Naja H Becher

7PUBLICATIONS
26CO-AUTHORS
GenomicsMedical biotechnology diagnostics (incl. biosensors)Cardiology (incl. cardiovascular diseases)Epigenetics (incl. genome methylation and epigenomics)Psychosocial aspects of childbirth and perinatal mental health
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Publications (7)

|Mar 23, 2025
Whole Genome Sequencing in Prenatal Diagnostics: The Danish Approach to Guideline Formation and Implementation Within Public Healthcare.

Ida Vogel, Lotte Andreasen, Marie Balslev-Harder

|Jul 21, 2023
A decade of change - lessons learned from prenatal diagnostics in Central Denmark region in 2008-2018.

Dorte Launholt Lildballe, Naja Becher, Else Marie Vestergaard

|May 18, 2023
How does cell-based non-invasive prenatal test (NIPT) perform against chorionic villus sampling and cell-free NIPT in detecting trisomies and copy number variations? A clinical study from Denmark.

Lotte Hatt, Katarina Ravn, Line Dahl Jeppesen

|May 12, 2021
A novel homozygous variant in C1QBP causes severe IUGR, edema, and cardiomyopathy in two fetuses.

Morten Alstrup, Ida Vogel, Puk Sandager

|Nov 24, 2020
National data on the early clinical use of non-invasive prenatal testing in public and private healthcare in Denmark 2013-2017.

Ida C B Lund, Olav B Petersen, Naja H Becher

|Apr 19, 2020
Implementation of exome sequencing in fetal diagnostics-Data and experiences from a tertiary center in Denmark.

Naja Becher, Lotte Andreasen, Puk Sandager

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Frequent Collaborators

6 joint publications

Ida Vogel

3 joint publications

Puk Sandager

3 joint publications

Olav Bjørn Petersen

3 joint publications

Lars Henning Pedersen