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Mike Barmada

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Mike Barmada
M Michael Barmada.jpg
Born(1969-11-14)November 14, 1969
December 2, 2016(2016-12-02) (aged 47)December 2, 2016(2016-12-02) (aged 47)
🏳️ NationalityAmerican
🎓 Alma materCarnegie Mellon University (BS)
Johns Hopkins University (M.A)
University of Pittsburgh (PhD)
💼 Occupation
Geneticist
🏢 OrganizationUniversity of Pittsburgh
👴 👵 Parents
  • Bicher barmada (father)
  • Mamdouha Ahdab-Barmada (mother)
👪 RelativesMustafa Bey Barmada (great grandfather)

Mahmud Muhieddine Barmada (Arabic: محمود محي الدين برمدا ; November 14, 1969 – December 2, 2016), known as Michael or Mike Barmada, was an American geneticist, professor, and academic administrator . He was the co-director of the Bioinformatics Resource Center in the Institute for Personalized Medicin[1][2]

Early life[edit]

Mike Barmada was born in Detroit MI, USA on November 14, 1969 . He is the son of Bicher Barmada, Thoracic Surgeon and Mamdouha Ahdab-Barmada, Pathologist.

Education[edit]

He obtained his BS from Carnegie Mellon University in Chemistry and Biological Sciences, Professional Minor in Piano Composition, an Honors Degree in Biological Research and his M.A in Molecular Genetics from Johns Hopkins University and Ph.D. in Human Genetics; Area of Specialization: Statistical and Computational Genetics from University of Pittsburgh.[1]

Career[edit]

Growing his scientific career at the University of Pittsburgh apace with his field, at the beginning of high throughput and data-intensive computing, using the cloud as a research tool , mentoring over 30 masters, doctorate, medical students and faculty, Barmada taught genetics, bioinformatics, and analysis at the graduate and postgraduate level and adjunct institutions. He served on over 25 committees since 2001 and as Director, Bioinformatics Resource Center, Institute for Personalized Medicine, since 2012, Associate Director, Center for Simulation and Modeling since 2012, Director, Center for Computational Genetics, GSPH since 2004, Director, Department Computational Resources Division, Department of Human Genetics, GSPH since 1999. [1][2]

Works[edit]

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[edit]

  1. 1.0 1.1 1.2 ORCID. "M Michael Barmada (0000-0002-3604-6460)". orcid.org. Retrieved 2020-11-23.
  2. 2.0 2.1 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. Unknown parameter |s2cid= ignored (help)
  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. Unknown parameter |s2cid= ignored (help)
  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. Unknown parameter |s2cid= ignored (help)
  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.

External links[edit]


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