Kyriacos Markianos, PhD

Affiliations: 
Harvard Medical School, Boston, MA, United States 
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"Kyriacos Markianos"
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Publications

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Crawford JE, Riehle MM, Markianos K, et al. (2016) Evolution of GOUNDRY, a cryptic subgroup of Anopheles gambiae s.l., and its impact on susceptibility to Plasmodium infection. Molecular Ecology
Markianos K, Bischoff E, Mitri C, et al. (2016) Genetic Structure of a Local Population of the Anopheles gambiae Complex in Burkina Faso. Plos One. 11: e0145308
Schmitz-Abe K, Ciesielski SJ, Schmidt PJ, et al. (2015) Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9. Blood
Redmond SN, Eiglmeier K, Mitri C, et al. (2015) Association mapping by pooled sequencing identifies TOLL 11 as a protective factor against Plasmodium falciparum in Anopheles gambiae. Bmc Genomics. 16: 779
Mitri C, Markianos K, Guelbeogo WM, et al. (2015) The kdr-bearing haplotype and susceptibility to Plasmodium falciparum in Anopheles gambiae: genetic correlation and functional testing. Malaria Journal. 14: 391
Nakayama T, Al-Maawali A, El-Quessny M, et al. (2015) Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination. American Journal of Human Genetics. 96: 709-19
Ahmed MY, Chioza BA, Rajab A, et al. (2015) Loss of PCLO function underlies pontocerebellar hypoplasia type III. Neurology. 84: 1745-50
Agrawal PB, Joshi M, Marinakis NS, et al. (2014) Expanding the phenotype associated with the NEFL mutation: neuromuscular disease in a family with overlapping myopathic and neurogenic findings. Jama Neurology. 71: 1413-20
Chakraborty PK, Schmitz-Abe K, Kennedy EK, et al. (2014) Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD). Blood. 124: 2867-71
Campagna DR, de Bie CI, Schmitz-Abe K, et al. (2014) X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutations. American Journal of Hematology. 89: 315-9
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