Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Allowing for missing data at highly polymorphic genes when testing for maternal, offspring and maternal-fetal genotype incompatibility effects.

Human heredity - 1 Jan 2006

Hsieh Hsin-Ju, Palmer Christina G S, Sinsheimer Janet S

Abstract excerpt

Genes can be associated with disease through an individual's inherited genotype, the maternal genotype or the interaction between these two. When the gene is highly polymorphic, it is more difficult to identify the gene's functional role than for less polymorphic loci, because different alleles a...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Algorithms
Share to Alleles
Share to Fetus

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Inheritance Patterns

Share to Models, Statistical

Share to Mothers

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 17065817
DOI: 10.1159/000096444

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17065817-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Allowing for missing data at highly polymorphic genes when testing for maternal, offspring and maternal-fetal genotype incompatibility effects.PMID 17065817Read ↗

The Quantitative-MFG Test: A Linear Mixed Effect Model to Detect Maternal-Offspring Gene Interactions.Semantic proximity Read ↗

Modeling maternal-offspring gene-gene interactions: the extended-MFG test.Semantic proximity Read ↗

Detecting genotype combinations that increase risk for disease: maternal-fetal genotype incompatibility test.Semantic proximity Read ↗

An exact maternal-fetal genotype incompatibility (MFG) test.Semantic proximity Read ↗

Rare variant association analysis in case-parents studies by allowing for missing parental genotypes.Semantic proximity Read ↗

A model for family-based case-control studies of genetic imprinting and epistasis.Semantic proximity Read ↗

The v-MFG test: investigating maternal, offspring and maternal-fetal genetic incompatibility effects on disease and viability.Semantic proximity Read ↗

Power evaluations for family-based tests of association with incomplete parental genotypes.Semantic proximity Read ↗

Human Birth Weight and Reproductive Immunology: Testing for Interactions between Maternal and Offspring KIR and HLA-C Genes.Semantic proximity Read ↗

Detection of intergenerational genetic effects with application to HLA-B matching as a risk factor for schizophrenia.Semantic proximity Read ↗

Nonparametric method for detecting imprinting effect using all members of general pedigrees with missing data.Semantic proximity Read ↗

Value of Mendelian laws of segregation in families: data quality control, imputation, and beyond.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.