Shaping the future of male reproductive health: fostering talent at the 14th Network of Young Researchers in Andrology meeting

por Marcu, Daniel, Egeberg, Dorte, Richer, Guillaume, Oud, Manon, Houston, Brendan, Berres, Sven, de la Iglesia, Alberto
Publicado 2023

A systematic review and standardized clinical validity assessment of male infertility genes

por Oud, Manon S, Volozonoka, Ludmila, Smits, Roos M, Vissers, Lisenka E L M, Ramos, Liliana, Veltman, Joris A
Publicado 2019

Phasing of de novo mutations using a scaled‐up multiple amplicon long‐read sequencing approach

por Holt, Giles S., Batty, Lois E., Alobaidi, Bilal K. S., Smith, Hannah E., Oud, Manon S., Ramos, Liliana, Xavier, Miguel J., Veltman, Joris A.
Publicado 2022

Programmed Cell Death 2-Like (Pdcd2l) Is Required for Mouse Embryonic Development

por Houston, Brendan J., Oud, Manon S., Aguirre, Daniel M., Merriner, D. Jo, O’Connor, Anne E., Okutman, Ozlem, Viville, Stéphane, Burke, Richard, Veltman, Joris A., O’Bryan, Moira K.
Publicado 2020

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

por 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
Publicado 2021

A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene–disease relationships

por Houston, Brendan J, Riera-Escamilla, Antoni, Wyrwoll, Margot J, Salas-Huetos, Albert, Xavier, Miguel J, Nagirnaja, Liina, Friedrich, Corinna, Conrad, Don F, Aston, Kenneth I, Krausz, Csilla, Tüttelmann, Frank, O’Bryan, Moira K, Veltman, Joris A, Oud, Manon S
Publicado 2021

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

por 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, Gilissen, Christian, Chinnery, Patrick F., Veltman, Joris A., Hoischen, Alexander
Publicado 2018

The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans

por Wyrwoll, Margot J., Gaasbeek, Channah M., Golubickaite, Ieva, Stakaitis, Rytis, Oud, Manon S., Nagirnaja, Liina, Dion, Camille, Sindi, Emad B., Leitch, Harry G., Jayasena, Channa N., Sironen, Anu, Dicke, Ann-Kristin, Rotte, Nadja, Stallmeyer, Birgit, Kliesch, Sabine, Grangeiro, Carlos H.P., Araujo, Thaís F., Lasko, Paul, D’Hauwers, Kathleen, Smits, Roos M., Ramos, Liliana, Xavier, Miguel J., Conrad, Don F., Almstrup, Kristian, Veltman, Joris A., Tüttelmann, Frank, van der Heijden, Godfried W.
Publicado 2022

Diverse monogenic subforms of human spermatogenic failure

por 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, Barros, Alberto, Carvalho, Filipa, Fernandes, Susana, Gonçalves, João, Gurnett, Christina A., Jørgensen, Niels, Jezek, Davor, Jungheim, Emily S., Kliesch, Sabine, McLachlan, Robert I., Omurtag, Kenan R., Pilatz, Adrian, Sandlow, Jay I., Smith, James, Eisenberg, Michael L., Hotaling, James M., Jarvi, Keith A., Punab, Margus, Rajpert-De Meyts, Ewa, Carrell, Douglas T., Krausz, Csilla, Laan, Maris, O’Bryan, Moira K., Schlegel, Peter N., Tüttelmann, Frank, Veltman, Joris A., Almstrup, Kristian, Aston, Kenneth I., Conrad, Donald F.
Publicado 2022