Pulvinar-posterior superior temporal sulcus connectivity contributes to non-conscious emotion processing in affective blindsight.
The 7 matches
- [1] § Materials and methods › Neuroimaging protocols › Bayesian statistical Modeling ↔ Codes/Bayesian_regression_ROI_analysis_version_8_LOO_PPC.r, lines 78–160 · score 0.94 · posterior predictive checks, adapt_delta, max_treedepth, brms, amygdala pathway, Full Model
- [2] § Materials and methods › Neuroimaging protocols › Bayesian statistical Modeling ↔ Logistic regression with SHAP/Bayesian_regression_ROI_analysis_version_7_LOO.r, lines 75–119 · score 0.92 · adapt_delta, max_treedepth, brms, amygdala pathway, Full Model, logistic regression
- [3] § Results › Bayesian model comparison reveals preservation of right-lateralized subcortical pathways supports affective blindsight ↔ Logistic regression with SHAP/Bayesian_regression_ROI_analysis_version_7_LOO.r, lines 165–213 · score 0.62 · pairwise Bayes factor, logistic regression, Model comparisons, bridge, heatmap, BF
- [4] § Materials and methods › Behavioral data analysis ↔ Codes/Binomial test_FWE_correction.py, lines 9–20 · score 0.61 · Static Emotion Recognition, Dynamic Emotion Recognition, PENN, AFC, binomial
- [5] § Results › Bayesian model comparison reveals preservation of right-lateralized subcortical pathways supports affective blindsight ↔ Logistic regression with SHAP/Bayesian_regression_ROI_analysis_version_7_LOO.r, lines 1–63 · score 0.61 · posterior predictive checks, logistic regression, model comparison, Bayesian, affective blindsight, pathways
- [6] § Materials and methods › Neuroimaging protocols › Region and tract of interests analysis ↔ Codes/Logistic Regression with Regularization Permuatation testing.py, lines 52–58 · score 0.60 · logistic regression, L1, Lasso, L2, Ridge, model
- [7] § Results › Bayesian model comparison reveals preservation of right-lateralized subcortical pathways supports affective blindsight ↔ Codes/Bayesian_regression_ROI_analysis_version_8_LOO_PPC.r, lines 78–160 · score 0.58 · posterior predictive checks, amygdala pathways, Full Model, affective blindsight, Bayesian, regression
Paper
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The authors' code
R · 213 lines · 9.8 KB · no license · 3 matches
- # Bayesian Model Comparison for Affective Blindsight Pathways
- # Version 6.0: Added posterior predictive checks and 95% credible intervals for all parameters
- # 1. Load Required Packages ---------------------------------------------------
- library(tidyverse) # Data manipulation
- library(brms) # Bayesian regression
- library(bridgesampling) # Marginal likelihood estimation
- library(pheatmap) # Heatmap visualization
- library(readxl) # Excel file reading
- library(bayesplot) # MCMC diagnostics
- library(cowplot) # Plot grids
- # Set plotting theme
- color_scheme_set("blue")
- theme_set(theme_minimal() + theme(
- panel.background = element_rect(fill = "white", colour = NA),
- plot.background = element_rect(fill = "white", colour = NA),
- legend.background = element_rect(fill = "white", colour = NA),
- panel.grid.major = element_line(colour = "lightgray"),
- panel.grid.minor = element_line(colour = "lightgray")
- ))
- # 2. Data Loading and Preparation ---------------------------------------------
- data_path <- "D:/PhD/Blindsight/ROI analysis in R/Blindsight_manual_Tract_TOI_Analysis_data_15N_july_2025.xlsx"
- data <- read_excel(data_path) %>%
- mutate(
- Affective_blindsight = factor(Affective_blindsight, levels = c("0", "1")),
- Calcrine = as.numeric(scale(Calcrine)),
- across(c(R_Pul_Amyg, L_Pul_Amyg, R_Pul_STS, L_Pul_STS), as.factor)
- )
- # Check predictor variance and factor levels
- predictor_vars <- c("Calcrine", "R_Pul_Amyg", "L_Pul_Amyg", "R_Pul_STS", "L_Pul_STS")
