| 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 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2014 |
Chakraborty PK, Schmitz-Abe K, Kennedy EK, Mamady H, Naas T, Durie D, Campagna DR, Lau A, Sendamarai AK, Wiseman DH, May A, Jolles S, Connor P, Powell C, Heeney MM, ... ... Markianos K, et al. Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD). Blood. 124: 2867-71. PMID 25193871 DOI: 10.1182/Blood-2014-08-591370 |
0.299 |
|
| 2016 |
Lichtenstein DA, Crispin AW, Sendamarai AK, Campagna DR, Schmitz-Abe K, Sousa CM, Kafina MD, Schmidt PJ, Niemeyer CM, Porter J, May A, Patnaik MM, Heeney MM, Kimmelman A, Bottomley SS, ... ... Markianos K, et al. A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemia. Blood. PMID 27488349 DOI: 10.1182/Blood-2016-05-719062 |
0.299 |
|
| 2013 |
Bartnikas TB, Wildt SJ, Wineinger AE, Schmitz-Abe K, Markianos K, Cooper DM, Fleming MD. A novel rat model of hereditary hemochromatosis due to a mutation in transferrin receptor 2. Comparative Medicine. 63: 143-55. PMID 23582421 DOI: 10.1182/Blood.V120.21.612.612 |
0.292 |
|
| 2018 |
Hofmann I, Geer MJ, Vögtle T, Crispin A, Campagna DR, Barr A, Calicchio ML, Heising S, van Geffen JP, Kuijpers MJE, Heemskerk JWM, Eble JA, Schmitz-Abe K, Obeng EA, Douglas M, ... ... Markianos K, et al. Congenital macrothrombocytopenia with focal myelofibrosis due to mutations in human G6b-B is rescued in humanized mice. Blood. PMID 29898956 DOI: 10.1182/Blood-2017-08-802769 |
0.281 |
|
| 2017 |
Jamuar SS, Schmitz-Abe K, D'Gama AM, Drottar M, Chan WM, Peeva M, Servattalab S, Lam AN, Delgado MR, Clegg NJ, Zayed ZA, Dogar MA, Alorainy IA, Jamea AA, Abu-Amero K, ... ... Markianos K, et al. Biallelic mutations in human DCC cause developmental split-brain syndrome. Nature Genetics. PMID 28250456 DOI: 10.1038/Ng.3804 |
0.279 |
|
| 2010 |
Paterson DS, Rivera KD, Broadbelt KG, Trachtenberg FL, Belliveau RA, Holm IA, Haas EA, Stanley C, Krous HF, Kinney HC, Markianos K. Lack of association of the serotonin transporter polymorphism with the sudden infant death syndrome in the San Diego Dataset. Pediatric Research. 68: 409-13. PMID 20661167 DOI: 10.1203/Pdr.0B013E3181F2Edf0 |
0.269 |
|
| 2013 |
Eran A, Li JB, Vatalaro K, McCarthy J, Rahimov F, Collins C, Markianos K, Margulies DM, Brown EN, Calvo SE, Kohane IS, Kunkel LM. Comparative RNA editing in autistic and neurotypical cerebella. Molecular Psychiatry. 18: 1041-8. PMID 22869036 DOI: 10.1038/Mp.2012.118 |
0.265 |
|
| 2017 |
Hofmann I, Crispin A, Campagna D, Calicchio M, Schmitz-Abe K, Obeng EA, Markianos K, Senis YA, Fleming MD. Congenital Thrombocytopenia and Myelofibrosis Due to Germline Mutations in G6b-B— a Megakaryocyte-Specific Immunoreceptor Tyrosine-Based Inhibitory Motif (ITIM) Receptor Blood. 130: 1630-1630. DOI: 10.1182/Blood.V130.Suppl_1.1630.1630 |
0.263 |
|
| 2015 |
Ahmed MY, Chioza BA, Rajab A, Schmitz-Abe K, Al-Khayat A, Al-Turki S, Baple EL, Patton MA, Al-Memar AY, Hurles ME, Partlow JN, Hill RS, Evrony GD, Servattalab S, Markianos K, et al. Loss of PCLO function underlies pontocerebellar hypoplasia type III. Neurology. 84: 1745-50. PMID 25832664 DOI: 10.1212/Wnl.0000000000001523 |
