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Publikationen

2024

pubs

  1. Schneider F., Calapai A., Mundry R., Báez-Mendoza R., Gail A., Kagan I., Treue S. (2024). Confidence over competence: Real-time integration of social information in human continuous perceptual decision-making. eLife 13:RP101021. doi.org/10.7554/eLife.101021.1
  2. Dang S., Antono J.E., Kagan I., Pooresmaeili A. (2024). Modality-specific and modality-general representations of subjective value in frontal cortex. Communications Biology 7:1550. doi.org/10.1038/s42003-024-07253-8
  3. Kaduk K., Wilke M., Kagan I. (2024). Dorsal pulvinar inactivation leads to spatial selection bias without perceptual deficit. Scientific Reports 14:12852. doi.org/10.1038/s41598-024-62056-5.
  4. Crayen M.A., Kagan I., Esghaei M., Hoehl D., Thomas U., Prückl R., Schaffelhofer S., Treue S. (2024) Using camera-guided electrode microdrive navigation for precise 3D targeting of macaque brain sites. PLOS ONE 19:e0301849. doi.org/10.1371/journal.pone.0301849.
  5. Ivanov V., Manenti G.L., Plewe S.S., Kagan I., Schwiedrzik C.M. (2024). Decision-making processes in perceptual learning depend on effectors. Scientific Reports 14:1–15. doi.org/10.1038/s41598-024-55508-5.
  6. Stinson C., Kagan I., Pooresmaeili A. (2024). The contribution of sensory information asymmetry and bias of attribution to egocentric tendencies in effort comparison tasks. Front. Psychol. 15:1304372. doi.org/10.3389/fpsyg.2024.1304372.

2023

  1. Schneider L., Dominguez-Vargas A.-U., Gibson L., Wilke M., Kagan I. (2023). Visual, delay, and oculomotor timing and tuning in macaque dorsal pulvinar during instructed and free choice memory saccades. Cerebral Cortex 33: 10877–10900. doi.org/10.1093/cercor/bhad333.
  2. Wilke M., Kagan I. (2023). Visuospatial and Motor Deficits Following Pulvinar Lesions. In: The Cerebral Cortex and Thalamus (Usrey WM, Sherman SM, eds), Oxford University Press. doi.org/10.1093/med/9780197676158.003.0071.
  3. Benedetto A., Kagan I. (2023). Active vision: How you look reflects what you are looking for. Current Biology 33:R303–R305. doi.org/10.1016/j.cub.2023.03.012.
  4. Moeller S., Unakafov A. M., Fischer J., Gail A., Treue S., Kagan I. (2023). Human and macaque pairs employ different coordination strategies in a transparent decision game. eLife 12:e81641. doi.org/10.7554/eLife.81641

2021

  1. The PRIMatE Data and Resource Exchange (PRIME-DRE) Global Collaboration Workshop and Consortium (2021). Toward next-generation primate neuroscience: A collaboration-based strategic plan for integrative neuroimaging. Neuron. doi.org/10.1016/j.neuron.2021.10.015.
  2. Kagan I., Gibson L., Spanou E., Wilke M. (2021). Effective connectivity and spatial selectivity-dependent fMRI changes elicited by microstimulation of pulvinar and LIP. NeuroImage 240, 118283. doi.org/10.1016/j.neuroimage.2021.118283.
  3. Klink P.C.*, Aubry J.-F., Ferrera V.P., Fox A.S., Froudist-Walsh S., Jarraya B., Konofagou E.E., Krauzlis R.J., Messinger A., Mitchell A.S., Ortiz-Rios M., Oya H., Roberts A.C., Roe A.W., Rushworth M.F.S., Sallet J., Schmid M.C., Schroeder C.E., Tasserie J., Tsao D.Y., Uhrig L., Vanduffel W., Wilke M., Kagan I.*, Petkov C.I.* (2021). Combining brain perturbation and neuroimaging in non-human primates. NeuroImage 235, 118017. doi.org/10.1016/j.neuroimage.2021.118017. * Shared corresponding authors

