Class information for:
Level 1: TRISOMY 9//TETRASOMY 9P//TRISOMY 9P

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
14190 786 22.4 62%


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
14190 1                   TRISOMY 9//TETRASOMY 9P//TRISOMY 9P 786

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 9 authKW 823137 4% 76% 28
2 TETRASOMY 9P authKW 667806 2% 90% 19
3 TRISOMY 9P authKW 575510 3% 74% 20
4 TRISOMY 8 MOSAICISM authKW 276248 1% 89% 8
5 PARTIAL TRISOMY 7Q authKW 199786 1% 86% 6
6 MOSAIC TETRASOMY 8P authKW 194238 1% 100% 5
7 LIFESPAN MED address 177054 2% 33% 14
8 TRISOMY 8 authKW 162107 3% 17% 24
9 TRISOMY 9 MOSAICISM authKW 161864 1% 83% 5
10 CHROMOSOME 8 authKW 160752 3% 17% 25

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 21104 67% 0% 528
2 Medical Ethics 2073 3% 0% 25
3 Obstetrics & Gynecology 617 9% 0% 72
4 Pediatrics 298 8% 0% 60
5 Multidisciplinary Sciences 129 2% 0% 19
6 Medical Laboratory Technology 119 2% 0% 18
7 Pathology 74 3% 0% 27
8 Medicine, Research & Experimental 60 4% 0% 35
9 Biotechnology & Applied Microbiology 37 4% 0% 35
10 Cell Biology 21 5% 0% 38

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 LIFESPAN MED 177054 2% 33% 14
2 CYTOGENET FISH GENOTOXICOL 51796 0% 67% 2
3 4901 AWAYACHO 38848 0% 100% 1
4 ABT REPROD MED 38848 0% 100% 1
5 ANAL SEZ CITOGENET 38848 0% 100% 1
6 ANNUNZIO FDN 38848 0% 100% 1
7 CARCINOGENE TARGET THER Y 38848 0% 100% 1
8 CATTEDRA UO GENET MEDUNIT MED GENET 38848 0% 100% 1
9 CLIN GENT UNIT 38848 0% 100% 1
10 CLIN PEDIAT MILANO BICOCCA 38848 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 46228 13% 1% 102
2 ANNALES DE GENETIQUE 32573 4% 3% 31
3 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 26714 8% 1% 63
4 GENETIC COUNSELING 25753 3% 3% 25
5 PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES 21958 4% 2% 34
6 JOURNAL OF MEDICAL GENETICS 18128 7% 1% 52
7 PRENATAL DIAGNOSIS 10538 5% 1% 39
8 CLINICAL GENETICS 10416 5% 1% 37
9 MOLECULAR CYTOGENETICS 9670 1% 2% 11
10 EUROPEAN JOURNAL OF MEDICAL GENETICS 4901 2% 1% 12

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 9 823137 4% 76% 28 Search TRISOMY+9 Search TRISOMY+9
2 TETRASOMY 9P 667806 2% 90% 19 Search TETRASOMY+9P Search TETRASOMY+9P
3 TRISOMY 9P 575510 3% 74% 20 Search TRISOMY+9P Search TRISOMY+9P
4 TRISOMY 8 MOSAICISM 276248 1% 89% 8 Search TRISOMY+8+MOSAICISM Search TRISOMY+8+MOSAICISM
5 PARTIAL TRISOMY 7Q 199786 1% 86% 6 Search PARTIAL+TRISOMY+7Q Search PARTIAL+TRISOMY+7Q
6 MOSAIC TETRASOMY 8P 194238 1% 100% 5 Search MOSAIC+TETRASOMY+8P Search MOSAIC+TETRASOMY+8P
7 TRISOMY 8 162107 3% 17% 24 Search TRISOMY+8 Search TRISOMY+8
8 TRISOMY 9 MOSAICISM 161864 1% 83% 5 Search TRISOMY+9+MOSAICISM Search TRISOMY+9+MOSAICISM
9 CHROMOSOME 8 160752 3% 17% 25 Search CHROMOSOME+8 Search CHROMOSOME+8
10 KANK1 155391 1% 100% 4 Search KANK1 Search KANK1

