Reply to: "No evidence of neural feature-specific pre-activation during the prediction of an upcoming stimulus".
The 3 matches
- [1] § Results and Discussion › Alternative approach to probe sound frequency specific neural preactivation patterns ↔ alajulienne/om_decode_timegen_trSNDteSND_alajulienne.m, lines 3–24 · score 0.70 · prediction related neural, random sequences, activation, complementary, activity, repetition
- [2] § Results and Discussion › Alternative approach to probe sound frequency specific neural preactivation patterns ↔ alajulienne/om_decode_timegen_trSNDteSND_alajulienne.m, lines 3–24 · score 0.61 · LDA classifier, random sequence, relabeled, transitions, probable, repetitions
- [3] § Results and Discussion › Novel data demonstrating feature-specific anticipatory auditory predictions ↔ 4and8tones/plot_stat_sequences.R, lines 184–228 · score 0.53 · mass, Intervals, probability, position, HDI, ROPE
Paper
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The authors' code
MATLAB · 381 lines · 14 KB · no license · 2 matches
- function om_decode_timegen_trSNDteSND_alajulienne(subJ,cfg_in)
- %% om_decode_timegen_trSNDteSND_alajulienne.m
- %%
- % This script implements two complementary decoding approaches to investigate prediction-related patterns
- % in the brain, as described more in details in Schubert et al. (2023) and
- % Topalidis et al. (2025) (https://doi.org/10.1016/j.cub.2025.03.064).
- %
- % In summary:
- % - We train a multiclass LDA classifier on tones from the random sequence, excluding tone repetitions (bottom-up classifier).
- % - We test this classifier on tone repetitions from both random and increasingly predictable sequences to detect pre-activation of stimulus-specific activity.
- % - We also relabel tone repetitions in the test set to the most likely (mp='most probable') expected next tone, capturing prediction-related neural activity.
- % - Separately, we train a second classifier (top-down classifier) on forward tone transitions from the predictable ('ordered') sequence (e.g., A/B, B/C).
- % - This top-down classifier is tested on random and increasingly more predictable most probable tone repetitions to identify top-down representations of expected transitions.
- %clear all; close all; restoredefaultpath; matlabrc;
- disp('Those are the inputs:')
- cfg_in
- OLDCFG = cfg_in;
- % Add user's version of FieldTrip or obob_ownft (update this path as needed)
- addpath('/path/to/your/fieldtrip'); % or obob_ownft
- ft_defaults;
- %% MVPALight
- % Add user's version of MVPA-Light (update this path as needed)
- addpath(genpath('/path/to/your/MVPA-Light/'));
- %%% the rest
- % Add user's analysis code directories (update these paths as needed)
- addpath('/path/to/your/omissionMarkov/decoding');
- addpath('/path/to/your/omissionMarkov/decoding/functions/');
- %% out things
