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Ancient human genomes suggest three ancestral populations for present-day EuropeansCommon variants in SLC17A3 gene affect intra-personal variation in serum uric acid levels in longitudinal time seriesThe peopling of Europe and the cautionary tale of Y chromosome lineage R-M269Genome-wide association analyses identify 18 new loci associated with serum urate concentrationsNew loci associated with kidney function and chronic kidney diseasePredictive value of 8 genetic loci for serum uric acid concentrationGenome-wide association study of biochemical traits in Korcula Island, CroatiaLarge-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repairMeta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levelsThe Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic LandscapeMultiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular diseaseGenome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohortsGenetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level.The OSR1 rs12329305 polymorphism contributes to the development of congenital malformations in cases of stillborn/neonatal deathGenome-wide association and functional follow-up reveals new loci for kidney functionMeta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.In search of a Croatian model of nursing education.Evidence of inbreeding depression on human height.IL12RB2 gene is associated with the age of type 1 diabetes onset in Croatian family Trios.The Greeks in the West: genetic signatures of the Hellenic colonisation in southern Italy and SicilyHistoric, demographic, and genetic evidence for increased population frequencies of CCR5Delta32 mutation in Croatian Island isolates after lethal 15th century epidemicsMeta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrationsEthical aspects of human biobanks: a systematic review.Association of NOS3 tag polymorphisms with hypoxic-ischemic encephalopathy.FokI polymorphism, vitamin D receptor, and interleukin-1 receptor haplotypes are associated with type 1 diabetes in the Dalmatian population.Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies.NeuroD1 gene and interleukin-18 gene polymorphisms in type 1 diabetes in Dalmatian population of Southern Croatia.Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.Molecular Characterization of Glucose-6-phosphate Dehydrogenase Deficiency in Families from the Republic of Macedonia and Genotype-phenotype Correlation.Discovery and fine mapping of serum protein loci through transethnic meta-analysisSixteen new lung function signals identified through 1000 Genomes Project reference panel imputationA meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.FTO genotype is associated with phenotypic variability of body mass indexIntegration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function.A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistanceFamily-based analysis of tumor necrosis factor and lymphotoxin-alpha tag polymorphisms with type 1 diabetes in the population of South Croatia.Common variants in Mendelian kidney disease genes and their association with renal function.Limited survivability of unbalanced progeny of carriers of a unique t(4;19)(p15.32;p13.3): a study in multiple generations.
P50
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P50
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Tatijana Zemunik
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P106
P21
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P496
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