Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
37024 | 68 | 30.5 | 76% |
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 |
642 | 3 | POLYCYSTIC KIDNEY DISEASE//AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE//HEDGEHOG | 12305 |
1658 | 2 | HEDGEHOG//GLI//CILIOPATHY | 6876 |
37024 | 1 | RAB23//CARPENTER SYNDROME//ACROCEPHALOPOLYSYNDACTYLY TYPE II | 68 |
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 | RAB23 | authKW | 5132032 | 29% | 57% | 20 |
2 | CARPENTER SYNDROME | authKW | 3403350 | 18% | 63% | 12 |
3 | ACROCEPHALOPOLYSYNDACTYLY TYPE II | authKW | 1796217 | 6% | 100% | 4 |
4 | OPEN BRAIN | authKW | 1010371 | 4% | 75% | 3 |
5 | CELLULAR SIGNALINGCANC | address | 598738 | 3% | 67% | 2 |
6 | ACROCEPHALOPOLYSYNDACTYLY SYNDROME | authKW | 449054 | 1% | 100% | 1 |
7 | CEREBROSPINAL MALFORMATIONS | authKW | 449054 | 1% | 100% | 1 |
8 | DEFECT OF LATERALIZATION | authKW | 449054 | 1% | 100% | 1 |
9 | DYSENCEPHALIA SPLANCHNOCYSTICA | authKW | 449054 | 1% | 100% | 1 |
10 | GTP BINDING PROTEIN A SUBUNITS | authKW | 449054 | 1% | 100% | 1 |
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 | 263 | 26% | 0% | 18 |
2 | Oncology | 53 | 16% | 0% | 11 |
3 | Medicine, Research & Experimental | 29 | 9% | 0% | 6 |
4 | Pediatrics | 24 | 7% | 0% | 5 |
5 | Cell Biology | 12 | 9% | 0% | 6 |
6 | Developmental Biology | 11 | 3% | 0% | 2 |
7 | Medicine, Legal | 11 | 1% | 0% | 1 |
8 | Biochemistry & Molecular Biology | 10 | 15% | 0% | 10 |
9 | Dentistry, Oral Surgery & Medicine | 6 | 3% | 0% | 2 |
10 | Surgery | 6 | 7% | 0% | 5 |
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 | CELLULAR SIGNALINGCANC | 598738 | 3% | 67% | 2 |
2 | PRENATAL DIAG CLIN | 449054 | 1% | 100% | 1 |
3 | SOBR AR | 449054 | 1% | 100% | 1 |
4 | FORENS NEUROPATHOL | 224526 | 1% | 50% | 1 |
5 | CLEFT LIP PALATE CRANIO IAL DEFORM | 179619 | 3% | 20% | 2 |
6 | INSERM GENETU781 | 149683 | 1% | 33% | 1 |
7 | OFF ASSOCIATE CHIEF MED EXAMINER | 149683 | 1% | 33% | 1 |
8 | COOPERAT DISCOVERY GENES COMMON HUMAN DIS | 49893 | 1% | 11% | 1 |
9 | RADIUMHOSPMED | 44904 | 1% | 10% | 1 |
10 | SKULL BASE SURG NEUROONCOL HUNAN | 44904 | 1% | 10% | 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 | JOURNAL OF DIAGNOSTIC MEDICAL SONOGRAPHY | 11512 | 1% | 3% | 1 |
2 | EXPERIMENTAL AND MOLECULAR MEDICINE | 2866 | 4% | 0% | 3 |
3 | CURRENT SIGNAL TRANSDUCTION THERAPY | 2067 | 1% | 0% | 1 |
4 | FORENSIC SCIENCE MEDICINE AND PATHOLOGY | 996 | 1% | 0% | 1 |
5 | TRAFFIC | 933 | 3% | 0% | 2 |
6 | AMERICAN JOURNAL OF MEDICAL GENETICS | 817 | 6% | 0% | 4 |
7 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 697 | 4% | 0% | 3 |
8 | TUMOR BIOLOGY | 655 | 4% | 0% | 3 |
9 | INTERNATIONAL JOURNAL OF OBSTETRIC ANESTHESIA | 448 | 1% | 0% | 1 |
10 | CLINICAL DYSMORPHOLOGY | 401 | 1% | 0% | 1 |
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 | RAB23 | 5132032 | 29% | 57% | 20 | Search RAB23 | Search RAB23 |
2 | CARPENTER SYNDROME | 3403350 | 18% | 63% | 12 | Search CARPENTER+SYNDROME | Search CARPENTER+SYNDROME |
3 | ACROCEPHALOPOLYSYNDACTYLY TYPE II | 1796217 | 6% | 100% | 4 | Search ACROCEPHALOPOLYSYNDACTYLY+TYPE+II | Search ACROCEPHALOPOLYSYNDACTYLY+TYPE+II |
4 | OPEN BRAIN | 1010371 | 4% | 75% | 3 | Search OPEN+BRAIN | Search OPEN+BRAIN |
