Class information for:
Level 2: PRADER WILLI SYNDROME//ANGELMAN SYNDROME//UBE3A

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
2900 2794 35.4 81%


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
2900 2             PRADER WILLI SYNDROME//ANGELMAN SYNDROME//UBE3A 2794
2365 1                   PRADER WILLI SYNDROME//ANGELMAN SYNDROME//UBE3A 2269
24691 1                   BTG2//BTG1//TOB 304
27801 1                   NECDIN//SASH1//REGULAT MACROMOL FUNCT 221

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 PRADER WILLI SYNDROME authKW 5987047 25% 79% 694
2 ANGELMAN SYNDROME authKW 2618294 11% 75% 321
3 UBE3A authKW 436456 2% 74% 54
4 CHROMOSOME 15 authKW 351897 3% 44% 74
5 PRADER WILLI authKW 306114 1% 68% 41
6 BTG2 authKW 223403 1% 66% 31
7 NECDIN authKW 208836 1% 66% 29
8 BTG1 authKW 199315 1% 79% 23
9 TOB authKW 156090 1% 71% 20
10 PWS authKW 153866 1% 54% 26

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 18153 34% 0% 946
2 Education, Special 6083 5% 0% 134
3 Pediatrics 3285 13% 0% 352
4 Rehabilitation 2309 6% 0% 177
5 Endocrinology & Metabolism 1652 10% 0% 292
6 Clinical Neurology 620 8% 0% 223
7 Cell Biology 275 7% 0% 200
8 Psychology, Developmental 243 2% 0% 54
9 Biochemistry & Molecular Biology 224 12% 0% 340
10 Oncology 215 7% 0% 188

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 REFERENCE SYNDROME PRADER WILLI 150371 1% 81% 17
2 AUXOL 135163 1% 35% 35
3 REGULAT MACROMOL FUNCT 101136 1% 51% 18
4 SECT MED GENET MOL MED 86493 1% 28% 28
5 UNIT AUTOIMMUNE ENDOCRINE DIS 80460 0% 82% 9
6 SECT DEV PSYCHIAT 72558 1% 24% 28
7 REGULAT NEURONAL DEV 71512 0% 55% 12
8 GASTROENTEROL SURG SURG 2 67728 1% 24% 26
9 RC PHILIPS UNIT 56195 0% 86% 6
10 PEDIAT AUTOIMMUNE ENDOCRINE DIS UNIT 54635 0% 100% 5

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 PART A 29950 5% 2% 126
2 AMERICAN JOURNAL OF MEDICAL GENETICS 27205 5% 2% 148
3 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 21599 2% 3% 62
4 CLINICAL GENETICS 7641 2% 1% 60
5 HUMAN MOLECULAR GENETICS 5702 3% 1% 72
6 JOURNAL OF NEURODEVELOPMENTAL DISORDERS 5025 0% 4% 11
7 AMERICAN JOURNAL ON MENTAL RETARDATION 4514 1% 2% 21
8 JOURNAL OF MEDICAL GENETICS 4275 2% 1% 48
9 EUROPEAN JOURNAL OF MEDICAL GENETICS 3808 1% 2% 20
10 JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM 3484 1% 1% 34

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 PRADER WILLI SYNDROME 5987047 25% 79% 694 Search PRADER+WILLI+SYNDROME Search PRADER+WILLI+SYNDROME
2 ANGELMAN SYNDROME 2618294 11% 75% 321 Search ANGELMAN+SYNDROME Search ANGELMAN+SYNDROME
3 UBE3A 436456 2% 74% 54 Search UBE3A Search UBE3A
4 CHROMOSOME 15 351897 3% 44% 74 Search CHROMOSOME+15 Search CHROMOSOME+15
5 PRADER WILLI 306114 1% 68% 41 Search PRADER+WILLI Search PRADER+WILLI
6 BTG2 223403 1% 66% 31 Search BTG2 Search BTG2
7 NECDIN 208836 1% 66% 29 Search NECDIN Search NECDIN
8 BTG1 199315 1% 79% 23 Search BTG1 Search BTG1
9 TOB 156090 1% 71% 20 Search TOB Search TOB
10 PWS 153866 1% 54% 26 Search PWS Search PWS

