Class information for:
Level 1: CRI DU CHAT SYNDROME//CRI DU CHAT//CHROMOSOME 5

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
24132 322 21.1 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
24132 1                   CRI DU CHAT SYNDROME//CRI DU CHAT//CHROMOSOME 5 322

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 CRI DU CHAT SYNDROME authKW 3459406 16% 69% 53
2 CRI DU CHAT authKW 975388 4% 86% 12
3 CHROMOSOME 5 authKW 627503 9% 22% 30
4 5P DELETION SYNDROME authKW 568979 2% 100% 6
5 TETRASOMY 5P authKW 568979 2% 100% 6
6 5P DELETION authKW 548651 3% 64% 9
7 HUNTER MCALPINE SYNDROME authKW 379319 1% 100% 4
8 ISOCHROMOSOME 5P authKW 338675 2% 71% 5
9 TRISOMY 5P authKW 338675 2% 71% 5
10 PARTIAL TRISOMY 5Q authKW 303454 1% 80% 4

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 9803 71% 0% 230
2 Rehabilitation 344 7% 0% 23
3 Audiology & Speech-Language Pathology 287 4% 0% 13
4 Medical Ethics 197 2% 0% 5
5 Linguistics 141 3% 0% 11
6 Education, Special 137 2% 0% 7
7 Obstetrics & Gynecology 117 7% 0% 21
8 Pediatrics 84 7% 0% 21
9 Clinical Neurology 10 4% 0% 13
10 Biotechnology & Applied Microbiology 8 4% 0% 12

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 N W BELFAST HLTH SOCIAL SERV TRUST 189660 1% 100% 2
2 AMBULATORIO GENET CLIN SOC PEDIAT 94830 0% 100% 1
3 CNRSUMR5292TIGER TEAM 94830 0% 100% 1
4 CONSULTANT MED GENET 94830 0% 100% 1
5 CRC EPIDEMIOL GRP 94830 0% 100% 1
6 CYTOGENET TESTING GRP 94830 0% 100% 1
7 CYTROGENET 94830 0% 100% 1
8 FISIOTER ISTA 94830 0% 100% 1
9 GENET CLIN 3 94830 0% 100% 1
10 GENET SEQUENCING 94830 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 26058 15% 1% 49
2 CLINICAL GENETICS 16774 9% 1% 30
3 EUROPEAN JOURNAL OF MEDICAL GENETICS 16334 4% 1% 14
4 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 11980 8% 0% 27
5 ANNALES DE GENETIQUE 8270 3% 1% 10
6 JOURNAL OF MEDICAL GENETICS 6543 6% 0% 20
7 PRENATAL DIAGNOSIS 3311 4% 0% 14
8 JOURNAL OF COMMUNICATION DISORDERS 2867 2% 1% 6
9 GENETIC COUNSELING 2509 2% 1% 5
10 CLINICAL LINGUISTICS & PHONETICS 1953 2% 0% 5

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 CRI DU CHAT SYNDROME 3459406 16% 69% 53 Search CRI+DU+CHAT+SYNDROME Search CRI+DU+CHAT+SYNDROME
2 CRI DU CHAT 975388 4% 86% 12 Search CRI+DU+CHAT Search CRI+DU+CHAT
3 CHROMOSOME 5 627503 9% 22% 30 Search CHROMOSOME+5 Search CHROMOSOME+5
4 5P DELETION SYNDROME 568979 2% 100% 6 Search 5P+DELETION+SYNDROME Search 5P+DELETION+SYNDROME
5 TETRASOMY 5P 568979 2% 100% 6 Search TETRASOMY+5P Search TETRASOMY+5P
6 5P DELETION 548651 3% 64% 9 Search 5P+DELETION Search 5P+DELETION
7 HUNTER MCALPINE SYNDROME 379319 1% 100% 4 Search HUNTER+MCALPINE+SYNDROME Search HUNTER+MCALPINE+SYNDROME
8 ISOCHROMOSOME 5P 338675 2% 71% 5 Search ISOCHROMOSOME+5P Search ISOCHROMOSOME+5P
9 TRISOMY 5P 338675 2% 71% 5 Search TRISOMY+5P Search TRISOMY+5P
10 PARTIAL TRISOMY 5Q 303454 1% 80% 4 Search PARTIAL+TRISOMY+5Q Search PARTIAL+TRISOMY+5Q