- % Set user's data and output directories (update these paths as needed)
- fileDir = '/path/to/your/data/sssoriginal/';
- outDirTGSND = '/path/to/your/data/decoding/matlab/alajulienne/';
- %%
- clear tmpdata data % to stay on the safe side
- conds={'random*','midminus*','midplus*','ordered*'};
- trialinfos = [];
- %%
- for iFile=1:length(conds) %only on orderer if 4
- tmpFile= dir([fileDir,'*',subJ,'_block*',conds{iFile}]);
- cur_file = [tmpFile.folder,'/',tmpFile.name];
- cfg = [];
- cfg.dataset = cur_file;
- cfg.trialdef.triallength = Inf; % infinite trial length for one trial
- cfg.trialdef.ntrials = 1; % one trial
- cfg = ft_definetrial(cfg);
- cfg.channel = cfg_in.chanType; % select channel type
- cfg.hpfilter = 'yes'; % high-pass filter
- cfg.hpfreq = 0.1;
- cfg.hpinstabilityfix = 'split';
- tmpdata = ft_preprocessing(cfg);
- cfg = [];
- cfg.channel = cfg_in.chanType;
- cfg.dataset=cur_file ;
- cfg.trialdef.prestim = 1;
- cfg.trialdef.poststim = 1;
- cfg.trialdef.eventtype = 'Trigger';
- cfg.trialdef.eventvalue = [1 2 3 4 10 20 30 40]; % only sounds needed
- cfg_wtrials = ft_definetrial(cfg);
- data{iFile}= ft_redefinetrial(cfg_wtrials, tmpdata);
- clear tmpdata;
- data{iFile}.trialinfo(:,2)= iFile;
- %%%
- % Low-pass filter at 30 Hz
- cfg=[];
- cfg.lpfilter = 'yes'; %usually is yes here
- cfg.lpfreq = 30;
- data{iFile} = ft_preprocessing(cfg,data{iFile});
- %% fix the stimulus delay
- cfg = [];
- cfg.offset = -24; % 24 samples at 1kHz (approx 23.5 ms delay), in the original study with the original pneumatic tubes
- data{iFile} = ft_redefinetrial(cfg,data{iFile});
- % Downsample if needed (if fsample > 100 (files on Zenode have Fs = 100))
- if data{iFile}.fsample > 100
- cfg=[];
- if iscell(cfg_in.Fs)
- cfg.resamplefs=str2num(cfg_in.Fs{1});
- else
- cfg.resamplefs=str2num(cfg_in.Fs); %
- end
- data{iFile}=ft_resampledata(cfg, data{iFile});
- else end
- trialinfos=[trialinfos; data{iFile}.trialinfo];
- if ~strcmp(cfg_in.chanType,'MEGMAG') % combine planar if not MEGMAG
- cfg=[];
- data{iFile}=ft_combineplanar(cfg, data{iFile});
- else end
- end
- %% Remove empty blocks if it happens and append data
- if max(size(data(~cellfun('isempty',data))))>1 % do not count the empty elements
- cfg = [];
- cfg.appenddim = 'rpt';
- data=ft_appenddata(cfg, data{:});
- else
- foo = data(~cellfun('isempty',data)); %take out the only non empty one
- data = foo{1};
- clear foo;
- end
- %% Remove cfg field to save disk space
- data = rmfield(data,'cfg');
- %% MVPA part
- clear acc* result* cfg*
- %% init the magic ....
- startup_MVPA_Light;
- %% find the indices of the different sounds and omissions
- allIdxRD = find(data.trialinfo(:,2)==1); %rd sounds and omissions
- allIdxMM = find(data.trialinfo(:,2)==2); %mm sounds and omissions
- allIdxMP = find(data.trialinfo(:,2)==3); %mp sounds and omissions
