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2017
Mark FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population
Kiiski, Johanna I. ; Tervasmäki, Anna ; Pelttari, Liisa M ; Khan, Sofia ; Mantere, Tuomo ; Pylkäs, Katri ; Mannermaa, Arto ; Tengström, Maria ; Kvist, Anders ^LU and Borg, Åke ^LU , et al. (2017) In Breast Cancer Research and Treatment 166(1). p.217-226
- Contribution to journal › Article
Mark Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing
Rohlin, Anna ^LU ; Rambech, Eva ^LU ; Kvist, Anders ^LU ; Törngren, Therese ^LU ; Eiengård, Frida ; Lundstam, Ulf ; Zagoras, Theofanis ; Gebre-Medhin, Samuel ^LU ; Borg, Åke ^LU and Björk, Jan , et al. (2017) In Familial Cancer 16(2). p.195-203
- Contribution to journal › Article
Mark Cytohesin 1 regulates homing and engraftment of human hematopoietic stem and progenitor cells
Rak, Justyna ^LU ; Foster, Katie ; Potrzebowska, Kasia ^LU ; Safaee Talkhoncheh, Mehrnaz ^LU ; Miharada, Natsumi ^LU ; Komorowska, Karolina ^LU ; Torngren, Therese ^LU ; Kvist, Anders ^LU ; Borg, Åke ^LU and Svensson, Lena ^LU , et al. (2017) In Blood 129(8). p.950-958
- Contribution to journal › Article
Mark NF1-mutated melanoma tumors harbor distinct clinical and biological characteristics
Cirenajwis, Helena ^LU ; Lauss, Martin ^LU ; Ekedahl, Henrik ^LU ; Törngren, Therese ^LU ; Kvist, Anders ^LU ; Saal, Lao H ^LU ; Olsson, Håkan ^LU ; Staaf, Johan ^LU ; Carneiro, Ana ^LU and Ingvar, Christian ^LU , et al. (2017) In Molecular Oncology 11(4). p.438-451
- Contribution to journal › Article
Mark Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility
Mantere, Tuomo ; Tervasmäki, Anna ; Nurmi, Anna ; Rapakko, Katrin ; Kauppila, Saila ; Tang, Jiangbo ; Schleutker, Johanna ; Kallioniemi, Anne ; Hartikainen, Jaana M and Mannermaa, Arto , et al. (2017) In Scientific Reports 7(1).
- Contribution to journal › Article
2016
Mark Targeted sequencing of BRCA1 and BRCA2 across a large unselected breast cancer cohort suggests that one-third of mutations are somatic
Winter, C ^LU ; Nilsson, M P ^LU ; Olsson, E ^LU ; George, A M ^LU ; Chen, Y ^LU ; Kvist, A ^LU ; Törngren, T ^LU ; Vallon-Christersson, J ^LU ; Hegardt, C ^LU and Häkkinen, J ^LU , et al. (2016) In Annals of Oncology 27(8). p.8-1532
- Contribution to journal › Article
Mark Multiregion whole-exome sequencing uncovers the genetic evolution and mutational heterogeneity of early-stage metastatic melanoma
Harbst, Katja ^LU ; Lauss, Martin ^LU ; Cirenajwis, Helena ^LU ; Isaksson, Karolin ^LU ; Rosengren, Frida ^LU ; Törngren, Therese ^LU ; Kvist, Anders ^LU ; Johansson, Maria C. ^LU ; Vallon-Christersson, Johan ^LU and Baldetorp, Bo ^LU , et al. (2016) In Cancer Research 76(16). p.4765-4774
- Contribution to journal › Article
Mark Genome-wide RNAi Screen Identifies Cohesin Genes as Modifiers of Renewal and Differentiation in Human HSCs
Galeev, Roman ^LU ; Baudet, Aurélie ^LU ; Kumar, Praveen ; Rundberg Nilsson, Alexandra ^LU ; Nilsson, Björn ^LU ; Soneji, Shamit ^LU ; Törngren, Therese ^LU ; Borg, Åke ^LU ; Kvist, Anders ^LU and Larsson, Jonas ^LU (2016) In Cell Reports 14(12). p.2988-3000
- Contribution to journal › Article
2015
Mark Molecular stratification of metastatic melanoma using gene expression profiling: prediction of survival outcome and benefit from molecular targeted therapy.
Cirenajwis, Helena ^LU ; Ekedahl, Henrik ^LU ; Lauss, Martin ^LU ; Harbst, Katja ^LU ; Carneiro, Ana ^LU ; Enoksson, Jens ^LU ; Rosengren, Frida ^LU ; Werner Hartman, Linda ^LU ; Törngren, Therese ^LU and Kvist, Anders ^LU , et al. (2015) In Oncotarget 6(14). p.12297-12309
- Contribution to journal › Article
Mark FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.
Peterlongo, Paolo ; Catucci, Irene ; Colombo, Mara ; Caleca, Laura ; Mucaki, Eliseos ; Bogliolo, Massimo ; Marin, Maria ; Damiola, Francesca ; Bernard, Loris and Pensotti, Valeria , et al. (2015) In Human Molecular Genetics 24(18). p.5345-5355
- Contribution to journal › Article

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