Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
33440 | 124 | 22.0 | 64% |
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 |
33440 | 1 | TRISOMY 20P//TRISOMY 6P//NEURENSIN 2 | 124 |
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 | TRISOMY 20P | authKW | 1432750 | 6% | 73% | 8 |
2 | TRISOMY 6P | authKW | 1026059 | 4% | 83% | 5 |
3 | NEURENSIN 2 | authKW | 985019 | 3% | 100% | 4 |
4 | PARTIAL TRISOMY 6P | authKW | 788013 | 3% | 80% | 4 |
5 | TRISOMY 20Q | authKW | 788013 | 3% | 80% | 4 |
6 | TETRASOMY 20P | authKW | 738764 | 2% | 100% | 3 |
7 | DUPLICATION 6P | authKW | 492509 | 2% | 100% | 2 |
8 | ISOCHROMOSOME 20P | authKW | 492509 | 2% | 100% | 2 |
9 | NEURENSIN | authKW | 492509 | 2% | 100% | 2 |
10 | NEURENSIN 1 | authKW | 492509 | 2% | 100% | 2 |
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 | 4739 | 80% | 0% | 99 |
2 | Medical Ethics | 82 | 2% | 0% | 2 |
3 | Obstetrics & Gynecology | 22 | 5% | 0% | 6 |
4 | Cell & Tissue Engineering | 8 | 1% | 0% | 1 |
5 | Pathology | 4 | 2% | 0% | 3 |
6 | Neurosciences | 3 | 6% | 0% | 7 |
7 | Medical Laboratory Technology | 1 | 1% | 0% | 1 |
8 | Medicine, Research & Experimental | 1 | 2% | 0% | 3 |
9 | Gastroenterology & Hepatology | 1 | 2% | 0% | 2 |
10 | Developmental Biology | 1 | 1% | 0% | 1 |
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 | CHU ESTAINGERTICAEA 4677 | 246255 | 1% | 100% | 1 |
2 | CINCINNATI DEV DISABIL | 246255 | 1% | 100% | 1 |
3 | CLIN GENET TRAINING PROGRAM | 246255 | 1% | 100% | 1 |
4 | COU OTORHINOLARYNGOL OTOSURG | 246255 | 1% | 100% | 1 |
5 | GRP HOSP COCHIN ST VINCENT DE PAUL MED | 246255 | 1% | 100% | 1 |
6 | GYNECOL OBSET | 246255 | 1% | 100% | 1 |
7 | INSERMU1028TIGER TEAM | 246255 | 1% | 100% | 1 |
8 | NEUROANAT MOL BIOL | 246255 | 1% | 100% | 1 |
9 | UNITE GENET MED ONCOGENET | 246255 | 1% | 100% | 1 |
10 | URTTS | 246255 | 1% | 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 | 31194 | 22% | 0% | 27 |
2 | ANNALES DE GENETIQUE | 30973 | 10% | 1% | 12 |
3 | CLINICAL GENETICS | 5855 | 9% | 0% | 11 |
4 | CLINICAL DYSMORPHOLOGY | 5516 | 4% | 0% | 5 |
5 | AMERICAN JOURNAL OF MEDICAL GENETICS | 4050 | 10% | 0% | 12 |
6 | JOURNAL OF MEDICAL GENETICS | 3444 | 7% | 0% | 9 |
7 | EUROPEAN JOURNAL OF MEDICAL GENETICS | 1945 | 2% | 0% | 3 |
8 | GENETIC COUNSELING | 1043 | 2% | 0% | 2 |
9 | INTERNATIONAL JOURNAL OF HUMAN GENETICS | 971 | 1% | 0% | 1 |
10 | PRENATAL DIAGNOSIS | 700 | 3% | 0% | 4 |
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 | TRISOMY 20P | 1432750 | 6% | 73% | 8 | Search TRISOMY+20P | Search TRISOMY+20P |
2 | TRISOMY 6P | 1026059 | 4% | 83% | 5 | Search TRISOMY+6P | Search TRISOMY+6P |
3 | NEURENSIN 2 | 985019 | 3% | 100% | 4 | Search NEURENSIN+2 | Search NEURENSIN+2 |
4 | PARTIAL TRISOMY 6P | 788013 | 3% | 80% | 4 | Search PARTIAL+TRISOMY+6P | Search PARTIAL+TRISOMY+6P |
5 | TRISOMY 20Q | 788013 | 3% | 80% | 4 | Search TRISOMY+20Q | Search TRISOMY+20Q |
6 | TETRASOMY 20P | 738764 | 2% | 100% | 3 | Search TETRASOMY+20P | Search TETRASOMY+20P |
7 | DUPLICATION 6P | 492509 | 2% | 100% | 2 | Search DUPLICATION+6P | Search DUPLICATION+6P |
8 | ISOCHROMOSOME 20P | 492509 | 2% | 100% | 2 | Search ISOCHROMOSOME+20P | Search ISOCHROMOSOME+20P |