- allIdxOR = find(data.trialinfo(:,2)==4); %or sounds and omissions
- %% find the self repetitions, see the function below
- tmpidx = findSelfRepetitions(data.trialinfo(allIdxRD,1));
- selfRepRD = allIdxRD(tmpidx);
- % same for the other entropies
- tmpidx = findSelfRepetitions(data.trialinfo(allIdxMM,1));
- selfRepMM = allIdxMM(tmpidx);
- tmpidx = findSelfRepetitions(data.trialinfo(allIdxMP,1));
- selfRepMP = allIdxMP(tmpidx);
- tmpidx = findSelfRepetitions(data.trialinfo(allIdxOR,1));
- selfRepOR = allIdxOR(tmpidx);
- % find the omissions and the trials immediately after
- % RD
- [tmpidx, tmpidy] = detectOmissions(data.trialinfo(allIdxRD,1));
- omIdxRD = allIdxRD(tmpidx); postOmIdxRD = allIdxRD(tmpidy);
- % MM
- [tmpidx, tmpidy] = detectOmissions(data.trialinfo(allIdxMM,1));
- omIdxMM = allIdxMM(tmpidx); postOmIdxMM = allIdxMM(tmpidy);
- % MP
- [tmpidx, tmpidy] = detectOmissions(data.trialinfo(allIdxMP,1));
- omIdxMP = allIdxMP(tmpidx); postOmIdxMP = allIdxMP(tmpidy);
- % OR
- [tmpidx, tmpidy] = detectOmissions(data.trialinfo(allIdxOR,1));
- omIdxOR = allIdxOR(tmpidx); postOmIdxOR = allIdxOR(tmpidy);
- %% create the 'classic' training set, i.e. wo omissions, and post omissions
- % RD
- normalIdxRD = setdiff(allIdxRD, union(omIdxRD, postOmIdxRD));
- cfg=[];
- cfg.keeptrials='yes';
- cfg.trials = [normalIdxRD];
- data_tl_snd_rd=ft_timelockanalysis(cfg, data);
- time=data_tl_snd_rd.time;
- % MM
- normalIdxMM = setdiff(allIdxMM, union(omIdxMM, postOmIdxMM));
- cfg=[];
- cfg.keeptrials='yes';
- cfg.trials = [normalIdxMM]; %
- data_tl_snd_mm=ft_timelockanalysis(cfg, data);
- % MP
- normalIdxMP = setdiff(allIdxMP, union(omIdxMP, postOmIdxMP));
- cfg=[];
- cfg.keeptrials='yes';
- cfg.trials = [normalIdxMP]; %
- data_tl_snd_mp=ft_timelockanalysis(cfg, data);
- % OR
- normalIdxOR = setdiff(allIdxOR, union(omIdxOR, postOmIdxOR));
- cfg=[];
- cfg.keeptrials='yes';
- cfg.trials = [normalIdxOR]; %
- data_tl_snd_or=ft_timelockanalysis(cfg, data);
- %% create the 'forward' training set, i.e. the one without self repetitions and omissions, and post omissions
- % RD
- forwardIdxRD = setdiff(allIdxRD, union(selfRepRD, union(omIdxRD, postOmIdxRD)));
- cfg=[];
- cfg.keeptrials='yes';
- cfg.trials = [forwardIdxRD]; %
- data_tl_rdFW=ft_timelockanalysis(cfg, data);
- % MM
- forwardIdxMM = setdiff(allIdxMM, union(selfRepMM, union(omIdxMM, postOmIdxMM)));
- cfg=[];
- cfg.keeptrials='yes';
- cfg.trials = [forwardIdxMM]; %
- data_tl_mmFW=ft_timelockanalysis(cfg, data);
- % MP
- forwardIdxMP = setdiff(allIdxMP, union(selfRepMP, union(omIdxMP, postOmIdxMP)));
- cfg=[];
- cfg.keeptrials='yes';
- cfg.trials = [forwardIdxMP]; %
- data_tl_mpFW=ft_timelockanalysis(cfg, data);
- % OR
- forwardIdxOR = setdiff(allIdxOR, union(selfRepOR, union(omIdxOR, postOmIdxOR)));
- cfg=[];
- cfg.keeptrials='yes';
- cfg.trials = [forwardIdxOR]; %
- data_tl_orFW=ft_timelockanalysis(cfg, data);
