Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
11862 | 884 | 33.3 | 76% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
1398 | 7605 | COMMON VARIABLE IMMUNODEFICIENCY//PRIMARY IMMUNODEFICIENCY//IGA DEFICIENCY |
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 | HUMAN GENET INFECT DIS | Address | 44 | 36% | 11% | 99 |
2 | PEDIAT HEMATOL IMMUNOL UNIT | Address | 30 | 49% | 5% | 44 |
3 | NECKER MED | Address | 29 | 39% | 7% | 58 |
4 | PEDIAT IMMUNOL HEMATOL UNIT | Address | 28 | 64% | 3% | 27 |
5 | ST GILES HUMAN GENET INFECT DIS | Address | 27 | 35% | 7% | 62 |
6 | ROCKEFELLER BRANCH | Address | 26 | 34% | 7% | 64 |
7 | NECKER BRANCH | Address | 21 | 35% | 5% | 48 |
8 | MENDELIAN SUSCEPTIBILITY TO MYCOBACTERIAL DISEASE | Author keyword | 21 | 85% | 1% | 11 |
9 | STUDY PRIMARY IMMUNODEFICIENCIES | Address | 20 | 44% | 4% | 35 |
10 | FRENCH CHINESE GENET LIFE SCI | Address | 17 | 100% | 1% | 8 |
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 | CALMETTE GUERIN INFECTION | 49 | 47% | 9% | 77 |
2 | ESSENTIAL MODULATOR MUTATION | 39 | 74% | 3% | 29 |
3 | SMALL DELETION HOTSPOT | 37 | 100% | 2% | 14 |
4 | INHERITED INTERLEUKIN 12 DEFICIENCY | 35 | 67% | 4% | 32 |
5 | RECEPTOR BETA 1 DEFICIENCY | 30 | 62% | 4% | 31 |
6 | ANHIDROTIC ECTODERMAL DYSPLASIA | 25 | 39% | 6% | 51 |
7 | DISSEMINATED BCG INFECTION | 23 | 79% | 2% | 15 |
8 | IRAK 4 DEFICIENCY | 21 | 69% | 2% | 18 |
9 | MYCOBACTERIAL INFECTION | 21 | 27% | 8% | 68 |
10 | IL 12R BETA 1 DEFICIENCY | 21 | 90% | 1% | 9 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Inborn errors of IL-12/23- and IFN-gamma-mediated immunity: molecular, cellular, and clinical features | 2006 | 131 | 126 | 75% |
Mendelian susceptibility to mycobacterial disease: Genetic, immunological, and clinical features of inborn errors of IFN-gamma immunity | 2014 | 6 | 265 | 72% |
Infectious Diseases in Patients with IRAK-4, MyD88, NEMO, or I kappa B alpha Deficiency | 2011 | 73 | 64 | 73% |
Genetic deficiencies of innate immune signalling in human infectious disease | 2009 | 45 | 128 | 65% |
The genetic heterogeneity of mendelian susceptibility to mycobacterial diseases | 2008 | 81 | 89 | 75% |
Inborn errors of interferon (IFN)-mediated immunity in humans: insights into the respective roles of IFN-alpha/beta, IFN-gamma, and IFN-lambda in host defense | 2008 | 119 | 112 | 53% |
Novel primary immunodeficiencies revealed by the investigation of paediatric infectious diseases | 2008 | 59 | 77 | 77% |
Genetic dissection of immunity to mycobacteria: The human model | 2002 | 479 | 162 | 33% |
Human interferon-gamma-mediated immunity is a genetically controlled continuous trait that determines the outcome of mycobacterial invasion | 2000 | 88 | 21 | 100% |
Primary immunodeficiencies of protective immunity to primary infections | 2010 | 37 | 43 | 56% |
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 | HUMAN GENET INFECT DIS | 44 | 36% | 11% | 99 |
2 | PEDIAT HEMATOL IMMUNOL UNIT | 30 | 49% | 5.0% | 44 |
3 | NECKER MED | 29 | 39% | 6.6% | 58 |
4 | PEDIAT IMMUNOL HEMATOL UNIT | 28 | 64% | 3.1% | 27 |
5 | ST GILES HUMAN GENET INFECT DIS | 27 | 35% | 7.0% | 62 |
6 | ROCKEFELLER BRANCH | 26 | 34% | 7.2% | 64 |
7 | NECKER BRANCH | 21 | 35% | 5.4% | 48 |
8 | STUDY PRIMARY IMMUNODEFICIENCIES | 20 | 44% | 4.0% | 35 |
9 | FRENCH CHINESE GENET LIFE SCI | 17 | 100% | 0.9% | 8 |
10 | GENET HUMAINE MALAD INFECT | 16 | 37% | 4.0% | 35 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000131082 | HYPER IGE SYNDROME//JOBS SYNDROME//JOB SYNDROME |
2 | 0.0000130222 | SLC11A1//NRAMP1//MCGILL STUDY HOST ISTANCE |
3 | 0.0000110379 | BCG//TUBERCULOSIS//LANZHOU TB |
4 | 0.0000106503 | TUBERCULIN SCREENING//HLTH EDUC HUMAN SERV//EX JEFE UNIDAD 9 |
5 | 0.0000094296 | OMENN SYNDROME//SEVERE COMBINED IMMUNODEFICIENCY//T CELL LYMPHOPENIA |
6 | 0.0000085899 | INCONTINENTIA PIGMENTI//HYPOMELANOSIS OF ITO//BLOCH SULZBERGER SYNDROME |
7 | 0.0000068042 | COMMON VARIABLE IMMUNODEFICIENCY//IGA DEFICIENCY//CVID |
8 | 0.0000065227 | TIR DOMAIN//PELLINO//INNATE IMMUN INFLAMMAT |
9 | 0.0000063270 | ICES UOTTAWA//VACCINATION AGE//TUBERCULIN RESPONSE |
10 | 0.0000058179 | CHILDHOOD TUBERCULOSIS//DESMOND TUTU TB//TUBERCULOSIS IN CHILDREN |