9 | NEURENSIN | 492509 | 2% | 100% | 2 | Search NEURENSIN | Search NEURENSIN |
10 | NEURENSIN 1 | 492509 | 2% | 100% | 2 | Search NEURENSIN+1 | Search NEURENSIN+1 |
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 | ENGELEN, JJM , MARCELIS, CLM , ALOFS, MGP , LONEUS, WH , PULLES-HEINTZBERGER, CFM , HAMERS, AJH , (2001) BRIEF CLINICAL REPORT - DE NOVO "PURE" PARTIAL TRISOMY (6)(P22.1 -> PTER) IN A CHROMOSOME 15 WITH AN ENLARGED SATELLITE, IDENTIFIED BY MICRODISSECTION.AMERICAN JOURNAL OF MEDICAL GENETICS. VOL. 99. ISSUE 1. P. 48-53 | 15 | 88% | 17 |
2 | CHEN, CP , CHEN, M , CHEN, CY , CHERN, SR , WU, PS , CHANG, SP , KUO, YL , CHEN, WL , PAN, CW , WANG, WS , (2014) PRENATAL DIAGNOSIS AND MOLECULAR CYTOGENETIC CHARACTERIZATION OF DE NOVO PURE PARTIAL TRISOMY 6P ASSOCIATED WITH MICROCEPHALY, CRANIOSYNOSTOSIS AND ABNORMAL MATERNAL SERUM BIOCHEMISTRY.GENE. VOL. 536. ISSUE 2. P. 425-429 | 15 | 58% | 0 |
3 | CASTIGLIONE, A , GUARAN, V , ASTOLFI, L , ORIOLI, E , ZERI, G , GEMMATI, D , BOVO, R , MONTALDI, A , ALGHISI, A , MARTINI, A , (2013) KARYOTYPE-PHENOTYPE CORRELATION IN PARTIAL TRISOMIES OF THE SHORT ARM OF CHROMOSOME 6: A FAMILY CASE REPORT AND REVIEW OF THE LITERATURE.CYTOGENETIC AND GENOME RESEARCH. VOL. 141. ISSUE 4. P. 243-259 | 29 | 29% | 3 |
4 | BLANC, P , GOUAS, L , FRANCANNET, C , GIOLLANT, M , VAGO, P , GOUMY, C , (2008) TRISOMY 20Q CAUSED BY INTERSTITIAL DUPLICATION 20Q13.2: CLINICAL REPORT AND LITERATURE REVIEW.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 146A. ISSUE 10. P. 1307-1311 | 10 | 91% | 5 |
5 | VILLA, A , GOMEZ, EG , RODRIGUEZ, L , RASTROLLO, RH , TALLO, MEM , MARTINEZ-FRIAS, ML , (2000) INTERSTITIAL TANDEM DUPLICATION OF 6P: A CASE WITH PARTIAL TRISOMY (6)(P12P21.3).AMERICAN JOURNAL OF MEDICAL GENETICS. VOL. 90. ISSUE 5. P. 369-375 | 13 | 87% | 18 |
6 | SEPULVEDA, W , BE, C , (2008) PARTIAL TRISOMY 20Q IN A FETUS WITH HYPOPLASTIC NASAL BONE, MILD VENTRICULOMEGALY, AND SHORT FEMUR.PRENATAL DIAGNOSIS. VOL. 28. ISSUE 9. P. 868-870 | 9 | 100% | 2 |
7 | KANG, JE , PARK, MY , CHEON, CK , LEE, HD , HWANG, SH , YI, J , (2012) A CASE OF PARTIAL TRISOMY 20P RESULTING FROM MEIOTIC RECOMBINATION OF A MATERNAL PERICENTRIC INVERSION.ANNALS OF LABORATORY MEDICINE. VOL. 32. ISSUE 1. P. 91-94 | 8 | 100% | 2 |
8 | STARR, LJ , TRUEMPER, EJ , PICKERING, DL , SANGER, WG , OLNEY, AH , (2014) DUPLICATION OF 20QTER AND DELETION OF 20PTER DUE TO PATERNAL PERICENTRIC INVERSION: PATIENT REPORT AND REVIEW OF 20QTER DUPLICATIONS.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 164. ISSUE 8. P. 2020 -2024 | 12 | 60% | 0 |
9 | CHAABOUNI, M , TURLEAU, C , KARBOUL, L , BEN JEMAA, L , MAAZOUL, F , ATTIE-BITACH, T , ROMANA, S , CHAABOUNI, H , (2007) CLINICAL REPORT - DE NOVO TRISOMY 20P OF PATERNAL ORIGIN.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 143A. ISSUE 10. P. 1100-1103 | 9 | 90% | 9 |
10 | GIARDINO, D , FINELLI, P , CAUFIN, D , GOTTARDI, G , LO VASCO, R , TUROLLA, L , LARIZZA, L , (2002) PURE 6P22-PTER TRISOMIC PATIENT: REFINED FISH CHARACTERIZATION AND GENOTYPE-PHENOTYPE CORRELATION.AMERICAN JOURNAL OF MEDICAL GENETICS. VOL. 108. ISSUE 1. P. 36 -40 | 11 | 85% | 13 |
Classes with closest relation at Level 1 |