Clonal hematopoiesis predicts development of therapy-related myeloid neoplasms post–autologous stem cell transplantation

Autor: Soerensen, Johannes Frasez, Aggerholm, Anni, Kerndrup, Gitte Birk, Hansen, Marcus Celik, Ewald, Ina Kathrine Lykke, Bill, Marie, Ebbesen, Lene Hyldahl, Rosenberg, Carina Agerbo, Hokland, Peter, Ludvigsen, Maja ^{*, *}, Stidsholt Roug, Anne ^*

Publikováno v: In Blood Advances 10 March 2020 4(5):885-892

Combination of RNA and exome sequencing:correlating somatic mutation between laboratory modalities in AML with normal karyotype

Autor: Hansen, Maria, Hansen, Marcus Celik

Publikováno v: Hansen, M & Hansen, M C 2017, ' Kombination af RNA-og exomsekventering : sammenligning af somatiske mutationer på tværs af laboratoriemodaliteter i AML med normal karyotype ', Best Practice, bind 7, nr. 20, 5, s. 22-23 .

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pure_au_____::60077bb1609ce5dbe890d975b21707d1
https://pure.au.dk/portal/da/publications/kombination-af-rna-og-exomsekventering(2f8adf4b-077b-4ecd-9d33-03c0bff0a6ef).html

Resolving copy number variations from existing exome SNP data without the need for sophisticated software

Autor: Hansen, Marcus Celik, Herborg, Laura Laine, Roug, Anne Stidsholt, Chotirat, Sadudee, Auewarakul, Chirayu Udomsakdi, Kjeldsen, Eigil, Hokland, Peter

Publikováno v: Hansen, M C, Herborg, L L, Roug, A S, Chotirat, S, Auewarakul, C U, Kjeldsen, E & Hokland, P 2016, ' Resolving copy number variations from existing exome SNP data without the need for sophisticated software ', AACR 107th Annual Meeting 2016, New Orleans, Louisiana, United States, 16/04/2016-20/04/2016 . https://doi.org/10.1158/1538-7445.AM2016-3648

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pure_au_____::a96f6ccb80a62acb10893742d953f03d
https://pure.au.dk/portal/da/publications/resolving-copy-number-variations-from-existing-exome-snp-data-without-the-need-for-sophisticated-software(27df0387-c946-42db-afe3-616408162f7a).html

Whole Genome Amplification and Exome Sequencing at the Single Cell Level:A Way to Address Clonal Heterogeneity and Very Sparse Clinical Material

Autor: Hokland, Peter, Simonsen, Anita Tranberg, Hansen, Marcus Celik, Hindkjær, Johnny, Aggerholm, Anni

Publikováno v: Hokland, P, Simonsen, A T, Hansen, M C, Hindkjær, J & Aggerholm, A 2016, ' Whole Genome Amplification and Exome Sequencing at the Single Cell Level : A Way to Address Clonal Heterogeneity and Very Sparse Clinical Material ', 58th ASH Annual Meeting & Exposition, San Diego, USA, 03/12/2016-06/12/2016 .

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pure_au_____::332df6c5be6bbce7af728fa386329a7a
https://pure.au.dk/portal/da/publications/whole-genome-amplification-and-exome-sequencing-at-the-single-cell-level(cc989146-9354-4666-92bf-66d9a7198188).html

Sensitive quantification of the intronless SOX11 mRNA from lymph nodes biopsies in mantle cell lymphoma

Autor: Nielsen, Per Ishøy, Hansen, Simone Valentin, Møller, Michael Boe, Kristensen, Thomas Kielsgaard, Cédile, Oriane, Hansen, Marcus Celik, Ebbesen, Lene Hyldahl, Haaber, Jacob, Abildgaard, Niels, Nyvold, Charlotte Guldborg

Publikováno v: In Leukemia Research March 2019 78:1-2