Ieva Miceikaite
6PUBLICATIONS
8CO-AUTHORS
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Publications (6)
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|Aug 23, 2025
Deep genome sequencing reveals extensive genetic heterogeneity in early human placentas.Ieva Miceikaite, Christina Fagerberg, Charlotte Brasch-Andersen
|Jun 25, 2023
Comprehensive prenatal diagnostics: Exome versus genome sequencing.Ieva Miceikaite, Christina Fagerberg, Charlotte Brasch-Andersen
|Feb 12, 2023
nanoNIPT: Short-fragment nanopore sequencing of cell-free DNA for non-invasive prenatal testing of fetal aneuploidies and sex chromosome aberrations.Maria Winther Jørgensen, Ieva Miceikaitė, Martin J Larsen
|Jul 26, 2021
Prenatal cases with rare RIT1 variants causing severe fetal hydrops and death.Ieva Miceikaite, Geske Sidsel Bak, Martin Jakob Larsen
|Mar 09, 2021
Total number of reads affects the accuracy of fetal fraction estimates in NIPT.Ieva Miceikaitė, Charlotte Brasch-Andersen, Christina Fagerberg
|Oct 15, 2020
Chromosomal translocation disrupting the SMAD4 gene resulting in the combined phenotype of Juvenile polyposis syndrome and Hereditary Hemorrhagic Telangiectasia.Katrine S Aagaard, Klaus Brusgaard, Ieva Miceikaite
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Frequent Collaborators
3 joint publications
Pernille Mathiesen Torring
3 joint publications
Martin Jakob Larsen
1 joint publications
Katrine S Aagaard
1 joint publications
Maria Winther Jørgensen
1 joint publications
Christina Fagerberg
1 joint publications
Charlotte Brasch-Andersen
1 joint publications
Britta Schlott Kristiansen
1 joint publications
Qin Hao
