Variable bleeding phenotype in an Amish pedigree with von Willebrand disease

av Gupta, Sweta, Heiman, Meadow, Duncan, Natalie, Hinckley, Jesse, Di Paola, Jorge, Shapiro, Amy D
I publikationen Am J Hematol (2016)

Quantitative trait locus linkage analysis in a large Amish pedigree identifies novel candidate loci for erythrocyte traits

av Hinckley, Jesse D, Abbott, Diana, Burns, Trudy L, Heiman, Meadow, Shapiro, Amy D, Wang, Kai, Di Paola, Jorge
Publicerad 2013

A null mutation in SERPINE1 protects against biological aging in humans

av Khan, Sadiya S., Shah, Sanjiv J., Klyachko, Ekaterina, Baldridge, Abigail S., Eren, Mesut, Place, Aaron T., Aviv, Abraham, Puterman, Eli, Lloyd-Jones, Donald M., Heiman, Meadow, Miyata, Toshio, Gupta, Sweta, Shapiro, Amy D., Vaughan, Douglas E.
I publikationen Sci Adv (2017)

Identification of Cardiac Fibrosis in Young Adults With a Homozygous Frameshift Variant in SERPINE1

av Khan, Sadiya S., Shah, Sanjiv J., Strande, Jennifer L., Baldridge, Abigail S., Flevaris, Panagiotis, Puckelwartz, Megan J., McNally, Elizabeth M., Rasmussen-Torvik, Laura J., Lee, Daniel C., Carr, James C., Benefield, Brandon C., Afzal, Muhammad Zeeshan, Heiman, Meadow, Gupta, Sweta, Shapiro, Amy D., Vaughan, Douglas E.
I publikationen JAMA Cardiol (2021)