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Baumann, Britta
32
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1
Pitfalls in the genetic testing of the OPN1LW-OPN1MW gene c..:
Wissinger, Bernd
;
Baumann, Britta
;
Buena-Atienza, Elena
..
npj Genomic Medicine. 9 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1038/..
?
2
Comprehensive variant spectrum of theCNGA3gene in patients ..:
Solaki, Maria
;
Baumann, Britta
;
Reuter, Peggy
...
Human Mutation. 43 (2022) 7 - p. 832-858 , 2022
Link:
https://doi.org/10.1002/..
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3
Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing De..:
Stingl, Katarina
;
Baumann, Britta
;
De Angeli, Pietro
...
International Journal of Molecular Sciences. 23 (2022) 12 - p. 6868 , 2022
Link:
https://doi.org/10.3390/..
?
4
The landscape of submicroscopic structural variants at theO..:
Wissinger, Bernd
;
Baumann, Britta
;
Buena-Atienza, Elena
...
Proceedings of the National Academy of Sciences. 119 (2022) 27 - p. , 2022
Link:
https://doi.org/10.1073/..
?
5
Paternal Uniparental Isodisomy of Chromosome 2 in a Patient..:
Kohl, Susanne
;
Baumann, Britta
;
Dassie, Francesca
...
International Journal of Molecular Sciences. 22 (2021) 15 - p. 7842 , 2021
Link:
https://doi.org/10.3390/..
?
6
Phenotype Variations Caused by Mutations in theRP1L1Gene in..:
Zobor, Ditta
;
Zobor, Gergely
;
Hipp, Stephanie
...
Investigative Opthalmology & Visual Science. 59 (2018) 7 - p. 3041 , 2018
Link:
https://doi.org/10.1167/..
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7
Multimodal imaging including semiquantitative short-wavelen..:
Matet, Alexandre
;
Kohl, Susanne
;
Baumann, Britta
...
Scientific Reports. 8 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1038/..
?
8
De novo intrachromosomal gene conversion from OPN1MW to OPN..:
Buena-Atienza, Elena
;
Rüther, Klaus
;
Baumann, Britta
...
Scientific Reports. 6 (2016) 1 - p. , 2016
Link:
https://doi.org/10.1038/..
?
9
A clinically complex form of dominant optic atrophy (OPA8) ..:
Carelli, Valerio
;
Schimpf, Simone
;
Fuhrmann, Nico
...
Human Molecular Genetics. 20 (2011) 10 - p. 1893-1905 , 2011
Link:
https://doi.org/10.1093/..
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10
A Homologous Genetic Basis of the Murine cpfl1 Mutant and H..:
Chang, Bo
;
Grau, Tanja
;
Dangel, Susann
...
Proceedings of the National Academy of Sciences of the United States of America. 106 (2009) 46 - p. 19581-19586 , 2009
Link:
https://www.jstor.org/st..
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11
A homologous genetic basis of the murinecpfl1mutant and hum..:
Chang, Bo
;
Grau, Tanja
;
Dangel, Susann
...
Proceedings of the National Academy of Sciences. 106 (2009) 46 - p. 19581-19586 , 2009
Link:
https://doi.org/10.1073/..
?
12
Functional analysis of human CNGA3 mutations associated wit..:
Koeppen, Katja
;
Reuter, Peggy
;
Kohl, Susanne
...
European Journal of Neuroscience. 27 (2008) 9 - p. 2391-2401 , 2008
Link:
https://doi.org/10.1111/..
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13
Human Rod Monochromacy: Linkage Analysis and Mapping of a C..:
Wissinger, Bernd
;
Jägle, Herbert
;
Kohl, Susanne
...
Genomics. 51 (1998) 3 - p. 325-331 , 1998
Link:
https://doi.org/10.1006/..
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14
Mutation Analysis of the ND6 Gene in Patients with Lebers H..:
Wissinger, Bernd
;
Besch, Dorothea
;
Baumann, Britta
...
Biochemical and Biophysical Research Communications. 234 (1997) 2 - p. 511-515 , 1997
Link:
https://doi.org/10.1006/..
?
15
Bacteria employ lysine acetylation of transcriptional regul..:
Kremer, Magdalena
;
Schulze, Sabrina
;
Eisenbruch, Nadja
...
Nature Communications. 15 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1038/..
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