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Year Number of Results
2000 1
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Page 1
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci.
Chang D, Nalls MA, Hallgrímsdóttir IB, Hunkapiller J, van der Brug M, Cai F; International Parkinson's Disease Genomics Consortium; 23andMe Research Team; Kerchner GA, Ayalon G, Bingol B, Sheng M, Hinds D, Behrens TW, Singleton AB, Bhangale TR, Graham RR. Chang D, et al. Among authors: hallgrimsdottir ib. Nat Genet. 2017 Oct;49(10):1511-1516. doi: 10.1038/ng.3955. Epub 2017 Sep 11. Nat Genet. 2017. PMID: 28892059 Free PMC article.
Association mapping from sequencing reads using k-mers.
Rahman A, Hallgrímsdóttir I, Eisen M, Pachter L. Rahman A, et al. Among authors: hallgrimsdottir i. Elife. 2018 Jun 13;7:e32920. doi: 10.7554/eLife.32920. Elife. 2018. PMID: 29897334 Free PMC article.
Placenta and appetite genes GDF15 and IGFBP7 are associated with hyperemesis gravidarum.
Fejzo MS, Sazonova OV, Sathirapongsasuti JF, Hallgrímsdóttir IB, Vacic V, MacGibbon KW, Schoenberg FP, Mancuso N, Slamon DJ, Mullin PM; 23andMe Research Team. Fejzo MS, et al. Among authors: hallgrimsdottir ib. Nat Commun. 2018 Mar 21;9(1):1178. doi: 10.1038/s41467-018-03258-0. Nat Commun. 2018. PMID: 29563502 Free PMC article.
The inheritance of hip osteoarthritis in Iceland.
Ingvarsson T, Stefánsson SE, Hallgrímsdóttir IB, Frigge ML, Jónsson H Jr, Gulcher J, Jónsson H, Ragnarsson JI, Lohmander LS, Stefánsson K. Ingvarsson T, et al. Among authors: hallgrimsdottir ib. Arthritis Rheum. 2000 Dec;43(12):2785-92. doi: 10.1002/1529-0131(200012)43:12<2785::AID-ANR19>3.0.CO;2-I. Arthritis Rheum. 2000. PMID: 11145037 Free article.
Human metabolic profiles are stably controlled by genetic and environmental variation.
Nicholson G, Rantalainen M, Maher AD, Li JV, Malmodin D, Ahmadi KR, Faber JH, Hallgrímsdóttir IB, Barrett A, Toft H, Krestyaninova M, Viksna J, Neogi SG, Dumas ME, Sarkans U, The Molpage Consortium, Silverman BW, Donnelly P, Nicholson JK, Allen M, Zondervan KT, Lindon JC, Spector TD, McCarthy MI, Holmes E, Baunsgaard D, Holmes CC. Nicholson G, et al. Among authors: hallgrimsdottir ib. Mol Syst Biol. 2011 Aug 30;7:525. doi: 10.1038/msb.2011.57. Mol Syst Biol. 2011. PMID: 21878913 Free PMC article.
Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes.
Lohmueller KE, Sparsø T, Li Q, Andersson E, Korneliussen T, Albrechtsen A, Banasik K, Grarup N, Hallgrimsdottir I, Kiil K, Kilpeläinen TO, Krarup NT, Pers TH, Sanchez G, Hu Y, Degiorgio M, Jørgensen T, Sandbæk A, Lauritzen T, Brunak S, Kristiansen K, Li Y, Hansen T, Wang J, Nielsen R, Pedersen O. Lohmueller KE, et al. Among authors: hallgrimsdottir i. Am J Hum Genet. 2013 Dec 5;93(6):1072-86. doi: 10.1016/j.ajhg.2013.11.005. Epub 2013 Nov 27. Am J Hum Genet. 2013. PMID: 24290377 Free PMC article.
13 results