Triin Kikas

Tartu, Estonia

Last Updated: 09/26/2026

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Found 12 publications

All-in-one exome sequencing approach for genetic testing of unexplained premature ovarian insufficiency.

All-in-one exome sequencing approach for genetic testing of unexplained premature ovarian insufficiency.

Journal: Human reproduction open

Published: March 10, 2026

The long (GGN)n repeat tract in the androgen receptor gene exerts a negative effect on quantitative sperm parameters.

The long (GGN)n repeat tract in the androgen receptor gene exerts a negative effect on quantitative sperm parameters.

Journal: Asian journal of andrology

Published: December 29, 2025

Microdeletion and microduplication syndromes, including recurrent rearrangements at 16p11.2 and 22q11.21, are enriched in unexplained male infertility.

Microdeletion and microduplication syndromes, including recurrent rearrangements at 16p11.2 and 22q11.21, are enriched in unexplained male infertility.

Journal: Human reproduction (Oxford, England)

Published: May 09, 2025

Microdeletions and microduplications linked to severe congenital disorders in infertile men.

Microdeletions and microduplications linked to severe congenital disorders in infertile men.

Journal: Scientific reports

Published: November 04, 2022

Novel Early Pregnancy Multimarker Screening Test for Preeclampsia Risk Prediction.

Novel Early Pregnancy Multimarker Screening Test for Preeclampsia Risk Prediction.

Journal: Frontiers in cardiovascular medicine

Published: April 29, 2022

Corrigendum to "Current knowledge on genetic variants shaping placental transcriptome and their link to gestational and postnatal health" [Placenta 116 (2021) 2-11].

Corrigendum to "Current knowledge on genetic variants shaping placental transcriptome and their link to gestational and postnatal health" [Placenta 116 (2021) 2-11].

Journal: Placenta

Published: April 22, 2022

Coordinated Expressional Landscape of the Human Placental miRNome and Transcriptome.

Coordinated Expressional Landscape of the Human Placental miRNome and Transcriptome.

Journal: Frontiers in cell and developmental biology

Published: April 20, 2021

Current knowledge on genetic variants shaping placental transcriptome and their link to gestational and postnatal health.

Current knowledge on genetic variants shaping placental transcriptome and their link to gestational and postnatal health.

Journal: Placenta

Published: October 31, 2020

C-allele of rs4769613 Near FLT1 Represents a High-Confidence Placental Risk Factor for Preeclampsia.

C-allele of rs4769613 Near FLT1 Represents a High-Confidence Placental Risk Factor for Preeclampsia.

Journal: Hypertension (Dallas, Tex. : 1979)

Published: August 07, 2020

The Effect of Genetic Variation on the Placental Transcriptome in Humans.

The Effect of Genetic Variation on the Placental Transcriptome in Humans.

Journal: Frontiers in genetics

Published: January 20, 2019

Stanniocalcin-1 Hormone in Nonpreeclamptic and Preeclamptic Pregnancy: Clinical, Life-Style, and Genetic Modulators.

Stanniocalcin-1 Hormone in Nonpreeclamptic and Preeclamptic Pregnancy: Clinical, Life-Style, and Genetic Modulators.

Journal: The Journal of clinical endocrinology and metabolism

Published: September 08, 2016

Extensive shift in placental transcriptome profile in preeclampsia and placental origin of adverse pregnancy outcomes.

Extensive shift in placental transcriptome profile in preeclampsia and placental origin of adverse pregnancy outcomes.

Journal: Scientific reports

Published: March 24, 2015

Showing 1-12 of 12

Last Updated: 09/26/2026