Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
11456 | 913 | 34.1 | 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 | OMENN SYNDROME | Author keyword | 86 | 82% | 5% | 50 |
2 | SEVERE COMBINED IMMUNODEFICIENCY | Author keyword | 65 | 40% | 14% | 130 |
3 | T CELL LYMPHOPENIA | Author keyword | 19 | 80% | 1% | 12 |
4 | SEVERE COMBINED IMMUNODEFICIENCY SCID | Author keyword | 16 | 56% | 2% | 19 |
5 | X SCID | Author keyword | 11 | 65% | 1% | 11 |
6 | JEFFREY MODELL DIAGNOST PRIMARY IMMUNOD | Address | 10 | 73% | 1% | 8 |
7 | SCID | Author keyword | 10 | 15% | 6% | 58 |
8 | RAG DEFICIENCY | Author keyword | 9 | 83% | 1% | 5 |
9 | RETICULAR DYSGENESIS | Author keyword | 9 | 83% | 1% | 5 |
10 | SEVERE COMBINED IMMUNE DEFICIENCY | Author keyword | 9 | 40% | 2% | 17 |
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 | OMENN SYNDROME | 86 | 82% | 5% | 50 | Search OMENN+SYNDROME | Search OMENN+SYNDROME |
2 | SEVERE COMBINED IMMUNODEFICIENCY | 65 | 40% | 14% | 130 | Search SEVERE+COMBINED+IMMUNODEFICIENCY | Search SEVERE+COMBINED+IMMUNODEFICIENCY |
3 | T CELL LYMPHOPENIA | 19 | 80% | 1% | 12 | Search T+CELL+LYMPHOPENIA | Search T+CELL+LYMPHOPENIA |
4 | SEVERE COMBINED IMMUNODEFICIENCY SCID | 16 | 56% | 2% | 19 | Search SEVERE+COMBINED+IMMUNODEFICIENCY+SCID | Search SEVERE+COMBINED+IMMUNODEFICIENCY+SCID |
5 | X SCID | 11 | 65% | 1% | 11 | Search X+SCID | Search X+SCID |
6 | SCID | 10 | 15% | 6% | 58 | Search SCID | Search SCID |
7 | RAG DEFICIENCY | 9 | 83% | 1% | 5 | Search RAG+DEFICIENCY | Search RAG+DEFICIENCY |
8 | RETICULAR DYSGENESIS | 9 | 83% | 1% | 5 | Search RETICULAR+DYSGENESIS | Search RETICULAR+DYSGENESIS |
9 | SEVERE COMBINED IMMUNE DEFICIENCY | 9 | 40% | 2% | 17 | Search SEVERE+COMBINED+IMMUNE+DEFICIENCY | Search SEVERE+COMBINED+IMMUNE+DEFICIENCY |
10 | IL2RG | 8 | 70% | 1% | 7 | Search IL2RG | Search IL2RG |
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 | OMENN SYNDROME | 39 | 48% | 6% | 59 |
2 | SCIDX1 | 24 | 91% | 1% | 10 |
3 | COMBINED IMMUNE DEFICIENCY | 20 | 20% | 10% | 87 |
4 | CONGENITAL IMMUNODEFICIENCIES | 18 | 83% | 1% | 10 |
5 | TERM IMMUNE RECONSTITUTION | 17 | 68% | 2% | 15 |
6 | RAG MUTATIONS | 15 | 54% | 2% | 19 |
7 | EUROPEAN EXPERIENCE | 13 | 36% | 3% | 30 |
8 | LINKED COMBINED IMMUNODEFICIENCY | 12 | 75% | 1% | 9 |
9 | ADENOSINE DEAMINASE DEFICIENCY | 9 | 15% | 6% | 53 |
10 | CLASS II DEFICIENCY | 8 | 36% | 2% | 18 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references |
% act. ref. to same field |
---|---|---|---|---|
Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution | 2004 | 233 | 75 | 48% |
The Case for Mandatory Newborn Screening for Severe Combined Immunodeficiency (SCID) | 2014 | 8 | 39 | 79% |
The long quest for neonatal screening for severe combined immunodeficiency | 2012 | 37 | 39 | 62% |
More than just SCID-The phenotypic range of combined immunodeficiencies associated with mutations in the recombinase activating genes (RAG) 1 and 2 | 2010 | 41 | 45 | 64% |
Guidelines for newborn screening of primary immunodeficiency diseases | 2013 | 14 | 19 | 63% |
Systematic Evidence Review of Newborn Screening and Treatment of Severe Combined Immunodeficiency | 2010 | 31 | 41 | 66% |
Educational paper | 2011 | 38 | 68 | 43% |
Hematopoietic stem cell transplantation for primary immunodeficiency disease | 2008 | 29 | 38 | 66% |
Reviewing Omenn syndrome | 2001 | 64 | 37 | 78% |
B-cell function in severe combined immunodeficiency after stem cell or gene therapy: A review | 2010 | 26 | 43 | 60% |
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 | JEFFREY MODELL DIAGNOST PRIMARY IMMUNOD | 10 | 73% | 0.9% | 8 |
2 | PEDIAT ALLERGY IMMUNOL BLOOD MARROW TRANS | 8 | 100% | 0.5% | 5 |
3 | ALLERGY IMMUNOL BLOOD MARROW TRANSPLANTAT | 4 | 75% | 0.3% | 3 |
4 | PEDIAT CLINTEC | 4 | 75% | 0.3% | 3 |
5 | JEFFREY MODELL DIAG PRIMARY IMMUNODEFICIE | 4 | 56% | 0.5% | 5 |
6 | CANADIAN PRIMARY IMMUNODEFICIENCY | 4 | 46% | 0.7% | 6 |
7 | PEDIAT IMMUNOL SERV | 3 | 39% | 0.8% | 7 |
8 | CLIN IMMUNOL TRANSFUS MED MED | 3 | 100% | 0.3% | 3 |
9 | IMMUNODEFICIENCY LEIPZIG IDCL | 3 | 100% | 0.3% | 3 |
10 | PEDIAT BONE MARROW TRANSPLANT SERV | 3 | 100% | 0.3% | 3 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000137567 | COMMON VARIABLE IMMUNODEFICIENCY//IGA DEFICIENCY//CVID |
2 | 0.0000119593 | TOFACITINIB//JAK3//CP 690 550 |
3 | 0.0000107222 | WISKOTT ALDRICH SYNDROME//X LINKED THROMBOCYTOPENIA//WISKOTT ALDRICH SYNDROME PROTEIN |
4 | 0.0000104959 | HYPER IGE SYNDROME//JOBS SYNDROME//JOB SYNDROME |
5 | 0.0000094296 | HUMAN GENET INFECT DIS//PEDIAT HEMATOL IMMUNOL UNIT//NECKER MED |
6 | 0.0000091732 | PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY//ADENOSINE DEAMINASE//CECR1 |
7 | 0.0000091255 | IN UTERO TRANSPLANTATION//FETAL GENE THERAPY//INUTERO TRANSPLANTATION |
8 | 0.0000083916 | LENTIVIRAL VECTOR//LENTIVIRAL VECTORS//EXPT HEMATOL |
9 | 0.0000082990 | LYMPHOCYTE RECOVERY//IMMUNE RECONSTITUTION//BMT RECIPIENTS |
10 | 0.0000080731 | INTERLEUKIN 7//IL 7//INTERLEUKIN 7 RECEPTOR |