Konrad Oexle

13PUBLICATIONS
57CO-AUTHORS
Comparative language studiesNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Medical microbiology not elsewhere classifiedEpidemiological methods
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Publications (13)

|Aug 20, 2025
De novo protein-coding gene variants in developmental stuttering.

Else Eising, Ivana Dzinovic, Arianna Vino

|Jul 05, 2025
Neurobiological correlates of schizophrenia-specific and highly pleiotropic genetic risk scores for neuropsychiatric disorders.

Lydia M Federmann, Lisa Sindermann, Sabrina Primus

|Jun 13, 2025
Beyond volume: Unraveling the genetics of human brain geometry.

Sabrina A Primus, Felix Hoffstaedter, Federico Raimondo

|Dec 11, 2024
Are there two disjunct episignatures for KMT2B-related disease?

Konrad Oexle

|Jun 05, 2024
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction.

Barbara Schormair, Chen Zhao, Steven Bell

|Jun 26, 2023
Episignature analysis of moderate effects and mosaics.

Konrad Oexle, Michael Zech, Lara G Stühn

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Frequent Collaborators

4 joint publications

Juliane Winkelmann

4 joint publications

Matias Wagner

3 joint publications

Barbara Schormair

2 joint publications

Felix Hoffstaedter