Britta Baumann

1.8k total citations
23 papers, 1.0k citations indexed

About

Britta Baumann is a scholar working on Molecular Biology, Ophthalmology and Cell Biology. According to data from OpenAlex, Britta Baumann has authored 23 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 8 papers in Ophthalmology and 5 papers in Cell Biology. Recurrent topics in Britta Baumann's work include Retinal Development and Disorders (16 papers), Retinal Diseases and Treatments (7 papers) and Photoreceptor and optogenetics research (4 papers). Britta Baumann is often cited by papers focused on Retinal Development and Disorders (16 papers), Retinal Diseases and Treatments (7 papers) and Photoreceptor and optogenetics research (4 papers). Britta Baumann collaborates with scholars based in Germany, United States and France. Britta Baumann's co-authors include Bernd Wissinger, Susanne Kohl, Mary Jane Potash, Georges Köhler, Thomas Rosenberg, Samuel G. Jacobson, Eberhart Zrenner, Birgit Lorenz, Maria Vadalà and Ulrich Kellner and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The EMBO Journal and Scientific Reports.

In The Last Decade

Britta Baumann

23 papers receiving 1.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Britta Baumann Germany 16 936 429 156 146 123 23 1.0k
Minghao Jin United States 20 1.0k 1.1× 475 1.1× 189 1.2× 244 1.7× 60 0.5× 37 1.3k
Benjamin J. Frankfort United States 18 894 1.0× 398 0.9× 165 1.1× 307 2.1× 86 0.7× 44 1.3k
Dominique Ducroq France 17 1.2k 1.2× 756 1.8× 161 1.0× 182 1.2× 246 2.0× 20 1.3k
Ralph J. Florijn Netherlands 21 1.0k 1.1× 470 1.1× 213 1.4× 208 1.4× 309 2.5× 46 1.3k
Lina Zelinger Israel 15 653 0.7× 246 0.6× 109 0.7× 135 0.9× 183 1.5× 19 733
Elena Marrocco Italy 18 839 0.9× 184 0.4× 56 0.4× 153 1.0× 261 2.1× 27 969
Alexander V. Kolesnikov United States 21 1.2k 1.3× 448 1.0× 173 1.1× 551 3.8× 41 0.3× 53 1.5k
Susanne Roosing Netherlands 24 1.6k 1.7× 716 1.7× 321 2.1× 221 1.5× 433 3.5× 68 1.9k
Diana van Driel Australia 13 635 0.7× 491 1.1× 67 0.4× 243 1.7× 37 0.3× 15 1.0k
Visvanathan Ramamurthy United States 23 1.4k 1.5× 383 0.9× 240 1.5× 400 2.7× 400 3.3× 55 1.6k

Countries citing papers authored by Britta Baumann

Since Specialization
Citations

This map shows the geographic impact of Britta Baumann's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Britta Baumann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Britta Baumann more than expected).

Fields of papers citing papers by Britta Baumann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Britta Baumann. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Britta Baumann. The network helps show where Britta Baumann may publish in the future.

