Class information for:
Level 1: 18Q SYNDROME//CHROMOSOME 18//TETRASOMY 18P

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
20269 468 20.5 63%


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
20269 1                   18Q SYNDROME//CHROMOSOME 18//TETRASOMY 18P 468

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 18Q SYNDROME authKW 1520890 6% 90% 26
2 CHROMOSOME 18 authKW 1121331 12% 31% 55
3 TETRASOMY 18P authKW 917513 3% 94% 15
4 18Q DELETION SYNDROME authKW 852539 3% 93% 14
5 ISOCHROMOSOME 18P authKW 799254 3% 88% 14
6 RING CHROMOSOME 18 authKW 734004 3% 75% 15
7 18P DELETION SYNDROME authKW 652455 2% 100% 10
8 MONOSOMY 18P authKW 648611 3% 76% 13
9 18Q DELETION authKW 521956 3% 67% 12
10 18P SYNDROME authKW 355222 1% 78% 7

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 13791 70% 0% 329
2 Medical Ethics 1090 3% 0% 14
3 Pediatrics 399 11% 0% 51
4 Obstetrics & Gynecology 140 6% 0% 28
5 Clinical Neurology 101 8% 0% 37
6 Biotechnology & Applied Microbiology 43 6% 0% 26
7 Medicine, Research & Experimental 36 4% 0% 21
8 Neuroimaging 26 1% 0% 5
9 Rheumatology 20 1% 0% 7
10 Education, Special 5 0% 0% 2

