Pathogenic gene variants in CCDC39, CCDC40, RSPH1, RSPH9, HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility.

Aprea, I; Wilken, A; Krallmann, C; Nöthe-Menchen, T; Olbrich, H; Loges, NT; Dougherty, GW; Bracht, D; Brenker, C; Kliesch, S; Strünker, T; Tüttelmann, F; Raidt, J; Omran, H (2023)

In: Frontiers in Genetics, 14.

Forschungsartikel (Zeitschrift)

Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility.

Aprea, Isabella; Raidt, Johanna; Höben, Inga Marlena; Loges, Niki Tomas; Nöthe-Menchen, Tabea; Pennekamp, Petra; Olbrich, Heike; Kaiser, Thomas; Biebach, Luisa; Tüttelmann, Frank; Horvath, Judit; Schubert, Maria; Krallmann, Claudia; Kliesch, Sabine; Omran, Heymut (2021)

In: PLOS Genetics, 17(2).

Forschungsartikel (Zeitschrift)

First reported nosocomial outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in a pediatric dialysis unit

Schwierzeck V, König JC, Kühn J, Mellmann A, Correa-Martinez CL, Omran H, Konrad M, Kaiser T, Kampmeier S (2020)

In: ((Bitte Journal prüfen)), 72(2).

Forschungsartikel (Zeitschrift)

DNAH11 localization in the proximal region of respiratory cilia defines distinct outer dynein arm complexes

Dougherty G., Loges N., Klinkenbusch J., Olbrich H., Pennekamp P., Menchen T., Raidt J., Wallmeier J., Werner C., Westermann C., Ruckert C., Mirra V., Hjeij R., Memari Y., Durbin R., Kolb-Kokocinski A., Praveen K., Kashef M., Kashef S., Eghtedari F., Häffner K., Valmari P., Baktai G., Aviram M., Bentur L., Amirav I., Davis E., Katsanis N., Brueckner M., Shaposhnykov A., Pigino G., Dworniczak B., Omran H. (2016)

In: American Journal of Respiratory Cell and Molecular Biology, 55(2).

Forschungsartikel (Zeitschrift)

A bumpy road to the diagnosis of a Kytococcus schroeteri shunt infection.

Schaumburg F, Schmalstieg C, Fiedler B, Brentrup A, Omran H, Becker K (2013)

In: Journal of Medical Microbiology, 62(Pt 1).

Forschungsartikel (Zeitschrift)

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Pathogenic gene variants in CCDC39, CCDC40, RSPH1, RSPH9, HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility. Aprea, I; Wilken, A; Krallmann, C; Nöthe-Menchen, T; Olbrich, H; Loges, NT; Dougherty, GW; Bracht, D; Brenker, C; Kliesch, S; Strünker, T; Tüttelmann, F; Raidt, J; Omran, H (2023) In: Frontiers in Genetics, 14. Forschungsartikel (Zeitschrift)
Mucociliary Wnt signaling promotes cilia biogenesis and beating Seidl, Carina; Da Silva, Fabio; Zhang, Kaiqing; Wohlgemuth, Kai; Omran, Heymut; Niehrs, Christof (2023) In: Nature Communications, 14, 1259. Forschungsartikel (Zeitschrift)
Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility. Aprea, Isabella; Raidt, Johanna; Höben, Inga Marlena; Loges, Niki Tomas; Nöthe-Menchen, Tabea; Pennekamp, Petra; Olbrich, Heike; Kaiser, Thomas; Biebach, Luisa; Tüttelmann, Frank; Horvath, Judit; Schubert, Maria; Krallmann, Claudia; Kliesch, Sabine; Omran, Heymut (2021) In: PLOS Genetics, 17(2). Forschungsartikel (Zeitschrift)
Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system. Aprea, Isabella; Nöthe-Menchen, Tabea; Dougherty, Gerard W; Raidt, Johanna; Loges, Niki T; Kaiser, Thomas; Wallmeier, Julia; Ulbrich, Heike; Strünker, Timo; Kliesch, Sabine; Pennekamp, Petra; Omran, Heymut (2021) In: Molecular Human Reproduction, 27(3). Forschungsartikel (Zeitschrift)
First reported nosocomial outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in a pediatric dialysis unit Schwierzeck V, König JC, Kühn J, Mellmann A, Correa-Martinez CL, Omran H, Konrad M, Kaiser T, Kampmeier S (2020) In: ((Bitte Journal prüfen)), 72(2). Forschungsartikel (Zeitschrift)
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry Wallmeier J, Frank D, Shoemark A, Nöthe-Menchen T, Cindric S, Olbrich H, Loges NT, Aprea I, Dougherty GW, Pennekamp P, Kaiser T, Mitchison HM, Hogg C, Carr SB, Zariwala MA, Ferkol T, Leigh MW, Davis SD, Atkinson J, Dutcher SK, Knowles MR, Thiele H, Altmüller J, Krenz H, Wöste M, Brentrup A, Ahrens F, Vogelberg C, Morris-Rosendahl DJ, Omran H (2019) In: American Journal of Human Genetics, 105(5). Forschungsartikel (Zeitschrift)
DNAH11 localization in the proximal region of respiratory cilia defines distinct outer dynein arm complexes Dougherty G., Loges N., Klinkenbusch J., Olbrich H., Pennekamp P., Menchen T., Raidt J., Wallmeier J., Werner C., Westermann C., Ruckert C., Mirra V., Hjeij R., Memari Y., Durbin R., Kolb-Kokocinski A., Praveen K., Kashef M., Kashef S., Eghtedari F., Häffner K., Valmari P., Baktai G., Aviram M., Bentur L., Amirav I., Davis E., Katsanis N., Brueckner M., Shaposhnykov A., Pigino G., Dworniczak B., Omran H. (2016) In: American Journal of Respiratory Cell and Molecular Biology, 55(2). Forschungsartikel (Zeitschrift)
Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia Raidt J., Wallmeier J., Hjeij R., Onnebrink J., Pennekamp P., Loges N., Olbrich H., Häffner K., Dougherty G., Omran H., Werner C. (2014) In: European Respiratory Journal, 44(6). Forschungsartikel (Zeitschrift)
A bumpy road to the diagnosis of a Kytococcus schroeteri shunt infection. Schaumburg F, Schmalstieg C, Fiedler B, Brentrup A, Omran H, Becker K (2013) In: Journal of Medical Microbiology, 62(Pt 1). Forschungsartikel (Zeitschrift)
ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry Hjeij R., Lindstrand A., Francis R., Zariwala M., Liu X., Li Y., Damerla R., Dougherty G., Abouhamed M., Olbrich H., Loges N., Pennekamp P., Davis E., Carvalho C., Pehlivan D., Werner C., Raidt J., Köhler G., Häffner K., Reyes-Mugica M., Lupski J., Leigh M., Rosenfeld M., Morgan L., Knowles M., Lo C., Katsanis N., Omran H. (2013) In: American Journal of Human Genetics, 93(2). Forschungsartikel (Zeitschrift)