Publications

2018 and 'in press'

  • Beste C, Münchau A (in press). Tics and Tourette Syndrome - surplus of actions rather than disorder? Mov Disord
  • Buse J, Beste C, Roessner V (in press). Neural correlates of prediction violations in boys with Tourette Syndrome - evidence from harmonic expectancy. World J Biol Psychiatry
  • Wolff N, Chmielewski WX, Beste C, Roessner V (in press). Working memory load affects repetitive behavior but not cognitive flexibility in adolescent autism spectrum disorder. World J Biol Psychiatry
  • Beste C, Arning L, Gerding WM, Epplen JT, Mertins A, Röder MC, Bless J, Hugdahl K, Westerhausen R, Güntürkün O, Ocklenburg S (in press). Cognitive control processes and functional cerebral asymmetries: association with Variation in the handedness-associated gene LRRTM1. Mol Neurobiol
  • Friedrich J, Mückschel M, Beste C (in press). Specific properties of the SI and SII somatosensory areas and their effects on motor control - a system neurophysiological study. Brain Struct Funct
  • Wolff N, Mückschel M, Ziemssen, T, Beste C (in press). The role of phasic norepinephrine modulations during task switching: evidence for specific effects in parietal areas. Brain Struct Funct
  • Bodmer B, Mückschel M, Roessner V, Beste (in press). Neurophysiological variability masks differences in functional neuroanatomical networks and their effectiveness to modulate response inhibition between children and adults. Brain Struct Funct

