(Q40767246)

23 September 2017

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Genome-wide association study of serum coenzyme Q10 levels identifies susceptibility loci linked to neuronal diseases (English)

1 reference

genome-wide association study

23 September 2017

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1 reference

8

Tõnu Esko

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23 September 2017

10

Andre Franke

1 reference

23 September 2017

Frauke Degenhardt

1

1 reference

23 September 2017

Petra Niklowitz

2

1 reference

23 September 2017

Silke Szymczak

3

1 reference

23 September 2017

Gunnar Jacobs

4

1 reference

23 September 2017

Wolfgang Lieb

5

1 reference

23 September 2017

Thomas Menke

6

1 reference

23 September 2017

Matthias Laudes

7

1 reference

23 September 2017

Stephan Weidinger

9

1 reference

23 September 2017

Frank Döring

11

1 reference

23 September 2017

Simone Onur

12

1 reference

23 September 2017

5 May 2016

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23 September 2017

Human Molecular Genetics

1 reference

23 September 2017

25

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23 September 2017

13

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23 September 2017

2881-2891

1 reference

describes a project that uses

23 September 2017

genome-wide association study

1 reference

based on heuristic

inferred from title

cites work

Biochemical functions of coenzyme Q10

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Coenzyme Q--biosynthesis and functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Coenzyme Q10 affects expression of genes involved in cell signalling, metabolism and transport in human CaCo-2 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Identification of LPS-inducible genes downregulated by ubiquinone in human THP-1 monocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

The impact of alpha-lipoic acid, coenzyme Q10 and caloric restriction on life span and gene expression patterns in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Effects of Coenzyme Q10 on TNF-alpha secretion in human and murine monocytic cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Influence of Coenzyme Q_{10} on release of pro-inflammatory chemokines in the human monocytic cell line THP-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

In Vitro Effects of the Reduced Form of Coenzyme Q(10) on Secretion Levels of TNF-alpha and Chemokines in Response to LPS in the Human Monocytic Cell Line THP-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Plasma membrane ubiquinone controls ceramide production and prevents cell death induced by serum withdrawal

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

N-acetylcysteine, coenzyme Q10 and superoxide dismutase mimetic prevent mitochondrial cell dysfunction and cell death induced by d-galactosamine in primary culture of human hepatocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

The diversity of coenzyme Q function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Biochemical, physiological and medical aspects of ubiquinone function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

The antioxidant role of coenzyme Q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Genetic bases and clinical manifestations of coenzyme Q10 (CoQ 10) deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Mutations in coenzyme Q10 biosynthetic genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

21 January 2018

Human CoQ10 deficiencies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Heterogeneity of coenzyme Q10 deficiency: patient study and literature review

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

An atlas of genetic influences on human blood metabolites

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Determination of the coenzyme Q10 status in a large Caucasian study population

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

The membrane-type collectin CL-P1 is a scavenger receptor on vascular endothelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Possible role of scavenger receptor SRCL in the clearance of amyloid-beta in Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Mutation analysis of the NRXN1 gene in a Chinese autism cohort.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Identification, molecular characterization, and chromosomal localization of the cDNA encoding a novel leucine zipper motif-containing protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Association between schizophrenia and genetic variation in DCC: a case-control study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Dynamin protein in stroke and vascular dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

DCC (deleted in colorectal carcinoma) gene variants confer increased susceptibility to gallbladder cancer (Ref. No.: Gene-D-12-01446).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

HNF4A mutation: switch from hyperinsulinaemic hypoglycaemia to maturity-onset diabetes of the young, and incretin response

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Identification and characterization of human endometase (Matrix metalloproteinase-26) from endometrial tumor

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Matrix metalloproteinase-26 (matrilysin-2) expression is high in endometrial hyperplasia and decreases with loss of histological differentiation in endometrial cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Biological, clinical and population relevance of 95 loci for blood lipids

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Isolation and expression profiling of genes upregulated in bone marrow-derived mononuclear cells of rheumatoid arthritis patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Association between genetic variants in the Coenzyme Q10 metabolism and Coenzyme Q10 status in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

PopGen: population-based recruitment of patients and controls for the analysis of complex genotype-phenotype relationships

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

IL-6 blockade by monoclonal antibodies inhibits apolipoprotein (a) expression and lipoprotein (a) synthesis in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

PLINK: a tool set for whole-genome association and population-based linkage analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Fast principal component analysis of large-scale genome-wide data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

A linear complexity phasing method for thousands of genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Genotype imputation for genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

A new multipoint method for genome-wide association studies by imputation of genotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

GWAMA: software for genome-wide association meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Genetic structure of Europeans: a view from the North-East

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

Defining the role of common variation in the genomic and biological architecture of adult human height

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

An integrated map of genetic variation from 1,092 human genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

LocusZoom: regional visualization of genome-wide association scan results

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW134

21 January 2018

Identifiers

0 references

1 reference