- Institut für Humangenetik, Universitätsklinikum Bonn
- human genetics
- male-pattern hair loss
- multifactorial diseases
Henne SK, Aldisi R, Sivalingam S, Hochfeld LM, Borisov O, Krawitz PM, Maj C, Nöthen MM, Heilmann-Heimbach S (2023) Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss. Nat Commun. 14(1):5492.
Hochfeld LM, Bertolini M, Broadley D, Botchkareva NV, Betz RC, Schoch S, Nöthen MM, Heilmann-Heimbach S (2021) Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness. PLoS One. 16(9):e0256846.
Heilmann-Heimbach S, Herold C, Hochfeld LM, Hillmer AM, Nyholt DR, Hecker J, Javed A, Chew EG, Pechlivanis S, Drichel D, Heng XT, Del Rosario RC, Fier HL, Paus R, Rueedi R, Galesloot TE, Moebus S, Anhalt T, Prabhakar S, Li R, Kanoni S, Papanikolaou G, Kutalik Z, Deloukas P, Philpott MP, Waeber G, Spector TD, Vollenweider P, Kiemeney LA, Dedoussis G, Richards JB, Nothnagel M, Martin NG, Becker T, Hinds DA, Nöthen MM. (2017) Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness. Nat Commun. 8:14694.
Heilmann S, Drichel D, Clarimon J, Fernández V, Lacour A, Wagner H, Thelen M, Hernández I, Fortea J, Algret M, Blesa R, Mauleón A, Roca MR, Kornhuber J, Peters P, Heun R, Föhlich L, Hüll M, Heneka MT, Rüther E, Riedel-Heller S, Scherer M, Wiltfang J, Jessen F, Becker T, Tárraga L, Boada M, Maier W, Lleó A, Ruiz A, Nöthen MM, Ramirez A (2015) PLD3 in non-familial Alzheimer’s disease. Nature 520(7545):E3-5.