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 CHROMOSOME CLIN 18 271855 1% 83% 5
2 MICRODISSECT 130491 0% 100% 2
3 AUDIOFON 65245 0% 100% 1
4 CITOGENOMICA 65245 0% 100% 1
5 CLIN IMMUNOL TRANSPLANTOL UNIT 65245 0% 100% 1
6 CONGENITAL IMMUNODEFICIENCIES 65245 0% 100% 1
7 CYTOGENET CECOS PICARDIE 65245 0% 100% 1
8 CYTOGENET HP 65245 0% 100% 1
9 DATA MANAGER 65245 0% 100% 1
10 DEV BEHAV PEDIAT DISABIL DEV 65245 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 ANNALES DE GENETIQUE 65864 7% 3% 34
2 AMERICAN JOURNAL OF MEDICAL GENETICS 22564 12% 1% 55
3 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 18092 9% 1% 40
4 GENETIC COUNSELING 13562 3% 1% 14
5 MOLECULAR CYTOGENETICS 8594 2% 2% 8
6 JOURNAL OF MEDICAL GENETICS 8201 6% 0% 27
7 CLINICAL GENETICS 7365 5% 0% 24
8 EUROPEAN JOURNAL OF MEDICAL GENETICS 6928 2% 1% 11
9 PRENATAL DIAGNOSIS 2270 3% 0% 14
10 JAPANESE JOURNAL OF HUMAN GENETICS 2027 1% 1% 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 18Q SYNDROME 1520890 6% 90% 26 Search 18Q+SYNDROME Search 18Q+SYNDROME
2 CHROMOSOME 18 1121331 12% 31% 55 Search CHROMOSOME+18 Search CHROMOSOME+18
3 TETRASOMY 18P 917513 3% 94% 15 Search TETRASOMY+18P Search TETRASOMY+18P
4 18Q DELETION SYNDROME 852539 3% 93% 14 Search 18Q+DELETION+SYNDROME Search 18Q+DELETION+SYNDROME
5 ISOCHROMOSOME 18P 799254 3% 88% 14 Search ISOCHROMOSOME+18P Search ISOCHROMOSOME+18P
6 RING CHROMOSOME 18 734004 3% 75% 15 Search RING+CHROMOSOME+18 Search RING+CHROMOSOME+18
7 18P DELETION SYNDROME 652455 2% 100% 10 Search 18P+DELETION+SYNDROME Search 18P+DELETION+SYNDROME
8 MONOSOMY 18P 648611 3% 76% 13 Search MONOSOMY+18P Search MONOSOMY+18P
9 18Q DELETION 521956 3% 67% 12 Search 18Q+DELETION Search 18Q+DELETION
10 18P SYNDROME 355222 1% 78% 7 Search 18P+SYNDROME Search 18P+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 SOILEAU, B , HASI, M , SEBOLD, C , HILL, A , O'DONNELL, L , HALE, DE , CODY, JD , (2015) ADULTS WITH CHROMOSOME 18 ABNORMALITIES.JOURNAL OF GENETIC COUNSELING. VOL. 24. ISSUE 4. P. 663 -674 33 94% 1
2 SEBOLD, C , ROEDER, E , ZIMMERMAN, M , SOILEAU, B , HEARD, P , CARTER, E , SCHATZ, M , WHITE, WA , PERRY, B , REINKER, K , ET AL (2010) TETRASOMY 18P: REPORT OF THE MOLECULAR AND CLINICAL FINDINGS OF 43 INDIVIDUALS.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 152A. ISSUE 9. P. 2164 -2172 25 86% 13
3 STANKIEWICZ, P , BROZEK, I , HELIAS-RODZEWICZ, Z , WIERZBA, J , PILCH, J , BOCIAN, E , BALCERSKA, A , WOZNIAK, A , KARDAS, I , WIRTH, J , ET AL (2001) CLINICAL AND MOLECULAR-CYTOGENETIC STUDIES IN SEVEN PATIENTS WITH RING CHROMOSOME 18.AMERICAN JOURNAL OF MEDICAL GENETICS. VOL. 101. ISSUE 3. P. 226-239 31 84% 36
4 BENINI, R , SAINT-MARTIN, C , SHEVELL, MI , BERNARD, G , (2012) ABNORMAL MYELINATION IN RING CHROMOSOME 18 SYNDROME.JOURNAL OF CHILD NEUROLOGY. VOL. 27. ISSUE 8. P. 1042-1047 23 85% 3
5 NGUYEN-MINH, S , DROSSEL, K , HORN, D , ROST, I , SPORS, B , KAINDL, AM , (2013) COMBINED DELETION 18Q22.2 AND DUPLICATION/TRIPLICATION 18Q22.1 CAUSES MICROCEPHALY, MENTAL RETARDATION AND LEUKENCEPHALOPATHY.GENE. VOL. 523. ISSUE 1. P. 92-98 21 84% 1
6 TAPIA, AJB , FIGUERA, L , CARDENAS, NAV , TORRES, VR , VELAZQUEZ, AIV , CONTRERAS, CG , DUENAS, MLR , (2010) THE VARIABLE PHENOTYPE IN TETRASOMY 18P SYNDROME. A PROPOS OF A SUBTLE DYSMORPHIC CASE.GENETIC COUNSELING. VOL. 21. ISSUE 3. P. 277 -283 18 100% 4
7 FEENSTRA, I , VISSERS, LELM , ORSEL, M , VAN KESSEL, AG , BRUNNER, HG , VELTMAN, JA , VAN RAVENSWAAIJ-ARTS, CMA , (2007) GENOTYPE-PHENOTYPE MAPPING OF CHROMOSOME 18Q DELETIONS BY HIGH-RESOLUTION ARRAY CGH: AN UPDATE OF THE PHENOTYPIC MAP.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 143A. ISSUE 16. P. 1858-1867 22 71% 65
8 GERELTZUL, E , BABA, Y , SUDA, N , SHIGA, M , INOUE, MS , TSUJI, M , SHIN, I , HIRATA, Y , OHYAMA, K , MORIYAMA, K , (2008) CASE REPORT OF DE NOVO DUP(18P)/DEL(18Q) AND R(18) MOSAICISM.JOURNAL OF HUMAN GENETICS. VOL. 53. ISSUE 10. P. 941 -946 21 81% 5
9 CELEP, F , SONMEZ, FM , KUL, S , UCAR, F , KARAGUZEL, A , (2011) RING CHROMOSOME 18 IN A CHILD WITH FEBRILE SEIZURES.GENETIC COUNSELING. VOL. 22. ISSUE 2. P. 165-171 17 85% 1
10 DOSTAL, A , NEMECKOVA, J , GAILLYOVA, R , (2009) THE 18Q DELETION SYNDROME AND ANALYSIS OF THE CRITICAL REGION FOR OROFACIAL CLEFT AT 18Q22.3.JOURNAL OF CRANIO-MAXILLOFACIAL SURGERY. VOL. 37. ISSUE 5. P. 272-275 18 75% 11

Classes with closest relation at Level 1


Rank Class id link
1 33440 TRISOMY 20P//TRISOMY 6P//NEURENSIN 2
2 10418 SUPERNUMERARY MARKER CHROMOSOME//MARKER CHROMOSOME//SMALL SUPERNUMERARY MARKER CHROMOSOME
3 24649 TRISOMY 18//TRISOMY 13//PATAU SYNDROME
4 14963 MONOSOMY 21//RING CHROMOSOME 21//RING CHROMOSOME 20
5 12166 HOLOPROSENCEPHALY//TGIF//CYCLOPIA
6 24132 CRI DU CHAT SYNDROME//CRI DU CHAT//CHROMOSOME 5
7 26502 PARACENTRIC INVERSION//PARTIAL TRISOMY 2P//TRISOMY 2P
8 29024 TRISOMY 10Q//MONOSOMY 10Q//DISTAL 10Q TRISOMY
9 14190 TRISOMY 9//TETRASOMY 9P//TRISOMY 9P
10 25706 PALLISTER KILLIAN SYNDROME//TETRASOMY 12P//ISOCHROMOSOME 12P

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