RP1 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "RP1" in English language version.

refsWebsite

Global rank English rank

12nih.gov

4^th place

6doi.org

2^nd place

2ensembl.org

1,626^th place

1,007^th place

2web.archive.org

1^st place

1unibas.ch

low place

1semanticscholar.org

11^th place

8^th place

doi.org

Blanton SH, Heckenlively JR, Cottingham AW, Friedman J, Sadler LA, Wagner M, et al. (Mar 1992). "Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8". Genomics. 11 (4): 857–69. doi:10.1016/0888-7543(91)90008-3. PMID 1783394.
Georgiou M, Grewal PS, Narayan A, Alser M, Ali N, Fujinami K, et al. (August 2020). "Sector Retinitis Pigmentosa: Extending the Molecular Genetics Basis and Elucidating the Natural History". American Journal of Ophthalmology. 221: 299–310. doi:10.1016/j.ajo.2020.08.004. PMC 7772805. PMID 32795431.
Ueno S, Koyanagi Y, Kominami T, Ito Y, Kawano K, Nishiguchi KM, et al. (September 2020). "Clinical characteristics and high resolution retinal imaging of retinitis pigmentosa caused by RP1 gene variants" (PDF). Japanese Journal of Ophthalmology. 64 (5): 485–496. doi:10.1007/s10384-020-00752-1. PMID 32627106. S2CID 220351273. Archived (PDF) from the original on 2022-05-19. Retrieved 2022-06-11.
Daiger SP, Sullivan LS, Bowne SJ, Kennan A, Humphries P, Birch DG, et al. (2003). "Identification of the RP1 and RP10 (IMPDH1) Genes Causing Autosomal Dominant RP". Retinal Degenerations. Advances in Experimental Medicine and Biology. Vol. 533. pp. 1–11. doi:10.1007/978-1-4615-0067-4_1. ISBN 978-1-4613-4909-9. PMC 2583078. PMID 15180241.
Daiger SP, Shankar SP, Schindler AB, Sullivan LS, Bowne SJ, King TM, et al. (2006). "Genetic factors modifying clinical expression of autosomal dominant RP". Retinal Degenerative Diseases. Advances in Experimental Medicine and Biology. Vol. 572. pp. 3–8. doi:10.1007/0-387-32442-9_1. ISBN 978-0-387-28464-4. PMC 2581449. PMID 17249547.
Wang DY, Chan WM, Tam PO, Baum L, Lam DS, Chong KK, et al. (January 2005). "Gene mutations in retinitis pigmentosa and their clinical implications". Clinica Chimica Acta; International Journal of Clinical Chemistry. 351 (1–2): 5–16. doi:10.1016/j.cccn.2004.08.004. PMID 15563868.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000104237 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000025900 – Ensembl, May 2017

nih.gov

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"RP1 axonemal microtubule associated". Archived from the original on 2021-01-17. Retrieved 2020-09-25.
Georgiou M, Grewal PS, Narayan A, Alser M, Ali N, Fujinami K, et al. (August 2020). "Sector Retinitis Pigmentosa: Extending the Molecular Genetics Basis and Elucidating the Natural History". American Journal of Ophthalmology. 221: 299–310. doi:10.1016/j.ajo.2020.08.004. PMC 7772805. PMID 32795431.
Daiger SP, Sullivan LS, Bowne SJ, Kennan A, Humphries P, Birch DG, et al. (2003). "Identification of the RP1 and RP10 (IMPDH1) Genes Causing Autosomal Dominant RP". Retinal Degenerations. Advances in Experimental Medicine and Biology. Vol. 533. pp. 1–11. doi:10.1007/978-1-4615-0067-4_1. ISBN 978-1-4613-4909-9. PMC 2583078. PMID 15180241.
Daiger SP, Shankar SP, Schindler AB, Sullivan LS, Bowne SJ, King TM, et al. (2006). "Genetic factors modifying clinical expression of autosomal dominant RP". Retinal Degenerative Diseases. Advances in Experimental Medicine and Biology. Vol. 572. pp. 3–8. doi:10.1007/0-387-32442-9_1. ISBN 978-0-387-28464-4. PMC 2581449. PMID 17249547.

