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2023
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 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 Genetic insights into resting heart rate and its role in cardiovascular disease
van de Vegte, Y.J. ; Ladenvall, C. ^LU ; Melander, O. ^LU ; Groop, L. ^LU ; Smith, J.G. ^LU and van der Harst, P. (2023) In Nature Communications 14(1).
- 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 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
Mark Revisiting Diagnosis and Treatment of Hypertrophic Cardiomyopathy : Current Practice and Novel Perspectives
Ottaviani, Andrea ; Mansour, Davide ; Molinari, Lorenzo V. ; Galanti, Kristian ; Mantini, Cesare ; Khanji, Mohammed Y. ; Chahal, Anwar A. ; Zimarino, Marco ; Renda, Giulia and Sciarra, Luigi , et al. (2023) In Journal of Clinical Medicine 12(17).
- Contribution to journal › Scientific review
Mark European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
Budu-Aggrey, A. ; Fadista, J. ^LU ; Standl, M. and Paternoster, L. (2023) In Nature Communications 14(1).
- 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

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