- for (var in predictor_vars) {
- if (is.numeric(data[[var]])) {
- var_val <- var(data[[var]], na.rm = TRUE)
- if (var_val < .Machine$double.eps) warning(sprintf("WARNING: Variable '%s' has near-zero variance.", var))
- } else {
- level_counts <- table(data[[var]])
- if (nlevels(data[[var]]) < 2 || any(level_counts < 1)) warning(sprintf("WARNING: Factor '%s' has issues with levels.", var))
- }
- }
- # 3. Set Up Output Directory --------------------------------------------------
- output_dir <- file.path(dirname(data_path), "Blindsight_Model_Comparison_Outputs-V7_PPC_CI")
- if (dir.exists(output_dir)) unlink(output_dir, recursive = TRUE) # Clear previous output directory
- dir.create(output_dir, showWarnings = FALSE)
- # 4. Define Priors ------------------------------------------------------------
- prior_params <- list(
- b_Intercept = list(mu = 0, sigma = 2.5),
- b_Calcrine = list(mu = 0, sigma = 2.5),
- b_R_Pul_Amyg1 = list(mu = 0, sigma = 2.5),
- b_L_Pul_Amyg1 = list(mu = 0, sigma = 2.5),
- b_R_Pul_STS1 = list(mu = 0, sigma = 2.5),
- b_L_Pul_STS1 = list(mu = 0, sigma = 2.5),
- `b_R_Pul_Amyg1:R_Pul_STS1` = list(mu = 0, sigma = 1.5),
- `b_L_Pul_Amyg1:L_Pul_STS1` = list(mu = 0, sigma = 1.5),
- `b_R_Pul_STS1:L_Pul_STS1` = list(mu = 0, sigma = 1.5),
- `b_R_Pul_Amyg1:L_Pul_Amyg1` = list(mu = 0, sigma = 1.5),
- `b_R_Pul_Amyg1:L_Pul_STS1` = list(mu = 0, sigma = 1.5),
- `b_L_Pul_Amyg1:R_Pul_STS1` = list(mu = 0, sigma = 1.5)
- )
- sample_prior_distribution <- function(param_name) {
- prior_info <- prior_params[[param_name]]
- if (!is.null(prior_info)) {
- rnorm(10000, prior_info$mu, prior_info$sigma)
- } else {
- warning(sprintf("No prior defined for %s", param_name))
- NULL
- }
- }
- # 5. Common brms Arguments ----------------------------------------------------
- n_iter <- 8000
- warmup <- 2000
- common_brm_args <- list(
- data = data,
- family = bernoulli(),
- chains = 4,
- iter = n_iter,
- warmup = warmup,
- cores = parallel::detectCores(),
- seed = 1234,
- control = list(adapt_delta = 0.95, max_treedepth = 12),
- file_refit = "always"
- )
- # 6. Model Specifications ----------------------------------------------------
- model_specs <- list(
- Model_0_Null = list(formula = Affective_blindsight ~ 1, file = "null_model",
- params = c("b_Intercept")),
- Model_Base_Covariate = list(formula = Affective_blindsight ~ Calcrine, file = "covar_model",
- params = c("b_Intercept", "b_Calcrine")),
- Model_Right_Sided = list(formula = Affective_blindsight ~ Calcrine + R_Pul_Amyg * R_Pul_STS,
- file = "right_model",
- params = c("b_Intercept", "b_Calcrine", "b_R_Pul_Amyg1", "b_R_Pul_STS1",
- "b_R_Pul_Amyg1:R_Pul_STS1")),
- Model_Left_Sided = list(formula = Affective_blindsight ~ Calcrine + L_Pul_Amyg * L_Pul_STS,
- file = "left_model",
- params = c("b_Intercept", "b_Calcrine", "b_L_Pul_Amyg1", "b_L_Pul_STS1",
- "b_L_Pul_Amyg1:L_Pul_STS1")),
- Model_STS_Pathways = list(formula = Affective_blindsight ~ Calcrine + R_Pul_STS * L_Pul_STS,
- file = "sts_model",
- params = c("b_Intercept", "b_Calcrine", "b_R_Pul_STS1", "b_L_Pul_STS1",
- "b_R_Pul_STS1:L_Pul_STS1")),
- Model_Amygdala_Pathways = list(formula = Affective_blindsight ~ Calcrine + R_Pul_Amyg * L_Pul_Amyg,
- file = "amyg_model",
- params = c("b_Intercept", "b_Calcrine", "b_R_Pul_Amyg1", "b_L_Pul_Amyg1",
- "b_R_Pul_Amyg1:L_Pul_Amyg1")),
- Model_Full_Model = list(formula = Affective_blindsight ~ Calcrine + (R_Pul_Amyg + L_Pul_Amyg + R_Pul_STS + L_Pul_STS)^2,
- file = "full_model",
- params = c("b_Intercept", "b_Calcrine", "b_R_Pul_Amyg1", "b_L_Pul_Amyg1",
- "b_R_Pul_STS1", "b_L_Pul_STS1", "b_R_Pul_Amyg1:R_Pul_STS1",
- "b_L_Pul_Amyg1:L_Pul_STS1", "b_R_Pul_STS1:L_Pul_STS1",
- "b_R_Pul_Amyg1:L_Pul_Amyg1", "b_R_Pul_Amyg1:L_Pul_STS1",
- "b_L_Pul_Amyg1:R_Pul_STS1"))
