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Kyriacos Markianos, PhD - Publications

Affiliations: 
Harvard Medical School, Boston, MA, United States 
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30 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Schmitz-Abe K, Sanchez-Schmitz G, Doan RN, Hill RS, Chahrour MH, Mehta BK, Servattalab S, Ataman B, Lam AN, Morrow EM, Greenberg ME, Yu TW, Walsh CA, Markianos K. Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder. Scientific Reports. 10: 14045. PMID 32820185 DOI: 10.1038/S41598-020-70656-0  0.339
2018 Renella R, Gagne K, Beauchamp E, Schlaeger T, Hofmann I, Shimamura A, Fogel J, Agarwal S, Ebert BL, Markianos K, Springer TA, Fleming MD, Williams DA. 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. DOI: 10.1182/Blood-2018-99-114682  0.356
2017 Pighi C, Compagno M, Cheong T, Poggio T, Wang Q, Langellotto F, Sendamarai A, Markianos K, Celle PFd, Zamò A, Chiarle R. Abstract PR10: FBXO11 is recurrently mutated in Burkitt lymphoma and its inactivation accelerates lymphomagenesis in Eμ-myc mice Clinical Cancer Research. 23. DOI: 10.1158/1557-3265.Hemmal17-Pr10  0.31
2016 Crawford JE, Riehle MM, Markianos K, Bischoff E, Guelbeogo WM, Gneme A, Sagnon N, Vernick KD, Nielsen R, Lazzaro BP. Evolution of GOUNDRY, a cryptic subgroup of Anopheles gambiae s.l., and its impact on susceptibility to Plasmodium infection. Molecular Ecology. PMID 26846876 DOI: 10.1111/Mec.13572  0.365
2016 Markianos K, Bischoff E, Mitri C, Guelbeogo WM, Gneme A, Eiglmeier K, Holm I, Sagnon N, Vernick KD, Riehle MM. Genetic Structure of a Local Population of the Anopheles gambiae Complex in Burkina Faso. Plos One. 11: e0145308. PMID 26731649 DOI: 10.1371/Journal.Pone.0145308  0.315
2015 Schmitz-Abe K, Ciesielski SJ, Schmidt PJ, Campagna DR, Rahimov F, Schilke BA, Cuijpers M, Rieneck K, Lausen B, Linenberger ML, Sendamarai AK, Guo C, Hofmann I, Newburger PE, Matthews D, ... ... Markianos K, et al. Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9. Blood. PMID 26491070 DOI: 10.1182/Blood-2015-09-659854  0.309
2015 Redmond SN, Eiglmeier K, Mitri C, Markianos K, Guelbeogo WM, Gneme A, Isaacs AT, Coulibaly B, Brito-Fravallo E, Maslen G, Mead D, Niare O, Traore SF, Sagnon N, Kwiatkowski D, et al. Association mapping by pooled sequencing identifies TOLL 11 as a protective factor against Plasmodium falciparum in Anopheles gambiae. Bmc Genomics. 16: 779. PMID 26462916 DOI: 10.1186/S12864-015-2009-Z  0.382
2015 Mitri C, Markianos K, Guelbeogo WM, Bischoff E, Gneme A, Eiglmeier K, Holm I, Sagnon N, Vernick KD, Riehle MM. The kdr-bearing haplotype and susceptibility to Plasmodium falciparum in Anopheles gambiae: genetic correlation and functional testing. Malaria Journal. 14: 391. PMID 26445487 DOI: 10.1186/S12936-015-0924-8  0.36
2015 Nakayama T, Al-Maawali A, El-Quessny M, Rajab A, Khalil S, Stoler JM, Tan WH, Nasir R, Schmitz-Abe K, Hill RS, Partlow JN, Al-Saffar M, Servattalab S, LaCoursiere CM, Tambunan DE, ... ... Markianos K, et al. Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination. American Journal of Human Genetics. 96: 709-19. PMID 25865492 DOI: 10.1016/J.Ajhg.2015.03.003  0.377
