Variable bleeding phenotype in an Amish pedigree with von Willebrand disease

Yazar: Gupta, Sweta, Heiman, Meadow, Duncan, Natalie, Hinckley, Jesse, Di Paola, Jorge, Shapiro, Amy D
Yayımlandı Am J Hematol (2016)

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

Yazar: Hinckley, Jesse D, Abbott, Diana, Burns, Trudy L, Heiman, Meadow, Shapiro, Amy D, Wang, Kai, Di Paola, Jorge
Baskı/Yayın Bilgisi 2013

A null mutation in SERPINE1 protects against biological aging in humans

Yazar: 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.
Yayımlandı Sci Adv (2017)

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

Yazar: 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.
Yayımlandı JAMA Cardiol (2021)