Andreas Tzschach

14PUBLICATIONS
161CO-AUTHORS
Gene mappingGene expression (incl. microarray and other genome-wide approaches)NeonatologyCancer geneticsCancer diagnosis
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Publications (14)

|Feb 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.

Benita Menden, Rana D Incebacak Eltemur, German Demidov

|Jun 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases.

Hellen Lesmann, Alexander Hustinx, Shahida Moosa

|Jul 19, 2023
Novel homozygous LAMB1 in-frame deletion in a pediatric patient with brain anomalies and cerebrovascular event.

Louiza Toutouna, Stefanie Beck-Woedl, Ursula Feige

|May 17, 2023
ABRAXAS1 orchestrates BRCA1 activities to counter genome destabilizing repair pathways-lessons from breast cancer patients.

Juliane Sachsenweger, Rebecca Jansche, Tatjana Merk

|Feb 09, 2023
Aberrant phase separation and nucleolar dysfunction in rare genetic diseases.

Martin A Mensah, Henri Niskanen, Alexandre P Magalhaes

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