Michael B. Hoffmann

3.1k total citations
110 papers, 2.1k citations indexed

About

Michael B. Hoffmann is a scholar working on Cognitive Neuroscience, Molecular Biology and Ophthalmology. According to data from OpenAlex, Michael B. Hoffmann has authored 110 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Cognitive Neuroscience, 45 papers in Molecular Biology and 40 papers in Ophthalmology. Recurrent topics in Michael B. Hoffmann's work include Visual perception and processing mechanisms (60 papers), Retinal Development and Disorders (45 papers) and Glaucoma and retinal disorders (35 papers). Michael B. Hoffmann is often cited by papers focused on Visual perception and processing mechanisms (60 papers), Retinal Development and Disorders (45 papers) and Glaucoma and retinal disorders (35 papers). Michael B. Hoffmann collaborates with scholars based in Germany, United Kingdom and United States. Michael B. Hoffmann's co-authors include Michael Bach, Antony B. Morland, Elisabeth von dem Hagen, Serge O. Dumoulin, Martin Kanowski, Sven P. Heinrich, Anthony T. Moore, D.J. Tolhurst, Jörg Stadler and Oliver Speck and has published in prestigious journals such as Neuron, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Michael B. Hoffmann

101 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael B. Hoffmann Germany 29 1.1k 805 597 357 303 110 2.1k
Antony B. Morland United Kingdom 30 1.6k 1.5× 666 0.8× 500 0.8× 349 1.0× 210 0.7× 89 2.3k
A Kriss United Kingdom 30 696 0.7× 908 1.1× 555 0.9× 210 0.6× 120 0.4× 81 2.4k
Carol A. Westall Canada 29 471 0.4× 934 1.2× 884 1.5× 386 1.1× 88 0.3× 106 2.4k
A Tormene Italy 9 676 0.6× 711 0.9× 620 1.0× 288 0.8× 50 0.2× 18 1.8k
Krystel R. Huxlin United States 29 896 0.8× 543 0.7× 573 1.0× 582 1.6× 95 0.3× 132 2.3k
Frank A. Proudlock United Kingdom 20 352 0.3× 328 0.4× 554 0.9× 201 0.6× 128 0.4× 60 1.2k
John J. Sloper United Kingdom 25 1.0k 1.0× 548 0.7× 373 0.6× 211 0.6× 66 0.2× 69 2.0k
William H. Ridder United States 26 690 0.6× 325 0.4× 442 0.7× 291 0.8× 81 0.3× 63 1.6k
Florian Gekeler Germany 33 763 0.7× 1.2k 1.5× 701 1.2× 515 1.4× 113 0.4× 143 3.9k
Patricia Apkarian Netherlands 20 725 0.7× 447 0.6× 260 0.4× 111 0.3× 239 0.8× 40 1.3k

Countries citing papers authored by Michael B. Hoffmann

Since Specialization
Citations

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

Fields of papers citing papers by Michael B. Hoffmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael B. Hoffmann. 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 Michael B. Hoffmann. The network helps show where Michael B. Hoffmann may publish in the future.

