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The Power of Gene-Based Rare Variant Methods to Detect Disease-Associated Variation and Test Hypotheses About Complex Disease (Power and Performance of Gene-Based Association Methods)

2015, Vol.11(4), p.e1005165 [Peer Reviewed Journal]

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Efficiency and Power as a Function of Sequence Coverage, SNP Array Density, and Imputation (Efficiency and Power of Genotyping Strategies)

PLoS Computational Biology, 2012, Vol.8(7), p.e1002604 [Peer Reviewed Journal]

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Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk

Gaudet, MM; Kuchenbaecker, KB; Vijai, J; Klein, RJ; Kirchhoff, T; McGuffog, L; Barrowdale, D; Dunning, AM; Lee, A; Dennis, J; +90 more... (2013) Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk. PLoS genetics, 9 (3) [Peer Reviewed Journal]

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Insight in Genome-Wide Association of Metabolite Quantitative Traits by Exome Sequence Analyses (Genetic Variants Influencing NMR Metabolome)

2015, Vol.11(1), p.e1004835 [Peer Reviewed Journal]

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Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population

Lim, E. T., P. Würtz, A. S. Havulinna, P. Palta, T. Tukiainen, K. Rehnström, T. Esko, et al. 2014. “Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population.” PLoS Genetics 10 (7): e1004494. doi:10.1371/journal.pgen.1004494. http://dx.doi.org/10.1371/journal.pgen.1004494. [Peer Reviewed Journal]

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Genetic Variation in the HSD17B1 Gene and Risk of Prostate Cancer ( HSD17B1 and Prostate Cancer)

PLoS Genetics, 2005, Vol.1(5), p.e68 [Peer Reviewed Journal]

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The Case for Selection at CCR5- Δ 32 (The Case for Selection at CCR5- Δ 32)

PLoS Biology, 2005, Vol.3(11), p.e378 [Peer Reviewed Journal]

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by this Author/Contributor:

  1. Altshuler, David
  2. Flannick, Jason
  3. Boehnke, Michael
  4. McCarthy, Mark I
  5. Groop, Leif

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