UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 228

Sortiert nach

Genetic and clinical characteristics of treatment-resistant depression using primary care records in two UK cohorts

Molecular psychiatry, 2021-07, Vol.26 (7), p.3363-3373

2021

Volltextzugriff (PDF)

Mendelian randomisation and causal inference in observational epidemiology

PLoS medicine, 2008-08, Vol.5 (8), p.e177-e177

2008

Volltextzugriff (PDF)

Genomic copy number variation, human health, and disease

The Lancet (British edition), 2009-07, Vol.374 (9686), p.340-350

2009

Volltextzugriff (PDF)

The sputum microbiome is distinct between COPD and health, independent of smoking history

Respiratory research, 2020-07, Vol.21 (1), p.183-183, Article 183

2020

Volltextzugriff (PDF)

Adjusting for treatment effects in studies of quantitative traits: antihypertensive therapy and systolic blood pressure

Statistics in medicine, 2005-10, Vol.24 (19), p.2911-2935

2005

Volltextzugriff (PDF)

Genome-wide gene-air pollution interaction analysis of lung function in 300,000 individuals

Environment international, 2022-01, Vol.159, p.107041, Article 107041

2022

Volltextzugriff (PDF)

A rapid RT-LAMP SARS-CoV-2 screening assay for collapsing asymptomatic COVID-19 transmission

PloS one, 2022-09, Vol.17 (9), p.e0273912

2022

Volltextzugriff (PDF)

Identifying potential causal effects of age at menarche: a Mendelian randomization phenome-wide association study

BMC medicine, 2020-03, Vol.18 (1), p.71-17, Article 71

2020

Volltextzugriff (PDF)

Genetic insights into smoking behaviours in 10,558 men of African ancestry from continental Africa and the UK

Scientific reports, 2022-11, Vol.12 (1), p.18828-18828, Article 18828

2022

Volltextzugriff (PDF)

How to design and implement a university-based COVID-19 testing programme? An evaluation of a novel RT-LAMP COVID-19 testing programme in a UK university

BMC health services research, 2022-12, Vol.22 (1), p.1502-8, Article 1502

2022

Volltextzugriff (PDF)

Access to personal protective equipment in healthcare workers during the COVID-19 pandemic in the United Kingdom: results from a nationwide cohort study (UK-REACH)

BMC health services research, 2022-07, Vol.22 (1), p.867-867, Article 867

2022

Volltextzugriff (PDF)

Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease

Nature communications, 2023-10, Vol.14 (1), p.6713-6713, Article 6713

2023

Volltextzugriff (PDF)

Healthcare workers’ views on mandatory SARS-CoV-2 vaccination in the UK: A cross-sectional, mixed-methods analysis from the UK-REACH study

EClinicalMedicine, 2022-04, Vol.46, p.101346, Article 101346

2022

Volltextzugriff (PDF)

Targeted Sequencing of Lung Function Loci in Chronic Obstructive Pulmonary Disease Cases and Controls

PloS one, 2017-01, Vol.12 (1), p.e0170222

2017

Volltextzugriff (PDF)

Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome)

Clinical science (1979), 2014-05, Vol.126 (10), p.721

2014

Volltextzugriff (PDF)

GSTCD and INTS12 regulation and expression in the human lung

PloS one, 2013-09, Vol.8 (9), p.e74630

2013

Volltextzugriff (PDF)

Improving ethnic diversity in respiratory genomics research

The European respiratory journal, 2021-10, Vol.58 (4), p.2101615

2021

Volltextzugriff (PDF)

Whole exome re-sequencing implicates CCDC38 and cilia structure and function in resistance to smoking related airflow obstruction

PLoS genetics, 2014-05, Vol.10 (5), p.e1004314-e1004314

2014

Volltextzugriff (PDF)

Persistent hesitancy for SARS-CoV-2 vaccines among healthcare workers in the United Kingdom: analysis of longitudinal data from the UK-REACH cohort study

