Variable bleeding phenotype in an Amish pedigree with von Willebrand disease

Por Gupta, Sweta, Heiman, Meadow, Duncan, Natalie, Hinckley, Jesse, Di Paola, Jorge, Shapiro, Amy D
Publicado no Am J Hematol (2016)

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

Por Hinckley, Jesse D, Abbott, Diana, Burns, Trudy L, Heiman, Meadow, Shapiro, Amy D, Wang, Kai, Di Paola, Jorge
Publicado em 2013

A null mutation in SERPINE1 protects against biological aging in humans

Por 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.
Publicado no Sci Adv (2017)

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

Por 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.
Publicado no JAMA Cardiol (2021)