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Mito-nuclear effects uncovered in admixed populations

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/0471142905.hg0123s76openalex-snapshot

Overview of Admixture Mapping

inferredcites →https://doi.org/10.1002/0471250953.bi1112s47openalex-snapshot

BEDTools: The Swiss‐Army Tool for Genome Feature Analysis

inferredcites →https://doi.org/10.1002/ajpa.10071openalex-snapshot

Unequal contributions of male and female gene pools from parental populations in the African descendants of the city of Melo, Uruguay

inferredcites →https://doi.org/10.1002/bies.200900162openalex-snapshot

Speciation through cytonuclear incompatibility: Insights from yeast and implications for higher eukaryotes

inferredcites →https://doi.org/10.1002/bies.201500008openalex-snapshot

Mitochondrial replacement therapy: Cautiously replace the master manipulator

inferredcites →https://doi.org/10.1002/humu.21382openalex-snapshot

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

inferredcites →https://doi.org/10.1002/pro.5560020202openalex-snapshot

The protein import machinery of mitochondria

inferredcites →https://doi.org/10.1007/s00125-009-1412-xopenalex-snapshot

Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes

inferredcites →https://doi.org/10.1007/s00439-006-0261-7openalex-snapshot

Elevated male European and female African contributions to the genomes of African American individuals

inferredcites →https://doi.org/10.1007/s00439-014-1458-9openalex-snapshot

Mitochondrial DNA copy number in peripheral blood cells declines with age and is associated with general health among elderly

inferredcites →https://doi.org/10.1016/bs.enz.2016.03.006openalex-snapshot

Animal Mitochondrial DNA Replication

inferredcites →https://doi.org/10.1016/j.ajhg.2013.06.020openalex-snapshot

RFMix: A Discriminative Modeling Approach for Rapid and Robust Local-Ancestry Inference

inferredcites →https://doi.org/10.1016/j.ajhg.2014.11.010openalex-snapshot

The Genetic Ancestry of African Americans, Latinos, and European Americans across the United States

inferredcites →https://doi.org/10.1016/j.ajhg.2017.03.004openalex-snapshot

Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations

inferredcites →https://doi.org/10.1016/j.bbadis.2013.10.016openalex-snapshot

Molecular and bioenergetic differences between cells with African versus European inherited mitochondrial DNA haplogroups: Implications for population susceptibility to diseases

inferredcites →https://doi.org/10.1016/j.biocel.2004.09.010openalex-snapshot

Mitochondrial biogenesis and mitochondrial DNA maintenance of mammalian cells under oxidative stress

inferredcites →https://doi.org/10.1016/j.cancergencyto.2006.10.010openalex-snapshot

Copy number increase of 1p36.33 and mitochondrial genome amplification in Epstein–Barr virus-transformed lymphoblastoid cell lines

inferredcites →https://doi.org/10.1016/j.cell.2008.06.016openalex-snapshot

A Mitochondrial Protein Compendium Elucidates Complex I Disease Biology

inferredcites →https://doi.org/10.1016/j.cell.2008.10.047openalex-snapshot

Incompatibility of Nuclear and Mitochondrial Genomes Causes Hybrid Sterility between Two Yeast Species

inferredcites →https://doi.org/10.1016/j.evolhumbehav.2011.10.008openalex-snapshot

Means, variances, and ranges in reproductive success: comparative evidence

inferredcites →https://doi.org/10.1016/j.lfs.2011.05.010openalex-snapshot

Generation, function and diagnostic value of mitochondrial DNA copy number alterations in human cancers

inferredcites →https://doi.org/10.1016/j.mito.2012.10.011openalex-snapshot

Is mitochondrial DNA content a potential biomarker of mitochondrial dysfunction?

