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 |