(Q30419441)

English

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

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16 February 2020

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

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16 February 2020

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Timothy A. Graubert

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16 February 2020

Nora Franceschini

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Nora Franceschini

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16 February 2020

James G. Wilson

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James G Wilson

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16 February 2020

Leslie A. Lange

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Leslie A Lange

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16 February 2020

Christopher J O'Donnell

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16 February 2020

Andrew D. Johnson

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Andrew D Johnson

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16 February 2020

Rebecca D. Jackson

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Rebecca D Jackson

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16 February 2020

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Paul L Auer

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16 February 2020

Jill M Johnsen

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16 February 2020

Benjamin A Logsdon

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16 February 2020

Michael A Nalls

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16 February 2020

Guosheng Zhang

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16 February 2020

Keolu Fox

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16 February 2020

Ethan M Lange

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16 February 2020

Stephen S Rich

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16 February 2020

Robert B Wallace

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16 February 2020

Zhao Chen

15

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16 February 2020

Hua Tang

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16 February 2020

Guillaume Lettre

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16 February 2020

Alex P Reiner

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16 February 2020

Santhi K Ganesh

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16 February 2020

Yun Li

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16 February 2020

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25 October 2012

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16 February 2020

American Journal of Human Genetics

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16 February 2020

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16 February 2020

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16 February 2020

794-808

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16 February 2020

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18 June 2022

https://europepmc.org/article/PMC/3487117

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Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative

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Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3487117

20 June 2018

Function of the chemokine receptor CXCR4 in haematopoiesis and in cerebellar development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3487117

20 June 2018

Design of the Women's Health Initiative clinical trial and observational study. The Women's Health Initiative Study Group

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3487117

20 June 2018

CARDIA: study design, recruitment, and some characteristics of the examined subjects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3487117

20 June 2018

The Atherosclerosis Risk in Communities (ARIC) Study: design and objectives. The ARIC investigators

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3487117

20 June 2018

Differential confounding of rare and common variants in spatially structured populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3487117

26 November 2018

The Asn505 mutation of the c-MPL gene, which causes familial essential thrombocythemia, induces autonomous homodimerization of the c-Mpl protein due to strong amino acid polarity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3487117

26 November 2018

Genome-wide analysis of transcript isoform variation in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3487117

26 November 2018

MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3487117

26 November 2018

A naturally occurring point mutation in the beta3 integrin MIDAS-like domain affects differently alphavbeta3 and alphaIIIbbeta3 receptor function.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3487117

26 November 2018

Developmental switching of messenger RNA expression from the human alpha-globin cluster: fetal/adult pattern of theta-globin gene expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3487117

26 November 2018

Pronounced thrombocytosis in transgenic mice expressing reduced levels of Mpl in platelets and terminally differentiated megakaryocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/23103231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Toward resolution of cardiovascular health disparities in African Americans: design and methods of the Jackson Heart Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/23103231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial thrombocytosis caused by the novel germ-line mutation p.Pro106Leu in the MPL gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/23103231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/23103231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.AJHG.2012.08.031

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23103231%20AND%20SRC:MED&resulttype=core&format=json

16 February 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23103231%20AND%20SRC:MED&resulttype=core&format=json

16 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23103231%20AND%20SRC:MED&resulttype=core&format=json

16 February 2020

ResearchGate publication ID

0 references

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