Cargando…

Evaluating the suitability of current mitochondrial DNA interpretation guidelines for multigenerational whole mitochondrial genome comparisons

Sanger sequencing of the mitochondrial DNA (mtDNA) control region was previously the only method available for forensic casework involving degraded samples from skeletal remains. The introduction of Next Generation Sequencing (NGS) has transformed genetic data generation and human identification usi...

Descripción completa

Detalles Bibliográficos
Autores principales:	Connell, Jasmine R., Benton, Miles C., Lea, Rodney A., Sutherland, Heidi G., Haupt, Larisa M., Wright, Kirsty M., Griffiths, Lyn R.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Original Papers
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543078/ https://www.ncbi.nlm.nih.gov/pubmed/35855536 http://dx.doi.org/10.1111/1556-4029.15097

Ejemplares similares

Gene‐centric analysis implicates nuclear encoded mitochondrial protein gene variants in migraine susceptibility
por: Stuart, Shani, et al.
Publicado: (2017)

Methylome-wide association study of whole blood DNA in the Norfolk Island isolate identifies robust loci associated with age
por: Benton, Miles C., et al.
Publicado: (2017)

Exploring the Functional Basis of Epigenetic Aging in Relation to Body Fat Phenotypes in the Norfolk Island Cohort
por: Cao, Thao Van, et al.
Publicado: (2023)

Genome-wide allele-specific methylation is enriched at gene regulatory regions in a multi-generation pedigree from the Norfolk Island isolate
por: Benton, Miles C., et al.
Publicado: (2019)

Pedigree derived mutation rate across the entire mitochondrial genome of the Norfolk Island population
por: Connell, J. R., et al.
Publicado: (2022)

Genetic and epigenetic variants in the MTHFR gene are not associated with non-Hodgkin lymphoma
por: Bradshaw, Gabrielle, et al.
Publicado: (2015)

Single Nucleotide Polymorphisms in MIR143 Contribute to Protection against Non-Hodgkin Lymphoma (NHL) in Caucasian Populations
por: Bradshaw, Gabrielle, et al.
Publicado: (2019)

Complete Mitochondrial Genome Sequencing Reveals Novel Haplotypes in a Polynesian Population
por: Benton, Miles, et al.
Publicado: (2012)

Correction: Complete Mitochondrial Genome Sequencing Reveals Novel Haplotypes in a Polynesian Population
por: Benton, Miles, et al.
Publicado: (2012)

Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes
por: Dunn, Paul, et al.
Publicado: (2018)

Ion torrent high throughput mitochondrial genome sequencing (HTMGS)
por: Harvey, N. R., et al.
Publicado: (2019)

Investigating a Genetic Link Between Alzheimer’s Disease and CADASIL-Related Cerebral Small Vessel Disease
por: Dunn, Paul J., et al.
Publicado: (2022)

Exonic mutations in cell–cell adhesion may contribute to CADASIL-related CSVD pathology
por: Dunn, Paul J., et al.
Publicado: (2023)

Dysregulated MicroRNA Expression Profiles and Potential Cellular, Circulating and Polymorphic Biomarkers in Non-Hodgkin Lymphoma
por: Bradshaw, Gabrielle, et al.
Publicado: (2016)

A CREB1 Gene Polymorphism (rs2253206) Is Associated with Prospective Memory in a Healthy Cohort
por: Avgan, Nesli, et al.
Publicado: (2017)

Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney disease
por: Tran, Ngan K., et al.
Publicado: (2021)

Comprehensive Exonic Sequencing of Known Ataxia Genes in Episodic Ataxia
por: Maksemous, Neven, et al.
Publicado: (2020)

The NRP1 migraine risk variant shows evidence of association with menstrual migraine
por: Pollock, Charmaine E., et al.
Publicado: (2018)

Exploring Neuronal Vulnerability to Head Trauma Using a Whole Exome Approach
por: Ibrahim, Omar, et al.
Publicado: (2020)

Exome Sequencing Diagnoses X-Linked Moesin-Associated Immunodeficiency in a Primary Immunodeficiency Case
por: Bradshaw, Gabrielle, et al.
Publicado: (2018)

Suitability of Chinese oak silkworm eggs for the multigenerational rearing of the parasitoid Trichogramma leucaniae
por: Xu, Wei, et al.
Publicado: (2020)

Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
por: Matovinovic, Elizabeth, et al.
Publicado: (2017)

Epigenetic Regulation of miR-92a and TET2 and Their Association in Non-Hodgkin Lymphoma
por: Elliott, Esther K., et al.
Publicado: (2021)

A Potential Epigenetic Marker Mediating Serum Folate and Vitamin B(12) Levels Contributes to the Risk of Ischemic Stroke
por: Keat Wei, Loo, et al.
Publicado: (2015)

Accounting for cell lineage and sex effects in the identification of cell-specific DNA methylation using a Bayesian model selection algorithm
por: White, Nicole, et al.
Publicado: (2017)

Genetic association analysis of miRNA SNPs implicates MIR145 in breast cancer susceptibility
por: Chacon-Cortes, Diego, et al.
Publicado: (2015)

Case-control study of ADARB1 and ADARB2 gene variants in migraine
por: Gasparini, Claudia F, et al.
Publicado: (2015)

Investigation of Mitochondrial Related Variants in a Cerebral Small Vessel Disease Cohort
por: Dunn, P. J., et al.
Publicado: (2022)

Investigating the influence of mtDNA and nuclear encoded mitochondrial variants on high intensity interval training outcomes
por: Harvey, N. R., et al.
Publicado: (2020)

Review: Alternative Splicing (AS) of Genes As An Approach for Generating Protein Complexity
por: Roy, Bishakha, et al.
Publicado: (2013)

Exploiting Heparan Sulfate Proteoglycans in Human Neurogenesis—Controlling Lineage Specification and Fate
por: Yu, Chieh, et al.
Publicado: (2017)

Comprehensive Exonic Sequencing of Hemiplegic Migraine-Related Genes in a Cohort of Suspected Probands Identifies Known and Potential Pathogenic Variants
por: Sutherland, Heidi G., et al.
Publicado: (2020)

The Multigenerational Sales Team
por: Shiver, Warren
Publicado: (2017)

Critical evaluation of linear regression models for cell-subtype specific methylation signal from mixed blood cell DNA
por: Kennedy, Daniel W., et al.
Publicado: (2018)

NTP Multigenerational Study of Environmental Estrogens
por: Barrett, Julia R.
Publicado: (2006)

A Multigenerational View of Inequality
por: Mare, Robert D.
Publicado: (2011)

Multigenerational and Transgenerational Effects of Dioxins
por: Viluksela, Matti, et al.
Publicado: (2019)

In silico analyses reveal common cellular pathways affected by loss of heterozygosity (LOH) events in the lymphomagenesis of Non-Hodgkin’s lymphoma (NHL)
por: Aya-Bonilla, Carlos, et al.
Publicado: (2014)

BDNF Variants May Modulate Long-Term Visual Memory Performance in a Healthy Cohort
por: Avgan, Nesli, et al.
Publicado: (2017)

Targeted next generation sequencing identifies novel NOTCH3 gene mutations in CADASIL diagnostics patients
por: Maksemous, Neven, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_i3kt11ah868fl3b1uol8og7m7n