Priit Palta

ORCID: 0000-0001-9320-7008 · 8 papers in corpus
2023
Nature ·doi:10.1038/s41586-022-05473-8

Population isolates such as those in Finland benefit genetic research because deleterious alleles are often concentrated on a small number of low-frequency variants (0.1% ≤ minor allele frequency < 5%). These variants survived the founding …

2023
Human molecular genetics ·doi:10.1093/hmg/ddad043

Genome-wide association studies (GWAS) have successfully identified associations for cervical cancer, but the underlying mechanisms of cervical biology and pathology remain uncharacterised. Our GWAS meta-analyses fill this gap, as we charac…

2023
Scientific reports ·doi:10.1038/s41598-023-40991-z

Expressional profiling of the endometrium enables the personalised timing of the window of implantation (WOI). This study presents and evaluates a novel analytical pipeline based on a TAC-seq (Targeted Allele Counting by sequencing) method …

2021
European journal of human genetics : EJHG ·doi:10.1038/s41431-020-00730-8

Multivariate methods are known to increase the statistical power to detect associations in the case of shared genetic basis between phenotypes. They have, however, lacked essential analytic tools to follow-up and understand the biology unde…

letter 2019
Biology of reproduction ·doi:10.1093/biolre/ioz072

Transcriptome profiling of 57 endometrial receptivity genes specifies the menstrual cycle phase of endometrial samples.

erratum 2019
Biology of reproduction ·doi:10.1093/biolre/ioz092
other 2012
Human Reproduction ·doi:10.1093/humrep/des125

BACKGROUND: De novo somatic copy number aberrations (SCNAs) in eutopic and ectopic endometria are thought to be involved in the pathogenesis of endometriosis. In this study we used, for the first time, high-density single nucleotide polymor…

article 2011
·doi:10.1093/humrep/26.s1.80