- %% create the self repetitions test set, i.e. the one with only self repetitions
- % RD
- SRidxRD = setdiff(selfRepRD, union(omIdxRD, postOmIdxRD)); %remove OMs as well
- cfg=[];
- cfg.keeptrials='yes';
- cfg.trials = SRidxRD;%
- data_tl_rdSR=ft_timelockanalysis(cfg, data);
- % MM
- SRidxMM = setdiff(selfRepMM, union(omIdxMM, postOmIdxMM)); %remove OMs as well
- cfg=[];
- cfg.keeptrials='yes';
- cfg.trials = [SRidxMM]; %
- data_tl_mmSR=ft_timelockanalysis(cfg, data);
- % MP
- SRidxMP = setdiff(selfRepMP, union(omIdxMP, postOmIdxMP)); %remove OMs as well
- cfg=[];
- cfg.keeptrials='yes';
- cfg.trials = [SRidxMP]; %
- data_tl_mpSR=ft_timelockanalysis(cfg, data);
- % OR
- SRidxOR = setdiff(selfRepOR, union(omIdxOR, postOmIdxOR)); %remove OMs as well
- cfg=[];
- cfg.keeptrials='yes';
- cfg.trials = [SRidxOR]; %
- data_tl_orSR=ft_timelockanalysis(cfg, data);
- %% 'classical' way a la Demarchi et al. 2019
- % RD train/test
- cfg = [];
- cfg.classifier = 'multiclass_lda';
- cfg.metric = 'accuracy';
- cfg.preprocessing = 'undersample';
- [accTG_SND_RD, result_accTG_SND_RD] = mv_classify_timextime(cfg, data_tl_snd_rd.trial, data_tl_snd_rd.trialinfo(:,1));
- % Cross decoding
- % Rd_SND to Mm_SND
- [accTG_SND_RD_MM, result_accTG_SND_RD_MM] = mv_classify_timextime(cfg, data_tl_snd_rd.trial, data_tl_snd_rd.trialinfo(:,1),data_tl_snd_mm.trial, data_tl_snd_mm.trialinfo(:,1));
- % Rd_SND to Mp_SND
- [accTG_SND_RD_MP, result_accTG_SND_RD_MP] = mv_classify_timextime(cfg,data_tl_snd_rd.trial, data_tl_snd_rd.trialinfo(:,1),data_tl_snd_mp.trial, data_tl_snd_mp.trialinfo(:,1));
- % Rd_SND to Or_SND
- [accTG_SND_RD_OR, result_accTG_SND_RD_OR] = mv_classify_timextime(cfg,data_tl_snd_rd.trial, data_tl_snd_rd.trialinfo(:,1),data_tl_snd_or.trial, data_tl_snd_or.trialinfo(:,1));
- %% train on ordered forward and test on self repetitions
- cfg = [];
- cfg.classifier = 'multiclass_lda';
- cfg.metric = 'accuracy';
- cfg.preprocessing = 'undersample';
- [accTG_SND_fwOR_srRD, result_acc_fwOR_srRD] = mv_classify_timextime(cfg, data_tl_orFW.trial, data_tl_orFW.trialinfo(:,1), data_tl_rdSR.trial, data_tl_rdSR.trialinfo(:,1));
- [accTG_SND_fwOR_srMM, result_acc_fwOR_srMM] = mv_classify_timextime(cfg, data_tl_orFW.trial, data_tl_orFW.trialinfo(:,1), data_tl_mmSR.trial, data_tl_mmSR.trialinfo(:,1));
- [accTG_SND_fwOR_srMP, result_acc_fwOR_srMP] = mv_classify_timextime(cfg, data_tl_orFW.trial, data_tl_orFW.trialinfo(:,1), data_tl_mpSR.trial, data_tl_mpSR.trialinfo(:,1));
- [accTG_SND_fwOR_srOR, result_acc_fwOR_srOR] = mv_classify_timextime(cfg, data_tl_orFW.trial, data_tl_orFW.trialinfo(:,1), data_tl_orSR.trial, data_tl_orSR.trialinfo(:,1));
- % relabeled / most probable
- % this is the one needed for the 'top down'/'negative training times' part of the plot
- cfg = [];
- cfg.classifier = 'multiclass_lda';
- cfg.metric = 'accuracy';
