Class information for:
Level 1: TRISOMY 20P//TRISOMY 6P//NEURENSIN 2

Basic class information

Class id #P Avg. number of
references
Database coverage
of references
33440 124 22.0 64%



Bar chart of Publication_year

Last years might be incomplete

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



Rank Class id link
1 33589 TRISOMY 16Q//TRISOMY 16P//DUPLICATION CHROMOSOME 16P
2 24663 TRISOMY 1Q//PARTIAL TRISOMY 1Q//3P SYNDROME
3 14190 TRISOMY 9//TETRASOMY 9P//TRISOMY 9P
4 25553 JACOBSEN SYNDROME//11Q SYNDROME//11Q TERMINAL DELETION DISORDER
5 20269 18Q SYNDROME//CHROMOSOME 18//TETRASOMY 18P
6 20402 ALAGILLE SYNDROME//ARTERIOHEPATIC DYSPLASIA//PAUCITY OF INTERLOBULAR BILE DUCTS
7 6924 SUBTELOMERIC REARRANGEMENTS//ARRAY CGH//MBD5
8 14963 MONOSOMY 21//RING CHROMOSOME 21//RING CHROMOSOME 20
9 10418 SUPERNUMERARY MARKER CHROMOSOME//MARKER CHROMOSOME//SMALL SUPERNUMERARY MARKER CHROMOSOME
10 20601 COMPLEX CHROMOSOMAL REARRANGEMENT//COMPLEX CHROMOSOME REARRANGEMENT//CHROMOTHRIPSIS

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