- )
- # 7. Fit Models --------------------------------------------------------------
- models <- list()
- for (model_name in names(model_specs)) {
- spec <- model_specs[[model_name]]
- priors <- lapply(spec$params, function(param) {
- prior_info <- prior_params[[param]]
- if (param == "b_Intercept") {
- set_prior(sprintf("student_t(%s, %s, %s)", 3, prior_info$mu, prior_info$sigma), class = "Intercept")
- } else {
- set_prior(sprintf("normal(%s, %s)", prior_info$mu, prior_info$sigma), class = "b", coef = gsub("b_", "", param))
- }
- })
- model <- do.call(brm, c(list(
- formula = spec$formula,
- file = file.path(output_dir, spec$file),
- prior = do.call(c, priors)
- ), common_brm_args))
- models[[model_name]] <- model
- # Save fixed effects summary with 95% credible intervals
- summary_df <- as.data.frame(posterior_summary(model, probs = c(0.025, 0.975))) %>%
- rownames_to_column("Parameter") %>%
- mutate(Model = model_name, .before = 1)
- write_csv(summary_df, file.path(output_dir, sprintf("%s_fixed_effects_with_CI.csv", model_name)))
- # Save model summary text
- sink(file.path(output_dir, sprintf("%s_summary.txt", model_name)))
- print(summary(model))
- sink()
- }
- # 8. Posterior Predictive Checks ---------------------------------------------
- for (model_name in names(models)) {
- model <- models[[model_name]]
- pp_hist <- pp_check(model, type = "hist") + ggtitle(paste(model_name, "PPC Histogram"))
- pp_dens <- pp_check(model, type = "dens_overlay") + ggtitle(paste(model_name, "PPC Density Overlay"))
- ggsave(file.path(output_dir, sprintf("%s_PPC_hist.png", model_name)), pp_hist, width = 6, height = 4, dpi = 300)
- ggsave(file.path(output_dir, sprintf("%s_PPC_density.png", model_name)), pp_dens, width = 6, height = 4, dpi = 300)
- }
- # 9. Compute Bayes Factors and Posterior Probabilities ------------------------
- log_marg_liks <- lapply(models, function(model) {
- tryCatch({
- bridge_sampler(model, silent = TRUE, maxiter = 1000)$logml
- }, error = function(e) NA)
- })
- valid_log_marg_liks <- log_marg_liks[!is.na(log_marg_liks)]
- log_marg_liks_vec <- unlist(valid_log_marg_liks)
- null_log_ml <- log_marg_liks_vec["Model_0_Null"]
- bf_results_df <- tibble(
- Model = names(log_marg_liks_vec),
- logML = log_marg_liks_vec,
- logBF = ifelse(Model == "Model_0_Null", 0, logML - null_log_ml),
- BF = exp(logBF)
- ) %>% arrange(desc(BF))
- posterior_probs <- bf_results_df %>%
- mutate(Posterior_Prob = BF / sum(BF)) %>%
- select(Model, BF, logBF, Posterior_Prob)
- write_csv(posterior_probs, file.path(output_dir, "bayes_factors_and_probs.csv"))
- # 10. Pairwise Bayes Factor Heatmap ------------------------------------------
- n_models <- length(log_marg_liks_vec)
- pairwise_log10_bf_matrix <- outer(log_marg_liks_vec, log_marg_liks_vec, FUN = function(x, y) (x - y)/log(10))
- pheatmap(pairwise_log10_bf_matrix,
- cluster_rows = FALSE,
- cluster_cols = FALSE,
- display_numbers = TRUE,
- number_format = "%.2f",
- main = "Pairwise log10 Bayes Factor",
- filename = file.path(output_dir, "pairwise_log10_bayes_factor_heatmap.png"),
- color = colorRampPalette(c("#4575b4", "white", "#d73027"))(100))
- # 11. Save All Results --------------------------------------------------------
- save(models, posterior_probs, bf_results_df, log_marg_liks_vec, data,
- file = file.path(output_dir, "blindsight_model_comparison_results.RData"))
- # 12. Completion Message ------------------------------------------------------
- cat("\nANALYSIS COMPLETE\n")
- cat(sprintf("All outputs saved to: %s\n", output_dir))
- cat("\nOutputs include:\n")
- cat("- Fixed effects summaries with 95% credible intervals (.csv)\n")
- cat("- Posterior predictive check plots (.png)\n")
- cat("- Bayes Factors and posterior probabilities (.csv)\n")
