Class information for:
Level 1: CHROMOSOME 6Q DELETION//SIM1 GENE//6Q DELETION

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
25018 245 30.8 76%


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 CHROMOSOME 6Q DELETION Author keyword 11 100% 2% 6
2 SIM1 GENE Author keyword 6 100% 2% 4
3 6Q DELETION Author keyword 4 41% 3% 7
4 CHROMOSOME 6 DUPLICATION Author keyword 3 100% 1% 3
5 CHROMOSOME 6Q DUPLICATION Author keyword 3 100% 1% 3
6 SIM1 Author keyword 3 35% 3% 7
7 SIM2 Author keyword 2 33% 2% 4
8 CHROMOSOME 6Q Author keyword 2 23% 2% 6
9 DUPLICATION 6Q Author keyword 1 100% 1% 2
10 INTERSTITIAL DELETION 6Q Author keyword 1 100% 1% 2

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 CHROMOSOME 6Q DELETION 11 100% 2% 6 Search CHROMOSOME+6Q+DELETION Search CHROMOSOME+6Q+DELETION
2 SIM1 GENE 6 100% 2% 4 Search SIM1+GENE Search SIM1+GENE
3 6Q DELETION 4 41% 3% 7 Search 6Q+DELETION Search 6Q+DELETION
4 CHROMOSOME 6 DUPLICATION 3 100% 1% 3 Search CHROMOSOME+6+DUPLICATION Search CHROMOSOME+6+DUPLICATION
5 CHROMOSOME 6Q DUPLICATION 3 100% 1% 3 Search CHROMOSOME+6Q+DUPLICATION Search CHROMOSOME+6Q+DUPLICATION
6 SIM1 3 35% 3% 7 Search SIM1 Search SIM1
7 SIM2 2 33% 2% 4 Search SIM2 Search SIM2
8 CHROMOSOME 6Q 2 23% 2% 6 Search CHROMOSOME+6Q Search CHROMOSOME+6Q
9 DUPLICATION 6Q 1 100% 1% 2 Search DUPLICATION+6Q Search DUPLICATION+6Q
10 INTERSTITIAL DELETION 6Q 1 100% 1% 2 Search INTERSTITIAL+DELETION+6Q Search INTERSTITIAL+DELETION+6Q

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 DRUG THERAPY TARGET 24 91% 4% 10
2 WILLI LIKE PHENOTYPE 6 37% 5% 13
3 2 MURINE HOMOLOGS 5 50% 3% 7
4 FACTOR BRN 2 3 20% 6% 14
5 SIM1 3 38% 2% 6
6 DISTAL DELETION 2 23% 3% 7
7 SINGLE MINDED GENE 2 11% 6% 14
8 SIM1 GENE 1 25% 2% 5
9 LONG ARM DELETION 1 15% 4% 9
10 6Q SYNDROME 1 100% 1% 2

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
CHROMOSOME-6Q DELETIONS - A REPORT OF 2 ADDITIONAL CASES AND A REVIEW OF THE LITERATURE 1990 49 16 81%
INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME-6 ASSOCIATED WITH UNUSUAL LIMB ANOMALIES - REPORT OF 2 NEW PATIENTS AND REVIEW OF THE LITERATURE 1995 23 16 81%
De novo microdeletions of chromosome 6q14.1-q14.3 and 6q12.1-q14.1 in two patients with intellectual disability - further delineation of the 6q14 microdeletion syndrome and review of the literature 2012 6 16 25%
Transcription factors in the development of medial hypothalamic structures 2009 9 37 24%
DELETIONS OF THE LONG ARM OF CHROMOSOME .6. 2 NEW CASES AND REVIEW OF THE LITERATURE 1985 49 3 100%
Looking for trouble: A search for developmental defects of the hypothalamus 2005 26 67 15%
Development of the Medial Hypothalamus: Forming a Functional Hypothalamic-Neurohypophyseal Interface 2013 10 150 11%
TRISOMY 6Q22-]6QTER DUE TO MATERNAL 6-21 TRANSLOCATION - CASE-REPORT AND REVIEW OF THE LITERATURE 1983 9 6 100%
Patterning, specification, and differentiation in the developing hypothalamus 2015 0 169 11%
Molecular genetics of the developing neuroendocrine hypothalamus 2010 20 99 5%

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 NEUROL DISABIL 1 33% 1.2% 3
2 AUSTRALIAN COUNCIL SPECIAL MOL GENET 1 40% 0.8% 2
3 RUDBECK SCI LIFE 1 50% 0.4% 1
4 ST ANTOINE PEDIAT HOSP 1 50% 0.4% 1
5 UNIT 862 1 50% 0.4% 1
6 UNIV CAMBRIDGE METAB S 1 50% 0.4% 1
7 BIOPHYS BIOCHEM GEN PATHOL 0 33% 0.4% 1
8 DINGLI CLIN MED 0 33% 0.4% 1
9 GENET HUMAN DEV 0 33% 0.4% 1
10 GENET HUMANA ENRIQUE CORONA RIVERA 0 33% 0.4% 1

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000148258 SUBTELOMERIC REARRANGEMENTS//IDIOPATHIC MENTAL RETARDATION//MBD5
2 0.0000140901 COMPLEX CHROMOSOMAL REARRANGEMENT//COMPLEX CHROMOSOME REARRANGEMENT CCR//COMPLEX CHROMOSOMAL REARRANGEMENTS
3 0.0000128883 NEONATAL DIABETES MELLITUS//NEONATAL DIABETES//WOLCOTT RALLISON SYNDROME
4 0.0000116927 AXENFELD RIEGER SYNDROME//PETERS ANOMALY//FOXC1
5 0.0000110539 CRI DU CHAT SYNDROME//CRI DU CHAT//3P DELETION SYNDROME
6 0.0000080706 BREATHLESS//TRACHEALESS//TRACHEAL SYSTEM
7 0.0000079011 ZEBRAFISH NEUROSCI CONSORTIUM//MORFOL CIENCIAS FISIOL//ZNRC
8 0.0000078498 TRISOMY 9P//TETRASOMY 9P//PARTIAL TRISOMY 7P
9 0.0000077168 RING CHROMOSOME 21//MONOSOMY 21//RING CHROMOSOME 15
10 0.0000070094 RUBINSTEIN TAYBI SYNDROME//CORNEAL KELOID//TRISOMY 16Q