Class information for:
Level 2: PRADER WILLI SYNDROME//ANGELMAN SYNDROME//PAR 4

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
2836 2461 34.4 79%


Bar chart of Publication_year

Last years might be incomplete

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