Christina R Fagerberg

14PUBLICATIONS
108CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Nutritional epidemiologyCancer geneticsDevelopmental genetics (incl. sex determination)
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Publications (14)

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

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

Ieva Miceikaite, Christina Fagerberg, Charlotte Brasch-Andersen

|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

4 joint publications

Martin Larsen

2 joint publications

Alix Paulet

2 joint publications

Francis Ramond

2 joint publications

Minna Kraatari-Tiri