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 MAINARDI, PC , (2006) CRI DU CHAT SYNDROME.ORPHANET JOURNAL OF RARE DISEASES. VOL. 1. ISSUE . P. - 52 79% 42
2 DE CARVALHO, AFL , BELLUCCO, FTD , KULIKOWSKI, LD , TORALLES, MBP , MELARAGNO, MI , (2008) PARTIAL 5P MONOSOMY OR TRISOMY IN 11 PATIENTS FROM A FAMILY WITH A T(5;15)(P13.3;P12) TRANSLOCATION.HUMAN GENETICS. VOL. 124. ISSUE 4. P. 387-392 26 93% 5
3 MAINARDI, PC , PASTORE, G , CASTRONOVO, C , GODI, M , GUALA, A , TAMIAZZO, S , PROVERA, S , PIERLUIGI, M , BRICARELLI, FD , (2006) THE NATURAL HISTORY OF CRI DU CHAT SYNDROME. A REPORT FROM THE ITALIAN REGISTER.EUROPEAN JOURNAL OF MEDICAL GENETICS. VOL. 49. ISSUE 5. P. 363-383 28 88% 23
4 FANG, JS , LEE, KF , HUANG, CT , SYU, CL , YANG, KJ , WANG, LH , LIAO, DL , CHEN, CH , (2008) CYTOGENETIC AND MOLECULAR CHARACTERIZATION OF A THREE-GENERATION FAMILY WITH CHROMOSOME 5P TERMINAL DELETION.CLINICAL GENETICS. VOL. 73. ISSUE 6. P. 585 -590 23 92% 8
5 NGUYEN, JM , QUALMANN, KJ , OKASHAH, R , REILLY, A , ALEXEYEV, MF , CAMPBELL, DJ , (2015) 5P DELETIONS: CURRENT KNOWLEDGE AND FUTURE DIRECTIONS.AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. VOL. 169. ISSUE 3. P. 224 -238 39 39% 4
6 KRGOVIC, D , BLATNIK, A , BURMAS, A , ZAGORAC, A , VOKAC, NK , (2014) A COALESCENCE OF TWO SYNDROMES IN A GIRL WITH TERMINAL DELETION AND INVERTED DUPLICATION OF CHROMOSOME 5.BMC MEDICAL GENETICS. VOL. 15. ISSUE . P. - 18 90% 2
7 ARENS, YHJM , ENGELEN, JJM , GOVAERTS, LCP , VAN RAVENSWAAY, CM , LONEUS, WH , VAN LENT-ALBRECHTS, JCM , VAN DER BLIJ-PHILIPSEN, M , HAMERS, AJH , SCHRANDER-STUMPEL, CTRM , (2004) FAMILIAL INSERTION (3;5)(Q25.3;Q22.1Q31.3) WITH DELETION OR DUPLICATION OF CHROMOSOME REGION 5Q22.1-5Q31.3 IN TEN UNBALANCED CARRIERS.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 130A. ISSUE 2. P. 128-133 29 69% 13
8 ZHANG, B , WILLING, M , GRANGE, DK , SHINAWI, M , MANWARING, L , VINEYARD, M , KULKARNI, S , COTTRELL, CE , (2016) MULTIGENERATIONAL AUTOSOMAL DOMINANT INHERITANCE OF 5P CHROMOSOMAL DELETIONS.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 170. ISSUE 3. P. 583 -593 18 67% 1
9 LEVY, B , DUNN, TM , KERN, JH , HIRSCHHORN, K , KARDON, NB , (2002) DELINEATION OF THE DUP 5Q PHENOTYPE BY MOLECULAR CYTOGENETIC ANALYSIS IN A PATIENT WITH DUP5Q/DEL 5P (CRI DU CHAT).AMERICAN JOURNAL OF MEDICAL GENETICS. VOL. 108. ISSUE 3. P. 192-197 24 75% 12
10 MAINARDI, PC , PERFUMO, C , CALI, A , COUCOURDE, G , PASTORE, G , CAVANI, S , ZARA, F , OVERHAUSER, J , PIERLUIGI, M , BRICARELLI, FD , (2001) CLINICAL AND MOLECULAR CHARACTERISATION OF 80 PATIENTS WITH 5P DELETION: GENOTYPE-PHENOTYPE CORRELATION.JOURNAL OF MEDICAL GENETICS. VOL. 38. ISSUE 3. P. 151-158 22 76% 81

Classes with closest relation at Level 1


Rank Class id link
1 26502 PARACENTRIC INVERSION//PARTIAL TRISOMY 2P//TRISOMY 2P
2 14190 TRISOMY 9//TETRASOMY 9P//TRISOMY 9P
3 24663 TRISOMY 1Q//PARTIAL TRISOMY 1Q//3P SYNDROME
4 20601 COMPLEX CHROMOSOMAL REARRANGEMENT//COMPLEX CHROMOSOME REARRANGEMENT//CHROMOTHRIPSIS
5 33589 TRISOMY 16Q//TRISOMY 16P//DUPLICATION CHROMOSOME 16P
6 25553 JACOBSEN SYNDROME//11Q SYNDROME//11Q TERMINAL DELETION DISORDER
7 20269 18Q SYNDROME//CHROMOSOME 18//TETRASOMY 18P
8 29024 TRISOMY 10Q//MONOSOMY 10Q//DISTAL 10Q TRISOMY
9 25706 PALLISTER KILLIAN SYNDROME//TETRASOMY 12P//ISOCHROMOSOME 12P
10 27158 ACROCALLOSAL SYNDROME//VICI SYNDROME//GREIG CEPHALOPOLYSYNDACTYLY SYNDROME

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