OGRE: calculate, visualize, and analyze overlap between genomic input regions and public annotations
Berres, Sven, Gromoll, Jörg, Wöste, Marius, Sandmann, Sarah, Laurentino, Sandra
Published in BMC bioinformatics (26.07.2023)
Published in BMC bioinformatics (26.07.2023)
Get full text
Journal Article
wg-blimp: an end-to-end analysis pipeline for whole genome bisulfite sequencing data
Wöste, Marius, Leitão, Elsa, Laurentino, Sandra, Horsthemke, Bernhard, Rahmann, Sven, Schröder, Christopher
Published in BMC bioinformatics (01.05.2020)
Published in BMC bioinformatics (01.05.2020)
Get full text
Journal Article
Reconstructing clonal evolution in relapsed and non-relapsed Burkitt lymphoma
Reutter, Katrin, Sandmann, Sarah, Rohde, Jonas, Müller, Stephanie, Wöste, Marius, Khanam, Tasneem, Michgehl, Ulf, Klapper, Wolfram, Wößmann, Wilhelm, Seggewiß, Jochen, Lenz, Georg, Dugas, Martin, Burkhardt, Birgit
Published in Leukemia (01.02.2021)
Published in Leukemia (01.02.2021)
Get full text
Journal Article
A GWAS in Idiopathic/Unexplained Infertile Men Detects a Genomic Region Determining Follicle-Stimulating Hormone Levels
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
Published in The journal of clinical endocrinology and metabolism (14.07.2022)
Published in The journal of clinical endocrinology and metabolism (14.07.2022)
Get full text
Journal Article
Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia
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.
Published in Human genetics (01.01.2021)
Published in Human genetics (01.01.2021)
Get full text
Journal Article
Publisher Correction: Reconstructing clonal evolution in relapsed and non-relapsed Burkitt lymphoma
Reutter, Katrin, Sandmann, Sarah, Rohde, Jonas, Müller, Stephanie, Wöste, Marius, Khanam, Tasneem, Michgehl, Ulf, Klapper, Wolfram, Wößmann, Wilhelm, Seggewiß, Jochen, Lenz, Georg, Dugas, Martin, Burkhardt, Birgit
Published in Leukemia (01.12.2021)
Published in Leukemia (01.12.2021)
Get full text
Journal Article
Correction to: Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia
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.
Published in Human genetics (2021)
Published in Human genetics (2021)
Get full text
Journal Article
TRIM71 Deficiency Causes Germ Cell Loss During Mouse Embryogenesis and Is Associated With Human Male Infertility
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
Published in Frontiers in cell and developmental biology (13.05.2021)
Published in Frontiers in cell and developmental biology (13.05.2021)
Get full text
Journal Article
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry
Wallmeier, Julia, Frank, Diana, Shoemark, Amelia, Nöthe-Menchen, Tabea, Cindric, Sandra, Olbrich, Heike, Loges, Niki T., Aprea, Isabella, Dougherty, Gerard W., Pennekamp, Petra, Kaiser, Thomas, Mitchison, Hannah M., Hogg, Claire, Carr, Siobhán B., Zariwala, Maimoona A., Ferkol, Thomas, Leigh, Margaret W., Davis, Stephanie D., Atkinson, Jeffrey, Dutcher, Susan K., Knowles, Michael R., Thiele, Holger, Altmüller, Janine, Krenz, Henrike, Wöste, Marius, Brentrup, Angela, Ahrens, Frank, Vogelberg, Christian, Morris-Rosendahl, Deborah J., Omran, Heymut
Published in American journal of human genetics (07.11.2019)
Published in American journal of human genetics (07.11.2019)
Get full text
Journal Article
Genetic Architecture of Azoospermia—Time to Advance the Standard of Care
