日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

The Genetics of Female and Male Infertility

女性和男性不育症的遗传学

Tüttelmann, Frank; Wyrwoll, Margot Julia; Steingröver, Johanna; Wieacker, Peter

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

林奇综合征女性患者中,生育力下降的肿瘤和手术发生率很高,但没有证据表明存在卵巢早衰。

Biermann, Sabine; Knapp, Michael; Wieacker, Peter; Aretz, Stefan; Steinke-Lange, Verena

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)

女性生殖器畸形的诊断和治疗(第一部分)。DGGG、OEGGG 和 SGGG 指南(S2k 级别,AWMF 注册号 015/052,2019 年 5 月)

Oppelt, Peter; Binder, Helge; Birraux, Jacques; Brucker, Sara; Dingeldein, Irene; Draths, Ruth; Eckoldt, Felicitas; Füllers, Ulrich; Hiort, Olaf; Hoffmann, Dorit; Hoopmann, Markus; Hucke, Jürgen; Korell, Matthias; Kühnert, Maritta; Ludwikowski, Barbara; Mentzel, Hans-Joachim; Mon OʼDey, Dan; Rall, Katharina; Riccabona, Michael; Rimbach, Stefan; Schäffeler, Norbert; Shavit, Sandra; Stein, Raimund; Utsch, Boris; Wenzl, Rene; Wieacker, Peter; Zeino, Mazen

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)

女性生殖器畸形的诊断和治疗(第二部分)。DGGG、OEGGG 和 SGGG 指南(S2k 级别,AWMF 注册号 015/052,2019 年 5 月)

Oppelt, Peter; Binder, Helge; Birraux, Jacques; Brucker, Sara; Dingeldein, Irene; Draths, Ruth; Eckoldt, Felicitas; Füllers, Ulrich; Hiort, Olaf; Hoffmann, Dorit; Hoopmann, Markus; Hucke, Jürgen; Korell, Matthias; Kühnert, Maritta; Ludwikowski, Barbara; Mentzel, Hans-Joachim; Mon OʼDey, Dan; Rall, Katharina; Riccabona, Michael; Rimbach, Stefan; Schäffeler, Norbert; Shavit, Sandra; Stein, Raimund; Utsch, Boris; Wenzl, Rene; Wieacker, Peter; Zeino, Mazen

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

女性X连锁ZC4H2基因的有害新生变异会导致神经源性多发性先天性关节挛缩症的表型变化。

Frints, Suzanna G M; Hennig, Friederike; Colombo, Roberto; Jacquemont, Sebastien; Terhal, Paulien; Zimmerman, Holly H; Hunt, David; Mendelsohn, Bryce A; Kordaß, Ulrike; Webster, Richard; Sinnema, Margje; Abdul-Rahman, Omar; Suckow, Vanessa; Fernández-Jaén, Alberto; van Roozendaal, Kees; Stevens, Servi J C; Macville, Merryn V E; Al-Nasiry, Salwan; van Gassen, Koen; Utzig, Norbert; Koudijs, Suzanne M; McGregor, Lesley; Maas, Saskia M; Baralle, Diana; Dixit, Abhijit; Wieacker, Peter; Lee, Marcus; Lee, Arthur S; Engle, Elizabeth C; Houge, Gunnar; Gradek, Gyri A; Douglas, Andrew G L; Longman, Cheryl; Joss, Shelagh; Velasco, Danita; Hennekam, Raoul C; Hirata, Hiromi; Kalscheuer, Vera M

The relevance of ANXA5 genetic variants on male fertility

ANXA5基因变异与男性生育能力的相关性

Lavorato, Heloisa Lopes; Markoff, Arseni; Altholz, Valeria; Bogdanova, Nadja; Wieacker, Peter; Kliesch, Sabine; Schlatt, Stefan

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

携带 ANXA5 M2 单倍型的母体患者发生胎盘介导的妊娠并发症的风险更高。

Aranda, Federico; Udry, Sebastián; Perés Wingeyer, Silvia; Amshoff, Lea Christina; Bogdanova, Nadja; Wieacker, Peter; Latino, José Omar; Markoff, Arseni; de Larrañaga, Gabriela

Assessment of M2/ANXA5 haplotype as a risk factor in couples with placenta-mediated pregnancy complications

评估 M2/ANXA5 单倍型作为胎盘介导妊娠并发症夫妇的风险因素

Rogenhofer, Nina; Nienaber, Lara R M; Amshoff, Lea C; Bogdanova, Nadia; Petroff, David; Wieacker, Peter; Thaler, Christian J; Markoff, Arseni

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

在 Mayer-Rokitansky-Küster-Hauser 患者中寻找改变的印记标记

Eggermann, Thomas; Ledig, Susanne; Begemann, Matthias; Elbracht, Miriam; Kurth, Ingo; Wieacker, Peter

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

Mayer-Rokitansky-Küster-Hauser综合征的临床和遗传学特征

Ledig, Susanne; Wieacker, Peter