Mitochondrial genetics

por Chinnery, Patrick Francis, Hudson, Gavin
Publicado 2013

Cell-free mitochondrial DNA in progressive multiple sclerosis

por Lowes, Hannah, Pyle, Angela, Duddy, Martin, Hudson, Gavin
Publicado 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...

por Lythgow, Kieren T., Hudson, Gavin, Andras, Peter, Chinnery, Patrick F.
Publicado 2011

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

por Lowes, Hannah, Pyle, Angela, Santibanez-Koref, Mauro, Hudson, Gavin
Publicado 2020

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

por Lowes, Hannah, Kurzawa-Akanbi, Marzena, Pyle, Angela, Hudson, Gavin
Publicado 2020

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

por Wei, Wei, Gomez-Duran, Aurora, Hudson, Gavin, Chinnery, Patrick F.
Publicado 2017

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

por Wei, Wei, Gomez-Duran, Aurora, Hudson, Gavin, Chinnery, Patrick F.
Publicado 2018

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

por Hudson, Gavin, Yu-Wai-Man, Patrick, Zeviani, Massimo, Chinnery, Patrick F.
Publicado 2009

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

por Hudson, Gavin, Gomez-Duran, Aurora, Wilson, Ian J., Chinnery, Patrick F.
Publicado 2014

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

por Carbutt, Sophia, Duff, Jennifer, Yarnall, Alison, Burn, David J., Hudson, Gavin
Publicado 2015

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

por Pyle, Angela, Anugrha, Haidyan, Kurzawa-Akanbi, Marzena, Yarnall, Alison, Burn, David, Hudson, Gavin
Publicado 2016

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

por Coxhead, Jonathan, Kurzawa-Akanbi, Marzena, Hussain, Rafiqul, Pyle, Angela, Chinnery, Patrick, Hudson, Gavin
Publicado 2016

Mitochondrial isolation: when size matters

por Bury, Alexander G., Vincent, Amy E., Turnbull, Doug M., Actis, Paolo, Hudson, Gavin
Publicado 2020

Mitochondrial DNA Damage and Brain Aging in Human Immunodeficiency Virus

por Roca-Bayerri, Carla, Robertson, Fiona, Pyle, Angela, Hudson, Gavin, Payne, Brendan A I
Publicado 2020

The genetics of mitochondrial disease: dissecting mitochondrial pathology using multi‐omic pipelines

por Alston, Charlotte L, Stenton, Sarah L, Hudson, Gavin, Prokisch, Holger, Taylor, Robert W
Publicado 2021

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

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

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

por Santibanez-Koref, Mauro, Griffin, Helen, Turnbull, Douglass M., Chinnery, Patrick F., Herbert, Mary, Hudson, Gavin
Publicado 2019

The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism

por Xia, Charley, Pickett, Sarah J., Liewald, David C. M., Weiss, Alexander, Hudson, Gavin, Hill, W. David
Publicado 2023

Mitochondrial DNA and traumatic brain injury

por Bulstrode, Harry, Nicoll, James A. R., Hudson, Gavin, Chinnery, Patrick F., Di Pietro, Valentina, Belli, Antonio
Publicado 2014

A subcellular cookie cutter for spatial genomics in human tissue

por Bury, Alexander G., Pyle, Angela, Marcuccio, Fabio, Turnbull, Doug M., Vincent, Amy E., Hudson, Gavin, Actis, Paolo
Publicado 2022