Center-Authored Papers

Filters: Author is Mitchell, Paul  [Clear All Filters]
2013
Sim X, Jensen RA, Ikram KM, Cotch MF, Li X, Macgregor S, Xie J, Smith AV, Boerwinkle E, Mitchell P et al..  2013.  Genetic loci for retinal arteriolar microcirculation.. PloS one. 8(6):e65804. Abstract
Jensen RA, Sim X, Li X, Cotch MF, Ikram KM, Holliday EG, Eiriksdottir G, Harris TB, Jonasson F, Klein BEK et al..  2013.  Genome-Wide Association Study of Retinopathy in Individuals without Diabetes.. PloS one. 8(2):e54232. Abstract
Holliday EG, Smith AV, Cornes BK, Buitendijk GHS, Jensen RA, Sim X, Aspelund T, Aung T, Baird PN, Boerwinkle E et al..  2013.  Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.. PloS one. 8(1):e53830. Abstract
2016
Pattaro C, Teumer A, Gorski M, Chu AY, Li M, Mijatovic V, Garnaas M, Tin A, Sorice R, Li Y et al..  2016.  Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.. Nature communications. 7:10023. Abstract
Li M, Li Y, Weeks O, Mijatovic V, Teumer A, Huffman JE, Tromp G, Fuchsberger C, Gorski M, Lyytikäinen L-P et al..  2016.  SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.. Journal of the American Society of Nephrology : JASN. Abstract
Jensen RA, Sim X, Smith AV, Li X, Jakobsdóttir J, Cheng C-Y, Brody JA, Cotch MF, McKnight B, Klein R et al..  2016.  Novel Genetic Loci Associated With Retinal Microvascular Diameter.. Circulation. Cardiovascular genetics. 9(1):45-54. Abstract
de Vries PS, Chasman DI, Sabater-Lleal M, Chen M-H, Huffman JE, Steri M, Tang W, Teumer A, Marioni RE, Grossmann V et al..  2016.  A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.. Human molecular genetics. 25(2):358-70. Abstract
2017
de Vries PS, Sabater-Lleal M, Chasman DI, Trompet S, Ahluwalia TS, Teumer A, Kleber ME, Chen M-H, Wang JJ, Attia JR et al..  2017.  Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study.. PloS one. 12(1):e0167742. Abstract
Marouli E, Graff M, Medina-Gomez C, Lo KS, Wood AR, Kjaer TR, Fine RS, Lu Y, Schurmann C, Highland HM et al..  2017.  Rare and low-frequency coding variants alter human adult height.. Nature. 542(7640):186-190. Abstract