inferredcites →https://doi.org/10.1016/j.mito.2014.01.002openalex-snapshot

Upregulation of TFAM and mitochondria copy number in human lymphoblastoid cells

inferredcites →https://doi.org/10.1016/j.molmed.2014.12.001openalex-snapshot

Mitochondrial replacement therapy in reproductive medicine

inferredcites →https://doi.org/10.1016/j.tree.2004.10.003openalex-snapshot

Cytonuclear coevolution: the genomics of cooperation

inferredcites →https://doi.org/10.1016/j.tree.2009.02.005openalex-snapshot

Bateman's principles and human sex roles

inferredcites →https://doi.org/10.1016/s0092-8674(00)80310-4openalex-snapshot

Neandertal DNA Sequences and the Origin of Modern Humans

inferredcites →https://doi.org/10.1016/s0092-8674(00)80611-xopenalex-snapshot

Mechanisms Controlling Mitochondrial Biogenesis and Respiration through the Thermogenic Coactivator PGC-1

inferredcites →https://doi.org/10.1038/35073006openalex-snapshot

Versatility of the mitochondrial protein import machinery

inferredcites →https://doi.org/10.1038/nature15393openalex-snapshot

A global reference for human genetic variation

inferredcites →https://doi.org/10.1038/ng0205-118openalex-snapshot

The beauty of admixture

inferredcites →https://doi.org/10.1038/nrm.2016.23openalex-snapshot

Mitonuclear communication in homeostasis and stress

inferredcites →https://doi.org/10.1038/srep35859openalex-snapshot

Altered mitochondrial DNA copy number contributes to human cancer risk: evidence from an updated meta-analysis

inferredcites →https://doi.org/10.1042/bst20120227openalex-snapshot

Beyond retrograde and anterograde signalling: mitochondrial–nuclear interactions as a means for evolutionary adaptation and contemporary disease susceptibility

inferredcites →https://doi.org/10.1042/bst20160162openalex-snapshot

Mitochondrial DNA replication: a PrimPol perspective

inferredcites →https://doi.org/10.1073/pnas.0136972100openalex-snapshot

Natural selection shaped regional mtDNA variation in humans

inferredcites →https://doi.org/10.1073/pnas.0510452103openalex-snapshot

Calorie restriction induces mitochondrial biogenesis and bioenergetic efficiency

inferredcites →https://doi.org/10.1073/pnas.202335899openalex-snapshot

Functional coadaptation between cytochrome c and cytochrome c oxidase within allopatric populations of a marine copepod

inferredcites →https://doi.org/10.1073/pnas.91.18.8334openalex-snapshot

Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio.

inferredcites →https://doi.org/10.1086/303004openalex-snapshot

The Ancestry of Brazilian mtDNA Lineages

inferredcites →https://doi.org/10.1086/316935openalex-snapshot

Population Structure in Admixed Populations: Effect of Admixture Dynamics on the Pattern of Linkage Disequilibrium

inferredcites →https://doi.org/10.1086/518564openalex-snapshot

A Genomewide Admixture Mapping Panel for Hispanic/Latino Populations

inferredcites →https://doi.org/10.1086/519795openalex-snapshot

PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses

inferredcites →https://doi.org/10.1093/gbe/evu208openalex-snapshot

Disrupting Mitochondrial–Nuclear Coevolution Affects OXPHOS Complex I Integrity and Impacts Human Health

inferredcites →https://doi.org/10.1093/gbe/evx114openalex-snapshot

The Mitonuclear Dimension of Neanderthal and Denisovan Ancestry in Modern Human Genomes

inferredcites →https://doi.org/10.1093/genetics/127.2.417openalex-snapshot

The genetic structure of admixed populations.

