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2023
Mark Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases
Kiiskinen, Tuomo ; Helkkula, Pyry ; Krebs, Kristi ; Karjalainen, Juha ; Saarentaus, Elmo ; Mars, Nina ; Lehisto, Arto ; Zhou, Wei ; Cordioli, Mattia and Jukarainen, Sakari , et al. (2023) In Nature Medicine 29(1). p.209-218
- Contribution to journal › Article
Mark Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
Oddsson, Asmundur ; Sulem, Patrick ; Sveinbjornsson, Gardar ; Arnadottir, Gudny A ; Steinthorsdottir, Valgerdur ; Halldorsson, Gisli H ; Atlason, Bjarni A ; Oskarsson, Gudjon R ; Helgason, Hannes and Nielsen, Henriette Svarre , et al. (2023) In Nature Communications 14(1). p.3453-3453
- Contribution to journal › Article
2022
Mark Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci
Fadista, João ^LU ; Skotte, Line ; Karjalainen, Juha ; Abner, Erik ; Sørensen, Erik ; Ullum, Henrik ; Werge, Thomas ; Esko, Tõnu ; Milani, Lili and Palotie, Aarno ^LU , et al. (2022) In Nature Communications 13(1).
- Contribution to journal › Article
2020
Mark Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
Bao, Erik L ; Nandakumar, Satish K ; Liao, Xiaotian ; Bick, Alexander G ; Karjalainen, Juha ; Tabaka, Marcin ; Gan, Olga I ; Havulinna, Aki S ; Kiiskinen, Tuomo T J and Lareau, Caleb A , et al. (2020) In Nature 586(7831). p.769-775
- 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
2017
Mark Rare variant, gene-based association study of hereditary melanoma using whole-exome sequencing
Artomov, Mykyta ; Stratigos, Alexander J. ; Kim, Ivana ; Kumar, Raj ; Lauss, Martin ^LU ; Reddy, Bobby Y. ; Miao, Benchun ; Robles-Espinoza, Carla Daniela ; Sankar, Aravind and Njauw, Ching Ni , et al. (2017) In Journal of the National Cancer Institute 109(12).
- Contribution to journal › Article
2016
Mark Association of Exome Sequences with Cardiovascular Traits among Blacks in the Jackson Heart Study
Peloso, Gina M. ; Lange, Leslie A. ; Varga, Tibor V. ^LU ; Nickerson, Deborah A. ; Smith, Joshua D. ; Griswold, Michael E. ; Musani, Solomon ; Polfus, Linda M. ; Mei, Hao and Gabriel, Stacey , et al. (2016) In Circulation: Cardiovascular Genetics 9(4). p.368-374
- Contribution to journal › Article
2015
Mark Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts
Ek, Weronica E. ; Reznichenko, Anna ; Ripke, Stephan ; Niesler, Beate ; Zucchelli, Marco ; Rivera, Natalia V. ; Schmidt, Peter T. ; Pedersen, Nancy L. ; Magnusson, Patrik and Talley, Nicholas J. , et al. (2015) In Gut 64(11). p.1774-1782
- Contribution to journal › Article
2014
Mark A Novel Test for Recessive Contributions to Complex Diseases Implicates Bardet-Biedl Syndrome Gene BBS10 in Idiopathic Type 2 Diabetes and Obesity
Lim, Elaine T. ; Liu, Yangfan P. ; Chan, Yingleong ; Tuomi, Tiinamaija ^LU ; Karajamaki, AnnMari ; Madsen, Erik ; Altshuler, David M. ; Raychaudhuri, Soumya ; Groop, Leif ^LU and Fannick, Jason , et al. (2014) In American Journal of Human Genetics 95(5). p.509-520
- Contribution to journal › Article
Mark Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population.
Lim, Elaine T ; Würtz, Peter ; Havulinna, Aki S ; Palta, Priit ; Tukiainen, Taru ; Rehnström, Karola ; Esko, Tõnu ; Mägi, Reedik ; Inouye, Michael and Lappalainen, Tuuli , et al. (2014) In PLoS Genetics 10(7).
- Contribution to journal › Article

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