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2017
Mark Polymorphisms in ADH1B and ALDH2 genes associated with the increased risk of gastric cancer in West Bengal, India
Ghosh, Sudakshina ; Bankura, Biswabandhu ; Ghosh, Soumee ; Saha, Makhan Lal ; Pattanayak, Arup Kumar ; Ghatak, Souvik ^LU ; Guha, Manalee ; Nachimuthu, Senthil Kumar ; Panda, Chinmoy Kumar and Maji, Suvendu , et al. (2017) In BMC Cancer 17(1).
- Contribution to journal › Article
2016
Mark Low-frequency and common genetic variation in ischemic stroke : The METASTROKE collaboration
Malik, Rainer ; Traylor, Matthew ; Pulit, Sara L ; Bevan, Steve ; Hopewell, Jemma C ; Holliday, Elizabeth G ; Zhao, Wei ; Abrantes, Patricia ; Amouyel, Philippe and Attia, John R , et al. (2016) In Neurology 86(13). p.26-1217
- Contribution to journal › Article
Mark Genetic variants in CETP increase risk of intracerebral hemorrhage
Anderson, Christopher D. ; Falcone, Guido J. ; Phuah, Chia-Ling ; Radmanesh, Farid ; Brouwers, H Bart ; Battey, Thomas W K ; Biffi, Alessandro ; Peloso, Gina M. ; Liu, Dajiang J and Ayres, Alison M. , et al. (2016) In Annals of Neurology 80(5). p.730-740
- Contribution to journal › Article
2015
Mark Identification of six new susceptibility loci for invasive epithelial ovarian cancer
Kuchenbaecker, Karoline B ; Ramus, Susan J ; Tyrer, Jonathan ; Lee, Andrew ; Shen, Howard C ; Beesley, Jonathan ; Lawrenson, Kate ; McGuffog, Lesley ; Healey, Sue and Lee, Janet M , et al. (2015) In Nature Genetics 47(2). p.71-164
- Contribution to journal › Article
Mark The role of tau in the pathological process and clinical expression of Huntington's disease
Vuono, Romina ; Winder-Rhodes, Sophie ; de Silva, Rohan ; Cisbani, Giulia ; Drouin-Ouellet, Janelle ^LU ; Spillantini, Maria G ; Cicchetti, Francesca and Barker, Roger A ^LU (2015) In Brain 138(7). p.18-1907
- Contribution to journal › Article
Mark Polymorphisms in DCDC2 and S100B associate with developmental dyslexia
Matsson, Hans ; Huss, Mikael ; Persson, Helena ^LU ; Einarsdottir, Elisabet ; Tiraboschi, Ettore ; Nopola-Hemmi, Jaana ; Schumacher, Johannes ; Neuhoff, Nina ; Warnke, Andreas and Lyytinen, Heikki , et al. (2015) In Journal of Human Genetics 60(7). p.399-401
- Contribution to journal › Article
Mark Risk of childhood asthma is associated with CpG-site polymorphisms, regional DNA methylation and mRNA levels at the GSDMB/ORMDL3 locus
Acevedo, Nathalie ; Reinius, Lovisa E ; Greco, Dario ; Gref, Anna ; Orsmark-Pietras, Christina ^LU ; Persson, Helena ^LU ; Pershagen, Göran ; Hedlin, Gunilla ; Melén, Erik and Scheynius, Annika , et al. (2015) In Human Molecular Genetics 24(3). p.90-875
- Contribution to journal › Article
Mark Early and exudative age-related macular degeneration is associated with increased plasma levels of soluble TNF receptor II
Faber, Carsten ; Jehs, Tina ; Juel, Helene Baek ; Singh, Amardeep ^LU ; Falk, Mads Krüger ; Sørensen, Torben Lykke and Nissen, Mogens Holst (2015) In Acta Ophthalmologica 93(3). p.7-242
- Contribution to journal › Article
Mark Genetic variation in caveolin-1 correlates with long-term pancreas transplant function
Hamilton, A ^LU ; Mittal, S ; Barnardo, M C N M ; Fuggle, S V ; Friend, P ; Gough, S C L ^LU and Simmonds, M J (2015) In American Journal of Transplantation 15(5). p.1392-1399
- Contribution to journal › Article
Mark Endothelial nitric oxide synthase single nucleotide polymorphism and left ventricular function in early chronic kidney disease
Chand, Sourabh ; Chue, Colin D ; Edwards, Nicola C ; Hodson, James ; Simmonds, Matthew J ; Hamilton, Alexander ^LU ; Gough, Stephen C L ; Harper, Lorraine ; Steeds, Rick P and Townend, Jonathan N , et al. (2015) In PLoS ONE 10(1).
- Contribution to journal › Article

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