Kyriacos Markianos, PhD
Affiliations: | Harvard Medical School, Boston, MA, United States |
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| Schmitz-Abe K, Sanchez-Schmitz G, Doan RN, et al. (2020) Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder. Scientific Reports. 10: 14045 |
| Renella R, Gagne K, Beauchamp E, et al. (2018) Congenital X-Linked Myelodysplasia with Tetraploidy Is Associated with De Novo Germline C-Terminal Mutation of SEPT6, a Septin Filament Protein Blood. 132: 644-644 |
| Pighi C, Compagno M, Cheong T, et al. (2017) Abstract PR10: FBXO11 is recurrently mutated in Burkitt lymphoma and its inactivation accelerates lymphomagenesis in Eμ-myc mice Clinical Cancer Research. 23 |
| 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 |
| 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 |