2017

  • Zhang R, Schrempf W, Brandt M, Mückschel M, Beste C, Stock, A-K (2017). RLS patients show better nocturnal performance in the Simon Task due to diminshed visuo-motor priming. Clin Neurophysiol, 129, 112-121.
  • Wolff N, Zink N, Stock A-K, Beste (2017). On the relevance of the alpha frequency oscillation's small-world network architecture for cognitive flexibility. Sci Rep, 7, 13910.
  • Petruo V, Zeißig S, Schmelz S, Hampe J, Beste (2017). Specific neurophysiological mechanisms underlie cognitive deficits in inflammatory bowel disease. Sci Rep, 7, 13943.
  • Friedrich P, Ocklenburg S, Heins N, Schlüter C, Fraenz C, Beste C, Güntürkün O, Genc E (2017). Callosal microstructure affects the timing of electrophysiological left-right differences. NeuroImage, 163, 310-318.
  • Zhang R, Stock AK, Rzepus A, Beste C (2017). Self-regulatory capacities are depleted in a domain-specific manner. Front Syst Neurosci, 28, 70.
  • Stock AK, Wolff N, Beste C (2017). Opposite effects of binge drinking on consciously vs. subliminally induced cognitive conflicts. NeuroImage, 162, 117-126.
  • Stock AK, Dajkic D, Köhling HL, Heintschel von Heinegg H, Fiedler M, Beste C (2017). Humans with latent toxoplasmosis display altered reward modulation of cognitive control. Sci Rep, 7, 10170.
  • Mückschel M, Dippel G, Beste C (2017). Distinguishing stimulus and response codes in theta oscillations in prefrontal areas during inhibitory control of automated responses. Hum Brain Mapp, 38, 5681-5690.
  • Letzner S, Güntürkün O, Beste C (2017). How birds outperform humans in multi-component behvior. Curr Biol, 27, R996-R998.
  • Brandt VC, Stock A-K, Münchau A, Beste C (2017). Evidence for enhanced multi-component behavior in Tourette syndrome - an EEG study. Sci Rep, 7, 7722
  • Gohil K, Bluschke A, Roessner V, Stock AK, Beste C (2017). Sensory processes modulate differences in multi-component behavior and cognitive control between childhood and adulthood. Hum Brain Mapp, 38, 4933-4945.
  • Dippel G, Mückschel M, Ziemssen T, Beste C (2017). Demands on response inhibition processes determine modulations of theta band activity in superior frontal areas and correlations with pupillometry - implications for the norepinephrine system. NeuroImage, 157, 575-585.
  • Zhang R, Brandt MD, Schrempf W, Beste C, Stock A (2017). Neurophysiological mechanisms of circadian cognitive control in RLS patients - an EEG source localization study. Neuroimage Clin, 15, 644-652.
  • Stock A-K (2017). Barking up the wrong tree: Why and how we may need to revise alcohol addiction therapy. Front Psychol, 8, 884.
  • Bluschke A, Chmielewski W, Mückschel M, Roessner V, Beste C (2017). Neuronal intra-individual variability masks response selection differences between ADHD subtypes - a need to change perspectives. Front Hum Neurosci, 11, 329.
  • Friedrich J, Mückschel M, Beste C (2017). Somatosensory lateral Inhibition processes modulate motor response inhibition - an EEG source localization study. Sci Rep,7, 4454.
  • Stock A-K, Gohil K, Huster R, Beste C (2017). On the effects of multimodal information integration in multitasking. Sci Rep, 7, 4927.
  • Beste C, Mückschel M, Rosales R, Domnigo A, Lee L, Ng A, Klein C, Münchau M (in press). The basal ganglia striosomes affect the modulation of conflicts by subliminal Information - evidence from X-linked dystonia parkinsonism. Cereb Cortex
  • Wolff N, Mückschel M, Beste C (2017). Neural mechanisms and functional neuroanatomical networks during memory and cue-based task switching as revealed by residue iteration decomposition (RIDE) based source localization. Brain Struct Funct, 222, 3819-3831.
  • Beste C, Mückschel M, Rosales R, Domingo A, Lee L, Ng A, Klein C, Münchau A (2017). Dysfunctions in striatal microstructure can enhance perceptual decision making through deficits in predictive coding. Brain Struct Funct, 222, 3807-3817.
  • Stock AK, Beste C (2017). On the necessity of translational cognitive-neurotoxicological research in methamphetamine abuse and addiction. Arch Toxicol, 91, 2707-2709.
  • Colzato L, Sellaro R, Beste C (2017). Darvin revisited: The vagus nerve is a causal element in controlling recognition of other's emotions. Cortex, 92, 95-102.
  • Fujakova-Lipski M, Kaping D, Sirova J, Horacek J, Palincek T, Zach P, Klaschka J, Kacer P, Syslova K, Vrajova M, Bubenikova-Vlesova V, Beste C, Slamberova R (2017). Trans-generational neurochemical Modulation of methamphetamine in the adult brain of the Wistar rat. Arch Toxicol, 91, 3373-3384.
  • Wolff N, Buse J, Handrick J, Roessner V, Beste C (2017). Modulations of cognitive flexibility in obsessive compulsive disorder reflect dysfunctions of perceptual categorization. J Child Psychol Psychiatry, 58, 939-949.
  • Jongkees BJ, Sellaro R, Beste C, Nitsche MA, Kühn S, Colzato L (2017). L-tyrosine administration modulates the effect of transcranial direct current stimulation on working memory in healthy humans. Cortex, 90, 103-114.
  • Bluschke A, von der Hagen M, Roessner V, Beste C (2017). Conflict processing in juvenile patients with neurofibromatosis type 1 (NF1) and healthy controls - two pathways to success. Neuroimage Clin, 14, 499-505.
  • Bluschke A, von der Hagen M, Papenhagen K, Roessner V, Beste C (2017). Response Inhibition in attention deficit hyperactivity disorder and neurofibromatosis type 1 - clinically similar, neurophysiologically different. Sci Rep, 7, 46929.
  • Stock AK, Gohil K, Beste C (2017). Blocking effects in non-conditioned goal-directed behavior. Brain Struct Funct, 222, 2807-2818.
  • Mückschel M, Chmielewski WX, Ziemssen, T, Beste C (2017). The norepinephrine system shows information-content specific properties during cognitive control - evidence from EEG and pupillary responses. NeuroImage, 149, 44-52.
  • Gohil K, Bluschke A, Roessner V, Stock A-K, Beste C (2017). ADHD patients fail to maintain task goals in face of subliminally and consciously induced cognitive conflicts. Psychol Med, 47, 1771-1783.
  • van Thriel C, Quetscher C, Pesch B, Lotz A, Lehnert M, Casjens C, Weiss T, Van Gelder R, Plitzke K, Brüning T, Beste C (2017). Are Multitasking abilities impaired in welders exposed to manganese? Translating cognitive neuroscience to neurotoxicology. Arch Toxicol, 91, 2865-1877.
  • Bodmer B, Beste C (2017). On the dependence of response inhibition processes on sensory modality. Hum Brain Mapp, 38, 1941-1951.
  • Beste C, Mückschel M, Rosales R, Domingo A, Lee LV, Ng A, Klein C, Münchau A (2017). Striosomal dysfunction affects behavioral adaptation but not impulsivity - evidence from XDP. Mov Disord, 32, 576-584.
  • Ocklenburg S, Gerding WM, Arning L, Genc E, Epplen JT, Güntürkün O, Beste C (2017). Myelin genes and the corpus callosum: Proteolipid protein 1 (PLP1) and contactin 1 (CNTN1) gene variation modulates interhemispheric Integration. Mol Neurobiol, 54, 7908-7916.
  • Chmielewski WX, Beste C (2017). Testing interactive effects of automatic and conflict control processes during response inhibition - a system neurophysiological study. NeuroImage, 146, 1149-1156.
  • Wolff N, Gussek P, Stock A-K, Beste C (2017). Effects of high-dose alcohol intoxication and hangover on cognitive flexibility. Addict Biol, 22, 1355-1365.
  • Mückschel M, Gohil K, Ziemssen T, Beste C (2017). The norepinephrine system and its relevance for multi-component behavior. NeuroImage, 146, 1062-1070.
  • Stock A-K, Mückschel M, Beste C (2017). Reversal of alcohol-induced effects on response control due to changes in proprioceptive information processing. Addict Biol, 22, 246-256.
  • Stock AK, Hoffmann S, Beste C (2017). Effects of binge drinking and hangover on response selection subprocesses - a study using EEG and drift diffusion modeling. Addict Biol, 22, 1355-1365.
  • Chmielewski WX, Mückschel M, Ziemssen T, Beste C (2017). The norepinephrine system affects neurophysiological subprocesses in the modulation of inhibitory control by working memory processes. Hum Brain Mapp, 38, 68-81.

