| scholarly article | Q13442814 |
| P50 | author | David Altshuler | Q5230746 |
| Vamsi Mootha | Q7913059 | ||
| Leif Groop | Q27214742 | ||
| Joel Hirschhorn | Q56277942 | ||
| Paul I W de Bakker | Q85643659 | ||
| Bo Isomaa | Q29839548 | ||
| Richa Saxena | Q30431575 | ||
| Mark Joseph Daly | Q39071290 | ||
| P2093 | author name string | Kristin G Ardlie | |
| Daniel Gaudet | |||
| Noel Burtt | |||
| Karyn Singer | |||
| P2860 | cites work | Classification of European mtDNAs from an analysis of three European populations | Q24533221 |
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| Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population. | Q54657414 | ||
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| Mitochondrial DNA polymorphism: its role in longevity of the Irish population | Q61054675 | ||
| Association of the mitochondrial DNA haplogroup J with longevity is population specific | Q61758423 | ||
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| Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits | Q29614876 | ||
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| Quality and completeness of SNP databases | Q34185532 | ||
| A cluster of metabolic defects caused by mutation in a mitochondrial tRNA. | Q34551734 | ||
| Mechanisms of insulin resistance in humans and possible links with inflammation | Q36095510 | ||
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| Effects of purifying and adaptive selection on regional variation in human mtDNA. | Q39413917 | ||
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| Mitochondrial genotypes and cytochrome b variants associated with longevity or Parkinson's disease | Q45055025 | ||
| Deficiency of subsarcolemmal mitochondria in obesity and type 2 diabetes | Q45199109 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | mitochondrial DNA | Q27075 |
| P304 | page(s) | 54-61 | |
| P577 | publication date | 2006-05-24 | |
| P1433 | published in | American Journal of Human Genetics | Q4744249 |
| P1476 | title | Comprehensive association testing of common mitochondrial DNA variation in metabolic disease | |
| P478 | volume | 79 |
| Q42974496 | Associating mitochondrial DNA variation with complex traits |
| Q90437799 | Association between mitochondrial genetic variation and breast cancer risk: The Multiethnic Cohort |
| Q37120483 | Association of genetic variation in the mitochondrial genome with blood pressure and metabolic traits |
| Q39081292 | Association study of mitochondrial DNA polymorphisms with type 2 diabetes in Tunisian population |
| Q30586031 | Association testing of the mitochondrial genome using pedigree data |
| Q48261445 | Associations of mitochondrial polymorphisms with sporadic colorectal adenoma. |
| Q37785510 | Bioenergetics and the epigenome: Interface between the environment and genes in common diseases |
| Q30645106 | Bioenergetics in human evolution and disease: implications for the origins of biological complexity and the missing genetic variation of common diseases |
| Q41690287 | Chronic Exposure to Proline Causes Aminoacidotoxicity and Impaired Beta-Cell Function: Studies In Vitro |
| Q92839200 | Clinical and molecular features of a Han Chinese family with maternally transmitted hypertension |
| Q21563350 | Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits |
| Q30428008 | Common mitochondrial sequence variants in ischemic stroke |
| Q30414654 | Common variants within oxidative phosphorylation genes influence risk of ischemic stroke and intracerebral hemorrhage |
| Q57730637 | Common variation in oxidative phosphorylation genes is not a major cause of insulin resistance or type 2 diabetes |
| Q34238839 | Complete mitochondrial genome sequencing reveals novel haplotypes in a Polynesian population. |
| Q37023886 | Comprehensive analysis of common mitochondrial DNA variants and colorectal cancer risk |
| Q48503421 | Deep sequencing of the mitochondrial genome reveals common heteroplasmic sites in NADH dehydrogenase genes |
| Q36662396 | Differences in mtDNA haplogroup distribution among 3 Jewish populations alter susceptibility to T2DM complications. |
| Q35946513 | Direct linkage of mitochondrial genome variation to risk factors for type 2 diabetes in conplastic strains |
| Q34472544 | Disrupting mitochondrial-nuclear coevolution affects OXPHOS complex I integrity and impacts human health. |
| Q36334137 | Effects of mitochondrial haplogroup N9a on type 2 diabetes mellitus and its associated complications |
| Q35632855 | Energetics, epigenetics, mitochondrial genetics |
| Q34372631 | European mitochondrial DNA haplogroups and metabolic changes during antiretroviral therapy in AIDS Clinical Trials Group Study A5142 |