- cfg.preprocessing = 'undersample';
- [accTG_SND_fwOR_srRDmp, result_acc_fwOR_srRDmp] = mv_classify_timextime(cfg, data_tl_orFW.trial, data_tl_orFW.trialinfo(:,1), data_tl_rdSR.trial, makeMostProbable(data_tl_rdSR.trialinfo(:,1)));
- [accTG_SND_fwOR_srMMmp, result_acc_fwOR_srMMmp] = mv_classify_timextime(cfg, data_tl_orFW.trial, data_tl_orFW.trialinfo(:,1), data_tl_mmSR.trial, makeMostProbable(data_tl_mmSR.trialinfo(:,1)));
- [accTG_SND_fwOR_srMPmp, result_acc_fwOR_srMPmp] = mv_classify_timextime(cfg, data_tl_orFW.trial, data_tl_orFW.trialinfo(:,1), data_tl_mpSR.trial, makeMostProbable(data_tl_mpSR.trialinfo(:,1)));
- [accTG_SND_fwOR_srORmp, result_acc_fwOR_srORmp] = mv_classify_timextime(cfg, data_tl_orFW.trial, data_tl_orFW.trialinfo(:,1), data_tl_orSR.trial, makeMostProbable(data_tl_orSR.trialinfo(:,1)));
- %% training on the random forward
- cfg = [];
- cfg.classifier = 'multiclass_lda';
- cfg.metric = 'accuracy'% {'accuracy', 'confusion', 'f1', 'mae'}; %
- cfg.output_type = 'dval'; %
- cfg.preprocessing = 'undersample';
- [accTG_SND_fwRD_srRD, result_acc_fwRD_srRD] = mv_classify_timextime(cfg, data_tl_rdFW.trial, data_tl_rdFW.trialinfo(:,1), data_tl_rdSR.trial, data_tl_rdSR.trialinfo(:,1));
- [accTG_SND_fwRD_srMM, result_acc_fwRD_srMM] = mv_classify_timextime(cfg, data_tl_rdFW.trial, data_tl_rdFW.trialinfo(:,1), data_tl_mmSR.trial, data_tl_mmSR.trialinfo(:,1));
- [accTG_SND_fwRD_srMP, result_acc_fwRD_srMP] = mv_classify_timextime(cfg, data_tl_rdFW.trial, data_tl_rdFW.trialinfo(:,1), data_tl_mpSR.trial, data_tl_mpSR.trialinfo(:,1));
- [accTG_SND_fwRD_srOR, result_acc_fwRD_srOR] = mv_classify_timextime(cfg, data_tl_rdFW.trial, data_tl_rdFW.trialinfo(:,1), data_tl_orSR.trial, data_tl_orSR.trialinfo(:,1));
- % relabeled / most probable
- % this is the one needed for the 'bottom up'/'positive training times' part of the plot
- cfg = [];
- cfg.classifier = 'multiclass_lda';
- cfg.metric = 'accuracy'% {'accuracy', 'confusion', 'f1', 'mae'}; %
- cfg.output_type = 'dval'; %
- cfg.preprocessing = 'undersample';
- [accTG_SND_fwRD_srRDmp, result_acc_fwRD_srRDmp] = mv_classify_timextime(cfg, data_tl_rdFW.trial, data_tl_rdFW.trialinfo(:,1), data_tl_rdSR.trial, makeMostProbable(data_tl_rdSR.trialinfo(:,1)));
- [accTG_SND_fwRD_srMMmp, result_acc_fwRD_srMMmp] = mv_classify_timextime(cfg, data_tl_rdFW.trial, data_tl_rdFW.trialinfo(:,1), data_tl_mmSR.trial, makeMostProbable(data_tl_mmSR.trialinfo(:,1)));
- [accTG_SND_fwRD_srMPmp, result_acc_fwRD_srMPmp] = mv_classify_timextime(cfg, data_tl_rdFW.trial, data_tl_rdFW.trialinfo(:,1), data_tl_mpSR.trial, makeMostProbable(data_tl_mpSR.trialinfo(:,1)));
- [accTG_SND_fwRD_srORmp, result_acc_fwRD_srORmp] = mv_classify_timextime(cfg, data_tl_rdFW.trial, data_tl_rdFW.trialinfo(:,1), data_tl_orSR.trial, makeMostProbable(data_tl_orSR.trialinfo(:,1)));
- %% and save!
