Genetic Evidence for Elevated Pathogenicity of Mitochondrial DNA Heteroplasmy in Autism Spectrum Disorder

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Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in Humans

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Extensive pathogenicity of mitochondrial heteroplasmy in healthy human individuals

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Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming

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Mitochondrial Dysfunction as a Neurobiological Subtype of Autism Spectrum Disorder

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Mitochondrial DNA Genetics and the Heteroplasmy Conundrum in Evolution and Disease

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Ultra-Sensitive Sequencing Reveals an Age-Related Increase in Somatic Mitochondrial Mutations That Are Inconsistent with Oxidative Damage

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Evidence of reactive oxygen species-mediated damage to mitochondrial DNA in children with typical autism

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Evaluating Mitochondrial DNA Variation in Autism Spectrum Disorders

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

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Experimental Evidence Supports a Sex-Specific Selective Sieve in Mitochondrial Genome Evolution

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Dynamics of mitochondrial heteroplasmy in three families investigated via a repeatable re-sequencing study

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Detecting Heteroplasmy from High-Throughput Sequencing of Complete Human Mitochondrial DNA Genomes

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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

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Can Association Between Preterm Birth and Autism be Explained by Maternal or Neonatal Morbidity?

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