UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

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)

Host genetic variation impacts microbiome composition across human body sites

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

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)

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)

The history of African gene flow into Southern Europeans, Levantines, and Jews

PLoS genetics, 2011-04, Vol.7 (4), p.e1001373-e1001373

2011

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)

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)

Integrating common and rare genetic variation in diverse human populations

Nature (London), 2010-09, Vol.467 (7311), p.52-58

2010

Volltextzugriff (PDF)

Analyses of X-linked and autosomal genetic variation in population-scale whole genome sequencing

Nature genetics, 2011-08, Vol.43 (8), p.741-743

2011

Volltextzugriff (PDF)

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

Molecular biology and evolution, 2016-07, Vol.33 (7), p.1726-1739

2016

Volltextzugriff (PDF)

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

Molecular biology and evolution, 2010-10, Vol.27 (10), p.2312-2321

2010

Volltextzugriff (PDF)

Rare LPL gene variants attenuate triglyceride reduction and HDL cholesterol increase in response to fenofibric acid therapy in individuals with mixed dyslipidemia

Atherosclerosis, 2014-06, Vol.234 (2), p.249-253

2014

Volltextzugriff (PDF)

Association of mitochondrial DNA variants with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) symptoms

Journal of translational medicine, 2016-12, Vol.14 (1), p.342-342, Article 342

2016

Volltextzugriff (PDF)

Combining Evidence of Natural Selection with Association Analysis Increases Power to Detect Malaria-Resistance Variants

American journal of human genetics, 2007-08, Vol.81 (2), p.234-242

2007

Volltextzugriff (PDF)

1 – 16 von 16

Suche als RSS-Feed

Aktive Filter

ThemaGenetic Variation

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(16)
Mit Volltextzugriff
(15)

Publikationsform

Artikel
(16)

Sprache

Englisch
(16)
Japanisch
(7)

Erscheinungsjahr

n.n

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

Host genetic variation impacts microbiome composition across human body sites

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

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

The history of African gene flow into Southern Europeans, Levantines, and Jews

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

Neutral genomic regions refine models of recent rapid human population growth

Integrating common and rare genetic variation in diverse human populations

Analyses of X-linked and autosomal genetic variation in population-scale whole genome sequencing

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?

Rare LPL gene variants attenuate triglyceride reduction and HDL cholesterol increase in response to fenofibric acid therapy in individuals with mixed dyslipidemia

Association of mitochondrial DNA variants with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) symptoms

Combining Evidence of Natural Selection with Association Analysis Increases Power to Detect Malaria-Resistance Variants

Aktive Filter

Suchergebnisse filtern