Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
4896 | 1637 | 33.1 | 54% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
332 | 17329 | COMPLEMENT//MANNOSE BINDING LECTIN//PAROXYSMAL NOCTURNAL HEMOGLOBINURIA |
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 | C2 DEFICIENCY | Author keyword | 17 | 70% | 1% | 14 |
2 | COMPLEMENT GENETICS | Author keyword | 15 | 77% | 1% | 10 |
3 | COMPLEMENT AND INFLAMMATION | Journal | 7 | 27% | 1% | 22 |
4 | COMPLEMENT COMPONENT C4 | Author keyword | 7 | 57% | 0% | 8 |
5 | C4 | Author keyword | 7 | 17% | 2% | 35 |
6 | NONEXPRESSED ALLELES | Author keyword | 6 | 80% | 0% | 4 |
7 | C4AQ0 | Author keyword | 6 | 71% | 0% | 5 |
8 | COMPLEMENT C4 DEFICIENCY | Author keyword | 6 | 100% | 0% | 4 |
9 | RCCX MODULES | Author keyword | 6 | 100% | 0% | 4 |
10 | COMPLEMENT C4 | Author keyword | 5 | 33% | 1% | 13 |
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 | C2 DEFICIENCY | 17 | 70% | 1% | 14 | Search C2+DEFICIENCY | Search C2+DEFICIENCY |
2 | COMPLEMENT GENETICS | 15 | 77% | 1% | 10 | Search COMPLEMENT+GENETICS | Search COMPLEMENT+GENETICS |
3 | COMPLEMENT COMPONENT C4 | 7 | 57% | 0% | 8 | Search COMPLEMENT+COMPONENT+C4 | Search COMPLEMENT+COMPONENT+C4 |
4 | C4 | 7 | 17% | 2% | 35 | Search C4 | Search C4 |
5 | NONEXPRESSED ALLELES | 6 | 80% | 0% | 4 | Search NONEXPRESSED+ALLELES | Search NONEXPRESSED+ALLELES |
6 | C4AQ0 | 6 | 71% | 0% | 5 | Search C4AQ0 | Search C4AQ0 |
7 | COMPLEMENT C4 DEFICIENCY | 6 | 100% | 0% | 4 | Search COMPLEMENT+C4+DEFICIENCY | Search COMPLEMENT+C4+DEFICIENCY |
8 | RCCX MODULES | 6 | 100% | 0% | 4 | Search RCCX+MODULES | Search RCCX+MODULES |
9 | COMPLEMENT C4 | 5 | 33% | 1% | 13 | Search COMPLEMENT+C4 | Search COMPLEMENT+C4 |
10 | C4B | 5 | 44% | 0% | 8 | Search C4B | Search C4B |
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 | 4TH COMPONENT | 110 | 62% | 7% | 113 |
2 | STEROID 21 HYDROXYLASE GENES | 56 | 61% | 4% | 60 |
3 | HUMAN C 4 | 26 | 100% | 1% | 11 |
4 | HUMAN COMPLEMENT C4 | 23 | 100% | 1% | 10 |
5 | COMPONENT C4 | 22 | 60% | 1% | 24 |
6 | HUMAN COMPLEMENT COMPONENT C4 | 21 | 71% | 1% | 17 |
7 | SEX LIMITED PROTEIN | 21 | 65% | 1% | 20 |
8 | SLP GENES | 20 | 100% | 1% | 9 |
9 | C2 DEFICIENCY | 20 | 58% | 1% | 23 |
10 | REFERENCE TYPING REPORT | 17 | 75% | 1% | 12 |
Journals |
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 | COMPLEMENT AND INFLAMMATION | 7 | 27% | 1% | 22 |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
The internal thioester and the covalent binding properties of the complement proteins C3 and C4 | 1997 | 157 | 71 | 73% |
The tick-over theory revisited: Is C3 a contact-activated protein? | 2012 | 14 | 35 | 43% |
GENETICS OF SYSTEMIC LUPUS-ERYTHEMATOSUS | 1992 | 123 | 156 | 43% |
Genetics of systemic lupus erythematosus | 1995 | 79 | 197 | 37% |
Dancing with complement C4 and the RP-C4-CYP21-TNX (RCCX) modules of the major histocompatibility complex | 2003 | 29 | 230 | 63% |
Sex, MHC and complement C4 in autoimmune diseases | 2004 | 30 | 34 | 35% |
Links between complement abnormalities and systemic lupus erythematosus | 2000 | 69 | 90 | 33% |
STRUCTURE, ORGANIZATION, AND REGULATION OF THE COMPLEMENT GENES | 1988 | 149 | 115 | 41% |
A STRUCTURAL MODEL FOR THE LOCATION OF THE RODGERS AND THE CHIDO ANTIGENIC DETERMINANTS AND THEIR CORRELATION WITH THE HUMAN-COMPLEMENT COMPONENT C4A C4B ISOTYPES | 1988 | 37 | 42 | 88% |
Ethnic diversity of class III genes in autoimmune disease | 2001 | 7 | 43 | 58% |
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 | GRP INFLAMMAT BIOL IMMUNGENOM | 1 | 100% | 0.1% | 2 |
2 | RUDBECK C5 3 | 1 | 33% | 0.1% | 2 |
3 | DEP IMMUNOL | 1 | 50% | 0.1% | 1 |
4 | EUDOWOOD IMMUNOL | 1 | 50% | 0.1% | 1 |
5 | HLTH SCI MED THYROID | 1 | 50% | 0.1% | 1 |
6 | HUS HUS | 1 | 50% | 0.1% | 1 |
7 | IMMUNOL CELLULARE IMMUNOGENET | 1 | 50% | 0.1% | 1 |
8 | INVESTIGAT PEDIAT CIPED | 1 | 50% | 0.1% | 1 |
9 | MED HOWARD HUGHES MED PEDIAT | 1 | 50% | 0.1% | 1 |
10 | MED IMMUNOL TB CANC | 1 | 50% | 0.1% | 1 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000218154 | COMPLEMENT SYNTHESIS//MRC TRANSPLANTAT TRANSPLANTAT IMMUNOL M//COMPLEMENTO |
2 | 0.0000170272 | C3 AND C4//COMPLEMENT AND INFLAMMATION//LUPUS EXCELLENCE |
3 | 0.0000161974 | COMPSTATIN//COBRA VENOM FACTOR//STELLAR CHANCE S 401 |
4 | 0.0000150101 | COMPLEMENT RECEPTOR 1//COMPLEMENT RECEPTOR TYPE 1//CR1 |
5 | 0.0000137232 | ATYPICAL HEMOLYTIC UREMIC SYNDROME//FACTOR H//C3 GLOMERULOPATHY |
6 | 0.0000128752 | MOL IMMUNOL RUMENTAT//GENOMIC MATCHING TECHNIQUE//HLA A ALLELES |
7 | 0.0000126126 | C8 ALPHA//C8 GAMMA//PROPERDIN DEFICIENCY |
8 | 0.0000086233 | C1Q//C1Q DEFICIENCY//ANTI C1Q ANTIBODIES |
9 | 0.0000070238 | CD21//COMPLEMENT RECEPTOR 2//CR2 |
10 | 0.0000067214 | IDDM2//INS VNTR//INSULIN GENE |