Complete mitochondrial DNA profile in stroke: A geographical matched case-control study in Spanish population

World Stroke Organization (WSO): Global Stroke Fact Sheet 2022

(2022) Valery L Feigin et al.   International Journal of Stroke

Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis

(2022) Ghada Al-Kafaji et al.   PLoS One

Editorial: Mitochondrial Dysfunction in Stroke

(2022) Feng Yan et al.   Frontiers in Aging Neuroscience

Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes

(2022) Wei Wei et al.   NATURE

A novel nonsense variant in MT-COX3 causes MELAS syndrome

(2021) Wei Wang et al.   NEUROMUSCULAR DISORDERS

Mitochondrial DNA Content Is Linked to Cardiovascular Disease Patient Phenotypes

(2021) Ruipeng Wei et al.   Journal of the American Heart Association

Avoiding Extinction: Recent Advances in Understanding Mechanisms of Mitochondrial DNA Purifying Selection in the Germline

(2021) Swathi P. Jeedigunta et al.   Annual Review of Genomics and Human Genetics

Interpretation of mitochondrial tRNA variants

(2020) Lee-Jun C. Wong et al.   GENETICS IN MEDICINE

The role of control region mitochondrial DNA mutations in cardiovascular disease: stroke and myocardial infarction

(2020) Miriam Umbria et al.   Scientific Reports

Mitochondrial Transfer as a Therapeutic Strategy Against Ischemic Stroke

(2020) Wei Chen et al.   Translational Stroke Research

Mitochondrial DNA copy number in human disease: the more the better?

(2020) Roberta Filograna et al.   FEBS LETTERS

Sensitivity of mitochondrial DNA heteroplasmy detection using Next Generation Sequencing

(2019) María del Mar González et al.   MITOCHONDRION

Mitochondrial uncoupling, ROS generation and cardioprotection

(2018) Susana Cadenas   BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS

The aetiology of cardiovascular disease: a role for mitochondrial DNA?

(2018) Marianne Venter et al.   Cardiovascular Journal of Africa

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

(2018) Vasileios I. Floros et al.   NATURE CELL BIOLOGY

Investigation of whole mitochondrial genome variation in normal tension glaucoma

(2018) Agnieszka Piotrowska-Nowak et al.   EXPERIMENTAL EYE RESEARCH

Association between mitochondrial DNA copy number and cardiovascular disease: Current evidence based on a systematic review and meta-analysis

(2018) Peng Yue et al.   PLoS One

Pandora's Box: mitochondrial defects in ischaemic heart disease and stroke

(2017) Sasan Andalib et al.   EXPERT REVIEWS IN MOLECULAR MEDICINE

A radical shift in perspective: mitochondria as regulators of reactive oxygen species

(2017) Daniel Munro et al.   JOURNAL OF EXPERIMENTAL BIOLOGY

Using MutPred derived mtDNA load scores to evaluate mtDNA variation in hypertension and diabetes in a two-population cohort: The SABPA study

(2017) Marianne Venter et al.   Journal of Genetics and Genomics

Stroke

(2017) Graeme J Hankey   LANCET

Involvement of mitochondrial haplogroups in myocardial infarction and stroke: A case-control study in Castile and Leon (Spain) population

(2017) Miriam Umbria et al.   MITOCHONDRION

Association of Mitochondrial DNA Copy Number With Cardiovascular Disease

(2017) Foram N. Ashar et al.   JAMA Cardiology

Analysis of Heteroplasmic Variants in the Cardiac Mitochondrial Genome of Individuals with Down Syndrome

(2016) Erik Hefti et al.   HUMAN MUTATION

Mitochondrial coupling and capacity of oxidative phosphorylation in skeletal muscle of Inuit and Caucasians in the arctic winter

(2015) E. Gnaiger et al.   SCANDINAVIAN JOURNAL OF MEDICINE & SCIENCE IN SPORTS

Cardiac Mitochondria and Reactive Oxygen Species Generation

(2014) Yeong-Renn Chen et al.   CIRCULATION RESEARCH

In D-loop: 40years of mitochondrial 7S DNA

(2014) Thomas J. Nicholls et al.   EXPERIMENTAL GERONTOLOGY

World Medical Association Declaration of Helsinki

(2013)   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Frequency and Pattern of Heteroplasmy in the Complete Human Mitochondrial Genome

(2013) Amanda Ramos et al.   PLoS One

Mitochondrial DNA Genetics and the Heteroplasmy Conundrum in Evolution and Disease

(2013) D. C. Wallace et al.   Cold Spring Harbor Perspectives in Biology

Mitochondrial Haplogroups H and J: Risk and Protective Factors for Ischemic Cardiomyopathy

(2012) Mariana Fernández-Caggiano et al.   PLoS One

Oxidative Stress in Atherosclerosis Development: The Central Role of LDL and Oxidative Burst

(2012) Ilaria Peluso et al.   Endocrine Metabolic & Immune Disorders-Drug Targets

Comparing Phylogeny and the Predicted Pathogenicity of Protein Variations Reveals Equal Purifying Selection across the Global Human mtDNA Diversity

(2011) Luísa Pereira et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The mitochondrial paradigm for cardiovascular disease susceptibility and cellular function: a complementary concept to Mendelian genetics

(2011) David M Krzywanski et al.   LABORATORY INVESTIGATION

Mitochondrial DNA variation in human metabolic rate and energy expenditure

(2011) Gregory J. Tranah et al.   MITOCHONDRION

Mitochondrial DNA haplogroups and risk of transient ischaemic attack and ischaemic stroke: a genetic association study

(2010) Patrick F Chinnery et al.   LANCET NEUROLOGY

Correcting for Purifying Selection: An Improved Human Mitochondrial Molecular Clock

(2009) Pedro Soares et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mitochondria and Reactive Oxygen Species

(2009) Francesco Addabbo et al.   HYPERTENSION

Evolutionary Pressure on Mitochondrial Cytochrome b Is Consistent with a Role of CytbI7T Affecting Longevity during Caloric Restriction

(2009) Wesley A. Beckstead et al.   PLoS One

Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients

(2008) Alexandra Rosa et al.   BMC Medical Genetics

Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation

(2008) Mannis van Oven et al.   HUMAN MUTATION