Peter Wieacker

Muenster, NW, Germany

Last Updated: 09/26/2026

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Found 42 publications

The Genetics of Female and Male Infertility.

The Genetics of Female and Male Infertility.

Journal: Deutsches Arzteblatt international

Published: June 29, 2024

High amount of fertility reducing tumors and procedures, but no evidence for premature ovarian failure in female Lynch syndrome patients.

High amount of fertility reducing tumors and procedures, but no evidence for premature ovarian failure in female Lynch syndrome patients.

Journal: Familial cancer

Published: December 11, 2023

ANKRD11 variants: KBG syndrome and beyond.

ANKRD11 variants: KBG syndrome and beyond.

Journal: Clinical genetics

Published: March 26, 2021

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).

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).

Journal: Geburtshilfe und Frauenheilkunde

Published: December 02, 2020

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).

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).

Journal: Geburtshilfe und Frauenheilkunde

Published: December 02, 2020

The relevance of ANXA5 genetic variants on male fertility.

The relevance of ANXA5 genetic variants on male fertility.

Journal: Journal of assisted reproduction and genetics

Published: March 11, 2019

Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita.

Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita.

Journal: Human mutation

Published: February 09, 2019

Sequence Variants in TBX6 Are Associated with Disorders of the Müllerian Ducts: An Update.

Sequence Variants in TBX6 Are Associated with Disorders of the Müllerian Ducts: An Update.

Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation

Published: September 03, 2018

Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patients.

Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patients.

Journal: Molecular genetics & genomic medicine

Published: March 13, 2018

Clinical and genetic aspects of Mayer-Rokitansky-Küster-Hauser syndrome.

Clinical and genetic aspects of Mayer-Rokitansky-Küster-Hauser syndrome.

Journal: Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V

Published: March 13, 2018

Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency.

Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency.

Journal: Trends in endocrinology and metabolism: TEM

Published: December 15, 2017

Maternal carriers of the ANXA5 M2 haplotype are exposed to a greater risk for placenta-mediated pregnancy complications.

Maternal carriers of the ANXA5 M2 haplotype are exposed to a greater risk for placenta-mediated pregnancy complications.

Journal: Journal of assisted reproduction and genetics

Published: November 07, 2017

Showing 1-12 of 42

Last Updated: 09/26/2026