UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...

Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humans

PLoS genetics, 2013-06, Vol.9 (6), p.e1003536-e1003536

2013

Link zum Volltext

Verfügbarkeit prüfen

Genome-Wide Pharmacogenetics of Antidepressant Response in the GENDEP Project

The American journal of psychiatry, 2010-05, Vol.167 (5), p.555-564

2010

Link zum Volltext

Verfügbarkeit prüfen

EIF2AK3 , encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome

Nature genetics, 2000-08, Vol.25 (4), p.406-409

2000

Link zum Volltext

Verfügbarkeit prüfen

Modulation of Malaria Phenotypes by Pyruvate Kinase (PKLR) Variants in a Thai Population

PloS one, 2015-12, Vol.10 (12), p.e0144555-e0144555

2015

Link zum Volltext

Verfügbarkeit prüfen

Untargeted Mass Spectrometry Lipidomics identifies correlation between serum sphingomyelins and plasma cholesterol

Lipids in health and disease, 2019-02, Vol.18 (1), p.38-38, Article 38

2019

Link zum Volltext

Verfügbarkeit prüfen

Association of the CpG methylation pattern of the proximal insulin gene promoter with type 1 diabetes

PloS one, 2012-05, Vol.7 (5), p.e36278-e36278

2012

Link zum Volltext

Verfügbarkeit prüfen

The Natural Metabolite 4-Cresol Improves Glucose Homeostasis and Enhances β-Cell Function

Cell reports (Cambridge), 2020-02, Vol.30 (7), p.2306-2320.e5

2020

Link zum Volltext

Verfügbarkeit prüfen

A General Framework for Interrogation of mRNA Stability Programs Identifies RNA-Binding Proteins that Govern Cancer Transcriptomes

Cell reports (Cambridge), 2018-05, Vol.23 (6), p.1639-1650

2018

Link zum Volltext

Verfügbarkeit prüfen

Intergenic Variants of HBS1L-MYB Are Responsible for a Major Quantitative Trait Locus on Chromosome 6q23 Influencing Fetal Hemoglobin Levels in Adults

Proceedings of the National Academy of Sciences - PNAS, 2007-07, Vol.104 (27), p.11346-11351

2007

Link zum Volltext

Verfügbarkeit prüfen

Gene–environment interactions in 7610 women with breast cancer: prospective evidence from the Million Women Study

The Lancet (British edition), 2010-06, Vol.375 (9732), p.2143-2151

2010

Link zum Volltext

Verfügbarkeit prüfen

An innate contribution of human nicotinic receptor polymorphisms to COPD-like lesions

Nature communications, 2021-11, Vol.12 (1), p.6384-6384, Article 6384

2021

Link zum Volltext

Verfügbarkeit prüfen

Integrated genomics point to immune vulnerabilities in pleural mesothelioma

Scientific reports, 2021-09, Vol.11 (1), p.19138-15, Article 19138

2021

Link zum Volltext

Verfügbarkeit prüfen

eQTL mapping identifies insertion- and deletion-specific eQTLs in multiple tissues

Nature communications, 2015-05, Vol.6 (1), p.6821, Article 6821

2015

Link zum Volltext

Verfügbarkeit prüfen

Cohort profile: genomic data for 26 622 individuals from the Canadian Longitudinal Study on Aging (CLSA)

BMJ open, 2022-03, Vol.12 (3), p.e059021-e059021

2022

Link zum Volltext

Verfügbarkeit prüfen

Y disruption, autosomal hypomethylation and poor male lung cancer survival

Scientific reports, 2021-06, Vol.11 (1), p.12453-12453, Article 12453

2021

Link zum Volltext

Verfügbarkeit prüfen

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Nature (London), 2010-04, Vol.464 (7289), p.713-720

2010

Link zum Volltext

Verfügbarkeit prüfen

Gene-environment interaction for childhood asthma and exposure to farming in Central Europe

Journal of allergy and clinical immunology, 2011-01, Vol.127 (1), p.138-144.e4

2011

Link zum Volltext

Verfügbarkeit prüfen

Estimating cell-type-specific DNA methylation effects in heterogeneous cellular populations

Epigenomics, 2021-01, Vol.13 (2), p.87

2021

Link zum Volltext

Verfügbarkeit prüfen

Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements

Nature communications, 2019-03, Vol.10 (1), p.1209-1209, Article 1209

2019

Link zum Volltext

Verfügbarkeit prüfen

HDR: a statistical two-step approach successfully identifies disease genes in autosomal recessive families

Journal of human genetics, 2016-11, Vol.61 (11), p.959-963

2016

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 852

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(831)
Mit Volltextzugriff
(737)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Nature Genetics
(100)
Human Molecular Genetics
(49)
Nature
(39)
American Journal Of Human Genetics
(38)
Nature Communications
(36)
Plos One
(36)
Genomics
(32)
European Journal Of Human Genetics : Ejhg
(28)
Plos Genetics
(27)
Diabetes
(17)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humans

Genome-Wide Pharmacogenetics of Antidepressant Response in the GENDEP Project

EIF2AK3 , encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome

Modulation of Malaria Phenotypes by Pyruvate Kinase (PKLR) Variants in a Thai Population

Untargeted Mass Spectrometry Lipidomics identifies correlation between serum sphingomyelins and plasma cholesterol

Association of the CpG methylation pattern of the proximal insulin gene promoter with type 1 diabetes

Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4

Homocysteine and coronary heart disease: meta-analysis of MTHFR case-control studies, avoiding publication bias

The Natural Metabolite 4-Cresol Improves Glucose Homeostasis and Enhances β-Cell Function

A General Framework for Interrogation of mRNA Stability Programs Identifies RNA-Binding Proteins that Govern Cancer Transcriptomes

Intergenic Variants of HBS1L-MYB Are Responsible for a Major Quantitative Trait Locus on Chromosome 6q23 Influencing Fetal Hemoglobin Levels in Adults

Gene–environment interactions in 7610 women with breast cancer: prospective evidence from the Million Women Study

An innate contribution of human nicotinic receptor polymorphisms to COPD-like lesions

Integrated genomics point to immune vulnerabilities in pleural mesothelioma

eQTL mapping identifies insertion- and deletion-specific eQTLs in multiple tissues

Genetics of venous thrombosis: insights from a new genome wide association study

Cohort profile: genomic data for 26 622 individuals from the Canadian Longitudinal Study on Aging (CLSA)

Y disruption, autosomal hypomethylation and poor male lung cancer survival

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Gene-environment interaction for childhood asthma and exposure to farming in Central Europe

Estimating cell-type-specific DNA methylation effects in heterogeneous cellular populations

Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements

A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis

HDR: a statistical two-step approach successfully identifies disease genes in autosomal recessive families

SLC2A9 is a high-capacity urate transporter in humans

Suchergebnisse filtern