Christina R Fagerberg
13PUBLICATIONS
104CO-AUTHORS
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Publications (13)
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|Aug 23, 2025
Deep genome sequencing reveals extensive genetic heterogeneity in early human placentas.Ieva Miceikaite, Christina Fagerberg, Charlotte Brasch-Andersen
|Apr 02, 2024
Correction: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study.Alix Paulet, Cavan Bennett-Ness, Faustine Ageorges
|Feb 15, 2024
Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study.Alix Paulet, Cavan Bennett-Ness, Faustine Ageorges
|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
|Dec 13, 2023
Complete or partial loss of the Y chromosome in an unselected cohort of 865 non-vasectomized, azoospermic men.J Fedder, C Fagerberg, M W Jørgensen
|Aug 29, 2023
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology.Henry Oppermann, Elia Marcos-Grañeda, Linnea A Weiss
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Frequent Collaborators
3 joint publications
Martin J Larsen
2 joint publications
Alix Paulet
2 joint publications
Francis Ramond
2 joint publications
Minna Kraatari-Tiri
2 joint publications
Andrew Green
2 joint publications
Wayne Lam
2 joint publications
Juliette Piard
2 joint publications
Rosalyn Jewell
2 joint publications
Marcello Scala
2 joint publications
Charlotte Brasch-Andersen
