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Nature Reviews. Genetics|April 10, 2008
Genome-wide association studies for complex traits: consensus, uncertainty and challengesMark I McCarthy, Gonçalo R Abecasis, Lon R Cardon, et al.Bioinformatics (Oxford, England)|March 19, 2008
Celestial3D: a novel method for 3D visualization of familial dataAngeline M Loh, Steven Wiltshire, Jon Emery, et al.American Journal of Hypertension|September 26, 2009
A single-nucleotide polymorphism in the gene encoding osteoprotegerin is associated with diastolic blood pressure in older menJonathan Golledge, Erik Biros, Paula Clancy, et al.Pituitary|March 11, 2025
FGFR1 variation in the divergent settings of congenital hypopituitarism and pituitary tumoursAndreas Orsmond, Gayathri Krishnan, Lyle J Palmer, et al.Atherosclerosis|October 13, 2009
Apolipoprotein E genotype is associated with serum C-reactive protein but not abdominal aortic aneurysmJonathan Golledge, Erik Biros, Matthew Cooper, et al.Australian Health Review : a Publication of the Australian Hospital Association|November 12, 2025
Navigating medication safety with electronic medical records: insights from a dual-phase implementation in paediatric, neonatal and maternity careDylan A Mordaunt, Nichola Johnson, Santosh Verghese, et al.American Journal of Medical Genetics|March 29, 2002
Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit/hyperactivity disorderErik G Willcutt, Bruce F Pennington, Shelley D Smith, et al.Nature Genetics|November 1, 2005
An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data setsEleftheria Zeggini, William Rayner, Andrew P Morris, et al.Genome Research|October 28, 2005
Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variantsRobert Lawrence, David M Evans, Andrew P Morris, et al.American Journal of Medical Genetics|September 5, 2002
Fine mapping of the IBD1 locus did not identify Crohn disease-associated NOD2 variants: implications for complex disease geneticsDavid A van Heel, Dermot P B McGovern, Lon R Cardon, et al.Pageof 29