Kontakt

Nottulner Landweg 33

48161 Münster

Tel: 02534-65283

mgrueter@comfood.com

Forschungsinteressen

Gesichtserkennung und ihre Störungen (Prosopagnosie), Prosopagnosie bei Kindern, magisches Denken, Verschwörungstheorien.

Ausgewählte Publikationen 2005 - 2011

Dinkelacker V, Grüter M, Klaver P, Grüter T, Specht K, Weis S, Kennerknecht I, Elger CE, Fernandez G. (2011) Congenital Prosopagnosia: Multistage Anatomical and Functional Deficits in Face Processing Circuitry. Journal of Neurology. 258(5) 770-82.

Grüter T, Grüter M, Carbon CC. (2011). Congenital prosopagnosia: diagnosis and mental imagery. Commentary on: Tree JJ and Wilkie J. Face and object imagery in congenital prosopagnosia: A case series. Cortex, 47(4) 511-513.

Carbon CC, Grüter T, Grüter M, Weber JE, Lueschow A. (2010). Dissociation of facial attractiveness and distinctiveness processing in congenital prosopagnosia. Visual Cognition, 18(5) 641-654.

Grüter T, Grüter M, Bell V, Carbon CC. (2009) Visual mental imagery in congenital prosopagnosia. Neuroscience Letters 453: 135-140.

Dinkelacker V, Grüter M, Klaver P, Grüter T, Specht K, Weis S, Kennerknecht I, Elger CE, Fernandez G. (2008) Congenital prosopagnosia: Multistage anatomical and functional deficits in face processing circuitry are overcome by emotional cues. Jahrestagung der Society for Neuroscience. Washington, D.C. (15.11 - 20.11.2008)

Grüter T, Grüter M. (2008) An underestimated handicap: congenital prosopagnosia. Invited speech. EUPO 2008, Genf (5.9. - 7.9.2008)

von Kriegstein K, Dogan Ö, Grüter M, Giraud AL, Kell CA, Grüter T, Kleinschmidt A, Kiebel SJ. (2008) Simulation of talking faces in the human brain improves auditory speech recognition. Proceedings of the National Academy of Science 105(18):6747-6752.

Carbon CC, Grüter M, Grüter T. (2008) Prosopagnosia. Transdisciplinary links between neuropsychology, genetics and cognitive neurosciences. Oral presentation, 36th Annual Meeting of the International Neuropsychological Society (INS), Waikoloa Hawaii, USA (6.2.-9.2.2008).

Grüter T, Grüter M, Carbon C. (2008) Neural and genetic foundations of face recognition and prosopagnosia. Journal of Neuropsychology 2:79-97.

Grüter T, Grüter M. (2007) Prosopagnosia in biographies and autobiographies.
Perception 36 (2) 299-301.

Schwarzer G, Huber S, Grüter M, Grüter T, Groß C, Hipfel M, Kennerknecht I.  (2007) Gaze behavior in hereditary prosopagnosia. Psychol Res. 71(5):583-590.

Grüter M, Grüter T, Bell V, Halligan P W, Horst J, Sperling K, Laskowski W, Ellis H D, Kennerknecht I. (2007) Hereditary Prosopagnosia, a first case series. Cortex 43(6):734-49.

Weber JE, Sander T, Carbon CC, Grüter T, Grüter M, Curio G, Trahms L, Lueschow A. (2006) Characterization of subjects with congenital prosopagnosia by combined electrophysiological and behavioural data. Journal of Vision, 6(6), 657a.

Kennerknecht I, Grüter T, Welling B, Wentzek S, Horst J, Edwards S, Grüter M. (2006). First report on the prevalence of non-syndromic hereditary prosopagnosia. Am. J. Med. Genet. Part A, 140 (15): 1617-1622.

Dinkelacker V, Grüter M, Klaver P, Weis S, Grüter T, Specht  K, Ruhlmann J, Kennerknecht I, Elger C, Fernandez G. (2006) Long term memory for faces in hereditary prosopagnosia: Emotional cues allow for normal performance via medial prefrontal processing. FENS, Forum of European Neuroscience 8-12. July 2006 Wien.

Weber JE, Sander T, Carbon CC, Grüter T, Grüter M, Trahms L, Curio G, Lueschow A. (2006)  Characterization of the impariment in congenital Prosopagnosia by combined elektrophysiolical an behavioural data. Neuroscience Forum 2006, 8-10. Juni.

Lueschow A, Weber JE, Sander T, Carbon CC, Grüter T, Grüter M, Curio G. (2006) A combination of electrophysiological and behavioural data as objective measure of the impairment in congenital prosopagnosia. Klin Neurophysiolog 37.

Grüter M, Welling B, Horst J, Kennerknecht I, Grüter T. (2005) Diagnostic procedure for assessment of hereditary prosopagnosia. Eur. J. Hum, Genet (Suppl. 1) 13: 381.

Kennerknecht I, Grüter T, Welling B., Horst J. Grüter M. (2005) Very high prevalence of hereditary prosopagnosia - a first report. Medgen 17:54.

Weber, J. E., Carbon, C. C., Grüter, M., Sander, T., Grüter, T., Curio, G., Trahms, L., & Lueschow, A. (2005) Characterization of face processing in patients with congenital prosopagnosia by simultaneous MEG/EEG recordings. Poster Presentation, Perception Conference, Tübingen (25.2.-27.2.2005).