Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
20347 | 402 | 27.7 | 80% |
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 |