"Collin RW"[Author] - Search Results

Year	Number of Results
2004	1
2005	2
2006	4
2007	4
2008	8
2009	10
2010	13
2011	9
2012	11
2013	9
2014	11
2015	12
2016	7
2017	1
2023	1
2025	0

1

Prenylation defects in inherited retinal diseases.

Roosing S, Collin RW, den Hollander AI, Cremers FP, Siemiatkowska AM. Roosing S, et al. Among authors: collin rw. J Med Genet. 2014 Mar;51(3):143-51. doi: 10.1136/jmedgenet-2013-102138. Epub 2014 Jan 8. J Med Genet. 2014. PMID: 24401286 Review.

2

Antisense Oligonucleotide Therapy for Inherited Retinal Dystrophies.

Gerard X, Garanto A, Rozet JM, Collin RW. Gerard X, et al. Among authors: collin rw. Adv Exp Med Biol. 2016;854:517-24. doi: 10.1007/978-3-319-17121-0_69. Adv Exp Med Biol. 2016. PMID: 26427454 Review.

3

Applications of antisense oligonucleotides for the treatment of inherited retinal diseases.

Collin RW, Garanto A. Collin RW, et al. Curr Opin Ophthalmol. 2017 May;28(3):260-266. doi: 10.1097/ICU.0000000000000363. Curr Opin Ophthalmol. 2017. PMID: 28151748 Review.

4

Unraveling the mysteries of pre-mRNA splicing in the retina via stem cell technology.

Collin RW. Collin RW. Stem Cell Investig. 2016 Nov 4;3:72. doi: 10.21037/sci.2016.10.05. eCollection 2016. Stem Cell Investig. 2016. PMID: 27868054 Free PMC article. No abstract available.

5

Genomic approaches for the discovery of genes mutated in inherited retinal degeneration.

Siemiatkowska AM, Collin RW, den Hollander AI, Cremers FP. Siemiatkowska AM, et al. Among authors: collin rw. Cold Spring Harb Perspect Med. 2014 Jun 17;4(8):a017137. doi: 10.1101/cshperspect.a017137. Cold Spring Harb Perspect Med. 2014. PMID: 24939053 Free PMC article. Review.

6

Next-generation genetic testing for retinitis pigmentosa.

Neveling K, Collin RW, Gilissen C, van Huet RA, Visser L, Kwint MP, Gijsen SJ, Zonneveld MN, Wieskamp N, de Ligt J, Siemiatkowska AM, Hoefsloot LH, Buckley MF, Kellner U, Branham KE, den Hollander AI, Hoischen A, Hoyng C, Klevering BJ, van den Born LI, Veltman JA, Cremers FP, Scheffer H. Neveling K, et al. Among authors: collin rw. Hum Mutat. 2012 Jun;33(6):963-72. doi: 10.1002/humu.22045. Epub 2012 Mar 19. Hum Mutat. 2012. PMID: 22334370 Free PMC article.

7

The pros and cons of vertebrate animal models for functional and therapeutic research on inherited retinal dystrophies.

Slijkerman RW, Song F, Astuti GD, Huynen MA, van Wijk E, Stieger K, Collin RW. Slijkerman RW, et al. Among authors: collin rw. Prog Retin Eye Res. 2015 Sep;48:137-59. doi: 10.1016/j.preteyeres.2015.04.004. Epub 2015 May 1. Prog Retin Eye Res. 2015. PMID: 25936606 Review.

8

CLRN1 mutations cause nonsyndromic retinitis pigmentosa.

Khan MI, Kersten FF, Azam M, Collin RW, Hussain A, Shah ST, Keunen JE, Kremer H, Cremers FP, Qamar R, den Hollander AI. Khan MI, et al. Among authors: collin rw. Ophthalmology. 2011 Jul;118(7):1444-8. doi: 10.1016/j.ophtha.2010.10.047. Epub 2011 Feb 18. Ophthalmology. 2011. PMID: 21310491

9

Gene augmentation of LCA5-associated Leber congenital amaurosis ameliorates bulge region defects of the photoreceptor ciliary axoneme.

Faber S, Mercey O, Junger K, Garanto A, May-Simera H, Ueffing M, Collin RW, Boldt K, Guichard P, Hamel V, Roepman R. Faber S, et al. Among authors: collin rw. JCI Insight. 2023 May 22;8(10):e169162. doi: 10.1172/jci.insight.169162. JCI Insight. 2023. PMID: 37071472 Free PMC article.

10

The power of homozygosity mapping: discovery of new genetic defects in patients with retinal dystrophy.

Littink KW, den Hollander AI, Cremers FP, Collin RW. Littink KW, et al. Among authors: collin rw. Adv Exp Med Biol. 2012;723:345-51. doi: 10.1007/978-1-4614-0631-0_45. Adv Exp Med Biol. 2012. PMID: 22183352 Review. No abstract available.

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