UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 78

Sortiert nach

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

Science (American Association for the Advancement of Science), 2012-05, Vol.336 (6082), p.740-743

2012

Volltextzugriff (PDF)

Extensive pathogenicity of mitochondrial heteroplasmy in healthy human individuals

Proceedings of the National Academy of Sciences - PNAS, 2014-07, Vol.111 (29), p.10654-10659

2014

Volltextzugriff (PDF)

Host genetic variation impacts microbiome composition across human body sites

Genome Biology, 2015-09, Vol.16 (1), p.191, Article 191

2015

Volltextzugriff (PDF)

Crowdsourced genealogies and genomes

Science (American Association for the Advancement of Science), 2018-04, Vol.360 (6385), p.153-154

2018

Volltextzugriff (PDF)

Contrasting X-Linked and Autosomal Diversity across 14 Human Populations

American journal of human genetics, 2014-06, Vol.94 (6), p.827-844

2014

Volltextzugriff (PDF)

Human population differentiation is strongly correlated with local recombination rate

PLoS genetics, 2010-03, Vol.6 (3), p.e1000886

2010

Volltextzugriff (PDF)

XWAS: A Software Toolset for Genetic Data Analysis and Association Studies of the X Chromosome

The Journal of heredity, 2015, Vol.106 (5), p.666-671

2015

Volltextzugriff (PDF)

Measurement of the human allele frequency spectrum demonstrates greater genetic drift in East Asians than in Europeans

Nature genetics, 2007-10, Vol.39 (10), p.1251-1255

2007

Volltextzugriff (PDF)

Principal component analysis characterizes shared pathogenetics from genome-wide association studies

PLoS computational biology, 2014-09, Vol.10 (9), p.e1003820-e1003820

2014

Volltextzugriff (PDF)

Accounting for eXentricities: analysis of the X chromosome in GWAS reveals X-linked genes implicated in autoimmune diseases

PloS one, 2014-12, Vol.9 (12), p.e113684-e113684

2014

Volltextzugriff (PDF)

Gene-based testing of interactions in association studies of quantitative traits

PLoS genetics, 2013-02, Vol.9 (2), p.e1003321-e1003321

2013

Volltextzugriff (PDF)

NRE: a tool for exploring neutral loci in the human genome

BMC bioinformatics, 2012-11, Vol.13 (1), p.301-301, Article 301

2012

Volltextzugriff (PDF)

Accelerated genetic drift on chromosome X during the human dispersal out of Africa

Nature genetics, 2009-01, Vol.41 (1), p.66-70

2009

Volltextzugriff (PDF)

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

Nature communications, 2019-09, Vol.10 (1), p.4141-15, Article 4141

2019

Volltextzugriff (PDF)

Incomplete Lineage Sorting and Hybridization Statistics for Large-Scale Retroposon Insertion Data

PLoS computational biology, 2016-03, Vol.12 (3), p.e1004812-e1004812

2016

Volltextzugriff (PDF)

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

Genome research, 2016-02, Vol.26 (2), p.151

2016

Volltextzugriff (PDF)

Neutral genomic regions refine models of recent rapid human population growth

Proceedings of the National Academy of Sciences - PNAS, 2014-01, Vol.111 (2), p.757-762

2014

Volltextzugriff (PDF)

Extracting replicable associations across multiple studies: Empirical Bayes algorithms for controlling the false discovery rate

PLoS computational biology, 2017-08, Vol.13 (8), p.e1005700-e1005700

2017

Volltextzugriff (PDF)

Combining Sparse Group Lasso and Linear Mixed Model Improves Power to Detect Genetic Variants Underlying Quantitative Traits

Frontiers in genetics, 2019-04, Vol.10, p.271-271

2019

Volltextzugriff (PDF)

Predicting signatures of "synthetic associations" and "natural associations" from empirical patterns of human genetic variation

PLoS computational biology, 2012-07, Vol.8 (7), p.e1002600-e1002600

2012

Volltextzugriff (PDF)

Knowledge-driven analysis identifies a gene-gene interaction affecting high-density lipoprotein cholesterol levels in multi-ethnic populations

PLoS genetics, 2012-05, Vol.8 (5), p.e1002714-e1002714

2012

Volltextzugriff (PDF)

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

Proceedings of the National Academy of Sciences - PNAS, 2014-10, Vol.111 (43), p.E4548-E4550

2014

Volltextzugriff (PDF)

Analysis of multiple association studies provides evidence of an expression QTL hub in gene-gene interaction network affecting HDL cholesterol levels

PloS one, 2014-03, Vol.9 (3), p.e92469-e92469

2014

Volltextzugriff (PDF)

Enhanced methods for local ancestry assignment in sequenced admixed individuals

PLoS computational biology, 2014-04, Vol.10 (4), p.e1003555-e1003555

2014

Volltextzugriff (PDF)

Gene-Based Nonparametric Testing of Interactions Using Distance Correlation Coefficient in Case-Control Association Studies

Genes, 2018-12, Vol.9 (12), p.608

2018

Volltextzugriff (PDF)

1 – 25 von 78

Suche als RSS-Feed

Aktive Filter

KollektionMIT Press Journals

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(76)
Mit Volltextzugriff
(72)

Publikationsform

Sprache

Englisch
(78)
Japanisch
(17)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

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

Contrasting X-Linked and Autosomal Diversity across 14 Human Populations

Human population differentiation is strongly correlated with local recombination rate

XWAS: A Software Toolset for Genetic Data Analysis and Association Studies of the X Chromosome

Measurement of the human allele frequency spectrum demonstrates greater genetic drift in East Asians than in Europeans

Principal component analysis characterizes shared pathogenetics from genome-wide association studies

Accounting for eXentricities: analysis of the X chromosome in GWAS reveals X-linked genes implicated in autoimmune diseases

Gene-based testing of interactions in association studies of quantitative traits

NRE: a tool for exploring neutral loci in the human genome

Accelerated genetic drift on chromosome X during the human dispersal out of Africa

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

Incomplete Lineage Sorting and Hybridization Statistics for Large-Scale Retroposon Insertion Data

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

Neutral genomic regions refine models of recent rapid human population growth

Extracting replicable associations across multiple studies: Empirical Bayes algorithms for controlling the false discovery rate

Combining Sparse Group Lasso and Linear Mixed Model Improves Power to Detect Genetic Variants Underlying Quantitative Traits

Predicting signatures of "synthetic associations" and "natural associations" from empirical patterns of human genetic variation

Knowledge-driven analysis identifies a gene-gene interaction affecting high-density lipoprotein cholesterol levels in multi-ethnic populations

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

Analysis of multiple association studies provides evidence of an expression QTL hub in gene-gene interaction network affecting HDL cholesterol levels

Enhanced methods for local ancestry assignment in sequenced admixed individuals

Gene-Based Nonparametric Testing of Interactions Using Distance Correlation Coefficient in Case-Control Association Studies

Aktive Filter

Suchergebnisse filtern