Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
21327 | 424 | 30.5 | 82% |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
0 | 4 | BIOCHEMISTRY & MOLECULAR BIOLOGY//CELL BIOLOGY//ONCOLOGY | 4064930 |
196 | 3 | GENETICS & HEREDITY//FRAGILE X SYNDROME//AMERICAN JOURNAL OF MEDICAL GENETICS | 53756 |
395 | 2 | GENETICS & HEREDITY//ANNALES DE GENETIQUE//HOLOPROSENCEPHALY | 16816 |
21327 | 1 | SATB1//SATB2//2Q DELETION | 424 |
Terms with highest relevance score |
rank | Term | termType | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|---|
1 | SATB1 | authKW | 3896224 | 16% | 78% | 69 |
2 | SATB2 | authKW | 1485562 | 9% | 54% | 38 |
3 | 2Q DELETION | authKW | 441099 | 2% | 88% | 7 |
4 | PARTIAL TRISOMY 2Q | authKW | 432099 | 1% | 100% | 6 |
5 | 2Q37 | authKW | 370369 | 1% | 86% | 6 |
6 | BDMR | authKW | 360082 | 1% | 100% | 5 |
7 | SPECIAL AT RICH SEQUENCE BINDING PROTEIN 1 | authKW | 320795 | 2% | 64% | 7 |
8 | CHROMOSOME 2 | authKW | 300551 | 6% | 17% | 24 |
9 | 2Q37 DELETION | authKW | 230451 | 1% | 80% | 4 |
10 | 2Q37 DELETION SYNDROME | authKW | 230451 | 1% | 80% | 4 |
Web of Science journal categories |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | Genetics & Heredity | 5328 | 46% | 0% | 197 |
2 | Medical Ethics | 295 | 2% | 0% | 7 |
3 | Oncology | 293 | 15% | 0% | 65 |
4 | Cell Biology | 242 | 14% | 0% | 59 |
5 | Pathology | 87 | 5% | 0% | 20 |
6 | Biochemistry & Molecular Biology | 85 | 16% | 0% | 68 |
7 | Medicine, Research & Experimental | 55 | 5% | 0% | 23 |
8 | Pediatrics | 14 | 3% | 0% | 13 |
9 | Developmental Biology | 11 | 1% | 0% | 6 |
10 | Ophthalmology | 9 | 2% | 0% | 8 |
Address terms |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | OSP L SPALLANZANI | 96021 | 0% | 67% | 2 |
2 | ACCESS GENOME ATG PC | 72016 | 0% | 100% | 1 |
3 | ANALYT DIAGNOST SCI | 72016 | 0% | 100% | 1 |
4 | CHILD DEV POTE | 72016 | 0% | 100% | 1 |
5 | CHR ORLEANSSERV GENET IMMUNOL NEUROGENET E | 72016 | 0% | 100% | 1 |
6 | CHU ESTAINGCYTOGENET MED | 72016 | 0% | 100% | 1 |
7 | DAQING LONGNAN HOSP | 72016 | 0% | 100% | 1 |
8 | DEV DISABIL STUDY SECT | 72016 | 0% | 100% | 1 |
9 | EXCELLENCE COE EPIGENET | 72016 | 0% | 100% | 1 |
10 | FUNCT GENOM JIANGSU PROV | 72016 | 0% | 100% | 1 |
Journals |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 17088 | 9% | 1% | 37 |
2 | AMERICAN JOURNAL OF MEDICAL GENETICS | 9496 | 8% | 0% | 34 |
3 | EUROPEAN JOURNAL OF MEDICAL GENETICS | 5117 | 2% | 1% | 9 |
4 | GENETIC COUNSELING | 3736 | 2% | 1% | 7 |
5 | JOURNAL OF MEDICAL GENETICS | 3168 | 4% | 0% | 16 |
6 | ANNALES DE GENETIQUE | 3071 | 2% | 1% | 7 |
7 | MOLECULAR CYTOGENETICS | 2368 | 1% | 1% | 4 |
8 | CLINICAL DYSMORPHOLOGY | 2315 | 1% | 1% | 6 |
9 | JAPANESE JOURNAL OF HUMAN GENETICS | 1257 | 1% | 1% | 3 |
10 | CLINICAL GENETICS | 1133 | 2% | 0% | 9 |
Author Key Words |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | SATB1 | 3896224 | 16% | 78% | 69 | Search SATB1 | Search SATB1 |
2 | SATB2 | 1485562 | 9% | 54% | 38 | Search SATB2 | Search SATB2 |
3 | 2Q DELETION | 441099 | 2% | 88% | 7 | Search 2Q+DELETION | Search 2Q+DELETION |
4 | PARTIAL TRISOMY 2Q | 432099 | 1% | 100% | 6 | Search PARTIAL+TRISOMY+2Q | Search PARTIAL+TRISOMY+2Q |
5 | 2Q37 | 370369 | 1% | 86% | 6 | Search 2Q37 | Search 2Q37 |
6 | BDMR | 360082 | 1% | 100% | 5 | Search BDMR | Search BDMR |
7 | SPECIAL AT RICH SEQUENCE BINDING PROTEIN 1 | 320795 | 2% | 64% | 7 | Search SPECIAL+AT+RICH+SEQUENCE+BINDING+PROTEIN+1 | Search SPECIAL+AT+RICH+SEQUENCE+BINDING+PROTEIN+1 |
