(Q34389694)

English

The case for the continuing use of the revised Cambridge Reference Sequence (rCRS) and the standardization of notation in human mitochondrial DNA studies

scientific article published on 5 December 2013

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

The case for the continuing use of the revised Cambridge Reference Sequence (rCRS) and the standardization of notation in human mitochondrial DNA studies (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

mitochondrial DNA

0 references

Martin B Richards

object named as

Martin B Richards

3

0 references

object named as

Yong-Gang Yao

4

0 references

Hans-Jürgen Bandelt

1

object named as

Hans-Jürgen Bandelt

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

author name string

Anita Kloss-Brandstätter

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Ian Logan

5

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

publication date

5 December 2013

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

59

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

66-77

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

A "Copernican" reassessment of the human mitochondrial DNA tree from its root

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

The role of selection in the evolution of human mitochondrial genomes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Mitochondrial genome variation and the origin of modern humans

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Harvesting the fruit of the human mtDNA tree

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

mtDNA tree Build 17 (18 Feb 2016)

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Median network analysis of defectively sequenced entire mitochondrial genomes from early and contemporary disease studies

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Normal variants of human mitochondrial DNA and translation products: the building of a reference data base

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

A novel mtDNA C11777A mutation in Leigh syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

New variants in the mitochondrial genomes of schizophrenic patients

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Exaggerated status of "novel" and "pathogenic" mtDNA sequence variants due to inadequate database searches

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Frequency of rare mitochondrial DNA mutations in patients with suspected Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Is cumulative frequency of mitochondrial DNA variants a biomarker for colorectal tumor progression?

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

The dawn of human matrilineal diversity

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Updating phylogeny of mitochondrial DNA macrohaplogroup m in India: dispersal of modern human in South Asian corridor

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Whole-mtDNA Genome Sequence Analysis of Ancient African Lineages

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Mitochondrial DNA signals of late glacial recolonization of Europe from near eastern refugia

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Is 8860 variation a rare polymorphism or associated as a secondary effect in HCM disease?

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Contrasting maternal and paternal histories in the linguistic context of Burkina Faso

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Mitochondrial DNA sequence variation in human evolution and disease.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Phylogeographic investigations: the role of trees in forensic genetics

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Consistent treatment of length variants in the human mtDNA control region: a reappraisal

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Transition m.3308T>C in the ND1 gene is associated with left ventricular hypertrabeculation/noncompaction.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Single nucleotide polymorphisms in the mitochondrial displacement loop and outcome of esophageal squamous cell carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Mitochondrial diversity within modern human populations

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

To trust or not to trust an idiosyncratic mitochondrial data set.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

mtDNA data mining in GenBank needs surveying

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Haplogrouping mitochondrial DNA sequences in Legal Medicine/Forensic Genetics

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Correcting for purifying selection: an improved human mitochondrial molecular clock

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

SNPedia: a wiki supporting personal genome annotation, interpretation and analysis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

ReseqChip: automated integration of multiple local context probe data from the MitoChip array in mitochondrial DNA sequence assembly

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Forensic application of the Affymetrix human mitochondrial resequencing array

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Mitochondrial variants in schizophrenia, bipolar disorder, and major depressive disorder

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Validation of microarray-based resequencing of 93 worldwide mitochondrial genomes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Mitochondrial genome sequence analysis: a custom bioinformatics pipeline substantially improves Affymetrix MitoChip v2.0 call rate and accuracy.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Insights into N-calls of mitochondrial DNA sequencing using MitoChip v2.0.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Analysis of mitochondrial DNA variants in Japanese patients with schizophrenia.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

No evidence that major mtDNA European haplogroups confer risk to schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Mitochondrial mutations and polymorphisms in psychiatric disorders

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

The role of mitochondrial dysfunction in psychiatric disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Functional effects of cancer mitochondria on energy metabolism and tumorigenesis: utility of transmitochondrial cybrids

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Impact of the mitochondrial genetic background in complex III deficiency

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Mitochondrial DNA G10398A polymorphism imparts maternal Haplogroup N a risk for breast and esophageal cancer.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Mitochondrial DNA G10398A variant is not associated with breast cancer in African-American women

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

mtDNA G10398A variant in African-American women with breast cancer provides resistance to apoptosis and promotes metastasis in mice

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

mtDNA sequence variants in subtypes of epithelial ovarian cancer stages in relation to ethnic and age difference

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Mitochondrial DNA haplogroups do not play a role in the variable phenotypic presentation of the A3243G mutation

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Multiplex genotyping system for efficient inference of matrilineal genetic ancestry with continental resolution

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Mitochondrial DNA backgrounds might modulate diabetes complications rather than T2DM as a whole

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Maternally inherited susceptibility to cancer

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Frequent mutations in the mitochondrial control region DNA in breast tissue

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Extended guidelines for mtDNA typing of population data in forensic science

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Median-joining networks for inferring intraspecific phylogenies

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Mitochondrial DNA recombination-no need to panic

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

A cautionary note on switching mitochondrial DNA reference sequences in forensic genetics

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

‘Distorted’ mitochondrial DNA sequences in schizophrenic patients

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Raising Doubts about the Pathogenicity of Mitochondrial DNA Mutation m.3308T>C in Left Ventricular Hypertraveculation/Noncompaction

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

Phylogeographic Analysis of Mitochondrial DNA in the Nogays: A Strong Mixture of Maternal Lineages from Eastern and Western Eurasia

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2013.120

21 January 2018

The acquisition of an inheritable 50-bp deletion in the human mtDNA control region does not affect the mtDNA copy number in peripheral blood cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Emerging Limbs and Twigs of the East Asian mtDNA Tree

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oxidative stress and sperm mitochondrial DNA mutation in idiopathic oligoasthenozoospermic men.

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA in pathogenesis of Alzheimer's and Parkinson's diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Direct detection of multiple point mutations in mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of mitochondrial DNA variations in Indian patients with congenital cataract

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA variant A4917G, smoking and spontaneous preterm birth

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Misanalysis gave false association of mtDNA mutations with infertility

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Do alterations in mitochondrial DNA play a role in breast carcinogenesis?

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequent D-loop polymorphism in mtDNA enables genotyping of 1400-year-old human remains from Merowingian graves

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High incidence of single nucleotide substitutions in the mitochondrial genome is associated with poor semen parameters in men

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Corrections to the human mitochondrial ribosomal RNA sequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phylogeography of mitochondrial DNA in western Europe

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of sequence polymorphism in the D-Loop region of mitochondrial DNA as a risk factor for hepatocellular carcinoma with distinct etiology

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A combination of three common inherited mitochondrial DNA polymorphisms promotes longevity in Finnish and Japanese subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifying potential pitfalls in interpreting mitochondrial DNA mutations of male infertility cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Necessity of nuclear and mitochondrial genome analysis prior to assisted reproductive techniques/intracytoplasmic sperm injection

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phylogeografic analysis of mitochondrial DNA Nogays: the high level of mixture of maternal lineages from Eastern and Western Eurasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Genographic Project public participation mitochondrial DNA database

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA analysis in primary congenital glaucoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence analysis of the entire mitochondrial genome in Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA mutations in patients with myelodysplastic syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of Y chromosome microdeletions and mitochondrial DNA mutations in male infertility patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial cardiomyopathy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The possible role of 10398A and 16189C mtDNA variants in providing susceptibility to T2DM in two North Indian populations: a replicative study

1 reference

https://pubmed.ncbi.nlm.nih.gov/24304692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/JHG.2013.120

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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