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  3. Schubert, Maria; Pérez Lanuza, Lina; Wöste, Marius; Dugas, Martin; Carmona, F David; Palomino-Morales, Rogelio J; Rassam, Yousif; Heilmann-Heimbach, Stefanie; Tüttelmann, Frank; Kliesch, Sabine; Gromoll, Jörg

    A GWAS in Idiopathic/Unexplained Infertile Men Detects a Genomic Region Determining Follicle-Stimulating Hormone Levels

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    The Endocrine Society, 2022

    Published in: The Journal of Clinical Endocrinology & Metabolism, 107 (2022) 8, Seite 2350-2361

  4. Di Persio, Sara; Leitão, Elsa; Wöste, Marius; Tekath, Tobias; Cremers, Jann-Frederik; Dugas, Martin; Li, Xiaolin; Meyer zu Hörste, Gerd; Kliesch, Sabine; Laurentino, Sandra; Neuhaus, Nina; Horsthemke, Bernhard

    Whole-genome methylation analysis of testicular germ cells from cryptozoospermic men points to recurrent and functionally relevant DNA methylation changes

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    Springer Science and Business Media LLC, 2021

    Published in: Clinical Epigenetics, 13 (2021) 1

  5. Siebert-Kuss, Lara M; Krenz, Henrike; Tekath, Tobias; Wöste, Marius; Di Persio, Sara; Terwort, Nicole; Wyrwoll, Margot J; Cremers, Jann-Frederik; Wistuba, Joachim; Dugas, Martin; Kliesch, Sabine; Schlatt, Stefan; Tüttelmann, Frank; Gromoll, Jörg; Neuhaus, Nina; Laurentino, Sandra

    Transcriptome analyses in infertile men reveal germ cell–specific expression and splicing patterns

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    Life Science Alliance, LLC, 2023

    Published in: Life Science Alliance, 6 (2023) 2, Seite e202201633

  6. Salas-Huetos, Albert; Tüttelmann, Frank; Wyrwoll, Margot J.; Kliesch, Sabine; Lopes, Alexandra M.; Gonçalves, João; Boyden, Steven E.; Wöste, Marius; Hotaling, James M.; Nagirnaja, Liina; Conrad, Donald F.; Carrell, Douglas T.; Aston, Kenneth I.

    Correction to: Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia

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    Springer Science and Business Media LLC, 2021

    Published in: Human Genetics, 140 (2021) 1, Seite 229-229

  7. Salas-Huetos, Albert; Tüttelmann, Frank; Wyrwoll, Margot J.; Kliesch, Sabine; Lopes, Alexandra M.; Goncalves, João; Boyden, Steven E.; Wöste, Marius; Hotaling, James M.; Nagirnaja, Liina; Conrad, Donald F.; Carrell, Douglas T.; Aston, Kenneth I.

    Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia

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    Springer Science and Business Media LLC, 2021

    Published in: Human Genetics, 140 (2021) 1, Seite 217-227

  8. Torres-Fernández, Lucia A.; Emich, Jana; Port, Yasmine; Mitschka, Sibylle; Wöste, Marius; Schneider, Simon; Fietz, Daniela; Oud, Manon S.; Di Persio, Sara; Neuhaus, Nina; Kliesch, Sabine; Hölzel, Michael; Schorle, Hubert; Friedrich, Corinna; Tüttelmann, Frank; Kolanus, Waldemar

    TRIM71 Deficiency Causes Germ Cell Loss During Mouse Embryogenesis and Is Associated With Human Male Infertility

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    Frontiers Media SA, 2021

    Published in: Frontiers in Cell and Developmental Biology, 9 (2021)

  9. Okutman, Ozlem; Muller, Jean; Skory, Valerie; Garnier, Jean Marie; Gaucherot, Angeline; Baert, Yoni; Lamour, Valérie; Serdarogullari, Munevver; Gultomruk, Meral; Röpke, Albrecht; Kliesch, Sabine; Herbepin, Viviana; Aknin, Isabelle; Benkhalifa, Moncef; Teletin, Marius; Bakircioglu, Emre; Goossens, Ellen; Charlet-Berguerand, Nicolas; Bahceci, Mustafa; Tüttelmann, Frank; Viville, STéphane

    A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family

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    Springer Science and Business Media LLC, 2017

    Published in: Journal of Assisted Reproduction and Genetics, 34 (2017) 5, Seite 683-694

  10. Wyrwoll, Margot J.; Temel, Şehime G.; Nagirnaja, Liina; Oud, Manon S.; Lopes, Alexandra M.; van der Heijden, Godfried W.; Heald, James S.; Rotte, Nadja; Wistuba, Joachim; Wöste, Marius; Ledig, Susanne; Krenz, Henrike; Smits, Roos M.; Carvalho, Filipa; Gonçalves, João; Fietz, Daniela; Türkgenç, Burcu; Ergören, Mahmut C.; Çetinkaya, Murat; Başar, Murad; Kahraman, Semra; McEleny, Kevin; Xavier, Miguel J.; Turner, Helen; [...]

    Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility

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    Elsevier BV, 2020

    Published in: The American Journal of Human Genetics, 107 (2020) 2, Seite 342-351

  11. Dougherty, Gerard W; Ostrowski, Lawrence E; Nöthe-Menchen, Tabea; Raidt, Johanna; Schramm, Andre; Olbrich, Heike; Yin, Weining; Sears, Patrick R.; Dang, Hong; Smith, Amanda J.; Beule, Achim G.; Hjeij, Rim; Rutjes, Niels; Haarman, Eric G; Maas, Saskia M.; Ferkol, Thomas W.; Noone, Peadar G; Olivier, Kenneth N.; Bracht, Diana C.; Barbry, Pascal; Zaragosi, Laure-Emmanuelle; Fierville, Morgane; Kliesch, Sabine; Wohlgemuth, Kai; [...]

    Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis

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    American Thoracic Society, 2024

    Published in: American Journal of Respiratory and Critical Care Medicine (2024)