(Q37948858)

25 August 2017

Do genome-wide association scans have potential for translation? (English)

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genome-wide association study

25 August 2017

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author

Eleftheria Zeggini

2

1 reference

PubMed ID

22022988

25 August 2017

Kalliope Panoutsopoulou

3

object named as

Kalliope Panoutsopoulou

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author name string

Margarida C Lopes

1

1 reference

PubMed ID

22022988

25 August 2017

Kalliope Panoutsopoulou

3

1 reference

25 August 2017

25 October 2011

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Clinical Chemistry and Laboratory Medicine

25 August 2017

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25 August 2017

50

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25 August 2017

2

1 reference

25 August 2017

255-260

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A polymorphic DNA marker genetically linked to Huntington's disease

25 August 2017

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Clinical implications of a molecular genetic classification of monogenic beta-cell diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Learning from molecular genetics: novel insights arising from the definition of genes for monogenic and type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

A genetic diagnosis of HNF1A diabetes alters treatment and improves glycaemic control in the majority of insulin-treated patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Contrasting diabetes phenotypes associated with hepatocyte nuclear factor-1alpha and -1beta mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

The continuum of translation research in genomic medicine: how can we accelerate the appropriate integration of human genome discoveries into health care and disease prevention?

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Translational research in cancer genetics: the road less traveled

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

The path from genome-based research to population health: development of an international public health genomics network

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Realizing the promise of genomics in biomedical research

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Soluble and tissue biomarkers in ankylosing spondylitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Where are you going, where have you been: a recent history of the direct-to-consumer genetic testing market

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Genetic correction of PSA values using sequence variants associated with PSA levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Common and rare variants in multifactorial susceptibility to common diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Prediction and interaction in complex disease genetics: experience in type 1 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Finding the missing heritability of complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Value of genetic profiling for the prediction of coronary heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

A common allele on chromosome 9 associated with coronary heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

A common variant on chromosome 9p21 affects the risk of myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Chromosome 9p21.3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Polymorphisms associated with cholesterol and risk of cardiovascular events

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Stimulation of adipogenesis in fibroblasts by PPAR gamma 2, a lipid-activated transcription factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Sulfated glycans stimulate endocytosis of the cellular isoform of the prion protein, PrPC, in cultured cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

A genome-wide association study identifies novel risk loci for type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

In vivo expression and functional characterization of the zinc transporter ZnT8 in glucose-induced insulin secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Phenotype-genotype relationships in monogenic disease: lessons from the thalassaemias.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Human fetal hemoglobin expression is regulated by the developmental stage-specific repressor BCL11A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Developmental and species-divergent globin switching are driven by BCL11A

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

In vitro differential sensitivity of melanomas to phenothiazines is based on the presence of codon 600 BRAF mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

HLA-B*5701 screening for hypersensitivity to abacavir

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Variation in TCF7L2 influences therapeutic response to sulfonylureas: a GoDARTs study

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

Integration of genetic, clinical, and INR data to refine warfarin dosing

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2011.748

21 January 2018

Identifiers

DOI

10.1515/CCLM.2011.748

1 reference

25 August 2017

1 reference

PubMed ID

22022988