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

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
25863 270 33.8 77%


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 BIOCHEMISTRY & MOLECULAR BIOLOGY//CELL BIOLOGY//ONCOLOGY 4064930
269 3       CELL BIOLOGY//CAVEOLIN 1//CAVEOLAE 44007
447 2             TRAFFIC//ENDOCYTOSIS//CLATHRIN 16170
25863 1                   LOWE SYNDROME//OCULOCEREBRORENAL SYNDROME//OCRL1 270

Terms with highest relevance score


rank Term termType Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 LOWE SYNDROME authKW 3673852 17% 69% 47
2 OCULOCEREBRORENAL SYNDROME authKW 1590378 6% 94% 15
3 OCRL1 authKW 1163246 4% 86% 12
4 OCULOCEREBRORENAL SYNDROME OF LOWE authKW 1017843 3% 100% 9
5 APPL1 authKW 995755 7% 46% 19
6 OCRL authKW 904741 4% 67% 12
7 OCRL1 GENE authKW 804220 3% 89% 8
8 APPL2 authKW 471222 2% 83% 5
9 DENT DISEASE 2 authKW 452375 1% 100% 4
10 OCRL GENE authKW 361898 1% 80% 4

Web of Science journal categories


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 Genetics & Heredity 618 21% 0% 56
2 Cell Biology 438 22% 0% 59
3 Pediatrics 338 13% 0% 35
4 Urology & Nephrology 216 9% 0% 24
5 Biochemistry & Molecular Biology 155 23% 0% 63
6 Ophthalmology 91 6% 0% 15
7 Clinical Neurology 56 8% 0% 21
8 Medicine, Research & Experimental 44 6% 0% 16
9 Endocrinology & Metabolism 28 5% 0% 14
10 Neuroimaging 16 1% 0% 3

Address terms


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 ABT NEONATAL 113094 0% 100% 1
2 CELLULAR COMPARTMENTALIZAT DYNAM 113094 0% 100% 1
3 CELLULAR MYOL PATHOL 113094 0% 100% 1
4 COCHIN CNRS UMR 8104 GENET DEV PATHO 113094 0% 100% 1
5 CR INSERM UJF CEA CHU 113094 0% 100% 1
6 EA 2411 UJF 113094 0% 100% 1
7 EA 2943MENRTCEA 113094 0% 100% 1
8 ETUDE MALADIES HEREDITAI METAB 113094 0% 100% 1
9 GENET DEV PATHOL MOLINSERMU567UMR8104 113094 0% 100% 1
10 GLICK EYE OPHTHALMOL 113094 0% 100% 1

Journals


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 TRAFFIC 2877 3% 0% 7
2 NEPHRON PHYSIOLOGY 2537 1% 1% 2
3 WORLD JOURNAL OF PEDIATRICS 1696 1% 1% 3
4 HUMAN MOLECULAR GENETICS 1147 4% 0% 10
5 AMERICAN JOURNAL OF HUMAN GENETICS 1128 3% 0% 9
6 JOURNAL OF MENTAL DEFICIENCY RESEARCH 969 1% 0% 2
7 PEDIATRIC NEPHROLOGY 906 3% 0% 7
8 PRENSA MEDICA ARGENTINA 637 0% 1% 1
9 JOURNAL OF PEDIATRIC OPHTHALMOLOGY & STRABISMUS 606 1% 0% 3
10 MOLECULAR BIOLOGY OF THE CELL 480 2% 0% 6

Author Key Words


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class		 LCSH search Wikipedia search
1 LOWE SYNDROME 3673852 17% 69% 47 Search LOWE+SYNDROME Search LOWE+SYNDROME
2 OCULOCEREBRORENAL SYNDROME 1590378 6% 94% 15 Search OCULOCEREBRORENAL+SYNDROME Search OCULOCEREBRORENAL+SYNDROME
3 OCRL1 1163246 4% 86% 12 Search OCRL1 Search OCRL1
4 OCULOCEREBRORENAL SYNDROME OF LOWE 1017843 3% 100% 9 Search OCULOCEREBRORENAL+SYNDROME+OF+LOWE Search OCULOCEREBRORENAL+SYNDROME+OF+LOWE
5 APPL1 995755 7% 46% 19 Search APPL1 Search APPL1
6 OCRL 904741 4% 67% 12 Search OCRL Search OCRL
7 OCRL1 GENE 804220 3% 89% 8 Search OCRL1+GENE Search OCRL1+GENE
8 APPL2 471222 2% 83% 5 Search APPL2 Search APPL2
9 DENT DISEASE 2 452375 1% 100% 4 Search DENT+DISEASE+2 Search DENT+DISEASE+2
10 OCRL GENE 361898 1% 80% 4 Search OCRL+GENE Search OCRL+GENE

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.


