Class information for:
Level 1: RETINITIS PIGMENTOSA//RPGR//AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
4434 1786 36.2 79%


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
360 3       RETINA//OPHTHALMOLOGY//PHOTORECEPTOR 34628
266 2             RETINITIS PIGMENTOSA//OPHTHALMOLOGY//RETINA 19390
4434 1                   RETINITIS PIGMENTOSA//RPGR//AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA 1786

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 RETINITIS PIGMENTOSA authKW 1741505 21% 27% 375
2 RPGR authKW 422849 2% 85% 29
3 AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA authKW 266895 1% 71% 22
4 X LINKED RETINITIS PIGMENTOSA authKW 221545 1% 72% 18
5 PRPF31 authKW 206363 1% 93% 13
6 RHODOPSIN GENE authKW 197094 1% 82% 14
7 BERMAN GUND STUDY RETINAL DEGENERAT address 175932 2% 29% 35
8 RP2 authKW 149697 1% 52% 17
9 RHODOPSIN authKW 122378 5% 8% 85
10 TAPETORETINAL DYSTROPHY authKW 104707 0% 88% 7

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 Ophthalmology 82810 58% 0% 1029
2 Genetics & Heredity 9359 31% 0% 546
3 Biochemistry & Molecular Biology 535 18% 0% 328
4 Medicine, Research & Experimental 227 5% 0% 96
5 Cell Biology 19 4% 0% 70
6 Neurosciences 17 5% 0% 83
7 Biotechnology & Applied Microbiology 13 3% 0% 49
8 Biology 5 1% 0% 22
9 Psychology, Biological 0 0% 0% 3
10 Medicine, General & Internal -0 2% 0% 32

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 BERMAN GUND STUDY RETINAL DEGENERAT 175932 2% 29% 35
2 BERMAN GUND 76147 0% 64% 7
3 UNIDAD RETINA 68381 0% 100% 4
4 OCULAR MOL GENET 64085 1% 25% 15
5 OPHTHALMOL 56835 33% 1% 591
6 UNIDAD CLIN GENET REPROD 52090 0% 38% 8
7 EIE EYE 48750 3% 6% 50
8 NEUROBIOL NEURODEGENERAT REPAIR 42198 1% 15% 17
9 STUDY RETINAL DEGENERAT 38463 0% 75% 3
10 MCGILL OCULAR GENET 36722 1% 18% 12

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 INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 53141 14% 1% 245
2 OPHTHALMIC GENETICS 33038 2% 6% 34
3 MOLECULAR VISION 31567 4% 2% 78
4 HUMAN MOLECULAR GENETICS 12874 5% 1% 86
5 OPHTHALMIC PAEDIATRICS AND GENETICS 8791 1% 4% 14
6 AMERICAN JOURNAL OF HUMAN GENETICS 7330 3% 1% 59
7 DOCUMENTA OPHTHALMOLOGICA 5947 2% 1% 28
8 ARCHIVES OF OPHTHALMOLOGY 5295 3% 1% 51
9 HUMAN MUTATION 5223 2% 1% 35
10 JOURNAL OF MEDICAL GENETICS 4906 2% 1% 41

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 RETINITIS PIGMENTOSA 1741505 21% 27% 375 Search RETINITIS+PIGMENTOSA Search RETINITIS+PIGMENTOSA
2 RPGR 422849 2% 85% 29 Search RPGR Search RPGR
3 AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA 266895 1% 71% 22 Search AUTOSOMAL+DOMINANT+RETINITIS+PIGMENTOSA Search AUTOSOMAL+DOMINANT+RETINITIS+PIGMENTOSA
4 X LINKED RETINITIS PIGMENTOSA 221545 1% 72% 18 Search X+LINKED+RETINITIS+PIGMENTOSA Search X+LINKED+RETINITIS+PIGMENTOSA
5 PRPF31 206363 1% 93% 13 Search PRPF31 Search PRPF31
6 RHODOPSIN GENE 197094 1% 82% 14 Search RHODOPSIN+GENE Search RHODOPSIN+GENE
7 RP2 149697 1% 52% 17 Search RP2 Search RP2
8 RHODOPSIN 122378 5% 8% 85 Search RHODOPSIN Search RHODOPSIN
9 TAPETORETINAL DYSTROPHY 104707 0% 88% 7 Search TAPETORETINAL+DYSTROPHY Search TAPETORETINAL+DYSTROPHY
10 RHODOPSIN MUTATION 103417 1% 55% 11 Search RHODOPSIN+MUTATION Search RHODOPSIN+MUTATION

