Theiß, SusanneUniversität HeidelbergHeidelberg
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Co-Autoren (Uni Heidelberg)
- Blattmann, Peter Nils (1)
- Paramasivam, Nagarajan (1)
- Steinbeisser, Herbert (1958-2014) (1)
- Ebrahimi-Fakhari, Darius (1)
- Wahlster, Lara (1)
- Stampfer, Miriam (1)
- Ibberson, David (1)
- Kumar, Rahul (1)
- Seitz, Angelika (1)
- Werenbeck-Ueding, Jennifer (1)
- Weber, Dominik (1)
- Ciprianidis, Anja (1)
- Thormälen, Aenne Solvejg (1)
- Pepperkok, Rainer (1)
- Sievers, Aaron (1)
- Hinderhofer, Katrin (1)
- Joggerst-Thomalla, Brigitte (1)
- Granzow, Martin (1)
- Marbach, Felix (1)
- Fischer, Christine (1)
- Laugsch, Magdalena (1)
- Schuberth, Christian (1)
- Evers, Christina (1)
- Bartram, Claus R. (1)
- Tängemo, Carolina (1)
Co-Autoren (extern)
- Pavlinic, Dinko (1)
- Benes, Vladimir (1)
- Haase, Bettina (1)
- Blake, Jonathon (1)
- Runz, Heiko (1)
- Riddell, Andrew (1)
- Gonzalez, Alexis Perez (1)
- Telegrafi, Aida (1)
- Person, Richard (1)
- Ceulemans, Sophia (1)
- Rosenfeld, Jill A. (1)
- Willaert, Rebecca (1)
- Torti, Erin (1)
- Stratakis, Constantine A. (1)
- Keller, Sigrid (1)
- Jiang, Xuntian (1)
- Amraoui, Yasmina (1)
- Yang, Mingxiao V. (1)
- Veeraragavan, Surabi (1)
- Strong, Theresa V. (1)
- Spanjaard, Melanie (1)
- Samaco, Rodney C. (1)
- Malovannaya, Anna (1)
- Jain, Antrix (1)
- Albelda de la Haza, Pedro (1)
- Reznik, Derek (1)
Publikationen in heiBIB 
- Reznik, Derek: Magel2 truncation alters select behavioral and physiological outcomes in a rat model of Schaaf-Yang syndrome / Derek L. Reznik, Mingxiao V. Yang, Pedro Albelda de la Haza, Antrix Jain, Melanie Spanjaard, Susanne… , February 2023. - 18 S. : Illustrationen
In: Disease models & mechanisms, ISSN 1754-8411. 16(2023), 2 vom: Feb., Artikel-ID dmm049829, Seite 1-18
DOI: 10.1242/dmm.049829
- Marbach, Felix: Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain / Felix Marbach, Georgi Stoyanov, Florian Erger, Constantine A. Stratakis, Nikolaos Settas, Edra Londo… , 08 April 2021. - 9 S.
In: Genetics in medicine, ISSN 1530-0366. 23(2021), 8, Seite 1465-1473
DOI: 10.1038/s41436-021-01152-7
- Ott, Tim: The frog Xenopus as a model to study Joubert syndrome : the case of a human patient with compound heterozygous variants in PIBF1 / Tim Ott, Lilian Kaufmann, Martin Granzow, Katrin Hinderhofer, Claus R. Bartram, Susanne Theiß, Angel… , 25 February 2019. - 13 S.
In: Frontiers in physiology, ISSN 1664-042X. 10(2019) Artikel-Nummer 134, 13 Seiten
DOI: 10.3389/fphys.2019.00134
- Kumar, Rahul: Nemo-like kinase 1 (Nlk1) and paraxial protocadherin (PAPC) cooperatively control Xenopus gastrulation through regulation of Wnt/planar cell polarity (PCP) signaling / Rahul Kumar, Anja Ciprianidis, Susanne Theiß, Herbert Steinbeißer, Lilian T. Kaufmann, 2017. - 12 S.
In: Differentiation, ISSN 1432-0436. 93(2017), Seite 27-38
DOI: 10.1016/j.diff.2016.10.002
- Ebrahimi-Fakhari, Darius: Reduction of TMEM97 increases NPC1 protein levels and restores cholesterol trafficking in Niemann-pick type C1 disease cells / Darius Ebrahimi-Fakhari, Lara Wahlster, Fabian Bartz, Jennifer Werenbeck-Ueding, Maria Praggastis, J… , 4 July 2016. - 12 S.
In: Human molecular genetics, ISSN 1460-2083. 25(2016), 16, Seite 3588-3599
DOI: 10.1093/hmg/ddw204
- Thormälen, Aenne Solvejg: Systematic cell-based phenotyping of missense alleles empowers rare variant association studies : a case for LDLR and myocardial infarction / Aenne S. Thormaehlen, Christian Schuberth, Hong-Hee Won, Peter Blattmann, Brigitte Joggerst-Thomalla… , February 3, 2015. - 23 S.
In: PLoS Genetics, ISSN 1553-7404. 11(2015,2) Artikel-Nummer e1004855, 23 Seiten
DOI: 10.1371/journal.pgen.1004855
- Blake, Jonathon: Sequencing of a patient with balanced chromosome abnormalities and neurodevelopmental disease identifies disruption of multiple high risk loci by structural variation / Jonathon Blake, Andrew Riddell, Susanne Theiss, Alexis Perez Gonzalez, Bettina Haase, Anna Jauch, Jo… , March 13, 2014
In: PLOS ONE, ISSN 1932-6203. 9(2014,3) Artikel-Nummer e90894, 11 Seiten
DOI: 10.1371/journal.pone.0090894
- Stampfer, Miriam: Niemann-Pick disease type C clinical database : cognitive and coordination deficits are early disease indicators / Miriam Stampfer, Susanne Theiss, Yasmina Amraoui, Xuntian Jiang, Sigrid Keller, Daniel S. Ory, Eugen… , 2013. - 11 S.
In: Orphanet journal of rare diseases, ISSN 1750-1172. 8(2013), Artikel-ID 35, Seite 1-11
DOI: 10.1186/1750-1172-8-35
- Tängemo, Carolina: Niemann-Pick Type C disease : characterizing lipid levels in patients with variant lysosomal cholesterol storage / Carolina Tängemo, Dominik Weber, Susanne Theiss, Eugen Mengel, and Heiko Runz, 17 January 2011. - 13 S.
In: Journal of lipid research, ISSN 1539-7262. 52(2011), 4 vom: Apr., Seite 813-825
DOI: 10.1194/jlr.P013524
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