N
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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Journal ArticleDOI
The first linkage disequilibrium (LD) maps: Delineation of hot and cold blocks by diplotype analysis
Nikolas Maniatis,Andrew Collins,Chun-Fang Xu,Linda McCarthy,Duncan R. Hewett,William J. Tapper,Sarah Ennis,Xiayi Ke,Newton E. Morton +8 more
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.
Journal ArticleDOI
The genomic and phenotypic diversity of Schizosaccharomyces pombe
Daniel C. Jeffares,Charalampos Rallis,Adrien Rieux,Doug Speed,Martin Převorovský,Tobias Mourier,Francesc Xavier Marsellach,Zamin Iqbal,Winston Lau,Tammy M. K. Cheng,Rodrigo Pracana,Michael Mülleder,Jonathan L.D. Lawson,Anatole Chessel,Sendu Bala,Garrett Hellenthal,Brendan D. O'Fallon,Thomas M. Keane,Jared T. Simpson,Leanne Bischof,Bartlomiej Tomiczek,Danny A. Bitton,Theodora C. Sideri,Sandra Codlin,Josephine E. E. U. Hellberg,Laurent van Trigt,Linda Jeffery,Juan Juan Li,Sophie R. Atkinson,Malte Thodberg,Melanie Febrer,Kirsten McLay,Nizar Drou,William Brown,Jacqueline Hayles,Rafael E. Carazo Salas,Markus Ralser,Nikolas Maniatis,David J. Balding,Francois Balloux,Richard Durbin,Jürg Bähler +41 more
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.
Journal ArticleDOI
Polymorphisms in A Disintegrin and Metalloprotease 33 (ADAM33) Predict Impaired Early-Life Lung Function
Angela Simpson,Nikolas Maniatis,Francine Jury,Julie A. Cakebread,Lesley Lowe,Stephen T. Holgate,Ashley Woodcock,William E R Ollier,Andrew Collins,Adnan Custovic,John W. Holloway,Sally John +11 more
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.
Journal ArticleDOI
Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration
Aspasia Angelakopoulou,Tina Shah,Reecha Sofat,Sonia Shah,Diane J. Berry,Jackie A. Cooper,Jutta Palmen,Ioanna Tzoulaki,Ioanna Tzoulaki,Andrew Wong,Barbara J. Jefferis,Nikolas Maniatis,Fotios Drenos,Bruna Gigante,Rebecca Hardy,Ross C. Laxton,Karin Leander,Anna Motterle,Iain A. Simpson,Liam Smeeth,A Thomson,Claudio J. Verzilli,Diana Kuh,Helen Ireland,John E. Deanfield,Mark J. Caulfield,Chris Wallace,Chris Wallace,Nilesh J. Samani,Nilesh J. Samani,Patricia B. Munroe,Mark Lathrop,F. Gerry R. Fowkes,Michael Marmot,Peter H. Whincup,John C. Whittaker,John C. Whittaker,Ulf de Faire,Mika Kivimäki,Meena Kumari,Elina Hyppönen,Chris Power,Steve E. Humphries,Philippa J. Talmud,Jackie F. Price,Richard W Morris,Shu Ye,Juan P. Casas,Juan P. Casas,Aroon D. Hingorani +49 more
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.
Journal ArticleDOI
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.