2016

  • Stock A-K, Friedrich J, Beste C (2016). Subliminally and consciously induced cognitive conflicts interact at several processing levels. Cortex, 85, 75-89.
  • Mückschel M, Beste C , Ziemssen T (2016). Immunmodulatory treatments and cognition in MS. Acta Neurol Scand, 134, Suppl 200, 55-59.
  • Beste C, Tübing J, Seeliger H, Bäumer T, Brandt V, Stock A-K, Münchau A (2016). Altered perceptual binding in Gilles de la Tourette Syndrome. Cortex, 83, 160-166.
  • Beste C, Steenbergen L, Sellaro R, Grigoriadou S, Zhang R, Chmielewski W, Stock A-K, Colzato, L (2016). Effects of concomitant Stimulation of the GABAergic and norepinephrine system on inhibitory control - a study using transcutaneous vagus nerve stimulation. Brain Stimul, 9, 811-818.
  • Stock A-K, Steenbergen L, Colzato L, Beste C (2016). The system neurophysiological basis of non-adaptive cognitive control: inhibition of implicit learning mediated by right prefrontal regions. Hum Brain Mapp, 37, 4511-4522.
  • Bluschke A, Broschwitz F, Kohl S, Roessner V, Beste C (2016). The neural mechanisms underlying improvement of impulsivity in ADHD by theta/beta neurofeedback. Sci Rep, 6, 31178.
  • Colzato LS, Steenbergen L, Sellaro R, Stock A-K, Arning L, Beste C (2016). Effects of L-tyrosine on working memory and inhibitory control are determined by DRD2 genotypes: a randomized controlled trial. Cortex, 82, 217-224.
  • Wolff N, Roessner V, Beste C (2016). Behavioural and neurophysiological evidence for increased cognitive flexibility in late childhood. Sci Rep, 6, 28954.
  • Gohil K, Hahne A, Beste C (2016). Improvements of sensorimotor processes during action cascading associated with changes in sensory processing architecture - insights from sensory deprivation. Sci Rep, 6, 28259.
  • Zhang R, Stock A-K, Beste C (2016). The neurophysiological basis of reward effects on backward inhibition processes. NeuroImage, 142, 163-171.
  • Petruo VA, Stock A-K, Münchau A, Beste C (2016). A system neurophysiology approach to voluntary event coding. NeuroImage, 135, 324-332.
  • Chmielewski WX, Beste C (2016). Perceptual conflict during sensorimotor integration processes - a neurophysiological study in response inhibition. Sci Rep, 6, 26289.
  • Beste C, Stock A-K, Epplen JT, Arning L (2016). Dissociable electrophysiological subprocesses during response Inhibition are differentially modulated by dopamine D1 and D2 receptors. Eur Neuropsychopharmacol, 26, 1029-1036.
  • Gohil K, Dippel G, Beste C (2016). Questioning the role of the frontopolar cortex in multi-component behavior - a TMS/EEG study. Sci Rep, 6, 22317.
  • Brandt VC, Beck C, Sajin V, Baaske MK, Bäumer T, Beste C, Anders S, Münchau A (2016). Temporal relationship between premonitory urges and tics in Gilles des la Tourette syndrome. Cortex, 77, 24-37.
  • Zhang R, Stock A-K, Fischer R, Beste C (2016). The system neurophysiological basis of backward Inhibition. Brain Struct Funct, 221, 4575-4587.
  • Stock A-K, Popescu F, Neuhaus AH, Beste C (2016). Single-subject prediction of response inhibition behavior by event-related potentials. J Neurophysiol, 115, 1252-1262.
  • Bluschke A, Roessner V, Beste C (2016). Editorial perspective: How to optimize frequency band neurofeedback in ADHD. J Child Psychol Psychiatry, 57, 457-461.
  • Bluschke A, Roessner V, Beste C (2016). Specific cognitive-neurophysiological processes predict impulsivity in the childhood ADHD combined subtype. Psychol Med, 46, 1277-1287.
  • Buse J, Beste C, Herrmann E, Roessner V (2016). Neural correlates of altered sensorimotor gating in boys with Tourette Syndrome: a combined EMG/fMRI study. World J Biol Psychiatry, 17, 187-197.
  • Dippel G, Chmielewski WX, Mückschel M, Beste C (2016). Response mode dependent differences in neurofunctional networks during response inhibition - an EEG-beamforming study. Brain Struct Funct, 221, 4091-4101.
  • Ocklenburg S, Arning L, Gerding WM, Hengstler JG, Epplen JT, Güntürkün O, Beste C, Akkad DA (2016). Left-right axis differentiation and functional lateralization: A haplotype in the methytransferase encoding gene SETDB2 might mediate handedness in healthy adults. Mol Neurobiol, 53, 6355-6361.
  • Chmielewski W, Mückschel M, Dippel G, Beste C (2016). Concurrent Information affects Response Inhibition processes via the modulation of theta oscillations in cognitive control networks. Brain Struct Funct, 221, 3949-3961.
  • Stock A-K, Riegler L, Chmielewski W, Beste C (2016). Paradox effects of binge-drinking on response Inhibition processes depending on mental workload. Arch Toxicol, 90, 1429-1436.
  • Stock A-K, Gohil K, Beste C (2016). Age-related differences in task goal processing strategies during action cascading. Brain Struct Funct, 221, 2767-2775.
  • Beste C, Ocklenburg S, von der Hagen M, Di Donato N (2016). Mammalian cadherins DCHS1-FAT4 affect functional cerebral architecture. Brain Struct Funct, 221, 2487-2491.
  • Mückschel M, Smitka M, Herman A, von der Hagen M, Beste C (2016). Deep brain stimulation in the globus pallidus compensates response inhibition deficits - evidence from pantothenate kinase-associated neurodegeneration. Brain Struct Funct, 221, 2251-2257.
  • Stock A-K, Schulz T, Lenhardt M, Blaszkewicz M, Beste C (2016). High-dose alcohol intoxication differentially modulates cognitive subprocesses involved in response inhibition. Addict Biol, 21, 136-145.
  • Stock A-K, Reuner U, Gohil K, Beste C (2016). Effects of copper toxicity on response inhibition processes: a study in Wilson's Disease. Arch Toxicol, 90, 1623-1630.
  • Mückschel M, Stock A-K, Dippel G, Chmielewski WX, Beste C (2016). Interacting sources of interference during sensorimotor integration processes. NeuroImage, 125, 342-349.

