UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 276

Sortiert nach

Genetic signatures of exceptional longevity in humans

PloS one, 2012-01, Vol.7 (1), p.e29848

2012

Volltextzugriff (PDF)

Comparison of multiple imputation and other methods for the analysis of imputed genotypes

BMC genomics, 2023-06, Vol.24 (1), p.303-303, Article 303

2023

Volltextzugriff (PDF)

GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21

Nature communications, 2018-01, Vol.9 (1), p.286-8, Article 286

2018

Volltextzugriff (PDF)

Iron status and the risk of sepsis and severe COVID-19: a two-sample Mendelian randomization study

Scientific reports, 2022-09, Vol.12 (1), p.16157-9, Article 16157

2022

Volltextzugriff (PDF)

Genome-Wide Gene by Environment Interaction Analysis Identifies Common SNPs at 17q21.2 that Are Associated with Increased Body Mass Index Only among Asthmatics

PloS one, 2015-12, Vol.10 (12), p.e0144114-e0144114

2015

Volltextzugriff (PDF)

Identification of genetic variants associated with dengue or West Nile virus disease: a systematic review and meta-analysis

BMC infectious diseases, 2018-06, Vol.18 (1), p.282-282, Article 282

2018

Volltextzugriff (PDF)

Type 2 cytokine genes as allergic asthma risk factors after viral bronchiolitis in early childhood

Frontiers in immunology, 2023-01, Vol.13, p.1054119

2023

Volltextzugriff (PDF)

The genetic contribution of the X chromosome in age-related hearing loss

Frontiers in genetics, 2023-02, Vol.14, p.1106328-1106328

2023

Volltextzugriff (PDF)

Explaining sex differences in risk of bloodstream infections using mediation analysis in the population-based HUNT study in Norway

Scientific reports, 2022-05, Vol.12 (1), p.8436-11, Article 8436

2022

Volltextzugriff (PDF)

Stage and gene specific signatures defined by histones H3K4me2 and H3K27me3 accompany mammalian retina maturation in vivo

PloS one, 2012-10, Vol.7 (10), p.e46867-e46867

2012

Volltextzugriff (PDF)

Genome‐Wide Association Study of Pre‐Eclampsia Detects Novel Maternal Single Nucleotide Polymorphisms and Copy‐Number Variants in Subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study Cohort

Annals of human genetics, 2013-07, Vol.77 (4), p.277-287

2013

Volltextzugriff (PDF)

Variants in JAZF1 are associated with asthma, type 2 diabetes, and height in the United Kingdom biobank population

Frontiers in genetics, 2023-06, Vol.14, p.1129389-1129389

2023

Volltextzugriff (PDF)

Neural-specific deletion of Htra2 causes cerebellar neurodegeneration and defective processing of mitochondrial OPA1

PloS one, 2014-12, Vol.9 (12), p.e115789-e115789

2014

Volltextzugriff (PDF)

Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients

BMC pregnancy and childbirth, 2012-06, Vol.12 (1), p.61-61, Article 61

2012

Volltextzugriff (PDF)

Exhaustive Genome-Wide Search for SNP-SNP Interactions Across 10 Human Diseases

G3 : genes - genomes - genetics, 2016-07, Vol.6 (7), p.2043-2050

2016

Volltextzugriff (PDF)

Microbiome links breast-feeding and asthma protection: A cohort study helps elucidate this underlying player

Journal of allergy and clinical immunology, 2022-09, Vol.150 (3), p.587-588

2022

Volltextzugriff (PDF)

Gene-based analysis identified the gene ZNF248 is associated with late-onset asthma in African Americans

Annals of allergy, asthma, & immunology, 2016-07, Vol.117 (1), p.50-55.e2

2016

Volltextzugriff (PDF)

A mediation analysis framework based on variance component to remove genetic confounding effect

Journal of human genetics, 2024-07, Vol.69 (7), p.301-309

2024

Volltextzugriff (PDF)

In-Depth Analysis of Genetic Variation Associated with Severe West Nile Viral Disease

Vaccines (Basel), 2020-12, Vol.8 (4), p.744

2020

Volltextzugriff (PDF)

Gene-Gene and Gene-Environment Interactions

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1793, p.89

DeWan, Andrew T

2018

Volltextzugriff (PDF)

