Publications | Lund University Publications

291 – 300 of 1995

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2021
Mark Morbidity, risk of cancer and mortality in 3645 HFE mutations carriers
Hagström, Hannes ; Ndegwa, Nelson ; Jalmeus, Molly ; Ekstedt, Mattias ; Posserud, Iris ; Rorsman, Fredrik ; Nyhlin, Nils ; Klintman, Daniel ^LU ; Werner, Mårten and Marschall, Hanns Ulrich , et al. (2021) In Liver International 41(3). p.545-553
- Contribution to journal › Article
Mark Gene therapy for infantile malignant osteopetrosis : review of pre-clinical research and proof-of-concept for phenotypic reversal
Moscatelli, Ilana ^LU ; Almarza, Elena ; Schambach, Axel ; Ricks, David ; Schulz, Ansgar ; Herzog, Christopher D. ; Henriksen, Kim ; Askmyr, Maria ^LU ; Schwartz, Jonathan D. and Richter, Johan ^LU (2021) In Molecular Therapy - Methods and Clinical Development 20. p.389-397
- Contribution to journal › Scientific review
Mark Sister chromatid cohesion defects are associated with chromosomal copy number heterogeneity in high hyperdiploid childhood acute lymphoblastic leukemia
Moura-Castro, Larissa H. ^LU ; Peña-Martínez, Pablo ^LU ; Castor, Anders ^LU ; Galeev, Roman ^LU ; Larsson, Jonas ^LU ; Järås, Marcus ^LU ; Yang, Minjun ^LU and Paulsson, Kajsa ^LU (2021) In Genes Chromosomes and Cancer 60(6). p.410-417
- Contribution to journal › Article
Mark Clinical and genomic characterization of patients diagnosed with the provisional entity Acute myeloid leukemia with BCR-ABL1, a Swedish population-based study
Orsmark-Pietras, Christina ^LU ; Landberg, Niklas ^LU ; Lorenz, Fryderyk ; Uggla, Bertil ; Höglund, Martin ; Lehmann, Sören ; Derolf, Åsa ; Deneberg, Stefan ; Antunovic, Petar and Cammenga, Jörg ^LU , et al. (2021) In Genes, Chromosomes and Cancer 60(6). p.426-433
- Contribution to journal › Article
Mark Molecular pathways in patients with systemic lupus erythematosus revealed by gene-centred DNA sequencing
Sandling, Johanna K. ; Pucholt, Pascal ; Hultin Rosenberg, Lina ; Farias, Fabiana H.G. ; Kozyrev, Sergey V. ; Eloranta, Maija Leena ; Alexsson, Andrei ; Bianchi, Matteo ; Padyukov, Leonid and Bengtsson, Christine ^LU , et al. (2021) In Annals of the Rheumatic Diseases 80(1). p.109-117
- Contribution to journal › Article
Mark Opportunistic genomic screening. Recommendations of the European Society of Human Genetics
de Wert, Guido ; Dondorp, Wybo ; Clarke, Angus ; Dequeker, Elisabeth M.C. ; Cordier, Christophe ; Deans, Zandra ; van El, Carla G. ; Fellmann, Florence ; Hastings, Ros and Hentze, Sabine , et al. (2021) In European Journal of Human Genetics 29(3). p.365-377
- Contribution to journal › Article
Mark Validation of prostate cancer risk variants rs10993994 and rs7098889 by CRISPR/Cas9 mediated genome editing
Wang, Xing ; Hayes, James E. ; Xu, Xing ; Gao, Xiaoni ; Mehta, Dipti ; Lilja, Hans G. ^LU and Klein, Robert J. (2021) In Gene 768.
- Contribution to journal › Article
Mark De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy
Klöckner, Chiara ; Lundgren, Johan ^LU and Platzer, Konrad (2021) In Genetics in Medicine 23(4). p.653-660
- Contribution to journal › Article
Mark Droplet digital PCR and mile-post analysis for the detection of F8 int1h inversions
Manderstedt, Eric ^LU ; Lind-Halldén, Christina ^LU ; Ljung, Rolf ^LU ; Astermark, Jan ^LU and Halldén, Christer ^LU (2021) In Journal of Thrombosis and Haemostasis 19(3). p.732-737
- Contribution to journal › Article
Mark The Association between Blood-Based Global DNA Methylation and Venous Thromboembolism
Wang, Xiao ^LU ; Memon, Ashfaque A. ^LU ; Palmér, Karolina ^LU ; Svensson, Peter J. ^LU ; Sundquist, Jan ^LU and Sundquist, Kristina ^LU (2021) In Seminars in Thrombosis and Hemostasis 47(6). p.662-668
- Contribution to journal › Article

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