Associate Professor
University of Michigan
Ann Arbor, Michigan, United States
I am an active clinician in Neonatal-Perinatal medicine at the University of Michigan, Ann Arbor. My laboratory investigates the genetic determinants of complex phenotypes that surround the maintenance of hemostasis and the avoidance of hemorrhage or excessive thrombosis. We have developed expertise in computational genetics (genome-wide association studies, rare variant association studies, mendelian randomization) and bench based genetic screens (phage display, deep mutational scanning, lentivirus delivered CRISPR targeting and proximity labeling proteomics). I train undergraduates, PhD and post-doctoral fellows in basic cell and molecular biology techniques to answer questions regarding the role of human genetic variation in thrombosis and hemostasis. I currently serve as an associate editor for the Journal of Thrombosis and Haemostasis focusing on manuscripts using genomic tools or pediatric populations. I serve on the variant curation expert panel for von Willebrand disease as a part of ClinGen.
OC 09.5 - Identification and validation of novel stabilin-2 plasma ligands
Saturday, June 24, 2023
14:00 – 14:15 ET
SOA 02.1 - Complex Trait Genetics in Thrombosis and Hemostasis
Sunday, June 25, 2023
08:00 – 08:25 ET