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Alisa Förster

4PUBLICATIONS

10CO-AUTHORS

HaematologyNeurology and neuromuscular diseasesHaematological tumoursEpigenetics (incl. genome methylation and epigenomics)

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Publications (4)

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|Jul 27, 2022

Beyond Pathogenic <i>RUNX1</i> 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

Frequent Collaborators

2 joint publications

Ruthild G Weber

2 joint publications

Tim Ripperger

1 joint publications

Nicolas Duployez

1 joint publications

Hildegunn Høberg-Vetti

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