Gian Andri Thun (Gian A Thun, Gian-Andri Thun)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 10

Top Venues

Vox sanguinis

Biomedicines

Proceedings of the National Academy of Sciences of the United States of America

Scientific reports

This page only lists publications with an associated author ORCID identifier.

Publications

Gian Andri Thun, Morgan Gueuning, Sonja Sigurdardottir, Eduardo Meyer, Elise Gourri, Linda Schneider, Yvonne Merki, Nadine Trost, Kathrin Neuenschwander, Charlotte Engström, Beat M Frey, Stefan Meyer, Maja P Mattle-Greminger
Novel regulatory variant in ABO intronic RUNX1 binding site inducing A 3 phenotype. Vox sanguinis 119 (4) (2024)
Morgan Gueuning, Gian Andri Thun, Nadine Trost, Linda Schneider, Sonja Sigurdardottir, Charlotte Engström, Naemi Larbes, Yvonne Merki, Beat M Frey, Christoph Gassner, Stefan Meyer, Maja P Mattle-Greminger
Resolving Genotype-Phenotype Discrepancies of the Kidd Blood Group System Using Long-Read Nanopore Sequencing. Biomedicines 12 (1) (2024)
Gian Andri Thun, Morgan Gueuning, Sonja Sigurdardottir, Eduardo Meyer, Elise Gourri, Linda Schneider, Yvonne Merki, Nadine Trost, Kathrin Neuenschwander, Charlotte Engström, Beat M Frey, Stefan Meyer, Maja P Mattle-Greminger
Novel regulatory variant in ABO intronic RUNX1 binding site inducing A 3 phenotype. Vox sanguinis 119 (4) (2024)
Gian Andri Thun, Morgan Gueuning, Sonja Sigurdardottir, Eduardo Meyer, Elise Gourri, Linda Schneider, Yvonne Merki, Nadine Trost, Kathrin Neuenschwander, Charlotte Engström, Beat M Frey, Stefan Meyer, Maja P Mattle-Greminger
Novel regulatory variant in ABO intronic RUNX1 binding site inducing A 3 phenotype. Vox sanguinis (2024)
Morgan Gueuning, Gian Andri Thun, Nadine Trost, Linda Schneider, Sonja Sigurdardottir, Charlotte Engström, Naemi Larbes, Yvonne Merki, Beat M Frey, Christoph Gassner, Stefan Meyer, Maja P Mattle-Greminger
Resolving Genotype-Phenotype Discrepancies of the Kidd Blood Group System Using Long-Read Nanopore Sequencing. Biomedicines 12 (1) (2024)
Adrian Belosevic, Anna-Elisabeth Minder, Morgan Gueuning, Franziska van Breemen, Gian Andri Thun, Maja P Mattle-Greminger, Stefan Meyer, Alessandra Baumer, Elisabeth I Minder, Xiaoye Schneider-Yin, Jasmin Barman-Aksözen
First Report of a Low-Frequency Mosaic Mutation in the Hydroxymethylbilane Synthase Gene Causing Acute Intermittent Porphyria. Life (Basel, Switzerland) 13 (9) (2023)
Morgan Gueuning, Gian Andri Thun, Michael Wittig, Anna-Lena Galati, Stefan Meyer, Nadine Trost, Elise Gourri, Janina Fuß, Sonja Sigurdardottir, Yvonne Merki, Kathrin Neuenschwander, Yannik Busch, Peter Trojok, Marco Schäfer, Jochen Gottschalk, Andre Franke, Christoph Gassner, Wolfgang Peter, Beat M Frey, Maja Patricia Mattle-Greminger
Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variants. Blood advances (2022)
Gerard Cantero-Recasens, Carla Burballa, Yuki Ohkawa, Tomohiko Fukuda, Yoichiro Harada, null null, Amy J Curwin, Nathalie Brouwers, Gian Andri Thun, Jianguo Gu, Ivo Gut, Naoyuki Taniguchi, Vivek Malhotra
The ulcerative colitis-associated gene FUT8 regulates the quantity and quality of secreted mucins. Proceedings of the National Academy of Sciences of the United States of America 119 (43) (2022)
Miranda D Stobbe, Gian Andri Thun, Andrea Diéguez-Docampo, Meritxell Oliva, Justin P Whalley, Emanuele Raineri, Ivo Glynne Gut
Recurrent somatic mutations reveal new insights into consequences of mutagenic processes in cancer. PLoS computational biology 15 (11) (2019)
Gian Andri Thun, Sophia Derdak, Francesc Castro Giner, Katherine Apunte-Ramos, Lidia Águeda, Matthias Wjst, Anne Boland-Auge, Jean-François Deleuze, Umme Kolsum, Marion S Heiss-Neumann, Adam Nowinski, Dorota Gorecka, Jens M Hohlfeld, Tobias Welte, Christopher E Brightling, David G Parr, Antje Prasse, Joachim Müller-Quernheim, Timm Greulich, Mariarita Stendardo, Piera Boschetto, Imre Barta, Balázs Döme, Marta Gut, Dave Singh, Loems Ziegler-Heitbrock, Ivo G Gut
High degree of polyclonality hinders somatic mutation calling in lung brush samples of COPD cases and controls. Scientific reports 9 (1) (2019)

Gian Andri Thun.css-eqlu8i{font-size:small;padding-left:4px;} (Gian A Thun, Gian-Andri Thun)

Publication Activity (10 Years)

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Gian Andri Thun (Gian A Thun, Gian-Andri Thun)