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Fadi Musfee

TitlePost Doctoral Fellow
InstitutionUniversity of Arkansas for Medical Sciences
DepartmentEpidemiology, College of Public Health
DivisionEpidemiology
Address220 UAMS Campus Dr.
Mail Slot # 820
Little Rock AR 72205
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions. Don't see publications published under other names? Login to add alternative names.
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    1. Musfee FI, Oluwafemi OO, Agopian AJ, Hakonarson H, Goldmuntz E, Mitchell LE. Maternal effect genes as risk factors for congenital heart defects. HGG Adv. 2022 Apr 14; 3(2):100098. PMID: 35345810.
      View in: PubMed
    2. Lamba HK, Musfee FI, Chatterjee S, Nair AP, Civitello AB, Simpson L, Frazier OH, Letsou GV. The influence of preoperative dialysis on survival after continuous-flow left ventricular assist device implantation. Interact Cardiovasc Thorac Surg. 2022 02 21; 34(3):470-477. PMID: 34966937.
      View in: PubMed
    3. Oluwafemi OO, Musfee FI, Mitchell LE, Goldmuntz E, Xie HM, Hakonarson H, Morrow BE, Guo T, Taylor DM, McDonald-McGinn DM, Emanuel BS, Agopian AJ. Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States. Genes (Basel). 2021 07 01; 12(7). PMID: 34356046.
      View in: PubMed
    4. Musfee FI, Agopian AJ, Goldmuntz E, Hakonarson H, Morrow BE, Taylor DM, Tristani-Firouzi M, Watkins WS, Yandell M, Mitchell LE. Common Variation in Cytoskeletal Genes is Associated with Conotruncal Heart Defects. Genes (Basel). 2021 04 27; 12(5). PMID: 33925651.
      View in: PubMed
    5. Lei Y, Ludorf KL, Yu X, Benjamin RH, Gu X, Lin Y, Finnell RH, Mitchell LE, Musfee FI, Malik S, Canfield MA, Morrison AC, Hobbs CA, Van Zutphen AR, Fisher S, Agopian AJ. Maternal Hypertension-Related Genotypes and Congenital Heart Defects. Am J Hypertens. 2021 02 18; 34(1):82-91. PMID: 32710738.
      View in: PubMed
    6. Musfee FI, Guo D, Pinard AC, Hostetler EM, Blue EE, Nickerson DA, Bamshad MJ, Milewicz DM, Prakash SK. 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. Mol Genet Genomic Med. 2020 10; 8(10):e1406. PMID: 32748548.
      View in: PubMed
    7. Letsou GV, Musfee FI, Lee AD, Cheema F, Delgado RM, Frazier OH. Ten-Year Survival With a Continuous-Flow Left Ventricular Assist Device and Aortic Valve Closure. Tex Heart Inst J. 2020 08 01; 47(4):325-328. PMID: 33472231.
      View in: PubMed
    8. Sewda A, Agopian AJ, Goldmuntz E, Hakonarson H, Morrow BE, Musfee F, Taylor D, Mitchell LE. Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects. PLoS One. 2020; 15(6):e0234357. PMID: 32516339.
      View in: PubMed
    9. Letsou GV, Musfee FI, Cheema FH, Lee AD, Loor G, Morgan J, Rosengart T, Frazier OH. Heterotopic Cardiac Transplantation: Long-term Results and Fate of the Native Heart. Ann Thorac Surg. 2020 10; 110(4):1316-1323. PMID: 32194033.
      View in: PubMed
    10. Zhao Y, Diacou A, Johnston HR, Musfee FI, McDonald-McGinn DM, McGinn D, Crowley TB, Repetto GM, Swillen A, Breckpot J, Vermeesch JR, Kates WR, Digilio MC, Unolt M, Marino B, Pontillo M, Armando M, Di Fabio F, Vicari S, van den Bree M, Moss H, Owen MJ, Murphy KC, Murphy CM, Murphy D, Schoch K, Shashi V, Tassone F, Simon TJ, Shprintzen RJ, Campbell L, Philip N, Heine-Suñer D, García-Miñaúr S, Fernández L, Bearden CE, Vingerhoets C, van Amelsvoort T, Eliez S, Schneider M, Vorstman JAS, Gothelf D, Zackai E, Agopian AJ, Gur RE, Bassett AS, Emanuel BS, Goldmuntz E, Mitchell LE, Wang T, Morrow BE. Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects. Am J Hum Genet. 2020 01 02; 106(1):26-40. PMID: 31870554.
      View in: PubMed
    11. Agopian AJ, Hoang TT, Goldmuntz E, Hakonarson H, Musfee FI, Mitchell LE. X-chromosome association studies of congenital heart defects. Am J Med Genet A. 2020 01; 182(1):250-254. PMID: 31729158.
      View in: PubMed
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