PD Nadine Hornig

J. Knerr, R. Werner, C. Schwan, H. Wang, P. Gebhardt, H. Grotsch, A. Caliebe, M. Spielmann, P. Holterhus, R. Grosse, and N. Hornig,
Formin-mediated nuclear actin at androgen receptors promotes transcription, Nature , 2023.

DOI:	10.1038/s41586-023-05981-1

H. Marko, N. Hornig, R. Betz, P. Holterhus, J. Altmuller, H. Thiele, M. Fabiano, H. Schweikert, D. Braun, and U. Schweizer,
Genomic variants reducing expression of two endocytic receptors in 46,XY differences of sex development, Hum Mutat , vol. 43, no. 3, pp. 420-433, 2022.

DOI:	10.1002/humu.24325

L. Tack, S. Straaten, S. Riedl, A. Springer, P. Holterhus, N. Hornig, Z. Kolesinska, M. Niedziela, F. Baronio, A. Balsamo, S. Hannema, A. Nordenstrom, S. Poyrazoglu, F. Darendeliler, R. Grinspon, R. Rey, F. Aljuraibah, J. Bryce, F. Ahmed, R. Tadokoro-Cuccaro, I. Hughes, G. Guaragna-Filho, A. Maciel-Guerra, G. Guerra-Junior, and M. Cools,
Growth, puberty and testicular function in boys born small for gestational age with a nonspecific disorder of sex development, Clin Endocrinol (Oxf) , vol. 96, no. 2, pp. 165-174, 2022.

DOI:	10.1111/cen.14614

N. Hornig, and P. Holterhus,
Molecular basis of androgen insensitivity syndromes, Mol Cell Endocrinol , vol. 523, pp. 111146, 2021.

DOI:	10.1016/j.mce.2020.111146

N. Hornig, J. Demiri, P. Rodens, E. Murga Penas, A. Caliebe, A. Eckstein, H. Schweikert, L. Audi, O. Hiort, R. Werner, A. Kulle, O. Ammerpohl, and P. Holterhus,
Reduced Androgen Receptor Expression in Genital Skin Fibroblasts From Patients With 45,X/46,XY Mosaicism, J Clin Endocrinol Metab , vol. 104, no. 10, pp. 4630-4638, 2019.

DOI:	10.1210/jc.2019-00108

N. Hornig, A. Kulle, and P. Holterhus,
Hormonal Control of Fetal Sex Development, in Encyclopedia of Endocrine Diseases (Second Edition) , Huhtaniemi, Ilpo and Martini, Luciano, Eds. Oxford: Academic Press, 2019, pp. 468-475.

DOI:	https://doi.org/10.1016/B978-0-12-801238-3.65372-2
ISBN:	978-0-12-812200-6

N. Hornig, P. Rodens, H. Dorr, N. Hubner, A. Kulle, H. Schweikert, M. Welzel, S. Bens, O. Hiort, R. Werner, S. Gonzalves, A. Eckstein, M. Cools, A. Verrijn-Stuart, H. Stunnenberg, R. Siebert, O. Ammerpohl, and P. Holterhus,
Epigenetic Repression of Androgen Receptor Transcription in Mutation-Negative Androgen Insensitivity Syndrome (AIS Type II), J Clin Endocrinol Metab , vol. 103, no. 12, pp. 4617-4627, 2018.

DOI:	10.1210/jc.2018-00052

N. Hornig, C. Beaufort, F. Denzer, M. Cools, M. Wabitsch, M. Ukat, A. Kulle, H. Schweikert, R. Werner, O. Hiort, L. Audi, R. Siebert, O. Ammerpohl, and P. Holterhus,
A Recurrent Germline Mutation in the 5'UTR of the Androgen Receptor Causes Complete Androgen Insensitivity by Activating Aberrant uORF Translation, PLoS One , vol. 11, no. 4, pp. e0154158, 2016.

DOI:	10.1371/journal.pone.0154158

N. Hornig, M. Ukat, H. Schweikert, O. Hiort, R. Werner, S. Drop, M. Cools, I. Hughes, L. Audi, S. Ahmed, J. Demiri, P. Rodens, L. Worch, G. Wehner, A. Kulle, D. Dunstheimer, E. Muller-Rossberg, T. Reinehr, A. Hadidi, A. Eckstein, C. Horst, C. Seif, R. Siebert, O. Ammerpohl, and P. Holterhus,
Identification of an AR Mutation-Negative Class of Androgen Insensitivity by Determining Endogenous AR Activity, J Clin Endocrinol Metab , vol. 101, no. 11, pp. 4468-4477, 2016.

DOI:	10.1210/jc.2016-1990