about
Significant genetic differentiation between Poland and Germany follows present-day political borders, as revealed by Y-chromosome analysisMandibular hypoplasia, deafness, progeroid features and lipodystrophy (MDPL) syndrome in the context of inherited lipodystrophiesGenome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markersLow-pass DNA sequencing of 1200 Sardinians reconstructs European Y-chromosome phylogenyVariants within the immunoregulatory CBLB gene are associated with multiple sclerosisRare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry.Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study.Genetic loci linked to type 1 diabetes and multiple sclerosis families in Sardinia.Mitogenome Diversity in Sardinians: A Genetic Window onto an Island's Past.Discovery of novel heart rate-associated loci using the Exome Chip.A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulationGenome-wide association study of susceptibility loci for breast cancer in Sardinian population.Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs.Height-reducing variants and selection for short stature in Sardinia.Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels.A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.Novel multiple sclerosis susceptibility loci implicated in epigenetic regulationTBK1 is associated with ALS and ALS-FTD in Sardinian patients.The burden of multiple sclerosis variants in continental Italians and Sardinians.Methods for association analysis and meta-analysis of rare variants in familiesExome-wide association study of plasma lipids in >300,000 individuals.The dependence of serum interleukin-6 level on PPAR-alpha polymorphism in men with coronary atherosclerosis.Allelic variant in CTLA4 is associated with thyroid failure and faster β-cell exhaustion in latent autoimmune diabetes in adults.A genome-wide association study by ImmunoChip reveals potential modifiers in myelodysplastic syndromesGenome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex DisordersGenomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibilitySNP-genotyping on human Y-chromosome for forensic purposes: comparison of two different methodsThree points detection of short fragments derived from the amelogenin gene for gender determination—new possibilities for the capillary electrophoresis systemGender determination in highly degraded DNA samplesUltimate shortening of the PCR product in the STR system TH01—a new perspective in testing of degraded forensic samples
P50
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P50
description
onderzoeker
@nl
name
Magdalena Zoledziewska
@ast
Magdalena Zoledziewska
@en
Magdalena Zoledziewska
@es
Magdalena Zoledziewska
@nl
Magdalena Zoledziewska
@sl
type
label
Magdalena Zoledziewska
@ast
Magdalena Zoledziewska
@en
Magdalena Zoledziewska
@es
Magdalena Zoledziewska
@nl
Magdalena Zoledziewska
@sl
prefLabel
Magdalena Zoledziewska
@ast
Magdalena Zoledziewska
@en
Magdalena Zoledziewska
@es
Magdalena Zoledziewska
@nl
Magdalena Zoledziewska
@sl