Martin Larsen

13PUBLICATIONS
72CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)HaematologyEpigenetics (incl. genome methylation and epigenomics)GenomicsCancer genetics
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Publications (13)

|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

|Jan 08, 2024
Variants in the WDR44 WD40-repeat domain cause a spectrum of ciliopathy by impairing ciliogenesis initiation.

Andrea Accogli, Saurabh Shakya, Taewoo Yang

|Jun 25, 2023
Comprehensive prenatal diagnostics: Exome versus genome sequencing.

Ieva Miceikaite, Christina Fagerberg, Charlotte Brasch-Andersen

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Frequent Collaborators

4 joint publications

Christina R Fagerberg

3 joint publications

Ieva Miceikaitė

2 joint publications

Pernille Mathiesen Tørring

2 joint publications

Qin Hao