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Human molecular genetics, ISSN 0964-6906, 08/2019, Volume 28, Issue 16, pp. 2675 - 2685
Alzheimer's disease (AD) is the most common neurodegenerative disease worldwide. Familial cases suggest genetic components; however, monogenetic causes are... 
Index Medicus | General
Journal Article
The Journal of investigative dermatology, ISSN 0022-202X, 05/2019
Hutchinson-Gilford progeria syndrome (HGPS) is the result of a defective form of the lamin A protein called progerin. While progerin is known to disrupt the... 
Index Medicus
Journal Article
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 3, pp. 294 - 298
Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 800 - 12
Journal Article
Nature, ISSN 0028-0836, 2013, Volume 497, Issue 7450, pp. 517 - 520
Journal Article
Journal Article
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 5, pp. 498 - 502
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 10/2015, Volume 24, Issue 19, pp. 5637 - 5643
Journal Article
Nature Genetics, ISSN 1061-4036, 03/2016, Volume 48, Issue 3, pp. 318 - 322
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 09/2011, Volume 89, Issue 3, pp. 446 - 450
Journal Article
by Stacey, S.N and Sulem, P and Jonasdottir, A and Masson, G and Gudmundsson, J and Gudbjartsson, D.F and Magnusson, O.T and Gudjonsson, S.A and Sigurgeirsson, B and Thorisdottir, K and Ragnarsson, R and Benediktsdottir, K.R and Nexo, B.A and Tjonneland, A and Overvad, K and Rudnai, P and Gurzau, E and Koppova, K and Hemminki, K and Corredera, C and Fuentelsaz, V and Grasa, P and Navarrete, S and Fuertes, F and Garcia-Prats, M.D and Sanambrosio, E and Panadero, A and Juan, A. de and Garcia, A and Rivera, F and Planelles, D and Soriano, V and Requena, C and Aben, K.K.H and Rossum, M.M. van and Cremers, R.G.H.M and Oort, I.M. van and Spronsen, D.J. van and Schalken, J.A and Peters, W.H.M and Helfand, B.T and Donovan, J.L and Hamdy, F.C and Badescu, D and Coeanu, O and Jinga, M and Csiki, I.E and Constantinescu, V and Badea, P and Mates, I.N and Dinu, D.E and Constantin, A and Mates, D and Kristjansdottir, S and Agnarsson, B.A and Jonsson, E and Barkardottir, R.B and Einarsson, G.V and Sigurdsson, F and Moller, P.H and Stefansson, T and Valdimarsson, T and Johannsson, O.T and Sigurdsson, H and Jonsson, T and Jonasson, J.G and Tryggvadottir, L and Rice, T and Hansen, H.M and Xiao, Y and Lachance, D.H and Kosel, M.L and Decker, P.A and Thorleifsson, G and Johannsdottir, H and Helgadottir, H.T and Sigurdsson, A and Steinthorsdottir, V and Lindblom, A and Sandler, R.S and Keku, T.O and Banasik, K and Jorgensen, T and Witte, D.R and Hansen, T and Pedersen, O and Jinga, V and Neal, D.E and Catalona, W.J and Wrensch, M and Wiencke, J and Jenkins, R.B and Nagore, E and Vogel, U and Kiemeney, L.A.L.M and Kumar, R and Mayordomo, J.I and Olafsson, J.H and et al and Swedish Low-Risk Colorectal Canc and Swedish Low-risk Colorectal Cancer Study Group and Medicinska och farmaceutiska vetenskapsområdet and Uppsala universitet and Medicinska och farmaceutiska vetenskapsområdet, centrumbildningar mm and Centrum för klinisk forskning, Västerås
Nature Genetics, ISSN 1061-4036, 2011, Volume 43, Issue 11, pp. 1098 - 1103
Journal Article
Nature Genetics, ISSN 1061-4036, 2011, Volume 43, Issue 11, pp. 1127 - 1130
We tested 16 million SNPs, identified through whole-genome sequencing of 457 Icelanders, for association with gout and serum uric acid levels. Genotypes were... 
GENOTYPES | SLC2A9 | URATE | IMPUTATION | METABOLISM | GENETICS & HEREDITY | CARDIOVASCULAR-DISEASE | RISK | CANCER | GENOME-WIDE ASSOCIATION | FAMILY | Gout - genetics | Polymorphism, Single Nucleotide | Uric Acid - blood | Mutation, Missense | Humans | Iceland | Urine | Genes | Genomes | Index Medicus
Journal Article