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

2013 ESH/ESC Guidelines for the management of arterial hypertension

(2013)   EUROPEAN HEART JOURNAL

Mitochondrial DNA haplogroup H as a risk factor for idiopathic dilated cardiomyopathy in Spanish population

(2013) M. Fernández-Caggiano et al.   MITOCHONDRION

Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease

(2013) G. Hudson et al.   NEUROLOGY

Mitochondrial Haplogroups Modify the Risk of Developing Hypertrophic Cardiomyopathy in a Danish Population

(2013) Christian M. Hagen et al.   PLoS One

No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controls

(2012) Gavin Hudson et al.   ANNALS OF THE RHEUMATIC DISEASES

Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy

(2012) Aurora Gómez-Durán et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

Estimating the current and future costs of Type 1 and Type 2 diabetes in the UK, including direct health costs and indirect societal and productivity costs

(2012) N. Hex et al.   DIABETIC MEDICINE

Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants

(2012) Wenqing Fu et al.   NATURE

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

(2012) Céline Bellenguez et al.   NATURE GENETICS

Recent Explosive Human Population Growth Has Resulted in an Excess of Rare Genetic Variants

(2012) A. Keinan et al.   SCIENCE

The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits

(2012) Benjamin F. Voight et al.   PLoS Genetics

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

(2011)   LANCET

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

(2011) David M Evans et al.   NATURE GENETICS

Principal-Component Analysis for Assessment of Population Stratification in Mitochondrial Medical Genetics

(2010) Alessandro Biffi et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Cancer cell mitochondria confer apoptosis resistance and promote metastasis

(2010) Mariola Kulawiec et al.   CANCER BIOLOGY & THERAPY

Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups

(2010) Aurora Gómez-Durán et al.   HUMAN MOLECULAR GENETICS

HaploGrep: a fast and reliable algorithm for automatic classification of mitochondrial DNA haplogroups

(2010) Anita Kloss-Brandstätter et al.   HUMAN MUTATION

Molecular-Clinical Correlation in a Family With a Novel Heteroplasmic Leigh Syndrome Missense Mutation in the Mitochondrial Cytochrome c Oxidase III Gene

(2010) Emna Mkaouar-Rebai et al.   JOURNAL OF CHILD NEUROLOGY

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

(2010) Patrick F Chinnery et al.   LANCET NEUROLOGY

Failure to Validate Association between 12p13 Variants and Ischemic Stroke

(2010)   NEW ENGLAND JOURNAL OF MEDICINE

Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor

(2009) Maria Ban et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Mitochondrial Variants in Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

(2009) Brandi Rollins et al.   PLoS One

Ancient mtDNA Genetic Variants Modulate mtDNA Transcription and Replication

(2009) Sarit Suissa et al.   PLoS Genetics

Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease

(2008) Rosa Pello et al.   HUMAN MOLECULAR GENETICS

Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation

(2008) Mannis van Oven et al.   HUMAN MUTATION

Meta-analyses of the incidence and prevalence of schizophrenia: conceptual and methodological issues

(2008) Sukanta Saha et al.   INTERNATIONAL JOURNAL OF METHODS IN PSYCHIATRIC RESEARCH

Mitochondrial DNA haplogroups and subhaplogroups are associated with Parkinson’s disease risk in a Polish PD cohort

(2008) Katarzyna Gaweda-Walerych et al.   JOURNAL OF NEURAL TRANSMISSION

Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease

(2008) Sheila A Fisher et al.   NATURE GENETICS

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

(2008) Manuel A R Ferreira et al.   NATURE GENETICS

Investigation of the Role of Mitochondrial DNA in Multiple Sclerosis Susceptibility

(2008) Maria Ban et al.   PLoS One