Author

Angela Risch

University of SalzburgORCID 0000-0002-8026-5505Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Evolutionary Biology· 1 Genetics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 4 Assay:DNA methylation· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Approach:experimental assay· 2 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:GWAS / association mapping· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Angelika LahnsteineriD· 4 shared Esther SchönaueriD· 2 shared Aage HaugeniD· 1 shared Adonina TardóniD· 1 shared Albert RosenbergeriD· 1 shared Angeline S. AndrewiD· 1 shared Anna Madeleine GnaigeriD· 1 shared Anna Oberlercher· 1 shared

Activity by Year

2023-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 13 mutual co-author links

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4 shared papersEvolutionary Biology

Angelika LahnsteinerORCID

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5 papers

Recent·Most cited

Genetic & Genomic MedicineCancer Epidemiology Biomarkers & PreventionPeer-reviewedOct 19, 2026

Large-scale association study identifies lung cancer susceptibility copy number variants and their potential functional role in genetic instability

Feifei Xiao, Fei Qin, Xizhi Luo…·Christopher Ian Amos

The paper identifies lung cancer susceptibility copy number variants (CNVs) and shows their potential role in genomic instability through association analyses and functional validation.

DOI 10.1158/1055-9965.epi-26-0120

humanwhole-genome sequencing

Evolutionary BiologybioRxivPreprintAug 5, 2026

G-quadruplex structures act as a novel recognition motif for the meiosis-specific histone methyltransferase PRDM9

Mia K. Hartge, Nuria Pfennig Hernández, Tomas Pavlik…·Angelika Lahnsteiner

This study shows PRDM9 binds G-quadruplex structures, enhancing meiotic recombination by creating chromatin accessibility.

DOI 10.64898/2026.07.31.742039

humanDNA methylation

Genetic & Genomic MedicinemedRxivPreprintJan 13, 2025

Genetic contributions to premenstrual symptoms: revisiting the role of the ESR1 gene

Angelika Lahnsteiner, Esmeralda Hidalgo‐Lopez, Isabel Asar Noachtar…·Belinda Angela Pletzer

This study examines the association between six SNPs in the ESR1 gene and premenstrual symptom severity, finding SNP-specific symptom profiles and interaction effects.

2 citations

humanstatistical model

GeneticsbioRxivPreprintMar 21, 2024

G-quadruplex formation in GCK and TM6SF2 are targets for differential DNA methylation in metabolic disease and hepatocellular carcinoma patients

Angelika Lahnsteiner, Victoria Ellmer, Anna Oberlercher…·Angela Risch

The paper investigates DNA methylation changes in GCK and TM6SF2 regions associated with metabolic diseases and hepatocellular carcinoma, revealing their impact on G-quadruplex formation and gene regulation.

DOI 10.1101/2024.03.21.585382

humanDNA methylation

Molecular BiologybioRxivPreprintNov 28, 2023

In vivo detection of DNA secondary structures using Permanganate/S1 Footprinting with Direct Adapter Ligation and Sequencing (PDAL-Seq)

Angelika Lahnsteiner, Sarah J. C. Craig, Kaivan Kamali…·Kateryna D. Makova

The paper introduces PDAL-Seq, a method to detect DNA secondary structures in vivo, and provides a standardized analysis pipeline.

DOI 10.1101/2023.11.28.569002

DNA methylationexperimental assay