Mattias Möller (M Möller)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 7

Top Topics

Dna Methylation

Electronic Health Record

Top Venues

Nature communications

Scientific reports

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

Publications

Ping Chun Wu, Yan Quan Lee, Mattias Möller, Jill R Storry, Martin L Olsson
Elucidation of the low-expressing erythroid CR1 phenotype by bioinformatic mining of the GATA1-driven blood-group regulome. Nature communications 14 (1) (2023)
Nicole M Thornton, Vanja Karamatic Crew, Louise Tilley, Carole A Green, Chwen Ling Tay, Rebecca E Griffiths, Belinda K Singleton, Frances Spring, Piers Walser, Abdul Ghani Alattar, Benjamin Jones, Rosalind Laundy, Jill R Storry, Mattias Möller, Lorna Wall, Richard Charlewood, Connie M Westhoff, Christine Lomas-Francis, Vered Yahalom, Ute Feick, Axel Seltsam, Beate Mayer, Martin L Olsson, David J Anstee
Disruption of the tumour-associated EMP3 enhances erythroid proliferation and causes the MAM-negative phenotype. Nature communications 11 (1) (2020)
Julia S Westman, Linn Stenfelt, Karina Malmros, Mattias Möller, Åsa Hellberg, Sven Kjellström, Martin L Olsson
Allele-selective RUNX1 binding regulates P1 blood group status by transcriptional control of A4GALT. Blood 131 (14) (2018)
Magnus Jöud, Mattias Möller, Martin L Olsson
Identification of human glycosyltransferase genes expressed in erythroid cells predicts potential carbohydrate blood group loci. Scientific reports 8 (1) (2018)
Mattias Möller, Yan Quan Lee, Karina Malmros, Sven Kjellström, Linda Björkman, Jill R Storry, Martin L Olsson
Disruption of a GATA1-binding motif upstream of XG/PBDX abolishes Xga expression and resolves the Xg blood group system. Blood 132 (3) (2018)
Mattias Möller, Åsa Hellberg, Martin L Olsson
Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project. Vox sanguinis 113 (2) (2017)
Mattias Möller, Magnus Jöud, Jill R Storry, Martin L Olsson
Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project. Blood advances 1 (3) (2016)