Class information for:
Level 1: RING CHROMOSOME 21//MONOSOMY 21//RING CHROMOSOME 15

Basic class information

ID Publications Average number
of references
Avg. shr. active
ref. in WoS
14697 686 22.2 60%



Bar chart of Publication_year

Last years might be incomplete

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