Mahmud Michael Barmada

Mahmud Michael Barmada (November 14, 1969 – December 2, 2016) Known as Michael Barmada , was an American geneticist and academic administrator from a Syrian descent ; served as associate director of the Center for Simulation and Modeling and co-director of the Bioinformatics Resource Center in the Institute for Personalized Medicine at University of Pittsburgh.[1][2]

Michael Barmada
Born(1969-11-14)November 14, 1969
DiedDecember 2, 2016(2016-12-02) (aged 47)
NationalityAmerican
Alma materCarnegie Mellon University (BS)
Johns Hopkins University (M.A)
University of Pittsburgh (PhD)
OccupationGeneticist
OrganizationUniversity of Pittsburgh
Parents
  • Bicher barmada (father)
  • Mamdouha Ahdab-Barmada (mother)
RelativesMustafa Bey Barmada (great grandfather)
Mahmoud Barmada (grandfather)

Education

He obtained his BS from Carnegie Mellon University in Chemistry and biology sciences, and his M.A in Molecular Genetic from Johns Hopkins University and PhD in statistical and computational genetic from University of Pittsburgh.[1]

Works

Research interests: Statistical Genetics, Genetic Epidemiology, Bioinformatics, Genome Informatics

Partial list:

  • Hereditary Lymphedema: Evidence for Linkage and Genetic Heterogeneity.[3]
  • Evidence for an inflammatory bowel disease locus on chromosome 3p26: linkage, transmission/disequilibrium and partitioning of linkage.[4]
  • A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.[5]
  • A new locus for hemiplegic migraine maps to chromosome 1q31.[6]
  • Learning genetic epistasis using Bayesian network scoring criteria.[7]
  • Comprehensive analysis of HLA-G: implications for recurrent spontaneous abortion.[8]
  • A Bayesian method for evaluating and discovering disease loci associations.[9]
  • The Serotonin Transporter: Sequence Variation in Macaca fascicularis and its Relationship to Dominance.[10]
  • Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.[11]

References
  1. ORCID. "M Michael Barmada (0000-0002-3604-6460)". orcid.org. Retrieved 2020-11-23.
  2. Webteam, University of Pittsburgh University Marketing Communications. "University Times » M. Michael Barmada". Retrieved 2020-11-23.
  3. E. Ferrell, Robert; Levinson, Kara L.; Esman, Judith H.; Kimak, Mark A.; Lawrence, Elizabeth C.; Barmada, M. Michael; Finegold, David N. (1998). "Hereditary Lymphedema: Evidence for Linkage and Genetic Heterogeneity". Human Molecular Genetics. 7 (13): 2073–2078. doi:10.1093/hmg/7.13.2073. PMID 9817924.
  4. Duerr, Richard H.; Barmada, M. Michael; Zhang, Leilei; Achkar, Jean-Paul; Cho, Judy H.; Hanauer, Stephen B.; Brant, Steven R.; Bayless, Theodore M.; Baldassano, Robert N.; Weeks, Daniel E. (2 October 2002). "Evidence for an inflammatory bowel disease locus on chromosome 3p26: linkage, transmission/disequilibrium and partitioning of linkage". Human Molecular Genetics. 11 (21): 2599–2606. doi:10.1093/hmg/11.21.2599. PMID 12354785.
  5. Duerr, Richard H; Taylor, Kent D; Barmada, M Michael; Brant, Steven R; Rioux, John D (2006). "A genome-wide association study identifies IL23R as an inflammatory bowel disease gene". Science. 314 (5804): 1461–1463. Bibcode:2006Sci...314.1461D. doi:10.1126/science.1135245. PMC 4410764. PMID 17068223.
  6. Gardner, Kathy; Barmada, M Michael; Ptacek, Louis J; Hoffman, Eric P (1997). "A new locus for hemiplegic migraine maps to chromosome 1q31". Neurology. 49 (5): 1231–1238. doi:10.1212/WNL.49.5.1231. PMID 9371899. S2CID 32611926.
  7. Jiang, Xia; Neapolitan, Richard E; Barmada, M Michael; Visweswaran, Shyam (2011). "Learning genetic epistasis using Bayesian network scoring criteria". BMC Bioinformatics. 12: 89. doi:10.1186/1471-2105-12-89. PMC 3080825. PMID 21453508.
  8. Berger, Dara S; Hogge, W Allen; Barmada, M Michael; Ferrell, Robert E (2010). "Comprehensive analysis of HLA-G: implications for recurrent spontaneous abortion". Reproductive Sciences. 17 (4): 331–338. doi:10.1177/1933719109356802. PMID 20228379. S2CID 11152568.
  9. Jiang, Xia; Barmada, M Michael; Cooper, Gregory F; Becich, Michael J (2011). "A Bayesian method for evaluating and discovering disease loci associations". PLOS ONE. 6 (8): e22075. Bibcode:2011PLoSO...622075J. doi:10.1371/journal.pone.0022075. PMC 3154195. PMID 21853025.
  10. Miller-Butterworth, Cassandra M.; Kaplan, Jay R.; Barmada, M. Michael; Manuck, Stephen B.; Ferrell, Robert E. (2007). "The Serotonin Transporter: Sequence Variation in Macaca fascicularis and its Relationship to Dominance". Behavior Genetics. 37 (5): 678–696. doi:10.1007/s10519-007-9162-3. PMID 17605101. S2CID 20668176.
  11. Barrett, Jeffrey C.; Hansoul, Sarah; Nicolae, Dan L.; Cho, Judy H.; Duerr, Richard H.; Rioux, John D.; Brant, Steven R.; Silverberg, Mark S.; Taylor, Kent D.; Barmada, M Michael; Bitton, Alain; Dassopoulos, Themistocles; Datta, Lisa Wu; Green, Todd; Griffiths, Anne M.; Kistner, Emily O.; Murtha, Michael T.; Regueiro, Miguel D.; Rotter, Jerome I.; Schumm, L Philip; Steinhart, A Hillary; Targan, Stephan R.; Xavier, Ramnik J.; Libioulle, Cécile; Sandor, Cynthia; Lathrop, Mark; Belaiche, Jacques; Dewit, Olivier; Gut, Ivo; et al. (2008). "Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease". Nature Genetics. 40 (8): 955–962. doi:10.1038/ng.175. PMC 2574810. PMID 18587394.
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