Alisa Förster
4PUBLICATIONS
10CO-AUTHORS
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Publications (4)
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|Jul 27, 2022
Beyond Pathogenic RUNX1 Germline Variants: The Spectrum of Somatic Alterations in RUNX1-Familial Platelet Disorder with Predisposition to Hematologic Malignancies.Alisa Förster, Melanie Decker, Brigitte Schlegelberger
|May 03, 2022
A SUMO4 initiator codon variant in amyotrophic lateral sclerosis reduces SUMO4 expression and alters stress granule dynamics.Alma Osmanovic, Alisa Förster, Maylin Widjaja
|Jan 13, 2022
Validation and clinical application of transactivation assays for RUNX1 variant classification.Melanie Decker, Anupriya Agarwal, Andreas Benneche
|Apr 30, 2021
Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial origin.Alisa Förster, Frank Brand, Rouzbeh Banan
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Frequent Collaborators
2 joint publications
Ruthild G Weber
2 joint publications
Tim Ripperger
1 joint publications
Nicolas Duployez
1 joint publications
Hildegunn Høberg-Vetti
1 joint publications
Adrianna Vlachos
1 joint publications
Brigitte Schlegelberger
1 joint publications
Thomas Illig
1 joint publications
Alma Osmanovic
1 joint publications
Frank Brand
1 joint publications
Susanne Petri