2014 Agrawal PB, Joshi M, Marinakis NS, Schmitz-Abe K, Ciarlini PD, Sargent JC, Markianos K, De Girolami U, Chad DA, Beggs AH. Expanding the phenotype associated with the NEFL mutation: neuromuscular disease in a family with overlapping myopathic and neurogenic findings. Jama Neurology. 71: 1413-20. PMID 25264603 DOI: 10.1001/Jamaneurol.2014.1432  0.381
2014 Campagna DR, de Bie CI, Schmitz-Abe K, Sweeney M, Sendamarai AK, Schmidt PJ, Heeney MM, Yntema HG, Kannengiesser C, Grandchamp B, Niemeyer CM, Knoers NV, Swart S, Marron G, van Wijk R, ... ... Markianos K, et al. X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutations. American Journal of Hematology. 89: 315-9. PMID 24166784 DOI: 10.1002/Ajh.23616  0.318
2013 Sankaran VG, Joshi M, Agrawal A, Schmitz-Abe K, Towne MC, Marinakis N, Markianos K, Berry GT, Agrawal PB. Rare complete loss of function provides insight into a pleiotropic genome-wide association study locus. Blood. 122: 3845-7. PMID 24288412 DOI: 10.1182/Blood-2013-09-528315  0.329
2013 Ceyhan-Birsoy O, Agrawal PB, Hidalgo C, Schmitz-Abe K, DeChene ET, Swanson LC, Soemedi R, Vasli N, Iannaccone ST, Shieh PB, Shur N, Dennison JM, Lawlor MW, Laporte J, Markianos K, et al. Recessive truncating titin gene, TTN, mutations presenting as centronuclear myopathy. Neurology. 81: 1205-14. PMID 23975875 DOI: 10.1212/Wnl.0B013E3182A6Ca62  0.333
2013 Yu TW, Chahrour MH, Coulter ME, Jiralerspong S, Okamura-Ikeda K, Ataman B, Schmitz-Abe K, Harmin DA, Adli M, Malik AN, D'Gama AM, Lim ET, Sanders SJ, Mochida GH, Partlow JN, ... ... Markianos K, et al. Using whole-exome sequencing to identify inherited causes of autism. Neuron. 77: 259-73. PMID 23352163 DOI: 10.1016/J.Neuron.2012.11.002  0.373
2013 Hofmann I, Kierstead D, Krasker J, Campagna D, Schmitz-Abe K, Markianos K, Lee MA, Sieff CA, Agarwal S, Clark JJ, Jeng M, Loh ML, Shereck E, Williams DA, Fleming MD. GATA2 Mutations In Pediatric Myelodysplastic Syndromes and Bone Marrow Failure Blood. 122: 1520-1520. DOI: 10.1182/Blood.V122.21.1520.1520  0.35
2013 Agrawal P, Joshi M, Marinakis N, Ciarlini P, Schmitz-Abe K, Markianos K, De Girolami U, Beggs A. P.9.5 A novel NEFL gene mutation is identified in a family diagnosed with Nemaline Myopathy Neuromuscular Disorders. 23: 784-785. DOI: 10.1016/J.Nmd.2013.06.518  0.375
2012 Agrawal P, Schmitz K, DeChene E, Ceyhan Ö, Mercier M, Viola M, Markianos K, Beggs A. C.O.6 Complete genetic analysis by whole exome sequencing of a cohort with centronuclear myopathy identifies titin gene mutations Neuromuscular Disorders. 22: 840. DOI: 10.1016/J.Nmd.2012.06.128  0.357
2011 Riehle MM, Guelbeogo WM, Gneme A, Eiglmeier K, Holm I, Bischoff E, Garnier T, Snyder GM, Li X, Markianos K, Sagnon N, Vernick KD. A cryptic subgroup of Anopheles gambiae is highly susceptible to human malaria parasites. Science (New York, N.Y.). 331: 596-8. PMID 21292978 DOI: 10.1126/Science.1196759  0.309
2009 Broadbelt KG, Barger MA, Paterson DS, Holm IA, Haas EA, Krous HF, Kinney HC, Markianos K, Beggs AH. Serotonin-related FEV gene variant in the sudden infant death syndrome is a common polymorphism in the African-American population. Pediatric Research. 66: 631-5. PMID 19707175 DOI: 10.1203/Pdr.0B013E3181Bd5A31  0.313