0.26 |
|
| 2016 |
Cattivelli K, Campagna DR, Schmitz-Abe K, Heeney MM, Yaish HM, Caruso Brown AE, Kearney S, Walkovich K, Markianos K, Fleming MD, Neufeld EJ. Ringed sideroblasts in β-thalassemia. Pediatric Blood & Cancer. PMID 27808451 DOI: 10.1002/Pbc.26324 |
0.252 |
|
| 2011 |
Riehle MM, Guelbeogo WM, Eiglmeier K, Holm I, Bischoff E, Garnier T, Markianos K, Sagnon N, Vernick KD. Outdoor-resting (exophilic) mosquitoes Science. 332: 420-421. DOI: 10.1126/Science.332.6028.420 |
0.235 |
|
| 1994 |
Gara A, Knapp BC, Christian D, Gutierrez G, Wehmann A, Felix J, Moreno G, Romero M, Sosa M, Berisso MC, Hartouni EP, Kreisler MN, Lee S, Markianos K, Wesson D. Light-meson spectroscopy in fermilab experiment E690 Il Nuovo Cimento A. 107: 1847-1855. DOI: 10.1007/Bf02823579 |
0.227 |
|
| 2008 |
Finberg KE, Heeney MM, Campagna DR, Aydinok Y, Pearson HA, Hartman KR, Mayo MM, Samuel SM, Strouse JJ, Markianos K, Andrews NC, Fleming MD. Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA). Nature Genetics. 40: 569-71. PMID 18408718 DOI: 10.1038/Ng.130 |
0.224 |
|
| 2024 |
Gorman BR, Francis M, Nealon CL, Halladay CW, Duro N, Markianos K, Genovese G, Hysi PG, Choquet H, Afshari NA, Li YJ, Gaziano JM, Hung AM, Wu WC, Greenberg PB, et al. A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation. Communications Biology. 7: 418. PMID 38582945 DOI: 10.1038/s42003-024-06046-3 |
0.221 |
|
| 2018 |
Heeney MM, Guo D, De Falco L, Campagna DR, Olbina G, Kao PP, Schmitz-Abe K, Rahimov F, Gutschow P, Westerman K, Ostland V, Jackson T, Klaassen RE, Markianos K, Finberg KE, et al. Normalizing hepcidin predicts mutation status in patients with chronic iron deficiency. Blood. PMID 29895660 DOI: 10.1182/Blood-2017-03-773028 |
0.219 |
|
| 1997 |
Reyes MA, Berisso MC, Christian D, Felix J, Gara A, Gottschalk E, Gutierrez G, Hartouni EP, Knapp B, Kreisler MN, Lee S, Markianos K, Moreno G, Sosa M, Wehmann A, et al. Spin-parity analysis of the centrally produced KsKs system at 800 GeV Nuclear Physics B - Proceedings Supplements. 56: 285-290. DOI: 10.1016/S0920-5632(97)00289-2 |
0.215 |
|
| 1994 |
Christian DC, Berisso MC, Gutierrez G, Holmes SD, Wehmann A, Avilez C, Felix J, Moreno G, Romero M, Sosa M, Forbush M, Huson FR, Wightman JA, Gara A, Knapp BC, ... ... Markianos K, et al. High rate drift chambers Nuclear Inst. and Methods in Physics Research, A. 345: 62-71. DOI: 10.1016/0168-9002(94)90972-5 |
0.214 |
|
| 2015 |
Riley LG, Rudinger-Thirion J, Schmitz-Abe K, Thorburn DR, Davis RL, Teo J, Arbuckle S, Cooper ST, Frugier M, Markianos K, Sue CM, Fleming MD, Christodoulou J. LARS2 variations can cause lethal infantile multisystem failure Mitochondrion. 24: S11-S12. DOI: 10.1016/J.Mito.2015.07.039 |
0.213 |
|
| 2001 |
Wang MH, Berisso MC, Christian DC, Félix J, Gara A, Gottschalk E, Gutiérrez G, Hartouni EP, Knapp BC, Kreisler MN, Lee S, Markianos K, Moreno G, Reyes MA, Sosa M, et al. Diffractively produced charm final states in 800-GeV/c pp collisions. Physical Review Letters. 87: 082002. PMID 11497936 DOI: 10.1103/Physrevlett.87.082002 |
0.209 |
|
| 2002 |
