Class information for:
Level 1: AARSKOG SCOTT SYNDROME//FGD1//FACIOGENITAL DYSPLASIA

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
183 3       NOONAN SYNDROME//PTEN//CELL BIOLOGY 56293
1653 2             RHO KINASE//FASUDIL//RHO GTPASES 7178
35963 1                   AARSKOG SCOTT SYNDROME//FGD1//FACIOGENITAL DYSPLASIA 105

Terms with highest relevance score



rank Category termType chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 AARSKOG SCOTT SYNDROME authKW 5417932 18% 95% 19
2 FGD1 authKW 3087383 11% 86% 12
3 FACIOGENITAL DYSPLASIA authKW 2401300 8% 100% 8
4 FGD1 GENE authKW 2401300 8% 100% 8
5 AARSKOG SYNDROME authKW 2269972 10% 69% 11
6 UOC MOL MED address 1200650 4% 100% 4
7 FRABIN authKW 686082 4% 57% 4
8 FACIODIGITOGENITAL SYNDROME authKW 600325 2% 100% 2
9 AARSKOG authKW 300163 1% 100% 1
10 AARSKOG SCOTT authKW 300163 1% 100% 1

Web of Science journal categories



chi_square_rank Category chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 Genetics & Heredity 1697 52% 0% 55
2 Pediatrics 140 13% 0% 14
3 Cell Biology 54 13% 0% 14
4 Biochemistry & Molecular Biology 41 20% 0% 21
5 Medical Ethics 24 1% 0% 1
6 Anatomy & Morphology 17 2% 0% 2
7 Developmental Biology 6 2% 0% 2
8 Biotechnology & Applied Microbiology 6 5% 0% 5
9 Peripheral Vascular Diseases 5 3% 0% 3
10 Medicine, Research & Experimental 5 4% 0% 4

Address terms



chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 UOC MOL MED 1200650 4% 100% 4
2 FAK COCUK HASTANESI INCIRALTI MED 300163 1% 100% 1
3 MOL CELL BIOL CANC CAMPAIGN 300163 1% 100% 1
4 MOL CELLULAR BIOLCHO KU 300163 1% 100% 1
5 PDIAT UROL 300163 1% 100% 1
6 UOC CHILD NEUROPSYCHIAT 300163 1% 100% 1
7 JCR PHARMACEUT CO LTDNISHI KU 300161 2% 50% 2
8 HUMAN GENET CYTOGENET 75039 1% 25% 1
9 CRC ONCOGENE SIGNAL TRANSDUCT GRP 60031 1% 20% 1
10 RIC DISABIL MENTALE MOTORIA 60031 1% 20% 1

Journals



chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 4044 9% 0% 9
2 AMERICAN JOURNAL OF MEDICAL GENETICS 3428 10% 0% 10
3 PADIATRIE UND PADOLOGIE 3371 1% 1% 1
4 GENES TO CELLS 2446 4% 0% 4
5 JOURNAL OF MEDICAL GENETICS 1841 6% 0% 6
6 CLINICAL GENETICS 1433 5% 0% 5
7 JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM 1298 4% 0% 4
8 HIROSHIMA JOURNAL OF MEDICAL SCIENCES 930 1% 0% 1
9 MINERVA PEDIATRICA 470 1% 0% 1
10 HUMAN MOLECULAR GENETICS 466 4% 0% 4

Author Key Words



chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass LCSH search Wikipedia search
1 AARSKOG SCOTT SYNDROME 5417932 18% 95% 19 Search AARSKOG+SCOTT+SYNDROME Search AARSKOG+SCOTT+SYNDROME
2 FGD1 3087383 11% 86% 12 Search FGD1 Search FGD1
3 FACIOGENITAL DYSPLASIA 2401300 8% 100% 8 Search FACIOGENITAL+DYSPLASIA Search FACIOGENITAL+DYSPLASIA
4 FGD1 GENE 2401300 8% 100% 8 Search FGD1+GENE Search FGD1+GENE
5 AARSKOG SYNDROME 2269972 10% 69% 11 Search AARSKOG+SYNDROME Search AARSKOG+SYNDROME
6 FRABIN 686082 4% 57% 4 Search FRABIN Search FRABIN
7 FACIODIGITOGENITAL SYNDROME 600325 2% 100% 2 Search FACIODIGITOGENITAL+SYNDROME Search FACIODIGITOGENITAL+SYNDROME
8 AARSKOG 300163 1% 100% 1 Search AARSKOG Search AARSKOG
9 AARSKOG SCOTT 300163 1% 100% 1 Search AARSKOG+SCOTT Search AARSKOG+SCOTT
10 AARSKOG SCOTT DISEASE 300163 1% 100% 1 Search AARSKOG+SCOTT+DISEASE Search AARSKOG+SCOTT+DISEASE

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 10602 X LINKED MENTAL RETARDATION//PQBP1//XLMR
2 9778 VAV//RHOGEF//VAV1
3 38275 POP EYE//TARDY FEATHERING//PEA COMB
4 14166 PODOSOME//INVADOPODIA//CORTACTIN
5 36930 HYPEROSTOSIS FRONTALIS INTERNA//INTRATHORACIC RIB//BIFID RIBS
6 20882 TRACHEAL SYSTEM//BREATHLESS//TRACHEALESS
7 34485 COMPUTER ASSISTED DIAGNOSIS COMPUTER AIDED//CONGENITAL MALFORMATION SYNDROMES//DYSMORPHOLOGY DATABASE
8 3236 RHO GTPASES//TIAM1//RHOB
9 16185 FRONTONASAL DYSPLASIA//MACROSTOMIA//PROBOSCIS LATERALIS
10 18777 FOXC1//AXENFELD RIEGER SYNDROME//RIEGER SYNDROME

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