Publications by authors named "Ronja Adam"

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Identifying colorectal cancer-specific vulnerabilities in the Wnt-driven long non-coding transcriptome.
Laura J Schwarzmueller, Ronja S Adam, Leandro F Moreno, Lisanne E Nijman, Adrian Logiantara

Gut· March 2025

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GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases.
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, Hannah Klinkhammer, Elaine Marchi, Ronja Adam

medRxiv· October 2024

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REEV: review, evaluate and explain variants.
Dzmitry Hramyka, Henrike Lisa Sczakiel, Max Xiaohang Zhao, Oliver Stolpe, Mikko Nieminen, Ronja Adam

Nucleic Acids Res· July 2024

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GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases.
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, Hannah Klinkhammer, Elaine Marchi, Ronja Adam

Res Sq· June 2024

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Development of a miRNA-based classifier for detection of colorectal cancer molecular subtypes.
Ronja S Adam, Dennis Poel, Leandro Ferreira Moreno, Joey M A Spronck, Tim R de Back

Mol Oncol· July 2022

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Variant profiling of colorectal adenomas from three patients of two families with MSH3-related adenomatous polyposis.
Claudia Perne, Sophia Peters, Maria Cartolano, Sukanya Horpaopan, Christina Grimm, Ronja Adam

PLoS One· December 2021

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The recurring features of molecular subtypes in distinct gastrointestinal malignancies-A systematic review.
Ronja S Adam, Ilse Blomberg, Sanne Ten Hoorn, Maarten F Bijlsma, Louis Vermeulen

Crit Rev Oncol Hematol· August 2021

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Intestinal region-specific Wnt signalling profiles reveal interrelation between cell identity and oncogenic pathway activity in cancer development.
Ronja S Adam, Sanne M van Neerven, Cayetano Pleguezuelos-Manzano, Salvatore Simmini, Nicolas Léveillé

Cancer Cell Int· December 2020

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Diagnostic yield and clinical utility of a comprehensive gene panel for hereditary tumor syndromes.
Jonas Henn, Isabel Spier, Ronja S Adam, Stefanie Holzapfel, Siegfried Uhlhaas

Hered Cancer Clin Pract· January 2019

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Stem cell functionality is microenvironmentally defined during tumour expansion and therapy response in colon cancer.
Kristiaan J Lenos, Daniël M Miedema, Sophie C Lodestijn, Lisanne E Nijman, Tom van den Bosch, Ronja S Adam

Nat Cell Biol· October 2018

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Prophylactic total gastrectomy in the management of hereditary tumor syndromes.
Dimitrios Pantelis, Robert Hüneburg, Ronja Adam, Stefanie Holzapfel, Heidrun Gevensleben

Int J Colorectal Dis· December 2016

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Chromoendoscopy in combination with random biopsies does not improve detection of gastric cancer foci in CDH1 mutation positive patients.
Robert Hüneburg, Tim Marwitz, Peer van Heteren, Tobias J Weismüller, Jonel Trebicka, Ronja Adam

Endosc Int Open· December 2016

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Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis.
Ronja Adam, Isabel Spier, Bixiao Zhao, Michael Kloth, Jonathan Marquez

Am J Hum Genet· August 2016

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Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis.
Isabel Spier, Martin Kerick, Dmitriy Drichel, Sukanya Horpaopan, Janine Altmüller, Ronja Adam

Fam Cancer· April 2016

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Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases.
Isabel Spier, Dmitriy Drichel, Martin Kerick, Jutta Kirfel, Sukanya Horpaopan, Ronja Adam

J Med Genet· March 2016

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Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas.
Isabel Spier, Stefanie Holzapfel, Janine Altmüller, Bixiao Zhao, Sukanya Horpaopan, Ronja Adam

Int J Cancer· July 2015

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Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis.
Sukanya Horpaopan, Isabel Spier, Alexander M Zink, Janine Altmüller, Stefanie Holzapfel, Ronja Adam

Int J Cancer· March 2015

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De novo duplication of chromosome 16p in a female infant with signs of neonatal hemochromatosis.
Eva Maria Christina Schwaibold, Iris Bartels, Helmut Küster, Michael Lorenz, Peter Burfeind, Ronja Adam

Mol Cytogenet· January 2014

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C-terminal fluorescent labeling impairs functionality of DNA mismatch repair proteins.
Angela Brieger, Guido Plotz, Inga Hinrichsen, Sandra Passmann, Ronja Adam

PLoS One· July 2012

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A CRM1-dependent nuclear export pathway is involved in the regulation of MutLα subcellular localization.
Angela Brieger, Ronja Adam, Sandra Passmann, Guido Plotz, Stefan Zeuzem

Genes Chromosomes Cancer· February 2011

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