2 CDG | Author keyword | 17 | 100% | 1% | 8 |
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 | CONGENITAL DISORDERS OF GLYCOSYLATION | 100 | 69% | 12% | 85 | Search CONGENITAL+DISORDERS+OF+GLYCOSYLATION | Search CONGENITAL+DISORDERS+OF+GLYCOSYLATION |
2 | CARBOHYDRATE DEFICIENT GLYCOPROTEIN SYNDROME | 91 | 85% | 7% | 47 | Search CARBOHYDRATE+DEFICIENT+GLYCOPROTEIN+SYNDROME | Search CARBOHYDRATE+DEFICIENT+GLYCOPROTEIN+SYNDROME |
3 | CDG | 79 | 74% | 8% | 59 | Search CDG | Search CDG |
4 | PMM2 | 38 | 93% | 2% | 14 | Search PMM2 | Search PMM2 |
5 | CDG IA | 37 | 100% | 2% | 14 | Search CDG+IA | Search CDG+IA |
6 | CONGENITAL DISORDER OF GLYCOSYLATION | 34 | 63% | 5% | 35 | Search CONGENITAL+DISORDER+OF+GLYCOSYLATION | Search CONGENITAL+DISORDER+OF+GLYCOSYLATION |
7 | PHOSPHOMANNOMUTASE DEFICIENCY | 20 | 100% | 1% | 9 | Search PHOSPHOMANNOMUTASE+DEFICIENCY | Search PHOSPHOMANNOMUTASE+DEFICIENCY |
8 | PHOSPHOMANNOMUTASE | 19 | 51% | 4% | 27 | Search PHOSPHOMANNOMUTASE | Search PHOSPHOMANNOMUTASE |
9 | PMM2 CDG | 17 | 100% | 1% | 8 | Search PMM2+CDG | Search PMM2+CDG |
10 | PHOSPHOMANNOSE ISOMERASE | 14 | 39% | 4% | 29 | Search PHOSPHOMANNOSE+ISOMERASE | Search PHOSPHOMANNOSE+ISOMERASE |
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 | DEFICIENT GLYCOPROTEIN SYNDROME | 200 | 69% | 25% | 172 |
2 | PHOSPHOMANNOSE ISOMERASE DEFICIENCY | 115 | 83% | 9% | 66 |
3 | CDG IA | 106 | 95% | 5% | 36 |
4 | PHOSPHOMANNOMUTASE DEFICIENCY | 102 | 95% | 5% | 35 |
5 | SYNDROME TYPE 1A | 89 | 100% | 4% | 27 |
6 | CDG | 81 | 83% | 6% | 45 |
7 | PMM2 | 73 | 89% | 5% | 33 |
8 | GLYCOSYLATION TYPE IA | 33 | 83% | 3% | 19 |
9 | CDG SYNDROME | 30 | 100% | 2% | 12 |
10 | CONGENITAL DISORDERS | 29 | 31% | 11% | 78 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Congenital Disorders of Glycosylation: An Update on Defects Affecting the Biosynthesis of Dolichol-Linked Oligosaccharides | 2009 | 74 | 112 | 76% |
The clinical spectrum of phosphomannomutase 2 deficiency (CDG-Ia) | 2009 | 36 | 104 | 95% |
Congenital disorders of glycosylation: a concise chart of glycocalyx dysfunction | 2015 | 5 | 70 | 26% |
Congenital disorders of glycosylation: A rapidly expanding disease family | 2007 | 126 | 67 | 61% |
Altered glycan structures: the molecular basis of congenital disorders of glycosylation | 2005 | 139 | 56 | 63% |
Congenital disorders of glycosylation: A review | 2002 | 87 | 75 | 85% |
Understanding Human Glycosylation Disorders: Biochemistry Leads the Charge | 2013 | 46 | 68 | 32% |
The clinical spectrum of phosphomannose isomerase deficiency, with an evaluation of mannose treatment for CDG-Ib | 2009 | 24 | 22 | 91% |
Genetic defects in the human glycome | 2006 | 180 | 99 | 29% |
Congenital disorders of glycosylation: review of their molecular bases, clinical presentations and specific therapies | 2003 | 150 | 126 | 47% |
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 | GLYCOBIOL CARBOHYDRATE CHEM PROGRAM | 17 | 63% | 2.4% | 17 |
2 | GENET DIS PROGRAM | 8 | 52% | 1.6% | 11 |
3 | KLIN POLIKLIN KINDER JUGENDMED ALLGEMEINE PAD | 3 | 50% | 0.6% | 4 |
4 | RIGSHOSP 4062 | 3 | 50% | 0.6% | 4 |
5 | GENET METAB ENDOCRINE DIS | 3 | 60% | 0.4% | 3 |
6 | KINDERHEILKUNDE 1 | 3 | 60% | 0.4% | 3 |
7 | SEKT METAB ENDOKRINOL ERKRANKUNGEN | 3 | 60% | 0.4% | 3 |
8 | AG PRAVENT KARDIOL | 2 | 67% | 0.3% | 2 |
9 | LEHRSTUHL ZELLBIOL PFLANZENBIOCHEM | 2 | 67% | 0.3% | 2 |
10 | UNITE GLYCOBIOL SIGNALISAT CELLULAIRE | 2 | 67% | 0.3% | 2 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000149372 | RHOMBENCEPHALOSYNAPSIS//PONTOCEREBELLAR HYPOPLASIA//GOMEZ LOPEZ HERNANDEZ SYNDROME |
2 | 0.0000142704 | DOLICHOL//POLYPRENOLS//POLYPRENOL |
3 | 0.0000135168 | CARBOHYDRATE DEFICIENT TRANSFERRIN//CDT//CARBOHYDRATE DEFICIENT TRANSFERRIN CDT |
4 | 0.0000115528 | UDP GALACTOSE TRANSPORTER//NUCLEOTIDE SUGAR TRANSPORTER//CMP SIALIC ACID TRANSPORTER |
5 | 0.0000100505 | UDP SUGAR HYDROLASE//PHOSPHOHEXOMUTASE//HAD SUPERFAMILY |
6 | 0.0000096595 | CONGENITAL DYSERYTHROPOIETIC ANEMIA//CONGENITAL DYSERYTHROPOIETIC ANAEMIA//HEMPAS |
7 | 0.0000082609 | TRANSALDOLASE DEFICIENCY//ESA 8080//NEONATAL HAEMORRHAGIC DIATHESIS |
8 | 0.0000065095 | OLIGOSACCHARYLTRANSFERASE//OLIGOSACCHARYL TRANSFERASE//STT3 |
9 | 0.0000064564 | GLYCOPROTEOMICS//GLYCOMICS//GLYC GLYCOPROTE |
10 | 0.0000061096 | CUTIS LAXA//MID DERMAL ELASTOLYSIS//ANNULAR ELASTOLYTIC GIANT CELL GRANULOMA |