Christian Hamel
Canterbury District Health Board(NZ)
Publications by Year
Research Areas
Retinal Development and Disorders, Mitochondrial Function and Pathology, Retinal Diseases and Treatments, ATP Synthase and ATPases Research, Metabolism and Genetic Disorders
Most-Cited Works
- → Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy(2000)1,421 cited
- → Cone rod dystrophies(2007)438 cited
- → The human dynamin‐related protein OPA1 is anchored to the mitochondrial inner membrane facing the inter‐membrane space(2002)411 cited
- → Mutation spectrum and splicing variants in the OPA1 gene(2001)379 cited
- → Leber congenital amaurosis: Comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype-phenotype correlations as a strategy for molecular diagnosis(2004)349 cited
- → Molecular cloning and expression of RPE65, a novel retinal pigment epithelium-specific microsomal protein that is post-transcriptionally regulated in vitro(1993)334 cited
- → Identification of a Novel BBS Gene (BBS12) Highlights the Major Role of a Vertebrate-Specific Branch of Chaperonin-Related Proteins in Bardet-Biedl Syndrome(2006)237 cited
- → TRPV4 channels mediate the infrared laser-evoked response in sensory neurons(2012)233 cited
- → OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution(2010)229 cited
- → OPA1 R445H mutation in optic atrophy associated with sensorineural deafness(2005)167 cited