Angela Bahr

687 total citations
16 papers, 254 citations indexed

About

Angela Bahr is a scholar working on Molecular Biology, Ophthalmology and Aquatic Science. According to data from OpenAlex, Angela Bahr has authored 16 papers receiving a total of 254 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Ophthalmology and 4 papers in Aquatic Science. Recurrent topics in Angela Bahr's work include Aquatic life and conservation (4 papers), Retinal Development and Disorders (4 papers) and Ocular Disorders and Treatments (3 papers). Angela Bahr is often cited by papers focused on Aquatic life and conservation (4 papers), Retinal Development and Disorders (4 papers) and Ocular Disorders and Treatments (3 papers). Angela Bahr collaborates with scholars based in Switzerland, Australia and Sweden. Angela Bahr's co-authors include Anthony B. Wilson, Wolfgang Berger, Christina Gerth‐Kahlert, Amit K. Tiwari, Stefan Sommer, Daniel Barthelmes, Martin S. Zinkernagel, John Neidhardt, Samuel Koller and Lieselotte Berger and has published in prestigious journals such as Scientific Reports, Human Molecular Genetics and Journal of Lipid Research.

In The Last Decade

Angela Bahr

15 papers receiving 252 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Angela Bahr Switzerland	9	135	74	65	43	32	16	254
Masatoshi Matsunami Japan	11	129 1.0×	15 0.2×	128 2.0×	18 0.4×	12 0.4×	29	269
Jeremy R. Charette United States	9	188 1.4×	67 0.9×	63 1.0×	183 4.3×	38 1.2×	16	428
Lanying Zhao China	9	126 0.9×	8 0.1×	90 1.4×	36 0.8×	13 0.4×	21	326
Luís Nunes Sweden	8	150 1.1×	62 0.8×	87 1.3×	11 0.3×	17 0.5×	17	283
Patrick Gilligan Singapore	8	295 2.2×	4 0.1×	69 1.1×	35 0.8×	37 1.2×	12	419
Malavika K. Adur United States	10	187 1.4×	13 0.2×	64 1.0×	61 1.4×	12 0.4×	24	439
Louise Pettitt United Kingdom	12	256 1.9×	99 1.3×	236 3.6×	7 0.2×	53 1.7×	21	452
D A McCullough United States	9	859 6.4×	71 1.0×	65 1.0×	16 0.4×	9 0.3×	14	931
Xinping Zhu China	12	229 1.7×	5 0.1×	174 2.7×	93 2.2×	8 0.3×	45	493
Wenzhao Yang China	10	94 0.7×	28 0.4×	7 0.1×	56 1.3×	58 1.8×	16	262

Countries citing papers authored by Angela Bahr

Since Specialization

Citations

This map shows the geographic impact of Angela Bahr'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 Angela Bahr with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Angela Bahr more than expected).

Fields of papers citing papers by Angela Bahr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Angela Bahr. 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 Angela Bahr. The network helps show where Angela Bahr may publish in the future.

Co-authorship network of co-authors of Angela Bahr

This figure shows the co-authorship network connecting the top 25 collaborators of Angela Bahr. A scholar is included among the top collaborators of Angela Bahr 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 Angela Bahr. Angela Bahr is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Hülsmeier, Andreas J., Sandra P. Toelle, Peter Bellstedt, et al.. (2023). The atypical sphingolipid SPB 18:1(14Z);O2 is a biomarker for DEGS1 related hypomyelinating leukodystrophy. Journal of Lipid Research. 64(12). 100464–100464. 6 indexed citations

Ivanovski, Ivan, Angela Bahr, Markus Zweier, et al.. (2023). A very mild phenotype in six individuals of a three‐generation family with the novel HRAS variant c.176C > G p.(Ala59Gly): Emergence of a new HRAS‐related RASopathy distinct from Costello syndrome. American Journal of Medical Genetics Part A. 191(8). 2074–2082.

Horn, Anselm H. C., Katharina Steindl, Alessandra Baumer, et al.. (2022). Assessing clinical utility of preconception expanded carrier screening regarding residual risk for neurodevelopmental disorders. npj Genomic Medicine. 7(1). 4 indexed citations

Lang, Elena, Samuel Koller, James V. M. Hanson, et al.. (2020). Genotype–phenotype spectrum in isolated and syndromic nanophthalmos. Acta Ophthalmologica. 99(4). e594–e607. 19 indexed citations

Lang, Elena, Samuel Koller, Marc Töteberg‐Harms, et al.. (2020). Exome Sequencing in a Swiss Childhood Glaucoma Cohort Reveals CYP1B1 and FOXC1 Variants as Most Frequent Causes. Translational Vision Science & Technology. 9(7). 47–47. 18 indexed citations

Koller, Samuel, James V. M. Hanson, Silke Feil, et al.. (2019). Atonal homolog 7 (ATOH7) loss-of-function mutations in predominant bilateral optic nerve hypoplasia. Human Molecular Genetics. 29(1). 132–148. 8 indexed citations

Gerth‐Kahlert, Christina, Samuel Koller, James V. M. Hanson, et al.. (2019). Genotype–Phenotype Analysis of a Novel Recessive and a Recurrent Dominant SNRNP200 Variant Causing Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 60(8). 2822–2822. 9 indexed citations

Gerth‐Kahlert, Christina, Amit K. Tiwari, Mathias Hauri‐Hohl, et al.. (2017). Unusual retinopathy in a child with severe combined immune deficiency. Ophthalmic Genetics. 39(1). 92–94. 1 indexed citations

Tiwari, Amit K., Angela Bahr, Johannes Fleischhauer, et al.. (2016). Next generation sequencing based identification of disease-associated mutations in Swiss patients with retinal dystrophies. Scientific Reports. 6(1). 28755–28755. 55 indexed citations

10.

Medeiros‐Domingo, Argelia, Ardan M. Saguner, I Magyar, et al.. (2016). 216-01: Arrhythmogenic Right Ventricular Cardiomyopathy: Implications of Next Generation Sequencing in Appropriate Diagnosis. EP Europace. 18(suppl_1). i141–i141. 2 indexed citations

11.

Vincent, Ajoy, Christina Gerth‐Kahlert, Erika Tavares, et al.. (2016). Biallelic Mutations inCRB1Underlie Autosomal Recessive Familial Foveal Retinoschisis. Investigative Ophthalmology & Visual Science. 57(6). 2637–2637. 33 indexed citations

12.

Medeiros‐Domingo, Argelia, Ardan M. Saguner, I Magyar, et al.. (2016). Arrhythmogenic right ventricular cardiomyopathy: implications of next-generation sequencing in appropriate diagnosis. EP Europace. 19(6). euw098–euw098. 23 indexed citations

13.

Wilson, Anthony B., Camilla M. Whittington, & Angela Bahr. (2014). High intralocus variability and interlocus recombination promote immunological diversity in a minimal major histocompatibility system. BMC Evolutionary Biology. 14(1). 273–273. 6 indexed citations

14.

Bahr, Angela & Anthony B. Wilson. (2012). The evolution of MHC diversity: Evidence of intralocus gene conversion and recombination in a single-locus system. Gene. 497(1). 52–57. 31 indexed citations

15.

Bahr, Angela, et al.. (2012). Mutual mate choice in the potbellied seahorse (Hippocampus abdominalis). Behavioral Ecology. 23(4). 869–878. 27 indexed citations

16.

Bahr, Angela & Anthony B. Wilson. (2011). The impact of sex-role reversal on the diversity of the major histocompatibility complex: Insights from the seahorse (Hippocampus abdominalis). BMC Evolutionary Biology. 11(1). 121–121. 12 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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