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 EL KHATTABI, L , JAILLARD, S , ANDRIEUX, J , PASQUIER, L , PERRIN, L , CAPRI, Y , BENMANSOUR, A , TOUTAIN, A , MARCORELLES, P , VINCENT-DELORME, C , ET AL (2015) CLINICAL AND MOLECULAR DELINEATION OF TETRASOMY 9P SYNDROME: REPORT OF 12 NEW CASES AND LITERATURE REVIEW.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 167. ISSUE 6. P. 1252 -1261 33 80% 0
2 WAT, MJ , SHCHELOCHKOV, OA , HOLDER, AM , BREMAN, AM , DAGLI, A , BACINO, C , SCAGLIA, F , ZORI, RT , CHEUNG, SW , SCOTT, DA , ET AL (2009) CHROMOSOME 8P23.1 DELETIONS AS A CAUSE OF COMPLEX CONGENITAL HEART DEFECTS AND DIAPHRAGMATIC HERNIA.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 149A. ISSUE 8. P. 1661-1677 42 58% 58
3 YU, SH , FIEDLER, S , STEGNER, A , GRAF, WD , (2010) GENOMIC PROFILE OF COPY NUMBER VARIANTS ON THE SHORT ARM OF HUMAN CHROMOSOME 8.EUROPEAN JOURNAL OF HUMAN GENETICS. VOL. 18. ISSUE 10. P. 1114 -1120 34 67% 14
4 KOWALCZYK, M , TOMASZEWSKA, A , PODBIOL-PALENTA, A , CONSTANTINOU, M , WAWRZKIEWICZ-WITKOWSKA, A , KOWALSKI, J , KALUZEWSKI, B , ZAJACZEK, S , SREBNIAK, MI , (2013) ANOTHER RARE CASE OF A CHILD WITH DE NOVO TERMINAL 9P DELETION AND CO-EXISTING INTERSTITIAL 9P DUPLICATION: CLINICAL FINDINGS AND MOLECULAR CYTOGENETIC STUDY BY ARRAY-CGH.CYTOGENETIC AND GENOME RESEARCH. VOL. 139. ISSUE 1. P. 9-16 21 91% 0
5 HULICK, PJ , NOONAN, KM , KULKARNI, S , DONOVAN, DJ , LISTEWNIK, M , IHM, C , STOLER, JM , WEREMOWICZ, S , (2009) CYTOGENETIC AND ARRAY-CGH CHARACTERIZATION OF A COMPLEX DE NOVO REARRANGEMENT INVOLVING DUPLICATION AND DELETION OF 9P AND CLINICAL FINDINGS IN A 4-MONTH-OLD FEMALE.CYTOGENETIC AND GENOME RESEARCH. VOL. 126. ISSUE 3. P. 305-312 23 82% 13
6 CHEN, CP , WANG, LK , CHERN, SR , WU, PS , CHEN, YT , KUO, YL , CHEN, WL , LEE, MS , WANG, W , (2014) MOSAIC TETRASOMY 9P AT AMNIOCENTESIS: PRENATAL DIAGNOSIS, MOLECULAR CYTOGENETIC CHARACTERIZATION, AND LITERATURE REVIEW.TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. VOL. 53. ISSUE 1. P. 79 -85 21 81% 2
7 CHEN, CP , SU, YN , CHERN, SR , HSU, CY , TSAI, FJ , WU, PC , LEE, CC , CHEN, YT , LEE, MS , WANG, WS , (2011) INV DUP DEL(9P): PRENATAL DIAGNOSIS AND MOLECULAR CYTOGENETIC CHARACTERIZATION BY FLUORESCENCE IN SITU HYBRIDIZATION AND ARRAY COMPARATIVE GENOMIC HYBRIDIZATION.TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. VOL. 50. ISSUE 1. P. 67-73 33 54% 9
8 DI BARTOLO, DL , EL NAGGAR, M , OWEN, R , SAHOO, T , GILBERT, F , PULIJAAL, VR , MATHEW, S , (2012) CHARACTERIZATION OF A COMPLEX REARRANGEMENT INVOLVING DUPLICATION AND DELETION OF 9P IN AN INFANT WITH CRANIOFACIAL DYSMORPHISM AND CARDIAC ANOMALIES.MOLECULAR CYTOGENETICS. VOL. 5. ISSUE . P. - 19 86% 4
9 BURNSIDE, RD , PAPPAS, JG , SACHAROW, S , APPLEGATE, C , HAMOSH, A , GADI, IK , JASWANEY, V , KEITGES, E , PHILLIPS, KK , POTLURI, VR , ET AL (2013) THREE CASES OF ISOLATED TERMINAL DELETION OF CHROMOSOME 8P WITHOUT HEART DEFECTS PRESENTING WITH A MILD PHENOTYPE.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 161A. ISSUE 4. P. 822-828 20 80% 0
10 GUILHERME, RS , MELONI, VA , PEREZ, ABA , PILLA, AL , DE RAMOS, MAP , DANTAS, AG , TAKERO, SS , KULIKOWSKI, LD , MELARAGNO, MI , (2014) DUPLICATION 9P AND THEIR IMPLICATION TO PHENOTYPE.BMC MEDICAL GENETICS. VOL. 15. ISSUE . P. - 20 74% 3

Classes with closest relation at Level 1


Rank Class id link
1 26502 PARACENTRIC INVERSION//PARTIAL TRISOMY 2P//TRISOMY 2P
2 33440 TRISOMY 20P//TRISOMY 6P//NEURENSIN 2
3 24132 CRI DU CHAT SYNDROME//CRI DU CHAT//CHROMOSOME 5
4 24663 TRISOMY 1Q//PARTIAL TRISOMY 1Q//3P SYNDROME
5 20601 COMPLEX CHROMOSOMAL REARRANGEMENT//COMPLEX CHROMOSOME REARRANGEMENT//CHROMOTHRIPSIS
6 29024 TRISOMY 10Q//MONOSOMY 10Q//DISTAL 10Q TRISOMY
7 25706 PALLISTER KILLIAN SYNDROME//TETRASOMY 12P//ISOCHROMOSOME 12P
8 18550 WOLF HIRSCHHORN SYNDROME//4P DELETION//CHROMOSOME 4
9 14963 MONOSOMY 21//RING CHROMOSOME 21//RING CHROMOSOME 20
10 33589 TRISOMY 16Q//TRISOMY 16P//DUPLICATION CHROMOSOME 16P

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