- cat("- Pairwise Bayes Factor heatmap (.png)\n")
- cat("- Model summaries (.txt) and RData for all models\n")
Bayesian_regression_ROI_analysis_version_7_LOO.r, no license · at the source
Overview
- Cognitive Neuroscience and Clinical Phenomenology Laboratory, Department of Neurological Sciences, University of Melbourne and Christian Medical College Vellore, Kilminnal, 632517, Ranipet District, Tamil nadu, India
- Melbourne School of Psychological Sciences, Redmond Barry Building, The University of Melbourne, Spencer Road, Parkville VIC 3010, Melbourne, Victoria, Australia
- Department of Radiology, Christian Medical College Vellore, Ida Scudder Road, 632004, Vellore, Tamil Nadu, India
- Department of Optometry and Vision Science, School of Allied Health, University of Western Australia, 2/39 Fairway, Crawley, WA 6009, Perth, Western Australia, Australia
- Lions Eye Institute, 2 Verdun St, Nedlands, WA 6009, Perth, Western Australia, Australia
- Department of Optometry & Vision Sciences, University of Melbourne, Grattan Street, Parkville, VIC 3010, Melbourne, Victoria, Australia
- Graeme Clark Institute for Biomedical Engineering, Grattan Street, Parkville, VIC 3010, Melbourne, Victoria, Australia
Abstract
Affective blindsight, the capacity to discriminate emotional stimuli despite bilateral damage to the primary visual cortex (V1) and without conscious awareness, offers a unique model of non-conscious visual processing. Subcortical pathways involving the pulvinar and amygdala have been proposed, but putative cortical contributions remain unclear. We examined 182 patients, including 31 with bilateral V1 lesions. Among these, 15 had cortical visual loss and seven showed affective blindsight. Using behavioral testing, lesion symptom mapping, and tractography, we found that preserved pulvinar connectivity with both the posterior superior temporal sulcus (pSTS) and the amygdala is necessary for affective blindsight. These findings provide causal evidence for a multi-route architecture, identifying the pulvinar–pSTS pathway, alongside the pulvinar–amygdala pathway, as a critical substrate for non-conscious affective processing.
Reproduced under the paper's license (CC BY-NC), from the paper cited above.
Repositories
Its files are read in the Code ↔ Paper reader above, with 7 matches between paragraphs and lines of code.
cogneuro-rgb
Availability: 1 check, the latest on 30 September 2026: the link answers (HTTP 200)
- 30 September 2026: the link answers (HTTP 200)
OSF xue3d
Availability: 1 check, the latest on 30 September 2026: the link answers (HTTP 200)
- 30 September 2026: the link answers (HTTP 200)
14 files
- Bayes factor matrix plot/
plot_both_quemark.py , Python, 29 lines - Bayes factor matrix plot/
plot_python.py , Python, 29 lines - Bayes factor matrix plot/
plot_r.r , R, 63 lines - Codes/
Bayesian_regression_ROI_ , R, 343 linesanalysis_version_5.4.r - Codes/
Bayesian_regression_ROI_ , R, 268 linesanalysis_version_6_LOO.r - Codes/
Bayesian_regression_ROI_ , R, 263 lines, 2 matchesanalysis_version_8_LOO_P PC.r - Codes/
Binomial test.py , Python, 47 lines - Codes/
Binomial test_FWE_correction.py , Python, 178 lines, 1 match - Codes/
Logistic Regression with Regularization Permuatation testing.py , Python, 228 lines, 1 match - Codes/
Negative_binomial_regres , Python, 91 linession_code_emotion_data.p y - Codes/
plot_python.py , Python, 29 lines - Logistic regression with SHAP/
Bayesian_regression_ROI_ , R, 343 linesanalysis_version_5.4.r - Logistic regression with SHAP/
Bayesian_regression_ROI_ , R, 213 lines, 3 matchesanalysis_version_7_LOO.r - Logistic regression with SHAP/
Bayesian_regression_ROI_ , R, 263 linesanalysis_version_8__PPC. r
The paper's code and data availability statement is in the Data section.
