Anna Wedell

45PUBLICATIONS
204CO-AUTHORS
NeurogeneticsMedical molecular engineering of nucleic acids and proteinsEpigenetics (incl. genome methylation and epigenomics)NeonatologyGene expression (incl. microarray and other genome-wide approaches)
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Publications (45)

|Sep 25, 2026
Deep Phenotyping in ReNU Syndrome Identifies a Recognizable Age-Dependent Clinical Trajectory.

|Jul 07, 2026
Genomic Medicine Sweden: Advancing precision medicine at the national level.

|May 25, 2026
Rare variants in TTC7A, ROCK2 and LIMK2 suggest a role for the ROCK-signaling pathway in isolated intestinal malrotation.

|Mar 27, 2026
First Reported Use of Recombinant Parathyroid Hormone in Kenny-Caffey Syndrome Type 2: A Case Report and Literature Review.

Maja Djordjevic Milosevic, Anita Skakic, Marina Andjelkovic

|Mar 25, 2026
Centromeric instability and chromoanasynthesis observed in nine supernumerary marker chromosomes resolved with long-read genome sequencing.

Kristine Bilgrav Saether, Angelo Salazar Mantero, Marlene Ek

|Feb 23, 2026
Flexible and rapid validation of structural variation using adaptive sampling.

Aida Paivandy, Felix Lenner, Jesper Eisfeldt

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Frequent Collaborators

12 joint publications

Ann Nordgren

9 joint publications

Maria Pettersson

6 joint publications

Kristina Lagerstedt-Robinson

6 joint publications

Fulya Taylan