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2017
Mark Variable Familial Exudative Vitreoretinopathy in a family harbouring variants in both FZD4 and TSPAN12
Schatz, Patrik ^LU and Khan, Arif O. (2017) In Acta Ophthalmologica 95(7). p.705-709
- Contribution to journal › Article
Mark New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals
Kraja, Aldi T. ; Cook, James P. ; Warren, Helen R. ; Surendran, Praveen ; Liu, Chunyu ; Evangelou, Evangelos ; Manning, Alisa K. ; Grarup, Niels ; Drenos, Fotios and Sim, Xueling , et al. (2017) In Circulation: Cardiovascular Genetics 10(5).
- Contribution to journal › Article
Mark Identification of new disease mechanisms and treatments for type 2 diabetes based on genetic variants and gene expression networks
Axelsson, Annika ^LU (2017)
- Thesis › Doctoral thesis (compilation)
Mark The P1 histo-blood group antigen is present on human red blood cell glycoproteins
Stenfelt, L. ^LU ; Westman, Julia ^LU and Olsson, M.L. ^LU (2017) 27th Regional Congress of the International Society of Blood Transfusion, ISBT 2017 In Vox Sanguinis 112(S1). p.25-25
- Contribution to journal › Published meeting abstract
Mark Impaired hepatic lipid synthesis from polyunsaturated fatty acids in TM6SF2 E167K variant carriers with NAFLD
Luukkonen, Panu K. ; Zhou, You ; Nidhina Haridas, P. A. ; Dwivedi, Om P. ; Hyötyläinen, Tuulia ; Ali, Ashfaq ; Juuti, Anne ; Leivonen, Marja ; Tukiainen, Taru and Ahonen, Linda , et al. (2017) In Journal of Hepatology 67(1). p.128-136
- Contribution to journal › Article
Mark A low-frequency inactivating AKT2 variant enriched in the finnish population is associated with fasting insulin levels and type 2 diabetes risk
Manning, Alisa ; Ladenvall, Claes ^LU ; Nilsson, Peter ^LU ; V. Varga, Tibor ^LU ; Franks, Paul ^LU ; Rosengren, Anders ^LU ; Melander, Olle ^LU ; Orho-Melander, Marju ^LU ; Kravic, Jasmina ^LU and Groop, Leif ^LU , et al. (2017) In Diabetes 66(7). p.2019-2032
- Contribution to journal › Article
Mark ECG-derived spatial QRS-T angle is strongly associated with hypertrophic cardiomyopathy
Cortez, Daniel ^LU ; Schlegel, Todd T. ; Ackerman, Michael J. and Bos, J. Martijn (2017) In Journal of Electrocardiology 50(2). p.195-202
- Contribution to journal › Article
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 Phenotype and genotype in 52 patients with Rubinstein–Taybi syndrome caused by EP300 mutations
Fergelot, Patricia ; Van Belzen, Martine ; Van Gils, Julien ; Afenjar, Alexandra ; Armour, Christine M. ; Arveiler, Benoit ; Beets, Lex ; Burglen, Lydie ; Busa, Tiffany and Collet, Marie , et al. (2016) In American Journal of Medical Genetics. Part A 170(12). p.3069-3082
- 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

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