2020

  1. Milham M., … Kagan I., … (2020). Accelerating the Evolution of Nonhuman Primate Neuroimaging. Neuron 105, 600–603. doi.org/10.1016/j.neuron.2019.12.023.
  2. Heins R.C., Mirza M.B., Parr T., Friston K., Kagan I., Pooresmaeili A. (2020). Deep Active Inference and Scene Construction. Front. Artif. Intell. 3. doi.org/10.3389/frai.2020.509354.
  3. Rollwage M., Pannach F., Stinson C., Toelch U., Kagan I.*, Pooresmaeili A.* (2020). Judgments of effort exerted by self and others are influenced by task contingent rewards. Scientific Reports 10: 1868. doi.org/10.1038/s41598-020-58686-0. * Shared senior authors
  4. Wilson V.A.D., Kade C., Moeller S., Treue S., Kagan I., Fischer J. (2020). Macaque Gaze Responses to the Primatar: A Virtual Macaque Head for Social Cognition Research. Front. Psychol. 11. doi.org/10.3389/fpsyg.2020.01645.
  5. Miloserdov K., Schmidt-Samoa C., Williams K., Weinrich C. A., Kagan I., Bürk K., Trenkwalder C., Bähr M., & Wilke M. (2020). Aberrant functional connectivity of resting state networks related to misperceptions and intra-individual variability in Parkinson‘s disease. NeuroImage: Clinical, 25: 102076. doi.org/10.1016/j.nicl.2019.102076.
  6. Schneider L., Domínguez-Vargas A. U., Gibson L., Kagan I.*, Wilke M.* (2020). Eye position signals in the dorsal pulvinar during fixation and goal-directed saccades. Journal of Neurophysiology, 123: 367-391. doi.org/10.1152/jn.00432.2019. * Shared senior authors
  7. Unakafov A. M., Schultze T., Gail A., Moeller S., Kagan I.*, Eule S.*, Wolf F.* (2020). Emergence and suppression of cooperation by action visibility in transparent games. PLOS Computational Biology, 16(1): e1007588. doi.org/10.1371/journal.pcbi.1007588. * Shared senior authors

2019

  1. Unakafov A. M., Schultze T., Kagan I., Moeller S., Gail A., Treue S., Eule S., Wolf F. (2019). Evolutionary successful strategies in a transparent iterated Prisoner’s Dilemma. EvoApplications 2019, Lecture Notes in Computer Science, 11454: 204–219. https://doi.org/10.1101/524348.
    See link.springer.com/chapter/10.1007/978-3-030-16692-2_14

     

2018

  1. Unakafov A.M., Möller S., Kagan I., Gail A., Treue S., Wolf F. (2018). Using imaging photoplethysmography for heart rate estimation in non-human primates. PLOS ONE 13(8): e0202581. https://doi.org/10.1371/journal.pone.0202581
  2. Hammerschmidt W., Kagan I., Kulke L., Schacht A. (2018). Implicit reward associations impact face processing: Time-resolved evidence from event-related brain potentials and pupil dilations. NeuroImage 179: 557-569. https://doi.org/10.1016/j.neuroimage.2018.06.055
  3. Christopoulos V.N., Kagan I., Andersen R.A. (2018). Lateral intraparietal area (LIP) is largely effector-specific in free-choice decisions. Scientific Reports 8: 8611. https://doi.org/10.1038/s41598-018-26366-9
  4. Moreira C.M., Rollwage M., Kaduk K., Wilke M., Kagan I. (2018). Post-decision wagering after perceptual judgments reveals bi-directional certainty readouts. Cognition 176: 40-52. https://doi.org/10.1016/j.cognition.2018.02.026
  5. Wilke M., Schneider L., Domínguez-Vargas A.U., Schmidt-Samoa C., Miloserdov K., Nazzal A., Dechent P., Cabral-Calderin Y., Scherberger H., Kagan I., Bähr M. (2018). Reach and grasp deficits following damage to the dorsal pulvinar. Cortex 99: 135-149. https://doi.org/10.1016/j.cortex.2017.10.011

2017

  1. Kagan I., Burr D.C. (2017). Active Vision: Dynamic Reformatting of Visual Information by the Saccade-Drift Cycle. Current Biology 27(9): R341-R343. https://doi.org/10.1016/j.cub.2017.03.042
  2. Domínguez-Vargas A.U., Schneider L., Wilke M.*, Kagan I.* (2017). Electrical Microstimulation of the Pulvinar Biases Saccade Choices and Reaction Times in a Time-Dependent Manner. Journal of Neuroscience 37(8):2234-2257. https://doi.org/10.1523/JNEUROSCI.1984-16.2016 

