Author

Anette‐Gabriele Ziegler

TUM KlinikumORCID 0000-0002-6290-5548Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Research Focus:differential expression· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1

Frequent Co-Authors

Christiane WinkleriD· 2 shared Ezio E. BonifacioiD· 2 shared Agnes Andersson SvärdiD· 1 shared Åke LernmarkiD· 1 shared Arancha de la Horra· 1 shared Beena AkolkariD· 1 shared Daniel AgardhiD· 1 shared Edward Choi· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Christiane WinklerORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genetic & Genomic MedicineeLifePeer-reviewedFeb 2, 2026

Polymorphisms in Intron 1 of HLA-DRA Differentially Associate with Type 1 Diabetes and Celiac Disease and Implicate Involvement of Complement System Genes C4A and C4B

Özkan Aydemir, Jeffrey A. Bailey, Daniel Agardh…·TEDDY Study Group

The paper identifies tri-SNP haplotypes in HLA-DRA associated with type 1 diabetes and celiac disease, and links them to differences in complement system genes C4A and C4B.

DOI 10.7554/elife.89068.2

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicineArchives of Disease in ChildhoodPeer-reviewedSep 28, 2022

Successful incorporation of a genetic risk prediction research platform into routine newborn screening

Owen Bendor-Samuel, Tabitha Wishlade, Louise Willis…·the GPPAD Study Group

The paper describes the integration of a genetic risk prediction platform into the NHS newborn screening program for Type 1 Diabetes, demonstrating a model for population-based genetic research.

4 citations

humanDNA methylation

𝕏 PostBluesky

GenomicsScientific ReportsPeer-reviewedApr 18, 2019

Common patterns of gene regulation associated with Cesarean section and the development of islet autoimmunity -- indications of immune cell activation

Michael Laimighofer, Ramona Lickert, R. Fuerst…·Jan Krumsiek

The paper identifies gene expression patterns linked to Cesarean section and islet autoimmunity, showing shared transcriptional changes associated with immune cell activation.

20 citations

humanbulk RNA-seq

𝕏 PostBluesky