| Q47551902 | Examining the role of common and rare mitochondrial variants in schizophrenia |
| Q35164588 | Facile transfer of [2Fe-2S] clusters from the diabetes drug target mitoNEET to an apo-acceptor protein |
| Q39946547 | Family-based mitochondrial association study of traits related to type 2 diabetes and the metabolic syndrome in adolescents. |
| Q43826118 | Fifteen novel mutations in the mitochondrial NADH dehydrogenase subunit 1, 2, 3, 4, 4L, 5 and 6 genes from Iranian patients with Leber's hereditary optic neuropathy (LHON). |
| Q33963912 | Gene expression pattern in transmitochondrial cytoplasmic hybrid cells harboring type 2 diabetes-associated mitochondrial DNA haplogroups |
| Q24600599 | Genetic association analysis of 13 nuclear-encoded mitochondrial candidate genes with type II diabetes mellitus: the DAMAGE study |
| Q33957933 | Genetic association study of common mitochondrial variants on body fat mass |
| Q33956859 | Genome-wide association study of exercise behavior in Dutch and American adults |
| Q35062730 | Higd1a is a positive regulator of cytochrome c oxidase |
| Q37648855 | Human mitochondrial DNA: roles of inherited and somatic mutations |
| Q42707401 | IL-1β hampers glucose-stimulated insulin secretion in Cohen diabetic rat islets through mitochondrial cytochrome c oxidase inhibition by nitric oxide |
| Q42059192 | Identification of lactate dehydrogenase as a mammalian pyrroloquinoline quinone (PQQ)-binding protein |
| Q35024031 | Inherited common variants in mitochondrial DNA and invasive serous epithelial ovarian cancer risk |
| Q33614087 | Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies |
| Q42160127 | Japanese Alzheimer’s Disease and Other Complex Disorders Diagnosis Based on Mitochondrial SNP Haplogroups |
| Q39766391 | Just in Time: An Update on Continuum Neurogenetics |
| Q46511881 | Lack of relationship between mitochondrial heteroplasmy or variation and childhood obesity. |
| Q34000675 | Leber's hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation |
| Q36156560 | Male-specific association between MT-ND4 11719 A/G polymorphism and ulcerative colitis: a mitochondria-wide genetic association study |
| Q34667750 | MitoLSDB: a comprehensive resource to study genotype to phenotype correlations in human mitochondrial DNA variations |
| Q36724311 | Mitochondria as chi. |
| Q35162982 | Mitochondria-wide association study of common variants in osteoporosis |
| Q58773352 | Mitochondrial DNA Haplogroup JT is Related to Impaired Glycaemic Control and Renal Function in Type 2 Diabetic Patients |
| Q21135340 | Mitochondrial DNA backgrounds might modulate diabetes complications rather than T2DM as a whole |
| Q33792687 | Mitochondrial DNA haplogroups and risk of transient ischaemic attack and ischaemic stroke: a genetic association study |
| Q24657699 | Mitochondrial DNA haplogroups and type 2 diabetes: a study of 897 cases and 1010 controls |
| Q36231680 | Mitochondrial DNA heteroplasmy in diabetes and normal adults: role of acquired and inherited mutational patterns in twins. |
| Q55052993 | Mitochondrial DNA mutations in disease and aging. |
| Q33603868 | Mitochondrial DNA sequence associations with dementia and amyloid-β in elderly African Americans |
| Q35729786 | Mitochondrial DNA sequence variation and risk of pancreatic cancer |
| Q34140769 | Mitochondrial DNA sequence variation associated with dementia and cognitive function in the elderly |
| Q41844017 | Mitochondrial DNA sequence variation in multiple sclerosis. |
| Q33718097 | Mitochondrial DNA variants in the pathogenesis of type 2 diabetes - relevance of asian population studies |
| Q33443895 | Mitochondrial DNA variants of respiratory complex I that uniquely characterize haplogroup T2 are associated with increased risk of age-related macular degeneration |
| Q37721270 | Mitochondrial DNA variation in human metabolic rate and energy expenditure |
| Q35760460 | Mitochondrial Haplogroup T Is Associated with Obesity in Austrian Juveniles and Adults |
| Q92836097 | Mitochondrial Polymorphisms, in The D-Loop Area, Are Associated with Brain Tumors |
| Q36762165 | Mitochondrial content is central to nuclear gene expression: Profound implications for human health. |
| Q35632864 | Mitochondrial energetics and therapeutics |
| Q21131961 | Mitochondrial genetic variants identified to be associated with BMI in adults |
| Q34428180 | Mitochondrial genomic analysis of late onset Alzheimer's disease reveals protective haplogroups H6A1A/H6A1B: the Cache County Study on Memory in Aging |
