Nikolas Maniatis
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Explore the profile of Nikolas Maniatis including associated specialties, affiliations and a list of published articles.
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Articles
22
Citations
455
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Recent Articles
1.
Lau W, Ali A, Maude H, Andrew T, Swallow D, Maniatis N
Genome Biol
. 2024 Jan;
25(1):7.
PMID: 38172955
Background: The cost-free increase in statistical power of using imputation to infer missing genotypes is undoubtedly appealing, but is it hazard-free? This case study of three type-2 diabetes (T2D) loci...
2.
Ali A, Liebert A, Lau W, Maniatis N, Swallow D
Ann Hum Genet
. 2021 Sep;
86(1):24-33.
PMID: 34523124
Although imputation of missing SNP results has been widely used in genetic studies, claims about the quality and usefulness of imputation have outnumbered the few studies that have questioned its...
3.
Maude H, Lau W, Maniatis N, Andrew T
Front Endocrinol (Lausanne)
. 2021 Aug;
12:694893.
PMID: 34456865
This study investigated the potential genetic mechanisms which underlie adipose tissue mitochondrial dysfunction in Type 2 diabetes (T2D), by systematically identifying nuclear-encoded mitochondrial genes (NEMGs) among the genes regulated by...
4.
Pomiankowski A, Thomas M, Jones S, Ekong R, van Dorp L, Maniatis N, et al.
Nature
. 2020 Apr;
580(7803):321.
PMID: 32286556
No abstract available.
5.
Habib A, Matsuyama A, Okorokov A, Santana-Varela S, Bras J, Aloisi A, et al.
Brain
. 2017 Dec;
141(2):365-376.
PMID: 29253101
Chronic pain is a major global public health issue causing a severe impact on both the quality of life for sufferers and the wider economy. Despite the significant clinical burden,...
6.
Liebert A, Lopez S, Jones B, Montalva N, Gerbault P, Lau W, et al.
Hum Genet
. 2017 Oct;
136(11-12):1445-1453.
PMID: 29063188
The genetic trait of lactase persistence (LP) is associated with at least five independent functional single nucleotide variants in a regulatory region about 14 kb upstream of the lactase gene...
7.
Lau W, Andrew T, Maniatis N
Am J Hum Genet
. 2017 May;
100(5):803-816.
PMID: 28475862
Interpretation of results from genome-wide association studies for T2D is challenging. Only very few loci have been replicated in African ancestry populations and the identification of the implicated functional genes...
8.
Jeffares D, Rallis C, Rieux A, Speed D, Prevorovsky M, Mourier T, et al.
Nat Genet
. 2015 Feb;
47(3):235-41.
PMID: 25665008
Natural variation within species reveals aspects of genome evolution and function. The fission yeast Schizosaccharomyces pombe is an important model for eukaryotic biology, but researchers typically use one standard laboratory...
9.
Direk K, Lau W, Small K, Maniatis N, Andrew T
Ann Hum Genet
. 2014 Aug;
78(5):333-44.
PMID: 25117150
Numerous functional studies have implicated PARL in relation to type 2 diabetes (T2D). We hypothesised that conflicting human association studies may be due to neighbouring causal variants being in linkage...
10.
Elding H, Lau W, Swallow D, Maniatis N
Am J Hum Genet
. 2012 Dec;
92(1):107-13.
PMID: 23246291
The risk of Crohn disease (CD) has a large genetic component. A recent meta-analysis of 6 genome-wide association studies reported 71 chromosomal intervals but does not account for all of...