Area of research
Genetics · Pediatrics, Perinatology and Child Health
Research interest
Research interests include Genetic Associations and Epidemiology, Birth, Development, and Health, Genetic Mapping and Diversity in Plants and Animals, and Genetic and phenotypic traits in livestock.
Multi-omic insights from a multi-ancestry genome-wide meta-analysis of ankylosing spondylitis reveal novel pathways of disease susceptibility
ABS0273 NEW PATHOGENIC PATHWAYS IN ANKYLOSING SPONDYLITIS IDENTIFIED THROUGH MULTI-ANCESTRY GENOMEWIDE ASSOCIATION STUDY
Serum proteomic profiling of physical activity reveals CD300LG as a novel exerkine with a potential causal link to glucose homeostasis
Educational attainment, health outcomes and mortality: a within-sibship Mendelian randomization study
Rare variant analyses across multiethnic cohorts identify novel genes for refractive error
Limb development genes underlie variation in human fingerprint patterns
Exploring the causal effect of maternal pregnancy adiposity on offspring adiposity: Mendelian randomisation using polygenic risk scores
<i>Dnmt3a</i> -mutated clonal hematopoiesis promotes osteoporosis
Osteocyte transcriptome mapping identifies a molecular landscape controlling skeletal homeostasis and susceptibility to skeletal disease
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color
Genome-wide association study of circulating interleukin 6 levels identifies novel loci
Direct and Indirect Effects of Maternal, Paternal, and Offspring Genotypes: Trio-GCTA
Fetal alleles predisposing to metabolically favorable adiposity are associated with higher birth weight
Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses
Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study
RSPO3 impacts body fat distribution and regulates adipose cell biology in vitro
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume
Exploring the role of genetic confounding in the association between maternal and offspring body mass index: evidence from three birth cohorts
Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
The MR-Base platform supports systematic causal inference across the human phenome
An atlas of genetic influences on osteoporosis in humans and mice
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects
Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study
Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference
Identification of Novel Loci Associated With Hip Shape: A Meta-Analysis of Genomewide Association Studies
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero