M. Groesbeek

1.4k total citations
28 papers, 1.2k citations indexed

About

M. Groesbeek is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Spectroscopy. According to data from OpenAlex, M. Groesbeek has authored 28 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Cellular and Molecular Neuroscience, 20 papers in Molecular Biology and 10 papers in Spectroscopy. Recurrent topics in M. Groesbeek's work include Photoreceptor and optogenetics research (23 papers), Retinal Development and Disorders (11 papers) and Neuroscience and Neuropharmacology Research (9 papers). M. Groesbeek is often cited by papers focused on Photoreceptor and optogenetics research (23 papers), Retinal Development and Disorders (11 papers) and Neuroscience and Neuropharmacology Research (9 papers). M. Groesbeek collaborates with scholars based in Netherlands, United States and Japan. M. Groesbeek's co-authors include Steven O. Smith, Johan Lugtenburg, Markus Eilers, Maryam M. Javadpour, Saburo Aimoto, Martine Ziliox, David Song, May Han, Thomas P. Sakmar and Hans Ippel and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and The Journal of Physical Chemistry B.

In The Last Decade

M. Groesbeek

28 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Groesbeek Netherlands 14 838 407 268 135 114 28 1.2k
Jean‐Michel Neumann France 25 1.9k 2.2× 334 0.8× 292 1.1× 152 1.1× 166 1.5× 89 2.2k
Olivier Soubias United States 22 1.3k 1.6× 408 1.0× 188 0.7× 86 0.6× 97 0.9× 39 1.6k
Martin Engelhard Germany 25 1.2k 1.4× 337 0.8× 334 1.2× 282 2.1× 349 3.1× 52 1.8k
Reto Bader United Kingdom 12 495 0.6× 281 0.7× 308 1.1× 293 2.2× 45 0.4× 15 982
Joseph Parello France 21 985 1.2× 293 0.7× 163 0.6× 144 1.1× 202 1.8× 46 1.4k
D.L. Worcester United States 14 1.3k 1.6× 179 0.4× 150 0.6× 145 1.1× 212 1.9× 26 1.6k
R. Kaptein Netherlands 15 804 1.0× 162 0.4× 156 0.6× 177 1.3× 35 0.3× 23 996
Andy LiWang United States 25 1.4k 1.7× 564 1.4× 170 0.6× 164 1.2× 45 0.4× 57 1.9k
Gregory V. Nikiforovich United States 26 1.4k 1.7× 597 1.5× 209 0.8× 140 1.0× 322 2.8× 92 1.9k
Andrei Leonov Germany 27 707 0.8× 310 0.8× 413 1.5× 165 1.2× 172 1.5× 55 1.7k