Wyrwoll, Margot J., Köckerling, Nils, Vockel, Matthias, Dicke, Ann-Kristin, Rotte, Nadja, Pohl, Eva, Emich, Jana, Wöste, Marius, Ruckert, Christian, Wabschke, Rebecca, Seggewiss, Jochen, Ledig, Susanne, Tewes, Ann-Christin, Stratis, Yvonne, Cremers, Jann F., Wistuba, Joachim, Krallmann, Claudia, Kliesch, Sabine, Röpke, Albrecht, Stallmeyer, Birgit, Friedrich, Corinna, Tüttelmann, Frank
Published in European urology (01.05.2023)
Published in European urology (01.05.2023)
Get full text
Journal Article
Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility
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, Pilatz, Adrian, Röpke, Albrecht, Dugas, Martin, Kliesch, Sabine, Neuhaus, Nina, Aston, Kenneth I., Conrad, Donald F., Veltman, Joris A., Friedrich, Corinna, Tüttelmann, Frank
Published in American journal of human genetics (06.08.2020)
Published in American journal of human genetics (06.08.2020)
Get full text
Journal Article
The sperm epigenome does not display recurrent epimutations in patients with severely impaired spermatogenesis
Leitão, Elsa, Di Persio, Sara, Laurentino, Sandra, Wöste, Marius, Dugas, Martin, Kliesch, Sabine, Neuhaus, Nina, Horsthemke, Bernhard
Published in Clinical epigenetics (06.05.2020)
Published in Clinical epigenetics (06.05.2020)
Get full text
Journal Article
Whole-genome methylation analysis of testicular germ cells from cryptozoospermic men points to recurrent and functionally relevant DNA methylation changes
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
Published in Clinical epigenetics (01.12.2021)
Published in Clinical epigenetics (01.12.2021)
Get full text
Journal Article
Calcitonin receptor‐like (CALCRL) is a marker of stemness and an independent predictor of outcome in pediatric AML
Angenendt, Linus, Wöste, Marius, Mikesch, Jan-Henrik, Arteaga, Maria Francisca, Angenendt, Adrian, Sandmann, Sarah, Berdel, Wolfgang E., Lenz, Georg, Dugas, Martin, Meshinchi, Soheil, Schliemann, Christoph, Rössig, Claudia
Published in Blood advances (09.11.2021)
Published in Blood advances (09.11.2021)
Get full text
Journal Article
CopyDetective: Detection threshold–aware copy number variant calling in whole-exome sequencing data
Sandmann, Sarah, Wöste, Marius, de Graaf, Aniek O, Burkhardt, Birgit, Jansen, Joop H, Dugas, Martin
Published in Gigascience (02.11.2020)
Published in Gigascience (02.11.2020)
Get full text
Journal Article
Transcriptome analyses in infertile men reveal germ cell-specific expression and splicing patterns
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
Published in Life science alliance (01.02.2023)
Published in Life science alliance (01.02.2023)
Get full text
Journal Article
TRIM71 deficiency causes germ cell loss during mouse embryogenesis and promotes human male infertility
Torres-Fernández, Lucia A, Emich, Jana, Port, Yasmine, Mitschka, Sibylle, Wöste, Marius, Schneider, Simon, Fietz, Daniela, Oud, Manon S, Sara Di Persio, Neuhaus, Nina, Kliesch, Sabine, Hölzel, Michael, Schorle, Hubert, Friedrich, Corinna, Tüttelmann, Frank, Kolanus, Waldemar
Published in bioRxiv (02.02.2021)
Published in bioRxiv (02.02.2021)
Get full text
Paper
Biallelic mutations in M1AP are a frequent cause of meiotic arrest leading to male infertility
Wyrwoll, Margot J, Temel, Şehime G, Nagirnaja, Liina, Oud, Manon S, Lopes, Alexandra M, Godfried W Van Der Heijden, 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, Pilatz, Adrian, Röpke, Albrecht, Dugas, Martin, Kliesch, Sabine, Neuhaus, Nina, Aston, Kenneth I, Conrad, Donald F, Veltman, Joris A, Friedrich, Corinna, Tüttelmann, Frank
Published in bioRxiv (15.10.2019)
Published in bioRxiv (15.10.2019)
Get full text
Paper