2015

  • Steenbergen L, Sellaro R, Stock A-K, Beste C, Colzato L (2015). Action video gaming and cognitive control: playing first person shooter games is associated with improved action cascading but not inhibition. Plos One, 10, 144364.
  • Stock A-K, Beste C (2015). Conscientiousness efficiency in multicomponent behavior. Sci Rep, 5, 15731.
  • Stock A-K, Ness V, Beste C (2015). Complex sensorimotor transformation processes required for response selection are facilitated by the striatum. NeuroImage, 123, 33-41.
  • Haag L, Quetscher C, Dharmadhikari S, Dydak U, Schmidt-Wilcke T, Beste C (2015). On the interrelation of resting state functional connectivity, striatal GABA levels and cognitive control processes. Hum Brain Mapp, 36, 4383-4393.
  • Steenbergen L, Sellaro R, Stock A-K, Beste C, Colzato L (2015). Gamma-aminobutyric acid (GABA) administration improves action selection processes. A randomized controlled trial. Sci Rep, 5, 12770.
  • Dharmadhikari S, Ma R, Yeh C-L, Stock A-K, Snyder S, Zauber SE, Dydak U, Beste C (2015). Striatal and thalamic GABA level concentrations play differential roles for the modulation of response selection processes by proprioceptive information. NeuroImage, 120, 36-42.
  • Finoia P, Mitchell DJ, Hauk O, Beste C, Pizzella V, Duncan J (2015). Concurrent brain responses to separate auditory and visual targets. J Neurophysiol, 114, 1239-1247.
  • Selpien H, Siebert C, Genc E, Beste C, Faustmann PM, Güntürkün O, Ocklenburg S (2015). Left dominance for language perception starts in the extrastriate cortex - and ERP and sLORETA study. Behav Brain Res, 291, 325-333.
  • Chmielewski WX, Roessner, V, Beste C (2015). Predictability and context determine differences in conflict Monitoring between adolescence and adulthood. Behav Brain Res, 292, 10-18.
  • Möckel T, Beste C, Wascher E (2015). The effects of time on task in response selection - an ERP study on mental fatigue. Sci Rep, 5, 10113.
  • Mückschel M, Stock A-K, Beste C (2015). Different strategies, but indifferent strategy adaptation during action cascading. Sci Rep, 5, 9992.
  • Steenbergen L, Sellaro R, Stock A-K, Verkuil B, Beste C, Colzato LS (2015). Transcutaneous vagus nerve Stimulation (tVNS) enhances response selection during action cascading processes. Eur Neuropsychopharmacol, 25, 773-778.
  • Gohil K, Stock AK, Beste C (2015). The importance of sensory Integration processes for action cascading. Sci Rep, 5, 9485.
  • Chmielewski W, Mückschel M, Stock AK, Beste C (2015). The impact of mental workload of response inhibition subprocesses. NeuroImage, 112, 96-104.
  • Dippel G, Beste C (2015). A causal role of the right inferior frontal cortex in the strategies of multi-component behaviour. Nat Commun, 6,6587.
  • Hoffmann S, Beste C (2015). A perspective on neural and cognitive mechanisms of error commission. Front Behav Neurosci, 9, 50.
  • Schroll H, Beste C, Hamker F (2015). Combined lesions of direct and indirect basal ganglia pathways but not changes in dopamine levels explain learning deficits in patients with Huntington's disease. Eur J Neurosci, 41, 1227-1244.
  • Beste C, Kneiphof J, Woitalla D (2015). Effects of fatigue on cognitive control in neurosarcoidosis. Eur Neuropsychopharmacol, 25, 522-530.
  • Quetscher C, Yildiz A, Dharmadhikari S, Glaubiz B, Schmidt-Wilcke T, Dydak U, Beste C (2015). Striatal GABA-MRS predicts response inhibition performance and its cortical electrophysiological correlates. Brain Struct Funct, 220, 3555-3564.
  • Yildiz A, Beste C (2015). Parallel and serial processing in dual-tasking differentially involves mechanisms in the striatum and the lateral prefrontal cortex. Brain Struct Funct, 220, 3131-3142.
  • Beste C, Mückschel M, Elben S, Hartmann C, McIntyre C, Saft C, Vesper J, Schnitzler A, Wojtecki L (2015). Behavioral and neurophysiological evidence for the enhancement of cognitive control under dorsal pallidal deep brain stimulation in Huntington's disease. Brain Struct Funct, 220, 2441-2448.
  • Beste C, Stock A-K, Ness V, Hoffmann R, Saft C. (2015). Evidence for divergent effects of neurodegeneration in Huntington's disease on attentional selection and neural plasticity - implications for excitotoxicity.Brain Strcut Funct, 220, 1437-1447.
  • Arning L, Ocklenburg S, Schulz S, Ness V, Gerding WM, Hengstler JG, Falkenstein M, Epplen JT, Güntürkün O, Beste C (2015). Handedness and the X chromosome: the role of androgen receptor CAG-repeat length. Sci Rep, 5, 8325
  • Farkas A, Bluschke A, Roessner V, Beste C (2015). Neurofeedback and its possible relevance for the treatment of Tourette Syndrome. Neurosci Biobehav Rev, 51, 87-99.
  • Mückschel M, Beste C (2015). Psychophysiological mechanisms underlying response selection in multidimensional space. Sci Rep, 5, 7759.
  • Beste C, Saft C. (2015). Action selection in a possible model of striatal medium spiny neuron dysfunction - behavioural and EEG data in a patient with benign hereditary chorea. Brain Struct Funct, 220, 221-228.
  • Chmielewski W, Beste C (2015). Action control processes in autism spectrum disorder - insights from a neurobiological and neuroanatomical perspective. Prog Neurobiol, 124, 49-83.