2015

  1. Paschke K., Kagan I., Wüstenberg T., Bähr M., Wilke M. (2015). Trunk rotation affects temporal order judgments with direct saccades: Influence of handedness. Neurophychologia 79: 123-137. doi.org/10.1016/j.neuropsychologia.2015.10.031
  2. Christopoulos V.N., Bonaiuto J., Kagan I., Andersen R.A. (2015). Inactivation of parietal reach region affects reaching but not saccade choices in internally guided decisions. Journal of Neuroscience 35(33): 11719-11728. doi.org/10.1523/JNEUROSCI.1068-15.2015

2014

  1. Przybyszewski A.W., Kagan I., Snodderly D.M. (2014). Primate area V1: largest response gain for receptive fields in the straight-ahead direction. Neuroreport 25(14):1109-1115. doi.org/10.1097/WNR.0000000000000235

2013

  1. Kagan I., Hafed Z.M. (2013). Active vision: microsaccades direct the eye to where it matters most. Current Biology 23(17): R712–R714. https://doi.org/10.1016/j.cub.2013.07.018
  2. Wilke M., Kagan I., Andersen R.A. (2013). Effects of pulvinar inactivation on spatial decision-making between equal and asymmetric reward options. Journal of Cognitive Neuroscience 25(8): 1270-1283. https://doi.org/10.1162/jocn_a_00399 

2012

  1. Kagan I. (2012). Microsaccades and image fading during natural vision. Response to McCamy et al. Microsaccadic efficacy and contribution to foveal and peripheral vision. Journal of Neuroscience www.jneurosci.org/content/32/27/9194/tab-e-letters
  2. Wilke M.*, Kagan I.*, Andersen R.A. (2012). Functional imaging reveals rapid reorganization of cortical activity after parietal inactivation in monkeys. Proc Natl Acad Sci USA 109(21): 8274-8279. doi.org/10.1073/pnas.1204789109 * Equal contribution
  3. Kagan I. (2012) Active vision: fixational eye movements help seeing space in time. Current Biology 22(6): R186 - R188. https://doi.org/10.1016/j.cub.2012.02.009 

1999-2010

  1. Kagan I., Iyer A., Lindner A., Andersen R.A. (2010). Space representation for eye movements is more contralateral in monkeys than in humans. Proc Natl Acad Sci USA 107(17): 7933-7938. https://doi.org/10.1073/pnas.1002825107
  2. Iyer A., Lindner A., Kagan I., Andersen R.A. (2010). Motor preparatory activity in posterior parietal cortex is modulated by subjective absolute value. PLoS Biol 8(8): e1000444. https://doi.org/10.1371/journal.pbio.1000444
  3. Lindner A., Iyer A., Kagan I., Andersen R.A. (2010). Human posterior parietal cortex plans where to reach and what to avoid. Journal of Neuroscience 30(35): 11715-11725. https://doi.org/10.1523/JNEUROSCI.2849-09.2010
  4. Snodderly D.M., Kagan I., Gur M. (2010). Linearity and selectivity of neuronal responses in awake visual cortex. Importance of the cell sample. Journal of Vision 9(9):12. https://doi.org/10.1167/9.9.12
  5. Kagan I., Gur M., Snodderly D.M. (2008). Saccades and drifts differentially modulate neuronal activity in V1: Effects of retinal image motion, position, and extraretinal influences. Journal of Vision 8(14):19: 1-25. https://doi.org/10.1167/8.14.19
  6. Gur M., Kagan I., Snodderly D.M. (2005). Orientation and direction selectivity of neurons in V1 of alert monkeys: Functional relationships and laminar distributions. Cerebral Cortex 15(8): 1207-1221. https://doi.org/10.1093/cercor/bhi003
  7. Kagan I., Shik M.L. (2004). How the mesencephalic “locomotor region” recruits hindbrain neurons. Progress in Brain Research 143: 221-230. https://doi.org/10.1016/S0079-6123(03)43022-7
  8. Kagan I., Gur M., Snodderly D.M. (2002). Spatial organization of receptive fields of V1 neurons of alert monkeys: a comparison with responses to gratings. Journal of Neurophysiology 88: 2557-2574. https://doi.org/10.1152/jn.00858.2001
  9. Snodderly D.M., Kagan I., Gur M. (2001). Selective activation of visual cortex neurons by fixational eye movements: Implications for neural coding. Visual Neuroscience 18(2): 259-277. https://doi.org/10.1017/S0952523801182118
  10. Bar-Gad I., Kagan I., Shik M.L. (1999). Behavior of hindbrain neurons during the transition from rest to evoked locomotion in a newt. Progress in Brain Research 123: 285-294. https://doi.org/10.1016/s0079-6123(08)62864-2