inferredcites →https://doi.org/10.1093/genetics/164.1.187openalex-snapshot

Mitochondrial Genotype Affects Fitness in Drosophila simulans

inferredcites →https://doi.org/10.1093/molbev/msh031openalex-snapshot

Evolution of Interacting Proteins in the Mitochondrial Electron Transport System in a Marine Copepod

inferredcites →https://doi.org/10.1093/molbev/msr211openalex-snapshot

Mitochondrial–Nuclear Interactions and Accelerated Compensatory Evolution: Evidence from the Primate Cytochrome c Oxidase Complex

inferredcites →https://doi.org/10.1093/molbev/mss228openalex-snapshot

Evidence for Compensatory Evolution of Ribosomal Proteins in Response to Rapid Divergence of Mitochondrial rRNA

inferredcites →https://doi.org/10.1093/molbev/msw246openalex-snapshot

Mitonuclear Interactions Mediate Transcriptional Responses to Hypoxia inDrosophila

inferredcites →https://doi.org/10.1093/nar/gkv1003openalex-snapshot

MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins

inferredcites →https://doi.org/10.1098/rspb.2009.0752openalex-snapshot

Climate shaped the worldwide distribution of human mitochondrial DNA sequence variation

inferredcites →https://doi.org/10.1098/rspb.2013.1521openalex-snapshot

Elevated oxidative damage is correlated with reduced fitness in interpopulation hybrids of a marine copepod

inferredcites →https://doi.org/10.1098/rspb.2015.1704openalex-snapshot

Mitonuclear linkage disequilibrium in human populations

inferredcites →https://doi.org/10.1098/rstb.2013.0443openalex-snapshot

Mitonuclear interactions: evolutionary consequences over multiple biological scales

inferredcites →https://doi.org/10.1101/095596openalex-snapshot

Mitochondrial-nuclear interactions maintain geographic separation of deeply diverged mitochondrial lineages in the face of nuclear gene flow

inferredcites →https://doi.org/10.1101/cshperspect.a012971openalex-snapshot

Human Mitochondrial DNA Replication

inferredcites →https://doi.org/10.1101/gr.094052.109openalex-snapshot

Fast model-based estimation of ancestry in unrelated individuals

inferredcites →https://doi.org/10.1101/gr.154831.113openalex-snapshot

Estimating and interpreting F ST : The impact of rare variants

inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb00243.xopenalex-snapshot

CYTONUCLEAR COADAPTATION IN DROSOPHILA: DISRUPTION OF CYTOCHROME C OXIDASE ACTIVITY IN BACKCROSS GENOTYPES

inferredcites →https://doi.org/10.1111/j.1420-9101.2009.01917.xopenalex-snapshot

Cytonuclear conflict in interpopulation hybrids: the role of RNA polymerase in mtDNA transcription and replication

inferredcites →https://doi.org/10.1111/j.1558-5646.2007.00305.xopenalex-snapshot

INTERPOPULATION HYBRID BREAKDOWN MAPS TO THE MITOCHONDRIAL GENOME

inferredcites →https://doi.org/10.1111/j.1558-5646.2010.01077.xopenalex-snapshot

MITOCHONDRIAL-NUCLEAR EPISTASIS AFFECTS FITNESS WITHIN SPECIES BUT DOES NOT CONTRIBUTE TO FIXED INCOMPATIBILITIES BETWEEN SPECIES OF DROSOPHILA

inferredcites →https://doi.org/10.1111/mec.12006openalex-snapshot

A disproportionate role for mt DNA in D obzhansky– M uller incompatibilities?

inferredcites →https://doi.org/10.1126/science.1078311openalex-snapshot

Genetic Structure of Human Populations

inferredcites →https://doi.org/10.1126/science.1237146openalex-snapshot

Mitochondrial Replacement, Evolution, and the Clinic

inferredcites →https://doi.org/10.1126/science.296.5566.261bopenalex-snapshot

A Human Genome Diversity Cell Line Panel

inferredcites →https://doi.org/10.1146/annurev.biochem.76.081205.150955openalex-snapshot

