Class information for:
Level 1: SMITH MAGENIS SYNDROME//RAI1//POTOCKI LUPSKI SYNDROME

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
16 4 DENTISTRY, ORAL SURGERY & MEDICINE//ORTHOPEDICS//DENT 796976
201 3       CLEFT PALATE-CRANIOFACIAL JOURNAL//CLEFT PALATE//CRANIOSYNOSTOSIS 52632
387 2             ARRAY CGH//GENETICS & HEREDITY//HOLOPROSENCEPHALY 17402
25172 1                   SMITH MAGENIS SYNDROME//RAI1//POTOCKI LUPSKI SYNDROME 312

Terms with highest relevance score



rank Category termType chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 SMITH MAGENIS SYNDROME authKW 6661283 27% 79% 84
2 RAI1 authKW 1836631 6% 91% 20
3 POTOCKI LUPSKI SYNDROME authKW 1414209 4% 100% 14
4 17P112 authKW 940212 4% 85% 11
5 CHROMOSOME 17P112 authKW 549967 2% 78% 7
6 DELETION 17P112 authKW 505075 2% 100% 5
7 SMITH MAGENIS SYNDROME SMS authKW 505075 2% 100% 5
8 17P112 DELETION authKW 449970 2% 64% 7
9 DUPLICATION 17P112 authKW 420894 2% 83% 5
10 PTLS authKW 404060 1% 100% 4

Web of Science journal categories



chi_square_rank Category chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 Genetics & Heredity 7561 64% 0% 199
2 Medical Ethics 297 2% 0% 6
3 Education, Special 236 3% 0% 9
4 Pediatrics 233 10% 0% 32
5 Rehabilitation 103 4% 0% 13
6 Biotechnology & Applied Microbiology 68 8% 0% 24
7 Psychology, Developmental 52 3% 0% 8
8 Biochemistry & Molecular Biology 28 13% 0% 39
9 Medicine, Research & Experimental 24 4% 0% 14
10 Clinical Neurology 20 5% 0% 16

Address terms



chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 ANOMALIES DEV 101015 0% 100% 1
2 BIOCHEM MOL BIOL ANTHROPOL 101015 0% 100% 1
3 CLIN CYTOGENET UCLH 101015 0% 100% 1
4 CLIN NEUROSCI POPULAT GENET EMMS 101015 0% 100% 1
5 CLIN PATHOL CYTOL HUMAN GENET 101015 0% 100% 1
6 CYST FIRBOSIS 101015 0% 100% 1
7 CYTOGENET FETAL PATHOL OBSTET GYNECOL 101015 0% 100% 1
8 CYTOGENET POSTNATALE 101015 0% 100% 1
9 GEN HUMANA 101015 0% 100% 1
10 HMRC 362 101015 0% 100% 1

Journals



chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 13174 9% 0% 28
2 AMERICAN JOURNAL OF MEDICAL GENETICS 9042 9% 0% 28
3 GENETIC COUNSELING 3745 2% 1% 6
4 AMERICAN JOURNAL OF HUMAN GENETICS 3581 5% 0% 17
5 ANNALES DE GENETIQUE 3167 2% 1% 6
6 JOURNAL OF MEDICAL GENETICS 2470 4% 0% 12
7 PHYSICAL & OCCUPATIONAL THERAPY IN PEDIATRICS 1625 1% 1% 2
8 CLINICAL GENETICS 1556 3% 0% 9
9 GENOMICS 1458 4% 0% 11
10 EUROPEAN JOURNAL OF MEDICAL GENETICS 1317 1% 0% 4

Author Key Words



chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass LCSH search Wikipedia search
1 SMITH MAGENIS SYNDROME 6661283 27% 79% 84 Search SMITH+MAGENIS+SYNDROME Search SMITH+MAGENIS+SYNDROME
2 RAI1 1836631 6% 91% 20 Search RAI1 Search RAI1
3 POTOCKI LUPSKI SYNDROME 1414209 4% 100% 14 Search POTOCKI+LUPSKI+SYNDROME Search POTOCKI+LUPSKI+SYNDROME
4 17P112 940212 4% 85% 11 Search 17P112 Search 17P112
5 CHROMOSOME 17P112 549967 2% 78% 7 Search CHROMOSOME+17P112 Search CHROMOSOME+17P112
6 DELETION 17P112 505075 2% 100% 5 Search DELETION+17P112 Search DELETION+17P112
7 SMITH MAGENIS SYNDROME SMS 505075 2% 100% 5 Search SMITH+MAGENIS+SYNDROME+SMS Search SMITH+MAGENIS+SYNDROME+SMS
8 17P112 DELETION 449970 2% 64% 7 Search 17P112+DELETION Search 17P112+DELETION
9 DUPLICATION 17P112 420894 2% 83% 5 Search DUPLICATION+17P112 Search DUPLICATION+17P112
10 PTLS 404060 1% 100% 4 Search PTLS Search PTLS

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 35817 FLIGHTLESS I//TTYH1//FLII
2 8049 SUBTELOMERIC REARRANGEMENTS//ARRAY CGH//MBD5
3 19087 COMPLEX CHROMOSOMAL REARRANGEMENT//COMPLEX CHROMOSOME REARRANGEMENT//CHROMOTHRIPSIS
4 14933 LISSENCEPHALY//LIS1//MILLER DIEKER SYNDROME
5 18658 CAT EYE SYNDROME//SMALL SUPERNUMERARY MARKER CHROMOSOME//SUPERNUMERARY MARKER CHROMOSOME
6 22614 SEGMENTAL DUPLICATION//DUF1220//NBPF
7 28901 TRISOMY 10Q//MONOSOMY 10Q//10P DUPLICATION
8 1438 CHARCOT MARIE TOOTH DISEASE//PMP22//CHARCOT MARIE TOOTH
9 18675 CRI DU CHAT SYNDROME//CRI DU CHAT//5P DELETION
10 22311 BIRT HOGG DUBE SYNDROME//FOLLICULIN//FIBROFOLLICULOMA

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