Markus Nöthen - Selected Publications#

H-Index (Web of Science 10/2023): 123

Henne SK, Aldisi R, Sivalingam S, Hochfeld LM, Borisov O, Krawitz PM, Maj C, Nöthen MM, Heilmann-Heimbach S. Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss. Nat Commun. 2023, 14:5492. doi: 10.1038/s41467-023-41186-w.

Hsieh TC, Bar-Haim A, Moosa S, Ehmke N, Gripp KW, Pantel JT, (...), Nöthen MM, Krawitz PM. GestaltMatcher facilitates rare disease matching using facial phenotype descriptors. Nat Genet. 2022, 54:349-357. doi: 10.1038/s41588-021-01010-x
Cited: 34 times

Heilmann-Heimbach S, Herold C, Hochfeld LM, Hillmer AM, Nyholt DR, Hecker J, (…), Nöthen MM. Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness, Nat Commun. 2017, 8:14694. doi: 10.1038/ncomms14694
Cited: 45 times

Mühleisen TW, Leber M, Schulze TG, Strohmaier J, Degenhardt F, Treutlein J, (...) Rietschel M*, Nöthen MM*, Cichon S*. Genome-wide association study reveals two new risk loci for bipolar disorder. Nat Commun. 2014, 5:3339. doi: 10.1038/ncomms4339 *corresponding authors
Cited: 237 times

Ludwig KU, Mangold E, Herms S, Nowak S, Reutter H, Paul A, (...), Nöthen MM. Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. Nat Genet. 2012 44:968-971
Cited: 250 times

Cichon S, Mühleisen TW, Degenhardt FA, Mattheisen M, Miró X, Strohmaier J, (...), Rietschel M*, Nöthen MM*. Genome-wide association study identifies genetic variation in neurocan as a susceptibility actor for bipolar disorder. Am J Hum Genet. 2011 88:372-38. doi: 10.1016/j.ajhg.2011.01.017.
Cited: 192 times

Mangold E, Ludwig KU, Birnbaum S, Baluardo C, Ferrian M, Herms S, (...), Nöthen MM. Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. Nat Genet. 2010 42:24-6. doi: 10.1038/ng.506.
Cited: 318 times

Cichon S, Martin L, Hennies HC, Müller F, Van Driessche K, Karpushova A, Stevens W, Colombo R, Renné T, Drouet C, Bork K, Nöthen MM. Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III. Am J Hum Genet. 2006, 79:1098-104. doi: 10.1086/509899.
Cited: 268 times

Hillmer AM, Brockschmidt FF, Hanneken S, Eigelshoven S, Steffens M, Flaquer A, (...), Nöthen MM. Susceptibility variants for male-pattern baldness on chromosome 20p11. Nat Genet. 2008 40:1279-81. doi: 10.1038/ng.228.
Cited: 92 times

Hillmer AM, Hanneken S, Ritzmann S, Becker T, Freudenberg J, Brockschmidt FF, (...) , Nöthen MM. Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia. Am J Hum Genet. 2005, 77:140-8. doi: 10.1086/431425.
Cited: 143 times