The Lancet regional health. Europe, 2022-02, Vol.13, p.100299, Article 100299

2022

Volltextzugriff (PDF)

Pleiotropic associations of heterozygosity for the SERPINA1 Z allele in the UK Biobank

ERJ open research, 2021-04, Vol.7 (2), p.49

2021

Volltextzugriff (PDF)

Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis

American journal of respiratory and critical care medicine, 2020-03, Vol.201 (5), p.564-574

2020

Volltextzugriff (PDF)

Identification and characterisation of a rare MTTP variant underlying hereditary non-alcoholic fatty liver disease

JHEP reports, 2023-08, Vol.5 (8), p.100764-100764, Article 100764

2023

Volltextzugriff (PDF)

Copy number variation of the beta-defensin genes in europeans: no supporting evidence for association with lung function, chronic obstructive pulmonary disease or asthma

PloS one, 2014-01, Vol.9 (1), p.e84192-e84192

2014

Volltextzugriff (PDF)

1 – 25 von 228

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(223)
Mit Volltextzugriff
(190)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(176)
Humans
(153)
Life Sciences & Biomedicine
(149)
Male
(77)
Female
(75)
Middle Aged
(67)
Genome-Wide Association Study
(53)
Adult
(50)
Genomes
(47)
Aged
(42)
Polymorphism, Single Nucleotide
(41)
Genetic Predisposition To Disease
(36)
Genetics
(36)
Risk Factors
(36)
Biological And Medical Sciences
(34)
Studies
(34)
Chronic Obstructive Pulmonary Disease
(33)
Genetics & Heredity
(32)
Respiratory System
(32)
Medical Sciences
(31)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Genetic and clinical characteristics of treatment-resistant depression using primary care records in two UK cohorts

Mendelian randomisation and causal inference in observational epidemiology

Genomic copy number variation, human health, and disease

The sputum microbiome is distinct between COPD and health, independent of smoking history

Adjusting for treatment effects in studies of quantitative traits: antihypertensive therapy and systolic blood pressure

Genome-wide gene-air pollution interaction analysis of lung function in 300,000 individuals

A rapid RT-LAMP SARS-CoV-2 screening assay for collapsing asymptomatic COVID-19 transmission

Identifying potential causal effects of age at menarche: a Mendelian randomization phenome-wide association study

Genetic insights into smoking behaviours in 10,558 men of African ancestry from continental Africa and the UK

How to design and implement a university-based COVID-19 testing programme? An evaluation of a novel RT-LAMP COVID-19 testing programme in a UK university

Access to personal protective equipment in healthcare workers during the COVID-19 pandemic in the United Kingdom: results from a nationwide cohort study (UK-REACH)

Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease

The United Kingdom Research study into Ethnicity And COVID-19 outcomes in Healthcare workers (UK-REACH): protocol for a prospective longitudinal cohort study of healthcare and ancillary workers in UK healthcare settings

Healthcare workers’ views on mandatory SARS-CoV-2 vaccination in the UK: A cross-sectional, mixed-methods analysis from the UK-REACH study

Targeted Sequencing of Lung Function Loci in Chronic Obstructive Pulmonary Disease Cases and Controls

Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome)

Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery disease

GSTCD and INTS12 regulation and expression in the human lung

Improving ethnic diversity in respiratory genomics research

Whole exome re-sequencing implicates CCDC38 and cilia structure and function in resistance to smoking related airflow obstruction

Persistent hesitancy for SARS-CoV-2 vaccines among healthcare workers in the United Kingdom: analysis of longitudinal data from the UK-REACH cohort study

Pleiotropic associations of heterozygosity for the SERPINA1 Z allele in the UK Biobank

Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis

Identification and characterisation of a rare MTTP variant underlying hereditary non-alcoholic fatty liver disease

Copy number variation of the beta-defensin genes in europeans: no supporting evidence for association with lung function, chronic obstructive pulmonary disease or asthma

Suchergebnisse filtern