Author

Zsófia Nemoda

Semmelweis UniversityORCID 0000-0002-9550-7730Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Approach:benchmark study· 1 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Alexander Maximilian MünchauiD· 1 shared Andrea DietrichiD· 1 shared Andreas HartmanniD· 1 shared Anette E. SchragiD· 1 shared Apostolia TopaloudiiD· 1 shared Arthur Jeremy WillseyiD· 1 shared Ástrid MoreriD· 1 shared Bastian HengereriD· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alexander Maximilian MünchauORCID

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2 papers

Recent·Most cited

Birth weight discordance, gene expression, and DNA methylation: A review of epigenetic twin studies

Dany Laure Wadji, Zsófia Nemoda, Chantal Martin-Söelch, Linda Booij, Chantal Wicky

This paper reviews epigenetic twin studies linking birth weight discordance to gene expression and DNA methylation, highlighting growth-related genes and epigenetic mechanisms.

PLoS ONE · Nov 19, 2025Peer-reviewedGenomics

Genome-wide Association Study identifies two novel loci for Gilles de la Tourette Syndrome

Fotis Tsetsos, Apostolia Topaloudi, Pritesh Jain, Zhiyu Yang, Dongmei Yu, Petros Kolovos, Zeynep Tümer, Renata Rizzo, Andreas Hartmann, Christel Depienne, Yulia Worbe, Kirsten Müller‐Vahl, Daniëlle C. Cath, Dorret Irene Boomsma, Tomasz Wolańczyk, , Peristera Paschou

This study identifies two novel genetic loci associated with Tourette Syndrome through a genome-wide meta-analysis and integrates functional data to implicate specific genes.

medRxiv · Dec 11, 2021 · PreprintGenetic & Genomic Medicine