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Genotype imputation
scientific article (publication date: 2009)
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
2925172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19715440%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
review article
1 reference
stated in
Europe PubMed Central
title
Genotype imputation
(English)
2 references
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19715440
retrieved
30 April 2017
stated in
Europe PubMed Central
PMCID
2925172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19715440%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
main subject
imputation
1 reference
based on heuristic
inferred from title
author
Cristen J. Willer
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
2925172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19715440%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
Serena Sanna
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
2925172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19715440%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
Gonçalo Abecasis
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
2925172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19715440%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
author name string
Yun Li
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
2925172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19715440%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
language of work or name
English
1 reference
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19715440
retrieved
30 April 2017
publication date
1 January 2009
1 reference
stated in
Europe PubMed Central
PMCID
2925172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19715440%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
published in
Annual Review of Genomics and Human Genetics
2 references
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19715440
retrieved
30 April 2017
stated in
Europe PubMed Central
PMCID
2925172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19715440%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
volume
10
2 references
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19715440
retrieved
30 April 2017
stated in
Europe PubMed Central
PMCID
2925172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19715440%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
page(s)
387-406
2 references
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19715440
retrieved
30 April 2017
stated in
Europe PubMed Central
PMCID
2925172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19715440%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
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Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits
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Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
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A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
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Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
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30 April 2017
CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration
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30 April 2017
Principal components analysis corrects for stratification in genome-wide association studies
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30 April 2017
A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase
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30 April 2017
A haplotype map of the human genome
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30 April 2017
Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers
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30 April 2017
Efficiency and power in genetic association studies
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30 April 2017
Susceptibility genes for age-related maculopathy on chromosome 10q26.
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Genome-wide association studies for common diseases and complex traits
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30 April 2017
Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation
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30 April 2017
The International HapMap Project
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30 April 2017
Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease
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30 April 2017
Score tests for association between traits and haplotypes when linkage phase is ambiguous
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30 April 2017
Merlin--rapid analysis of dense genetic maps using sparse gene flow trees
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30 April 2017
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
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30 April 2017
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
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30 April 2017
Genomic control for association studies
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30 April 2017
A New Statistical Method for Haplotype Reconstruction from Population Data
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30 April 2017
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
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30 April 2017
Initial sequencing and analysis of the human genome
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30 April 2017
The Sequence of the Human Genome
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30 April 2017
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30 April 2017
Parametric and nonparametric linkage analysis: a unified multipoint approach
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30 April 2017
Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics
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30 April 2017
Disease gene mapping in isolated human populations: the example of Finland
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30 April 2017
Genetic dissection of complex traits
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30 April 2017
Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population
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30 April 2017
Multilocus linkage analysis in humans: detection of linkage and estimation of recombination
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30 April 2017
DNA sequencing with chain-terminating inhibitors
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30 April 2017
Genotype-based matching to correct for population stratification in large-scale case-control genetic association studies.
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3 June 2018
On Jim Watson's APOE status: genetic information is hard to hide.
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3 June 2018
Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.
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3 June 2018
Gene variants influencing measures of inflammation or predisposing to autoimmune and inflammatory diseases are not associated with the risk of type 2 diabetes
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3 June 2018
Extending genome-wide association studies to copy-number variation.
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3 June 2018
Common variants at CD40 and other loci confer risk of rheumatoid arthritis
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3 June 2018
A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose
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retrieved
3 June 2018
Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
LDL-cholesterol concentrations: a genome-wide association study.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Common variants in the GDF5-UQCC region are associated with variation in human height
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
A statistical method for predicting classical HLA alleles from SNP data.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Family-based association tests for genomewide association scans.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Imputation-based analysis of association studies: candidate regions and quantitative traits
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Leveraging the HapMap correlation structure in association studies.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
A tutorial on statistical methods for population association studies.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Heritability of cardiovascular and personality traits in 6,148 Sardinians
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
In silico method for inferring genotypes in pedigrees.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Multilocus association mapping using variable-length Markov chains.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Mapping determinants of human gene expression by regional and genome-wide association
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Genome-wide association studies: theoretical and practical concerns.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Haplotype variation and linkage disequilibrium in 313 human genes.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Efficient multipoint linkage analysis through reduction of inheritance space.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
A general test of association for quantitative traits in nuclear families.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Combined linkage and association sib-pair analysis for quantitative traits
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Linkage disequilibrium mapping in isolated populations: the example of Finland revisited.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Markov chain Monte Carlo segregation and linkage analysis for oligogenic models.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Extensions to pedigree analysis. V. Optimal calculation of Mendelian likelihoods.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
A general model for the genetic analysis of pedigree data.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Construction of multilocus genetic linkage maps in humans.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Two point mutations are responsible for G6PD polymorphism in Sardinia.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Inference of haplotypes from PCR-amplified samples of diploid populations.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
Measurement of erythrocyte glucose-6-phosphate dehydrogenase activity with a centrifugal analyzer.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
3 June 2018
A functional polymorphism in the 5' UTR of GDF5 is associated with susceptibility to osteoarthritis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
26 November 2018
Testing untyped alleles (TUNA)-applications to genome-wide association studies.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
26 November 2018
The value of relatives with phenotypes but missing genotypes in association studies for quantitative traits
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
26 November 2018
Association testing with Mendel.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
26 November 2018
Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
26 November 2018
Testing association of statistically inferred haplotypes with discrete and continuous traits in samples of unrelated individuals.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
26 November 2018
Faster multipoint linkage analysis using Fourier transforms.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
26 November 2018
Influence of hemoglobin precipitation on erythrocyte metabolism in alpha and beta thalassemia.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
26 November 2018
The use of measured genotype information in the analysis of quantitative phenotypes in man. I. Models and analytical methods.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2925172
retrieved
26 November 2018
Identifiers
DOI
10.1146/ANNUREV.GENOM.9.081307.164242
3 references
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19715440
retrieved
30 April 2017
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
906850
stated in
Europe PubMed Central
PMCID
2925172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19715440%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
OpenCitations bibliographic resource ID
906850
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
906850
PMCID
2925172
3 references
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19715440
retrieved
30 April 2017
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
906850
stated in
Europe PubMed Central
PMCID
2925172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19715440%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
PubMed ID
19715440
3 references
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19715440
retrieved
30 April 2017
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
906850
stated in
Europe PubMed Central
PMCID
2925172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19715440%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
ResearchGate publication ID
26775265
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