Why Do We Still Have a Maternally Inherited Mitochondrial DNA? Insights from Evolutionary Medicine

inferredcites →https://doi.org/10.1186/1471-2148-8-213openalex-snapshot

Genetic origin, admixture, and asymmetry in maternal and paternal human lineages in Cuba

inferredcites →https://doi.org/10.1186/1471-2164-13-477openalex-snapshot

In depth comparison of an individual’s DNA and its lymphoblastoid cell line using whole genome sequencing

inferredcites →https://doi.org/10.1186/s12864-017-3539-3openalex-snapshot

Implications of human evolution and admixture for mitochondrial replacement therapy

inferredcites →https://doi.org/10.1186/s13742-015-0047-8openalex-snapshot

Second-generation PLINK: rising to the challenge of larger and richer datasets

inferredcites →https://doi.org/10.1201/9781317952268openalex-snapshot

Human Evolutionary Genetics

inferredcites →https://doi.org/10.1353/hub.2007.0024openalex-snapshot

Sex-Specific Genetic Admixture of Mestizos, Amerindian Kichwas, and Afro-Ecuadorans from Ecuador

inferredcites →https://doi.org/10.1371/journal.pbio.0020057openalex-snapshot

No Evidence of Neandertal mtDNA Contribution to Early Modern Humans

inferredcites →https://doi.org/10.1371/journal.pbio.1000432openalex-snapshot

Multiple Molecular Mechanisms Cause Reproductive Isolation between Three Yeast Species

inferredcites →https://doi.org/10.1371/journal.pgen.1000474openalex-snapshot

Ancient mtDNA Genetic Variants Modulate mtDNA Transcription and Replication

inferredcites →https://doi.org/10.1371/journal.pgen.1003238openalex-snapshot

An Incompatibility between a Mitochondrial tRNA and Its Nuclear-Encoded tRNA Synthetase Compromises Development and Fitness in Drosophila

inferredcites →https://doi.org/10.1371/journal.pgen.1003925openalex-snapshot

Reconstructing the Population Genetic History of the Caribbean

inferredcites →https://doi.org/10.1371/journal.pgen.1004572openalex-snapshot

Admixture in Latin America: Geographic Structure, Phenotypic Diversity and Self-Perception of Ancestry Based on 7,342 Individuals

inferredcites →https://doi.org/10.1371/journal.pgen.1005602openalex-snapshot

Genomic Insights into the Ancestry and Demographic History of South America

inferredcites →https://doi.org/10.1371/journal.pgen.1006517openalex-snapshot

Evolved genetic and phenotypic differences due to mitochondrial-nuclear interactions

inferredcites →https://doi.org/10.1371/journal.pmed.1001779openalex-snapshot

UK Biobank: An Open Access Resource for Identifying the Causes of a Wide Range of Complex Diseases of Middle and Old Age

inferredcites →https://doi.org/10.1534/genetics.105.052050openalex-snapshot

Intergenomic Epistasis for Fitness: Within-Population Interactions Between Cytoplasmic and Nuclear Genes in Drosophila melanogaster

inferredcites →https://doi.org/10.1534/genetics.113.154914openalex-snapshot

Pleiotropic Effects of a Mitochondrial–Nuclear Incompatibility Depend upon the Accelerating Effect of Temperature in Drosophila

inferredcites →https://doi.org/10.1534/genetics.116.196436openalex-snapshot

Mitochondrial Replacement Therapy: Are Mito-nuclear Interactions Likely To Be a Problem?

inferredcites →https://doi.org/10.1554/06-210.1openalex-snapshot

DISRUPTION OF MITOCHONDRIAL FUNCTION IN INTERPOPULATION HYBRIDS OF TIGRIOPUS CALIFORNICUS

inferredcites →https://doi.org/10.2147/agg.s128824openalex-snapshot

Differences between the genomes of lymphoblastoid cell lines and blood-derived samples

inferredcites →https://doi.org/10.3389/fgene.2014.00448openalex-snapshot

Mito-nuclear co-evolution: the positive and negative sides of functional ancient mutations

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1111/brv.12493openalex-snapshot

Assessing the fitness consequences of mitonuclear interactions in natural populations

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