2014

  • Ocklenburg S, Beste C, Arning L (2014). Handedness genetics: considering the phenotype. Front Psychol, 5, 1300.
  • Beste C, Kneiphof J, Woitalla D (2014). Modulatory effects of proinflammatory cytokines on action cascading processes - evidence from neurosarcoidosis. Brain Behav Immun, 41, 126-133.
  • Ocklenburg S, Hirnstein M, Beste C, Güntürkün O (2014). Lateralization and cognitive systems. Front Psychol, 5, 1143.
  • Yildiz A, Quetscher C, Dharmadhikari S, Chmielewski W, Glaubiz B, Schmidt-Wilcke T, Edden R, Dydak U, Beste C. (2014). Feeling safe in the plane: neural mechanisms underlying superior action control in airplane pilot trainees - a combined EEG/MRS study. Hum Brain Mapp, 35, 5040-5051.
  • Beste C, Stock A-K, Epplen JT, Arning L (2014). On the relevance of the NPY2-receptor variation for modes of action cascading processes. NeuroImage, 102, 588-564.
  • Chmielewski W, Mückschel M, Roessner V, Beste C (2014). Expectancy effects during response selection modulate attentional selection and response inhibition networks. Behav Brain Res, 274, 53-61.
  • Chmielewski W, Yildiz A, Beste C (2014). The neural architecture of age-related dual-task interferences. Front Aging Neurosci, 6, 193.
  • Arning L, Stock A-K, Kloster E, Epplen JT, Beste C (2014). NPY2-receptor Variation modulates iconic memory processes. Eur Neuropsychopharmacology, 24,1298-1302.
  • Mückschel M, Stock A-K, Beste C. (2014). Psychophysiological mechanisms of interindividual differences in goal activation modes during action cascading. Cereb Cortex, 24, 2120-2129.
  • Lenk S, Bluschke A, Beste C, Ianilli E, Roessner V, Hummel T, Bender S. (2014). Olfactory short-term memory encoding and maintenance - an event-related potential study. NeuroImage, 98, 475-486.
  • Beste C, Saft C. (2014). Benign hereditary chorea as an experimental model to investigate the role of medium spiny neurons for response adaptation. Neuropsychologia, 59C, 124-129.
  • Hoffmann R, Stüwe SH, Goetze O, Banasch M, Klotz P, Lukas C, Tegenthoff M, Beste C, Orth M, Saft C. (2014). Progressive hepatic mitochondrial dysfunction in premanifest Huntington's disease. Mov Disord, 29, 831-834.
  • Ocklenburg S, Beste C, Arning L, Peterburs J, Güntürkün O. (2014). The ontogenesis of language lateralization and its relation to handedness. Neurosci Biobehav Rev, 43, 191-198.
  • Beste C, Humphries MD, Saft C. (2014). Striatal disorders dissociate mechanisms of enhanced and impaired response selection - evidence from cognitive-neurophysiology and computational modelling. Neuroimage Clin, 4, 623-634.
  • Stock A-K, Arning L, Epplen JT, Beste C. (2014). DRD1 and DRD2 genotypes modulate processing modes of goal activation processes during action cascading. J Neurosci, 34, 5335-5341.
  • Ness V, Bestgen A-K, Saft C, Beste C. (2014). Changes in cognitive control in pre-manifest Huntington's disease examined using pre-saccadic EEG potentials - a longitudinal study. J Huntingtons Dis, 3, 33-43.
  • Stock A-K, Beste C. (2014). Lateralization of spatial Information processing in response monitoring. Front Psychol, 5, 22.
  • Stock A-K, Heintschel v. H E, Köhling H-L, Beste C. (2014). Latent toxoplasma gondii infection leads to increased action control. Brain Behav Immun, 37, 103-108.
  • Yildiz A, Wolf OT, Beste C. (2014). Stress intensities demands on esponse selection during action cascading processes. Psychoneuroendocrinology, 42, 178-187.
  • Hoffmann S, Labrenz F, Themann M, Wascher E, Beste C. (2014) Error-related theta-activity predicts error-related BOLD signal changes during simultaneous EEG-fMRI. Brain Struct Funct, 219, 595-605.
  • Tomkins A, Vasilaki E, Beste C, Gurney K, Humphries M. (2014). Transient and steady-state selection in the striatal microcircuit. Front Comp Neurosci, 7, 192.
  • Beste C, Getzmann S, Gajewski PD, Golka K, Falkenstein M. (2014). Latent toxoplasma gondii infection leads to deficits in goal-directed behaviour in healthy elderly. Neurobiol Aging, 35, 1037-1044.
  • Stock AK, Blaszkewicz M, Beste C. (2014). Effects of binge drinking on action cascading processes – an EEG study. Arch Toxicol, 88, 475-488.
  • Stock A-K., Beste C. (2014). Binge drinking and the differential influence of Ethanol on cognitive control subprocesses - a novel field of neurotoxicology. Arch Toxicol, 88, 9-10.

