Martin Larsen

15PUBLICATIONS
88CO-AUTHORS
Psychosocial aspects of childbirth and perinatal mental healthMedical molecular engineering of nucleic acids and proteinsGene expression (incl. microarray and other genome-wide approaches)HaematologyEpigenetics (incl. genome methylation and epigenomics)
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Publications (15)

|Nov 11, 2026
Five years of nationwide use of whole genome sequencing in ongoing pregnancies: Diagnostic yield, timing, and implementation.

|Oct 02, 2026
Reappraising the topology of cell-free fetal DNA in maternal blood toward improved prenatal genetic diagnostics.

|Sep 01, 2026
Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

|Oct 30, 2025
Multiple lesion-specific somatic mutations and bi-allelic loss of ACVRL1 in a single patient with hereditary haemorrhagic telangiectasia.

Pernille Darre Haahr, Qin Hao, Klaus Brusgaard

|Aug 23, 2025
Deep genome sequencing reveals extensive genetic heterogeneity in early human placentas.

Ieva Miceikaite, Christina Fagerberg, Charlotte Brasch-Andersen

|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

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Frequent Collaborators

4 joint publications

Christina R Fagerberg

3 joint publications

Pernille Mathiesen Tørring

3 joint publications

Ieva Miceikaitė

2 joint publications

Ida Charlotte Bay Lund