Markus Perola (Former)

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2021
Mark The genomics of heart failure : design and rationale of the HERMES consortium
Lumbers, R. Thomas ; Shah, Sonia ; Lin, Honghuang ; Czuba, Tomasz ^LU ; Henry, Albert ; Swerdlow, Daniel I. ; Mälarstig, Anders ; Andersson, Charlotte ; Verweij, Niek and Holmes, Michael V. , et al. (2021) In ESC Heart Failure 8(6). p.5531-5541
- Contribution to journal › Article
Mark Genome-Wide Association Study of Peripheral Artery Disease
van Zuydam, Natalie R. ; Stiby, Alexander ; Abdalla, Moustafa ; Austin, Erin ; Dahlström, Emma H. ; McLachlan, Stela ; Vlachopoulou, Efthymia ; Ahlqvist, Emma ^LU ; Di Liao, Chen and Sandholm, Niina , et al. (2021) In Circulation. Genomic and precision medicine 14(5). p.002862-002862
- Contribution to journal › Article
Mark A Web Portal for Communicating Polygenic Risk Score Results for Health Care Use—The P5 Study
Marjonen, Heidi ; Marttila, Minttu ; Paajanen, Teemu ; Vornanen, Marleena ; Brunfeldt, Minna ; Joensuu, Anni ; Halmesvaara, Otto ; Aro, Kimmo ; Alanne-Kinnunen, Mervi and Jousilahti, Pekka , et al. (2021) In Frontiers in Genetics 12.
- Contribution to journal › Article
2020
Mark Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
Li, Chen ; Perola, Markus ^LU ; Franks, Paul ^LU ; Eriksson, Johan Gunnar ^LU ; Melander, Olle ^LU ; Nilsson, Peter ^LU and Codd, Veryan (2020) In American Journal of Human Genetics 106(3). p.389-404
- Contribution to journal › Article
2019
Mark Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium
Merino, Jordi ^LU ; Dashti, Hassan S. ; Li, Sherly X. ; Sarnowski, Chloé ; Justice, Anne E. ; Graff, Misa ; Papoutsakis, Constantina ; Smith, Caren E. ; Dedoussis, George V. and Lemaitre, Rozenn N. , et al. (2019) In Molecular Psychiatry 24(12). p.1920-1932
- Contribution to journal › Article
Mark A catalog of genetic loci associated with kidney function from analyses of a million individuals
Wuttke, Matthias ; Almgren, Peter ^LU ; Lindgren, Cecilia M ^LU ; Melander, Olle ^LU ; Orho-Melander, Marju ^LU ; Perola, Markus ^LU ; Schulz, Christina-Alexandra ^LU ; Thomsen, Hauke ^LU ; Wallentin, Lars ^LU and Pattaro, Cristian (2019) In Nature Genetics 51(6). p.957-972
- Contribution to journal › Article
2018
Mark Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland
Martin, Alicia R ; Karczewski, Konrad J ; Kerminen, Sini ; Kurki, Mitja I ; Sarin, Antti-Pekka ; Artomov, Mykyta ; Eriksson, Johan G ; Esko, Tõnu ; Genovese, Giulio and Havulinna, Aki S , et al. (2018) In American Journal of Human Genetics 102(5). p.760-775
- Contribution to journal › Article
2016
Mark Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Surendran, Praveen ; Drenos, Fotios ; Young, Robin ; Warren, Helen ; Cook, James P. ; Manning, Alisa K. ; Grarup, Niels ; Sim, Xueling ; Barnes, Daniel R. and Witkowska, Kate , et al. (2016) In Nature Genetics 48(10). p.1151-1161
- Contribution to journal › Article
Mark Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease
Stitziel, Nathan O. ; Stirrups, Kathleen E. ; Masca, Nicholas G D ; Erdmann, Jeanette ; Ferrario, Paola G. ; König, Inke R. ; Weeke, Peter E. ; Webb, Thomas R. ; Auer, Paul L. and Schick, Ursula M. , et al. (2016) In New England Journal of Medicine 374(12). p.1134-1144
- Contribution to journal › Article
Mark A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease
Scott, Robert A. ; Freitag, Daniel F. ; Li, Li ^LU ; Chu, Audrey Y. ; Surendran, Praveen ; Young, Robin ; Grarup, Niels ; Stancáková, Alena ; Chen, Yuning and Varga, Tibor V. ^LU , et al. (2016) In Science Translational Medicine 8(341).
- Contribution to journal › Article

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