2008 Morrow EM, Yoo SY, Flavell SW, Kim TK, Lin Y, Hill RS, Mukaddes NM, Balkhy S, Gascon G, Hashmi A, Al-Saad S, Ware J, Joseph RM, Greenblatt R, Gleason D, ... ... Markianos K, et al. Identifying autism loci and genes by tracing recent shared ancestry. Science (New York, N.Y.). 321: 218-23. PMID 18621663 DOI: 10.1126/Science.1157657  0.339
2007 Riehle MM, Markianos K, Lambrechts L, Xia A, Sharakhov I, Koella JC, Vernick KD. A major genetic locus controlling natural Plasmodium falciparum infection is shared by East and West African Anopheles gambiae. Malaria Journal. 6: 87. PMID 17612409 DOI: 10.1186/1475-2875-6-87  0.372
2006 Riehle MM, Markianos K, Niaré O, Xu J, Li J, Touré AM, Podiougou B, Oduol F, Diawara S, Diallo M, Coulibaly B, Ouatara A, Kruglyak L, Traoré SF, Vernick KD. Natural malaria infection in Anopheles gambiae is regulated by a single genomic control region. Science (New York, N.Y.). 312: 577-9. PMID 16645095 DOI: 10.1126/Science.1124153  0.549
2004 Ostrander EA, Markianos K, Stanford JL. Finding prostate cancer susceptibility genes. Annual Review of Genomics and Human Genetics. 5: 151-75. PMID 15485346 DOI: 10.1146/Annurev.Genom.5.061903.180044  0.343
2004 Abecasis G, Cox N, Daly MJ, Kruglyak L, Laird N, Markianos K, Patterson N. No bias in linkage analysis. American Journal of Human Genetics. 75: 722-3; author reply . PMID 15338460 DOI: 10.1086/424757  0.543
2004 Mukhopadhyay I, Feingold E, Weeks DE, Visscher PM, Wray NR, Sieberts SK, Broman KW, Gudbjartsson DF, Abecasis G, Cox N, Daly MJ, Kruglyak L, Laird N, Markianos K, Patterson N, et al. No "bias" toward the null hypothesis in most conventional multipoint nonparametric linkage analyses [1] (multiple letters) American Journal of Human Genetics. 75: 716-727. PMID 15338457 DOI: 10.1086/424754  0.519
2004 Furman I, Rieder MJ, Da Ponte S, Carrington DP, Nickerson DA, Kruglyak L, Markianos K. Sequence-based linkage analysis. American Journal of Human Genetics. 75: 647-53. PMID 15329798 DOI: 10.1086/424888  0.653
2003 Matise TC, Sachidanandam R, Clark AG, Kruglyak L, Wijsman E, Kakol J, Buyske S, Chui B, Cohen P, de Toma C, Ehm M, Glanowski S, He C, Heil J, Markianos K, et al. A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set. American Journal of Human Genetics. 73: 271-84. PMID 12844283 DOI: 10.1086/377137  0.535
2002 Niaré O, Markianos K, Volz J, Oduol F, Touré A, Bagayoko M, Sangaré D, Traoré SF, Wang R, Blass C, Dolo G, Bouaré M, Kafatos FC, Kruglyak L, Touré YT, et al. Genetic loci affecting resistance to human malaria parasites in a West African mosquito vector population. Science (New York, N.Y.). 298: 213-6. PMID 12364806 DOI: 10.1126/Science.1073420  0.542
2001 Markianos K, Carlson S, Gibbs M, Kruglyak L. A joint analysis of asthma affection status and IgE levels in multiple data sets collected for asthma. Genetic Epidemiology. 21: S148-53. PMID 11793658 DOI: 10.1002/Gepi.2001.21.S1.S148  0.506
2001 Markianos K, Daly MJ, Kruglyak L. Efficient multipoint linkage analysis through reduction of inheritance space. American Journal of Human Genetics. 68: 963-77. PMID 11254453 DOI: 10.1086/319507  0.56
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