Minjun Yang

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10 Artikel i vetenskaplig tidskrift
2 Letter

Single base substitution and insertion/deletion mutational signatures in adult core binding factor acute myeloid leukemia
Gunnarsson, R., Yang, M., Biloglav, A., Lazarevic, V., Paulsson, K. & Johansson, B., 2022 apr. 1, I: Leukemia. 4 s.
Forskningsoutput: Tidskriftsbidrag › Letter › Peer review

Öppen tillgång
Pan-genomic sequencing reveals actionable cdkn2a/2b deletions and kataegis in anaplastic thyroid carcinoma
Stenman, A., Yang, M., Paulsson, J. O., Zedenius, J., Paulsson, K. & Juhlin, C. C., 2021 dec., I: Cancers. 13, 24, 6340.
Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

Öppen tillgång
Single base substitution mutational signatures in pediatric acute myeloid leukemia based on whole genome sequencing
Gunnarsson, R., Yang, M., Olsson-Arvidsson, L., Biloglav, A., Behrendtz, M., Castor, A., Paulsson, K. & Johansson, B., 2021 maj 1, I: Leukemia. 35, 5, s. 1485–1489 5 s.
Forskningsoutput: Tidskriftsbidrag › Letter › Peer review

Öppen tillgång
Sister chromatid cohesion defects are associated with chromosomal copy number heterogeneity in high hyperdiploid childhood acute lymphoblastic leukemia
Moura-Castro, L. H., Peña-Martínez, P., Castor, A., Galeev, R., Larsson, J., Järås, M., Yang, M. & Paulsson, K., 2021 juni 1, I: Genes Chromosomes and Cancer. 60, 6, s. 410-417 8 s.
Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

Öppen tillgång
13q12.2 deletions in acute lymphoblastic leukemia lead to upregulation of FLT3 through enhancer hijacking
Yang, M., Safavi, S., Woodward, E. L., Duployez, N., Olsson-arvidsson, L., Ungerbäck, J., Sigvardsson, M., Zaliova, M., Zuna, J., Fioretos, T., Johansson, B., Nord, K. H. & Paulsson, K., 2020 aug. 20, I: Blood. 136, 8, s. 946-956 11 s.
Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

Minjun Yang

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Nätverk

Se detaljer

Single base substitution and insertion/deletion mutational signatures in adult core binding factor acute myeloid leukemia

Pan-genomic sequencing reveals actionable cdkn2a/2b deletions and kataegis in anaplastic thyroid carcinoma

Single base substitution mutational signatures in pediatric acute myeloid leukemia based on whole genome sequencing

Sister chromatid cohesion defects are associated with chromosomal copy number heterogeneity in high hyperdiploid childhood acute lymphoblastic leukemia

13q12.2 deletions in acute lymphoblastic leukemia lead to upregulation of FLT3 through enhancer hijacking

Minjun Yang

Fingeravtryck

Nätverk

Forskningsoutput

Single base substitution and insertion/deletion mutational signatures in adult core binding factor acute myeloid leukemia

Pan-genomic sequencing reveals actionable cdkn2a/2b deletions and kataegis in anaplastic thyroid carcinoma

Single base substitution mutational signatures in pediatric acute myeloid leukemia based on whole genome sequencing

Sister chromatid cohesion defects are associated with chromosomal copy number heterogeneity in high hyperdiploid childhood acute lymphoblastic leukemia

13q12.2 deletions in acute lymphoblastic leukemia lead to upregulation of FLT3 through enhancer hijacking