Minjun Yang

E-postadressminjun.yangmed.luse

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1 Liknande profiler

9 Artikel i vetenskaplig tidskrift
1 Letter

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

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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 jun 1, I: Genes Chromosomes and Cancer. 60, 6, s. 410-417 8 s.
Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

Öppen tillgång
1 Citering (SciVal)
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
7 Citeringar (SciVal)
Global RNA expression and DNA methylation patterns in primary anaplastic thyroid cancer
Ravi, N., Yang, M., Mylona, N., Wennerberg, J. & Paulsson, K., 2020 mar 13, I: Cancers. 12, 3, 680.
Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

Öppen tillgång
3 Citeringar (SciVal)
A urinary extracellular vesicle microRNA biomarker discovery pipeline; from automated extracellular vesicle enrichment by acoustic trapping to microRNA sequencing
Ku, A., Ravi, N., Yang, M., Evander, M., Laurell, T., Lilja, H. & Ceder, Y., 2019, I: PLoS ONE. 14, 5, e0217507.
Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

Öppen tillgång
11 Citeringar (SciVal)

Minjun Yang

Fingeravtryck

Nätverk

Se detaljer

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

Global RNA expression and DNA methylation patterns in primary anaplastic thyroid cancer

A urinary extracellular vesicle microRNA biomarker discovery pipeline; from automated extracellular vesicle enrichment by acoustic trapping to microRNA sequencing

Minjun Yang

Fingeravtryck

Nätverk

Forskningsoutput

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

Global RNA expression and DNA methylation patterns in primary anaplastic thyroid cancer

A urinary extracellular vesicle microRNA biomarker discovery pipeline; from automated extracellular vesicle enrichment by acoustic trapping to microRNA sequencing