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2019
Mark Atrial Fibrillation in Long QT Syndrome by Genotype
Platonov, Pyotr G. ^LU ; McNitt, Scott ; Polonsky, Bronislava ; Rosero, Spencer Z. and Zareba, Wojciech (2019) In Circulation: Arrhythmia and Electrophysiology 12(10).
- Contribution to journal › Article
Mark The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
Figlioli, Gisella ; Brenner, Hermann ^LU ; Ellberg, Carolina ^LU ; Hall, Per ^LU ; Olsson, Håkan ^LU and Peterlongo, Paolo (2019) In npj Breast Cancer 5(1).
- Contribution to journal › Article
Mark SSD1 suppresses phenotypes induced by the lack of Elongator-dependent tRNA modifications
Xu, Fu ; Byström, Anders S and Johansson, Marcus J O ^LU (2019) In PLoS Genetics 15(8).
- Contribution to journal › Article
2018
Mark Risk Stratification of Type 2 Long-QT Syndrome Mutation Carriers with Normal QTc Interval : The Value of Sex, T-Wave Morphology, and Mutation Type
Platonov, Pyotr G. ^LU ; McNitt, Scott ; Polonsky, Bronislava ; Rosero, Spencer Z. ; Kutyifa, Valentina ; Huang, Allison ; Moss, Arthur J. and Zareba, Wojciech (2018) In Circulation: Arrhythmia and Electrophysiology 11(7).
- Contribution to journal › Article
Mark Differential distribution of IgA-protease genotypes in mucosal and invasive isolates of Haemophilus influenzae in Sweden
Resman, Fredrik ^LU ; Manat, Guillaume ^LU ; Lindh, Victor ; Murphy, Timothy F. and Riesbeck, Kristian ^LU (2018) In BMC Infectious Diseases 18(1).
- Contribution to journal › Article
Mark Contrasting results from GWAS and QTL mapping on wing length in great reed warblers
Hansson, Bengt ^LU ; Sigeman, Hanna ^LU ; Stervander, Martin ^LU ; Tarka, Maja ^LU ; Ponnikas, Suvi ^LU ; Strandh, Maria ^LU ; Westerdahl, Helena ^LU and Hasselquist, Dennis ^LU (2018) In Molecular Ecology Resources 18(4). p.867-876
- Contribution to journal › Article
Mark TSC-associated neuropsychiatric disorders (TAND) : findings from the TOSCA natural history study
de Vries, Petrus J and Jansen, Anna C (2018) In Orphanet Journal of Rare Diseases 13(1). p.157-157
- Contribution to journal › Article
Mark ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepancies
Wu, Ping Chun ^LU ; Lin, Yin-Hung ; Tsai, Lei Fang ; Chen, Ming Hung ; Chen, Pei-Lung and Pai, Shun-Chung (2018) In Transfusion 58(9). p.2232-2242
- Contribution to journal › Article
2017
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 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

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