Stephanie A. Schubert

Utrecht, UT 3584CH, Netherlands

Last Updated: 09/26/2026

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Found 14 publications

Differential Wnt/β-catenin signaling via TCF7L2/LEF1 binding specificity shapes cellular and tumor phenotypes.

Differential Wnt/β-catenin signaling via TCF7L2/LEF1 binding specificity shapes cellular and tumor phenotypes.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: June 10, 2026

High-plex imaging of hepatoblastoma and adjacent liver in pediatric patients reveals a predominant myeloid infiltrate expressing immune-checkpoints.

High-plex imaging of hepatoblastoma and adjacent liver in pediatric patients reveals a predominant myeloid infiltrate expressing immune-checkpoints.

Journal: Cancer immunology, immunotherapy : CII

Published: May 04, 2025

Mechanisms of dexamethasone-induced bone toxicity in developing bone: a single-cell perspective.

Mechanisms of dexamethasone-induced bone toxicity in developing bone: a single-cell perspective.

Journal: JBMR plus

Published: January 27, 2025

Germline NPAT inactivating variants as cause of hereditary colorectal cancer.

Germline NPAT inactivating variants as cause of hereditary colorectal cancer.

Journal: European journal of human genetics : EJHG

Published: February 05, 2024

Divergent WNT signaling and drug sensitivity profiles within hepatoblastoma tumors and organoids.

Divergent WNT signaling and drug sensitivity profiles within hepatoblastoma tumors and organoids.

Journal: Nature communications

Published: October 25, 2023

Germline biallelic Mcm8 variants are associated with early-onset Lynch-like syndrome.

Germline biallelic Mcm8 variants are associated with early-onset Lynch-like syndrome.

Journal: JCI insight

Published: May 27, 2020

Germline variant affecting p53β isoforms predisposes to familial cancer.

Germline variant affecting p53β isoforms predisposes to familial cancer.

Journal: Nature communications

Published: May 08, 2020

Digenic inheritance of MSH6 and MUTYH variants in familial colorectal cancer.

Digenic inheritance of MSH6 and MUTYH variants in familial colorectal cancer.

Journal: Genes, chromosomes & cancer

Published: March 04, 2020

The missing heritability of familial colorectal cancer.

The missing heritability of familial colorectal cancer.

Journal: Mutagenesis

Published: June 20, 2019

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.

Journal: British journal of cancer

Published: January 24, 2018

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.

Journal: British journal of cancer

Published: March 21, 2017

Proton Magnetic Resonance Spectroscopy Indicates Preserved Cerebral Biochemical Composition in Duchenne Muscular Dystrophy Patients.

Proton Magnetic Resonance Spectroscopy Indicates Preserved Cerebral Biochemical Composition in Duchenne Muscular Dystrophy Patients.

Journal: Journal of neuromuscular diseases

Published: March 09, 2017

Showing 1-12 of 14

Last Updated: 09/26/2026