Alisa H. Forster

Carl Neuberg Str. 1
Hannover, NI 30625, Germany

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 18 publications

Characterization of CTNND2-related neurodevelopmental disease, phenotype-genotype spectrum and WNT dynamics in early neurogenesis.

Characterization of CTNND2-related neurodevelopmental disease, phenotype-genotype spectrum and WNT dynamics in early neurogenesis.

Journal: Research square
Published: January 08, 2026

Germline variants in ATM, BRCA2, other cancer predisposition and novel candidate genes are implicated in glioma risk in adult glioma patients with a familial or personal history of tumors.

Germline variants in ATM, BRCA2, other cancer predisposition and novel candidate genes are implicated in glioma risk in adult glioma patients with a familial or personal history of tumors.

Journal: Acta neuropathologica
Published: August 26, 2025

Genomic variant profiling in blast-phase paediatric chronic myeloid leukaemia: Predisposing and driving alterations.

Genomic variant profiling in blast-phase paediatric chronic myeloid leukaemia: Predisposing and driving alterations.

Journal: British journal of haematology
Published: February 14, 2025

Measurements regarding a combined therapy concept for ophthalmic tumors consisting of brachytherapy and x-rays.

Measurements regarding a combined therapy concept for ophthalmic tumors consisting of brachytherapy and x-rays.

Journal: Biomedical physics & engineering express
Published: September 11, 2023

Germline variants in patients developing second malignant neoplasms after therapy for pediatric acute lymphoblastic leukemia-a case-control study.

Germline variants in patients developing second malignant neoplasms after therapy for pediatric acute lymphoblastic leukemia-a case-control study.

Journal: Leukemia
Published: September 10, 2023

Rare germline variants in POLE and POLD1 encoding the catalytic subunits of DNA polymerases ε and δ in glioma families.

Rare germline variants in POLE and POLD1 encoding the catalytic subunits of DNA polymerases ε and δ in glioma families.

Journal: Acta neuropathologica communications
Published: August 23, 2023

Beyond Pathogenic RUNX1 Germline Variants: The Spectrum of Somatic Alterations in RUNX1-Familial Platelet Disorder with Predisposition to Hematologic Malignancies.

Beyond Pathogenic RUNX1 Germline Variants: The Spectrum of Somatic Alterations in RUNX1-Familial Platelet Disorder with Predisposition to Hematologic Malignancies.

Journal: Cancers
Published: June 16, 2022

Sustained response to bevacizumab in a patient with mosaic neurofibromatosis type 2 carrying the NF2:c.784C>T p.(Arg262*) variant.

Sustained response to bevacizumab in a patient with mosaic neurofibromatosis type 2 carrying the NF2:c.784C>T p.(Arg262*) variant.

Journal: Clinical neuropathology
Published: April 21, 2022

European standard clinical practice - Key issues for the medical care of individuals with familial leukemia.

European standard clinical practice - Key issues for the medical care of individuals with familial leukemia.

Journal: European journal of medical genetics
Published: March 22, 2022

A SUMO4 initiator codon variant in amyotrophic lateral sclerosis reduces SUMO4 expression and alters stress granule dynamics.

A SUMO4 initiator codon variant in amyotrophic lateral sclerosis reduces SUMO4 expression and alters stress granule dynamics.

Journal: Journal of neurology
Published: January 14, 2022

Validation and clinical application of transactivation assays for RUNX1 variant classification.

Validation and clinical application of transactivation assays for RUNX1 variant classification.

Journal: Blood advances
Published: September 14, 2021

Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial origin.

Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial origin.

Journal: Acta neuropathologica
Published: January 26, 2021
Showing 1-12 of 18

Last Updated: 09/26/2026