Class information for:
Level 1: MARFAN SYNDROME//FIBRILLIN//FBN1

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
2605 2122 32.4 74%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
1680 6226 MARFAN SYNDROME//FIBRILLIN//LYSYL OXIDASE

Terms with highest relevance score


Rank Term Type of term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 MARFAN SYNDROME Author keyword 517 62% 25% 537
2 FIBRILLIN Author keyword 160 62% 8% 164
3 FBN1 Author keyword 138 83% 4% 78
4 LOEYS DIETZ SYNDROME Author keyword 129 83% 3% 73
5 FIBRILLIN 1 Author keyword 117 66% 5% 109
6 CONGENITAL CONTRACTURAL ARACHNODACTYLY Author keyword 50 88% 1% 23
7 FBN1 GENE Author keyword 45 90% 1% 19
8 MARFAN GRP Address 44 100% 1% 16
9 REFERENCE SYNDROME MARFAN PARENTES Address 41 87% 1% 20
10 CENT BIOCHIM HORMONOL GENET MOL Address 34 93% 1% 13

Web of Science journal categories

Author Key Words


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class		 LCSH search Wikipedia search
1 MARFAN SYNDROME 517 62% 25% 537 Search MARFAN+SYNDROME Search MARFAN+SYNDROME
2 FIBRILLIN 160 62% 8% 164 Search FIBRILLIN Search FIBRILLIN
3 FBN1 138 83% 4% 78 Search FBN1 Search FBN1
4 LOEYS DIETZ SYNDROME 129 83% 3% 73 Search LOEYS+DIETZ+SYNDROME Search LOEYS+DIETZ+SYNDROME
5 FIBRILLIN 1 117 66% 5% 109 Search FIBRILLIN+1 Search FIBRILLIN+1
6 CONGENITAL CONTRACTURAL ARACHNODACTYLY 50 88% 1% 23 Search CONGENITAL+CONTRACTURAL+ARACHNODACTYLY Search CONGENITAL+CONTRACTURAL+ARACHNODACTYLY
7 FBN1 GENE 45 90% 1% 19 Search FBN1+GENE Search FBN1+GENE
8 NEONATAL MARFAN SYNDROME 29 88% 1% 14 Search NEONATAL+MARFAN+SYNDROME Search NEONATAL+MARFAN+SYNDROME
9 MARFANS SYNDROME 27 39% 3% 54 Search MARFANS+SYNDROME Search MARFANS+SYNDROME
10 ECTOPIA LENTIS 26 54% 2% 34 Search ECTOPIA+LENTIS Search ECTOPIA+LENTIS

Key Words Plus


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 MARFAN SYNDROME 208 31% 27% 567
2 FBN1 MUTATIONS 155 89% 3% 71
3 EXTRACELLULAR MICROFIBRILS 146 80% 4% 90
4 RICH MICROFIBRILS 103 97% 1% 30
5 FBN1 99 80% 3% 61
6 FIBRILLIN 88 49% 6% 129
7 ELASTIN ASSOCIATED MICROFIBRILS 82 77% 3% 56
8 FBN1 GENE 61 88% 1% 29
9 FIBRILLINOPATHIES 60 100% 1% 20
10 FIBRILLIN GENE 56 75% 2% 41

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Cardiovascular manifestations in Marfan syndrome and related diseases; multiple genes causing similar phenotypes 2015 2 79 81%
Elastic fibres 2002 370 107 54%
Biogenesis and function of fibrillin assemblies 2010 62 102 78%
Marfan's syndrome 2005 331 94 66%
Role of Mechanotransduction in Vascular Biology Focus on Thoracic Aortic Aneurysms and Dissections 2015 5 160 26%
The molecular genetics of Marfan syndrome and related disorders 2006 150 228 76%
Heritable thoracic aortic disorders 2014 9 38 53%
The Marfan syndrome 2000 184 104 72%
MUTATIONS IN THE HUMAN GENE FOR FIBRILLIN-1 (FBN1) IN THE MARFAN-SYNDROME AND RELATED DISORDERS 1995 285 71 85%
Dissecting the Fibrillin Microfibril: Structural Insights into Organization and Function 2012 17 93 85%

Address terms


Rank Address term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 MARFAN GRP 44 100% 0.8% 16
2 REFERENCE SYNDROME MARFAN PARENTES 41 87% 0.9% 20
3 CENT BIOCHIM HORMONOL GENET MOL 34 93% 0.6% 13
4 REFERENCE SYNDROMES MARFAN PARENTES 17 100% 0.4% 8
5 MUNROE HUMAN GENET 9 83% 0.2% 5
6 SECT FUNCT STRUCTSAWARA KU 8 100% 0.2% 5
7 TRS OURCE RARE DISORDERS 6 53% 0.4% 8
8 BIOCHIM HORMONOL GENET MOL 4 47% 0.3% 7
9 U827 3 18% 0.8% 17
10 SONALEE MARFAN SYNDROME RELATED DISORDERS 3 100% 0.1% 3

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000144119 BICUSPID AORTIC VALVE//AORTIC VALVE REPAIR//AORTIC ROOT
2 0.0000138774 LTBP//ALPHA V BETA 6//INTEGRIN ALPHAVBETA6
3 0.0000137050 FIBULIN 1//EFEMP1//FIBULIN 3
4 0.0000106955 MYHRE SYNDROME//MICROSPHEROPHAKIA//GELEOPHYSIC DYSPLASIA
5 0.0000068431 EHLERS DANLOS SYNDROME//EHLERS DANLOS SYNDROME TYPE IV//JOINT HYPERMOBILITY
6 0.0000059909 ISODESMOSINE//ELASTIN LAMININ RECEPTOR//DESMOSINE
7 0.0000059317 CIAPIN1//NOB1//MG7 AG
8 0.0000055631 CUTIS LAXA//MID DERMAL ELASTOLYSIS//ANNULAR ELASTOLYTIC GIANT CELL GRANULOMA
9 0.0000051441 BETHLEM MYOPATHY//COLLAGEN VI//TYPE VI COLLAGEN
10 0.0000050824 NEUHAUSER SYNDROME//MEGALOCORNEA//ANTERIOR MEGALOPHTHALMOS