Tewes AC, Rall KK, Römer T, Wieacker P, Ledig S, et al. (2015) Variations in RBM8A and TBX6 are associated with disorders of the müllerian ducts.
Fertil Steril 103: 1313-1318.
Hu H, Haas SA, Chelly J, Van Esch H, Raynaud M, et al. (2016) X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes. Mol Psychiatry 21: 133-148.
Waschk DE, Tewes AC, Römer T, Hucke J, Wieacker P, et al. (2016) Mutations in WNT9B are associated with Mayer-Rokitansky-Küster-Hauser syndrome. Clin Genet 89: 590-596.
Seidl R, Bogdanova N, Röpke A, Wieacker P, Am Zehnhoff-Dinnesen A, et al. (2016) Intrafamilial phenotypic variability of Specific Language Impairment. Brain Lang 159: 102-108.
Abdullah WZ, Bogdanova N, Wieacker P, Markoff A, Tang TH, et al. (2017) Genetic analysis of the M2/ANXA5 haplotype as recurrent pregnancy loss predisposition in the Malay population. J Assist Reprod Genet 34: 517-524.