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 CASSIDY, SB , SCHWARTZ, S , MILLER, JL , DRISCOLL, DJ , (2012) PRADER-WILLI SYNDROME.GENETICS IN MEDICINE. VOL. 14. ISSUE 1. P. 10 -26 134 91% 202
2 GOLDSTONE, AP , HOLLAND, AJ , HAUFFA, BP , HOKKEN-KOELEGA, AC , TAUBER, M , (2008) RECOMMENDATIONS FOR THE DIAGNOSIS AND MANAGEMENT OF PRADER-WILLI SYNDROME.JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. VOL. 93. ISSUE 11. P. 4183 -4197 130 93% 145
3 ANGULO, MA , BUTLER, MG , CATALETTO, ME , (2015) PRADER-WILLI SYNDROME: A REVIEW OF CLINICAL, GENETIC, AND ENDOCRINE FINDINGS.JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION. VOL. 38. ISSUE 12. P. 1249 -1263 109 88% 24
4 HURREN, BJ , FLACK, NAMS , (2016) PRADER-WILLI SYNDROME: A SPECTRUM OF ANATOMICAL AND CLINICAL FEATURES.CLINICAL ANATOMY. VOL. 29. ISSUE 5. P. 590 -605 125 91% 1
5 DEAL, CL , TONY, M , HOYBYE, C , ALLEN, DB , TAUBER, M , CHRISTIANSEN, JS , (2013) GROWTH HORMONE RESEARCH SOCIETY WORKSHOP SUMMARY: CONSENSUS GUIDELINES FOR RECOMBINANT HUMAN GROWTH HORMONE THERAPY IN PRADER-WILLI SYNDROME.JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. VOL. 98. ISSUE 6. P. E1072-E1087 104 87% 37
6 BUITING, K , (2010) PRADER-WILLI SYNDROME AND ANGELMAN SYNDROME.AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. VOL. 154C. ISSUE 3. P. 365-376 93 94% 101
7 BUITING, K , WILLIAMS, C , HORSTHEMKE, B , (2016) ANGELMAN SYNDROME - INSIGHTS INTO A RARE NEUROGENETIC DISORDER.NATURE REVIEWS NEUROLOGY. VOL. 12. ISSUE 10. P. 584 -593 91 92% 2
8 GRUGNI, G , MARZULLO, P , (2016) DIAGNOSIS AND TREATMENT OF GH DEFICIENCY IN PRADER-WILLI SYNDROME.BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM. VOL. 30. ISSUE 6. P. 785 -794 88 96% 0
9 HOGART, A , WU, D , LASALLE, JM , SCHANEN, NC , (2010) THE COMORBIDITY OF AUTISM WITH THE GENOMIC DISORDERS OF CHROMOSOME 15Q11.2-Q13.NEUROBIOLOGY OF DISEASE. VOL. 38. ISSUE 2. P. 181-191 102 70% 88
10 CASSIDY, SB , DRISCOLL, DJ , (2009) PRADER-WILLI SYNDROME.EUROPEAN JOURNAL OF HUMAN GENETICS. VOL. 17. ISSUE 1. P. 3-13 64 100% 176

Classes with closest relation at Level 2


Rank Class id link
1 2439 GENOMIC IMPRINTING//BECKWITH WIEDEMANN SYNDROME//SILVER RUSSELL SYNDROME
2 3091 WILLIAMS SYNDROME//WILLIAMS BEUREN SYNDROME//SUPRAVALVULAR AORTIC STENOSIS
3 395 GENETICS & HEREDITY//ANNALES DE GENETIQUE//HOLOPROSENCEPHALY
4 1566 FRAGILE X SYNDROME//RETT SYNDROME//FRAGILE X
5 493 AUTISM//JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS//AUTISM SPECTRUM DISORDER
6 3109 VELOCARDIOFACIAL SYNDROME//DIGEORGE SYNDROME//22Q112 DELETION SYNDROME
7 3882 SOTOS SYNDROME//NSD1//WEAVER SYNDROME
8 2731 DOWN SYNDROME//DYRK1A//TS65DN
9 3382 LISSENCEPHALY//SECKEL SYNDROME//LIS1
10 1334 INTELLECTUAL DISABILITY//EDUCATION, SPECIAL//JOURNAL OF INTELLECTUAL DISABILITY RESEARCH

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