Rank Reference # ref.
in cl.		 Shr. of ref. in
cl.		 Citations
1 BOKENKAMP, A , LUDWIG, M , (2016) THE OCULOCEREBRORENAL SYNDROME OF LOWE: AN UPDATE.PEDIATRIC NEPHROLOGY. VOL. 31. ISSUE 12. P. 2201 -2212 50 68% 1
2 HICHRI, H , RENDU, J , MONNIER, N , COUTTON, C , DORSEUIL, O , POUSSOU, RV , BAUJAT, G , BLANCHARD, A , NOBILI, F , RANCHIN, B , ET AL (2011) FROM LOWE SYNDROME TO DENT DISEASE: CORRELATIONS BETWEEN MUTATIONS OF THE OCRL1 GENE AND CLINICAL AND BIOCHEMICAL PHENOTYPES.HUMAN MUTATION. VOL. 32. ISSUE 4. P. 379 -388 39 83% 31
3 MEHTA, ZB , PIETKA, G , LOWE, M , (2014) THE CELLULAR AND PHYSIOLOGICAL FUNCTIONS OF THE LOWE SYNDROME PROTEIN OCRL1.TRAFFIC. VOL. 15. ISSUE 5. P. 471-487 46 46% 22
4 PIRRUCCELLO, M , SWAN, LE , FOLTA-STOGNIEW, E , DE CAMILLI, P , (2011) RECOGNITION OF THE F&H MOTIF BY THE LOWE SYNDROME PROTEIN OCRL.NATURE STRUCTURAL & MOLECULAR BIOLOGY. VOL. 18. ISSUE 7. P. 789 -U63 31 78% 14
5 MONTJEAN, R , AOIDI, R , DESBOIS, P , RUCCI, J , TRICHET, M , SALOMON, R , RENDU, J , FAURE, J , LUNARDI, J , GACON, G , ET AL (2015) OCRL-MUTATED FIBROBLASTS FROM PATIENTS WITH DENT-2 DISEASE EXHIBIT INPP5B-INDEPENDENT PHENOTYPIC VARIABILITY RELATIVELY TO LOWE SYNDROME CELLS.HUMAN MOLECULAR GENETICS. VOL. 24. ISSUE 4. P. 994 -1006 36 61% 1
6 ERDMANN, KS , SKOWRONEK, A , SHARMA, S , (2015) THE ROLE OF THE LOWE SYNDROME PROTEIN OCRL IN THE ENDOCYTIC PATHWAY.BIOLOGICAL CHEMISTRY. VOL. 396. ISSUE 12. P. 1293 -1300 32 62% 1
7 ALIA, A , BARABAN, SC , HURLSTONE, AFL , LOWE, M , RAMIREZ, IBR , PIETKA, G , JONES, DR , DIVECHA, N , (2012) IMPAIRED NEURAL DEVELOPMENT IN A ZEBRAFISH MODEL FOR LOWE SYNDROME.HUMAN MOLECULAR GENETICS. VOL. 21. ISSUE 8. P. 1744 -1759 30 63% 17
8 TIAN, X , ZOU, H , XING, J , CHE, GH , TIAN, J , ZHANG, YF , (2016) A NOVEL OCRL1 MUTATION IN A CHINESE CHILD WITH LOWE SYNDROME.INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE. VOL. 9. ISSUE 8. P. 16907 -16912 21 88% 0
9 OLTRABELLA, F , PIETKA, G , RAMIREZ, IBR , MIRONOV, A , STARBORG, T , DRUMMOND, IA , HINCHLIFFE, KA , LOWE, M , (2015) THE LOWE SYNDROME PROTEIN OCRL1 IS REQUIRED FOR ENDOCYTOSIS IN THE ZEBRAFISH PRONEPHRIC TUBULE.PLOS GENETICS. VOL. 11. ISSUE 4. P. - 29 54% 9
10 BOTHWELL, SP , CHAN, E , BERNARDINI, IM , KUO, YM , GAHL, WA , NUSSBAUM, RL , (2011) MOUSE MODEL FOR LOWE SYNDROME/DENT DISEASE 2 RENAL TUBULOPATHY.JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY. VOL. 22. ISSUE 3. P. 443 -448 26 70% 15

Classes with closest relation at Level 1


Rank Class id link
1 11107 DENTS DISEASE//CLCN5//CHLORIDE CHANNEL
2 14683 SHIP2//SHIP1//DOK
3 7540 PHOSPHOINOSITIDE//PIKFYVE//SECT MOL SIGNAL TRANSDUCT
4 31620 FANCONI BICKEL SYNDROME//GLYCOGEN STORAGE DISEASE TYPE XI//FANCONI BICKEL
5 24510 ENPP1//PC 1//PLASMA CELL MEMBRANE GLYCOPROTEIN 1
6 35936 DYGGVE MELCHIOR CLAUSEN SYNDROME//DYMECLIN//AXIAL OSTEOMALACIA
7 30096 MARINESCO SJOGREN SYNDROME//SIL1//WARBURG MICRO SYNDROME
8 2031 RAB//RAB PROTEINS//RAB27A
9 18529 MACROPINOCYTOSIS//PHAGOSOME//RECYCLING FROM PHAGOSOMES
10 437 ADIPONECTIN//ADIPONECTIN RECEPTOR//ADIPOQ

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