Genetic analysis of the M2/ANXA5 haplotype as recurrent pregnancy loss predisposition in the Malay population

Ang K., Kathirgamanathan S., Ch’ng E., Lee Y., Roslani A., Naidu B., Kumar K., Abdullah R., Kadir S., Yusoff N., Abdullah W., Bogdanova N., Wieacker P., Markoff A., Tang T. (2017)
In: Journal of Assisted Reproduction and Genetics, null(null)
Type of Publication: Research article (journal)

New Territory for an Old Disease: 5-Alpha-Reductase Type 2 Deficiency in Bulgaria

Andonova S., Robeva R., Vazharova R., Ledig S., Grozdanova L., Stefanova E., Bradinova I., Todorov T., Hadjidekov G., Sirakov M., Wieacker P., Kumanov P., Savov A. (2017)
In: Sexual Development, 11(1)
Type of Publication: Research article (journal)

Mosaicism for an unbalanced Y;21 translocation in an infertile man: A case report

Röpke A., Stratis Y., Dossow-Scheele D., Wieacker P., Kliesch S., Tüttelmann F. (2013)
In: Journal of Assisted Reproduction and Genetics, 30(12)
Type of Publication: Research article (journal)

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.

Rauch A, Wieczorek D, Graf E, Wieland T, Endele S, Schwarzmayr T, Albrecht B, Bartholdi D, Beygo J, Di Donato N, Dufke A, Cremer K, Hempel M, Horn D, Hoyer J, Joset P, Röpke A, Moog U, Riess A, Thiel CT, Tzschach A, Wiesener A, Wohlleber E, Zweier C, Ekici AB, Zink AM, Rump A, Meisinger C, Grallert H, Sticht H, Schenck A, Engels H, Rappold G, Schröck E, Wieacker P, Riess O, Meitinger T, Reis A, Strom TM (2012)
In: Lancet, 380(9854)
Type of Publication: Research article (journal)

Gastrointestinal stromal tumor presenting as a rectovaginal mass. Clinicopathologic and molecular-genetic characterization of a rare tumor with a literature review

Pelz A-F, Agaimy A, Daniels M, Evert M, Schulz H-U, Lüders P, Müller G, Lasota J, Röpke A, Wieacker P, Miettinen M, Schneider-Stock R (2011)
In: Human Pathology
Type of Publication: Research article (journal)

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Four novel NR5A1 mutations in 46,XY gonadal dysgenesis patients including frameshift mutations with altered subcellular SF-1 localization Rehkämper J., Tewes A., Horvath J., Scherer G., Wieacker P., Ledig S. (2018) In: Sexual Development, 11(null) Type of Publication: Research article (journal)
Genetic analysis of the M2/ANXA5 haplotype as recurrent pregnancy loss predisposition in the Malay population Ang K., Kathirgamanathan S., Ch’ng E., Lee Y., Roslani A., Naidu B., Kumar K., Abdullah R., Kadir S., Yusoff N., Abdullah W., Bogdanova N., Wieacker P., Markoff A., Tang T. (2017) In: Journal of Assisted Reproduction and Genetics, null(null) Type of Publication: Research article (journal)
Elevated annexin A5 plasma levels in term pregnancies of M2/ANXA5 carriers Ang K., Kathirgamanathan S., Ch'ng E., Abdullah W., Yusoff N., Jahnke C., Schmitz R., Bogdanova N., Wieacker P., Tang T., Markoff A. (2017) In: Thrombosis Research, 156(null) Type of Publication: Research article (journal)
New Territory for an Old Disease: 5-Alpha-Reductase Type 2 Deficiency in Bulgaria Andonova S., Robeva R., Vazharova R., Ledig S., Grozdanova L., Stefanova E., Bradinova I., Todorov T., Hadjidekov G., Sirakov M., Wieacker P., Kumanov P., Savov A. (2017) In: Sexual Development, 11(1) Type of Publication: Research article (journal)
Intrafamilial phenotypic variability of Specific Language Impairment Bartha-Doering L., Regele S., Deuster D., Seidl R., Bogdanova N., Röpke A., Wieacker P., am Zehnhoff-Dinnesen A. (2016) In: Brain and Language, 159(null) Type of Publication: Research article (journal)
Mosaicism for an unbalanced Y;21 translocation in an infertile man: A case report Röpke A., Stratis Y., Dossow-Scheele D., Wieacker P., Kliesch S., Tüttelmann F. (2013) In: Journal of Assisted Reproduction and Genetics, 30(12) Type of Publication: Research article (journal)
Comprehensive sequence analysis of the NR5A1 gene encoding steroidogenic factor 1 in a large group of infertile males Röpke A., Tewes A., Gromoll J., Kliesch S., Wieacker P., Tüttelmann F. (2013) In: European Journal of Human Genetics, 21(9) Type of Publication: Research article (journal)
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study. Rauch A, Wieczorek D, Graf E, Wieland T, Endele S, Schwarzmayr T, Albrecht B, Bartholdi D, Beygo J, Di Donato N, Dufke A, Cremer K, Hempel M, Horn D, Hoyer J, Joset P, Röpke A, Moog U, Riess A, Thiel CT, Tzschach A, Wiesener A, Wohlleber E, Zweier C, Ekici AB, Zink AM, Rump A, Meisinger C, Grallert H, Sticht H, Schenck A, Engels H, Rappold G, Schröck E, Wieacker P, Riess O, Meitinger T, Reis A, Strom TM (2012) In: Lancet, 380(9854) Type of Publication: Research article (journal)
Recurrent aberrations identified by array-CGH in patients with Mayer-Rokitansky-Küster-Hauser syndrome. Ledig S, Schippert C, Strick R, Beckmann MW, Oppelt PG, Wieacker P (2011) In: Fertility and Sterility, 95(5) Type of Publication: Research article (journal)
Gastrointestinal stromal tumor presenting as a rectovaginal mass. Clinicopathologic and molecular-genetic characterization of a rare tumor with a literature review Pelz A-F, Agaimy A, Daniels M, Evert M, Schulz H-U, Lüders P, Müller G, Lasota J, Röpke A, Wieacker P, Miettinen M, Schneider-Stock R (2011) In: Human Pathology Type of Publication: Research article (journal)