Class information for:
Level 1: SATB1//2Q DELETION//SATB2

Basic class information

ID Publications Average number
of references
Avg. shr. active
ref. in WoS
20347 402 27.7 80%



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 SATB1 Author keyword 65 72% 13% 51
2 2Q DELETION Author keyword 15 88% 2% 7
3 SATB2 Author keyword 13 46% 5% 22
4 PARTIAL TRISOMY 2Q Author keyword 11 100% 1% 6
5 2Q37 Author keyword 9 83% 1% 5
6 TERMINAL DELETION 2Q Author keyword 9 83% 1% 5
7 BDMR Author keyword 8 100% 1% 5
8 SPECIAL AT RICH SEQUENCE BINDING PROTEIN 1 Author keyword 7 64% 2% 7
9 2Q37 DELETION Author keyword 6 80% 1% 4
10 2Q37 DELETION SYNDROME Author keyword 6 80% 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 SATB1 65 72% 13% 51 Search SATB1 Search SATB1
2 2Q DELETION 15 88% 2% 7 Search 2Q+DELETION Search 2Q+DELETION
3 SATB2 13 46% 5% 22 Search SATB2 Search SATB2
4 PARTIAL TRISOMY 2Q 11 100% 1% 6 Search PARTIAL+TRISOMY+2Q Search PARTIAL+TRISOMY+2Q
5 2Q37 9 83% 1% 5 Search 2Q37 Search 2Q37
6 TERMINAL DELETION 2Q 9 83% 1% 5 Search TERMINAL+DELETION+2Q Search TERMINAL+DELETION+2Q
7 BDMR 8 100% 1% 5 Search BDMR Search BDMR
8 SPECIAL AT RICH SEQUENCE BINDING PROTEIN 1 7 64% 2% 7 Search SPECIAL+AT+RICH+SEQUENCE+BINDING+PROTEIN+1 Search SPECIAL+AT+RICH+SEQUENCE+BINDING+PROTEIN+1
9 2Q37 DELETION 6 80% 1% 4 Search 2Q37+DELETION Search 2Q37+DELETION
10 2Q37 DELETION SYNDROME 6 80% 1% 4 Search 2Q37+DELETION+SYNDROME Search 2Q37+DELETION+SYNDROME

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 46 XY DEL2Q37 26 100% 3% 11
2 DOMAIN MEDIATED DIMERIZATION 12 86% 1% 6
3 BREAST CANCER PATHOGENESIS 11 100% 1% 6
4 BINDING PROTEIN SATB1 11 69% 2% 9
5 2Q32 Q33 9 67% 2% 8
6 SATB1 8 39% 4% 17
7 PARTIAL TRISOMY 2Q 8 100% 1% 5
8 TSSC5 8 100% 1% 5
9 MAR BINDING PROTEIN 8 50% 3% 11
10 CHARACTERISTIC PHENOTYPE 6 80% 1% 4

Journals

Reviews



Title Publ. year Cit. Active references % act. ref.
to same field
The role of SATB2 in skeletogenesis and human disease 2014 6 47 49%
Genome organizing function of SATB1 in tumor progression 2013 20 89 35%
Chromosome 2q duplications: Case report of a de novo interstitial duplication and review of the literature 2001 17 25 92%
A REVIEW OF PHENOTYPE-KARYOTYPE CORRELATIONS IN INDIVIDUALS WITH INTERSTITIAL DELETIONS OF THE LONG ARM OF CHROMOSOME-2 1989 39 11 100%
The third dimension of gene regulation: organization of dynamic chromatin loopscape by SATB1 2007 77 25 24%
Ocular anomalies associated with interstitial deletion of chromosome 2q31: case report and review 2007 4 8 75%
SATB1 and 2 in colorectal cancer 2015 0 69 58%
Interstitial Deletion 2p11.2-p12: Report of a Patient with Mental Retardation and Review of the Literature 2009 5 8 50%
Chromatin organizer SATB1 is an important determinant of T-cell differentiation 2012 5 60 28%
Chromatin Organizer SATB1 As a Novel Molecular Target for Cancer Therapy 2012 9 145 20%

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 OSP L SPALLANZANI 2 67% 0.5% 2
2 HUMAN FUNCT GENOM JIANGSU PROVINCE 1 40% 0.5% 2
3 EXCELLENCE EPIGENET 1 27% 0.7% 3
4 CHRU NANCY BRABOIS 1 50% 0.2% 1
5 DISCIPLINE CELLULAR MOL BIOL 1 50% 0.2% 1
6 HUMAN GENET UNITMOL MED 1 50% 0.2% 1
7 ISRAEL R HAEL RECANATI GENET 1 50% 0.2% 1
8 ONCOL MINIST EDUC 1 50% 0.2% 1
9 PEOPLE HOSP AFFILIATED 3 1 50% 0.2% 1
10 PRENATAL DIAGNOST GENET CLIN 1 50% 0.2% 1

Related classes at same level (level 1)



Rank Relatedness score Related classes
1 0.0000198464 PULMONARY AGENESIS//LUNG AGENESIS//PARTIAL TRISOMY 2P
2 0.0000132004 TRISOMY 10Q//MONOSOMY 10Q//10P TRISOMY
3 0.0000126742 SUBTELOMERIC REARRANGEMENTS//IDIOPATHIC MENTAL RETARDATION//MBD5
4 0.0000111600 TRISOMY 9P//TETRASOMY 9P//PARTIAL TRISOMY 7P
5 0.0000107064 JACOBSEN SYNDROME//11Q SYNDROME//11Q TERMINAL DELETION DISORDER
6 0.0000094856 CRI DU CHAT SYNDROME//CRI DU CHAT//3P DELETION SYNDROME
7 0.0000090216 RING CHROMOSOME 21//MONOSOMY 21//RING CHROMOSOME 15
8 0.0000089982 WOLF HIRSCHHORN SYNDROME//4P DELETION//PITT ROGERS DANKS SYNDROME
9 0.0000086875 NUCLEAR MATRIX//MATRIX ATTACHMENT REGION//NUCLEAR SCAFFOLD
10 0.0000082476 WAARDENBURG SYNDROME//WAARDENBURGS SYNDROME//KLEIN WAARDENBURG SYNDROME