- cfg_in = OLDCFG; % to keep the original cfg_in
- if iscell(cfg_in.Fs)
- Fs = cfg_in.Fs{1};
- else
- Fs = cfg_in.Fs;
- end
- outFile = [ subJ '_' cfg_in.chanType '_timegen_trRdSND_teSND_Fs' num2str(Fs) '_alajulienne.mat' ];
- if iscell(outFile)
- outFile = [outFile{:}];
- else end
- save(fullfile(outDirTGSND, outFile),'acc*','result*','time','cfg_in' ,'-v7.3');
- disp(['Saved: ',fullfile(outDirTGSND, outFile)]);
- end
- %% local functions
- function repetition_indices = findSelfRepetitions(sequence)
- % Initialize an empty array to store indices of the first self-repetitions
- repetition_indices = [];
- % Flag to track if we're in a repetition sequence
- inRepetition = false;
- % Loop through the sequence starting from the second element
- for i = 2:length(sequence)
- % Check if the current element is equal to the previous element
- if sequence(i) == sequence(i-1)
- % If not already in a repetition, this is the first repetition
- if ~inRepetition
- repetition_indices = [repetition_indices, i];
- inRepetition = true; % Mark that we're now in a repetition
- end
- else
- % If the current element is different, reset the repetition flag
- inRepetition = false;
- end
- end
- end
- function [omIdx, postOmIdx] = detectOmissions(sequence)
- % Find indices where elements are 10 or more (detect omissions)
- omIdx = find(sequence >= 10);
- % Initialize array to store the indices following the omissions
- postOmIdx = omIdx + 1;
- % Ensure indices are within bounds
- postOmIdx(postOmIdx > length(sequence)) = [];
- end
- function shifted_sequence = makeMostProbable(sequence)
- % mod to perform the cyclic shift
- % 2 -> 1, 3 -> 2, 4 -> 3, 1 -> 4, ...
- shifted_sequence = mod(sequence - 2, 4) + 1;
- end
om_decode_timegen_trSNDteSND_alajulienne.m at commit 25f86b2, no license · at the source
Overview
- Centre for Cognitive Neuroscience, Department of Psychology, Paris-Lodron-University of Salzburg, Salzburg, Austria
- Neuroscience Institute, Christian Doppler University Hospital, Paracelsus Medical University Salzburg, Salzburg, Austria
Abstract
No abstract was found for this paper: the paper, at the publisher.
Repository
Its files are read in the Code ↔ Paper reader above, with 3 matches between paragraphs and lines of code.
gdemarchi/Markov2.0
25f86b286e5d5fdabbb35a450d40e5f8caef79d9, 12 April 2026Availability: 1 check, the latest on 28 September 2026: the link answers
- 28 September 2026: the link answers
8 files
- 4and8tones/
mtng_decode_timegen_trSN , MATLAB, 292 linesDteSND.m - 4and8tones/
plot_mtng_SNDtoSND.m , MATLAB, 378 lines - 4and8tones/
plot_stat_sequences.R , R, 347 lines, 1 match - 4and8tones/
run_mtng_decode_timegen_ , MATLAB, 64 linestrSNDteSND.m - alajulienne/
om_decode_timegen_trSNDt , MATLAB, 381 lines, 2 matcheseSND_alajulienne.m - alajulienne/
plot_TG_trSNDteSND_MVPAL , MATLAB, 233 linesight_mr_alajulienne.m - alajulienne/
run_om_decode_timegen_tr , MATLAB, 56 linesSNDteSND_alajulienne.m - README.TXT, Text, 46 lines
The paper's code and data availability statement is in the Data section.
Tracing map
Proposed by the machine: these links were found in the paper and verified at the source, without human review. The map will receive a Zenodo DOI once one of the paper's authors has validated it with their ORCID.
