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

Lowes, Hannah ; Pyle, Angela ; Santibanez-Koref, Mauro ; Hudson, Gavin

Molecular neurodegeneration, 2020-02, Vol.15 (1), p.10-10, Article 10 [Periódico revisado por pares]

England: BioMed Central Ltd

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2
Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos
Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos
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Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos

Floros, Vasileios I ; Pyle, Angela ; Dietmann, Sabine ; Wei, Wei ; Tang, Walfred C W ; Irie, Naoko ; Payne, Brendan ; Capalbo, Antonio ; Noli, Laila ; Coxhead, Jonathan ; Hudson, Gavin ; Crosier, Moira ; Strahl, Henrik ; Khalaf, Yacoub ; Saitou, Mitinori ; Ilic, Dusko ; Surani, M Azim ; Chinnery, Patrick F

Nature cell biology, 2018-02, Vol.20 (2), p.144-151 [Periódico revisado por pares]

England: Nature Publishing Group

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3
Nanobiopsy investigation of the subcellular mtDNA heteroplasmy in human tissues
Nanobiopsy investigation of the subcellular mtDNA heteroplasmy in human tissues
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Nanobiopsy investigation of the subcellular mtDNA heteroplasmy in human tissues

Bury, Alexander ; Pyle, Angela ; Vincent, Amy E ; Actis, Paolo ; Hudson, Gavin

Scientific reports, 2024-06, Vol.14 (1), p.13789-12 [Periódico revisado por pares]

London: Nature Publishing Group

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4
Somatic mtDNA variation is an important component of Parkinson's disease
Somatic mtDNA variation is an important component of Parkinson's disease
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Somatic mtDNA variation is an important component of Parkinson's disease

Coxhead, Jonathan ; Kurzawa-Akanbi, Marzena ; Hussain, Rafiqul ; Pyle, Angela ; Chinnery, Patrick ; Hudson, Gavin

Neurobiology of aging, 2016-02, Vol.38, p.217.e1-217.e6 [Periódico revisado por pares]

United States: Elsevier Inc

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5
Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations
Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations
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Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations

Wei, Wei ; Gomez-Duran, Aurora ; Hudson, Gavin ; Chinnery, Patrick F Larsson, Nils-Göran

PLoS genetics, 2017-12, Vol.13 (12), p.e1007126-e1007126 [Periódico revisado por pares]

United States: Public Library of Science

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6
Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases
Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases
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Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases

Hudson, Gavin ; Gomez-Duran, Aurora ; Wilson, Ian J ; Chinnery, Patrick F Gojobori, Takashi

PLoS genetics, 2014-05, Vol.10 (5), p.e1004369-e1004369 [Periódico revisado por pares]

United States: Public Library of Science

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7
Reduced cerebrospinal fluid mitochondrial DNA is a biomarker for early-stage Parkinson's disease
Reduced cerebrospinal fluid mitochondrial DNA is a biomarker for early-stage Parkinson's disease
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Reduced cerebrospinal fluid mitochondrial DNA is a biomarker for early-stage Parkinson's disease

Pyle, Angela ; Brennan, Rebecca ; Kurzawa-Akanbi, Marzena ; Yarnall, Alison ; Thouin, Anais ; Mollenhauer, Brit ; Burn, David ; Chinnery, Patrick F. ; Hudson, Gavin

Annals of neurology, 2015-12, Vol.78 (6), p.1000-1004 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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8
Assessing mitochondrial heteroplasmy using next generation sequencing: A note of caution
Assessing mitochondrial heteroplasmy using next generation sequencing: A note of caution
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Assessing mitochondrial heteroplasmy using next generation sequencing: A note of caution

Santibanez-Koref, Mauro ; Griffin, Helen ; Turnbull, Douglass M ; Chinnery, Patrick F ; Herbert, Mary ; Hudson, Gavin

Mitochondrion, 2019-05, Vol.46, p.302-306 [Periódico revisado por pares]

Netherlands: Elsevier Science

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9
The Prevalence and Natural History of Dominant Optic Atrophy Due to OPA1 Mutations
The Prevalence and Natural History of Dominant Optic Atrophy Due to OPA1 Mutations
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The Prevalence and Natural History of Dominant Optic Atrophy Due to OPA1 Mutations

Yu-Wai-Man, Patrick, MRCOphth ; Griffiths, Philip G., FRCOphth ; Burke, Ailbhe, MBBS ; Sellar, Peter W., FRCOphth ; Clarke, Michael P., FRCOphth ; Gnanaraj, Lawrence, FRCOphth ; Ah-Kine, Desiree, FRCOphth ; Hudson, Gavin, PhD ; Czermin, Birgit, PhD ; Taylor, Robert W., PhD ; Horvath, Rita, PhD ; Chinnery, Patrick F., FRCP

Ophthalmology (Rochester, Minn.), 2010-08, Vol.117 (8), p.1538-1546.e1 [Periódico revisado por pares]

United States: Elsevier Inc

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10
metabolic profiling of Parkinson's disease and mild cognitive impairment
metabolic profiling of Parkinson's disease and mild cognitive impairment
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metabolic profiling of Parkinson's disease and mild cognitive impairment

Burté, Florence ; Houghton, David ; Lowes, Hannah ; Pyle, Angela ; Nesbitt, Sarah ; Yarnall, Alison ; Yu‐Wai‐Man, Patrick ; Burn, David J. ; Santibanez‐Koref, Mauro ; Hudson, Gavin

Movement disorders, 2017-06, Vol.32 (6), p.927-932 [Periódico revisado por pares]

United States: John Wiley and Sons Inc

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