Mitochondrial genetics

gan Chinnery, Patrick Francis, Hudson, Gavin
Cyhoeddwyd 2013

Cell-free mitochondrial DNA in progressive multiple sclerosis

gan Lowes, Hannah, Pyle, Angela, Duddy, Martin, Hudson, Gavin
Cyhoeddwyd yn Mitochondrion (2019)

A critical analysis of the combined usage of protein localization prediction methods: Increasing the number of independent data sets can reduce the accuracy of predicted mitochondr...

gan Lythgow, Kieren T., Hudson, Gavin, Andras, Peter, Chinnery, Patrick F.
Cyhoeddwyd 2011

Circulating cell-free mitochondrial DNA levels in Parkinson’s disease are influenced by treatment

gan Lowes, Hannah, Pyle, Angela, Santibanez-Koref, Mauro, Hudson, Gavin
Cyhoeddwyd yn Mol Neurodegener (2020)

Post-mortem ventricular cerebrospinal fluid cell-free-mtDNA in neurodegenerative disease

gan Lowes, Hannah, Kurzawa-Akanbi, Marzena, Pyle, Angela, Hudson, Gavin
Cyhoeddwyd yn Sci Rep (2020)

Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations

gan Wei, Wei, Gomez-Duran, Aurora, Hudson, Gavin, Chinnery, Patrick F.
Cyhoeddwyd yn PLoS Genet (2017)

Correction: Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations

gan Wei, Wei, Gomez-Duran, Aurora, Hudson, Gavin, Chinnery, Patrick F.
Cyhoeddwyd yn PLoS Genet (2018)

Genetic variation in the methylenetetrahydrofolate reductase gene, MTHFR, does not alter the risk of visual failure in Leber’s hereditary optic neuropathy

gan Hudson, Gavin, Yu-Wai-Man, Patrick, Zeviani, Massimo, Chinnery, Patrick F.
Cyhoeddwyd 2009

Recent Mitochondrial DNA Mutations Increase the Risk of Developing Common Late-Onset Human Diseases

gan Hudson, Gavin, Gomez-Duran, Aurora, Wilson, Ian J., Chinnery, Patrick F.
Cyhoeddwyd 2014

Variation in complement protein C1q is not a major contributor to cognitive impairment in Parkinson’s disease

gan Carbutt, Sophia, Duff, Jennifer, Yarnall, Alison, Burn, David J., Hudson, Gavin
Cyhoeddwyd yn Neurosci Lett (2015)

Reply: Parsing the differences in affected with LHON: genetic versus environmental triggers of disease conversion

gan Yu-Wai-Man, Patrick, Hudson, Gavin, Klopstock, Thomas, Chinnery, Patrick F.
Cyhoeddwyd yn Brain (2016)

Interactions between nuclear and mitochondrial SNPs and Parkinson’s disease risk

gan Pickett, Sarah J., Deen, Dasha, Pyle, Angela, Santibanez-Koref, Mauro, Hudson, Gavin
Cyhoeddwyd yn Mitochondrion (2022)

Reduced mitochondrial DNA copy number is a biomarker of Parkinson's disease

gan Pyle, Angela, Anugrha, Haidyan, Kurzawa-Akanbi, Marzena, Yarnall, Alison, Burn, David, Hudson, Gavin
Cyhoeddwyd yn Neurobiol Aging (2016)

Somatic mtDNA variation is an important component of Parkinson's disease

gan Coxhead, Jonathan, Kurzawa-Akanbi, Marzena, Hussain, Rafiqul, Pyle, Angela, Chinnery, Patrick, Hudson, Gavin
Cyhoeddwyd yn Neurobiol Aging (2016)

Mitochondrial isolation: when size matters

gan Bury, Alexander G., Vincent, Amy E., Turnbull, Doug M., Actis, Paolo, Hudson, Gavin
Cyhoeddwyd yn Wellcome Open Res (2020)

Mitochondrial DNA Damage and Brain Aging in Human Immunodeficiency Virus

gan Roca-Bayerri, Carla, Robertson, Fiona, Pyle, Angela, Hudson, Gavin, Payne, Brendan A I
Cyhoeddwyd yn Clin Infect Dis (2020)

Epigenetics, epidemiology and mitochondrial DNA diseases

gan Chinnery, Patrick F, Elliott, Hannah R, Hudson, Gavin, Samuels, David C, Relton, Caroline L
Cyhoeddwyd 2012

Raised Intraocular Pressure as a Potential Risk Factor for Visual Loss in Leber Hereditary Optic Neuropathy

gan Thouin, Anais, Griffiths, Philip G., Hudson, Gavin, Chinnery, Patrick F., Yu-Wai-Man, Patrick
Cyhoeddwyd 2013

Assessing mitochondrial heteroplasmy using next generation sequencing: A note of caution

gan Santibanez-Koref, Mauro, Griffin, Helen, Turnbull, Douglass M., Chinnery, Patrick F., Herbert, Mary, Hudson, Gavin
Cyhoeddwyd yn Mitochondrion (2019)

No evidence of substantia nigra telomere shortening in Parkinson’s disease

gan Hudson, Gavin, Faini, David, Stutt, Andrea, Eccles, Martin, Robinson, Louise, Burn, David J., Chinnery, Patrick F.
Cyhoeddwyd 2011