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2023
Mark Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake
Williamson, A. ; Hatem, G. ^LU ; Aly, D.M. ^LU ; Ahlqvist, E. ^LU ; Prasad, R.B. ^LU ; Groop, L. ^LU ; Meigs, J.B. and Langenberg, C. (2023) In Nature Genetics 55(6). p.973-983
- Contribution to journal › Article
Mark Obesity-associated changes in molecular biology of primary breast cancer
Nguyen, H.-L. ; Borg, A. ^LU and Desmedt, C. (2023) In Nature Communications 14(1).
- Contribution to journal › Article
Mark Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis
Medina-Gomez, Carolina ; McGuigan, F.E. ^LU ; Akesson, K.E. ^LU and Rivadeneira, F. (2023) In Communications Biology 6(1).
- Contribution to journal › Article
Mark The impact of sex, age at onset, recurrence, mode of ascertainment and medical complications on the family genetic risk score profiles for alcohol use disorder
Kendler, Kenneth S. ; Ohlsson, Henrik ^LU ; Sundquist, Jan ^LU and Sundquist, Kristina ^LU (2023) In Psychological Medicine 53(5). p.1732-1740
- Contribution to journal › Article
Mark Differences in genetic risk score profiles for drug use disorder, major depression, and ADHD as a function of sex, age at onset, recurrence, mode of ascertainment, and treatment
Kendler, Kenneth S. ^LU ; Ohlsson, Henrik ^LU ; Bacanu, Silviu ; Sundquist, Jan ^LU and Sundquist, Kristina ^LU (2023) In Psychological Medicine 53(8). p.3448-3460
- Contribution to journal › Article
Mark The moderation of the genetic risk for alcohol and drug use disorders in a Swedish national sample by the genetic aptitude for educational attainment
Kendler, Kenneth S. ; Ohlsson, Henrik ^LU ; Sundquist, Jan ^LU and Sundquist, Kristina ^LU (2023) In Psychological Medicine 53(7). p.3077-3084
- Contribution to journal › Article
Mark Gene Therapy with Etranacogene Dezaparvovec for Hemophilia B
Pipe, Steven W. ; Leebeek, Frank W.G. ; Recht, Michael ; Key, Nigel S. ; Castaman, Giancarlo ; Miesbach, Wolfgang ; Lattimore, Susan ; Peerlinck, Kathelijne ; Van Der Valk, Paul and Coppens, Michiel , et al. (2023) In New England Journal of Medicine 388(8). p.706-718
- Contribution to journal › Article
Mark Factor B Mutation in Monozygotic Twins Discordant for Atypical Hemolytic Uremic Syndrome
Aradottir, Sigridur Sunna ^LU ; Kristoffersson, Ann Charlotte ^LU ; Jensson, Brynjar O. ; Sulem, Patrick ; Gong, Henning ; Palsson, Runolfur and Karpman, Diana ^LU (2023) In Kidney International Reports 8(5). p.1097-1101
- Contribution to journal › Article
Mark Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk
Wilcox, N. ; Wahlström, C. ^LU ; Kvist, A. ^LU and Simard, J. (2023) In Nature Genetics 55(9). p.1435-1439
- Contribution to journal › Article
Mark Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease Project
Vollstedt, E.-J. ; Puschmann, A. ^LU and Klein, C. (2023) In PLoS ONE 18(10 October).
- Contribution to journal › Article

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