| Q28390920 | Mitochondrial genomic variation associated with higher mitochondrial copy number: the Cache County Study on Memory Health and Aging |
| Q36937849 | Mitochondrial genomics and antiretroviral therapy-associated metabolic complications in HIV-infected Black South Africans: a pilot study |
| Q42930492 | Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation |
| Q35677807 | Mitochondrial haplogroup N9a confers resistance against type 2 diabetes in Asians |
| Q51788256 | Mitochondrial haplogroups associated with Japanese Alzheimer's patients |
| Q53303487 | Mitochondrial haplogroups associated with Japanese centenarians, Alzheimer's patients, Parkinson's patients, type 2 diabetic patients and healthy non-obese young males |
| Q64948586 | Mitochondrial miR-762 regulates apoptosis and myocardial infarction by impairing ND2. |
| Q22241837 | Mitochondrial modulators for bipolar disorder: A pathophysiologically informed paradigm for new drug development |
| Q33503932 | MtSNPscore: a combined evidence approach for assessing cumulative impact of mitochondrial variations in disease |
| Q33622660 | Multiplex analysis of mitochondrial DNA pathogenic and polymorphic sequence variants. |
| Q35327135 | Mutational analysis of the mitochondrial tRNA genes and flanking regions in umbilical cord tissue from uninfected infants receiving AZT-based therapies for prophylaxis of HIV-1. |
| Q35874327 | NADPH Inhibits [2Fe-2S] Cluster Protein Transfer from Diabetes Drug Target MitoNEET to an Apo-acceptor Protein |
| Q30532736 | No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controls |
| Q24624194 | Novel susceptibility loci for second primary tumors/recurrence in head and neck cancer patients: large-scale evaluation of genetic variants |
| Q38827762 | Ovarian ageing: the role of mitochondria in oocytes and follicles. |
| Q33470046 | Parental diabetes status reveals association of mitochondrial DNA haplogroup J1 with type 2 diabetes |
| Q26853274 | Perspectives on pharmacogenomics of antiretroviral medications and HIV-associated comorbidities |
| Q24647983 | Polymorphisms in mitochondrial genes and prostate cancer risk |
| Q36700182 | Power and SNP tagging in whole mitochondrial genome association studies |
| Q33301926 | Power to detect risk alleles using genome-wide tag SNP panels |
| Q34544496 | Principal-component analysis for assessment of population stratification in mitochondrial medical genetics |
| Q93649975 | Reply to Elson et al |
| Q60304737 | Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease |
| Q34658774 | Studies on the pathophysiology and genetic basis of migraine. |
| Q54188363 | Study on heteroplasmic variation and the effect of chicken mitochondrial ND2. |
| Q37080100 | The association of the mitochondrial DNA OriB variant (16184-16193 polycytosine tract) with type 2 diabetes in Europid populations |
| Q46675663 | The expression characteristics of mt-ND2 gene in chicken |
| Q34372347 | The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits |
| Q33434473 | The mitochondrial A10398G polymorphism, interaction with alcohol consumption, and breast cancer risk |
| Q33813322 | The mitochondrial T16189C polymorphism is associated with coronary artery disease in Middle European populations |
| Q27027887 | The other genome: a systematic review of studies of mitochondrial DNA haplogroups and outcomes of HIV infection and antiretroviral therapy |
| Q37287583 | The pathophysiology of mitochondrial disease as modeled in the mouse |
| Q34591630 | The role of the mitochondrial genome in ageing and carcinogenesis |
| Q34267442 | The saga of the many studies wrongly associating mitochondrial DNA with breast cancer |
| Q34829027 | The search for genetic risk factors of type 2 diabetes mellitus |
| Q40072966 | The use of common mitochondrial variants to detect and characterise population structure in the Australian population: implications for genome-wide association studies |
| Q41689696 | Transcribing β-cell mitochondria in health and disease |
| Q34831919 | Two common genetic variants near nuclear-encoded OXPHOS genes are associated with insulin secretion in vivo |
| Q33917423 | Using molecular classification to predict gains in maximal aerobic capacity following endurance exercise training in humans |
| Q43177334 | Variation and association to diabetes in 2000 full mtDNA sequences mined from an exome study in a Danish population |
| Q34525212 | mtDNA haplogroup and single nucleotide polymorphisms structure human microbiome communities |
| Q46210004 | mtDNA lineages reveal coronary artery disease-associated structures in the Lebanese population |
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