Dagmar Wieczorek
8PUBLICATIONS
153CO-AUTHORS
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Publications (8)
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|Mar 30, 2026
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.Elsa Leitão, Amandine Santini, Benjamin Cogne
|Jul 23, 2025
Structural variation in 1,019 diverse humans based on long-read sequencing.Siegfried Schloissnig, Samarendra Pani, Jana Ebler
|Jul 05, 2023
Natural History and Developmental Trajectories of Individuals With Disease-Causing Variants in STXBP1.Kim M Thalwitzer, Jan H Driedger, Julie Xian
|Dec 23, 2022
Clinical and Cytogenetic Characterization of Early and Late Relapses in Patients Allografted for Myeloid Neoplasms with a Myelodysplastic Component.Victoria Platte, Anika Bergmann, Barbara Hildebrandt
|Nov 26, 2022
Episignature Mapping of TRIP12 Provides Functional Insight into Clark-Baraitser Syndrome.Liselot van der Laan, Kathleen Rooney, Mariëlle Alders
|Oct 18, 2021
Correction to: The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype.Luisa Averdunk, Heinrich Sticht, Harald Surowy
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Frequent Collaborators
2 joint publications
Anne-Sophie Denomme-Pichon
1 joint publications
Ilaria Parenti
1 joint publications
Cristina Gervasini
1 joint publications
Emanuele Agolini
1 joint publications
Denise Horn
1 joint publications
A Micheil Innes
1 joint publications
Chiara Leoni
1 joint publications
Sally Ann Lynch
1 joint publications
Milena Mariani
1 joint publications
Donatella Milani
