Search Results - Merki, Yvonne

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  1. 1
    Resolving Genotype-Phenotype Discrepancies of the Kidd Blood Group System Using Long-Read Nanopore Sequencing

    Resolving Genotype-Phenotype Discrepancies of the Kidd Blood Group System Using Long-Read Nanopore Sequencing by Gueuning, Morgan, Thun, Gian Andri, Trost, Nadine, Schneider, Linda, Sigurdardottir, Sonja, Engström, Charlotte, Larbes, Naemi, Merki, Yvonne, Frey, Beat M, Gassner, Christoph, Meyer, Stefan, Mattle-Greminger, Maja P

    Published in Biomedicines
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  2. 2
    Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variants

    Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variants by Gueuning, Morgan, Thun, Gian Andri, Wittig, Michael, Galati, Anna-Lena, Meyer, Stefan, Trost, Nadine, Gourri, Elise, Fuss, Janina, Sigurdardottir, Sonja, Merki, Yvonne, Neuenschwander, Kathrin, Busch, Yannik, Trojok, Peter, Schäfer, Marco, Gottschalk, Jochen, Franke, Andre, Gassner, Christoph, Peter, Wolfgang, Frey, Beat M., Mattle-Greminger, Maja P.

    Published in Blood advances
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  3. 3
    Novel regulatory variant in ABO intronic RUNX1 binding site inducing A 3 phenotype

    Novel regulatory variant in ABO intronic RUNX1 binding site inducing A 3 phenotype by Thun, Gian Andri, Gueuning, Morgan, Sigurdardottir, Sonja, Meyer, Eduardo, Gourri, Elise, Schneider, Linda, Merki, Yvonne, Trost, Nadine, Neuenschwander, Kathrin, Engström, Charlotte, Frey, Beat M, Meyer, Stefan, Mattle-Greminger, Maja P

    Published in Vox sanguinis
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  4. 4
    Novel regulatory variant in ABO intronic RUNX1 binding site inducing A3 phenotype

    Novel regulatory variant in ABO intronic RUNX1 binding site inducing A3 phenotype by Thun, Gian Andri, Gueuning, Morgan, Sigurdardottir, Sonja, Meyer, Eduardo, Gourri, Elise, Schneider, Linda, Merki, Yvonne, Trost, Nadine, Neuenschwander, Kathrin, Engström, Charlotte, Frey, Beat M., Meyer, Stefan, Mattle‐Greminger, Maja P.

    Published in Vox sanguinis
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  5. 5
    Genetic background of the rare Yus and Gerbich blood group phenotypes: homologous regions of the GYPC gene contribute to deletion alleles

    Genetic background of the rare Yus and Gerbich blood group phenotypes: homologous regions of the GYPC gene contribute to deletion alleles by Gourri, Elise, Denomme, Gregory A., Merki, Yvonne, Scharberg, Erwin A., Vrignaud, Cedric, Frey, Beat M., Peyrard, Thierry, Gassner, Christoph

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  6. 6
    Stepwise partitioning of Xp21: a profiling method for XK deletions causative of the McLeod syndrome

    Stepwise partitioning of Xp21: a profiling method for XK deletions causative of the McLeod syndrome by Gassner, Christoph, Brönnimann, Chantal, Merki, Yvonne, Mattle‐Greminger, Maja P., Sigurdardottir, Sonja, Meyer, Eduardo, Engström, Charlotte, O'Sullivan, John D., Jung, Hans H., Frey, Beat M.

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  7. 7
    Low-Frequency Blood Group Antigens in Switzerland

    Low-Frequency Blood Group Antigens in Switzerland by Gassner, Christoph, Degenhardt, Frauke, Meyer, Stefan, Vollmert, Caren, Trost, Nadine, Neuenschwander, Kathrin, Merki, Yvonne, Portmann, Claudia, Sigurdardottir, Sonja, Zorbas, Antigoni, Engström, Charlotte, Gottschalk, Jochen, Amar el Dusouqui, Soraya, Waldvogel-Abramovski, Sophie, Rigal, Emmanuel, Tissot, Jean-Daniel, Tinguely, Caroline, Mauvais, Simon M., Sarraj, Amira, Bessero, Daniel, Stalder, Michele, Infanti, Laura, Buser, Andreas, Sigle, Jörg, Weingand, Tina, Castelli, Damiano, Braisch, Monica C., Thierbach, Jutta, Heer, Sonja, Schulzki, Thomas, Krawczak, Michael, Franke, Andre, Frey, Beat M.

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