Whole-exome sequencing of a pedigree segregating asthma

BMC medical genetics, 2012-10, Vol.13 (1), p.95-95, Article 95

2012

Volltextzugriff (PDF)

Dyslipidemia and Risk of Preeclampsia: A Multiancestry Mendelian Randomization Study

Hypertension (Dallas, Tex. 1979), 2023-05, Vol.80 (5), p.1067-1076

2023

Volltextzugriff (PDF)

LDER-GE estimates phenotypic variance component of gene–environment interactions in human complex traits accurately with GE interaction summary statistics and full LD information

Briefings in bioinformatics, 2024-07, Vol.25 (4)

2024

Volltextzugriff (PDF)

Paired Indoor and Outdoor Nitrogen Dioxide Associated With Childhood Asthma Outcomes in a Mixed Rural-Urban Setting: A Feasibility Study

Journal of primary care & community health, 2023-01, Vol.14, p.21501319231173813-21501319231173813

2023

Volltextzugriff (PDF)

Discovery and Mediation Analysis of Cross-Phenotype Associations Between Asthma and Body Mass Index in 12q13.2

American journal of epidemiology, 2021-01, Vol.190 (1), p.85-94

2021

Volltextzugriff (PDF)

1 – 25 von 276

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(250)
Mit Volltextzugriff
(242)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Englisch
(273)
Japanisch
(24)

Erscheinungsjahr

n.n

Thema

Science & Technology
(211)
Humans
(154)
Life Sciences & Biomedicine
(142)
Female
(107)
Male
(77)
Science & Technology - Other Topics
(54)
Multidisciplinary Sciences
(53)
Polymorphism, Single Nucleotide
(53)
Adult
(45)
Risk Factors
(44)
Middle Aged
(40)
Genome-Wide Association Study
(39)
Genomes
(39)
Genetic Predisposition To Disease
(38)
Genotype
(38)
Genes
(36)
Case-Control Studies
(34)
Aged
(31)
Medicine
(31)
Studies
(31)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

Genetic signatures of exceptional longevity in humans

Comparison of multiple imputation and other methods for the analysis of imputed genotypes

GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21

Iron status and the risk of sepsis and severe COVID-19: a two-sample Mendelian randomization study

Genome-Wide Gene by Environment Interaction Analysis Identifies Common SNPs at 17q21.2 that Are Associated with Increased Body Mass Index Only among Asthmatics

Identification of genetic variants associated with dengue or West Nile virus disease: a systematic review and meta-analysis

Type 2 cytokine genes as allergic asthma risk factors after viral bronchiolitis in early childhood

The genetic contribution of the X chromosome in age-related hearing loss

Explaining sex differences in risk of bloodstream infections using mediation analysis in the population-based HUNT study in Norway

Stage and gene specific signatures defined by histones H3K4me2 and H3K27me3 accompany mammalian retina maturation in vivo

Genome‐Wide Association Study of Pre‐Eclampsia Detects Novel Maternal Single Nucleotide Polymorphisms and Copy‐Number Variants in Subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study Cohort

Variants in JAZF1 are associated with asthma, type 2 diabetes, and height in the United Kingdom biobank population

Neural-specific deletion of Htra2 causes cerebellar neurodegeneration and defective processing of mitochondrial OPA1

Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients

Exhaustive Genome-Wide Search for SNP-SNP Interactions Across 10 Human Diseases

Microbiome links breast-feeding and asthma protection: A cohort study helps elucidate this underlying player

Gene-based analysis identified the gene ZNF248 is associated with late-onset asthma in African Americans

A mediation analysis framework based on variance component to remove genetic confounding effect

In-Depth Analysis of Genetic Variation Associated with Severe West Nile Viral Disease

Gene-Gene and Gene-Environment Interactions

Whole-exome sequencing of a pedigree segregating asthma

Dyslipidemia and Risk of Preeclampsia: A Multiancestry Mendelian Randomization Study

LDER-GE estimates phenotypic variance component of gene–environment interactions in human complex traits accurately with GE interaction summary statistics and full LD information

Paired Indoor and Outdoor Nitrogen Dioxide Associated With Childhood Asthma Outcomes in a Mixed Rural-Urban Setting: A Feasibility Study

Discovery and Mediation Analysis of Cross-Phenotype Associations Between Asthma and Body Mass Index in 12q13.2

Suchergebnisse filtern