sameAs
Genome-wide association studies in an isolated founder population from the Pacific Island of KosraeCommon inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traitsVariation in genome-wide mutation rates within and between human familiesGenome sequence, comparative analysis and haplotype structure of the domestic dogInitial sequencing and comparative analysis of the mouse genomeGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's diseaseHost-microbe interactions have shaped the genetic architecture of inflammatory bowel diseaseMeta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorderMethods for high-density admixture mapping of disease genesGenome-wide detection and characterization of positive selection in human populationsThe common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetesIDDM17: polymorphisms in the AMACO gene are associated with dominant protection against type 1A diabetes in a Bedouin Arab familyCa2+/calmodulin-dependent protein kinase II is a modulator of CARMA1-mediated NF-kappaB activationAcheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene.A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16Genome-wide mapping of DNase hypersensitive sites using massively parallel signature sequencing (MPSS)Common variants at five new loci associated with early-onset inflammatory bowel diseaseVariation near complement factor I is associated with risk of advanced AMDDeep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel diseaseTwelve type 2 diabetes susceptibility loci identified through large-scale association analysisGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility lociGenetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosisUlcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association studyDisruption of neurexin 1 associated with autism spectrum disorder.Genome-wide association scan of the time to onset of attention deficit hyperactivity disorderGenome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.The role of the CD58 locus in multiple sclerosisCommon SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13A second generation human haplotype map of over 3.1 million SNPsA high-density association screen of 155 ion transport genes for involvement with common migraineGenome-wide association analysis of metabolic traits in a birth cohort from a founder populationCollaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorderGenome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesisMeta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility lociPLINK: a tool set for whole-genome association and population-based linkage analysesAnalysis of protein-coding genetic variation in 60,706 humansThe structure of haplotype blocks in the human genomeThe Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing dataHaploview: analysis and visualization of LD and haplotype mapsGenome-wide association identifies multiple ulcerative colitis susceptibility loci
P50
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P50
description
geneticist at Harvard University and the University of Helsinki
@en
onderwijzer
@nl
name
Mark Daly
@ast
Mark Daly
@es
Mark Daly
@nl
Mark Joseph Daly
@en
type
label
Mark Daly
@ast
Mark Daly
@es
Mark Daly
@nl
Mark Joseph Daly
@en
altLabel
Daly MJ
@en
Mark Daly
@en
Mark J Daly
@ast
Mark J Daly
@en
Mark J Daly
@es
Mark J Daly
@nl
prefLabel
Mark Daly
@ast
Mark Daly
@es
Mark Daly
@nl
Mark Joseph Daly
@en
P106
P166
P21
P31
P4012
P496
0000-0002-0949-8752
P569
1967-09-15T00:00:00Z