Sandra Cindrić

Mutation of serine/threonine protein kinase 36 (STK36) causes primary ciliary dyskinesia with a central pair defect

H. Omran, P. Pennekamp, I. Amirav, 2017, Human mutation.

Label-Free Multi Parameter Optical Interrogation of Endothelial Activation in Single Cells using a Lab on a Disc Platform

J. Ducrée, A. Llobera, P. Cahill, 2019, Scientific Reports.

SPEF2- and HYDIN-mutant Cilia Lack the Central Pair Associated Protein SPEF2 Aiding PCD Diagnostics.

H. Omran, B. Dworniczak, P. Pennekamp, 2019, American journal of respiratory cell and molecular biology.

CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module

H. Mussaffi, H. Omran, S. Letteboer, 2020, Nature Communications.

Immunofluorescence Analysis and Diagnosis of Primary Ciliary Dyskinesia with Radial Spoke Defects.

R. Durbin, H. Omran, S. Sauer, 2015, American journal of respiratory cell and molecular biology.

Recessive Mutations in CFAP74 Cause Primary Ciliary Dyskinesia with Normal Ciliary Ultrastructure

H. Omran, J. Schreiber, H. Olbrich, 2022, American journal of respiratory cell and molecular biology.

Immunofluorescence analysis and diagnosis of primary ciliary dyskinesia with radial spoke defects

H. Omran, M. Boon, Y. Memari, 2015 .