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)
Art der Publikation: Forschungsartikel (Zeitschrift)

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)
Art der Publikation: Forschungsartikel (Zeitschrift)

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)
Art der Publikation: Forschungsartikel (Zeitschrift)

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)
Art der Publikation: Forschungsartikel (Zeitschrift)

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
Art der Publikation: Forschungsartikel (Zeitschrift)

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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) Art der Publikation: Forschungsartikel (Zeitschrift)
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) Art der Publikation: Forschungsartikel (Zeitschrift)
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) Art der Publikation: Forschungsartikel (Zeitschrift)
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) Art der Publikation: Forschungsartikel (Zeitschrift)
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) Art der Publikation: Forschungsartikel (Zeitschrift)
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) Art der Publikation: Forschungsartikel (Zeitschrift)
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) Art der Publikation: Forschungsartikel (Zeitschrift)
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) Art der Publikation: Forschungsartikel (Zeitschrift)
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) Art der Publikation: Forschungsartikel (Zeitschrift)
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 Art der Publikation: Forschungsartikel (Zeitschrift)