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Showing 1–7 of 7
Uniparental analysis of Deep Maniot Greeks reveals genetic continuity from the pre-Medieval era
Davranoglou LR, Kofinakos AP, Mariolis AD, Runfeldt G, Maier PA, Sager M, Soulioti P, Mariolis-Sapsakos T, Heraclides A.
Communications biology · doi:10.1038/s42003-026-09597-9 · PMC12873217
Sephardic origins revealed for rare skin disorder, recessive dystrophic epidermolysis bullosa, in individuals carrying the unique c.6527insC mutation
Warshauer EM, Maier PA, Runfeldt G, Fuentes I, Escamez MJ, Valinotto L, Natale M, Manzur G, Illera N, Garcia M, Del Rio M, Mencia A, Holguin A, Larcher F, He…
Journal of medical genetics · doi:10.1136/jmg-2025-110967 · PMC12716802
Unearthing who and Y at Harewood Cemetery and inference of George Washington's Y-chromosomal haplotype
Cavagnino C, Runfeldt G, Sager M, Estes R, Tillmar A, Greytak EM, Thomas JT, Anderson E, Daniels-Higginbotham J, Kjelland K, Sturk-Andreaggi K, Parsons TJ, M…
iScience · doi:10.1016/j.isci.2024.109353 · PMC11074960
Delineating the dispersal of Y-chromosome sub-haplogroup O2a2b-P164 among Austronesian-speaking populations
Luis JR, Palencia-Madrid L, Runfeldt G, Garcia-Bertrand R, Herrera RJ.
Scientific reports · doi:10.1038/s41598-024-52293-z · PMC10808098
Low Genetic Impact of the Roman Occupation of Britain in Rural Communities
Scheib CL, Hui R, Rose AK, D'Atanasio E, Inskip SA, Dittmar J, Cessford C, Griffith SJ, Solnik A, Wiseman R, Neil B, Biers T, Harknett SJ, Sasso S, Biagini S…
Molecular biology and evolution · doi:10.1093/molbev/msae168 · PMC11393495
African mitochondrial haplogroup L7: a 100,000-year-old maternal human lineage discovered through reassessment and new sequencing
Maier PA, Runfeldt G, Estes RJ, Vilar MG.
Scientific reports · doi:10.1038/s41598-022-13856-0 · PMC9232647
Determination of the phylogenetic origins of the Árpád Dynasty based on Y chromosome sequencing of Béla the Third
Nagy PL, Olasz J, Neparáczki E, Rouse N, Kapuria K, Cano S, Chen H, Di Cristofaro J, Runfeldt G, Ekomasova N, Maróti Z, Jeney J, Litvinov S, Dzhaubermezov M,…
European journal of human genetics : EJHG · doi:10.1038/s41431-020-0683-z · PMC7809292