Class information for:
Level 1: PRADER WILLI SYNDROME//ANGELMAN SYNDROME//UBE3A

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
2735 2084 33.3 77%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
2836 2461 PRADER WILLI SYNDROME//ANGELMAN SYNDROME//PAR 4

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 871 75% 30% 627
2 ANGELMAN SYNDROME Author keyword 375 72% 14% 297
3 UBE3A Author keyword 62 73% 2% 47
4 CHROMOSOME 15 Author keyword 43 44% 4% 75
5 PRADER WILLI Author keyword 34 63% 2% 35
6 REFERENCE SYNDROME PRADER WILLI Address 29 88% 1% 14
7 PRADER LABHART WILLI SYNDROME Author keyword 21 90% 0% 9
8 PRADER WILLI SYNDROME PWS Author keyword 19 74% 1% 14
9 ANGELMAN Author keyword 18 67% 1% 16
10 INV DUP15 Author keyword 17 79% 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 PRADER WILLI SYNDROME 871 75% 30% 627 Search PRADER+WILLI+SYNDROME Search PRADER+WILLI+SYNDROME
2 ANGELMAN SYNDROME 375 72% 14% 297 Search ANGELMAN+SYNDROME Search ANGELMAN+SYNDROME
3 UBE3A 62 73% 2% 47 Search UBE3A Search UBE3A
4 CHROMOSOME 15 43 44% 4% 75 Search CHROMOSOME+15 Search CHROMOSOME+15
5 PRADER WILLI 34 63% 2% 35 Search PRADER+WILLI Search PRADER+WILLI
6 PRADER LABHART WILLI SYNDROME 21 90% 0% 9 Search PRADER+LABHART+WILLI+SYNDROME Search PRADER+LABHART+WILLI+SYNDROME
7 PRADER WILLI SYNDROME PWS 19 74% 1% 14 Search PRADER+WILLI+SYNDROME+PWS Search PRADER+WILLI+SYNDROME+PWS
8 ANGELMAN 18 67% 1% 16 Search ANGELMAN Search ANGELMAN
9 INV DUP15 17 79% 1% 11 Search INV+DUP15 Search INV+DUP15
10 IMPRINTING CENTER 15 82% 0% 9 Search IMPRINTING+CENTER Search IMPRINTING+CENTER

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% 3% 61
2 BIRTH INCIDENCE 118 95% 2% 39
3 ANGELMAN SYNDROMES 106 64% 5% 104
4 CHROMOSOME 15 89 43% 8% 157
5 15Q11 13 86 80% 3% 53
6 15Q11 Q13 83 67% 4% 74
7 UBE3A E6 AP 79 91% 2% 32
8 ANGELMAN SYNDROME 78 30% 11% 222
9 15Q DELETIONS 77 96% 1% 24
10 PROXIMAL 15Q 76 63% 4% 77

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%
Angelman syndrome: a review of the clinical and genetic aspects 2003 215 67 79%
Neurologic Manifestations of Angelman Syndrome 2013 19 79 91%
Angelman syndrome: insights into genomic imprinting and neurodevelopmental phenotypes 2011 62 97 60%
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 62%
Prader-Willi syndrome: advances in genetics, pathophysiology and treatment 2004 196 79 68%
The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13 2010 71 145 69%

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% 0.7% 14
2 UNIT AUTOIMMUNE ENDOCRINE DIS 15 82% 0.4% 9
3 AUXOL 13 34% 1.5% 31
4 RC PHILIPS UNIT 12 86% 0.3% 6
5 SECT MED GENET MOL MED 9 28% 1.3% 28
6 PEDIAT AUTOIMMUNE ENDOCRINE DIS UNIT 8 100% 0.2% 5
7 SECT DEV PSYCHIAT 7 22% 1.2% 26
8 PRADER WILLI SYNDROME CLIN 6 80% 0.2% 4
9 ENDOCRINOL METAB DIABETOL 5 33% 0.6% 13
10 ENDOCRINOL GENET GYNAECOL BONE DIS 5 63% 0.2% 5

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000204406 NECDIN//REGULAT MACROMOL FUNCT//REGULAT NEURONAL DEV
2 0.0000134159 CAT EYE SYNDROME//SUPERNUMERARY MARKER CHROMOSOMES//SMALL SUPERNUMERARY MARKER CHROMOSOME
3 0.0000079209 WS HALL PSYCHIAT//BROAD AUTISM PHENOTYPE//HYPERSEROTONEMIA
4 0.0000074008 GENOMIC IMPRINTING//H19//BECKWITH WIEDEMANN SYNDROME
5 0.0000064201 SMITH MAGENIS SYNDROME//RAI1//POTOCKI LUPSKI SYNDROME
6 0.0000062938 CONFINED PLACENTAL MOSAICISM//UNIPARENTAL DISOMY//TRISOMY 9
7 0.0000041235 COHEN SYNDROME//COH1//VPS13B
8 0.0000038693 SUBTELOMERIC REARRANGEMENTS//IDIOPATHIC MENTAL RETARDATION//MBD5
9 0.0000036668 ZNF804A//MCLAUGHLIN//MOL CLIN NEUROBIOL
10 0.0000032915 ALBINISM//OCULOCUTANEOUS ALBINISM//OCULAR ALBINISM