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2024
Mark A genomic mutational constraint map using variation in 76,156 human genomes
Chen, S. ; Groop, L. ^LU ; Melander, O. ^LU ; Nilsson, P.M. ^LU ; Smith, J. Gustav ^LU ; MacArthur, D.G. and Karczewski, K.J. (2024) In Nature 625(7993). p.92-100
- Contribution to journal › Article
2023
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 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
Mark A saturated map of common genetic variants associated with human height
Yengo, L. ; Hindy, G. ^LU ; Kurbasic, A. ^LU ; Lyssenko, V. ^LU ; Poveda, A. ^LU ; Elmståhl, S. ^LU ; Franks, P.W. ^LU ; Smith, J. Gustav ^LU ; Tuomi, T. ^LU and Consortium, The PRACTICAL , et al. (2022) In Nature p.704-712
- Contribution to journal › Article
Mark Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
Hindy, George ^LU ; Groop, Leif ^LU ; Lyssenko, Valeriya ^LU ; Melander, Olle ^LU ; Nilsson, Peter M ^LU ; Orho-Melander, Marju ^LU and Peloso, Gina M. (2022) In American Journal of Human Genetics 109(1). p.81-96
- Contribution to journal › Article
2021
Mark The trans-ancestral genomic architecture of glycemic traits
Chen, J. ; Lyssenko, Valeriya ^LU ; Franks, Paul ^LU ; Elmståhl, Sölve ^LU ; Groop, Leif ^LU and van Duijn, C. (2021) In Nature Genetics 53(6). p.840-860
- Contribution to journal › Article
Mark The power of genetic diversity in genome-wide association studies of lipids
Graham, Sarah E. ; Poveda, Alaitz ^LU ; Kurbasic, Azra ^LU ; Lyssenko, Valeriya ^LU ; Franks, Paul ^LU and Willer, Cristen J. (2021) In Nature 600(7890). p.675-679
- Contribution to journal › Article
2020
Mark Protein-altering germline mutations implicate novel genes related to lung cancer development
Ji, Xuemei ; Brunnström, Hans ^LU ; Manjer, Jonas ^LU ; Melander, Olle ^LU ; Overvad, Kim and Amos, Christopher I. (2020) In Nature Communications 11(1).
- Contribution to journal › Article
2019
Mark PATJ Low Frequency Variants Are Associated With Worse Ischemic Stroke Functional Outcome
Mola-Caminal, Marina ; Lindgren, Arne ^LU ; Fernandez-Cadenas, Israel and Jimenez-Conde, Jordi (2019) In Circulation Research 124(1). p.114-120
- 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

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