Class information for:
Level 1: JOUBERT SYNDROME//BARDET BIEDL SYNDROME//INTRAFLAGELLAR TRANSPORT

Basic class information

ID Publications Average number
of references
Avg. shr. active
ref. in WoS
2195 2250 48.1 85%



Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)



ID, lev.
above
Publications Label for level above
1566 6734 AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE//POLYCYSTIC KIDNEY DISEASE//ADPKD

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 JOUBERT SYNDROME Author keyword 137 74% 4% 101
2 BARDET BIEDL SYNDROME Author keyword 128 67% 5% 114
3 INTRAFLAGELLAR TRANSPORT Author keyword 120 74% 4% 90
4 PRIMARY CILIA Author keyword 110 57% 6% 131
5 CILIOPATHY Author keyword 107 68% 4% 94
6 MOLAR TOOTH SIGN Author keyword 51 83% 1% 29
7 CILIA Author keyword 46 19% 10% 216
8 PRIMARY CILIUM Author keyword 44 47% 3% 70
9 NEPHRONOPHTHISIS Author keyword 34 45% 3% 57
10 CILIOPATHIES Author keyword 31 55% 2% 39

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 JOUBERT SYNDROME 137 74% 4% 101 Search JOUBERT+SYNDROME Search JOUBERT+SYNDROME
2 BARDET BIEDL SYNDROME 128 67% 5% 114 Search BARDET+BIEDL+SYNDROME Search BARDET+BIEDL+SYNDROME
3 INTRAFLAGELLAR TRANSPORT 120 74% 4% 90 Search INTRAFLAGELLAR+TRANSPORT Search INTRAFLAGELLAR+TRANSPORT
4 PRIMARY CILIA 110 57% 6% 131 Search PRIMARY+CILIA Search PRIMARY+CILIA
5 CILIOPATHY 107 68% 4% 94 Search CILIOPATHY Search CILIOPATHY
6 MOLAR TOOTH SIGN 51 83% 1% 29 Search MOLAR+TOOTH+SIGN Search MOLAR+TOOTH+SIGN
7 CILIA 46 19% 10% 216 Search CILIA Search CILIA
8 PRIMARY CILIUM 44 47% 3% 70 Search PRIMARY+CILIUM Search PRIMARY+CILIUM
9 NEPHRONOPHTHISIS 34 45% 3% 57 Search NEPHRONOPHTHISIS Search NEPHRONOPHTHISIS
10 CILIOPATHIES 31 55% 2% 39 Search CILIOPATHIES Search CILIOPATHIES

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 INTRAFLAGELLAR TRANSPORT 301 53% 18% 399
2 BARDET BIEDL SYNDROME 196 44% 15% 337
3 JOUBERT SYNDROME 157 50% 10% 228
4 KINESIN II 153 70% 6% 126
5 HUMAN OBESITY SYNDROME 132 85% 3% 71
6 SENSORY CILIA 106 65% 4% 100
7 CILIOGENESIS 102 46% 7% 168
8 PRIMARY CILIUM 87 30% 11% 241
9 INTRAFLAGELLAR TRANSPORT PROTEIN 71 77% 2% 49
10 CILIOPATHIES 68 57% 4% 81

Journals

Reviews



Title Publ. year Cit. Active references % act. ref.
to same field
Mechanisms of Disease: Ciliopathies 2011 278 77 73%
Ciliogenesis: building the cell's antenna 2011 217 143 83%
The primary cilium: a signalling centre during vertebrate development 2010 473 156 53%
The Vertebrate Primary Cilium in Development, Homeostasis, and Disease 2009 280 107 64%
The Primary Cilium as a Complex Signaling Center 2009 202 102 68%
Primary Cilia in the Developing and Mature Brain 2014 16 93 69%
INTRAFLAGELLAR TRANSPORT (IFT): ROLE IN CILIARY ASSEMBLY, RESORPTION AND SIGNALLING 2008 232 180 78%
Primary cilia in neurodevelopmental disorders 2014 15 115 65%
joubert syndrome: congenital cerebellar ataxia with the molar tooth 2013 28 105 90%
Intraflagellar transport 2002 744 70 51%

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 HUMAN DIS MODELING 15 32% 1.8% 40
2 SECT OPHTHALMOL NEUROSCI 8 27% 1.1% 24
3 GENET MED EA3949 6 100% 0.2% 4
4 REFERENCE AFFECT RA GENET OPHTALMOL CARGO 5 50% 0.3% 7
5 SERV CYTOGENET GENET MOL BIOL REPROD 4 67% 0.2% 4
6 U983 4 25% 0.6% 14
7 U574 4 19% 0.8% 18
8 TRYPANOSOME CELL BIOL UNIT 3 31% 0.4% 9
9 REFERENCE AFFECT GENET OPHTALMOL 3 100% 0.1% 3
10 EA 3949 3 60% 0.1% 3

Related classes at same level (level 1)



Rank Relatedness score Related classes
1 0.0000184498 ALSTROM SYNDROME//ALMS1//TUBBY
2 0.0000169168 ELLIS VAN CREVELD SYNDROME//SHORT RIB POLYDACTYLY SYNDROME//JEUNE SYNDROME
3 0.0000135605 RPGR//X LINKED RETINITIS PIGMENTOSA//RP2
4 0.0000115316 LEFT RIGHT ASYMMETRY//LEFT RIGHT PATTERNING//NODAL FLOW
5 0.0000096561 AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE//ADPKD//POLYCYSTIC KIDNEY DISEASE
6 0.0000086586 CENTROSOME//CENTRIOLE//CENTRIN
7 0.0000084833 RHOMBENCEPHALOSYNAPSIS//PONTOCEREBELLAR HYPOPLASIA//GOMEZ LOPEZ HERNANDEZ SYNDROME
8 0.0000081302 UROMODULIN//TAMM HORSFALL PROTEIN//FAMILIAL JUVENILE HYPERURICEMIC NEPHROPATHY
9 0.0000076365 AXONEME//DYNEIN//MICROTUBULE SLIDING
10 0.0000072719 NIMA//NEK6//NEK2