Fritz Benseler

Staff Status
campusgoe
 

1-6 of 6
 
The bibliographical data in your publication list are complete
You can correct existing data in the blue highlighted fields.To do this, please click on the coloured field. It is not possible to delete data here.
Fields that are not marked in colour (e. g. the authors) can be edited using the input form. To do so, click on the in front of the respective publication.
The bibliographic data in your publication list may be incomplete. You can
  • add any missing data in the fields marked in red or
  • correct existing data in the blue highlighted fields.
To do this, please click on the coloured field. It is not possible to delete data here.
Fields that are not marked in colour (e. g. the authors) can be edited using the input form. To do so, click on the in front of the respective publication.
Check/Uncheck all
  • 2023 Journal Article
    ​ ​Ca2+-binding to the C2E domain of otoferlin is required for hair cell exocytosis and hearing​
    Chen, H.; Monga, M.; Fang, Q.; Slitin, L.; Neef, J. ; Chepurwar, S. S & Mingroni Netto, R. C. et al.​ (2023) 
    Protein & cell, art. pwad058​.​ DOI: https://doi.org/10.1093/procel/pwad058 
    Details  DOI 
  • 2015 Journal Article | Research Paper | 
    ​ ​Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes​
    Stepniak, B. ; Kastner, A.; Poggi, G.; Mitjans, M.; Begemann, M. ; Hartmann, A. M. & Van der Auwera, S. et al.​ (2015) 
    EMBO Molecular Medicine7(12) pp. 1565​-1579​.​ DOI: https://doi.org/10.15252/emmm.201505696 
    Details  DOI  PMID  PMC  WoS 
  • 2011 Journal Article | Research Paper | 
    ​ ​A CAG repeat polymorphism of KCNN3 predicts SK3 channel function and cognitive performance in schizophrenia​
    Grube, S.; Gerchen, M. F.; Adamcio, B. ; Pardo, L. A. ; Martin, S. ; Malzahn, D.   & Papiol, S.  et al.​ (2011) 
    EMBO Molecular Medicine3(6) pp. 309​-319​.​ DOI: https://doi.org/10.1002/emmm.201100135 
    Details  DOI  PMID  PMC  WoS 
  • 2011 Journal Article
    ​ ​A phenotype-based genetic association study reveals the contribution of neuregulin1 gene variants to age of onset and positive symptom severity in schizophrenia​
    Papiol, S. ; Begemann, M. ; Rosenberger, A. ; Friedrichs, H. ; Ribbe, K. ; Grube, S. & Schwab, M. H. et al.​ (2011) 
    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics156B(3) pp. 340​-345​.​ DOI: https://doi.org/10.1002/ajmg.b.31168 
    Details  DOI  PMID  PMC 
  • 2010 Journal Article | 
    ​ ​Modification of cognitive performance in schizophrenia by complexin 2 gene polymorphisms​
    Begemann, M. ; Grube, S.; Papiol, S. ; Malzahn, D. ; Krampe, H. ; Ribbe, K.   & Friedrichs, H.  et al.​ (2010) 
    Archives of General Psychiatry67(9) pp. 879​-888​.​ DOI: https://doi.org/10.1001/archgenpsychiatry.2010.107 
    Details  DOI 
  • 1997 Journal Article | Research Paper
    ​ ​Rat homologues of yeast sec7p​
    Telemenakis, I. ; Benseler, F. ; Stenius, K.; Südhof, T. C. & Brose, N. ​ (1997) 
    European Journal of Cell Biology74(2) pp. 143​-149​.​
    Details  PMID  PMC  WoS 

Publication List

Type

Subtype

Date issued

Author

Project

Peer-Reviewed

Organization

Language

Fulltext

Options

Citation Style

https://publications.goettingen-research-online.de URI: /cris/rp/rp04384
ID: 0000000
PREF: default TOKEN:

0

Sort

Issue Date
Title

Embed

JavaScript
Link

Export

Activate Export Mode
Deactivate Export Mode

Select some or all items (max. 800 for CSV/Excel) from the publications list, then choose an export format below.