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Nikolas Maniatis

Researcher at University College London

Publications -  31
Citations -  1507

Nikolas Maniatis is an academic researcher from University College London. The author has contributed to research in topics: Linkage disequilibrium & Association mapping. The author has an hindex of 20, co-authored 31 publications receiving 1410 citations. Previous affiliations of Nikolas Maniatis include University of Southampton & Southampton General Hospital.

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The first linkage disequilibrium (LD) maps: Delineation of hot and cold blocks by diplotype analysis

TL;DR: In this article, the authors present a theory to construct an additive LD map for which distances are additive and population-specific maps are expected to be approximately proportional, for a random sample and trustworthy map, which can be predicted reliably from information over a small distance and does not depend on the evolutionary variance unless the sample size approaches the population size.
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The genomic and phenotypic diversity of Schizosaccharomyces pombe

TL;DR: The fission yeast Schizosaccharomyces pombe is an important model for eukaryotic biology, but researchers typically use one standard laboratory strain, so this analysis represents a rich resource to examine genotype-phenotype relationships in a tractable model.
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Polymorphisms in A Disintegrin and Metalloprotease 33 (ADAM33) Predict Impaired Early-Life Lung Function

TL;DR: Polymorphisms in ADAM33 predict impaired early-life lung function and there is evidence of a significant causal location between BC+1 and F1 SNPs, at the 5' end of the gene.
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Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration

TL;DR: In this paper, the associations of genome-wide association study-derived coronary heart disease (CHD)-associated single nucleotide polymorphisms (SNPs) with established and emerging risk factors, and the association of genomewide-association study derived lipid-associated SNPs with other risk factors and CHD events were evaluated.
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A map of the human genome in linkage disequilibrium units

TL;DR: The authors used a subset of single nucleotide polymorphisms from the HapMap Project to create a genome-wide map in LDU and found that recombination accounts for 96.8% of the LDU variance in chromosome arms and 92.4% in their deciles.