2013

  • Ocklenburg S, Ness V, Güntürkün O, Suchan B, Beste C. (2013).Response inhibition is modulated by functional cerebral asymmetries for facial expression perception. Front Psychol, 4, 879.
  • Ocklenburg S, Beste C, Güntürkün O. (2013). Handedness: a neurogenetic shift in perspective. Neurosci Biobehav Rev, 37, 278-2793.
  • Gajewski PD, Hengstler JG, Golka K, Falkenstein M, Beste C. (2013). The functional tumor necrosis factor (TNF)-α (308G/A) polymorphism modulates attentional selection in aging. Neurobiol Aging, 34, 2694.e1-2694.e12.
  • Ness V, Beste C. (2013). The role of the striatum in goal activation of cascaded actions. Neuropsychologia, 51, 2562-2571.
  • Ocklenburg S, Arning L, Gerding WM, Epplen JT, Güntürkün O, Beste C. (2013). FOXP2 variation modulates functional hemispheric asymmetries for speech perception. Brain Lang, 126, 279-284.
  • Beste C, Yildiz A, Meissner TW, Wolf OT. (2013) Stress improves task processing efficiency in dual-tasks. Behav Brain Res, 252C, 260-265.
  • Arning L, Ocklenburg S, Schulz S, Ness V, Gerding WM, Hengstler JG, Falkenstein M, Epplen JT, Güntürkün O, Beste C. (2013). PCSK6 VNTR polymorphism is associated with handedness. PloS One, 8, e67251.
  • Yildiz A, Chmielewski W, Beste C. (2013). Rewards and punishments differentially modulate dual-tasking. Behav Brain Res, 250, 304-307.
  • Beste C, Dinse HR (2013). Learning without training. Curr Biol, 23, R489-499.
  • Beste C, Stock A-K, Ness V, Hoffmann R, Lukas C, Saft C. (2013). A novel cognitive-neurophysiological state biomarker in pre-manifest Huntington’s disease validated on longitudinal data. Sci Rep 3, 1797.
  • Stock A-K, Wascher E, Beste C. (2013) Differential effects of motor-efference copies and proprioceptive information on response evaluation processes. PloS One 8, e:62335.
  • Ocklenburg S, Arning L, Gerding WM, Epplen JT, Güntürkün O, Beste C. (2013). Cholecystokinin A receptor (CCKAR) gene variation is associated with language lateralization. PloS One, 8, e:53643.
  • Beste C, Konrad C, Uhlmann C, Arolt V, Zwanzger P, Domschke K. (2013). Neuropeptide S receptor (NPSR1) gene variation modulates response inhibition and error monitoring. NeuroImage, 71, C1-9.
  • Getzmann S, Gajewski P, Hengstler J, Falkenstein M, Beste C. (2013). BDNF Val66Met polymorphism and goal-directed behaviour in healthy elderly – evidence from auditory distraction. NeuroImage, 64C, 290-298.

2012

  • Gajewski PD, Hengstler JG, Golka K, Falkenstein M, Beste C. (2012). The Met-genotype of the BDNF Val66Met polymorphism is associated with reduced Stroop interference in elderly. Neuropsychologia, 50, 3554-63.
  • Beste C, Stock AK, Ness V, Epplen JT, Arning L. (2012). Differential effects of ADORA2A gene variations in pre-attentive visual sensory memory subprocesses. Eur Neuropsychopharmacol, 22, 555-61.
  • van Thriel C, Westerink R, Beste C, Bale AS, Lein PJ, Leist M. (2012). Translating neurobehavioural endpoints of developmental neurotoxicity tests into in vitro assays and readouts. Neurotoxicology, 33, 911-24.
  • Wascher E, Schneider D, Hoffmann S, Beste C, Sänger J. (2012). When compensation fails: attentional deficits in healthy ageing caused by visual distraction. Neuropsychologia, 50, 3185-3192.
  • Schneider D, Beste C, Wascher E. (2012). On the time course of bottom-up and top-down processes in selective visual attention: An EEG study. Psychophysiology, 49, 1660-1667.
  • Beste C, Wascher E, Dinse HR, Saft C. (2012). Faster perceptual learning through excitotoxic neurodegeneration. Curr Biol, 22, 1914-1917.
  • Labrenz F, Themann M, Wascher E, Beste C, Pfleiderer B. (2012). Neural Correlates of Individual Performance Differences in Resolving Perceptual Conflict. PLoS ONE, 7: e42849.
  • Schulz S, Arning L, Pinnow M, Epplen JT, Beste C. (2012). N-methyl-d-aspartate receptor 2B subunit (GRIN2B) gene variation is associated with alerting, but not with orienting and conflicting in the attention network test. Neuropharmacology, 63, 259-265.
  • Schneider D, Beste C, Wascher E. (2012). Attentional capture by irrelevant transients leads to perceptual error in a competitive change detection task. Front Psychol, 3, 164.
  • Beste C, Ness V, Lukas C, Hoffmann R, Stüwe S, Falkenstein M, Saft C. (2012). Mechanisms mediating parallel action monitoring in fronto-striatal circuits. NeuroImage, 62, 137-146.
  • Ocklenburg S, Güntürkün O, Beste C. (2012). Hemispheric asymmetries and cognitive flexibility: an ERP and sLORETA study. Brain Cogn, 78, 148-155.
  • Schulz S, Arning L, Pinnow M, Wascher E, Epplen JT, Beste C. (2012). When control fails: Influence of the prefrontal but not striatal dopaminergic system on behavioural flexibility in a change detection task. Neuropharmacology, 62, 1028-1033.

