Ralf Werner

11PUBLICATIONS
36CO-AUTHORS
Analytical spectrometryInfant and child healthDevelopmental genetics (incl. sex determination)Predictive and prognostic markersSolid tumours
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Publications (11)

|Aug 04, 2026
Exonisation of an Alu element in the 3'-UTR contributes to SRD5A2 deficiency.

|Mar 08, 2026
Clinical Characterization and Molecular Profiling by Targeted Next-Generation Sequencing in a Large Indian Cohort With 46,XY Differences in Sex Development.

Vandana Jain, Sukanya Priyadarshini, Rajni Sharma

|May 27, 2023
DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis.

Felipe Rodrigues de Oliveira, Taís Nitsch Mazzola, Maricilda Palandi de Mello

|Mar 27, 2023
Formin-mediated nuclear actin at androgen receptors promotes transcription.

Julian Knerr, Ralf Werner, Carsten Schwan

|Feb 01, 2023
Persistence of foetal testicular features in patients with defective androgen signalling.

Mostafa Al-Sharkawi, Verónica Calonga-Solís, Franz F Dressler

|Jan 08, 2023
A Novel Look at Dosage-Sensitive Sex Locus Xp21.2 in a Case of 46,XY Partial Gonadal Dysgenesis without NR0B1 Duplication.

Ana Paula Francese-Santos, Jakob A Meinel, Cristiane S C Piveta

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Frequent Collaborators

5 joint publications

Hauke Busch

5 joint publications

Olaf Hiort

4 joint publications

Axel Künstner

2 joint publications

Nadine C Hornig