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Ober, Carole
One or more keywords matched the following items that are connected to
Ober, Carole
Item Type
Name
Concept
Pedigree
Academic Article
HLA-G1 protein expression is not essential for fetal survival.
Academic Article
Broad and narrow heritabilities of quantitative traits in a founder population.
Academic Article
Quantitative-trait homozygosity and association mapping and empirical genomewide significance in large, complex pedigrees: fasting serum-insulin level in the Hutterites.
Academic Article
A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.
Academic Article
Sequence variation in the promoter region of the cholinergic receptor muscarinic 3 gene and asthma and atopy.
Academic Article
Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin.
Academic Article
The genetic dissection of complex traits in a founder population.
Academic Article
Multilocus linkage disequilibrium mapping by the decay of haplotype sharing with samples of related individuals.
Academic Article
Correlation of intergenerational family sizes suggests a genetic component of reproductive fitness.
Academic Article
High-resolution mapping of crossovers reveals extensive variation in fine-scale recombination patterns among humans.
Academic Article
Best linear unbiased allele-frequency estimation in complex pedigrees.
Academic Article
Variation in ITGB3 has sex-specific associations with plasma lipoprotein(a) and whole blood serotonin levels in a population-based sample.
Academic Article
Accurate imputation of rare and common variants in a founder population from a small number of sequenced individuals.
Academic Article
Estimating the human mutation rate using autozygosity in a founder population.
Academic Article
Variation in conserved non-coding sequences on chromosome 5q and susceptibility to asthma and atopy.
Academic Article
Evaluating the evidence for transmission distortion in human pedigrees.
Academic Article
Genome-wide association study identifies candidate genes for male fertility traits in humans.
Academic Article
Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility.
Academic Article
Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13.
Academic Article
A population-based study of autosomal-recessive disease-causing mutations in a founder population.
Academic Article
Estimation of variance components of quantitative traits in inbred populations.
Academic Article
Major loci influencing serum triglyceride levels on 2q14 and 9p21 localized by homozygosity-by-descent mapping in a large Hutterite pedigree.
Academic Article
A genome-wide screen for hyposmia susceptibility Loci.
Academic Article
Fine mapping of a locus for nonsyndromic mental retardation on chromosome 19p13.
Academic Article
A genomewide screen for chronic rhinosinusitis genes identifies a locus on chromosome 7q.
Academic Article
Human leukocyte antigen matching and fetal loss: results of a 10 year prospective study.
Academic Article
An estimate of the average number of recessive lethal mutations carried by humans.
Academic Article
PRIMAL: Fast and accurate pedigree-based imputation from sequence data in a founder population.
Academic Article
Parent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions.
Academic Article
Parent-of-origin effects on quantitative phenotypes in a large Hutterite pedigree.
Academic Article
Parent-of-origin effects on quantitative phenotypes in a large Hutterite pedigree.
Grant
CHARACTERIZING A 5P-LINKED BHR SUSCEPTIBILITY LOCUS
Search Criteria
Pedigree