Rebecca Hanna
David Moore
Professor Mark Birch-Machin
| Optimised detection of mitochondrial DNA strand breaks | 2019 |
|
David Moore
Dr Florence Burte
Dr Patrick Yu Wai Man
| A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions | 2017 |
|
David Moore
Dr Florence Burte
Dr Patrick Yu Wai Man
| Corrigendum: A novel CISD2 mutation associated with a classical wolfram syndrome phenotype alters Ca21 homeostasis and ER-mitochondria interactions. [Human Molecular Genetics (2017)], doi: 10.1093/hmg/ddx060 | 2017 |
|
Dr Patrick Yu Wai Man
David Moore
Dr Florence Burte
| Evaluating the therapeutic potential of idebenone and related quinone analogues in Leber hereditary optic neuropathy | 2017 |
|
David Moore
Dr Patrick Yu Wai Man
| Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China | 2016 |
|
David Moore
Professor Patrick Chinnery
Dr Patrick Yu Wai Man
| Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies | 2015 |
|
David Moore
| Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis | 2015 |
|
David Moore
| Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis? | 2015 |
|
David Moore
Dr Patrick Yu Wai Man
| A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement | 2014 |
|
Dr Gerald Pfeffer
Professor Grainne Gorman
Dr Helen Griffin
Dr Marzena Kurzawa-Akanbi
Dr Ian Wilson
et al. | Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance | 2014 |
|
David Moore
Dr Patrick Yu Wai Man
| Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis? | 2014 |
|
David Moore
Dr Patrick Yu Wai Man
| Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis | 2014 |
|
David Moore
Dr Patrick Yu Wai Man
| Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease | 2014 |
|
