Huanan Ren

Huanan Ren

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Huanan Ren

Huanan Ren

Publications by authors named "Huanan Ren"

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18Publications

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

Invest Ophthalmol Vis Sci 2015 Dec;56(13):8297-305

The McGill Ocular Genetics Laboratory Paediatric Ophthalmology Division, Montreal Children's Hospital, McGill University Health Centre, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1167/iovs.15-17104DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4699406PMC
December 2015

Comprehensive analysis of patients with Stargardt macular dystrophy reveals new genotype-phenotype correlations and unexpected diagnostic revisions.

Genet Med 2015 Apr 4;17(4):262-70. Epub 2014 Dec 4.

1] Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA [2] Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA [3] Structural and Computational Biology and Molecular Biophysics Graduate Program, Baylor College of Medicine, Houston, Texas, USA [4] Program in Developmental Biology, Baylor College of Medicine, Houston, Texas, USA.

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http://www.nature.com/articles/gim2014174
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http://dx.doi.org/10.1038/gim.2014.174DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4385427PMC
April 2015

Novel insights into the molecular pathogenesis of CYP4V2-associated Bietti's retinal dystrophy.

Mol Genet Genomic Med 2015 Jan 15;3(1):14-29. Epub 2014 Sep 15.

McGill Ocular Genetics Laboratory, Departments of Paediatric Surgery, Human Genetics and Ophthalmology, Montreal Children's Hospital, McGill University Health Centre Montreal, Quebec, Canada.

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http://dx.doi.org/10.1002/mgg3.109DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299712PMC
January 2015

A Review of Secondary Photoreceptor Degenerations in Systemic Disease.

Cold Spring Harb Perspect Med 2014 Dec 4;5(11). Epub 2014 Dec 4.

Department of Paediatric Surgery, Human Genetics and Ophthalmology, McGill University, Montreal, Quebec H3A 1A1, Canada McGill Ocular Genetics Laboratory, Montreal, Quebec H3H 1P3, Canada Faculty of Medicine, Human Genetics, McGill University, Montreal, Quebec H3A 1B1, Canada Montreal Children's Hospital Research Institute, Montreal, Quebec H3H 1P3, Canada.

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http://perspectivesinmedicine.cshlp.org/lookup/doi/10.1101/c
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http://dx.doi.org/10.1101/cshperspect.a025825DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632864PMC
December 2014

A dominant mutation in hexokinase 1 (HK1) causes retinitis pigmentosa.

Invest Ophthalmol Vis Sci 2014 Sep 4;55(11):7147-58. Epub 2014 Sep 4.

Human Genetics Center, University of Texas Health Science Center, Houston, Texas, United States Department of Ophthalmology and Visual Sciences, University of Texas Health Science Center, Houston, Texas, United States.

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http://dx.doi.org/10.1167/iovs.14-15419DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4224580PMC
September 2014

Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling.

Cell 2012 Aug;150(3):533-48

Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, MI 48109, USA.

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http://dx.doi.org/10.1016/j.cell.2012.06.028DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3433835PMC
August 2012