Publications by authors named "Peter Wieacker"

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The Genetics of Female and Male Infertility.
Frank Tüttelmann, Margot Julia Wyrwoll, Johanna Steingröver, Peter Wieacker

Dtsch Arztebl Int· March 2025

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High amount of fertility reducing tumors and procedures, but no evidence for premature ovarian failure in female Lynch syndrome patients.
Sabine Biermann, Michael Knapp, Peter Wieacker, Stefan Aretz, Verena Steinke-Lange

Fam Cancer· November 2024

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Diagnosis and Therapy of Female Genital Malformations (Part 1). Guideline of the DGGG, OEGGG and SGGG (S2k Level, AWMF Registry Number 015/052, May 2019).
Peter Oppelt, Helge Binder, Jacques Birraux, Sara Brucker, Irene Dingeldein, Peter Wieacker

Geburtshilfe Frauenheilkd· December 2021

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Diagnosis and Therapy of Female Genital Malformations (Part 2). Guideline of the DGGG, OEGGG and SGGG (S2k Level, AWMF Registry Number 015/052, May 2019).
Peter Oppelt, Helge Binder, Jacques Birraux, Sara Brucker, Irene Dingeldein, Peter Wieacker

Geburtshilfe Frauenheilkd· December 2021

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ANKRD11 variants: KBG syndrome and beyond.
Ilaria Parenti, Mark B Mallozzi, Irina Hüning, Cristina Gervasini, Alma Kuechler, Peter Wieacker

Clin Genet· August 2021

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Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita.
Suzanna G M Frints, Friederike Hennig, Roberto Colombo, Sebastien Jacquemont, Paulien Terhal, Peter Wieacker

Hum Mutat· December 2019

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Sequence Variants in TBX6 Are Associated with Disorders of the Müllerian Ducts: An Update.
Ann-Christin Tewes, Jürgen Hucke, Thomas Römer, Karina Kapczuk, Cordula Schippert, Peter Wieacker

Sex Dev· August 2019

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The relevance of ANXA5 genetic variants on male fertility.
Heloisa Lopes Lavorato, Arseni Markoff, Valeria Altholz, Nadja Bogdanova, Peter Wieacker

J Assist Reprod Genet· July 2019

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Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patients.
Thomas Eggermann, Susanne Ledig, Matthias Begemann, Miriam Elbracht, Ingo Kurth, Peter Wieacker

Mol Genet Genomic Med· November 2018

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Four Novel NR5A1 Mutations in 46,XY Gonadal Dysgenesis Patients Including Frameshift Mutations with Altered Subcellular SF-1 Localization.
Jan Rehkämper, Ann-Christin Tewes, Judit Horvath, Gerd Scherer, Peter Wieacker

Sex Dev· October 2018

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Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency.
Ilpo Huhtaniemi, Outi Hovatta, Antonio La Marca, Gabriel Livera, Danielle Monniaux, Peter Wieacker

Trends Endocrinol Metab· June 2018

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Maternal carriers of the ANXA5 M2 haplotype are exposed to a greater risk for placenta-mediated pregnancy complications.
Federico Aranda, Sebastián Udry, Silvia Perés Wingeyer, Lea Christina Amshoff, Nadja Bogdanova, Peter Wieacker

J Assist Reprod Genet· May 2018

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Prevalence of pathogenic BRCA1/2 germline mutations among 802 women with unilateral triple-negative breast cancer without family cancer history.
Christoph Engel, Kerstin Rhiem, Eric Hahnen, Sibylle Loibl, Karsten E Weber, Peter Wieacker

BMC Cancer· March 2018

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Clinical and genetic aspects of Mayer-Rokitansky-Küster-Hauser syndrome.
Susanne Ledig, Peter Wieacker

Med Genet· February 2018

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Assessment of M2/ANXA5 haplotype as a risk factor in couples with placenta-mediated pregnancy complications.
Nina Rogenhofer, Lara R M Nienaber, Lea C Amshoff, Nadia Bogdanova, David Petroff, Peter Wieacker

J Assist Reprod Genet· January 2018

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New Territory for an Old Disease: 5-Alpha-Reductase Type 2 Deficiency in Bulgaria.
Silvia Andonova, Ralitsa Robeva, Radoslava Vazharova, Susanne Ledig, Liliana Grozdanova, Peter Wieacker

Sex Dev· November 2017

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Elevated annexin A5 plasma levels in term pregnancies of M2/ANXA5 carriers.
Kai-Cheen Ang, Sushilnathan Kathirgamanathan, Ewe Seng Ch'ng, Wan Zaidah Abdullah, Narazah Mohd Yusoff, Peter Wieacker

Thromb Res· August 2017

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Genetic analysis of the M2/ANXA5 haplotype as recurrent pregnancy loss predisposition in the Malay population.
Kai-Cheen Ang, Sushilnathan Kathirgamanathan, Ewe Seng Ch'ng, Yan-Yeow Lee, Anna-Liza Roslani, Peter Wieacker

J Assist Reprod Genet· April 2017

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Intrafamilial phenotypic variability of Specific Language Impairment.
Lisa Bartha-Doering, Sabrina Regele, Dirk Deuster, Rainer Seidl, Nadja Bogdanova, Peter Wieacker

Brain Lang· August 2016

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Premature ovarian failure caused by a heterozygous missense mutation in POF1B and a reciprocal translocation 46,X,t(X;3)(q21.1;q21.3).
Susanne Ledig, Sabine Preisler-Adams, Susanne Morlot, Thomas Liehr, Peter Wieacker

Sex Dev· February 2016

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Variations in RBM8A and TBX6 are associated with disorders of the müllerian ducts.
Ann-Christin Tewes, Kristin Katharina Rall, Thomas Römer, Jürgen Hucke, Karina Kapczuk, Peter Wieacker

Fertil Steril· May 2015

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Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex development.
Gwang-Jin Kim, Elisabeth Sock, Astrid Buchberger, Walter Just, Friederike Denzer, Peter Wieacker

J Med Genet· April 2015

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M2/ANXA5 haplotype as a predisposition factor in Malay women and couples experiencing recurrent spontaneous abortion: a pilot study.
Tang Thean Hock, Nadja Bogdanova, Ang Kai Cheen, Sushilnathan Kathirgamanathan, Ridzuan Bin Abdullah, Peter Wieacker

Reprod Biomed Online· April 2015

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DMRT1 mutations are rarely associated with male infertility.
Ann-Christin Tewes, Susanne Ledig, Frank Tüttelmann, Sabine Kliesch, Peter Wieacker

Fertil Steril· September 2014

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Novel associations in disorders of sex development: findings from the I-DSD Registry.
Kathryn Cox, Jillian Bryce, Jipu Jiang, Martina Rodie, Richard Sinnott, Peter Wieacker

J Clin Endocrinol Metab· February 2014

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