Kreutz, Michael R.
University Medical Center Hamburg-Eppendorf · Leibniz Institute for Neurobiology
18 papers on CoChatORCID 0000-0003-0575-6950
Most cited papers
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Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Trubetskoy, V., Pardiñas, A. F., Qi, T., Panagiotaropoulou, G., Awasthi, S., Bigdeli, T. B., Bryois, J., Chen, C.-Y., Dennison, C. A., Hall, L. S., et al. (2022) · Nature
Schizophrenia research and treatmentGenetic Associations and Epidemiology
Cited by 2,964
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SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the Synapse
Koopmans, F., van Nierop, P., Andres-Alonso, M., Byrnes, A., Cijsouw, T., Coba, M. P., Cornelisse, L. N., Farrell, R. J., Goldschmidt, H. L., Howrigan, D. P., et al. (2019) · Neuron
Biomedical Text Mining and OntologiesBioinformatics and Genomic Networks
Cited by 938
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Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2
Schmeisser, M. J., Ey, E., Wegener, S., Bockmann, J., Stempel, A. V., Kuebler, A., Janssen, A.-L., Udvardi, P. T., Shiban, E., Spilker, C., et al. (2012) · Nature
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 638
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ProSAP/Shank proteins – a family of higher order organizing molecules of the postsynaptic density with an emerging role in human neurological disease
Boeckers, T. M., Bockmann, J., Kreutz, M. R., & Gundelfinger, E. D. (2002) · Journal of Neurochemistry
Neuroscience and Neuropharmacology ResearchGenetics and Neurodevelopmental Disorders
Cited by 349
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Brevican-Deficient Mice Display Impaired Hippocampal CA1 Long-Term Potentiation but Show No Obvious Deficits in Learning and Memory
Brakebusch, C., Seidenbecher, C. I., Asztely, F., Rauch, U., Matthies, H., Meyer, H., Krug, M., Böckers, T. M., Zhou, X., Kreutz, M. R., et al. (2002) · Molecular and Cellular Biology
Proteoglycans and glycosaminoglycans researchNeuroscience and Neuropharmacology Research
Cited by 264
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Proline-Rich Synapse-Associated Protein-1/Cortactin Binding Protein 1 (ProSAP1/CortBP1) Is a PDZ-Domain Protein Highly Enriched in the Postsynaptic Density
Boeckers, T. M., Kreutz, M. R., Winter, C., Zuschratter, W., Smalla, K.-H., Sanmarti-Vila, L., Wex, H., Langnaese, K., Bockmann, J., Garner, C. C., et al. (1999) · The Journal of Neuroscience
Neuroscience and Neuropharmacology ResearchGenetics and Neurodevelopmental Disorders
Cited by 257
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Concerted action of zinc and ProSAP/Shank in synaptogenesis and synapse maturation
Grabrucker, A. M., Knight, M. J., Proepper, C., Bockmann, J., Joubert, M., Rowan, M., Nienhaus, G. U., Garner, C. C., Bowie, J. U., Kreutz, M. R., et al. (2011) · The EMBO Journal
Neuroscience and Neuropharmacology ResearchGenetics and Neurodevelopmental Disorders
Cited by 228
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Proline-Rich Synapse-Associated Proteins ProSAP1 and ProSAP2 Interact with Synaptic Proteins of the SAPAP/GKAP Family
Boeckers, T. M., Winter, C., Smalla, K.-H., Kreutz, M. R., Bockmann, J., Seidenbecher, C., Garner, C. C., & Gundelfinger, E. D. (1999) · Biochemical and Biophysical Research Communications
Neuroscience and Neuropharmacology ResearchGenetics and Neurodevelopmental Disorders
Cited by 200
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Zinc deficiency dysregulates the synaptic ProSAP/Shank scaffold and might contribute to autism spectrum disorders
Grabrucker, S., Jannetti, L., Eckert, M., Gaub, S., Chhabra, R., Pfaender, S., Mangus, K., Reddy, P. P., Rankovic, V., Schmeisser, M. J., et al. (2014) · Brain