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 TEE, JJL , SMITH, AJ , HARDCASTLE, AJ , MICHAELIDES, M , (2016) RPGR-ASSOCIATED RETINOPATHY: CLINICAL FEATURES, MOLECULAR GENETICS, ANIMAL MODELS AND THERAPEUTIC OPTIONS.BRITISH JOURNAL OF OPHTHALMOLOGY. VOL. 100. ISSUE 8. P. 1022 -1027 64 73% 1
2 KABIR, F , ULLAH, I , ALI, S , GOTTSCH, ADH , NAEEM, MA , ASSIR, MZ , KHAN, SN , AKRAM, J , RIAZUDDIN, S , AYYAGARI, R , ET AL (2016) LOSS OF FUNCTION MUTATIONS IN RP1 ARE RESPONSIBLE FOR RETINITIS PIGMENTOSA IN CONSANGUINEOUS FAMILIAL CASES.MOLECULAR VISION. VOL. 22. ISSUE . P. 610 -625 72 68% 0
3 BELTRAN, WA , CIDECIYAN, AV , LEWIN, AS , HAUSWIRTH, WW , JACOBSON, SG , AGUIRRE, GD , (2015) GENE AUGMENTATION FOR X-LINKED RETINITIS PIGMENTOSA CAUSED BY MUTATIONS IN RPGR.COLD SPRING HARBOR PERSPECTIVES IN MEDICINE. VOL. 5. ISSUE 2. P. - 64 76% 0
4 DAIGER, SP , BOWNE, SJ , SULLIVAN, LS , (2015) GENES AND MUTATIONS CAUSING AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA.COLD SPRING HARBOR PERSPECTIVES IN MEDICINE. VOL. 5. ISSUE 10. P. - 47 80% 6
5 LYRAKI, R , MEGAW, R , HURD, T , (2016) DISEASE MECHANISMS OF X-LINKED RETINITIS PIGMENTOSA DUE TO RP2 AND RPGR MUTATIONS.BIOCHEMICAL SOCIETY TRANSACTIONS. VOL. 44. ISSUE . P. 1235 -1244 62 65% 0
6 GAL, A , APFELSTEDTSYLLA, E , JANECKE, AR , ZRENNER, E , (1997) RHODOPSIN MUTATIONS IN INHERITED RETINAL DYSTROPHIES AND DYSFUNCTIONS.PROGRESS IN RETINAL AND EYE RESEARCH. VOL. 16. ISSUE 1. P. 51-79 75 80% 81
7 XU, Y , GUAN, LP , SHEN, T , ZHANG, JG , XIAO, XS , JIANG, H , LI, SQ , YANG, JH , JIA, XY , YIN, Y , ET AL (2014) MUTATIONS OF 60 KNOWN CAUSATIVE GENES IN 157 FAMILIES WITH RETINITIS PIGMENTOSA BASED ON EXOME SEQUENCING.HUMAN GENETICS. VOL. 133. ISSUE 10. P. 1255 -1271 48 63% 26
8 SHU, XH , BLACK, GC , RICE, JM , HART-HOLDEN, N , JONES, A , O'GRADY, A , RAMSDEN, S , WRIGHT, AE , (2007) RPGR MUTATION ANALYSIS AND DISEASE: AN UPDATE.HUMAN MUTATION. VOL. 28. ISSUE 4. P. 322 -328 46 87% 46
9 PELLETIER, V , JAMBOU, M , DELPHIN, N , ZINOVIEVA, E , STUM, M , GIGAREL, N , DOLLFUS, H , HAMEL, C , TOUTAIN, A , DUFIER, JL , ET AL (2007) COMPREHENSIVE SURVEY OF MUTATIONS IN RP2 AND RPGR IN PATIENTS AFFECTED WITH DISTINCT RETINAL DYSTROPHIES: GENOTYPE-PHENOTYPE CORRELATIONS AND IMPACT ON GENETIC COUNSELING.HUMAN MUTATION. VOL. 28. ISSUE 1. P. 81 -91 43 91% 47
10 CHURCHILL, JD , BOWNE, SJ , SULLIVAN, LS , LEWIS, RA , WHEATON, DK , BIRCH, DG , BRANHAM, KE , HECKENLIVELY, JR , DAIGER, SP , (2013) MUTATIONS IN THE X-LINKED RETINITIS PIGMENTOSA GENES RPGR AND RP2 FOUND IN 8.5% OF FAMILIES WITH A PROVISIONAL DIAGNOSIS OF AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA.INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. VOL. 54. ISSUE 2. P. 1411-1416 32 94% 36

Classes with closest relation at Level 1


Rank Class id link
1 9747 LEBER CONGENITAL AMAUROSIS//RPE65//LEBERS CONGENITAL AMAUROSIS
2 16231 CELL DEV DIS//RETINAL DEGENERATION//N METHYL N NITROSOUREA
3 37544 PIGMENTED PARAVENOUS RETINOCHOROIDAL ATROPHY//HELICOID PERIPAPILLARY CHORIORETINAL DEGENERATION//PARAVENOUS
4 21767 PROGRESSIVE RETINAL ATROPHY//PROGRESSIVE ROD CONE DEGENERATION//GENERALISED PROGRESSIVE RETINAL ATROPHY
5 11222 INTERPHOTORECEPTOR MATRIX//PERIPHERIN RDS//OUTER SEGMENT
6 10743 ELECTRORETINOGRAM//OSCILLATORY POTENTIALS//CONGENITAL STATIONARY NIGHT BLINDNESS
7 30188 TUBBY//TULP1//ORF PHAGE DISPLAY
8 10225 USHER SYNDROME//USH2A//MYO7A
9 8532 STARGARDT DISEASE//ABCA4//FUNDUS AUTOFLUORESCENCE
10 25093 CHOROIDEREMIA//POU3F4//CHM GENE

Go to start page