Class information for:
Level 2: 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
24317 1                   BTG2//BTG3//BTG1 339
29583 1                   NECDIN//REGULAT MACROMOL FUNCT//GASTROENTEROL SURG SURG 2 201

Terms with highest relevance score


rank Category termType chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 PRADER WILLI SYNDROME authKW 6091571 25% 78% 709
2 ANGELMAN SYNDROME authKW 2695397 12% 74% 330
3 UBE3A authKW 490096 2% 73% 61
4 CHROMOSOME 15 authKW 381317 3% 45% 77
5 PRADER WILLI authKW 304881 1% 67% 41
6 BTG2 authKW 216976 1% 63% 31
7 NECDIN authKW 206762 1% 64% 29
8 BTG3 authKW 190200 1% 90% 19
9 BTG1 authKW 184651 1% 76% 22
10 TOB authKW 174255 1% 75% 21

Web of Science journal categories


chi_square_rank Category chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 Genetics & Heredity 17491 33% 0% 937
2 Education, Special 5886 5% 0% 134
3 Pediatrics 3365 13% 0% 359
4 Rehabilitation 2421 6% 0% 183
5 Endocrinology & Metabolism 1780 11% 0% 304
6 Clinical Neurology 638 8% 0% 228
7 Cell Biology 360 8% 0% 222
8 Neurosciences 267 8% 0% 235
9 Biochemistry & Molecular Biology 260 13% 0% 357
10 Psychology, Developmental 225 2% 0% 53

Address terms


chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 REFERENCE SYNDROME PRADER WILLI 145339 1% 77% 17
2 AUXOL 142850 1% 35% 37
3 REGULAT MACROMOL FUNCT 102408 1% 51% 18
4 GASTROENTEROL SURG SURG 2 89307 1% 26% 31
5 SECT MED GENET MOL MED 87581 1% 28% 28
6 UNIT AUTOIMMUNE ENDOCRINE DIS 81471 0% 82% 9
7 SECT DEV PSYCHIAT 73470 1% 24% 28
8 REGULAT NEURONAL DEV 72411 0% 55% 12
9 RC PHILIPS UNIT 56901 0% 86% 6
10 ANGELMAN SYNDROME CLIN 55322 0% 100% 5

Journals


chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 27724 4% 2% 123
2 AMERICAN JOURNAL OF MEDICAL GENETICS 26074 5% 2% 144
3 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 21253 2% 3% 62
4 JOURNAL OF NEURODEVELOPMENTAL DISORDERS 7477 0% 5% 14
5 CLINICAL GENETICS 7292 2% 1% 59
6 HUMAN MOLECULAR GENETICS 5524 3% 1% 72
7 JOURNAL OF MEDICAL GENETICS 4276 2% 1% 48
8 AMERICAN JOURNAL ON MENTAL RETARDATION 4144 1% 2% 20
9 EUROPEAN JOURNAL OF MEDICAL GENETICS 3958 1% 2% 21
10 HUMAN GENETICS 3508 2% 1% 51

Author Key Words


chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass LCSH search Wikipedia search
1 PRADER WILLI SYNDROME 6091571 25% 78% 709 Search PRADER+WILLI+SYNDROME Search PRADER+WILLI+SYNDROME
2 ANGELMAN SYNDROME 2695397 12% 74% 330 Search ANGELMAN+SYNDROME Search ANGELMAN+SYNDROME
3 UBE3A 490096 2% 73% 61 Search UBE3A Search UBE3A
4 CHROMOSOME 15 381317 3% 45% 77 Search CHROMOSOME+15 Search CHROMOSOME+15
5 PRADER WILLI 304881 1% 67% 41 Search PRADER+WILLI Search PRADER+WILLI
6 BTG2 216976 1% 63% 31 Search BTG2 Search BTG2
7 NECDIN 206762 1% 64% 29 Search NECDIN Search NECDIN
8 BTG3 190200 1% 90% 19 Search BTG3 Search BTG3
9 BTG1 184651 1% 76% 22 Search BTG1 Search BTG1
10 TOB 174255 1% 75% 21 Search TOB Search TOB

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 2


rank cluster_id2 link
1 2580 GENOMIC IMPRINTING//IMPRINTING//SILVER RUSSELL SYNDROME
2 387 ARRAY CGH//GENETICS & HEREDITY//HOLOPROSENCEPHALY
3 2127 RETT SYNDROME//MECP2//X CHROMOSOME INACTIVATION
4 2136 FRAGILE X SYNDROME//FRAGILE X//FMR1
5 3276 VELOCARDIOFACIAL SYNDROME//DIGEORGE SYNDROME//22Q112 DELETION SYNDROME
6 487 AUTISM//JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS//AUTISM SPECTRUM DISORDER
7 3403 PSEUDOHYPOPARATHYROIDISM//FAHRS DISEASE//ALBRIGHT HEREDITARY OSTEODYSTROPHY
8 2623 DOWN SYNDROME//DYRK1A//TS65DN
9 2571 DRAVET SYNDROME//FEBRILE SEIZURES//SCN1A
10 634 INTELLECTUAL DISABILITY//EDUCATION, SPECIAL//REHABILITATION

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