Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
18873 | 466 | 28.0 | 69% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
1298 | 8144 | TRANSFUSION//ABO INCOMPATIBLE//VOX SANGUINIS |
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 | MCLEOD SYNDROME | Author keyword | 103 | 93% | 8% | 39 |
2 | CHOREA ACANTHOCYTOSIS | Author keyword | 85 | 85% | 10% | 45 |
3 | NEUROACANTHOCYTOSIS | Author keyword | 73 | 77% | 11% | 50 |
4 | CHOREIN | Author keyword | 29 | 88% | 3% | 14 |
5 | ACANTHOCYTOSIS | Author keyword | 25 | 70% | 5% | 21 |
6 | XK GENE | Author keyword | 21 | 90% | 2% | 9 |
7 | VPS13A | Author keyword | 20 | 100% | 2% | 9 |
8 | HUNTINGTONS DISEASE LIKE 2 | Author keyword | 6 | 80% | 1% | 4 |
9 | KELL BLOOD GROUP | Author keyword | 6 | 80% | 1% | 4 |
10 | KELL BLOOD GROUP ANTIGENS | Author keyword | 6 | 100% | 1% | 4 |
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 | MCLEOD SYNDROME | 103 | 93% | 8% | 39 | Search MCLEOD+SYNDROME | Search MCLEOD+SYNDROME |
2 | CHOREA ACANTHOCYTOSIS | 85 | 85% | 10% | 45 | Search CHOREA+ACANTHOCYTOSIS | Search CHOREA+ACANTHOCYTOSIS |
3 | NEUROACANTHOCYTOSIS | 73 | 77% | 11% | 50 | Search NEUROACANTHOCYTOSIS | Search NEUROACANTHOCYTOSIS |
4 | CHOREIN | 29 | 88% | 3% | 14 | Search CHOREIN | Search CHOREIN |
5 | ACANTHOCYTOSIS | 25 | 70% | 5% | 21 | Search ACANTHOCYTOSIS | Search ACANTHOCYTOSIS |
6 | XK GENE | 21 | 90% | 2% | 9 | Search XK+GENE | Search XK+GENE |
7 | VPS13A | 20 | 100% | 2% | 9 | Search VPS13A | Search VPS13A |
8 | HUNTINGTONS DISEASE LIKE 2 | 6 | 80% | 1% | 4 | Search HUNTINGTONS+DISEASE+LIKE+2 | Search HUNTINGTONS+DISEASE+LIKE+2 |
9 | KELL BLOOD GROUP | 6 | 80% | 1% | 4 | Search KELL+BLOOD+GROUP | Search KELL+BLOOD+GROUP |
10 | KELL BLOOD GROUP ANTIGENS | 6 | 100% | 1% | 4 | Search KELL+BLOOD+GROUP+ANTIGENS | Search KELL+BLOOD+GROUP+ANTIGENS |
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 | NEUROACANTHOCYTOSIS | 111 | 77% | 16% | 76 |
2 | CHOREA ACANTHOCYTOSIS | 55 | 62% | 12% | 56 |
3 | MCLEOD SYNDROME | 39 | 67% | 8% | 35 |
4 | CHOREOACANTHOCYTOSIS | 31 | 92% | 3% | 12 |
5 | KX PROTEIN | 26 | 100% | 2% | 11 |
6 | AMYOTROPHIC CHOREA | 22 | 81% | 3% | 13 |
7 | XK | 19 | 71% | 3% | 15 |
8 | DISEASE LIKE 2 | 17 | 79% | 2% | 11 |
9 | JUNCTOPHILIN 3 | 13 | 80% | 2% | 8 |
10 | GROUP PROTEIN | 13 | 44% | 5% | 22 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Neuroacanthocytosis Syndromes | 2011 | 21 | 39 | 82% |
Neurologic phenotypes associated with acanthocytosis | 2007 | 39 | 82 | 67% |
Developments in neuroacanthocytosis: Expanding the spectrum of choreatic syndromes | 2006 | 20 | 94 | 56% |
Clinical features and molecular bases of neuroacanthocytosis | 2002 | 60 | 144 | 54% |
McLeod syndrome: a neurohaematological disorder | 2007 | 14 | 53 | 81% |
The neuropsychiatry of neuroacanthocytosis syndromes | 2011 | 9 | 82 | 50% |
Huntington's disease and Huntington's disease-like syndromes: an overview | 2013 | 4 | 67 | 45% |
Abnormal red cell features associated with hereditary neurodegenerative disorders: the neuroacanthocytosis syndromes | 2014 | 1 | 77 | 48% |
THE KELL BLOOD-GROUP SYSTEM - A REVIEW | 1990 | 42 | 14 | 79% |
Brain, blood, and iron: Perspectives on the roles of erythrocytes and iron in neurodegeneration | 2012 | 12 | 198 | 28% |
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 MOL GENET UNIT 2A3 | 1 | 100% | 0.4% | 2 |
2 | INHERITED CARDIAC DIS SECT | 1 | 50% | 0.4% | 2 |
3 | NEUROBIOL GENET NEUROBIOL | 1 | 40% | 0.4% | 2 |
4 | AFFECT MYELINE | 1 | 50% | 0.2% | 1 |
5 | CNRGS INSERM U665 | 1 | 50% | 0.2% | 1 |
6 | DAY HOSP TALASSEMICI | 1 | 50% | 0.2% | 1 |
7 | GROUPEMENT INTERET PUBL | 1 | 50% | 0.2% | 1 |
8 | NEUROIMAGING DEV DISORDERS UNIT | 1 | 50% | 0.2% | 1 |
9 | PLANT BIOTECHNOL GEN | 1 | 50% | 0.2% | 1 |
10 | ZENTRUM NEUROPATHOL PRIONFOR UNG | 1 | 50% | 0.2% | 1 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000177450 | PKAN//HALLERVORDEN SPATZ SYNDROME//NBIA |
2 | 0.0000159145 | WEAK D//RH BLOOD GROUP SYSTEM//RH BLOOD GROUP |
3 | 0.0000141344 | COHEN SYNDROME//COH1//VPS13B |
4 | 0.0000117396 | MNSS BLOOD GROUP SYSTEM//GLYCOPHORIN//VICIA UNIJUGA LECTIN |
5 | 0.0000082812 | ALLOIMMUNIZATION//TRANSFUS CELLULAR THER IES//DELAYED HEMOLYTIC TRANSFUSION REACTION |
6 | 0.0000082139 | FETAL ANEMIA//INTRAUTERINE TRANSFUSION//FETOMATERNAL HEMORRHAGE |
7 | 0.0000072731 | HUNTINGTONS DISEASE//HUNTINGTON DISEASE//NEUROGENET RARE DIS |
8 | 0.0000064806 | ENDOTHELIN CONVERTING ENZYME//PHOSPHORAMIDON//BIG ENDOTHELIN |
9 | 0.0000064752 | DUFFY BLOOD GROUP//DARC//DUFFY ANTIGEN |
10 | 0.0000050427 | MACHADO JOSEPH DISEASE//SPINOCEREBELLAR ATAXIA//SCA2 |