2011

  • Beste C, Schüttke A, Pfleiderer B, Saft C. (2011). Music perception and movement deterioration in Huntington's disease. PloS Curr, RRN1252.
  • Gajewski PD, Hengstler JG, Golka K, Falkenstein M, Beste C. (2011). The Met-allele of the BDNF Val66Met polymorphism enhances task switching in elderly. Neurobiol Aging, 32, 2327.e7-2327.e19.
  • Beste C, Ness V, Falkenstein M, Saft C. (2011). On the role of fronto-striatal neural synchronization processes for response inhibition – evidence from ERP phase synchronization analyses in pre-manifest Huntington's disease gene mutation carriers. Neuropsychologia, 49, 3484-3493.
  • Ocklenburg S, Arning L, Hahn C, Gerding WM, Epplen JT, Güntürkün O, Beste C. (2011). Variation in the NMDA receptor 2B subunit gene GRIN2B is associated with differential language lateralization. Behav Brain Res, 225, 284-289.
  • Ness V, Arning L, Niesert HE, Stüttgen MC, Epplen JT, Beste C. (2011). Variations in GRN2B gene are associated with risky decision making. Neuropharmacology, 61, 950-956.
  • Beste C, Domschke K, Radenz B, Falkenstein M, Konrad C. (2011). The functional 5-HT1A receptor polymorphism affects response inhibition processes in a context-dependent manner. Neuropsychologia, 49, 2664-2672.
  • Beste C, Wascher E, Güntürkün O, Dinse HR. (2011). Improvement and impairment of visually guided behavior through LTP- and LTD-like exposure-based visual learning. Curr Biol, 21, 876-882.
  • Ocklenburg S, Güntürkün O, Beste C. (2011). Lateralized neural mechanisms underlying the modulation of response inhibition processes. NeuroImage, 55, 1771-1778.
  • Heil M, Kavsek M, Rolke B, Beste C, Jansen P. (2011). Mental rotation in female twins: evidence for intra-uterine hormone transfer? Biol Psychol, 86, 90-93.
  • Beste C, Güntürkün O, Baune BT, Domschke K, Falkenstein M, Konrad C. (2011). Double dissociated effects of the functional TNF-alpha -308G/A polymorphism on processes of cognitive control. Neuropsychologia, 49, 196-202.
  • Beste C, Schneider D, Epplen JT, Arning L. (2011). The functional BDNF Val66Met polymorphism affects functions of pre-attentive visual sensory memory processes. Neuropharmacology, 60, 467-471.
  • Willemssen R, Schwarz M, Müller T, Falkenstein M, Beste C. (2011). Effects of ageing, Parkinson's Disease and medication on conflict processing functions. Neurobiol Aging, 32, 327-335.

2010

  • Beste C, Otto T, Hoffmann S. (2010). The Biopsychology - Nonlinear Analysis Toolbox: A free, open-source Matlab-toolbox for the non-linear analysis of time series data. Neuroinformatics, 8, 197-200.
  • Beste, C, Baune BT, Falkenstein M, Konrad C. (2010). Variations in the TNF-alpha gene (TNF-alpha -308G/A) affect attention and action selection mechanisms in a double-dissociated fashion. J Neurophysiol, 104, 2523-2531.
  • Beste C, Heil M, Domschke K, Baune BT, Konrad C. (2010). Associations between the tumor necrosis factor alpha gene (-308G->A) and event-related potential indices of attention and mental rotation. Neuroscience, 170, 742-748.
  • Baune BT, Konrad C, Suslow T, Domschke K, Birosiva E, Sehlmeyer C, Beste C. (2010). The Reelin (RELN) gene is associated with executive function in healthy individuals. Neurobiol Learn Mem, 94, 446-451.
  • Sehlmeyer C, Konrad C, Zwitserlood P, Arolt V, Falkenstein M, Beste C. (2010). Executive functions and emotional traits: ERP indices for response inhibition are related to anxiety-related personality traits. Neuropsychologia, 48, 2488-2495.
  • Beste C, Kolev V, Yordanova J, Domschke K, Falkenstein M, Baune BT, Konrad C. (2010). The role of the BDNF Val66Met polymorphism for the synchronization of error- specific neural networks. J Neurosci, 30, 10727-10733.
  • Beste C, Baune BT, Domschke K, Falkenstein M, Konrad C. (2010). Dissociable influences of NR2B-receptor related neural transmission on functions of distinct associative basal ganglia circuits. NeuroImage, 52, 309-315. 
  • Baune BT, Suslow T, Beste C, Birosova E, Domschke K, Sehlmeyer C, & Konrad C. (2010). Association between genetic variants of the metabotropic glutamate receptor 3 (GRM3) and cognitive set shifting in healthy individuals. Genes Brain Behav, 9, 459-466.
  • Beste C, Domschke K, Kolev V, Yordanova J, Baffa A, Falkenstein M, & Konrad C. (2010). Functional 5-HT1a receptor polymorphism selectively modulates error-specific subprocesses of performance monitoring, Hum Brain Mapp, 31, 621-630.
  • Beste C, Willemssen R, Saft C, & Falkenstein M. (2010). Response inhibition subprocesses and dopaminergic pathways: basal ganglia disease effects. Neuropsychologia, 48, 366-373.
  • Pogatzki-Zahn EM, Wagner C, Meinhardt-Renner A, Burgmer M, Beste C, Zahn PK, & Pfleiderer B. (2010). Coding of incisional pain in the brain: a functional magnetic resonance imaging study in human volunteers. Anesthesiology, 112, 406-417.
  • Wascher E, & Beste C. (2010). Tuning perceptual competition. J Neurophysiol, 103, 1057-1065.
  • Beste C, Baune BT, Domschke K, Falkenstein M, & Konrad C. (2010). Paradoxical association of the brain-derived-neurotrophic factor val66met genotype with response inhibition. Neuroscience, 166, 178-184.
  • Beste C, Heil, M, Domschke K, & Konrad C. (2010). The relevance of the functional 5-HT1A receptor polymorphism for attention and working memory processes during mental rotation of characters, Neuropsychologia, 48, 1248-1254.
  • Beste C, Domschke K, Falkenstein, M, & Konrad C. (2010). Differential modulations of response control processes by 5-HT1A gene variation. NeuroImage, 50, 764-771.

