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

Basic class information
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 ONCOLOGY//CELL BIOLOGY//BIOCHEMISTRY & MOLECULAR BIOLOGY 2934640
304 3       DNA METHYLATION//FRAGILE X SYNDROME//RETT SYNDROME 41307
2979 2             PRADER WILLI SYNDROME//ANGELMAN SYNDROME//UBE3A 2848
2359 1                   PRADER WILLI SYNDROME//ANGELMAN SYNDROME//UBE3A 2308

Terms with highest relevance score


rank Category termType chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 PRADER WILLI SYNDROME authKW 7327489 30% 77% 700
2 ANGELMAN SYNDROME authKW 3326190 14% 74% 330
3 UBE3A authKW 604791 3% 73% 61
4 CHROMOSOME 15 authKW 470569 3% 45% 77
5 PRADER WILLI authKW 340418 2% 64% 39
6 PWS authKW 199046 1% 54% 27
7 PRADER WILLI SYNDROME PWS authKW 179352 1% 77% 17
8 REFERENCE SYNDROME PRADER WILLI address 179352 1% 77% 17
9 AUXOL address 176290 2% 35% 37
10 INV DUP15 authKW 170666 1% 83% 15

Web of Science journal categories


chi_square_rank Category chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 Genetics & Heredity 19076 38% 0% 875
2 Education, Special 7325 6% 0% 134
3 Pediatrics 4307 16% 0% 359
4 Rehabilitation 3068 8% 0% 183
5 Endocrinology & Metabolism 2138 13% 0% 293
6 Clinical Neurology 863 10% 0% 227
7 Psychology, Developmental 299 2% 0% 53
8 Neurosciences 233 8% 0% 195
9 Psychiatry 214 5% 0% 106
10 Medical Ethics 171 1% 0% 13

Address terms


chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 REFERENCE SYNDROME PRADER WILLI 179352 1% 77% 17
2 AUXOL 176290 2% 35% 37
3 SECT MED GENET MOL MED 108086 1% 28% 28
4 UNIT AUTOIMMUNE ENDOCRINE DIS 100537 0% 82% 9
5 SECT DEV PSYCHIAT 90673 1% 24% 28
6 RC PHILIPS UNIT 70217 0% 86% 6
7 ANGELMAN SYNDROME CLIN 68268 0% 100% 5
8 PEDIAT AUTOIMMUNE ENDOCRINE DIS UNIT 68268 0% 100% 5
9 PRADER WILLI SYNDROME CLIN 68268 0% 100% 5
10 ENDOCRINOL BONE DIS GENET GYNAECOL 54615 0% 100% 4

Journals


chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 34268 5% 2% 123
2 AMERICAN JOURNAL OF MEDICAL GENETICS 32242 6% 2% 144
3 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 26254 3% 3% 62
4 JOURNAL OF NEURODEVELOPMENTAL DISORDERS 9233 1% 5% 14
5 CLINICAL GENETICS 9026 3% 1% 59
6 HUMAN MOLECULAR GENETICS 6658 3% 1% 71
7 JOURNAL OF MEDICAL GENETICS 5299 2% 1% 48
8 AMERICAN JOURNAL ON MENTAL RETARDATION 5123 1% 2% 20
9 EUROPEAN JOURNAL OF MEDICAL GENETICS 4894 1% 2% 21
10 JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM 4224 1% 1% 34

Author Key Words


chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass LCSH search Wikipedia search
1 PRADER WILLI SYNDROME 7327489 30% 77% 700 Search PRADER+WILLI+SYNDROME Search PRADER+WILLI+SYNDROME
2 ANGELMAN SYNDROME 3326190 14% 74% 330 Search ANGELMAN+SYNDROME Search ANGELMAN+SYNDROME
3 UBE3A 604791 3% 73% 61 Search UBE3A Search UBE3A
4 CHROMOSOME 15 470569 3% 45% 77 Search CHROMOSOME+15 Search CHROMOSOME+15
5 PRADER WILLI 340418 2% 64% 39 Search PRADER+WILLI Search PRADER+WILLI
6 PWS 199046 1% 54% 27 Search PWS Search PWS
7 PRADER WILLI SYNDROME PWS 179352 1% 77% 17 Search PRADER+WILLI+SYNDROME+PWS Search PRADER+WILLI+SYNDROME+PWS
8 INV DUP15 170666 1% 83% 15 Search INV+DUP15 Search INV+DUP15
9 UNIPARENTAL DISOMY 158373 3% 18% 65 Search UNIPARENTAL+DISOMY Search UNIPARENTAL+DISOMY
10 ANGELMAN 146132 1% 63% 17 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.

Classes with closest relation at Level 1


rank cluster_id2 link
1 29583 NECDIN//REGULAT MACROMOL FUNCT//GASTROENTEROL SURG SURG 2
2 18658 CAT EYE SYNDROME//SMALL SUPERNUMERARY MARKER CHROMOSOME//SUPERNUMERARY MARKER CHROMOSOME
3 593 GENOMIC IMPRINTING//SILVER RUSSELL SYNDROME//H19
4 25172 SMITH MAGENIS SYNDROME//RAI1//POTOCKI LUPSKI SYNDROME
5 8114 BROAD AUTISM PHENOTYPE//BROADER AUTISM PHENOTYPE//AUTISM
6 16770 MONOSOMY 21//RING CHROMOSOME 21//RING CHROMOSOME 20
7 8049 SUBTELOMERIC REARRANGEMENTS//ARRAY CGH//MBD5
8 28816 MOTOR STEREOTYPIES//REPETITIVE BEHAVIOR//TIC NEURODEV MOVEMENTS TANDEM
9 32012 COHEN SYNDROME//COH1//VPS13B
10 4703 ZNF804A//CACNA1C//ANK3

Go to start page