Class information for:
Level 1: LOWE SYNDROME//OCULOCEREBRORENAL SYNDROME//OCRL1

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
25041 244 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
625 13166 PTEN//MTOR//LHERMITTE DUCLOS DISEASE

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 LOWE SYNDROME Author keyword 44 67% 16% 39
2 OCULOCEREBRORENAL SYNDROME Author keyword 31 92% 5% 12
3 OCRL1 Author keyword 21 85% 5% 11
4 OCRL1 GENE Author keyword 18 89% 3% 8
5 OCULOCEREBRORENAL SYNDROME OF LOWE Author keyword 18 89% 3% 8
6 APPL1 Author keyword 10 48% 6% 15
7 OCRL Author keyword 9 64% 4% 9
8 PHOSPHATIDYLINOSITOL 4 5 BISPHOSPHATE 5 PHOSPHATASE Author keyword 6 80% 2% 4
9 APPL2 Author keyword 6 100% 2% 4
10 DENT DISEASE 2 Author keyword 3 100% 1% 3

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 LOWE SYNDROME 44 67% 16% 39 Search LOWE+SYNDROME Search LOWE+SYNDROME
2 OCULOCEREBRORENAL SYNDROME 31 92% 5% 12 Search OCULOCEREBRORENAL+SYNDROME Search OCULOCEREBRORENAL+SYNDROME
3 OCRL1 21 85% 5% 11 Search OCRL1 Search OCRL1
4 OCRL1 GENE 18 89% 3% 8 Search OCRL1+GENE Search OCRL1+GENE
5 OCULOCEREBRORENAL SYNDROME OF LOWE 18 89% 3% 8 Search OCULOCEREBRORENAL+SYNDROME+OF+LOWE Search OCULOCEREBRORENAL+SYNDROME+OF+LOWE
6 APPL1 10 48% 6% 15 Search APPL1 Search APPL1
7 OCRL 9 64% 4% 9 Search OCRL Search OCRL
8 PHOSPHATIDYLINOSITOL 4 5 BISPHOSPHATE 5 PHOSPHATASE 6 80% 2% 4 Search PHOSPHATIDYLINOSITOL+4+5+BISPHOSPHATE+5+PHOSPHATASE Search PHOSPHATIDYLINOSITOL+4+5+BISPHOSPHATE+5+PHOSPHATASE
9 APPL2 6 100% 2% 4 Search APPL2 Search APPL2
10 DENT DISEASE 2 3 100% 1% 3 Search DENT+DISEASE+2 Search DENT+DISEASE+2

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 OCULOCEREBRORENAL SYNDROME 100 77% 28% 69
2 SYNDROME PROTEIN OCRL1 22 53% 12% 29
3 BAR PH 12 86% 2% 6
4 LOWE SYNDROME 11 31% 11% 28
5 XQ24 Q26 10 73% 3% 8
6 DENT DISEASE 10 61% 5% 11
7 PROTEIN APPL1 9 83% 2% 5
8 OCRL1 GENE 9 67% 3% 8
9 INOSITOL POLYPHOSPHATE 5 PHOSPHATASE 7 20% 13% 32
10 OCRL1 6 47% 4% 9

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
The Cellular and Physiological Functions of the Lowe Syndrome Protein OCRL1 2014 10 100 46%
Lowe syndrome 2006 41 18 89%
Inositol 5-phosphatases: insights from the Lowe syndrome protein OCRL 2012 29 79 37%
Lowe Syndrome: Report of a Case and Brief Literature Review 2009 0 8 88%
Structure and function of the Lowe syndrome protein OCRL1 2005 89 65 23%
Inositol polyphosphate 5-phosphatases; new players in the regulation of cilia and ciliopathies 2012 14 140 26%
Inherited cerebrorenal syndromes 2009 16 60 32%
Endosomal crosstalk: meeting points for signaling pathways 2012 20 80 4%
Endocytosis and spatial restriction of cell signaling 2009 20 106 3%

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 CNRSUNITE MIXTE RECH 144 1 50% 0.4% 1
2 NEUROBIOLKAVLI NEUROSCI 1 50% 0.4% 1
3 REFERENCE MALAD RENALES 1 50% 0.4% 1
4 SERV NEPHROL PEDIAT MED INTERNE 1 50% 0.4% 1
5 UMR U765 1 50% 0.4% 1
6 OTTO HEUBNER CENTRUM KINDER JUGENDMED 0 20% 0.8% 2
7 COCHIN GENET DEV PATHOL MOL 0 33% 0.4% 1
8 EA 2019 UJF 0 33% 0.4% 1
9 HOWARD HUGHES MED PROGRAM CELLULAR NEUROSCI 0 33% 0.4% 1
10 IQUIFIB FARM BIOQUIM 0 33% 0.4% 1

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000251886 SHIP2//INOSITOL 5 PHOSPHATASE//SHIP1
2 0.0000201825 DENTS DISEASE//CLCN5//MYOTONIA CONGENITA
3 0.0000186225 PIKFYVE//PTDINS5P//GOLPH3
4 0.0000088093 FANCONI BICKEL SYNDROME//GLYCOGEN STORAGE DISEASE TYPE XI//GLUT2 GENE
5 0.0000086471 ENPP1//PLASMA CELL MEMBRANE GLYCOPROTEIN 1//PC 1
6 0.0000062948 CUBILIN//AMNIONLESS//MEGALIN
7 0.0000062131 RAB25//RAB//RAB PROTEINS
8 0.0000057051 MARINESCO SJOGREN SYNDROME//MICRO SYNDROME//WARBURG MICRO SYNDROME
9 0.0000051735 TRIBBLES//TRB3//TRIB3
10 0.0000049933 DYNAMIN//F BAR DOMAIN//AMPHIPHYSIN