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2023
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 Genetic liability to suicide attempt, suicide death, and psychiatric and substance use disorders on the risk for suicide attempt and suicide death : A Swedish national study
Kendler, Kenneth S. ; Ohlsson, Henrik ^LU ; Mościcki, Eve K. ; Sundquist, Jan ^LU ; Edwards, Alexis C. ^LU and Sundquist, Kristina ^LU (2023) In Psychological Medicine 53(4). p.1639-1648
- 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 Cerebellar and subcortical atrophy contribute to psychiatric symptoms in frontotemporal dementia
Bussy, Aurélie ; Levy, Jake P. ; Best, Tristin ; Patel, Raihaan ; Cupo, Lani ; Van Langenhove, Tim ; Nielsen, Jørgen E. ; Pijnenburg, Yolande ; Waldö, Maria Landqvist ^LU and Remes, Anne M. , et al. (2023) In Human Brain Mapping 44(7). p.2684-2700
- Contribution to journal › Article
Mark Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes : A genetic association study in Europeans
Uglebjerg, Nicoline ; Ahmadizar, Fariba ; Aly, Dina M. ^LU ; Cañadas-Garre, Marisa ; Hill, Claire ; Naber, Annemieke ; Oddsson, Asmundur ; Singh, Sunny S. ; Smyth, Laura and Trégouët, David Alexandre , et al. (2023) In Frontiers in Endocrinology 14.
- Contribution to journal › Article
Mark The etiology of Parkinson's disease. Genetic and non-genetic risk factors for a multifactorial disease
Brolin, Kajsa ^LU (2023) In Lund University, Faculty of Medicine Doctoral Dissertation Series
- Thesis › Doctoral thesis (compilation)
Mark HNF1B variant without hyperglycaemia as a cause of isolated profound hypomagnesaemia
Vollmer, Shobitha ; Katzman, Per ^LU and Londahl, Magnus ^LU (2023) In BMJ Case Reports 16(2).
- 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 Contribution of rare and common coding variants to haematological malignancies in the UK biobank
Zöller, Bengt ^LU ; Manderstedt, Eric ^LU ; Lind-Halldén, Christina ^LU and Halldén, Christer (2023) In Leukemia Research Reports 19.
- Contribution to journal › Article

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