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Page 1
Novel regulatory variant in ABO intronic RUNX1 binding site inducing A3 phenotype.
Thun GA, Gueuning M, Sigurdardottir S, Meyer E, Gourri E, Schneider L, Merki Y, Trost N, Neuenschwander K, Engström C, Frey BM, Meyer S, Mattle-Greminger MP. Thun GA, et al. Among authors: gourri e. Vox Sang. 2024 Apr;119(4):377-382. doi: 10.1111/vox.13580. Epub 2024 Jan 16. Vox Sang. 2024. PMID: 38226545
Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variants.
Gueuning M, Thun GA, Wittig M, Galati AL, Meyer S, Trost N, Gourri E, Fuss J, Sigurdardottir S, Merki Y, Neuenschwander K, Busch Y, Trojok P, Schäfer M, Gottschalk J, Franke A, Gassner C, Peter W, Frey BM, Mattle-Greminger MP. Gueuning M, et al. Among authors: gourri e. Blood Adv. 2023 Mar 28;7(6):878-892. doi: 10.1182/bloodadvances.2022007133. Blood Adv. 2023. PMID: 36129841 Free PMC article.
Automatic computation of bone defective volume from tomographic images.
Ezzahmouly M, Essakhi A, El Ouahli A, El Byad H, Ed-Dhahraouy M, Hakim S, Gourri E, ELmoutaouakkil A, Hatim Z. Ezzahmouly M, et al. Among authors: gourri e. Heliyon. 2022 May 30;8(6):e09594. doi: 10.1016/j.heliyon.2022.e09594. eCollection 2022 Jun. Heliyon. 2022. PMID: 35669543 Free PMC article.
Clonal hematopoiesis in donors and long-term survivors of related allogeneic hematopoietic stem cell transplantation.
Boettcher S, Wilk CM, Singer J, Beier F, Burcklen E, Beisel C, Ventura Ferreira MS, Gourri E, Gassner C, Frey BM, Schanz U, Skoda RC, Ebert BL, Brummendorf TH, Beerenwinkel N, Manz MG. Boettcher S, et al. Among authors: gourri e. Blood. 2020 Apr 30;135(18):1548-1559. doi: 10.1182/blood.2019003079. Blood. 2020. PMID: 32181816 Free article.