Co-authorship network of co-authors of Britta Baumann

This figure shows the co-authorship network connecting the top 25 collaborators of Britta Baumann. A scholar is included among the top collaborators of Britta Baumann based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Britta Baumann. Britta Baumann is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Štingl, Katarína, Britta Baumann, Pietro De Angeli, et al.. (2022). Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction. International Journal of Molecular Sciences. 23(12). 6868–6868. 4 indexed citations
2.
Khateb, Samer, Ruth Sheffer, Tamar Ben‐Yosef, et al.. (2022). Relatively mild blue cone monochromacy phenotype caused by various haplotypes in the L- and M-cone opsin genes.. PubMed. 28. 21–28. 1 indexed citations
3.
Kohl, Susanne, Britta Baumann, Francesca Dassie, et al.. (2021). Paternal Uniparental Isodisomy of Chromosome 2 in a Patient with CNGA3-Associated Autosomal Recessive Achromatopsia. International Journal of Molecular Sciences. 22(15). 7842–7842. 3 indexed citations
4.
Matet, Alexandre, Susanne Kohl, Britta Baumann, et al.. (2018). Multimodal imaging including semiquantitative short-wavelength and near-infrared autofluorescence in achromatopsia. Scientific Reports. 8(1). 5665–5665. 8 indexed citations
5.
Zobor, Ditta, Stephanie Hipp, Britta Baumann, et al.. (2018). Phenotype Variations Caused by Mutations in theRP1L1Gene in a Large Mainly German Cohort. Investigative Ophthalmology & Visual Science. 59(7). 3041–3041. 26 indexed citations
6.
Zobor, Ditta, et al.. (2014). Homozygosity mapping reveals new nonsense mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in a Palestinian family.. PubMed. 20. 178–82. 17 indexed citations
7.
Wawrocka, Anna, et al.. (2014). Five novel CNGB3 gene mutations in Polish patients with achromatopsia.. PubMed. 20. 1732–9. 7 indexed citations
8.
Greenberg, Jonathan P., Jerome Sherman, Sandrine Zweifel, et al.. (2014). Spectral-Domain Optical Coherence Tomography Staging and Autofluorescence Imaging in Achromatopsia. JAMA Ophthalmology. 132(4). 437–437. 53 indexed citations
9.
Koeppen, Katja, Thomas Ladewig, Susanne Kohl, et al.. (2010). Dissecting the pathogenic mechanisms of mutations in the pore region of the human cone photoreceptor cyclic nucleotide-gated channel. Human Mutation. 31(7). 830–839. 19 indexed citations
10.
Chang, Bo, R.E. Hurd, Bernhard Jurklies, et al.. (2009). A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene. Proceedings of the National Academy of Sciences. 106(46). 19581–19586. 154 indexed citations
11.
Koeppen, Katja, et al.. (2008). Mutations in CNGA3 impair trafficking or function of cone cyclic nucleotide-gated channels, resulting in achromatopsia. Human Mutation. 29(10). 1228–1236. 51 indexed citations
12.
Koeppen, Katja, et al.. (2008). Functional analysis of human CNGA3 mutations associated with colour blindness suggests impaired surface expression of channel mutants A3R427C and A3R563C. European Journal of Neuroscience. 27(9). 2391–2401. 29 indexed citations
13.
Wissinger, Bernd, Lars Hestbjerg Hansen, Britta Baumann, et al.. (2008). Cone Dystrophy with Supernormal Rod Response Is Strictly Associated with Mutations inKCNV2. Investigative Ophthalmology & Visual Science. 49(2). 751–751. 64 indexed citations
14.
Carelli, Valério, Simone Schimpf, Maria Lucia Valentino, et al.. (2007). Dominant Optic Atrophy (DOA) and Sensorineural Hearing Loss: Clinical, Biochemical, Spectroscopic and Molecular Genetic Study of a Large Italian Pedigree Linked to a New Locus on Chromosome 16. Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna). 68. 4 indexed citations
15.
Rosenberg, Thomas, Britta Baumann, Susanne Kohl, et al.. (2004). Variant Phenotypes of Incomplete Achromatopsia in Two Cousins withGNAT2Gene Mutations. Investigative Ophthalmology & Visual Science. 45(12). 4256–4256. 41 indexed citations
16.
Kohl, Susanne, Britta Baumann, Thomas Rosenberg, et al.. (2002). Mutations in the Cone Photoreceptor G-Protein α-Subunit Gene GNAT2 in Patients with Achromatopsia. The American Journal of Human Genetics. 71(2). 422–425. 197 indexed citations
17.
Wissinger, Bernd, Herbert Jägle, Susanne Kohl, et al.. (1998). Human Rod Monochromacy: Linkage Analysis and Mapping of a Cone Photoreceptor Expressed Candidate Gene on Chromosome 2q11. Genomics. 51(3). 325–331. 53 indexed citations
18.
Wissinger, Bernd, Dorothea Besch, Britta Baumann, et al.. (1997). Mutation Analysis of the ND6 Gene in Patients with Lebers Hereditary Optic Neuropathy. Biochemical and Biophysical Research Communications. 234(2). 511–515. 48 indexed citations
19.
Leo‐Kottler, Beate, et al.. (1996). Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.. PubMed. 5(4). 233–40. 21 indexed citations
20.
Köhler, Georges, Britta Baumann, Antonio Iglesias, et al.. (1984). Different ways to modify monoclonal antibodies. Medical Oncology and Tumor Pharmacotherapy. 1(4). 227–233. 9 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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