Class information for:
Level 1: SUBTELOMERIC REARRANGEMENTS//IDIOPATHIC MENTAL RETARDATION//MBD5

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
7426 1289 32.9 85%


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 SUBTELOMERIC REARRANGEMENTS Author keyword 47 88% 2% 22
2 IDIOPATHIC MENTAL RETARDATION Author keyword 34 93% 1% 13
3 MBD5 Author keyword 33 100% 1% 13
4 ARRAY CGH Author keyword 23 14% 12% 152
5 1P36 DELETION SYNDROME Author keyword 17 75% 1% 12
6 MONOSOMY 1P36 Author keyword 15 67% 1% 14
7 17Q2131 MICRODELETION SYNDROME Author keyword 14 100% 1% 7
8 CHROMOSOMAL MICROARRAY ANALYSIS Author keyword 11 50% 1% 16
9 CHROMOSOMAL MICROARRAY Author keyword 10 41% 2% 20
10 GLOBAL DEVELOPMENTAL DELAY Author keyword 9 44% 1% 16

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 SUBTELOMERIC REARRANGEMENTS 47 88% 2% 22 Search SUBTELOMERIC+REARRANGEMENTS Search SUBTELOMERIC+REARRANGEMENTS
2 IDIOPATHIC MENTAL RETARDATION 34 93% 1% 13 Search IDIOPATHIC+MENTAL+RETARDATION Search IDIOPATHIC+MENTAL+RETARDATION
3 MBD5 33 100% 1% 13 Search MBD5 Search MBD5
4 ARRAY CGH 23 14% 12% 152 Search ARRAY+CGH Search ARRAY+CGH
5 1P36 DELETION SYNDROME 17 75% 1% 12 Search 1P36+DELETION+SYNDROME Search 1P36+DELETION+SYNDROME
6 MONOSOMY 1P36 15 67% 1% 14 Search MONOSOMY+1P36 Search MONOSOMY+1P36
7 17Q2131 MICRODELETION SYNDROME 14 100% 1% 7 Search 17Q2131+MICRODELETION+SYNDROME Search 17Q2131+MICRODELETION+SYNDROME
8 CHROMOSOMAL MICROARRAY ANALYSIS 11 50% 1% 16 Search CHROMOSOMAL+MICROARRAY+ANALYSIS Search CHROMOSOMAL+MICROARRAY+ANALYSIS
9 CHROMOSOMAL MICROARRAY 10 41% 2% 20 Search CHROMOSOMAL+MICROARRAY Search CHROMOSOMAL+MICROARRAY
10 GLOBAL DEVELOPMENTAL DELAY 9 44% 1% 16 Search GLOBAL+DEVELOPMENTAL+DELAY Search GLOBAL+DEVELOPMENTAL+DELAY

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 IDIOPATHIC MENTAL RETARDATION 112 61% 9% 121
2 MONOSOMY 1P36 50 65% 4% 47
3 SUBTELOMERIC REARRANGEMENTS 49 61% 4% 51
4 DYSMORPHIC FEATURES 47 49% 5% 69
5 CHROMOSOMAL MICROARRAY 43 57% 4% 51
6 ARRAY CGH 37 19% 13% 173
7 DEVELOPMENTAL DELAY 33 22% 10% 131
8 GLOBAL DEVELOPMENTAL DELAY 24 60% 2% 26
9 UNEXPLAINED MENTAL RETARDATION 23 72% 1% 18
10 MULTIPLE MALFORMATIONS 22 53% 2% 29

Journals


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 MOLECULAR CYTOGENETICS 4 11% 3% 39

Reviews


Title Publ. year Cit. Active
references		 % act. ref.
to same field
Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysis 2015 1 46 70%
Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis 2013 26 29 93%
Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis 2011 85 20 65%
Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects 2009 86 28 75%
Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation 2007 153 54 52%
Genomic Microarrays in Mental Retardation: A Practical Workflow for Diagnostic Applications 2009 79 51 59%
Implementation of genomic arrays in prenatal diagnosis: The Belgian approach to meet the challenges 2014 6 26 42%
Implementation of High Resolution Whole Genome Array CGH in the Prenatal Clinical Setting: Advantages, Challenges, and Review of the Literature 2013 8 25 84%
Novel microdeletion syndromes detected by chromosome microarrays 2008 115 50 36%
The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature 2013 8 26 81%

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 SIGNATURE GENOM S 6 27% 1.6% 20
2 CGH MICROARRAY 6 100% 0.3% 4
3 PAW PRINT GENET 5 54% 0.5% 7
4 OXFORD GENET KNOWLEDGE PK 3 60% 0.2% 3
5 FULLERTON GENET 3 35% 0.5% 6
6 CHROMOSOME REGISTRY SOC 18 2 67% 0.2% 2
7 JOINT UTRECHT UNIV GENET CORE 2 67% 0.2% 2
8 PEDIAT NEUROL PSYCHIAT 2 67% 0.2% 2
9 UK NEQAS CLIN CYTOGENET 2 43% 0.2% 3
10 MED GENET S 2 16% 0.7% 9

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000244213 COMPLEX CHROMOSOMAL REARRANGEMENT//COMPLEX CHROMOSOME REARRANGEMENT CCR//COMPLEX CHROMOSOMAL REARRANGEMENTS
2 0.0000216568 ZNF804A//MCLAUGHLIN//MOL CLIN NEUROBIOL
3 0.0000211654 QF PCR//UNCULTURED AMNIOCYTES//RAPID ANEUPLOIDY DETECTION
4 0.0000198633 SMITH MAGENIS SYNDROME//RAI1//POTOCKI LUPSKI SYNDROME
5 0.0000180362 COPY NUMBER VARIATION//CCL3L1//PENNCNV
6 0.0000170589 PELGER HUET ANOMALY//PELGER HUET//INTERSTITIAL 1Q DELETION
7 0.0000165575 TRISOMY 10Q//MONOSOMY 10Q//10P TRISOMY
8 0.0000163713 CRI DU CHAT SYNDROME//CRI DU CHAT//3P DELETION SYNDROME
9 0.0000157908 TRISOMY 9P//TETRASOMY 9P//PARTIAL TRISOMY 7P
10 0.0000148258 CHROMOSOME 6Q DELETION//SIM1 GENE//6Q DELETION