Regina C Betz

33PUBLICATIONS
148CO-AUTHORS
Medical infection agents (incl. prions)Sociological methodology and research methodsOrthodontics and dentofacial orthopaedicsEpigenetics (incl. genome methylation and epigenomics)Neurogenetics
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Publications (33)

|Apr 13, 2026
Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot.

Sheetal Kumar, Sohail Ahmed, Pietro Incardona

|Jul 23, 2025
Statement from the frontal fibrosing alopecia international expert alliance: SOFFIA 2024.

Nekma Meah, Jane Li, Dmitri Wall

|Jul 17, 2025
Beneath the surface: delineating the subtypes of Dowling-Degos disease.

Sheetal Kumar, Damian J Ralser, Joerg Wenzel

|Jul 22, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

Axel Schmidt, Magdalena Danyel, Kathrin Grundmann

|Jul 19, 2024
A nonsense variant in KRT31 is associated with autosomal dominant monilethrix.

Xing Xiong, Nicole Cesarato, Yasmina Gossmann

|Jun 05, 2024
Recent advances in the genetics of alopecia areata.

F Buket Basmanav, Regina C Betz

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Frequent Collaborators

4 joint publications

Markus Nöthen

3 joint publications

Jean Tori Pantel

3 joint publications

Axel Schmidt

3 joint publications

Hannah Klinkhammer