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David G. Moore

A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement
2014 · Sylvie Bannwarth, Samira Ait-El-Mkadem, et al. · Brain · 488
CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis
2015 · Emmanuelle C Genin, Morgane Plutino, et al. · EMBO Molecular Medicine · 199
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Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance
2014 · Gerald Pfeffer, Gráinne S Gorman, et al. · Brain · 175
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Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies
2015 · Claire Angebault, Pierre-Olivier Guichet, et al. · The American Journal of Human Genetics · 76
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A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions
2017 · Cécile Rouzier, David Moore, et al. · Human Molecular Genetics · 75
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Evaluating the therapeutic potential of idebenone and related quinone analogues in Leber hereditary optic neuropathy
2017 · Patrick Yu-Wai-Man, Devorah Soiferman, et al. · Mitochondrion · 73
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A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions
2017 · Cécile Rouzier, David Moore, et al. · Human Molecular Genetics · 52
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Behr's Syndrome is Typically Associated with Disturbed Mitochondrial Translation and Mutations in the C12orf65 Gene
2014 · Angela Pyle, Venkateswaran Ramesh, et al. · Journal of Neuromuscular Diseases · 28
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Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?
2014 · Sylvie Bannwarth, Samira Ait-El-Mkadem, et al. · Brain · 13
Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections
2023 · Lauren Jeffries, Emily K. Mis, et al. · Genetics in Medicine · 12
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Leber Hereditary Optic Neuropathy and Longitudinally Extensive Transverse Myelitis
2017 · C. Bursle, K. Riney, et al. · JIMD Reports · 11
Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying aCHCHD10mutation: Table 1
2015 · Sylvie Bannwarth, Samira Ait-El-Mkadem, et al. · Brain · 4
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Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis
2014 · Sylvie Bannwarth, Samira Ait-El-Mkadem, et al. · Brain · 4
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Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease
2014 · Sylvie Bannwarth, Samira Ait-El-Mkadem, et al. · Brain · 4
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Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies
2015 · Claire Angebault, Pierre-Olivier Guichet, et al. · The American Journal of Human Genetics · 3
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Reply: IsCHCHD10Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?
2015 · Sylvie Bannwarth, Samira Ait-El-Mkadem, et al. · Brain · 3
Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.
2015 · Bannwarth, Sylvie, Ait-El-Mkadem, Samira, et al. · HAL (Le Centre pour la Communication Scientifique Directe) · 1
Reply:CHCHD10mutations in Italian patients with sporadic amyotrophic lateral sclerosis
2015 · Sylvie Bannwarth, Samira Ait-El-Mkadem, et al. · Brain · 1
Disturbed interactions between mitochondria and the endoplasmic reticulum : implications for human disease
2017 · David Moore
Reply: High prevalence ofCHCHD10mutations in patients with frontotemporal dementia from China: Table 1
2015 · Sylvie Bannwarth, Samira Ait-El-Mkadem, et al. · Brain
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement
2014 · Sylvie Bannwarth, Samira Ait-El-Mkadem, et al. · Newcastle University ePrints (Newcastle Univesity)
P32 Mutations in SPG7 cause chronic progressive external ophthalmoplegia through disordered mtDNA maintenance
2014 · G.S. Gorman, G. Pfeffer, et al. · Neuromuscular Disorders
073 Hereditary spastic paraplegia caused by spastin (SPAST, SPG4) mutations is found more often in males: report of novel mutations from one centre, and review of published literature
2012 · C Proukakis, D Moore, et al. · Journal of Neurology Neurosurgery & Psychiatry
P3.49 Myopathy associated with mutations in CHKB in three UK patients
2011 · R. Quinlivan, I. Nishino, et al. · Neuromuscular Disorders
Works count: 24
Citation count: 1,222
H-index: 11
I10-index: 11
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