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Author/Creator Hostetler, Ellen M.

1. Expanding ACTA2 genotypes with corresponding phenotypes overlapping with smooth muscle dysfunction syndrome. Issue 8 (14th May 2022)

Authors:
Kaw, Anita; Kaw, Kaveeta; Hostetler, Ellen M.; Beleza‐Meireles, Ana; Smith‐Collins, Adam; Armstrong, Catherine; Scurr, Ingrid; Cotts, Timothy; Aatre, Rajani; Bamshad, Michael J.; Earl, Dawn; Groner, Abraham; Agre, Katherine; Raveh, Yehuda; Kwartler, Callie S.; Milewicz, Dianna M.
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 8(2022)
Page Start:
2389
Record Type:
Journal Article
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2. LOX Mutations Predispose to Thoracic Aortic Aneurysms and Dissections. Issue 6 (18th March 2016)

Authors:
Guo, Dong-chuan; Regalado, Ellen S.; Gong, Limin; Duan, Xueyan; Santos-Cortez, Regie Lyn P.; Arnaud, Pauline; Ren, Zhao; Cai, Bo; Hostetler, Ellen M.; Moran, Rocio; Liang, David; Estrera, Anthony; Safi, Hazim J.; Leal, Suzanne M.; Bamshad, Michael J.; Shendure, Jay; Nickerson, Deborah A.; Jondeau...
Journal:
Circulation research
Issue:
Volume 118:Issue 6(2016)
Page Start:
Record Type:
Journal Article
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3. Rare deleterious variants of NOTCH1, GATA4, SMAD6, and ROBO4 are enriched in BAV with early onset complications but not in BAV with heritable thoracic aortic disease. Issue 10 (3rd August 2020)

Authors:
Musfee, Fadi I.; Guo, Dongchuan; Pinard, Amélie C.; Hostetler, Ellen M.; Blue, Elizabeth E.; Nickerson, Deborah A.; Bamshad, Michael J.; Milewicz, Dianna M.; Prakash, Siddharth K.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 8:Issue 10(2020)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