What the map holds:
- 1 repository of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
- 7 scripts, each with its path and the digest of its content;
- 3 matches between paragraphs of the paper and lines of the code (method lexical-v1);
- neither the text of the paper nor the code itself.
Its JSON (tracing-map.json) is deposited on Zenodo with its DOI once the map is validated.
Data
Datasets cited
- zenodo:3268713, at Zenodo; found in “Data availability”
Code and data availability statement
The paper has a code and data availability statement. Its license (CC BY-NC-ND) does not allow reproducing it here; in short, from what the harvester recognized in it:
- it points to a dataset: Zenodo 3268713
- it points to the authors' code: gdemarchi/
Markov2.0 - it says that the data are available on request
Read it in the paper: doi.org/10.1038/s41467-026-73567-2.
Versions
The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.
Version 1, 28 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 10 authors, 3 keywords, 1 funder, 8 references.
Cite
This paper
Demarchi, G., Hartmann, T., Hauswald, A., Schubert, J., Reisinger, L., Topalidis, P., Benz, K., Schmidt, F., Gehmacher, Q., & Weisz, N. (2026). Reply to: "No evidence of neural feature-specific pre-activation during the prediction of an upcoming stimulus". Nature communications, 17(1), 4638. https://
BibTeX
@article{demarchi2026rep
author = {Demarchi, Gianpaolo and Hartmann, Thomas and Hauswald, Anne and Schubert, Juliane and Reisinger, Lisa and Topalidis, Pavlos and Benz, Kaja and Schmidt, Fabian and Gehmacher, Quirin and Weisz, Nathan},
title = {{Reply to: "No evidence of neural feature-specific pre-activation during the prediction of an upcoming stimulus"}},
journal = {Nature communications},
year = {2026},
month = may,
volume = {17},
number = {1},
pages = {4638},
publisher = {Nature Publishing Group},
issn = {2041-1723},
doi = {10.1038/
url = {https://
pmid = {42191730},
pmcid = {PMC13212686}
}
RIS
TY - JOUR
AU - Demarchi, Gianpaolo
AU - Hartmann, Thomas
AU - Hauswald, Anne
AU - Schubert, Juliane
AU - Reisinger, Lisa
AU - Topalidis, Pavlos
AU - Benz, Kaja
AU - Schmidt, Fabian
AU - Gehmacher, Quirin
AU - Weisz, Nathan
TI - Reply to: "No evidence of neural feature-specific pre-activation during the prediction of an upcoming stimulus"
T2 - Nature communications
J2 - Nat Commun
PY - 2026
DA - 2026/
VL - 17
IS - 1
SP - 4638
SN - 2041-1723
PB - Nature Publishing Group
DO - 10.1038/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.1038/
"type": "article-journal",
"title": "Reply to: \"No evidence of neural feature-specific pre-activation during the prediction of an upcoming stimulus\"",
"container-title": "Nature communications",
"author": [
{
"family": "Demarchi",
"given": "Gianpaolo"
},
{
"family": "Hartmann",
"given": "Thomas"
},
{
"family": "Hauswald",
"given": "Anne"
},
{
"family": "Schubert",
"given": "Juliane"
},
{
"family": "Reisinger",
"given": "Lisa"
},
{
"family": "Topalidis",
"given": "Pavlos"
},
{
"family": "Benz",
"given": "Kaja"
},
{
"family": "Schmidt",
"given": "Fabian"
},
{
"family": "Gehmacher",
"given": "Quirin"
},
{
"family": "Weisz",
"given": "Nathan"
}
],
"container-title-short":
"volume": "17",
"issue": "1",
"page": "4638",
"DOI": "10.1038/
"PMID": "42191730",
"PMCID": "PMC13212686",
"ISSN": "2041-1723",
"publisher": "Nature Publishing Group",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
5,
26
]
]
}
}
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