Félix J, Berisso MC, Christian DC, Gara A, Gottschalk EE, Gutiérrez G, Hartouni EP, Knapp BC, Kreisler MN, Lee S, Markianos K, Moreno G, Reyes MA, Sosa M, Wang MH, et al. Lambda(0) polarization in 800-GeV/cpp --> p(f)(Lambda0K+). Physical Review Letters. 88: 061801. PMID 11863796 DOI: 10.1103/Physrevlett.88.061801 |
0.206 |
|
| 1998 |
Reyes MA, Berisso MC, Christian DC, Felix J, Gara A, Gottschalk E, Gutierrez G, Hartouni EP, Knapp BC, Kreisler MN, Lee S, Markianos K, Moreno G, Sosa M, Wang MHLS, et al. Partial wave analysis of the centrally produced KSKS system at 800 GeV/c Physical Review Letters. 81: 4079-4082. DOI: 10.1103/Physrevlett.81.4079 |
0.204 |
|
| 2023 |
Peachey N, Gorman B, Francis M, Nealon C, Halladay C, Duro N, Markianos K, Genovese G, Hysi P, Choquet H, Afshari N, Li YJ, Gaziano JM, Hung A, Wu WC, et al. Multi-ancestry GWAS of Fuchs corneal dystrophy highlights roles of laminins, collagen, and endothelial cell regulation. Research Square. PMID 37205546 DOI: 10.21203/rs.3.rs-2762003/v1 |
0.202 |
|
| 1999 |
Sosa M, Berisso MC, Christian DC, Félix J, Gara A, Gottschalk E, Gutiérrez G, Hartouni EP, Knapp BC, Kreisler MN, Lee S, Markianos K, Moreno G, Reyes MA, Wang M, et al. Spin-parity analysis of the centrally produced KS 0K±π∓ system at 800 GeV/c Physical Review Letters. 83: 913-916. DOI: 10.1103/Physrevlett.83.913 |
0.2 |
|
| 2021 |
Renella R, Gagne K, Beauchamp E, Fogel J, Perlov A, Sola M, Schlaeger T, Hofmann I, Shimamura A, Ebert BL, Schmitz-Abe K, Markianos K, Murphy K, Sun L, Rockowitz S, et al. Congenital X-linked Neutropenia with Myelodysplasia and Somatic Tetraploidy due to a Germline Mutation in SEPT6. American Journal of Hematology. PMID 34677878 DOI: 10.1002/ajh.26382 |
0.199 |
|
| 1992 |
Hartouni EP, Jensen DA, Klima B, Kreisler MN, Lee S, Markianos K, Nordberg M, Rabin MSZ, Uribe J, Wesson D, Church M, Gara A, Gottschalk E, Hylton R, Knapp BC, et al. High speed simultaneous measurement of pulse area and time-of-flight for photomultiplier signals Nuclear Inst. and Methods in Physics Research, A. 317: 161-169. DOI: 10.1016/0168-9002(92)90605-4 |
0.198 |
|
| 2003 |
Felix J, Berisso MC, Christian DC, Gara A, Gottschalk EE, Gutierrez G, Hartouni EP, Knapp BC, Kreisler MN, Lee S, Markianos K, Moreno G, Reyes MA, Wang MHLS, Wehmann A, et al. Resonances and Λ0 polarization in 800 GeV/c pp → pdif fracted Λ0 K + Nuclear Physics A. 721: 805c-808c. DOI: 10.1016/S0375-9474(03)01186-2 |
0.195 |
|
| 2016 |
Morton SU, Neilan EG, Peake RW, Shi J, Schmitz-Abe K, Towne M, Markianos K, Prabhu SP, Agrawal PB. Hyperammonemia as a Presenting Feature in Two Siblings with FBXL4 Variants. Jimd Reports. PMID 27858371 DOI: 10.1007/8904_2016_17 |
0.193 |
|
| 2023 |
Markianos K, Dong F, Gorman B, Shi Y, Dochtermann D, Saxena U, Devineni P, Moser J, Muralidhar S, Ramoni R, Tsao P, Pyarajan S, Przygodzki R. Pharmacogenetic allele variant frequencies: An analysis of the VA's Million Veteran Program (MVP) as a representation of the diversity in US population. Plos One. 18: e0274339. PMID 36827430 DOI: 10.1371/journal.pone.0274339 |
0.187 |
|
| 2015 |