Genetics and Neurodevelopmental DisordersTrace Elements in Health
Cited by 175
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Differential expression and dendritic transcript localization of Shank family members: identification of a dendritic targeting element in the 3′ untranslated region of Shank1 mRNA
Böckers, T. M., Segger-Junius, M., Iglauer, P., Bockmann, J., Gundelfinger, E. D., Kreutz, M. R., Richter, D., Kindler, S., & Kreienkamp, H.-J. (2004) · Molecular and Cellular Neuroscience
Neuroscience and Neuropharmacology ResearchGenetics and Neurodevelopmental Disorders
Cited by 149
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Synaptic Scaffolding Proteins in Rat Brain
Böckers, T. M., Mameza, M. G., Kreutz, M. R., Bockmann, J., Weise, C., Buck, F., Richter, D., Gundelfinger, E. D., & Kreienkamp, H.-J. (2001) · Journal of Biological Chemistry
Neuroscience and Neuropharmacology ResearchGenetics and Neurodevelopmental Disorders
Cited by 137
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Abelson interacting protein 1 (Abi‐1) is essential for dendrite morphogenesis and synapse formation
Proepper, C., Johannsen, S., Liebau, S., Dahl, J., Vaida, B., Bockmann, J., Kreutz, M. R., Gundelfinger, E. D., & Boeckers, T. M. (2007) · The EMBO Journal
Neuroscience and Neuropharmacology ResearchGenetics and Neurodevelopmental Disorders
Cited by 124
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Brevican-containing perineuronal nets of extracellular matrix in dissociated hippocampal primary cultures
John, N., Krügel, H., Frischknecht, R., Smalla, K.-H., Schultz, C., Kreutz, M. R., Gundelfinger, E. D., & Seidenbecher, C. I. (2006) · Molecular and Cellular Neuroscience
Proteoglycans and glycosaminoglycans researchNeuroscience and Neuropharmacology Research
Cited by 122
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C‐terminal synaptic targeting elements for postsynaptic density proteins ProSAP1/Shank2 and ProSAP2/Shank3
Boeckers, T. M., Liedtke, T., Spilker, C., Dresbach, T., Bockmann, J., Kreutz, M. R., & Gundelfinger, E. D. (2005) · Journal of Neurochemistry
Neuroscience and Neuropharmacology ResearchGenetics and Neurodevelopmental Disorders
Cited by 113
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The needs of a synapse—How local organelles serve synaptic proteostasis
Grochowska, K. M., Andres‐Alonso, M., Karpova, A., & Kreutz, M. R. (2022) · The EMBO Journal
Cellular transport and secretionNeuroscience and Neuropharmacology Research
Cited by 38
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Autism-associated SHANK3 missense point mutations impact conformational fluctuations and protein turnover at synapses
Bucher, M., Niebling, S., Han, Y., Molodenskiy, D., Hassani Nia, F., Kreienkamp, H.-J., Svergun, D., Kim, E., Kostyukova, A. S., Kreutz, M. R., et al. (2021) · eLife
Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research
Cited by 33
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MicroRNA-92a–CPEB3 axis protects neurons against inflammatory neurodegeneration
Winkler, I., Engler, J. B., Vieira, V., Bauer, S., Liu, Y.-H., Di Liberto, G., Grochowska, K. M., Wagner, I., Bier, J., Bal, L. C., et al. (2023) · Science Advances
Multiple Sclerosis Research StudiesMicroRNA in disease regulation
Cited by 22
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Transgenic modeling of Ndr2 gene amplification reveals disturbance of hippocampus circuitry and function
Madencioglu, D. A., Çalışkan, G., Yuanxiang, P., Rehberg, K., Demiray, Y. E., Kul, E., Engler, A., Hayani, H., Bergado-Acosta, J. R., Kummer, A., et al. (2021) · iScience
Genetics and Neurodevelopmental DisordersNeurogenesis and neuroplasticity mechanisms
Cited by 8
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