publication venue for
- Examination of a novel expression-based gene-SNP annotation strategy to identify tissue-specific contributions to heritability in multiple traits 2024
- Imputation of behavioral candidate gene repeat variants in 486,551 publicly-available UK Biobank individuals 2019
- A fast and accurate method for detection of IBD shared haplotypes in genome-wide SNP data 2017
- An omnibus test for family-based association studies with multiple SNPs and multiple phenotypes 2010
- A recurrent homozygous single amino acid deletion (p.Glu133del) in MED22 leads to a progressive neurodevelopmental disorder with microcephaly, dystonia, seizures and neurodegeneration 2024