Maria Pettersson

12PUBLICATIONS
22CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Adolescent healthCell and nuclear divisionGene mapping
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Publications (12)

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

|Apr 05, 2023
Expanding the phenotype of Seckel syndrome associated with biallelic loss-of-function variants in CEP63.

Nadja Pekkola Pacheco, Maria Pettersson, Anna Lindstrand

|Nov 09, 2022
Copy number variants suggest different molecular pathways for the pathogenesis of bladder exstrophy.

Agneta Nordenskjöld, Samara Arkani, Maria Pettersson

|Jul 17, 2022
Multi-omics analysis reveals multiple mechanisms causing Prader-Willi like syndrome in a family with a X;15 translocation.

Jesper Eisfeldt, Fatemah Rezayee, Maria Pettersson

|Sep 09, 2020
Cytogenetically visible inversions are formed by multiple molecular mechanisms.

Maria Pettersson, Christopher M Grochowski, Josephine Wincent

|Mar 04, 2020
Whole-genome sequencing reveals complex chromosome rearrangement disrupting NIPBL in infant with Cornelia de Lange syndrome.

Morasha Plesser Duvdevani, Maria Pettersson, Jesper Eisfeldt

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Frequent Collaborators

9 joint publications

Anna Lindstrand

4 joint publications

Jesper Eisfeldt

3 joint publications

Claudia M B Carvalho

2 joint publications

Daniel Nilsson