Koenekoop RK - Search Results

1

Genotype and Phenotype Studies in Autosomal Dominant Retinitis Pigmentosa (adRP) of the French Canadian Founder Population.

Coussa RG, Chakarova C, Ajlan R, Taha M, Kavalec C, Gomolin J, Khan A, Lopez I, Ren H, Waseem N, Kamenarova K, Bhattacharya SS, Koenekoop RK. Coussa RG, et al. Among authors: koenekoop rk. Invest Ophthalmol Vis Sci. 2015 Dec;56(13):8297-305. doi: 10.1167/iovs.15-17104. Invest Ophthalmol Vis Sci. 2015. PMID: 26720483 Free PMC article.

2

The management of age-related macular degeneration: patterns of referral and compliance in seeking low-vision aids.

Koenekoop RK, Gomolin JE. Koenekoop RK, et al. Can J Ophthalmol. 1995 Jun;30(4):208-10. Can J Ophthalmol. 1995. PMID: 7585314 No abstract available.

3

Presumed photic retinopathy after cataract surgery: an angiographic study.

Gomolin JE, Koenekoop RK. Gomolin JE, et al. Among authors: koenekoop rk. Can J Ophthalmol. 1993 Aug;28(5):221-4. Can J Ophthalmol. 1993. PMID: 8221370 Clinical Trial.

4

Prevalence of AIPL1 mutations in inherited retinal degenerative disease.

Sohocki MM, Perrault I, Leroy BP, Payne AM, Dharmaraj S, Bhattacharya SS, Kaplan J, Maumenee IH, Koenekoop R, Meire FM, Birch DG, Heckenlively JR, Daiger SP. Sohocki MM, et al. Mol Genet Metab. 2000 Jun;70(2):142-50. doi: 10.1006/mgme.2000.3001. Mol Genet Metab. 2000. PMID: 10873396

5

Novel RPGR mutations with distinct retinitis pigmentosa phenotypes in French-Canadian families.

Koenekoop RK, Loyer M, Hand CK, Al Mahdi H, Dembinska O, Beneish R, Racine J, Rouleau GA. Koenekoop RK, et al. Am J Ophthalmol. 2003 Oct;136(4):678-87. doi: 10.1016/s0002-9394(03)00331-3. Am J Ophthalmol. 2003. PMID: 14516808

6

The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations.

Dharmaraj S, Leroy BP, Sohocki MM, Koenekoop RK, Perrault I, Anwar K, Khaliq S, Devi RS, Birch DG, De Pool E, Izquierdo N, Van Maldergem L, Ismail M, Payne AM, Holder GE, Bhattacharya SS, Bird AC, Kaplan J, Maumenee IH. Dharmaraj S, et al. Among authors: koenekoop rk. Arch Ophthalmol. 2004 Jul;122(7):1029-37. doi: 10.1001/archopht.122.7.1029. Arch Ophthalmol. 2004. PMID: 15249368

7

Genotyping microarray (disease chip) for Leber congenital amaurosis: detection of modifier alleles.

Zernant J, Külm M, Dharmaraj S, den Hollander AI, Perrault I, Preising MN, Lorenz B, Kaplan J, Cremers FP, Maumenee I, Koenekoop RK, Allikmets R. Zernant J, et al. Among authors: koenekoop rk. Invest Ophthalmol Vis Sci. 2005 Sep;46(9):3052-9. doi: 10.1167/iovs.05-0111. Invest Ophthalmol Vis Sci. 2005. PMID: 16123401

8

Sequencing arrays for screening multiple genes associated with early-onset human retinal degenerations on a high-throughput platform.

Mandal MN, Heckenlively JR, Burch T, Chen L, Vasireddy V, Koenekoop RK, Sieving PA, Ayyagari R. Mandal MN, et al. Among authors: koenekoop rk. Invest Ophthalmol Vis Sci. 2005 Sep;46(9):3355-62. doi: 10.1167/iovs.05-0007. Invest Ophthalmol Vis Sci. 2005. PMID: 16123440

9

A new locus (RP31) for autosomal dominant retinitis pigmentosa maps to chromosome 9p.

Papaioannou M, Chakarova CF, Prescott DC, Waseem N, Theis T, Lopez I, Gill B, Koenekoop RK, Bhattacharya SS. Papaioannou M, et al. Among authors: koenekoop rk. Hum Genet. 2005 Dec;118(3-4):501-3. doi: 10.1007/s00439-005-0063-3. Epub 2005 Sep 28. Hum Genet. 2005. PMID: 16189705

10

CRB1 heterozygotes with regional retinal dysfunction: implications for genetic testing of leber congenital amaurosis.

Yzer S, Fishman GA, Racine J, Al-Zuhaibi S, Chakor H, Dorfman A, Szlyk J, Lachapelle P, van den Born LI, Allikmets R, Lopez I, Cremers FP, Koenekoop RK. Yzer S, et al. Among authors: koenekoop rk. Invest Ophthalmol Vis Sci. 2006 Sep;47(9):3736-44. doi: 10.1167/iovs.05-1637. Invest Ophthalmol Vis Sci. 2006. PMID: 16936081

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