Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
3229 | 1493 | 40.0 | 69% |
Classes in level above (level 3) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
96 | 73697 | DNA METHYLATION//FRAGILE X SYNDROME//RETT SYNDROME |
Classes in level below (level 1) |
ID, lev. below |
Publications | Label for level below |
---|---|---|
5883 | 1493 | WILLIAMS SYNDROME//WILLIAMS BEUREN SYNDROME//SUPRAVALVULAR AORTIC STENOSIS |
Terms with highest relevance score |
Rank | Term | Type of term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|---|
1 | WILLIAMS SYNDROME | Author keyword | 828 | 79% | 35% | 528 |
2 | WILLIAMS BEUREN SYNDROME | Author keyword | 154 | 75% | 8% | 112 |
3 | SUPRAVALVULAR AORTIC STENOSIS | Author keyword | 66 | 70% | 4% | 55 |
4 | GTF2IRD1 | Author keyword | 41 | 100% | 1% | 15 |
5 | GTF2I | Author keyword | 32 | 88% | 1% | 15 |
6 | HYPERSOCIABILITY | Author keyword | 21 | 90% | 1% | 9 |
7 | 7Q1123 | Author keyword | 19 | 80% | 1% | 12 |
8 | TFII I | Author keyword | 17 | 57% | 1% | 20 |
9 | SUPRAVALVAR AORTIC STENOSIS | Author keyword | 15 | 73% | 1% | 11 |
10 | ELASTIN GENE | Author keyword | 13 | 69% | 1% | 11 |
Web of Science journal categories |
Author Key Words |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | WILLIAMS SYNDROME | 828 | 79% | 35% | 528 | Search WILLIAMS+SYNDROME | Search WILLIAMS+SYNDROME |
2 | WILLIAMS BEUREN SYNDROME | 154 | 75% | 8% | 112 | Search WILLIAMS+BEUREN+SYNDROME | Search WILLIAMS+BEUREN+SYNDROME |
3 | SUPRAVALVULAR AORTIC STENOSIS | 66 | 70% | 4% | 55 | Search SUPRAVALVULAR+AORTIC+STENOSIS | Search SUPRAVALVULAR+AORTIC+STENOSIS |
4 | GTF2IRD1 | 41 | 100% | 1% | 15 | Search GTF2IRD1 | Search GTF2IRD1 |
5 | GTF2I | 32 | 88% | 1% | 15 | Search GTF2I | Search GTF2I |
6 | HYPERSOCIABILITY | 21 | 90% | 1% | 9 | Search HYPERSOCIABILITY | Search HYPERSOCIABILITY |
7 | 7Q1123 | 19 | 80% | 1% | 12 | Search 7Q1123 | Search 7Q1123 |
8 | TFII I | 17 | 57% | 1% | 20 | Search TFII+I | Search TFII+I |
9 | SUPRAVALVAR AORTIC STENOSIS | 15 | 73% | 1% | 11 | Search SUPRAVALVAR+AORTIC+STENOSIS | Search SUPRAVALVAR+AORTIC+STENOSIS |
10 | ELASTIN GENE | 13 | 69% | 1% | 11 | Search ELASTIN+GENE | Search ELASTIN+GENE |
Key Words Plus |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | BEUREN SYNDROME | 341 | 87% | 11% | 165 |
2 | HEMIZYGOSITY | 189 | 84% | 7% | 102 |
3 | SUPRAVALVULAR AORTIC STENOSIS | 160 | 55% | 14% | 202 |
4 | HYPERSOCIABILITY | 114 | 86% | 4% | 59 |
5 | 7Q1123 | 114 | 86% | 4% | 57 |
6 | LINGUISTIC ABILITIES | 93 | 91% | 3% | 39 |
7 | ELASTIN LOCUS | 90 | 96% | 2% | 27 |
8 | ELFIN FACIES SYNDROME | 79 | 91% | 2% | 32 |
9 | IDIOPATHIC INFANTILE HYPERCALCEMIA | 65 | 76% | 3% | 45 |