8 | CHROMOSOME 2 | 300551 | 6% | 17% | 24 | Search CHROMOSOME+2 | Search CHROMOSOME+2 |
9 | 2Q37 DELETION | 230451 | 1% | 80% | 4 | Search 2Q37+DELETION | Search 2Q37+DELETION |
10 | 2Q37 DELETION SYNDROME | 230451 | 1% | 80% | 4 | Search 2Q37+DELETION+SYNDROME | Search 2Q37+DELETION+SYNDROME |
Core articles |
The table includes core articles in the class. The following variables is taken into account for the relevance score of an article in a cluster c: (1) Number of references referring to publications in the class. (2) Share of total number of active references referring to publications in the class. (3) Age of the article. New articles get higher score than old articles. (4) Citation rate, normalized to year. |
Rank | Reference | # ref. in cl. |
Shr. of ref. in cl. |
Citations |
---|---|---|---|---|
1 | ZARATE, YA , FISH, JL , (2017) SATB2-ASSOCIATED SYNDROME: MECHANISMS, PHENOTYPE, AND PRACTICAL RECOMMENDATIONS.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 173. ISSUE 2. P. 327 -337 | 34 | 76% | 1 |
2 | BROCATO, J , COSTA, M , (2015) SATB1 AND 2 IN COLORECTAL CANCER.CARCINOGENESIS. VOL. 36. ISSUE 2. P. 186 -191 | 45 | 65% | 3 |
3 | FROMBERG, A , RABE, M , AIGNER, A , (2014) MULTIPLE EFFECTS OF THE SPECIAL AT-RICH BINDING PROTEIN 1 (SATB1) IN COLON CARCINOMA.INTERNATIONAL JOURNAL OF CANCER. VOL. 135. ISSUE 11. P. 2537 -2546 | 32 | 70% | 6 |
4 | SENGA, T , NAGINO, M , UEHARA, K , KOKURYO, T , AKTER, KA , HYODO, T , MANSOUR, MA , (2016) SATB1 AND SATB2 PLAY OPPOSING ROLES IN C-MYC EXPRESSION AND PROGRESSION OF COLORECTAL CANCER.ONCOTARGET. VOL. 7. ISSUE 4. P. 4993 -5006 | 28 | 68% | 2 |
5 | ROSENFELD, JA , BALLIF, BC , LUCAS, A , SPENCE, EJ , POWELL, C , AYLSWORTH, AS , TORCHIA, BA , SHAFFER, LG , (2009) SMALL DELETIONS OF SATB2 CAUSE SOME OF THE CLINICAL FEATURES OF THE 2Q33.1 MICRODELETION SYNDROME.PLOS ONE. VOL. 4. ISSUE 8. P. - | 25 | 83% | 37 |
6 | KOBIERZYCKI, C , WOJNAR, A , DZIEGIEL, P , (2013) EXPRESSION OF SATB1 PROTEIN IN THE DUCTAL BREAST CARCINOMA TISSUE MICROARRAYS - PRELIMINARY STUDY.FOLIA HISTOCHEMICA ET CYTOBIOLOGICA. VOL. 51. ISSUE 4. P. 333-338 | 25 | 81% | 5 |
7 | FROMBERG, A , RABE, M , OPPERMANN, H , GAUNITZ, F , AIGNER, A , (2017) ANALYSIS OF CELLULAR AND MOLECULAR ANTITUMOR EFFECTS UPON INHIBITION OF SATB1 IN GLIOBLASTOMA CELLS.BMC CANCER. VOL. 17. ISSUE . P. - | 30 | 63% | 0 |
8 | ELEBRO, J , HEBY, M , GABER, A , NODIN, B , JONSSON, L , FRISTEDT, R , UHLEN, M , JIRSTROM, K , EBERHARD, J , (2014) PROGNOSTIC AND TREATMENT PREDICTIVE SIGNIFICANCE OF SATB1 AND SATB2 EXPRESSION IN PANCREATIC AND PERIAMPULLARY ADENOCARCINOMA.JOURNAL OF TRANSLATIONAL MEDICINE. VOL. 12. ISSUE . P. - | 21 | 84% | 8 |
9 | ZHANG, Y , WANG, L , LIU, YD , MENG, FL , WANG, SX , SHANG, P , GAO, Y , CHEN, XW , (2015) OVEREXPRESSION OF SPECIAL AT-RICH SEQUENCE-BINDING PROTEIN 1 IN ENDOMETRIAL CANCER A CLINICOPATHOLOGIC STUDY.INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER. VOL. 25. ISSUE 1. P. 4 -11 | 22 | 79% | 1 |
10 | WANG, SX , WANG, L , ZHANG, Y , LIU, YD , MENG, FL , MA, JQ , SHANG, P , GAO, Y , HUANG, Q , CHEN, XW , (2015) SPECIAL AT-RICH SEQUENCE-BINDING PROTEIN 1: A NOVEL BIOMARKER PREDICTING CERVICAL SQUAMOUS CELL CARCINOMA PROGNOSIS AND LYMPH NODE METASTASIS.JAPANESE JOURNAL OF CLINICAL ONCOLOGY. VOL. 45. ISSUE 9. P. 812 -818 | 21 | 81% | 1 |
Classes with closest relation at Level 1 |