P. Hofmann

Loss of ADAMTS19 causes progressive non-syndromic heart valve disease

M. Hurles, A. McCallion, A. Franco‐Cereceda, 2019, Nature Genetics.

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

R. Siebert, J. Coselli, K. Devriendt, 2020, bioRxiv.

The oestrogen receptor 2 (ESR2) gene in female‐pattern hair loss: replication of association with rs10137185 in German patients

T. Becker, R. Tazi-Ahnini, D. Drichel, 2014, The British journal of dermatology.