UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 144

Sortiert nach

An atlas of genetic associations in UK Biobank

Nature genetics, 2018-11, Vol.50 (11), p.1593-1599

2018

Link zum Volltext

Verfügbarkeit prüfen

Mendelian randomization study of whole blood viscosity and cardiovascular diseases

PloS one, 2024-04, Vol.19 (4), p.e0294095-e0294095

2024

Link zum Volltext

Verfügbarkeit prüfen

The heritability of human disease: estimation, uses and abuses

Nature reviews. Genetics, 2013-02, Vol.14 (2), p.139

2013

Link zum Volltext

Verfügbarkeit prüfen

Evidence for sex-specific genetic architectures across a spectrum of human complex traits

Genome Biology, 2016-07, Vol.17 (1), p.166-166, Article 166

2016

Link zum Volltext

Verfügbarkeit prüfen

Indirect assortative mating for human disease and longevity

Heredity, 2019-08, Vol.123 (2), p.106-116

2019

Link zum Volltext

Verfügbarkeit prüfen

Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability

Nature communications, 2018-12, Vol.9 (1), p.5271-10, Article 5271

2018

Link zum Volltext

Verfügbarkeit prüfen

Plasma Vitamin D Concentration Influences Survival Outcome After a Diagnosis of Colorectal Cancer

Journal of clinical oncology, 2014-08, Vol.32 (23), p.2430-2439

2014

Link zum Volltext

Verfügbarkeit prüfen

Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

Nature communications, 2019-03, Vol.10 (1), p.1383-1383, Article 1383

2019

Link zum Volltext

Verfügbarkeit prüfen

Effect of aspirin and NSAIDs on risk and survival from colorectal cancer

Gut, 2010-12, Vol.59 (12), p.1670-1679

2010

Link zum Volltext

Verfügbarkeit prüfen

Functional annotation of the cattle genome through systematic discovery and characterization of chromatin states and butyrate-induced variations

BMC biology, 2019-08, Vol.17 (1), p.68-68, Article 68

2019

Link zum Volltext

Verfügbarkeit prüfen

Evidence of horizontal indirect genetic effects in humans

Nature human behaviour, 2021-03, Vol.5 (3), p.399

2021

Link zum Volltext

Verfügbarkeit prüfen

Genetic contributions to stability and change in intelligence from childhood to old age

Nature (London), 2012-02, Vol.482 (7384), p.212-215

2012

Link zum Volltext

Verfügbarkeit prüfen

Epigenomics and genotype-phenotype association analyses reveal conserved genetic architecture of complex traits in cattle and human

BMC biology, 2020-07, Vol.18 (1), p.80-80, Article 80

2020

Link zum Volltext

Verfügbarkeit prüfen

Recent human effective population size estimated from linkage disequilibrium

Genome Research, 2007-04, Vol.17 (4), p.520-526

2007

Link zum Volltext

Verfügbarkeit prüfen

Identification and Survival of Carriers of Mutations in DNA Mismatch-Repair Genes in Colon Cancer

The New England journal of medicine, 2006-06, Vol.354 (26), p.2751-2763

2006

Link zum Volltext

Verfügbarkeit prüfen

Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone

Nature genetics, 2010-06, Vol.42 (6), p.520-524

2010

Link zum Volltext

Verfügbarkeit prüfen

Dietary Flavonoids and the Risk of Colorectal Cancer

Cancer epidemiology, biomarkers & prevention, 2007-04, Vol.16 (4), p.684-693

2007

Link zum Volltext

Verfügbarkeit prüfen

Comparative transcriptome in large-scale human and cattle populations

Genome Biology, 2022-08, Vol.23 (1), p.176-176, Article 176

2022

Link zum Volltext

Verfügbarkeit prüfen

The association of dietary intake of purine-rich vegetables, sugar-sweetened beverages and dairy with plasma urate, in a cross-sectional study

PloS one, 2012-06, Vol.7 (6), p.e38123

2012

Link zum Volltext

Verfügbarkeit prüfen

Gene expression and RNA splicing explain large proportions of the heritability for complex traits in cattle

Cell genomics, 2023-10, Vol.3 (10), p.100385-100385, Article 100385

2023

Link zum Volltext

Verfügbarkeit prüfen

Improved Genetic Profiling of Anthropometric Traits Using a Big Data Approach

PloS one, 2016-12, Vol.11 (12), p.e0166755-e0166755

2016

Link zum Volltext

Verfügbarkeit prüfen

Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits

PLoS genetics, 2020-07, Vol.16 (7), p.e1008785-e1008785

2020

Link zum Volltext

Verfügbarkeit prüfen

Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

Nature communications, 2019-05, Vol.10 (1), p.2069-2069, Article 2069

2019

Link zum Volltext

Verfügbarkeit prüfen

Germline Susceptibility to Colorectal Cancer Due to Base-Excision Repair Gene Defects

American journal of human genetics, 2005-07, Vol.77 (1), p.112-119

2005

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 144

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(141)
Mit Volltextzugriff
(125)

Publikationsform

Sprache

Englisch
(143)
Japanisch
(33)
Spanisch
(1)
Russisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

An atlas of genetic associations in UK Biobank

Mendelian randomization study of whole blood viscosity and cardiovascular diseases

The heritability of human disease: estimation, uses and abuses

Evidence for sex-specific genetic architectures across a spectrum of human complex traits

Indirect assortative mating for human disease and longevity

Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability

Plasma Vitamin D Concentration Influences Survival Outcome After a Diagnosis of Colorectal Cancer

Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

Effect of aspirin and NSAIDs on risk and survival from colorectal cancer

Functional annotation of the cattle genome through systematic discovery and characterization of chromatin states and butyrate-induced variations

Evidence of horizontal indirect genetic effects in humans

Genetic contributions to stability and change in intelligence from childhood to old age

Epigenomics and genotype-phenotype association analyses reveal conserved genetic architecture of complex traits in cattle and human

Recent human effective population size estimated from linkage disequilibrium

Identification and Survival of Carriers of Mutations in DNA Mismatch-Repair Genes in Colon Cancer

Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone

Dietary Flavonoids and the Risk of Colorectal Cancer

Comparative transcriptome in large-scale human and cattle populations

The association of dietary intake of purine-rich vegetables, sugar-sweetened beverages and dairy with plasma urate, in a cross-sectional study

Gene expression and RNA splicing explain large proportions of the heritability for complex traits in cattle

Improved Genetic Profiling of Anthropometric Traits Using a Big Data Approach

Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits

Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

Germline Susceptibility to Colorectal Cancer Due to Base-Excision Repair Gene Defects

Common genetic variants at the CRAC1 ( HMPS ) locus on chromosome 15q13.3 influence colorectal cancer risk

Suchergebnisse filtern