(Q37689829)

22 August 2017

0 references

Lessons and Implications from Genome-Wide Association Studies (GWAS) Findings of Blood Cell Phenotypes (English)

1 reference

genome-wide association study

22 August 2017

0 references

author name string

Nathalie Chami

series ordinal

1

1 reference

PMC publication ID

3978511

22 August 2017

Guillaume Lettre

series ordinal

2

1 reference

22 August 2017

27 January 2014

1 reference

22 August 2017

1 reference

22 August 2017

5

1 reference

22 August 2017

1

1 reference

22 August 2017

51-64

1 reference

Creative Commons Attribution 4.0 International

22 August 2017

start time

27 January 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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23 August 2017

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JAK2 Allele Burden in the Myeloproliferative Neoplasms: Effects on Phenotype, Prognosis and Change with Treatment.

23 August 2017

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Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network

23 August 2017

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GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children

23 August 2017

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Seventy-five genetic loci influencing the human red blood cell

23 August 2017

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Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.

23 August 2017

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Linking disease associations with regulatory information in the human genome

23 August 2017

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Systematic localization of common disease-associated variation in regulatory DNA

23 August 2017

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An integrated encyclopedia of DNA elements in the human genome

23 August 2017

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Cyclin D3 coordinates the cell cycle during differentiation to regulate erythrocyte size and number

23 August 2017

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Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study

23 August 2017

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A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans

23 August 2017

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New gene functions in megakaryopoiesis and platelet formation

23 August 2017

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HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants

23 August 2017

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Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network

23 August 2017

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Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry

23 August 2017

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Correction of sickle cell disease in adult mice by interference with fetal hemoglobin silencing

23 August 2017

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A high-resolution map of human evolutionary constraint using 29 mammals

23 August 2017

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Multiple loci are associated with white blood cell phenotypes

23 August 2017

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Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).

23 August 2017

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Identification of nine novel loci associated with white blood cell subtypes in a Japanese population

23 August 2017

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Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans.

23 August 2017

1 reference

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Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation

23 August 2017

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The NIH Roadmap Epigenomics Mapping Consortium

23 August 2017

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A method and server for predicting damaging missense mutations

23 August 2017

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Advances in the understanding of haemoglobin switching

23 August 2017

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A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E

23 August 2017

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Genome-wide association study of hematological and biochemical traits in a Japanese population

23 August 2017

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BioGPS: an extensible and customizable portal for querying and organizing gene annotation resources

23 August 2017

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Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

23 August 2017

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Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels

23 August 2017

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A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium

23 August 2017

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Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

23 August 2017

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Mapping complex disease traits with global gene expression

23 August 2017

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A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function

23 August 2017

1 reference

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Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

A genome-wide association study identifies three loci associated with mean platelet volume

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

Hematopoiesis: an evolving paradigm for stem cell biology

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

Mendelian randomization: can genetic epidemiology help redress the failures of observational epidemiology?

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

Heritability of cardiovascular and personality traits in 6,148 Sardinians

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

Leukocytes and coronary heart disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

An erythroid enhancer of BCL11A subject to genetic variation determines fetal hemoglobin level.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

The search for genetic modifiers of disease severity in the β-hemoglobinopathies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

Ischaemic stroke: a thrombo-inflammatory disease?

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

JAK2 V617F and beyond: role of genetics and aberrant signaling in the pathogenesis of myeloproliferative neoplasms

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

Modifier genes in Mendelian disorders: the example of hemoglobin disorders

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

Pathophysiology of anemia

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

Genetics. GWAS to therapy by genome edits?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

The genetic basis of myeloproliferative disorders

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humans.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

Determinants and characteristics of mean corpuscular volume and hemoglobin concentration in white HFE C282Y homozygotes in the hemochromatosis and iron overload screening study.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

Evidence for linkage of red blood cell size and count: genome-wide scans in the Framingham Heart Study

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

Genetics of Hb F/F cell variance in adults and heterocellular hereditary persistence of fetal hemoglobin.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

Mortality in sickle cell disease. Life expectancy and risk factors for early death.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978511

Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus

1 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.3390%2FGENES5010051

The acute chest syndrome in sickle cell disease: incidence and risk factors. The Cooperative Study of Sickle Cell Disease

21 January 2018

1 reference

12 December 2020

Etiology of differences in hematocrit between males and females: sequence-based polymorphisms in erythropoietin and its receptor

1 reference

12 December 2020

Assessment of mean platelet volume in coronary artery disease - what does it mean?

1 reference

12 December 2020

Genetic influences on F cells and other hematologic variables: a twin heritability study

1 reference

12 December 2020

Pain in sickle cell disease. Rates and risk factors

1 reference

12 December 2020

Identifiers

DOI

10.3390/GENES5010051

1 reference

22 August 2017

1 reference

PMC publication ID

3978511

22 August 2017

PubMed publication ID

24705286

1 reference

PMC publication ID

3978511