Works by Oud, Manon S.

Results: 11
    1

    Innovative all‐in‐one exome sequencing strategy for diagnostic genetic testing in male infertility: Validation and 10‐month experience.

    Published in:
    Andrology, 2025, v. 13, n. 5, p. 1078, doi. 10.1111/andr.13742
    By:
    • Oud, Manon S.;
    • de Leeuw, Nicole;
    • Smeets, Dominique F. C. M.;
    • Ramos, Liliana;
    • van der Heijden, Godfried W.;
    • Timmermans, Raoul G. J.;
    • van de Vorst, Maartje;
    • Hofste, Tom;
    • Kempers, Marlies J. E.;
    • Stokman, Marijn F.;
    • D'Hauwers, Kathleen W. M.;
    • Faas, Brigitte H. W.;
    • Westra, Dineke
    Publication type:
    Article
    2

    WWC2 expression in the testis: Implications for spermatogenesis and male fertility.

    Published in:
    FASEB Journal, 2023, v. 37, n. 5, p. 1, doi. 10.1096/fj.202200960R
    By:
    • Höffken, Verena;
    • Di Persio, Sara;
    • Laurentino, Sandra;
    • Wyrwoll, Margot J.;
    • Terwort, Nicole;
    • Hermann, Anke;
    • Röpke, Albrecht;
    • Oud, Manon S.;
    • Wistuba, Joachim;
    • Kliesch, Sabine;
    • Pavenstädt, Hermann J.;
    • Tüttelmann, Frank;
    • Neuhaus, Nina;
    • Kremerskothen, Joachim
    Publication type:
    Article
    3
    4
    5
    6

    Diverse monogenic subforms of human spermatogenic failure.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-35661-z
    By:
    • Nagirnaja, Liina;
    • Lopes, Alexandra M.;
    • Charng, Wu-Lin;
    • Miller, Brian;
    • Stakaitis, Rytis;
    • Golubickaite, Ieva;
    • Stendahl, Alexandra;
    • Luan, Tianpengcheng;
    • Friedrich, Corinna;
    • Mahyari, Eisa;
    • Fadial, Eloise;
    • Kasak, Laura;
    • Vigh-Conrad, Katinka;
    • Oud, Manon S.;
    • Xavier, Miguel J.;
    • Cheers, Samuel R.;
    • James, Emma R.;
    • Guo, Jingtao;
    • Jenkins, Timothy G.;
    • Riera-Escamilla, Antoni
    Publication type:
    Article
    7

    Linking human Dead end 1 (DND1) variants to male infertility employing zebrafish embryos.

    Published in:
    Human Reproduction, 2023, v. 38, n. 4, p. 655, doi. 10.1093/humrep/dead031
    By:
    • Westerich, Kim Joana;
    • Reinecke, Solveig;
    • Emich, Jana;
    • Wyrwoll, Margot Julia;
    • Stallmeyer, Birgit;
    • Meyer, Matthias;
    • Oud, Manon S;
    • Fietz, Daniela;
    • Pilatz, Adrian;
    • Kliesch, Sabine;
    • Reichman-Fried, Michal;
    • Tarbashevich, Katsiaryna;
    • Limon, Tamara;
    • Stehling, Martin;
    • Friedrich, Corinna;
    • Tüttelmann, Frank;
    • Raz, Erez
    Publication type:
    Article
    8
    9

    Somatic variants in autosomal dominant genes are a rare cause of sporadic Alzheimer's disease.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, n. 12, p. 1632, doi. 10.1016/j.jalz.2018.06.3056
    By:
    • Nicolas, Gaël;
    • Acuña‐Hidalgo, Rocío;
    • Keogh, Michael J.;
    • Quenez, Olivier;
    • Steehouwer, Marloes;
    • Lelieveld, Stefan;
    • Rousseau, Stéphane;
    • Richard, Anne‐Claire;
    • Oud, Manon S.;
    • Marguet, Florent;
    • Laquerrière, Annie;
    • Morris, Chris M.;
    • Attems, Johannes;
    • Smith, Colin;
    • Ansorge, Olaf;
    • Al Sarraj, Safa;
    • Frebourg, Thierry;
    • Campion, Dominique;
    • Hannequin, Didier;
    • Wallon, David
    Publication type:
    Article
    10
    11

    Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia.

    Published in:
    Human Mutation, 2017, v. 38, n. 11, p. 1592, doi. 10.1002/humu.23312
    By:
    • Oud, Manon S.;
    • Ramos, Liliana;
    • O'Bryan, Moira K.;
    • McLachlan, Robert I.;
    • Okutman, Özlem;
    • Viville, Stephane;
    • Vries, Petra F.;
    • Smeets, Dominique F.C.M.;
    • Lugtenberg, Dorien;
    • Hehir‐Kwa, Jayne Y.;
    • Gilissen, Christian;
    • de Vorst, Maartje;
    • Vissers, Lisenka E.L.M.;
    • Hoischen, Alexander;
    • Meijerink, Aukje M.;
    • Fleischer, Kathrin;
    • Veltman, Joris A.;
    • Noordam, Michiel J.
    Publication type:
    Article