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Publications by Bart P. Leroy

Correction: Mapping the Genomic Landscape of Inherited Retinal Disease Genes Prioritizes Genes Prone to Coding and Noncoding Copy-Number Variations

Genetics in Medicine
MedicineGenetics
2018English

ABCA4-associated Disease as a Model for Missing Heritability in Autosomal Recessive Disorders: Novel Noncoding Splice, Cis-Regulatory, Structural, and Recurrent Hypomorphic Variants

Genetics in Medicine
MedicineGenetics
2019English

In This Issue

Genetics in Medicine
MedicineGenetics
2012English

Characterization of Cardiovascular Involvement in Pseudoxanthoma Elasticum FamiliesSignificance

Arteriosclerosis, Thrombosis, and Vascular Biology
Cardiovascular MedicineCardiology
2013English

Clinical Characterization of 66 Patients With Congenital Retinal Disease Due to the Deep-Intronic C.2991+1655A>G Mutation in CEP290

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2018English

Analysis of KERA in Four Families With Cornea Plana Identifies Two Novel Mutations

Acta Ophthalmologica
MedicineOphthalmology
2017English

Is Oral Moxifloxacin Associated With Bilateral Acute Iris Transillumination?

Acta Ophthalmologica
MedicineOphthalmology
2017English

Detailed Functional and Structural Phenotype of Bietti Crystalline Dystrophy Associated With Mutations in CYP4V2 Complicated by Choroidal Neovascularization

Ophthalmic Genetics
Child HealthOphthalmologyPediatricsPerinatologyGenetics
2016English

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