Evidence for extensive transmission distortion in the human genome - Wikidata - wikimedia - TriplyDB

Evidence for extensive transmission distortion in the human genome

Evidence for extensive transmission distortion in the human genome

http://www.wikidata.org/entity/Q33909560

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Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings Evidence of a linkage between matrilin-1 gene (MATN1) and idiopathic scoliosis Increasing incidence of Type 1 diabetes--role for genes?Spam1-associated transmission ratio distortion in mice: elucidating the mechanism.A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication The emergence of human-evolutionary medical genomics Linkage disequilibrium between MSX1 and non-syndromic cleft lip/palate in the Chilean population.A regression based transmission/disequilibrium test for binary traits: the power of joint tests for linkage and association Forward-time simulations of human populations with complex diseases Design considerations in a sib-pair study of linkage for susceptibility loci in cancer.Markers typed in genome-wide analysis identify regions showing deviation from Hardy-Weinberg equilibrium.Genetic selection? A study of individual variation in the enzymes of folate metabolism.Usefulness of Mendelian randomization in observational epidemiology.Transmission-ratio distortion and allele sharing in affected sib pairs: a new linkage statistic with reduced bias, with application to chromosome 6q25.3.Mathematical assumptions versus biological reality: myths in affected sib pair linkage analysis Contrasting methods of quantifying fine structure of human recombination.Assessment of transmission distortion on chromosome 6p in healthy individuals using tagSNPs.Identification of two maternal transmission ratio distortion loci in pedigrees of the Framingham heart study.Variance calculations for identity-by-descent estimation Estimation of linkage disequilibrium and interspecific gene flow in Ficedula flycatchers by a newly developed 50k single-nucleotide polymorphism array.HLA and genomewide allele sharing in dizygotic twins.Orofacial cleft risk is increased with maternal smoking and specific detoxification-gene variants.Scrambling eggs: meiotic drive and the evolution of female recombination rates.Evaluating the evidence for transmission distortion in human pedigrees.Correlation of intergenerational family sizes suggests a genetic component of reproductive fitness.Genetics of Crohn disease, an archetypal inflammatory barrier disease.Parental effect of DNA (Cytosine-5) methyltransferase 1 on grandparental-origin-dependent transmission ratio distortion in mouse crosses and human families.Genome-wide single-cell analysis of recombination activity and de novo mutation rates in human sperm.Identification of susceptibility genes for cancer in a genome-wide scan: results from the colon neoplasia sibling study Detection of intergenerational genetic effects with application to HLA-B matching as a risk factor for schizophrenia Analysis of Case-Parent Trios Using a Loglinear Model with Adjustment for Transmission Ratio Distortion Transmission-ratio distortion in the Framingham Heart Study Transmission ratio distortion: review of concept and implications for genetic association studies.A prezygotic transmission distorter acting equally in female and male zebra finches Taeniopygia guttata.Analysis of case-parent trios for imprinting effect using a loglinear model with adjustment for sex-of-parent-specific transmission ratio distortion.A novel sampling design to explore gene-longevity associations: the ECHA study.Genetic overlap of schizophrenia and bipolar disorder in a high-density linkage survey in the Portuguese Island population.Analysis of IL10 haplotypic associations with severe malaria.Recombination rate plasticity: revealing mechanisms by design.An investigation of transmission ratio distortion in the central region of the human MHC.

P2860

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P2860

Evidence for extensive transmission distortion in the human genome

http://www.wikidata.org/entity/Q33909560

description

2003 nî lūn-bûn

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2003 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

Evidence for extensive transmission distortion in the human genome

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Evidence for extensive transmission distortion in the human genome

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type

label

Evidence for extensive transmission distortion in the human genome

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Evidence for extensive transmission distortion in the human genome

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prefLabel

Evidence for extensive transmission distortion in the human genome

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Evidence for extensive transmission distortion in the human genome

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American Journal of Human Genetics

P1476

Evidence for extensive transmission distortion in the human genome

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P2093

Jonathan K Pritchard

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Mark A Herbert

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Neil A Hanchard

http://www.w3.org/2001/XMLSchema#string

Sebastian Zöllner

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P2860

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

Inbreeding effects on fertility in humans: evidence for reproductive compensation.

A genomic screen of autism: evidence for a multilocus etiology.

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion

Parametric and nonparametric linkage analysis: a unified multipoint approach

A high-resolution recombination map of the human genome

Comprehensive human genetic maps: individual and sex-specific variation in recombination

Natural selection and the function of genome imprinting: beyond the silenced minority.

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10.1086/381131

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1

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