UB Paderborn / Katalog / Suche / in CDI

Philosophical transactions of the Royal Society of London. Series A: Mathematical, physical, and engineering sciences, 2003-10, Vol.361 (1811), p.2123-2144

2003

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Clustered mutations in hominid genome evolution are consistent with APOBEC3G enzymatic activity

Genome research, 2016-05, Vol.26 (5), p.579

2016

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Selection for translation efficiency on synonymous polymorphisms in recent human evolution

Genome biology and evolution, 2011-01, Vol.3, p.749-761

2011

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Fair localization of function via multi-lesion analysis

Neuroinformatics (Totowa, N.J.), 2004, Vol.2 (2), p.163-168

2004

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Biological knowledge-driven analysis of epistasis in human GWAS with application to lipid traits

Methods in molecular biology (Clifton, N.J.), 2015, Vol.1253, p.35

2015

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Recent Explosive Human Population Growth Has Resulted in an Excess of Rare Genetic Variants

Extensive pathogenicity of mitochondrial heteroplasmy in healthy human individuals

Host genetic variation impacts microbiome composition across human body sites

Crowdsourced genealogies and genomes

Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations

Indigenous Arabs are descendants of the earliest split from ancient Eurasian populations

Neutral genomic regions refine models of recent rapid human population growth

Reply to Just et al.: Mitochondrial DNA heteroplasmy could be reliably detected with massively parallel sequencing technologies

Inference of Super-exponential Human Population Growth via Efficient Computation of the Site Frequency Spectrum for Generalized Models

Interaction between SNPs in the RXRA and near ANGPTL3 gene region inhibits apoB reduction after statin-fenofibric acid therapy in individuals with mixed dyslipidemia

Crowdsourced genealogies and genomes: Genealogical study provides insight into history and life span and heralds crowdsourced genetic research

Fair Attribution of Functional Contribution in Artificial and Biological Networks

X-inactivation informs variance-based testing for X-linked association of a quantitative trait

Principal Component Analysis Characterizes Shared Pathogenetics from Genome-Wide Association Studies: e1003820

Regional dietary adaptation of FADS genes in humans: molecular mechanism and functional consequences

Population growth inflates the per-individual number of deleterious mutations and reduces their mean effect

Strong Constraint on Human Genes Escaping X-Inactivation Is Modulated by their Expression Level and Breadth in Both Sexes

Positive Selection on a Regulatory Insertion-Deletion Polymorphism in FADS2 Influences Apparent Endogenous Synthesis of Arachidonic Acid

Can a sex-biased human demography account for the reduced effective population size of chromosome X in non-Africans?

Human Population Differentiation Is Strongly Correlated with Local Recombination Rate: e1000886

Controlled analysis of neurocontrollers with informational lesioning

Clustered mutations in hominid genome evolution are consistent with APOBEC3G enzymatic activity

Selection for translation efficiency on synonymous polymorphisms in recent human evolution

Fair localization of function via multi-lesion analysis

Biological knowledge-driven analysis of epistasis in human GWAS with application to lipid traits

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