Area of research
Genetics · Pediatrics, Perinatology and Child Health
Research interest
Research interests include Genetic Associations and Epidemiology, Birth, Development, and Health, Chronic Kidney Disease and Diabetes, and Nutrition, Genetics, and Disease.
Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
A saturated map of common genetic variants associated with human height
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Early-life respiratory tract infections and the risk of school-age lower lung function and asthma: a meta-analysis of 150 000 European children
Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies
Urinary Proteomics Identifies Cathepsin D as a Biomarker of Rapid eGFR Decline in Type 1 Diabetes
Genome-wide study of early and severe childhood asthma identifies interaction between CDHR3 and GSDMB
A Saturated Map of Common Genetic Variants Associated with Human Height from 5.4 Million Individuals of Diverse Ancestries
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
The trans-ancestral genomic architecture of glycemic traits
Genetic association study of childhood aggression across raters, instruments, and age
Genome-wide association study of circulating interleukin 6 levels identifies novel loci
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4
Repositioning of the global epicentre of non-optimal cholesterol
Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
FUT2–ABO epistasis increases the risk of early childhood asthma and Streptococcus pneumoniae respiratory illnesses
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen
GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI
A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity
Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function
Metabolomic Assessment Reveals Alteration in Polyols and Branched Chain Amino Acids Associated With Present and Future Renal Impairment in a Discovery Cohort of 637 Persons With Type 1 Diabetes
Protein-coding variants contribute to the risk of atopic dermatitis and skin-specific gene expression
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume
Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group