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New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing.
Keller A, Graefen A, Ball M, Matzas M, Boisguerin V, Maixner F, Leidinger P, Backes C, Khairat R, Forster M, Stade B, Franke A, Mayer J, Spangler J, McLaughlin S, Shah M, Lee C, Harkins TT, Sartori A, Moreno-Estrada A, Henn B, Sikora M, Semino O, Chiaroni J, Rootsi S, Myres NM, Cabrera VM, Underhill PA, Bustamante CD, Vigl EE, Samadelli M, Cipollini G, Haas J, Katus H, O'Connor BD, Carlson MR, Meder B, Blin N, Meese E, Pusch CM, Zink A. Keller A, et al. Among authors: khairat r. Nat Commun. 2012 Feb 28;3:698. doi: 10.1038/ncomms1701. Nat Commun. 2012. PMID: 22426219 Free article.
Ancestry and pathology in King Tutankhamun's family.
Hawass Z, Gad YZ, Ismail S, Khairat R, Fathalla D, Hasan N, Ahmed A, Elleithy H, Ball M, Gaballah F, Wasef S, Fateen M, Amer H, Gostner P, Selim A, Zink A, Pusch CM. Hawass Z, et al. Among authors: khairat r. JAMA. 2010 Feb 17;303(7):638-47. doi: 10.1001/jama.2010.121. JAMA. 2010. PMID: 20159872
Bioarcheology: Medicine, Biology, and Forensic Sciences.
Appenzeller O, Bromage TG, Khairat R, Nerlich AG, Rühli FJ. Appenzeller O, et al. Among authors: khairat r. Biomed Res Int. 2015;2015:671206. doi: 10.1155/2015/671206. Epub 2015 Aug 6. Biomed Res Int. 2015. PMID: 26346711 Free PMC article. No abstract available.
Expansion of the phenotypic and mutational spectrum of Carpenter syndrome.
Khairat R, Elhossini R, Sobreira N, Wohler E, Otaify G, Mohamed AM, Abdel Raouf ER, Sayed I, Aglan M, Ismail S, Temtamy SA. Khairat R, et al. Eur J Med Genet. 2022 Jan;65(1):104377. doi: 10.1016/j.ejmg.2021.104377. Epub 2021 Nov 5. Eur J Med Genet. 2022. PMID: 34748996