Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Fadi I. Musfee"'
Autor:
Fadi I. Musfee, Omobola O. Oluwafemi, A.J. Agopian, Hakon Hakonarson, Elizabeth Goldmuntz, Laura E. Mitchell
Publikováno v:
HGG Advances, Vol 3, Iss 2, Pp 100098- (2022)
Summary: Maternal effect genes (MEGs) encode factors (e.g., RNA) in the oocyte that control embryonic development prior to activation of the embryonic genome. Over 80 mammalian MEGs have been identified, including several that have been associated wi
Externí odkaz:
https://doaj.org/article/4736ac8353cb4ac88f8f87d2492e5918
Autor:
Fadi I. Musfee, Dongchuan Guo, Amélie C. Pinard, Ellen M. Hostetler, Elizabeth E. Blue, Deborah A. Nickerson, University of Washington Center for Mendelian Genomics (UW‐CMG), Michael J. Bamshad, Dianna M. Milewicz, Siddharth K. Prakash
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Abstract Background Bicuspid aortic valve (BAV) is the most common cardiovascular malformation in adults, with a prevalence of 0.5%–2%. The prevalence of BAV in cohorts who were ascertained due to thoracic aortic aneurysms or acute aortic dissectio
Externí odkaz:
https://doaj.org/article/1d158b20e0ea44649fa7e87963d23e6a
Stroke and mortality rates after off-pump vs. pump-assisted/no-clamp coronary artery bypass grafting
Publikováno v:
The Journal of Cardiovascular Surgery. 63
Ascending aorta manipulation during on-pump coronary artery bypass grafting (CABG) surgery can release embolic matter and may cause stroke. Strategies for lowering the stroke rate associated with coronary artery bypass grafting surgery include off-pu
Autor:
A. J. Agopian, Sadia Malik, Ying Lin, Alanna C. Morrison, Xiao Yu, Richard H. Finnell, Renata H. Benjamin, Sarah C. Fisher, Katherine L. Ludorf, Fadi I Musfee, Yunping Lei, Laura E. Mitchell, Alissa R. Van Zutphen, Xue Gu, Mark A. Canfield, Charlotte A. Hobbs
Publikováno v:
Am J Hypertens
BACKGROUND Maternal hypertension has been associated with congenital heart defect occurrence in several studies. We assessed whether maternal genotypes associated with this condition were also associated with congenital heart defect occurrence. METHO
Autor:
Reynolds M Delgado, O H Frazier, Faisal H. Cheema, Andrew D Lee, Fadi I Musfee, George V. Letsou
Publikováno v:
Tex Heart Inst J
We report the long-term survival of a 46-year-old man supported with a HeartMate II continuous-flow left ventricular assist device after complex repair of a bicuspid aortic valve, anomalous left main coronary artery, and dilated aorta. He has been ma
Autor:
Fadi I Musfee, randa hamden, Mrinalini Buddha, Hayden Naizer, Alexandra Q Zingg Guzman, Cecilia M Ganduglia Cazaban, George V Letsou
Publikováno v:
Circulation. 144
Introduction: The incidence of left ventricular assist device (LVAD) implantation in heart failure (HF) patients across various racial groups has not been examined in large databases. We present an analysis of racial groups and LVAD implantation usin
Autor:
Elizabeth Goldmuntz, Beverly S. Emanuel, Omobola O. Oluwafemi, Fadi I Musfee, A. J. Agopian, Hongbo Xie, Tingwei Guo, Hakon Hakonarson, Laura E. Mitchell, Deanne Taylor, Donna M McDonald-McGinn, Bernice E. Morrow
Publikováno v:
Genes
Volume 12
Issue 7
Genes, Vol 12, Iss 1030, p 1030 (2021)
Volume 12
Issue 7
Genes, Vol 12, Iss 1030, p 1030 (2021)
Conotruncal defects with normally related great vessels (CTD-NRGVs) occur in both patients with and without 22q11.2 deletion syndrome (22q11.2DS), but it is unclear to what extent the genetically complex etiologies of these heart defects may overlap
Autor:
Thanh T. Hoang, Hakon Hakonarson, Elizabeth Goldmuntz, A. J. Agopian, Fadi I Musfee, Laura E. Mitchell
Publikováno v:
Am J Med Genet A
Autor:
Harveen K Lamba, Fadi I Musfee, Subhasis Chatterjee, Ajith P Nair, Andrew B Civitello, Leo Simpson, O H Frazier, George V Letsou
Publikováno v:
Interactive cardiovascular and thoracic surgery. 34(3)
OBJECTIVES Dialysis is considered a contraindication to continuous-flow left ventricular assist device (CF-LVAD) implantation. We evaluated clinical outcomes and survival in carefully selected, low-risk patients with renal failure who required dialys
Autor:
Deanne Taylor, Mark Yandell, Hakon Hakonarson, Elizabeth Goldmuntz, Fadi I Musfee, Martin Tristani-Firouzi, Bernice E. Morrow, W. Scott Watkins, Laura E. Mitchell, A. J. Agopian
Publikováno v:
Genes
Volume 12
Issue 5
Genes, Vol 12, Iss 655, p 655 (2021)
Volume 12
Issue 5
Genes, Vol 12, Iss 655, p 655 (2021)
There is strong evidence for a genetic contribution to non-syndromic congenital heart defects (CHDs). However, exome- and genome-wide studies conducted at the variant and gene-level have identified few genome-wide significant CHD-related genes. Gene-