Author

André Fienemann

University of LübeckORCID 0009-0004-9594-3673Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:GWAS / association mapping· 1 Assay:long-read sequencing· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Christine KleiniD· 2 shared Joanne TrinhiD· 2 shared Katja LohmanniD· 2 shared Samia Ben SassiiD· 2 shared Ai Huey TaniD· 1 shared Allison Ann DilliottiD· 1 shared Ana WestenbergeriD· 1 shared Andrew SingletoniD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Christine KleinORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJun 22, 2026

Repeat expansions in Parkinson's disease and parkinsonism across ancestries: insights from a global genetic cohort

Lara Mariah Lange, Catalina Cerquera‐Cleves, Ai Huey Tan…·the Global Parkinson’s Genetic Program (GP2)

This study identifies pathogenic and intermediate repeat expansions in Parkinson's disease and parkinsonism across 11 ancestries, highlighting ATXN2's role in PD risk and ancestry-specific patterns.

DOI 10.64898/2026.06.12.26354932

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintAug 20, 2025

Complementarity of long-read sequencing and optical genome mapping in Parkinson's disease

André Fienemann, Theresa Lüth, Susen Schaake…·Joanne Trinh

This study compares long-read sequencing and optical genome mapping in detecting structural variants in Parkinson's disease, finding OGM better detects large variants while ONT provides high-resolution refinement.

DOI 10.1101/2025.08.20.25333965

humanlong-read sequencing

𝕏 PostBluesky