Author

Indrajit Nanda

University of Würzburg

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1 Approach:statistical model· 1 Organism:zebrafish· 1

Frequent Co-Authors

Barbara VonaiD· 2 shared Daniel LiedtkeiD· 2 shared Thomas HaafiD· 2 shared Amanda M. LaueriD· 1 shared Caroline LekszasiD· 1 shared Cordula Neuner· 1 shared Daniel Bengl· 1 shared Erik de VriezeiD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Barbara VonaORCID

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2 papers

Recent·Most cited

FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss

Daniel Liedtke, K Rak, Katrina M. Schrode, Philip Hehlert, Niloofar Chamanrou, Daniel Bengl, Radoslaw Katana, Soganad Heydaran, Julia Doll, Mei Han, Indrajit Nanda, Pingkalai R. Senthilan, Lukas Juergens, Linda Bieniussa, Johannes Voelker, , Barbara Vona

The paper identifies FRMPD4 as a causal gene for X-linked non-syndromic hearing loss through genetic analysis and cross-species functional studies.

medRxiv · Mar 30, 2026 · PreprintGenetic & Genomic Medicine

Biallelic TANGO1 mutations cause a novel syndromal disease due to hampered cellular collagen secretion

Caroline Lekszas, Ombretta Foresti, Ishier Raote, Daniel Liedtke, Eva‐Maria König, Indrajit Nanda, Barbara Vona, Peter De Coster, Rita G. E. C. Cauwels, Vivek Malhotra, Thomas Haaf

This paper identifies biallelic TANGO1 mutations causing a novel syndromal collagenopathy in humans, leading to multiple systemic abnormalities.

eLife · Feb 26, 2020Peer-reviewedGenetics