Default: Genetic Epidemiology

ISSN: 0741-0395

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Genetic Epidemiology Q2 Unclaimed

Wiley-Liss Inc. United States
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Genetic Epidemiology is a journal indexed in SJR in Epidemiology and Genetics (clinical) with an H index of 102. It has a price of 2500 €. It has an SJR impact factor of 1,06 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 1,06.

Genetic Epidemiology focuses its scope in these topics and keywords: association, genomewide, genetic, selection, identify, haplotypesstability, individuals, interactions, largest, leverage, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Price

2500 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

Genetic Epidemiology

1,06

SJR Impact factor

102

H Index

38

Total Docs (Last Year)

196

Total Docs (3 years)

1908

Total Refs

424

Total Cites (3 years)

193

Citable Docs (3 years)

2.05

Cites/Doc (2 years)

50.21

Ref/Doc

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Aims and Scope


association, genomewide, genetic, selection, identify, haplotypesstability, individuals, interactions, largest, leverage, main, megaanalysis, approachpedigree, model, multilocus, phenotypes, quantitative, analysisgeneral, rarevariant, regions, effects, associationutilizing, averaging, bayes, collapsing, considerations, constructing, datacontemporary, disequilibrium, associationusing, exome, framework, g, gene, genomic,



Best articles by citations

Maternal exposure to paternal HLA does not explain the postpartum increase in rheumatoid arthritis

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Erratum: Broman KW. 2001. Estimation of Allele Frequencies With Data on Sibships. Genet Epidemiol 20:307-15.

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Detecting low-quality markers using map expanders

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Preferential transmission of type 1 diabetes from parents to offspring: fact or artifact?

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Logistic regression of family data from retrospective study designs

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Sum statistics for the joint detection of multiple disease loci in case-control association studies with SNP markers

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Power estimation of multiple SNP association test of case-control study and application

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Analysis of metabolic syndrome phenotypes in Framingham Heart Study families from Genetic Analysis Workshop 13

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Testing for association with a case-parents design in the presence of genotyping errors

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Increased power for case-control studies of single nucleotide polymorphisms through incorporation of family history and genetic constraints

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Stoppage: An issue for segregation analysis

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Affected-sib-pair test for linkage based on constraints for identical-by-descent distributions corresponding to disease models with imprinting

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Candidate gene association analysis for a quantitative trait, using parent-offspring trios

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Bias in Mendelian randomization due to assortative mating

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Evaluating bias due to population stratification in case-control association studies of admixed populations

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Bayesian trio models for association in the presence of genotyping errors

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Efficient Simulation ofP Values for Linkage Analysis

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Estimation of allele frequencies with data on sibships

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Consistency of genetic analyses in longitudinal data: Observations from the GAW13 Framingham Heart Study data

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Quantitative trait linkage analysis by generalized estimating equations: Unification of variance components and Haseman-Elston regression

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Modeling and dissection of longitudinal blood pressure and hypertension phenotypes in genetic epidemiological studies

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On planning of samples for linkage analysis: Two ways of a sample size reduction

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Parameter estimation in ascertainment adjustment in complex diseases

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Genetic analysis of phenotypes derived from longitudinal data: Presentation Group 1 of Genetic Analysis Workshop 13

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