Countries citing papers authored by M. Groesbeek

Since Specialization
Citations

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

Fields of papers citing papers by M. Groesbeek

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Groesbeek

This figure shows the co-authorship network connecting the top 25 collaborators of M. Groesbeek. A scholar is included among the top collaborators of M. Groesbeek 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 M. Groesbeek. M. Groesbeek 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.
Smith, Steven O., Markus Eilers, David Song, et al.. (2002). Implications of Threonine Hydrogen Bonding in the Glycophorin A Transmembrane Helix Dimer. Biophysical Journal. 82(5). 2476–2486. 94 indexed citations
2.
Makino, Clint L., M. Groesbeek, Johan Lugtenburg, & D. A. Baylor. (1999). Spectral Tuning in Salamander Visual Pigments Studied with Dihydroretinal Chromophores. Biophysical Journal. 77(2). 1024–1035. 34 indexed citations
3.
Javadpour, Maryam M., Markus Eilers, M. Groesbeek, & Steven O. Smith. (1999). Helix Packing in Polytopic Membrane Proteins: Role of Glycine in Transmembrane Helix Association. Biophysical Journal. 77(3). 1609–1618. 241 indexed citations
4.
Imamoto, Yasushi, Hiroo Imai, Hideki Kandori, et al.. (1999). Effect of Anion Binding on Iodopsin Studied by Low-Temperature Fourier Transform Infrared Spectroscopy. Biochemistry. 38(36). 11749–11754. 5 indexed citations
5.
Lin, Steven, M. Groesbeek, Ineke van der Hoef, et al.. (1998). Vibrational Assignment of Torsional Normal Modes of Rhodopsin:  Probing Excited-State Isomerization Dynamics along the Reactive C11C12 Torsion Coordinate. The Journal of Physical Chemistry B. 102(15). 2787–2806. 89 indexed citations
6.
Han, May, M. Groesbeek, Steven O. Smith, & Thomas P. Sakmar. (1998). Role of the C9 Methyl Group in Rhodopsin Activation:  Characterization of Mutant Opsins with the Artificial Chromophore 11-cis-9-Demethylretinal. Biochemistry. 37(2). 538–545. 41 indexed citations
7.
Huang, Li‐Hua, Hua Deng, Yiannis Koutalos, et al.. (1997). A Resonance Raman Study Of the C=C Stretch Modes in Bovine and Octopus Visual Pigments with Isotopically Labeled Retinal Chromophores. Photochemistry and Photobiology. 66(6). 747–754. 9 indexed citations
8.
Groesbeek, M. & Steven O. Smith. (1997). Synthesis of 19-Fluororetinal and 20-Fluororetinal. The Journal of Organic Chemistry. 62(11). 3638–3641. 13 indexed citations
9.
Smith, Steven O., et al.. (1996). Magic angle spinning NMR spectroscopy of membrane proteins. Quarterly Reviews of Biophysics. 29(4). 395–449. 87 indexed citations
10.
Huang, Li‐Hua, Hua Deng, Gezhi Weng, et al.. (1996). A Resonance Raman Study of the CN Configurations of Octopus Rhodopsin, Bathorhodopsin, and Isorhodopsin. Biochemistry. 35(26). 8504–8510. 6 indexed citations
11.
Sasaki, Jun, Akio Maeda, Tôru Yoshizawa, et al.. (1995). Changes in structure of the chromophore in the photochemical process of bovine rhodopsin as revealed by FTIR spectroscopy for hydrogen out-of-plane vibrations. Biophysical Chemistry. 56(1-2). 71–78. 17 indexed citations
12.
Peersen, Olve B., M. Groesbeek, Saburo Aimoto, & Steven O. Smith. (1995). Analysis of Rotational Resonance Magnetization Exchange Curves from Crystalline Peptides. Journal of the American Chemical Society. 117(27). 7228–7237. 42 indexed citations
13.
Groesbeek, M. & Johan Lugtenburg. (1995). Synthesis of nitroxide containing polyenes: Two chemically modified retinals and their interaction with bacterioopsin. Recueil des Travaux Chimiques des Pays-Bas. 114(9-10). 403–409. 6 indexed citations
14.
Groesbeek, M., et al.. (1994). Synthesis of six novel retinals and their interaction with bacterioopsin. Recueil des Travaux Chimiques des Pays-Bas. 113(1). 45–52. 6 indexed citations
15.
Deng, Hua, Li‐Hua Huang, M. Groesbeek, Johan Lugtenburg, & Robert Callender. (1994). Vibrational Analysis of a Retinal Protonated Schiff Base Analog. The Journal of Physical Chemistry. 98(18). 4776–4779. 11 indexed citations
16.
17.
Sasaki, Jun, Akio Maeda, Yoshinori Shichida, et al.. (1992). STRUCTURE OF HYPSORHODOPSIN: ANALYSIS BY FOURIER TRANSFORM INFRARED SPECTROSCOPY AT 10 K. Photochemistry and Photobiology. 56(6). 1063–1071. 4 indexed citations
18.
Grip, Willem J. de, et al.. (1990). 10,20‐Methanorhodopsins: (7E, 9E, 13E)‐10, 20‐methanorhodopsin and (7E, 9Z, 13Z)‐10, 20‐methanorhodopsin. European Journal of Biochemistry. 191(1). 211–220. 41 indexed citations
19.
Groesbeek, M., et al.. (1989). Synthesis of three retinal models, including the 10‐s‐cis‐locked retinal, all‐E‐12,19‐methanoretinal. Recueil des Travaux Chimiques des Pays-Bas. 108(12). 427–436. 3 indexed citations
20.

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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