Ieva Miceikaite (Ieva Miceikaitė)

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 10

Top Topics

Transforming Growth Factor

Single Molecule

Epithelial Mesenchymal Transition

Mass Spectrometry

Top Venues

Prenatal diagnosis

Molecular genetics & genomic medicine

Clinical case reports

This page only lists publications with an associated author ORCID identifier.

Publications

Maria Winther Jørgensen, Ieva Miceikaite, Martin Jakob Larsen
nanoNIPT: Short-fragment nanopore sequencing of cell-free DNA for non-invasive prenatal testing of fetal aneuploidies and sex chromosome aberrations. Prenatal diagnosis (2023)
Maria Winther Jørgensen, Ieva Miceikaite, Martin Jakob Larsen
nanoNIPT: Short-fragment Nanopore Sequencing of Cell-free DNA for Non-invasive Prenatal testing of Fetal Aneuploidies and Sex Chromosome Aberrations. Prenatal diagnosis (2023)
Maria Winther Jørgensen, Ieva Miceikaite, Martin Jakob Larsen
nanoNIPT: Short-fragment nanopore sequencing of cell-free DNA for non-invasive prenatal testing of fetal aneuploidies and sex chromosome aberrations. Prenatal diagnosis 43 (3) (2023)
Maria Winther Jørgensen, Ieva Miceikaite, Martin Jakob Larsen
nanoNIPT: Short-fragment nanopore sequencing of cell-free DNA for non-invasive prenatal testing of fetal aneuploidies and sex chromosome aberrations. Prenatal diagnosis 43 (3) (2023)
Maria Winther Jørgensen, Ieva Miceikaite, Martin Jakob Larsen
nanoNIPT: Short-fragment nanopore sequencing of cell-free DNA for non-invasive prenatal testing of fetal aneuploidies and sex chromosome aberrations. Prenatal diagnosis 43 (3) (2023)
Maria Winther Jørgensen, Ieva Miceikaite, Martin Jakob Larsen
nanoNIPT: Short-fragment nanopore sequencing of cell-free DNA for non-invasive prenatal testing of fetal aneuploidies and sex chromosome aberrations. Prenatal diagnosis 43 (3) (2023)
Ieva Miceikaite, Christina Fagerberg, Charlotte Brasch-Andersen, Pernille Mathiesen Torring, Britta Schlott Kristiansen, Qin Hao, Lene Sperling, Mette Holm Ibsen, Katrin Löser, Eske Alf Bendsen, Lilian Bomme Ousager, Martin Jakob Larsen
Comprehensive prenatal diagnostics: Exome versus genome sequencing. Prenatal diagnosis (2023)
Ieva Miceikaite, Charlotte Brasch-Andersen, Christina Fagerberg, Martin Jakob Larsen
Total number of reads affects the accuracy of fetal fraction estimates in NIPT. Molecular genetics & genomic medicine 9 (4) (2021)
Ieva Miceikaite, Geske Sidsel Bak, Martin Jakob Larsen, Britta Schlott Kristiansen, Pernille Mathiesen Torring
Prenatal cases with rare RIT1 variants causing severe fetal hydrops and death. Clinical case reports 9 (7) (2021)
Katrine S Aagaard, Klaus Brusgaard, Ieva Miceikaite, Martin J Larsen, Anette D Kjeldsen, Emilie B Lester, Lilian B Ousager, Pernille Mathiesen Torring
Chromosomal translocation disrupting the SMAD4 gene resulting in the combined phenotype of Juvenile polyposis syndrome and Hereditary Hemorrhagic Telangiectasia. Molecular genetics & genomic medicine 8 (11) (2020)