Author details

Full Name

Loukas Moutsianas

Affiliation

ORCID

Career Start Year

2007

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
29360107	Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2018
29876894	Genetic Association in the HLA Region.	Methods in Molecular Biology	2018
28067910	Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7.	Nat Genet	2017
28341696	A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.	Diabetes	2017
29257133	Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2017
28067908	Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.	Nat Genet	2017
27398621	The genetic architecture of type 2 diabetes.	Nature	2016
26343388	Class II HLA interactions modulate genetic risk for multiple sclerosis.	Nat Genet	2015
25906071	The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease.	PLoS Genet	2015
25605240	Hypoxia induces a lipogenic cancer cell phenotype via HIF1Î±-dependent and -independent pathways.	Oncotarget	2015
24916163	Methodology for the analysis of rare genetic variation in genome-wide association and re-sequencing studies of complex human traits.	Brief Funct Genomics	2014
24412096	Revisiting the thrifty gene hypothesis via 65 loci associated with susceptibility to type 2 diabetes.	Am J Hum Genet	2014
23459081	Multi-population classical HLA type imputation.	PLoS Comput Biol	2013
23860716	Assessing association between protein truncating variants and quantitative traits.	Bioinformatics	2013
24076602	Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.	Nat Genet	2013
24343240	A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates.	Nat Commun	2013
21596858	Multiple Hodgkin lymphoma-associated loci within the HLA region at chromosome 6p21.3.	Blood	2011
21300701	HLA*IMP--an integrated framework for imputing classical HLA alleles from SNP genotypes.	Bioinformatics	2011
21059899	MHC variation and risk of childhood B-cell precursor acute lymphoblastic leukemia.	Blood	2011
21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Nature	2011
20810666	Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging.	Genome Res	2010
20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Nat Genet	2010
20811451	Integrating common and rare genetic variation in diverse human populations.	Nature	2010
19420052	Approximate Bayesian feature selection on a large meta-dataset offers novel insights on factors that effect siRNA potency.		2009
17695752	Grid methodology for identifying co-regulated genes and transcription factor binding sites.	IEEE Trans Nanobioscience	2007