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Genetic and phenotypic profiling of supranormal ejection fraction reveals decreased survival and underdiagnosed heart failure

European journal of heart failure, 2022-11, Vol.24 (11), p.2118-2127

2022

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Population-Based Penetrance of Deleterious Clinical Variants

JAMA : the journal of the American Medical Association, 2022-01, Vol.327 (4), p.350

2022

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A machine learning model identifies patients in need of autoimmune disease testing using electronic health records

Nature communications, 2023-04, Vol.14 (1), p.2385-12, Article 2385

2023

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

eLife, 2023-03, Vol.12

2023

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Derivation and Validation of Genome-Wide Polygenic Score for Ischemic Heart Failure

Journal of the American Heart Association, 2021-11, Vol.10 (22), p.e021916-e021916

2021

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A tissue-level phenome-wide network map of colocalized genes and phenotypes in the UK Biobank

Communications biology, 2022-08, Vol.5 (1), p.849-9, Article 849

2022

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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

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Machine learning-based markers for CAD – Authors' reply

The Lancet (British edition), 2023-07, Vol.402 (10397), p.184-184

2023

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Penetrance of Deleterious Clinical Variants-Reply

JAMA : the journal of the American Medical Association, 2022-05, Vol.327 (19), p.1927

2022

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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

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Cholesterol Contributes to Risk, Severity, and Machine Learning-Driven Diagnosis of Lyme Disease

Clinical infectious diseases, 2023-09, Vol.77 (6), p.839-847

2023

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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

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

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

2021

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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

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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

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Non-invasive ventilation versus mechanical ventilation in hypoxemic patients with COVID-19

Infection, 2021-10, Vol.49 (5), p.989-997

2021

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Genome-first evaluation with exome sequence and clinical data uncovers underdiagnosed genetic disorders in a large healthcare system

Cell reports. Medicine, 2024-05, Vol.5 (5), p.101518, Article 101518

2024

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Tissue-specific genetic features inform prediction of drug side effects in clinical trials

Science advances, 2020-09, Vol.6 (37)

2020

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Genetic pleiotropy of ERCC6 loss‐of‐function and deleterious missense variants links retinal dystrophy, arrhythmia, and immunodeficiency in diverse ancestries

Human mutation, 2021-08, Vol.42 (8), p.969-977

2021

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

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

2024

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Dermestes maculatus: an intermediate-germ beetle model system for evo-devo

EvoDevo, 2015-10, Vol.6 (1), p.32-32, Article 32

2015

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Muesli Intake May Protect Against Coronary Artery Disease

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

2024

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Systematic Control of the Orientation of Organic Phosphorescent Pt Complexes in Thin Films for Increased Optical Outcoupling

Advanced materials (Weinheim), 2019-08, Vol.31 (32), p.e1900921-n/a

2019

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Rapid implementation of SARS-CoV-2 sequencing to investigate cases of health-care associated COVID-19: a prospective genomic surveillance study

The Lancet infectious diseases, 2020-11, Vol.20 (11), p.1263-1271

2020

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The hypoxic cancer secretome induces pre-metastatic bone lesions through lysyl oxidase

Nature (London), 2015-06, Vol.522 (7554), p.106-110

2015

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Genetic and phenotypic profiling of supranormal ejection fraction reveals decreased survival and underdiagnosed heart failure

Population-Based Penetrance of Deleterious Clinical Variants

A machine learning model identifies patients in need of autoimmune disease testing using electronic health records

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

Derivation and Validation of Genome-Wide Polygenic Score for Ischemic Heart Failure

A tissue-level phenome-wide network map of colocalized genes and phenotypes in the UK Biobank

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

Machine learning-based markers for CAD – Authors' reply

Penetrance of Deleterious Clinical Variants-Reply

Coronary Risk Estimation Based on Clinical Data in Electronic Health Records

Cholesterol Contributes to Risk, Severity, and Machine Learning-Driven Diagnosis of Lyme Disease

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

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

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

Non-invasive ventilation versus mechanical ventilation in hypoxemic patients with COVID-19

Genome-first evaluation with exome sequence and clinical data uncovers underdiagnosed genetic disorders in a large healthcare system

Tissue-specific genetic features inform prediction of drug side effects in clinical trials

Genetic pleiotropy of ERCC6 loss‐of‐function and deleterious missense variants links retinal dystrophy, arrhythmia, and immunodeficiency in diverse ancestries

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

Dermestes maculatus: an intermediate-germ beetle model system for evo-devo

Muesli Intake May Protect Against Coronary Artery Disease

Systematic Control of the Orientation of Organic Phosphorescent Pt Complexes in Thin Films for Increased Optical Outcoupling

Rapid implementation of SARS-CoV-2 sequencing to investigate cases of health-care associated COVID-19: a prospective genomic surveillance study

The hypoxic cancer secretome induces pre-metastatic bone lesions through lysyl oxidase

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