University of Tartu
103 papers found
Response to “Annexin A5 haplotype M2 is not a risk factor for recurrent miscarriages in Northern Europe, is there sufficient evidence?”
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
Extensive shift in placental transcriptome profile in preeclampsia and placental origin of adverse pregnancy outcomes
Annexin A5 Promoter Haplotype M2 Is Not a Risk Factor for Recurrent Pregnancy Loss in Northern Europe
Haplotype Phasing and Inheritance of Copy Number Variants in Nuclear Families
‘Carriers of V-LH among 1593 Baltic men have significantly higher serum LH’
A Meta-analysis of Gene Expression Signatures of Blood Pressure and Hypertension
Extensive load of somatic CNVs in the human placenta
CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs
Effects of Long-Term Averaging of Quantitative Blood Pressure Traits on the Detection of Genetic Associations
Structural genomic variation as risk factor for idiopathic recurrent miscarriage
Reproductive Physiology in Young Men Is Cumulatively Affected by FSH-Action Modulating Genetic Variants: FSHR -29G/A and c.2039 A/G, FSHB -211G/T
Gene-age interactions in blood pressure regulation: A large-scale investigation with the CHARGE, Global BPgen, and ICBP consortia.
Developmental programming of growth: Genetic variant in GH2 gene encoding placental growth hormone contributes to adult height determination
A modest but significant effect of CGB5 gene promoter polymorphisms in modulating the risk of recurrent miscarriage
Increased placental expression and maternal serum levels of apoptosis-inducing TRAIL in recurrent miscarriage
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
Study in 1790 Baltic men: FSHR Asn680Ser polymorphism affects total testes volume.
Mid-Gestational Gene Expression Profile in Placenta and Link to Pregnancy Complications
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