Martin Larsen
12PUBLICATIONS
68CO-AUTHORS
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Publications (12)
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|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
|Nov 22, 2023
Comprehensive Noninvasive Fetal Screening by Deep Trio-Exome Sequencing.Ieva Miceikaitė, Qin Hao, Charlotte Brasch-Andersen
|Jun 25, 2023
Comprehensive prenatal diagnostics: Exome versus genome sequencing.Ieva Miceikaite, Christina Fagerberg, Charlotte Brasch-Andersen
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Frequent Collaborators
3 joint publications
Ieva Miceikaitė
3 joint publications
Christina R Fagerberg
2 joint publications
Pernille Mathiesen Tørring
2 joint publications
Qin Hao
2 joint publications
Marcello Scala
1 joint publications
Christian Gilissen
1 joint publications
Corrado Romano
1 joint publications
Mohammed A Al Balwi
1 joint publications
Weilong Li
1 joint publications
Afsaneh Mohammadnejad
