Christina L. McHenry

Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration.

Debra A. Thompson, P Gyürüs, L L Fleischer et al. · PubMed · 2000 · 253 citations

Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy

Andreas Janecke, Debra A. Thompson, Gerd Utermann et al. · Nature Genetics · 2004 · 244 citations

Photoreceptor Cell, Mendelian Disorder, Genetic Disorder +5

Role of Double-Stranded RNA Pattern Recognition Receptors in Rhinovirus-Induced Airway Epithelial Cell Responses

Qiong Wang, Deepti R. Nagarkar, Emily Bowman et al. · The Journal of Immunology · 2009 · 243 citations · Full text

Viral Replication, Inflammatory Lung Disease, Respiratory Diseases +14

Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy

Debra A. Thompson, Yun Li, Christina L. McHenry et al. · Nature Genetics · 2001 · 183 citations

Ocular Disease, Retina, Mendelian Disorder +8

Retinal Dystrophy Due to Paternal Isodisomy for Chromosome 1 or Chromosome 2, with Homoallelism for Mutations in RPE65 or MERTK, Respectively

Debra A. Thompson, Christina L. McHenry, Yun Li et al. · The American Journal of Human Genetics · 2002 · 151 citations · Full text

Paternal Isodisomy, Retina, Ophthalmology +9