Sandra Cindrić

ORCID

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 5

Top Venues

American journal of respiratory cell and molecular biology

PLoS genetics

Human mutation

Nature communications

Universitätsklinikum Münster (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Universitätsklinikum Münster Mar 01 2016 - Aug 31 2019

Germany

PHD :: Department of General Pediatrics

Westfälische Wilhelms-Universität Münster Oct 01 2013 - Feb 29 2016

Germany

MSC :: Biotechnology

Publications

Luisa Biebach, Sandra Cindrić, Julia Koenig, Isabella Aprea, Gerard W Dougherty, Johanna Raidt, Diana Bracht, Renate Ruppel, Jens Schreiber, Rim Hjeij, Heike Olbrich, Heymut Omran
Recessive Mutations in CFAP74 Cause Primary Ciliary Dyskinesia with Normal Ciliary Ultrastructure. American journal of respiratory cell and molecular biology 67 (3) (2022)
Gerard W Dougherty, Katsutoshi Mizuno, Tabea Nöthe-Menchen, Yayoi Ikawa, Karsten Boldt, Asaf Ta-Shma, Isabella Aprea, Katsura Minegishi, Yuan-Ping Pang, Petra Pennekamp, Niki T Loges, Johanna Raidt, Rim Hjeij, Julia Wallmeier, Huda Mussaffi, Zeev Perles, Orly Elpeleg, Franziska Rabert, Hidetaka Shiratori, Stef J Letteboer, Nicola Horn, Samuel Young, Timo Strünker, Friederike Stumme, Claudius Werner, Heike Olbrich, Katsuyoshi Takaoka, Takahiro Ide, Wang Kyaw Twan, Luisa Biebach, Jörg Große-Onnebrink, Judith A Klinkenbusch, Kavita Praveen, Diana C Bracht, Inga M Höben, Katrin Junger, Jana Gützlaff, Sandra Cindrić, Micha Aviram, Thomas Kaiser, Yasin Memari, Petras P Dzeja, Bernd Dworniczak, Marius Ueffing, Ronald Roepman, Kerstin Bartscherer, Nicholas Katsanis, Erica E Davis, Israel Amirav, Hiroshi Hamada, Heymut Omran
CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module. Nature communications 11 (1) (2020)
Sandra Cindrić, Gerard W Dougherty, Heike Olbrich, Rim Hjeij, Niki Tomas Loges, Israel Amirav, Maria C Philipsen, June K Marthin, Kim G Nielsen, Sivagurunathan Sutharsan, Johanna Raidt, Claudius Werner, Petra Pennekamp, Bernd Dworniczak, Heymut Omran
SPEF2- and HYDIN-Mutant Cilia Lack the Central Pair-associated Protein SPEF2, Aiding Primary Ciliary Dyskinesia Diagnostics. American journal of respiratory cell and molecular biology 62 (3) (2020)
Asaf Ta-Shma, Rim Hjeij, Zeev Perles, Gerard W Dougherty, Ibrahim Abu Zahira, Stef J F Letteboer, Dinu Antony, Alaa Darwish, Dorus A Mans, Sabrina Spittler, Christine Edelbusch, Sandra Cindrić, Tabea Nöthe-Menchen, Heike Olbrich, Friederike Stuhlmann, Isabella Aprea, Petra Pennekamp, Niki T Loges, Oded Breuer, Avraham Shaag, Azaria J J T Rein, Elif Yilmaz Gulec, Alper Gezdirici, Revital Abitbul, Nael Elias, Israel Amirav, Miriam Schmidts, Ronald Roepman, Orly Elpeleg, Heymut Omran
Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility. PLoS genetics 14 (8) (2018)
Christine Edelbusch, Sandra Cindrić, Gerard W Dougherty, Niki T Loges, Heike Olbrich, Joseph Rivlin, Julia Wallmeier, Petra Pennekamp, Israel Amirav, Heymut Omran
Mutation of serine/threonine protein kinase 36 (STK36) causes primary ciliary dyskinesia with a central pair defect. Human mutation 38 (8) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Sandra Cindrić