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Data
Datasets cited
- dataverse.harvard.edu/
dataset.xhtml , at dataverse.harvard.edu; found in the references - dataverse.harvard.edu/
dataverse/ , at dataverse.harvard.edu; found in the text, “Lesion network mapping”gsp - doi:10.7910/
dvn/ , at the source; found in the references25833
Data availability
De-identified data and analysis code are available https://
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Version 1, 30 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 16 authors, 5 keywords, 16 MeSH terms, 1 funder, 71 references.
Cite
This paper
Prabhakar, A. T., Margabandhu, K., Bosco, C. J., Jepegnanam, R. T., Prasad, T., Sampathkumar, S., Sunderraj, E. S., Prasad, J. D., Abraham Ninan, G., Bal, D., Vanjare, H., Jasper, A., Mannam, P., M McKendrick, A., Carter, O., & Garrido, M. I. (2026). Pulvinar-posterior superior temporal sulcus connectivity contributes to non-conscious emotion processing in affective blindsight. Cerebral cortex (New York, N.Y. : 1991), 36(3), bhag032. https://
BibTeX
@article{prabhakar2026pu
author = {Prabhakar, Appaswamy Thirumal and Margabandhu, Kavitha and Bosco, Christilda John and Jepegnanam, Rohan Thomas and Prasad, Thanusha and Sampathkumar, Sowmiya and Sunderraj, Evelyn Sheena and Prasad, John Davis and Abraham Ninan, George and Bal, Deepti and Vanjare, Harshad and Jasper, Anitha and Mannam, Pavithra and M McKendrick, Allison and Carter, Olivia and Garrido, Marta Isabel},
title = {{Pulvinar-posterior superior temporal sulcus connectivity contributes to non-conscious emotion processing in affective blindsight}},
journal = {Cerebral cortex (New York, N.Y. : 1991)},
year = {2026},
month = mar,
volume = {36},
number = {3},
pages = {bhag032},
publisher = {Oxford University Press},
issn = {1047-3211},
doi = {10.1093/
url = {https://
pmid = {41902577},
pmcid = {PMC13168818}
}
RIS
TY - JOUR
AU - Prabhakar, Appaswamy Thirumal
AU - Margabandhu, Kavitha
AU - Bosco, Christilda John
AU - Jepegnanam, Rohan Thomas
AU - Prasad, Thanusha
AU - Sampathkumar, Sowmiya
AU - Sunderraj, Evelyn Sheena
AU - Prasad, John Davis
AU - Abraham Ninan, George
AU - Bal, Deepti
AU - Vanjare, Harshad
AU - Jasper, Anitha
AU - Mannam, Pavithra
AU - M McKendrick, Allison
AU - Carter, Olivia
AU - Garrido, Marta Isabel
TI - Pulvinar-posterior superior temporal sulcus connectivity contributes to non-conscious emotion processing in affective blindsight
T2 - Cerebral cortex (New York, N.Y. : 1991)
J2 - Cereb Cortex
PY - 2026
DA - 2026/
VL - 36
IS - 3
SP - bhag032
SN - 1047-3211
PB - Oxford University Press
DO - 10.1093/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.1093/
"type": "article-journal",
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"DOI": "10.1093/
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You validate the map as this page shows it: 2 repositories of the authors' code, each at its verified commit and with its license, 14 scripts, and 7 matches between paragraphs and code (see the Code and Map sections). It then receives a DOI on Zenodo, with you (your ORCID iD) and OSCR as its creators; the code itself is not deposited.
The map's fingerprint: sha256:38fc4bd268384348…
Add the badge to its README
The badge links the code to this page. Copy one of these into the README of the paper's code: only you decide where it goes, and nothing is changed for you.
Markdown
[, paste the snippet at the top, then “Commit changes…” and, to review it first, “Create a new branch and start a pull request”. You open the pull request; OSCR asks for no permission.
Request its removal
To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).
Discussion, reproductions, activity
Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.
Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.
Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.
