Universität zu Köln

2023

Salamon, Sarah ORCID: 0009-0005-7435-405X (2023). CaV1.3 gating modulation by S1475 phosphorylation and disease-associated CACNA1D missense mutations. PhD thesis, Universität zu Köln.

2022

Despang, Patrick, Salamon, Sarah ORCID: 0009-0005-7435-405X, Breitenkamp, Alexandra, Kuzmenkina, Elza and Matthes, Jan ORCID: 0000-0003-2754-1555 (2022). Inhibitory effects on L- and N-type calcium channels by a novel Ca-V beta(1) variant identified in a patient with autism spectrum disorder. Naunyn-Schmiedebergs Arch. Pharmacol., 395 (4). S. 459 - 471. NEW YORK: SPRINGER. ISSN 1432-1912

2020

Despang, Patrick, Salamon, Sarah, Breitenkamp, Alexandra F., Kuzmenkina, Elza, Herzig, Stefan and Matthes, Jan ORCID: 0000-0003-2754-1555 (2020). Autism-associated mutations in the Ca-v beta(2) calcium-channel subunit increase Ba2+-currents and lead to differential modulation by the RGK-protein Gem. Neurobiol. Dis., 136. SAN DIEGO: ACADEMIC PRESS INC ELSEVIER SCIENCE. ISSN 1095-953X

Scaplen, Kristin M., Talay, Mustafa, Nunez, Kavin M., Salamon, Sarah, Waterman, Amanda G., Gang, Sydney, Song, Sophia L., Barnea, Gilad and Kaun, Karla R. (2020). Circuits that encode and guide alcohol-associated preference. eLife, 9. CAMBRIDGE: ELIFE SCIENCES PUBLICATIONS LTD. ISSN 2050-084X

2018

Salamon, Sarah, Santelmann, Hanno, Franklin, Jeremy ORCID: 0000-0003-1536-0925 and Baethge, Christopher (2018). Test-retest reliability of the diagnosis of schizoaffective disorder in childhood and adolescence - A systematic review and meta-analysis. J. Affect. Disord., 230. S. 28 - 34. AMSTERDAM: ELSEVIER SCIENCE BV. ISSN 1573-2517

2017

Sukumaran, Salil K., Stumpf, Maria, Salamon, Sarah, Ahmad, Ilyas, Bhattacharya, Kurchi, Fischer, Sarah ORCID: 0000-0001-6227-3950, Mueller, Rolf, Altmueller, Janine, Budde, Birgit, Thiele, Holger, Tariq, Muhammad ORCID: 0000-0002-5334-403X, Malik, Naveed Altaf, Nuernberg, Peter, Baig, Shahid Mahmood, Hussain, Muhammad Sajid ORCID: 0000-0002-1353-8809 and Noegel, Angelika A. (2017). CDK5RAP2 interaction with components of the Hippo signaling pathway may play a role in primary microcephaly. Mol. Genet. Genomics, 292 (2). S. 365 - 384. HEIDELBERG: SPRINGER HEIDELBERG. ISSN 1617-4623