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Publications by Vincent Plagnol

Dense Genotyping Identifies and Localizes Multiple Common and Rare Variant Association Signals in Celiac Disease

Nature Genetics

English

Whole-Exome Sequencing in the Investigation of Retinal Dystrophy

English

Plasma Urate Concentration and Risk of Coronary Heart Disease: A Mendelian Randomisation Analysis

The Lancet Diabetes and Endocrinology

Internal Medicine

English

Bi-Allelic Loss-Of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

American Journal of Human Genetics

English

Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita

American Journal of Human Genetics

English

Limited Clinical Utility of Non-Invasive Prenatal Testing for Subchromosomal Abnormalities

American Journal of Human Genetics

English

Correction: Insights Into the Genetic Epidemiology of Crohn's and Rare Diseases in the Ashkenazi Jewish Population

Molecular Biology

Cancer Research

English

Variants Génétiques Associés Au Diabète De Type 1 Et Contrôle De L’expression Du Récepteur De L’IL-2

Medecine/Sciences

Molecular Biology

English

A Robust Statistical Method for Case-Control Association Testing With Copy Number Variation

Nature Genetics

English

Fluorescence Intensity Normalisation: Correcting for Time Effects in Large-Scale Flow Cytometric Analysis

Advances in Bioinformatics

Biomedical Engineering

Computer Science Applications

Molecular Biology

English