Co-authorship network of co-authors of Michael B. Hoffmann

This figure shows the co-authorship network connecting the top 25 collaborators of Michael B. Hoffmann. A scholar is included among the top collaborators of Michael B. Hoffmann 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 Michael B. Hoffmann. Michael B. Hoffmann 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.
Jarrar, Zakariya, Katie Williams, Sobha Sivaprasad, et al.. (2024). Temporal-to-Nasal Macular Ganglion Cell and Inner Plexiform Layer Ratios in a Large Adult Twin Cohort: Correlations With Age and Heritability. Investigative Ophthalmology & Visual Science. 65(2). 26–26. 2 indexed citations
2.
Behrens, Martin, et al.. (2024). Gaze behavior in open-angle glaucoma patients during visuo-cognitive-motor tasks: a cross-sectional study. Scientific Reports. 14(1). 20978–20978.
3.
Hoffmann, Michael B., et al.. (2024). Assessing Visual Crowding in Participants With Preperimetric Glaucoma Using Eye Movement and Manual Response Paradigms. Translational Vision Science & Technology. 13(9). 8–8. 1 indexed citations
4.
Molz, Barbara, Heidi A. Baseler, Noa Raz, et al.. (2023). Achromatopsia—Visual Cortex Stability and Plasticity in the Absence of Functional Cones. Investigative Ophthalmology & Visual Science. 64(13). 23–23. 3 indexed citations
5.
McLean, Rebecca J., Sebastian Stober, Sarim Ather, et al.. (2023). CHIASM-Net: Artificial Intelligence-Based Direct Identification of Chiasmal Abnormalities in Albinism. Investigative Ophthalmology & Visual Science. 64(13). 14–14. 2 indexed citations
6.
Hoffmann, Michael B., et al.. (2021). Non-invasive electrophysiology in glaucoma, structure and function—a review. Eye. 35(9). 2374–2385. 12 indexed citations
7.
Hamilton, Ruth, Michael Bach, Sven P. Heinrich, et al.. (2020). VEP estimation of visual acuity: a systematic review. Documenta Ophthalmologica. 142(1). 25–74. 64 indexed citations
8.
Kaufmann, Jörn, et al.. (2019). Quantifying nerve decussation abnormalities in the optic chiasm. NeuroImage Clinical. 24. 102055–102055. 20 indexed citations
9.
Bach, Michael, et al.. (2018). Retinal conduction speed analysis reveals different origins of the P50 and N95 components of the (multifocal) pattern electroretinogram. Experimental Eye Research. 169. 48–53. 22 indexed citations
10.
Yakupov, Renat, et al.. (2017). False fMRI activation after motion correction. Human Brain Mapping. 38(9). 4497–4510. 9 indexed citations
11.
Arngrim, Nanna, Anders Hougaard, Mark B. Vestergaard, et al.. (2017). Heterogenous migraine aura symptoms correlate with visual cortex functional magnetic resonance imaging responses. Annals of Neurology. 82(6). 925–939. 41 indexed citations
12.
Hoffmann, Michael B. & Serge O. Dumoulin. (2014). Congenital visual pathway abnormalities: a window onto cortical stability and plasticity. Trends in Neurosciences. 38(1). 55–65. 51 indexed citations
13.
Thieme, Hagen, et al.. (2014). Differential effects of optic media opacities on simultaneous multifocal pattern electroretinograms and visual evoked potentials. Clinical Neurophysiology. 125(12). 2418–2426. 5 indexed citations
14.
Schega, Lutz, et al.. (2013). Differential effects of head-mounted displays on visual performance. Ergonomics. 57(1). 1–11. 20 indexed citations
15.
Bridge, Holly, et al.. (2012). Changes in brain morphology in albinism reflect reduced visual acuity. Cortex. 56. 64–72. 38 indexed citations
16.
Mühler, Roland, et al.. (2010). Motion-onset auditory-evoked potentials critically depend on history. Experimental Brain Research. 203(1). 159–168. 13 indexed citations
17.
Heinrich, Sven P., Maarten J. van der Smagt, Michael Bach, & Michael B. Hoffmann. (2004). Electrophysiological evidence for independent speed channels in human motion processing. Journal of Vision. 4(6). 6–6. 31 indexed citations
18.
Hoffmann, Michael B., et al.. (2001). Directional tuning of human motion adaptation as reflected by the motion VEP. Vision Research. 41(17). 2187–2194. 66 indexed citations
19.
Bach, Michael & Michael B. Hoffmann. (2000). Visual motion detection in man is governed by non-retinal mechanisms. Vision Research. 40(18). 2379–2385. 36 indexed citations
20.
Hoffmann, Michael B., et al.. (1994). Deprivation myopia and its relation to the retinal dopamine/melatonin system in chickens. Acta Neurobiologiae Experimentalis. 54. 1 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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