Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
2836 | 2461 | 34.4 | 79% |
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 |
---|---|---|
2735 | 2084 | PRADER WILLI SYNDROME//ANGELMAN SYNDROME//UBE3A |
25658 | 228 | PAR 4//AATF//PROSTATE APOPTOSIS RESPONSE 4 |
29658 | 149 | NECDIN//REGULAT MACROMOL FUNCT//REGULAT NEURONAL DEV |
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 | PRADER WILLI SYNDROME | Author keyword | 912 | 76% | 26% | 636 |
2 | ANGELMAN SYNDROME | Author keyword | 375 | 72% | 12% | 297 |
3 | PAR 4 | Author keyword | 63 | 64% | 3% | 62 |
4 | UBE3A | Author keyword | 62 | 73% | 2% | 47 |
5 | CHROMOSOME 15 | Author keyword | 43 | 44% | 3% | 75 |
6 | PRADER WILLI | Author keyword | 40 | 66% | 2% | 37 |
7 | NECDIN | Author keyword | 32 | 69% | 1% | 27 |
8 | REFERENCE SYNDROME PRADER WILLI | Address | 29 | 88% | 1% | 14 |
9 | PRADER LABHART WILLI SYNDROME | Author keyword | 21 | 90% | 0% | 9 |
10 | PRADER WILLI SYNDROME PWS | Author keyword | 19 | 74% | 1% | 14 |
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 | PRADER WILLI SYNDROME | 912 | 76% | 26% | 636 | Search PRADER+WILLI+SYNDROME | Search PRADER+WILLI+SYNDROME |
2 | ANGELMAN SYNDROME | 375 | 72% | 12% | 297 | Search ANGELMAN+SYNDROME | Search ANGELMAN+SYNDROME |
3 | PAR 4 | 63 | 64% | 3% | 62 | Search PAR+4 | Search PAR+4 |
4 | UBE3A | 62 | 73% | 2% | 47 | Search UBE3A | Search UBE3A |
5 | CHROMOSOME 15 | 43 | 44% | 3% | 75 | Search CHROMOSOME+15 | Search CHROMOSOME+15 |
6 | PRADER WILLI | 40 | 66% | 2% | 37 | Search PRADER+WILLI | Search PRADER+WILLI |
7 | NECDIN | 32 | 69% | 1% | 27 | Search NECDIN | Search NECDIN |
8 | PRADER LABHART WILLI SYNDROME | 21 | 90% | 0% | 9 | Search PRADER+LABHART+WILLI+SYNDROME | Search PRADER+LABHART+WILLI+SYNDROME |
9 | PRADER WILLI SYNDROME PWS | 19 | 74% | 1% | 14 | Search PRADER+WILLI+SYNDROME+PWS | Search PRADER+WILLI+SYNDROME+PWS |
10 | ANGELMAN | 18 | 67% | 1% | 16 | Search ANGELMAN | Search ANGELMAN |
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 | HAPPY PUPPET SYNDROME | 157 | 92% | 2% | 61 |
2 | BIRTH INCIDENCE | 118 | 95% | 2% | 39 |
3 | ANGELMAN SYNDROMES | 106 | 64% | 4% | 104 |
4 | CHROMOSOME 15 | 89 | 43% | 6% | 157 |
5 | PRADER WILLI SYNDROME | 87 | 21% | 15% | 363 |
6 | 15Q11 13 | 86 | 80% | 2% | 53 |
7 | 15Q11 Q13 | 83 | 67% | 3% | 74 |
8 | UBE3A E6 AP | 79 | 91% | 1% | 32 |
9 | ANGELMAN SYNDROME | 78 | 30% | 9% | 222 |
10 | 15Q DELETIONS | 77 | 96% | 1% | 24 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Prader-Willi syndrome | 2012 | 119 | 147 | 86% |
Recommendations for the Diagnosis and Management of Prader-Willi Syndrome | 2008 | 118 | 140 | 89% |
Angelman Syndrome | 2015 | 1 | 70 | 70% |
Neurologic Manifestations of Angelman Syndrome | 2013 | 19 | 79 | 91% |
Angelman syndrome: insights into genomic imprinting and neurodevelopmental phenotypes | 2011 | 62 | 97 | 60% |
Angelman syndrome: a review of the clinical and genetic aspects | 2003 | 215 | 67 | 79% |
Mechanisms of imprinting of the Prader-Willi/Angelman region | 2008 | 115 | 47 | 70% |
Genome organization, function and imprinting in Prader-Willi and Angelman syndromes | 2001 | 326 | 79 | 63% |
Prader-Willi syndrome: advances in genetics, pathophysiology and treatment | 2004 | 196 | 79 | 72% |
The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13 | 2010 | 71 | 145 | 70% |
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 | REFERENCE SYNDROME PRADER WILLI | 29 | 88% | 0.6% | 14 |
2 | UNIT AUTOIMMUNE ENDOCRINE DIS | 15 | 82% | 0.4% | 9 |
3 | AUXOL | 13 | 34% | 1.3% | 31 |
4 | REGULAT MACROMOL FUNCT | 13 | 51% | 0.7% | 18 |
5 | RC PHILIPS UNIT | 12 | 86% | 0.2% | 6 |
6 | SECT MED GENET MOL MED | 9 | 28% | 1.1% | 28 |
7 | PEDIAT AUTOIMMUNE ENDOCRINE DIS UNIT | 8 | 100% | 0.2% | 5 |
8 | REGULAT NEURONAL DEV | 7 | 53% | 0.4% | 10 |
9 | SECT DEV PSYCHIAT | 7 | 22% | 1.1% | 26 |
10 | PRADER WILLI SYNDROME CLIN | 6 | 80% | 0.2% | 4 |
Related classes at same level (level 2) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000058082 | GENOMIC IMPRINTING//H19//BECKWITH WIEDEMANN SYNDROME |
2 | 0.0000025100 | WILLIAMS SYNDROME//WILLIAMS BEUREN SYNDROME//SUPRAVALVULAR AORTIC STENOSIS |
3 | 0.0000019764 | WOLF HIRSCHHORN SYNDROME//HOLOPROSENCEPHALY//ANNALES DE GENETIQUE |
4 | 0.0000017059 | RETT SYNDROME//MECP2//MECP2 GENE |
5 | 0.0000011285 | FRAGILE X SYNDROME//FRAGILE X//FMR1 |
6 | 0.0000010957 | AUTISM//JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS//AUTISM SPECTRUM DISORDERS |
7 | 0.0000010804 | DOWN SYNDROME//JOURNAL OF INTELLECTUAL DISABILITY RESEARCH//INTELLECTUAL DISABILITY |
8 | 0.0000010693 | HERMANSKY PUDLAK SYNDROME//CHEDIAK HIGASHI SYNDROME//GRISCELLI SYNDROME |
9 | 0.0000010040 | SOTOS SYNDROME//WEAVER SYNDROME//CEREBRAL GIGANTISM |
10 | 0.0000009532 | GHRELIN//OBESTATIN//NESFATIN 1 |