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Detection of human adaptation during the past 2000 years

Science (American Association for the Advancement of Science), 2016-11, Vol.354 (6313), p.760-764

2016

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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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A survey about methods dedicated to epistasis detection

Frontiers in genetics, 2015-09, Vol.6 (Article 285), p.285-285

2015

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SMMB: a stochastic Markov blanket framework strategy for epistasis detection in GWAS

Bioinformatics, 2018-08, Vol.34 (16), p.2773-2780

2018

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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 genome-wide association study identifies novel risk loci for type 2 diabetes

Nature, 2007-02, Vol.445 (7130), p.881-885

2007

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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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Jointly Modelling Single Nucleotide Polymorphisms With Longitudinal and Time-to-Event Trait: An Application to Type 2 Diabetes and Fasting Plasma Glucose

Frontiers in genetics, 2018-06, Vol.9, p.210-210

2018

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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.849-849, Article 849

2022

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Aging and Diets Regulate the Rat Anterior Pituitary and Hypothalamic Transcriptome

Neuroendocrinology, 2013-01, Vol.97 (2), p.146-159

2013

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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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Abstract P1179: Evaluation Of A Machine Learning-based Metabolic Marker For Coronary Artery Disease In The UK Biobank

Circulation research, 2023-08, Vol.133 (Suppl_1)

2023

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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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A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

Nature genetics, 2012-06, Vol.44 (6), p.659-669

2012

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The Lin28/let-7 Axis Regulates Glucose Metabolism

Cell, 2011-09, Vol.147 (1), p.81-94

2011

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Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

Nature genetics, 2010-07, Vol.42 (7), p.579-589

2010

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CA-075 - Variants génétiques associés à la trajectoire de la glycémie à jeun et à l’incidence du diabète de type 2 : Une approche par modèle joint

Diabetes & metabolism, 2017-03, Vol.43 (2), p.A76-A76

2017

Volltextzugriff (PDF)

Variants génétiques associés à la trajectoire de la glycémie à jeun et à l’incidence du diabète de type 2 : Une approche par modèle joint

Diabetes & metabolism, 2017-03, Vol.43 (2), p.A76

2017

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Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians

Nature genetics, 2012-01, Vol.44 (1), p.67-72

2012

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Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits

PLoS genetics, 2011-03, Vol.7 (3), p.e1001324-e1001324

2011

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Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis

Nature genetics, 2012-05, Vol.44 (5), p.483-489

2012

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ALDH2 Polymorphism rs671, but Not ADH1B Polymorphism rs1229984, Increases Risk for Hypo‐HDL‐Cholesterolemia in a/a Carriers Compared to the G/G Carriers

Lipids, 2018-08, Vol.53 (8), p.797-807

2018

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Use of Diagnostic Codes for Primary Open-Angle Glaucoma Polygenic Risk Score Construction in Electronic Health Record–Linked Biobanks

American journal of ophthalmology, 2024-11, Vol.267, p.204-212

2024

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Detection of human adaptation during the past 2000 years

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

A survey about methods dedicated to epistasis detection

SMMB: a stochastic Markov blanket framework strategy for epistasis detection in GWAS

Population-Based Penetrance of Deleterious Clinical Variants

A genome-wide association study identifies novel risk loci for type 2 diabetes

Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes

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

Jointly Modelling Single Nucleotide Polymorphisms With Longitudinal and Time-to-Event Trait: An Application to Type 2 Diabetes and Fasting Plasma Glucose

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

Aging and Diets Regulate the Rat Anterior Pituitary and Hypothalamic Transcriptome

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

Abstract P1179: Evaluation Of A Machine Learning-based Metabolic Marker For Coronary Artery Disease In The UK Biobank

Coronary Risk Estimation Based on Clinical Data in Electronic Health Records

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

The Lin28/let-7 Axis Regulates Glucose Metabolism

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

CA-075 - Variants génétiques associés à la trajectoire de la glycémie à jeun et à l’incidence du diabète de type 2 : Une approche par modèle joint

Variants génétiques associés à la trajectoire de la glycémie à jeun et à l’incidence du diabète de type 2 : Une approche par modèle joint

Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians

Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits

Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis

ALDH2 Polymorphism rs671, but Not ADH1B Polymorphism rs1229984, Increases Risk for Hypo‐HDL‐Cholesterolemia in a/a Carriers Compared to the G/G Carriers

Use of Diagnostic Codes for Primary Open-Angle Glaucoma Polygenic Risk Score Construction in Electronic Health Record–Linked Biobanks

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