5 | ACROCEPHALOPOLYSYNDACTYLY SYNDROME | 449054 | 1% | 100% | 1 | Search ACROCEPHALOPOLYSYNDACTYLY+SYNDROME | Search ACROCEPHALOPOLYSYNDACTYLY+SYNDROME |
6 | CEREBROSPINAL MALFORMATIONS | 449054 | 1% | 100% | 1 | Search CEREBROSPINAL+MALFORMATIONS | Search CEREBROSPINAL+MALFORMATIONS |
7 | DEFECT OF LATERALIZATION | 449054 | 1% | 100% | 1 | Search DEFECT+OF+LATERALIZATION | Search DEFECT+OF+LATERALIZATION |
8 | DYSENCEPHALIA SPLANCHNOCYSTICA | 449054 | 1% | 100% | 1 | Search DYSENCEPHALIA+SPLANCHNOCYSTICA | Search DYSENCEPHALIA+SPLANCHNOCYSTICA |
9 | GTP BINDING PROTEIN A SUBUNITS | 449054 | 1% | 100% | 1 | Search GTP+BINDING+PROTEIN+A+SUBUNITS | Search GTP+BINDING+PROTEIN+A+SUBUNITS |
10 | MACROSSOMIA | 449054 | 1% | 100% | 1 | Search MACROSSOMIA | Search MACROSSOMIA |
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 | VICTORINE, AS , WEIDA, J , HINES, KA , ROBINSON, B , TORRES-MARTINEZ, W , WEAVER, DD , (2014) PRENATAL DIAGNOSIS OF CARPENTER SYNDROME: LOOKING BEYOND CRANIOSYNOSTOSIS AND POLYSYNDACTYLY.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 164. ISSUE 3. P. 820-823 | 9 | 100% | 1 |
2 | ALTUNHAN, H , ANNAGUR, A , ORS, R , (2011) THE ASSOCIATION OF CARPENTER SYNDROME AND SITUS INVERSUS TOTALIS: FIRST CASE REPORT.TURKIYE KLINIKLERI TIP BILIMLERI DERGISI. VOL. 31. ISSUE 2. P. 464-467 | 9 | 100% | 2 |
3 | KADAKIA, S , HELMAN, SN , HEALY, NJ , SAMAN, M , WOOD-SMITH, D , (2014) CARPENTER SYNDROME: A REVIEW FOR THE CRANIOFACIAL SURGEON.JOURNAL OF CRANIOFACIAL SURGERY. VOL. 25. ISSUE 5. P. 1653 -1657 | 18 | 44% | 0 |
4 | HAYE, D , COLLET, C , SEMBELY-TAVEAU, C , HADDAD, G , DENIS, C , SOULE, N , SUC, AL , LISTRAT, A , TOUTAIN, A , (2014) PRENATAL FINDINGS IN CARPENTER SYNDROME AND A NOVEL MUTATION IN RAB23.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 164. ISSUE 11. P. 2926 -2930 | 7 | 100% | 2 |
5 | CHANG, JK , XU, WB , LIU, GC , DU, XY , LI, XD , (2017) DOWNREGULATION OF RAB23 IN PROSTATE CANCER INHIBITS TUMOR GROWTH IN VITRO AND IN VIVO.ONCOLOGY RESEARCH. VOL. 25. ISSUE 2. P. 241 -248 | 12 | 55% | 0 |
6 | RAMOS, J , DAVIS, G , HUNSAKER, J , BALKO, M , (2009) SUDDEN DEATH IN A CHILD WITH CARPENTER SYNDROME. CASE REPORT AND LITERATURE REVIEW.FORENSIC SCIENCE MEDICINE AND PATHOLOGY. VOL. 5. ISSUE 4. P. 313 -317 | 8 | 67% | 2 |
7 | SUN, HJ , LIU, YJ , LI, N , SUN, ZY , ZHAO, HW , WANG, C , LI, H , MA, FM , SHI, SM , XU, XQ , ET AL (2012) SUBLOCALIZATION OF RAB23, A MEDIATOR OF SONIC HEDGEHOG SIGNALING PATHWAY, IN HEPATOCELLULAR CARCINOMA CELL LINES.MOLECULAR MEDICINE REPORTS. VOL. 6. ISSUE 6. P. 1276-1280 | 12 | 40% | 7 |
8 | CHEN, YA , NG, F , TANG, BL , (2016) RAB23 ACTIVITIES AND HUMAN CANCER-EMERGING CONNECTIONS AND MECHANISMS.TUMOR BIOLOGY. VOL. 37. ISSUE 10. P. 12959 -12967 | 19 | 19% | 0 |
9 | CHENG, LN , YANG, F , ZHOU, BX , YANG, H , YUAN, Y , LI, XL , HAN, SY , (2016) RAB23, REGULATED BY MIR-92B, PROMOTES THE PROGRESSION OF ESOPHAGEAL SQUAMOUS CELL CARCINOMA.GENE. VOL. 595. ISSUE 1. P. 31 -38 | 7 | 47% | 0 |
10 | ALESSANDRI, JL , DAGONEAU, N , LAVILLE, JM , BARUTEAU, J , HEBERT, JC , CORMIER-DAIRE, V , (2010) RAB23 MUTATION IN A LARGE FAMILY FROM COMOROS ISLANDS WITH CARPENTER SYNDROME.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 152A. ISSUE 4. P. 982-986 | 5 | 63% | 15 |
Classes with closest relation at Level 1 |