Gavin Hudson

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Senior Lecturer

Newcastle University

United Kingdom

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About

Gavin Hudson is a Senior Lecturer at Newcastle University in the United Kingdom. His research focuses on mitochondrial genetics, with recent articles discussing topics such as mitochondrial DNA mutations in HIV-exposed children and the role of mitochondrial variations in neurodegenerative diseases like Parkinson's. He also investigates genomic strategies for mitochondrial diagnostics and the impacts of genetic factors on various clinical conditions.

Recent Grants

Grant: Close

Wellcome Centre for Mitochondrial Research

Open Date: 2022-05-01

Close Date: 2024-04-01

Grant: Close

The role of acylcarnitines in the development and progression of Parkinson's disease

Open Date: 2021-04-01

Close Date: 2023-05-01

Grant: Close

The role of circular RNAs in Parkinson's disease and dementia

Open Date: 2020-10-01

Close Date: 2023-09-01

Grant: Close

The role of circular RNAs in complex disease

Open Date: 2020-01-01

Close Date: 2024-05-01

Grant: Close

Nanobiopsy as a tool to study the clonal expansion on mtDNA variation

Open Date: 2018-10-01

Close Date: 2022-06-01

Articles (20)

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2020

Collaborators (26)

kathleen freson

Prof

Katholieke Universiteit Leuven

BELGIUM

Gavin Hudson

Research Interests

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About

Recent Grants

Articles (20)

Relationships of mitochondrial DNA mutations and select clinical diagnoses in perinatally HIV- and ART-exposed uninfected children

Parkinson’s disease neurons exhibit alterations in mitochondrial quality control proteins

Feasibility and impact of haplogroup matching for mitochondrial replacement treatment

Single-cell multiomic analyses sheds light on mitochondrial mutational selection.

The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism.

Genomic Strategies in Mitochondrial Diagnostics.

GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements.

Interactions between nuclear and mitochondrial SNPs and Parkinson's disease risk.

A subcellular cookie cutter for spatial genomics in human tissue

GBA and APOE Impact Cognitive Decline in Parkinson's Disease: A 10-Year Population-Based Study.

Heteroplasmic mitochondrial DNA variants in cardiovascular diseases.

Author Correction: Age-associated mitochondrial DNA mutations cause metabolic remodeling that contributes to accelerated intestinal tumorigenesis (Nature Cancer, (2020), 1, 10, (976-989), 10.1038/s43018-020-00112-5)

Imaging mass cytometry reveals generalised deficiency in OXPHOS complexes in Parkinson’s disease

Maternal germline factors associated with aneuploid pregnancy loss: A systematic review

Mitochondrial DNA Damage and Brain Aging in Human Immunodeficiency Virus

Neuropathological and biochemical investigation of Hereditary Ferritinopathy cases with ferritin light chain mutation: Prominent protein aggregation in the absence of major mitochondrial or oxidative stress

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

Age-associated mitochondrial DNA mutations cause metabolic remodelling that contributes to accelerated intestinal tumorigenesis.

Mitochondrial isolation: when size matters.

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

Collaborators (26)

kathleen freson

Carl Counsell

Andrea Olschewski

Wendy Erber

Mary Herbert

Peter Dixon

Daniel Erskine

Timothy Aitman

Amy E. Vincent

Paolo Actis

David Allsup

Jodi Maple‐Grødem

Marzena Kurzawa-Akanbi

Robert Taylor

Inês Cebola

Adam Levine

Michael Keogh

Michael Simpson

Lorraine Ochieng

Christopher Morris

David Michael Gay

Oliver Russell

Eleni Louka

Ian Wilson

Tim @timjph Hubbard

Laura C. Greaves

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