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...

Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association

Circulation (New York, N.Y.), 2022-08, Vol.146 (8), p.e93-e118

2022

Volltextzugriff (PDF)

Functionally informed fine-mapping and polygenic localization of complex trait heritability

Nature genetics, 2020-12, Vol.52 (12), p.1355-1363

2020

Volltextzugriff (PDF)

Multiethnic polygenic risk scores improve risk prediction in diverse populations

Genetic epidemiology, 2017-12, Vol.41 (8), p.811-823

2017

Volltextzugriff (PDF)

Phenome-wide Mendelian randomization study of plasma triglyceride levels and 2600 disease traits

eLife, 2023-03, Vol.12

2023

Volltextzugriff (PDF)

Genetic architecture of cardiometabolic risks in people living with HIV

BMC medicine, 2020-10, Vol.18 (1), p.288-288, Article 288

2020

Volltextzugriff (PDF)

Machine Learning Identifies Plasma Metabolites Associated With Heart Failure in Underrepresented Populations With the TTR V122I Variant

Journal of the American Heart Association, 2023-04, Vol.12 (8), p.e027736

2023

Volltextzugriff (PDF)

Correction to: Genetic architecture of cardiometabolic risks in people living with HIV

BMC medicine, 2021-05, Vol.19 (1), p.114-114, Article 114

2021

Volltextzugriff (PDF)

Improving the informativeness of Mendelian disease-derived pathogenicity scores for common disease

Nature communications, 2020-12, Vol.11 (1), p.6258-6258, Article 6258

2020

Volltextzugriff (PDF)

Short-term prediction of coronary artery disease using serum metabolomic patterns

American heart journal plus, 2022-12, Vol.24, p.100232, Article 100232

2022

Volltextzugriff (PDF)

Coronary Risk Estimation Based on Clinical Data in Electronic Health Records

Journal of the American College of Cardiology, 2022-03, Vol.79 (12), p.1155-1166

2022

Volltextzugriff (PDF)

Development of a human genetics-guided priority score for 19,365 genes and 399 drug indications

Nature genetics, 2024-01, Vol.56 (1), p.51-59

2024

Volltextzugriff (PDF)

Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets

Nature communications, 2021-10, Vol.12 (1), p.6052-6052, Article 6052

2021

Volltextzugriff (PDF)

Exome sequence analysis identifies rare coding variants associated with a machine learning-based marker for coronary artery disease

Nature genetics, 2024-07, Vol.56 (7), p.1412-1419

2024

Volltextzugriff (PDF)

Reconciling S-LDSC and LDAK functional enrichment estimates

Nature genetics, 2019-08, Vol.51 (8), p.1202-1204

2019

Volltextzugriff (PDF)

Machine learning-based marker for coronary artery disease: derivation and validation in two longitudinal cohorts

The Lancet (British edition), 2023-01, Vol.401 (10372), p.215-225

2023

Volltextzugriff (PDF)

Online Education in Times of COVID: Adapting and Deploying a Data Science Program in Mexico

Harvard Data Science Review, 2022-04

2022

Volltextzugriff (PDF)

Genome-wide polygenic risk score for retinopathy of type 2 diabetes

Human molecular genetics, 2021-05, Vol.30 (10), p.952-960

2021

Volltextzugriff (PDF)

Genome-first recall of healthy individuals by polygenic risk score reveals differences in coronary artery calcium

The American heart journal, 2022-08, Vol.250, p.29-33

2022

Volltextzugriff (PDF)

Muesli Intake May Protect Against Coronary Artery Disease

JACC. Advances (Online), 2024-04, Vol.3 (4), p.100888, Article 100888

2024

Volltextzugriff (PDF)

Founder effect and ancestral origin of the spinocerebellar ataxia type 7 (SCA7) mutation in Mexican families

Neurogenetics, 2014-03, Vol.15 (1), p.13-17

2014

Volltextzugriff (PDF)

Muesli Intake May Protect Against Coronary Artery Disease: Mendelian Randomization on 13 Dietary Traits

JACC. Advances (Online), 2024-04, Vol.3 (4)

2024

Volltextzugriff (PDF)

Leveraging Functional Annotations and Multiethnic Data to Improve Polygenic Risk Prediction

Marquez Luna, Carla

2018

Volltextzugriff (PDF)

Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico

Nature (London), 2014-02, Vol.506 (7486), p.97-101

2014

Volltextzugriff (PDF)

Multi-ethnic polygenic risk scores improve risk prediction in diverse populations

Genetic epidemiology, 2017-11, Vol.41 (8), p.811-823

2017

Volltextzugriff (PDF)

Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes

Proceedings of the National Academy of Sciences - PNAS, 2014-09, Vol.111 (36), p.13127-13132

2014

Volltextzugriff (PDF)

1 – 25 von 26

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(25)
Mit Volltextzugriff
(21)

Publikationsform

Artikel
(25)
Dissertationen
(1)

Sprache

Englisch
(26)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association

Functionally informed fine-mapping and polygenic localization of complex trait heritability

Multiethnic polygenic risk scores improve risk prediction in diverse populations

Phenome-wide Mendelian randomization study of plasma triglyceride levels and 2600 disease traits

Genetic architecture of cardiometabolic risks in people living with HIV

Machine Learning Identifies Plasma Metabolites Associated With Heart Failure in Underrepresented Populations With the TTR V122I Variant

Correction to: Genetic architecture of cardiometabolic risks in people living with HIV

Improving the informativeness of Mendelian disease-derived pathogenicity scores for common disease

Short-term prediction of coronary artery disease using serum metabolomic patterns

Coronary Risk Estimation Based on Clinical Data in Electronic Health Records

Development of a human genetics-guided priority score for 19,365 genes and 399 drug indications

Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets

Exome sequence analysis identifies rare coding variants associated with a machine learning-based marker for coronary artery disease

Reconciling S-LDSC and LDAK functional enrichment estimates

Machine learning-based marker for coronary artery disease: derivation and validation in two longitudinal cohorts

Online Education in Times of COVID: Adapting and Deploying a Data Science Program in Mexico

Genome-wide polygenic risk score for retinopathy of type 2 diabetes

Genome-first recall of healthy individuals by polygenic risk score reveals differences in coronary artery calcium

Muesli Intake May Protect Against Coronary Artery Disease

Founder effect and ancestral origin of the spinocerebellar ataxia type 7 (SCA7) mutation in Mexican families

Muesli Intake May Protect Against Coronary Artery Disease: Mendelian Randomization on 13 Dietary Traits

Leveraging Functional Annotations and Multiethnic Data to Improve Polygenic Risk Prediction

Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico

Multi-ethnic polygenic risk scores improve risk prediction in diverse populations

Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes

Suchergebnisse filtern