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

Proceedings of the National Academy of Sciences - PNAS, 2014-09, Vol.111 (38), p.E4033-E4042

2014

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Mitochondrial energy deficiency leads to hyperproliferation of skeletal muscle mitochondria and enhanced insulin sensitivity

Proceedings of the National Academy of Sciences - PNAS, 2017-03, Vol.114 (10), p.2705-2710

2017

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Association Between Mitochondrial DNA Haplogroup Variation and Autism Spectrum Disorders

JAMA psychiatry (Chicago, Ill.), 2017-11, Vol.74 (11), p.1161

2017

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Mitochondrial DNA variant associated with Leber hereditary optic neuropathy and high-altitude Tibetans

Proceedings of the National Academy of Sciences - PNAS, 2012-05, Vol.109 (19), p.7391-7396

2012

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Traces of Early Eurasians in the Mansi of Northwest Siberia Revealed by Mitochondrial DNA Analysis

American journal of human genetics, 2002-04, Vol.70 (4), p.1009-1014

2002

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Analysis of Mitochondrial DNA Diversity in the Aleuts of the Commander Islands and Its Implications for the Genetic History of Beringia

American journal of human genetics, 2002-08, Vol.71 (2), p.415-421

2002

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Mitochondrial DNA associations with East Asian metabolic syndrome

Biochimica et biophysica acta. Bioenergetics, 2018-09, Vol.1859 (9), p.878-892

2018

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Cytoskeletal mitochondrial interactions in collagen VI related disorders

Biochimica et biophysica acta. Bioenergetics, 2016-08, Vol.1857, p.e102-e102

2016

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The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J

Human genetics, 2002-02, Vol.110 (2), p.130-138

2002

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

Proceedings of the National Academy of Sciences - PNAS, 2014-09, Vol.111 (38), p.13689-13689

2014

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Preterm birth is associated with mitochondrial DNA variation

Mitochondrion, 2013-11, Vol.13 (6), p.929-930

2013

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19-OR: TOWARDS ALLELE LEVEL HLA GENOTYPING: A COMPARISON OF NEXT-GENERATION SEQUENCING PLATFORMS – ION TORRENT PGM AND ILLUMINA MiSeq

Human immunology, 2012-10, Vol.73, p.16-16

2012

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19-OR

Human immunology, 2012-10, Vol.73, p.16-16

2012

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Leber Hereditary Optic Neuropathy (LHON) associated mutation 3394 is also a high-altitude adaptive polymorphism

Mitochondrion, 2012-09, Vol.12 (5), p.584

2012

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Clinical and functional characterization of a human ORNT1 mutation (T32R) in the hyperornithinemia-hyperammonemia- homocitrullinuria (HHH) syndrome

Pediatric research, 2006-10, Vol.60 (4), p.423-429

2006

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Association between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohort: Alzheimer's Disease Neuroimaging Initiative (ADNI) Studies

Neurobiology of aging, 2010, Vol.31 (8), p.1355-1363

2010

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117 Asian mitochondrial DNA (mtDNA) lineage F4 is associated with increased risk of developing metabolic syndrome

Mitochondrion, 2010-03, Vol.10 (2), p.233

2010

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77 Somatic mtDNA control region mutations and their effects in down syndrome with Alzheimer dementia

Mitochondrion, 2007-12, Vol.7 (6), p.426

2007

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Traces of early Eurasians in the Mansi of Northwest Siberia revealed by mitochondrial DNA analysis

American journal of human genetics, 2002, Vol.70 (4), p.1009-1014

2002

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

Mitochondrial energy deficiency leads to hyperproliferation of skeletal muscle mitochondria and enhanced insulin sensitivity

Association Between Mitochondrial DNA Haplogroup Variation and Autism Spectrum Disorders

Mitochondrial DNA variant associated with Leber hereditary optic neuropathy and high-altitude Tibetans

Traces of Early Eurasians in the Mansi of Northwest Siberia Revealed by Mitochondrial DNA Analysis

Analysis of Mitochondrial DNA Diversity in the Aleuts of the Commander Islands and Its Implications for the Genetic History of Beringia

Mitochondrial DNA associations with East Asian metabolic syndrome

Cytoskeletal mitochondrial interactions in collagen VI related disorders

The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J

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

Preterm birth is associated with mitochondrial DNA variation

19-OR: TOWARDS ALLELE LEVEL HLA GENOTYPING: A COMPARISON OF NEXT-GENERATION SEQUENCING PLATFORMS – ION TORRENT PGM AND ILLUMINA MiSeq

19-OR

Leber Hereditary Optic Neuropathy (LHON) associated mutation 3394 is also a high-altitude adaptive polymorphism

Clinical and functional characterization of a human ORNT1 mutation (T32R) in the hyperornithinemia-hyperammonemia- homocitrullinuria (HHH) syndrome

Association between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohort: Alzheimer's Disease Neuroimaging Initiative (ADNI) Studies

117 Asian mitochondrial DNA (mtDNA) lineage F4 is associated with increased risk of developing metabolic syndrome

77 Somatic mtDNA control region mutations and their effects in down syndrome with Alzheimer dementia

Traces of early Eurasians in the Mansi of Northwest Siberia revealed by mitochondrial DNA analysis

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