Priit Palta

NIPTmer: rapid k-mer-based software package for detection of fetal aneuploidies

Nathalie Brison, Lauris Kaplinski, Martin Sauk, 2018, Scientific Reports.

Computational framework for targeted high-coverage sequencing based NIPT

Priit Paluoja, Hindrek Teder, Priit Palta, 2019, PloS one.

Creating basis for introducing NIPT in the Estonian public health setting

Lauris Kaplinski, Martin Sauk, Olga Žilina, 2018, bioRxiv.

Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples

Joris Robert Vermeesch, Amin Ardeshirdavani, Priit Paluoja, 2021, PLoS Comput. Biol..

Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population

Andres Metspalu, Mark I. McCarthy, Alex P. Reiner, 2014, PLoS genetics.

Genome-wide methylation analyses of primary human leukocyte subsets identifies functionally important cell-type-specific hypomethylated regions.

Aarno Palotie, Priit Palta, Alison J Coffey, 2013, Blood.

Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms

Eric S. Lander, Andres Metspalu, Mart Kals, 2016, Proceedings of the National Academy of Sciences.

Genome-wide meta-analysis identifies new susceptibility loci for migraine

Thomas Meitinger, Dorret I. Boomsma, M. Arfan Ikram, 2013, Nature Genetics.