publication venue for
- Evaluation of power of the Illumina HumanOmni5M-4v1 BeadChip to detect risk variants for human complex diseases.. 24:1029-34. 2015
- No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia.. 23:555-7. 2014
- Gene by stress genome-wide interaction analysis and path analysis identify EBF1 as a cardiovascular and metabolic risk gene.. 23:854-62. 2014
- A gene-centric analysis of activated partial thromboplastin time and activated protein C resistance using the HumanCVD focused genotyping array.. 21:779-83. 2012
- Characterization of autosomal copy-number variation in African Americans: the HyperGEN Study.. 19:1271-5. 2011
- Genome-Wide Association Study of Postoperative Cognitive Dysfunction in older surgical patients 2020
- Genome-Wide Association Study of Postoperative Cognitive Dysfunction in older surgical patients 2020