2009

  • Kolev V, Beste C, Falkenstein M, Yordanova Y. (2009). Error-related oscillations: effects of aging on neural systems for behavioural monitoring. J Psychophysiol, 23, 216-223.
  • Beste C, Heil M, Arolt V, Konrad C. (2009). ERPs during mental rotation of characters: lateralization, and performance level. Brain and Cognition [Epub ahead of print]
  • Willemssen R, Müller T, Schwarz M, Falkenstein M, Beste C. (2009). Response monitoring in de novo patients with Parkinson’s Disease. PloS One e:4898.
  • Beste C, Schüttke A, Konrad C, Saft C, Andrich J, Pfleiderer B (2009). Functional connectivity during auditory processing in Huntington’s Disease. J Psychophyiol, 22, 195-201.
  • Beste C, Willemssen R, Falkenstein M (2009). Error processing in healthy aging and basal ganglia disorders. Neuroscience, 159, 143-149.
  • Beste C, Konrad C, Saft C, Ukas T, Andrich J, Gold R, Pfleiderer B, Hausmann M, Falkenstein M. (2009). Alterations in voluntary movement execution in Huntington's disease are related to the dominant motor system - evidence from event-related potentials. Exp Neurol, 216, 148-157.
  • Beste C, Dziobek I, Hielscher H, Willemssen R, Falkenstein M. (2009). Effects of stimulus-response compatibility on inhibitory processes in Parkinson’s disease. Eur J Neurosci, 29, 855-860.

2008

  • Beste C, Saft C, Güntürkün O, Falkenstein M. (2008). Increased cognitive functioning in symptomatic Huntington’s disease as revealed by behavioral and event-related potential indices of auditory sensory memory and attention. J Neurosci, 28, 45, 11695-11702.
  • Wild-Wall N, Willemssen R, Falkenstein M, Beste C. (2008). Time estimation in healthy aging and neurodegenerative basal ganglia disorders. Neuroscience Lett, 442, 44-48.
  • Beste C, Saft C, Andrich J, Gold R, Falkenstein M. (2008) Stimulus-response compatibility in Huntington’s Disease: a cognitive-neurophysiological analysis. J Neurophysiol , 99, 1213-1223.
  • Saft C, Schüttke A, Beste C, Andrich J, Heindel W, Pfleiderer B (2008). fMRI reveals altered auditory processing in manifest and premanifest Huntington’s disease. Neuropsychologia, 46, 1279-1289.
  • Beste C, Saft C, Andrich J, Gold R, Falkenstein M (2008). Response inhibition in Huntington’s Disease – a study using ERPs and sLORETA. Neuropsychologia , 46, 1290-1297.
  • Beste C, Saft C, Konrad C, Andrich J, Habbel A, Schepers I, Jansen A, Pfleiderer B, Falkenstein M. (2008). Levels of error processing in Huntington’s Disease: a combined study using event-related potentials and voxel-based morphometry. Hum Brain Mapp, 29, 2, 212-230.

2007

  • Beste C, Saft C, Andrich J, Gold R, Müller T, Falkenstein M (2007). Time processing in Huntington’s disease – a group-control study. PLoS One, e:1263
  • Hellwig K, Beste C, Brune N, Haghikia A, Müller T, Schimrigk S, Gold, R. (2007). Increased MS relapse rate during assisted reproduction technique. J Neurol , 255, 592-593.
  • Beste C, Saft C, Yordanova J, Andrich J, Gold R, Falkenstein M, Kolev V. (2007). Functional compensation or pathology in cortico-subcortical interactions in preclinical Huntington’s disease? Neuropsychologia, 45, 2922-2930.

2006

  • Beste C, Saft C, Andrich J, Gold R, Falkenstein M. (2006). Error processing in Huntington’s Disease. PloS One 1(1): e86
  • Beste C, Hamm JP, Hausmann M. (2006). Developmental changes in line bisection during adulthood. Dev Neuropsychol, 30, 753-767.