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Resolving Genotype-Phenotype Discrepancies of the Kidd Blood Group System Using Long-Read Nanopore Sequencing.
Biomedicines. 2024 Jan 19;12(1):225. doi: 10.3390/biomedicines12010225.
Biomedicines. 2024.
PMID: 38275395
Free PMC article.
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: merki y.
Vox Sang. 2024 Apr;119(4):377-382. doi: 10.1111/vox.13580. Epub 2024 Jan 16.
Vox Sang. 2024.
PMID: 38226545
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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: merki y.
Blood Adv. 2023 Mar 28;7(6):878-892. doi: 10.1182/bloodadvances.2022007133.
Blood Adv. 2023.
PMID: 36129841
Free PMC article.
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Low-Frequency Blood Group Antigens in Switzerland.
Gassner C, Degenhardt F, Meyer S, Vollmert C, Trost N, Neuenschwander K, Merki Y, Portmann C, Sigurdardottir S, Zorbas A, Engström C, Gottschalk J, Amar El Dusouqui S, Waldvogel-Abramovski S, Rigal E, Tissot JD, Tinguely C, Mauvais SM, Sarraj A, Bessero D, Stalder M, Infanti L, Buser A, Sigle J, Weingand T, Castelli D, Braisch MC, Thierbach J, Heer S, Schulzki T, Krawczak M, Franke A, Frey BM.
Gassner C, et al. Among authors: merki y.
Transfus Med Hemother. 2018 Jul;45(4):239-250. doi: 10.1159/000490714. Epub 2018 Jul 10.
Transfus Med Hemother. 2018.
PMID: 30283273
Free PMC article.
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Stepwise partitioning of Xp21: a profiling method for XK deletions causative of the McLeod syndrome.
Gassner C, Brönnimann C, Merki Y, Mattle-Greminger MP, Sigurdardottir S, Meyer E, Engström C, O'Sullivan JD, Jung HH, Frey BM.
Gassner C, et al. Among authors: merki y.
Transfusion. 2017 Sep;57(9):2125-2135. doi: 10.1111/trf.14172. Epub 2017 May 28.
Transfusion. 2017.
PMID: 28555782
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Genetic background of the rare Yus and Gerbich blood group phenotypes: homologous regions of the GYPC gene contribute to deletion alleles.
Gourri E, Denomme GA, Merki Y, Scharberg EA, Vrignaud C, Frey BM, Peyrard T, Gassner C.
Gourri E, et al. Among authors: merki y.
Br J Haematol. 2017 May;177(4):630-640. doi: 10.1111/bjh.14578. Epub 2017 Mar 8.
Br J Haematol. 2017.
PMID: 28272739
Free article.
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