Mark Daly (Former)

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2023
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
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
2014
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
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
2011
Mark Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers
Im, Kate M ; Kirchhoff, Tomas ; Wang, Xianshu ; Green, Todd ; Chow, Clement Y ; Vijai, Joseph ; Korn, Joshua ; Gaudet, Mia M ; Fredericksen, Zachary and Shane Pankratz, V , et al. (2011) In Human Genetics 130(5). p.99-685
- Contribution to journal › Article
2007
Mark Age at first birth and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers.
Kotsopoulos, J ; Lubinski, J ; Lynch, HT ; Klijn J, Ghadirian, P ; Neuhausen, SL ; Kim-Sing, C ; Foulkes, WD ; Moller, P ; Isaacs, C and Domchek, S , et al. (2007) In Breast Cancer Research and Treatment 105(2). p.221-228
- Contribution to journal › Article
1995
Mark A genetic linkage map of the laboratory rat, Rattus norvegicus
Jacob, Howard J. ; Brown, Donna M. ; Bunker, Ruth K. ; Daly, Mark J. ^LU ; Dzau, Victor J. ; Goodman, Alec ; Koike, George ; Kren, Vladimir ; Kurtz, Theodore and Lernmark, Åke ^LU , et al. (1995) In Nature Genetics 9(1). p.63-69
- Contribution to journal › Article