Avdelningen för klinisk genetik

Organisation: avdelning

Fler filtreringsmöjligheter
  1. Whole chromosome gain does not in itself confer cancer-like chromosomal instability.

    Anders Valind, Jin, Y., Bo Baldetorp & David Gisselsson Nord, 2013, I : Proceedings of the National Academy of Sciences. 110, 52, s. 21119-21123

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  2. Whole-exome sequencing exploration of acquired uniparental disomies in B-cell precursor acute lymphoblastic leukemia

    Kristina B. Lundin-Ström, Biloglav, A., Henrik Lilljebjörn, Rissler, M., Thoas Fioretos, Markus Hansson, Behrendtz, M., Anders Castor, Linda Olsson & Bertil Johansson, 2018 sep, I : Leukemia. 32, 9, s. 2058-2062

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  3. Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke

    Andreea Ilinca, Martinez-Majander, N., Sofie Samuelsson, Paul Piccinelli, Truvé, K., Cole, J., Kittner, S., Soller, M., Ulf Kristoffersson, Tatlisumak, T., Andreas Puschmann, Putaala, J. & Arne Lindgren, 2020, I : Stroke. 51, 4, s. 1056-1063 8 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  4. Whole-exome sequencing of pediatric acute lymphoblastic leukemia.

    Henrik Lilljebjörn, Rissler, M., Lassen, C., Heldrup, J., Behrendtz, M., Felix Mitelman, Bertil Johansson & Thoas Fioretos, 2012, I : Leukemia. 26, s. 1602-1607

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  5. Whole-genome-amplified DNA as a source for mutational analysis underestimates the frequency of mutations in pediatric acute myeloid leukemia

    Rosenquist, R., Hans Ehrencrona, Hasle, H., Palle, J. & Kanduri, M., 2013, I : Leukemia. 27, 2, s. 510-512

    Forskningsoutput: TidskriftsbidragLetter

  6. Whole-genome sequencing of triple-negative breast cancers in a population-based clinical study

    Staaf, J., Glodzik, D., Bosch, A., Vallon-Christersson, J., Reuterswärd, C., Häkkinen, J., Degasperi, A., Amarante, T. D., Saal, L. H., Hegardt, C., Stobart, H., Ehinger, A., Larsson, C., Rydén, L., Loman, N., Malmberg, M., Kvist, A., Ehrencrona, H., Davies, H. R., Borg, Å. & 1 andra, Nik-Zainal, S., 2019, I : Nature Medicine. 25, s. 1526–1533

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  7. Whole-genome sequencing of triple negative breast cancers in a standard population-based clinical setting

    Staaf, J., Glodzik, D., Bosch Campos, A., Vallon-Christersson, J., Reuterswärd, C., Häkkinen, J., Degasperi, A., Amarante, T. D., Saal, L., Hegardt, C., Stobart, H., Ehinger, A., Larsson, C., Ryden, L., Loman, N., Malmberg, M., Kvist, A., Ehrencrona, H., Davies, H. R., Borg, Å. & 1 andra, Nik-Zainal, S., 2020 feb 6, I : Breast Cancer Research and Treatment. 180, s. 531-532

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  8. Why classical cytogenetics still matters in acute myeloid leukemia

    Lazarevic, V. L. & Bertil Johansson, 2020, I : Expert Review of Hematology. 13, 2, s. 95-97 3 s.

    Forskningsoutput: TidskriftsbidragDebate/Note/Editorial

  9. Wilms tumors develop through two distinct karyotypic pathways.

    Mattias Höglund, David Gisselsson Nord, Hansen, G. B. & Felix Mitelman, 2004, I : Cancer Genetics and Cytogenetics. 150, 1, s. 9-15

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  10. World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone

    Fletcher, C. D. M. (red.), Unni, K. (red.) & Fredrik Mertens (red.), 2002, IARC Press. 432 s.

    Forskningsoutput: Bok/rapportAntologi (redaktör)