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List of works by Kaarel Krjutškov

A novel amplification strategy for genotyping with liquid chromatography-electrospray ionization mass spectrometry

scientific article published on November 21, 2012

Analysis of allele and haplotype diversity across 25 genomic regions in three Eastern European populations

scientific article published in April 2009

Characterization and target genes of nine human PRD-like homeobox domain genes expressed exclusively in early embryos

scientific article published on 14 July 2016

Combined immunodeficiency and hypoglycemia associated with mutations in hypoxia upregulated 1.

scientific article published on 29 November 2016

Comparison of DNA extraction methods for multiplex polymerase chain reaction.

scientific article

Complementary seminovaginal microbiome in couples

scientific article published on 11 April 2015

Comprehensive mapping of the effects of azacitidine on DNA methylation, repressive/permissive histone marks and gene expression in primary cells from patients with MDS and MDS-related disease

scientific article

Corrigendum: Characterization and target genes of nine human PRD-like homeobox domain genes expressed exclusively in early embryos

scientific article published on 2 September 2016

Creating basis for introducing non-invasive prenatal testing in the Estonian public health setting

scientific article published on 06 November 2019

Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypes

scientific article published on 20 January 2017

Development of a single tube 640-plex genotyping method for detection of nucleic acid variations on microarrays

scientific article published on 5 June 2008

Estrogen receptor β, a regulator of androgen receptor signaling in the mouse ventral prostate

scientific article

Evaluation of the 124-plex SNP typing microarray for forensic testing.

scientific article

Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study

scientific article

From late fatherhood to prenatal screening of monogenic disorders: evidence and ethical concerns

scientific article published on 02 July 2021

Gene-Expression Profiling Suggests Impaired Signaling via the Interferon Pathway in Cstb-/- Microglia

scientific article

Generation of RNA sequencing libraries for transcriptome analysis of globin-rich tissues of the domestic dog

scientific article published on 12 December 2021

Genetic evidence of assortative mating in humans

scholarly article

Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate

scientific article published in September 2010

Globin mRNA reduction for whole-blood transcriptome sequencing

scientific article published on 12 August 2016

Human pluripotent reprogramming with CRISPR activators.

scientific article published on 6 July 2018

Impact of polyols on Oral microbiome of Estonian schoolchildren

scientific article published on 18 April 2019

Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation

scientific article published on 19 April 2017

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

scientific article

MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate

scientific article published on June 2010

Meta-signature of human endometrial receptivity: a meta-analysis and validation study of transcriptomic biomarkers

scientific article published on 30 August 2017

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

scientific article published on 4 April 2018

Optimizing bone morphogenic protein 4-mediated human embryonic stem cell differentiation into trophoblast-like cells using fibroblast growth factor 2 and transforming growth factor-β/activin/nodal signalling inhibition

scientific article published on 12 June 2017

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

scientific article published on 20 December 2021

TAC-seq: targeted DNA and RNA sequencing for precise biomarker molecule counting

scientific article published in 2018

The human PRD-like homeobox gene LEUTX has a central role in embryo genome activation

scientific article published on 30 August 2016

The pruritus- and TH2-associated cytokine IL-31 promotes growth of sensory nerves

scientific article published on 6 April 2016

Tissue-specific mitochondrial heteroplasmy at position 16,093 within the same individual

scientific article published on 11 July 2013

Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate

scientific article published on 01 April 2011

Whole-exome sequencing identifies a polymorphism in the BMP5 gene associated with SSRI treatment response in major depression.

scientific article published on 7 August 2013