Riley LG, Rudinger-Thirion J, Schmitz-Abe K, Thorburn DR, Davis RL, Teo J, Arbuckle S, Cooper ST, Campagna DR, Frugier M, Markianos K, Sue CM, Fleming MD, Christodoulou J. LARS2 Variants Associated with Hydrops, Lactic Acidosis, Sideroblastic Anemia, and Multisystem Failure. Jimd Reports. PMID 26537577 DOI: 10.1007/8904_2015_515 |
0.172 |
|
| 2023 |
Talwar JV, Laub D, Pagadala MS, Castro A, Lewis M, Luebeck GE, Gorman BR, Pan C, Dong FN, Markianos K, Teerlink CC, Lynch J, Hauger R, Pyarajan S, Tsao PS, et al. Autoimmune alleles at the major histocompatibility locus modify melanoma susceptibility. American Journal of Human Genetics. PMID 37339630 DOI: 10.1016/j.ajhg.2023.05.013 |
0.157 |
|
| 2016 |
Joshi M, Anselm I, Shi J, Bale TA, Towne M, Schmitz-Abe K, Crowley L, Giani FC, Kazerounian S, Markianos K, Lidov HG, Folkerth R, Sankaran VG, Agrawal PB. Mutations in the substrate binding glycine-rich loop of the mitochondrial processing peptidase-α protein (PMPCA) cause a severe mitochondrial disease. Cold Spring Harbor Molecular Case Studies. 2: a000786. PMID 27148589 DOI: 10.1101/mcs.a000786 |
0.14 |
|
| 2013 |
Hofmann I, Krasker J, Campagna D, Kierstead D, Schmitz-Abe K, Markianos K, Lee M, Sieff C, Williams D, Fleming M. O-025 GATA2 mutations in pediatric myelodysplastic syndrome and bone marrow failure disorders Leukemia Research. 37: S20. DOI: 10.1016/S0145-2126(13)70047-X |
0.086 |
|
| 2007 |
Castorena J, Félix J, Berisso MC, Christian DC, Gara A, Gottschalk EE, Gutiérrez G, Hartouni EP, Knapp BC, Kreisler MN, Lee S, Markianos K, Moreno G, Reyes MA, Wang MHLS, et al. Λ0 polarization in pp→pfp sΛ0anti-Λ0 at 800-GeV/c Aip Conference Proceedings. 917: 413. DOI: 10.1063/1.2751987 |
0.042 |
|
| 2008 |
Valencia E, Félix J, Wang MHLS, Berisso MC, Christian DC, Gara A, Gottschalk E, Gutiérrez G, Hartouni EP, Knapp BC, Kreisler MN, Lee S, Markianos K, Reyes MA, Wehmann A, et al. Λ0 Polarization in pp→pΛ0K + at 800 GeV/c Aip Conference Proceedings. 1026: 315-317. DOI: 10.1063/1.2965073 |
0.041 |
|
| 2002 |
Félix J, Berisso MC, Christian DC, Gara A, Gottschalk EE, Gutiérrez G, Hartouni EP, Knapp BC, Kreisler MN, Lee S, Markianos K, Moreno G, Reyes MA, Sosa M, Wang MHLS, et al. Λ0 polarization in 800-GeV/cpp → pf(Λ0K+) Physical Review Letters. 88: 061801/1-061801/4. |
0.023 |
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| 2009 |
Félix J, Berisso MC, Christian DC, Gara A, Gottschalk EE, Gutierrez G, Hartouni EP, Knapp BC, Kreisler MN, Lee S, Markianos K, Moreno G, Reyes MA, Wang MHLS, Wehmann A, et al. A0 polarization in exclusive pp reactions from the FNAL e690 experiment Aip Conference Proceedings. 1116: 97-100. DOI: 10.1063/1.3131611 |
0.014 |
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| 2006 |
M. R, Markianos K. Le gène de la résistance au paludisme Revue Francophone Des Laboratoires. 2006: 17. DOI: 10.1016/S1773-035X(06)80298-4 |
0.01 |
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| 2006 |
M. R. R, Markianos K. Editorial | Le gène de la résistance au paludisme Revue Francophone Des Laboratoires. 2006: 17. |
0.01 |
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