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Publications

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
Type of Publication: Research article (journal)

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)
Type of Publication: Research article (journal)

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)
Type of Publication: Research article (journal)

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: Clin. Infect. Dis., 72(2)
Type of Publication: Research article (journal)

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)
Type of Publication: Research article (journal)

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)
Type of Publication: Research article (journal)

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)
Type of Publication: Research article (journal)

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)
Type of Publication: Research article (journal)

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)
Type of Publication: Research article (journal)

DYX1C1 is required for axonemal dynein assembly and ciliary motility

Tarkar A., Loges N., Slagle C., Francis R., Dougherty G., Tamayo J., Shook B., Cantino M., Schwartz D., Jahnke C., Olbrich H., Werner C., Raidt J., Pennekamp P., Abouhamed M., Hjeij R., Köhler G., Griese M., Li Y., Lemke K., Klena N., Liu X., Gabriel G., Tobita K., Jaspers M., Morgan L., Shapiro A., Letteboer S., Mans D., Carson J., Leigh M., Wolf W., Chen S., Lucas J., Onoufriadis A., Plagnol V., Schmidts M., Boldt K., Roepman R., Zariwala M., Lo C., Mitchison H., Knowles M., Burdine R., Loturco J., Omran H. (2013)
In: Nature Genetics, 45(9)
Type of Publication: Research article (journal)