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2025
Mark Clinical and Metabolic Signatures of FAM47E–SHROOM3 Haplotypes in a General Population Sample
Ghasemi-Semeskandeh, Dariush ; König, Eva ; Foco, Luisa ; Dordevic, Nikola ; Gögele, Martin ; Rainer, Johannes ; Ralser, Markus ; Acoba, Dianne ^LU ; Domingues, Francisco S. and Peters, Dorien J.M. , et al. (2025) In Kidney International Reports 10(5). p.1495-1508
- Contribution to journal › Article
2024
Mark Outcomes from the International Society of Nephrology Hemolytic Uremic Syndromes International Forum
Kavanagh, D. ; Gerogianni, A. ^LU ; Karpman, D. ^LU and Greenbaum, Larry A. (2024) In Kidney International 106(6). p.1038-1050
- Contribution to journal › Article
2023
Mark Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci
de las Fuentes, L. ; Poveda, A. ^LU ; Franks, P.W. ^LU and Rotter, J.I. (2023) In Frontiers in Genetics 14.
- Contribution to journal › Article
Mark A large meta-analysis identifies genes associated with anterior uveitis
Gelfman, S. ; Melander, O. ^LU and Coppola, G. (2023) In Nature Communications 14(1).
- Contribution to journal › Article
2022
Mark Genetic variation of the blood coagulation regulator tissue factor pathway inhibitor and venous thromboembolism among middle-aged and older adults: A population-based cohort study
Manderstedt, E. ; Elf, J. ^LU ; Svensson, P.J. ^LU ; Engström, G. ^LU ; Melander, O. ^LU and Zöller, B. ^LU (2022) In Research and practice in thrombosis and haemostasis 6(7).
- Contribution to journal › Letter
Mark Complement component C4 structural variation and quantitative traits contribute to sex-biased vulnerability in systemic sclerosis
Kerick, M. ; Hesselstrand, R. ^LU and Martin, Javier (2022) In npj Genomic Medicine 7(1).
- Contribution to journal › Article
2021
Mark Poorly Expressed Alleles of Several Human Immunoglobulin Heavy Chain Variable Genes are Common in the Human Population
Ohlin, Mats ^LU (2021) In Frontiers in Immunology 11.
- Contribution to journal › Article
2017
Mark Parallel antibody germline gene and haplotype analyses support the validity of immunoglobulin germline gene inference and discovery
Kirik, Ufuk ^LU ; Greiff, Lennart ^LU ; Levander, Fredrik ^LU and Ohlin, Mats ^LU (2017) In Molecular Immunology 87. p.12-22
- Contribution to journal › Article
2015
Mark Haemophilia in Sweden – Studies on mutations and clinical implications
Mårtensson, Annika ^LU (2015) In Lund University Faculty of Medicine Doctoral Dissertation Series 2015:103.
- Thesis › Doctoral thesis (compilation)
2013
Mark GNAL mutations cause adult-onset primary dystonia
Vemula, Satya R ; Puschmann, Andreas ^LU ; Xiao, Jianfeng ; Zhao, Yu-Xia ; Rudzinska, Monika ; Wszolek, Zbigniew K and LeDoux, Mark S. (2013) In Neurology 80(1).
- Contribution to journal › Published meeting abstract

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