Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
14697 | 686 | 22.2 | 60% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
409 | 16055 | WOLF HIRSCHHORN SYNDROME//HOLOPROSENCEPHALY//ANNALES DE GENETIQUE |
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 | RING CHROMOSOME 21 | Author keyword | 24 | 82% | 2% | 14 |
2 | MONOSOMY 21 | Author keyword | 19 | 63% | 3% | 19 |
3 | RING CHROMOSOME 15 | Author keyword | 18 | 89% | 1% | 8 |
4 | RING CHROMOSOME 20 | Author keyword | 15 | 71% | 2% | 12 |
5 | 13Q SYNDROME | Author keyword | 11 | 78% | 1% | 7 |
6 | 13Q DELETION SYNDROME | Author keyword | 9 | 83% | 1% | 5 |
7 | CHROMOSOME 13Q DELETION | Author keyword | 9 | 83% | 1% | 5 |
8 | RING 20 SYNDROME | Author keyword | 8 | 75% | 1% | 6 |
9 | RING CHROMOSOME 20 SYNDROME | Author keyword | 8 | 100% | 1% | 5 |
10 | RING CHROMOSOME | Author keyword | 8 | 26% | 4% | 25 |
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 | RING CHROMOSOME 21 | 24 | 82% | 2% | 14 | Search RING+CHROMOSOME+21 | Search RING+CHROMOSOME+21 |
2 | MONOSOMY 21 | 19 | 63% | 3% | 19 | Search MONOSOMY+21 | Search MONOSOMY+21 |
3 | RING CHROMOSOME 15 | 18 | 89% | 1% | 8 | Search RING+CHROMOSOME+15 | Search RING+CHROMOSOME+15 |
4 | RING CHROMOSOME 20 | 15 | 71% | 2% | 12 | Search RING+CHROMOSOME+20 | Search RING+CHROMOSOME+20 |
5 | 13Q SYNDROME | 11 | 78% | 1% | 7 | Search 13Q+SYNDROME | Search 13Q+SYNDROME |
6 | 13Q DELETION SYNDROME | 9 | 83% | 1% | 5 | Search 13Q+DELETION+SYNDROME | Search 13Q+DELETION+SYNDROME |
7 | CHROMOSOME 13Q DELETION | 9 | 83% | 1% | 5 | Search CHROMOSOME+13Q+DELETION | Search CHROMOSOME+13Q+DELETION |
8 | RING 20 SYNDROME | 8 | 75% | 1% | 6 | Search RING+20+SYNDROME | Search RING+20+SYNDROME |
9 | RING CHROMOSOME 20 SYNDROME | 8 | 100% | 1% | 5 | Search RING+CHROMOSOME+20+SYNDROME | Search RING+CHROMOSOME+20+SYNDROME |
10 | RING CHROMOSOME | 8 | 26% | 4% | 25 | Search RING+CHROMOSOME | Search RING+CHROMOSOME |
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 | 21 MONOSOMY | 20 | 100% | 1% | 9 |
2 | NONCONVULSIVE STATUS | 17 | 100% | 1% | 8 |
3 | 14Q323 | 15 | 82% | 1% | 9 |
4 | SUBTELOMERIC SEQUENCES | 13 | 71% | 1% | 10 |
5 | T5P 21Q | 12 | 86% | 1% | 6 |
6 | 21Q | 10 | 73% | 1% | 8 |
7 | 14 CHROMOSOME | 8 | 100% | 1% | 5 |
8 | 13Q DELETION | 7 | 56% | 1% | 9 |
9 | 13Q SYNDROME | 6 | 80% | 1% | 4 |
10 | 14Q112Q13 | 6 | 80% | 1% | 4 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references |
% act. ref. to same field |
---|---|---|---|---|
The ring 14 syndrome | 2012 | 6 | 14 | 79% |
Epilepsy in ring 14 chromosome syndrome | 2012 | 4 | 28 | 89% |
Chromosome deletions in 13q33-34: Report of four patients and review of the literature | 2008 | 31 | 16 | 56% |
Distal 13q deletion syndrome and the VACTERL association: Case report, literature review, and possible implications | 2001 | 38 | 42 | 48% |
Mosaic ring 20 with no detectable deletion by FISH analysis: Characteristic seizure disorder and literature review | 2006 | 25 | 65 | 49% |
Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency: Molecular cytogenetic analysis and review of the literature | 2010 | 6 | 17 | 65% |
Complete monosomy mosaic of chromosome 21: Case report and review of literature | 2012 | 3 | 8 | 50% |
First trimester diagnosis of 13q-syndrome associated with increased fetal nuchal translucency thickness. Clinical findings and systematic review | 2012 | 1 | 15 | 73% |
BRIEF CLINICAL REPORT AND REVIEW - 2 PATIENTS WITH RING CHROMOSOME-15 SYNDROME | 1988 | 39 | 11 | 100% |
MONOSOMY-21Q - 2 CASES OF DEL(21Q) AND REVIEW OF THE LITERATURE | 1995 | 36 | 30 | 77% |
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 | ATENCAO INTEGRAL SAUDE DA MULHER | 1 | 50% | 0.1% | 1 |
2 | CHILD MOTHER HLTH | 1 | 50% | 0.1% | 1 |
3 | CLIN GENETMED | 1 | 50% | 0.1% | 1 |
4 | DIPARTIMENTO SCI GENET PERINATALI GINECOL | 1 | 50% | 0.1% | 1 |
5 | GENET SOC PROGRAM | 1 | 50% | 0.1% | 1 |
6 | INTELLECTUAL DEV DISABIL BRANCH | 1 | 50% | 0.1% | 1 |
7 | MED ISSEMYM | 1 | 50% | 0.1% | 1 |
8 | MINIST EDUC CULTURA DEPORTE | 1 | 50% | 0.1% | 1 |
9 | OBSTET GYNE IN KOU MED | 1 | 50% | 0.1% | 1 |
10 | PEDIAT DIABETOL ENDOCRINOL UNIT | 1 | 50% | 0.1% | 1 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000230784 | TRISOMY 10Q//MONOSOMY 10Q//10P TRISOMY |
2 | 0.0000223094 | CAT EYE SYNDROME//SUPERNUMERARY MARKER CHROMOSOMES//SMALL SUPERNUMERARY MARKER CHROMOSOME |
3 | 0.0000209821 | TRISOMY 9P//TETRASOMY 9P//PARTIAL TRISOMY 7P |
4 | 0.0000164776 | WOLF HIRSCHHORN SYNDROME//4P DELETION//PITT ROGERS DANKS SYNDROME |
5 | 0.0000158249 | PITT HOPKINS SYNDROME//18Q DELETION SYNDROME//18Q SYNDROME |
6 | 0.0000130637 | JACOBSEN SYNDROME//11Q SYNDROME//11Q TERMINAL DELETION DISORDER |
7 | 0.0000122573 | PALLISTER KILLIAN SYNDROME//TETRASOMY 12P//TRISOMY 12P |
8 | 0.0000122037 | PELGER HUET ANOMALY//PELGER HUET//INTERSTITIAL 1Q DELETION |
9 | 0.0000119527 | CRI DU CHAT SYNDROME//CRI DU CHAT//3P DELETION SYNDROME |
10 | 0.0000112797 | COMPLEX CHROMOSOMAL REARRANGEMENT//COMPLEX CHROMOSOME REARRANGEMENT CCR//COMPLEX CHROMOSOMAL REARRANGEMENTS |