pubmed.ncbi.nlm.nih.gov

Blanton SH, Heckenlively JR, Cottingham AW, Friedman J, Sadler LA, Wagner M, et al. (Mar 1992). "Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8". Genomics. 11 (4): 857–69. doi:10.1016/0888-7543(91)90008-3. PMID 1783394.
Georgiou M, Grewal PS, Narayan A, Alser M, Ali N, Fujinami K, et al. (August 2020). "Sector Retinitis Pigmentosa: Extending the Molecular Genetics Basis and Elucidating the Natural History". American Journal of Ophthalmology. 221: 299–310. doi:10.1016/j.ajo.2020.08.004. PMC 7772805. PMID 32795431.
Ueno S, Koyanagi Y, Kominami T, Ito Y, Kawano K, Nishiguchi KM, et al. (September 2020). "Clinical characteristics and high resolution retinal imaging of retinitis pigmentosa caused by RP1 gene variants" (PDF). Japanese Journal of Ophthalmology. 64 (5): 485–496. doi:10.1007/s10384-020-00752-1. PMID 32627106. S2CID 220351273. Archived (PDF) from the original on 2022-05-19. Retrieved 2022-06-11.
Daiger SP, Sullivan LS, Bowne SJ, Kennan A, Humphries P, Birch DG, et al. (2003). "Identification of the RP1 and RP10 (IMPDH1) Genes Causing Autosomal Dominant RP". Retinal Degenerations. Advances in Experimental Medicine and Biology. Vol. 533. pp. 1–11. doi:10.1007/978-1-4615-0067-4_1. ISBN 978-1-4613-4909-9. PMC 2583078. PMID 15180241.
Daiger SP, Shankar SP, Schindler AB, Sullivan LS, Bowne SJ, King TM, et al. (2006). "Genetic factors modifying clinical expression of autosomal dominant RP". Retinal Degenerative Diseases. Advances in Experimental Medicine and Biology. Vol. 572. pp. 3–8. doi:10.1007/0-387-32442-9_1. ISBN 978-0-387-28464-4. PMC 2581449. PMID 17249547.
Wang DY, Chan WM, Tam PO, Baum L, Lam DS, Chong KK, et al. (January 2005). "Gene mutations in retinitis pigmentosa and their clinical implications". Clinica Chimica Acta; International Journal of Clinical Chemistry. 351 (1–2): 5–16. doi:10.1016/j.cccn.2004.08.004. PMID 15563868.

semanticscholar.org

api.semanticscholar.org

Ueno S, Koyanagi Y, Kominami T, Ito Y, Kawano K, Nishiguchi KM, et al. (September 2020). "Clinical characteristics and high resolution retinal imaging of retinitis pigmentosa caused by RP1 gene variants" (PDF). Japanese Journal of Ophthalmology. 64 (5): 485–496. doi:10.1007/s10384-020-00752-1. PMID 32627106. S2CID 220351273. Archived (PDF) from the original on 2022-05-19. Retrieved 2022-06-11.

unibas.ch

edoc.unibas.ch

Ueno S, Koyanagi Y, Kominami T, Ito Y, Kawano K, Nishiguchi KM, et al. (September 2020). "Clinical characteristics and high resolution retinal imaging of retinitis pigmentosa caused by RP1 gene variants" (PDF). Japanese Journal of Ophthalmology. 64 (5): 485–496. doi:10.1007/s10384-020-00752-1. PMID 32627106. S2CID 220351273. Archived (PDF) from the original on 2022-05-19. Retrieved 2022-06-11.

web.archive.org

"RP1 axonemal microtubule associated". Archived from the original on 2021-01-17. Retrieved 2020-09-25.
Ueno S, Koyanagi Y, Kominami T, Ito Y, Kawano K, Nishiguchi KM, et al. (September 2020). "Clinical characteristics and high resolution retinal imaging of retinitis pigmentosa caused by RP1 gene variants" (PDF). Japanese Journal of Ophthalmology. 64 (5): 485–496. doi:10.1007/s10384-020-00752-1. PMID 32627106. S2CID 220351273. Archived (PDF) from the original on 2022-05-19. Retrieved 2022-06-11.