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Clinical Genetics|June 22, 2021
How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policiesJasmijn E Klapwijk, Malgorzata I Srebniak, Attie T J I Go, et al.
Breast Cancer Research and Treatment|December 25, 2010
A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicingMads Thomassen, Inge Søkilde Pedersen, Ida Vogel, et al.
Prenatal Diagnosis|April 27, 2022
Factors that impact on women's decision-making around prenatal genomic tests: An international discrete choice surveyJames Buchanan, Melissa Hill, Caroline M Vass, et al.
Ugeskrift for Laeger|May 13, 2025
[Genetics in fetal medicine]Simon Horsholt Thomsen, Tina Duelund Hjortshøj, Malou Barbosa, et al.
European Journal of Medical Genetics|July 1, 2018
Is MED13L-related intellectual disability a recognizable syndrome?Pernille Mathiesen Tørring, Martin Jakob Larsen, Charlotte Brasch-Andersen, et al.
Acta Obstetricia Et Gynecologica Scandinavica|November 24, 2020
National data on the early clinical use of non-invasive prenatal testing in public and private healthcare in Denmark 2013-2017Ida C B Lund, Olav B Petersen, Naja H Becher, et al.
Prenatal Diagnosis|March 23, 2025
Whole Genome Sequencing in Prenatal Diagnostics: The Danish Approach to Guideline Formation and Implementation Within Public HealthcareIda Vogel, Lotte Andreasen, Marie Balslev-Harder, et al.
Prenatal Diagnosis|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 DenmarkLotte Hatt, Katarina Ravn, Line Dahl Jeppesen, et al.
Obstetrics and Gynecology|August 24, 2012
Cytokines and the risk of preterm delivery in twin pregnanciesLine Rode, Katharina Klein, Helle Larsen, et al.
Journal of Assisted Reproduction and Genetics|March 7, 2021
Cell-based non-invasive prenatal testing for monogenic disorders: confirmation of unaffected fetuses following preimplantation genetic testingChristian Liebst Frisk Toft, Hans Jakob Ingerslev, Ulrik Schiøler Kesmodel, et al.
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