This laboratory has recently contributed to the large-scale association based human genetics studies identifying coronary heart disease (CHD) risk loci. Post-genomics studies in this laboratory employing bioinformatics, in vitro cell culture, and mouse genetic models, are being employed to identify the mechanisms by which CHD-associated alleles contribute to disease risk.
In particular, interest is focused on transcription factors that are active in the blood vessel wall, and high throughput methods are being employed to characterize the gene regulatory program that is mediated by these disease factors.
Postdoctoral fellows are sought with experience in the study of transcriptional regulatory mechanisms, high throughput methods such as ChIPseq and RNAseq, bioinformatic analysis of such genomic data, or smooth muscle cell biology.
The Division of Cardiovascular Medicine and the Stanford University School of Medicine provide superlative training opportunities at the post-doctoral level in a highly stimulating and interactive environment.
To apply, please forward your CV and a personal statement to Thomas Quertermous (tomq1@stanford.edu).
Stanford University is an equal opportunity employer and minority applicants are encouraged to apply
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