10 | EXTENDED AORTOPLASTY | 57 | 95% | 1% | 19 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
MEDICAL PROGRESS Williams-Beuren Syndrome | 2010 | 148 | 77 | 95% |
Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype | 2008 | 124 | 191 | 95% |
Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour | 2006 | 173 | 131 | 74% |
Cardiovascular and Genitourinary Anomalies in Patients With Duplications Within the Williams Syndrome Critical Region: Phenotypic Expansion and Review of the Literature | 2014 | 3 | 10 | 90% |
Language abilities in Williams syndrome: A critical review | 2007 | 79 | 127 | 73% |
The genomic basis of the Williams - Beuren syndrome | 2009 | 63 | 167 | 65% |
Mechanisms and treatment of cardiovascular disease in Williams-Beuren syndrome | 2008 | 56 | 102 | 71% |
Copy number variants at Williams-Beuren syndrome 7q11.23 region | 2010 | 38 | 207 | 63% |
Defining the social phenotype in Williams syndrome: A model for linking gene, the brain, and behavior | 2008 | 48 | 109 | 72% |
Biochemistry and biology of the inducible multifunctional transcription factor TFII-I: 10 years later | 2012 | 19 | 84 | 56% |
Address terms |
Rank | Address term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | NEUROCOGNIT DEV UNIT | 11 | 31% | 2.1% | 31 |
2 | BIRKBECK BRAIN COGNIT DEV | 5 | 50% | 0.5% | 7 |
3 | DEV NEUROCOGNIT | 4 | 38% | 0.6% | 9 |
4 | BRAIN CHILD DEV | 4 | 75% | 0.2% | 3 |
5 | SERV NEUROL RIABILITAZ | 4 | 50% | 0.4% | 6 |
6 | INTEGRATED NEUROSCI HUMAN BEHAV | 4 | 56% | 0.3% | 5 |
7 | NEURODEV SCI | 4 | 31% | 0.7% | 10 |
8 | SECT INTEGRAT NEUROIMAGING | 3 | 28% | 0.7% | 10 |
9 | CIPSI | 3 | 19% | 1.0% | 15 |
10 | NEUROPSYCHOPHYSIOL | 3 | 16% | 1.0% | 15 |
Related classes at same level (level 2) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000025100 | PRADER WILLI SYNDROME//ANGELMAN SYNDROME//PAR 4 |
2 | 0.0000016055 | SPECIFIC LANGUAGE IMPAIRMENT//INTERNATIONAL JOURNAL OF LANGUAGE & COMMUNICATION DISORDERS//SPECIFIC LANGUAGE IMPAIRMENT SLI |
3 | 0.0000015505 | VELOCARDIOFACIAL SYNDROME//DIGEORGE SYNDROME//PSEUDOHYPOPARATHYROIDISM |
4 | 0.0000015099 | FRAGILE X SYNDROME//FRAGILE X//FMR1 |
5 | 0.0000014558 | DOWN SYNDROME//JOURNAL OF INTELLECTUAL DISABILITY RESEARCH//INTELLECTUAL DISABILITY |
6 | 0.0000013861 | AUTISM//JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS//AUTISM SPECTRUM DISORDERS |
7 | 0.0000013084 | MARFAN SYNDROME//FIBRILLIN//LYSYL OXIDASE |
8 | 0.0000012161 | SOTOS SYNDROME//WEAVER SYNDROME//CEREBRAL GIGANTISM |
9 | 0.0000008926 | INTERNATIONAL JOURNAL OF ART & DESIGN EDUCATION//JOURNAL OF ART & DESIGN EDUCATION//CHILDRENS DRAWINGS |
10 | 0.0000007874 | DYSLEXIA//FOXP2//DEVELOPMENTAL DYSLEXIA |