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

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
2365 2269 34.4 78%


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

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 7182649 30% 78% 685
2 ANGELMAN SYNDROME authKW 3224262 14% 75% 321
3 UBE3A authKW 537468 2% 74% 54
4 CHROMOSOME 15 authKW 433353 3% 44% 74
5 PRADER WILLI authKW 341078 2% 65% 39
6 PWS authKW 189479 1% 54% 26
7 REFERENCE SYNDROME PRADER WILLI address 185171 1% 81% 17
8 INV DUP15 authKW 168193 1% 83% 15
9 AUXOL address 166454 2% 35% 35
10 PRADER WILLI SYNDROME PWS authKW 164025 1% 76% 16

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 19587 39% 0% 880
2 Education, Special 7551 6% 0% 134
3 Pediatrics 4194 16% 0% 352
4 Rehabilitation 2920 8% 0% 177
5 Endocrinology & Metabolism 1991 12% 0% 282
6 Clinical Neurology 828 10% 0% 221
7 Psychology, Developmental 321 2% 0% 54
8 Psychiatry 226 5% 0% 107
9 Neurosciences 177 8% 0% 177
10 Medical Ethics 174 1% 0% 13

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 185171 1% 81% 17
2 AUXOL 166454 2% 35% 35
3 SECT MED GENET MOL MED 106519 1% 28% 28
4 UNIT AUTOIMMUNE ENDOCRINE DIS 99081 0% 82% 9
5 SECT DEV PSYCHIAT 89359 1% 24% 28
6 RC PHILIPS UNIT 69200 0% 86% 6
7 PEDIAT AUTOIMMUNE ENDOCRINE DIS UNIT 67279 0% 100% 5
8 PRADER WILLI SYNDROME CLIN 67279 0% 100% 5
9 AUTOIMMUNE ENDOCRINE DIS UNIT 60548 0% 75% 6
10 ANGELMAN SYNDROME CLIN 53823 0% 100% 4

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 36938 6% 2% 126
2 AMERICAN JOURNAL OF MEDICAL GENETICS 33568 7% 2% 148
3 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 26625 3% 3% 62
4 CLINICAL GENETICS 9122 3% 1% 59
5 HUMAN MOLECULAR GENETICS 6858 3% 1% 71
6 JOURNAL OF NEURODEVELOPMENTAL DISORDERS 6193 0% 4% 11
7 AMERICAN JOURNAL ON MENTAL RETARDATION 5568 1% 2% 21
8 JOURNAL OF MEDICAL GENETICS 5286 2% 1% 48
9 EUROPEAN JOURNAL OF MEDICAL GENETICS 4699 1% 2% 20
10 JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM 4306 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 7182649 30% 78% 685 Search PRADER+WILLI+SYNDROME Search PRADER+WILLI+SYNDROME
2 ANGELMAN SYNDROME 3224262 14% 75% 321 Search ANGELMAN+SYNDROME Search ANGELMAN+SYNDROME
3 UBE3A 537468 2% 74% 54 Search UBE3A Search UBE3A
4 CHROMOSOME 15 433353 3% 44% 74 Search CHROMOSOME+15 Search CHROMOSOME+15
5 PRADER WILLI 341078 2% 65% 39 Search PRADER+WILLI Search PRADER+WILLI
6 PWS 189479 1% 54% 26 Search PWS Search PWS
7 INV DUP15 168193 1% 83% 15 Search INV+DUP15 Search INV+DUP15
8 PRADER WILLI SYNDROME PWS 164025 1% 76% 16 Search PRADER+WILLI+SYNDROME+PWS Search PRADER+WILLI+SYNDROME+PWS
9 UNIPARENTAL DISOMY 156918 3% 18% 64 Search UNIPARENTAL+DISOMY Search UNIPARENTAL+DISOMY
10 ANGELMAN 132476 1% 62% 16 Search ANGELMAN Search ANGELMAN

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 CASSIDY, SB , DRISCOLL, DJ , (2009) PRADER-WILLI SYNDROME.EUROPEAN JOURNAL OF HUMAN GENETICS. VOL. 17. ISSUE 1. P. 3-13 64 100% 176
10 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. 181-191 101 70% 88

Classes with closest relation at Level 1


Rank Class id link
1 27801 NECDIN//SASH1//REGULAT MACROMOL FUNCT
2 1779 GENOMIC IMPRINTING//H19//IGF2
3 10418 SUPERNUMERARY MARKER CHROMOSOME//MARKER CHROMOSOME//SMALL SUPERNUMERARY MARKER CHROMOSOME
4 24588 SMITH MAGENIS SYNDROME//RAI1//POTOCKI LUPSKI SYNDROME
5 9519 SILVER RUSSELL SYNDROME//BECKWITH WIEDEMANN SYNDROME//UNIPARENTAL DISOMY
6 5364 AUTISM//BROAD AUTISM PHENOTYPE//MOLECULAR AUTISM
7 6924 SUBTELOMERIC REARRANGEMENTS//ARRAY CGH//MBD5
8 27098 ACRO CARDIO FACIAL SYNDROME//CHROMOSOME 6Q DELETION//SIM1 GENE
9 5669 WILLIAMS SYNDROME//WILLIAMS BEUREN SYNDROME//SUPRAVALVULAR AORTIC STENOSIS
10 14963 MONOSOMY 21//RING CHROMOSOME 21//RING CHROMOSOME 20

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