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Parallel palaeogenomic transects reveal complex genetic history of early European farmers.
Lipson M, Szécsényi-Nagy A, Mallick S, Pósa A, Stégmár B, Keerl V, Rohland N, Stewardson K, Ferry M, Michel M, Oppenheimer J, Broomandkhoshbacht N, Harney E, Nordenfelt S, Llamas B, Gusztáv Mende B, Köhler K, Oross K, Bondár M, Marton T, Osztás A, Jakucs J, Paluch T, Horváth F, Csengeri P, Koós J, Sebők K, Anders A, Raczky P, Regenye J, Barna JP, Fábián S, Serlegi G, Toldi Z, Gyöngyvér Nagy E, Dani J, Molnár E, Pálfi G, Márk L, Melegh B, Bánfai Z, Domboróczki L, Fernández-Eraso J, Antonio Mujika-Alustiza J, Alonso Fernández C, Jiménez Echevarría J, Bollongino R, Orschiedt J, Schierhold K, Meller H, Cooper A, Burger J, Bánffy E, Alt KW, Lalueza-Fox C, Haak W, Reich D. Lipson M, et al. Among authors: Marton T. Nature. 2017 Nov 16;551(7680):368-372. doi: 10.1038/nature24476. Epub 2017 Nov 8. Nature. 2017. PMID: 29144465 Free PMC article.
Possible cases of leprosy from the Late Copper Age (3780-3650 cal BC) in Hungary.
Köhler K, Marcsik A, Zádori P, Biro G, Szeniczey T, Fábián S, Serlegi G, Marton T, Donoghue HD, Hajdu T. Köhler K, et al. Among authors: Marton T. PLoS One. 2017 Oct 12;12(10):e0185966. doi: 10.1371/journal.pone.0185966. eCollection 2017. PLoS One. 2017. PMID: 29023477 Free PMC article.
Tracing the genetic origin of Europe's first farmers reveals insights into their social organization.
Szécsényi-Nagy A, Brandt G, Haak W, Keerl V, Jakucs J, Möller-Rieker S, Köhler K, Mende BG, Oross K, Marton T, Osztás A, Kiss V, Fecher M, Pálfi G, Molnár E, Sebők K, Czene A, Paluch T, Šlaus M, Novak M, Pećina-Šlaus N, Ősz B, Voicsek V, Somogyi K, Tóth G, Kromer B, Bánffy E, Alt KW. Szécsényi-Nagy A, et al. Among authors: Marton T. Proc Biol Sci. 2015 Apr 22;282(1805):20150339. doi: 10.1098/rspb.2015.0339. Proc Biol Sci. 2015. PMID: 25808890 Free PMC article.
Evolution of a prenatal genetic clinic-A 10-year cohort study.
Mone F, O'Connor C, Hamilton S, Quinlan-Jones E, Allen S, Marton T, Williams D, Kilby MD. Mone F, et al. Among authors: Marton T. Prenat Diagn. 2020 Feb 10. doi: 10.1002/pd.5661. Online ahead of print. Prenat Diagn. 2020. PMID: 32037575
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Lord J, McMullan DJ, Eberhardt RY, Rinck G, Hamilton SJ, Quinlan-Jones E, Prigmore E, Keelagher R, Best SK, Carey GK, Mellis R, Robart S, Berry IR, Chandler KE, Cilliers D, Cresswell L, Edwards SL, Gardiner C, Henderson A, Holden ST, Homfray T, Lester T, Lewis RA, Newbury-Ecob R, Prescott K, Quarrell OW, Ramsden SC, Roberts E, Tapon D, Tooley MJ, Vasudevan PC, Weber AP, Wellesley DG, Westwood P, White H, Parker M, Williams D, Jenkins L, Scott RH, Kilby MD, Chitty LS, Hurles ME, Maher ER; Prenatal Assessment of Genomes and Exomes Consortium. Lord J, et al. Lancet. 2019 Feb 23;393(10173):747-757. doi: 10.1016/S0140-6736(18)31940-8. Epub 2019 Jan 31. Lancet. 2019. PMID: 30712880 Free PMC article. Clinical Trial.
Pathophysiological Mechanism of Extravasation via Umbilical Venous Catheters.
Hargitai B, Toldi G, Marton T, Ramalingam V, Ewer AK, Bedford Russell AR. Hargitai B, et al. Among authors: Marton T. Pediatr Dev Pathol. 2019 Jul-Aug;22(4):340-343. doi: 10.1177/1093526619826714. Epub 2019 Jan 25. Pediatr Dev Pathol. 2019. PMID: 30683018
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