Is the whole more than the sum of its parts? Considering global and local features of the connectome improves prediction of individuals and phenotypes.
The 1 match
- [1] § Methods › Predictive modeling with CRAM ↔ get_embedding.m, lines 10–38 · score 0.56 · classic MDS, landmark MDS
Paper
Loaded from Europe PMC by your browser, not stored by OSCR: doi.org · Europe PMC
The paper is loaded when this pane is shown.
The authors' code
MATLAB · 38 lines · 1.5 KB · no license · 1 match
- % SUMMARY: This function implements the landmark MDS (Multi-Dimensional
- % Scaling) algorithm to compute the embedding of data points based on a
- % distance matrix.
- function [L, dim] = get_embedding(distmatrix)
- [L, e] = cmdscale(distmatrix, length(distmatrix));
- dim = round(find(e > mean(e), 1, 'last'), 0);
- end
- function embedding = landmark_MDS()
- % Calculate the embedding using the landmark MDS algorithm
- % Extract the distance matrix for the landmarks
- landmark_distmatrix = distmatrix(1:n_landmarks, 1:n_landmarks);
- landmark_distmatrix_sq = landmark_distmatrix.^2;
- % Perform classical MDS on the landmark distance matrix
- [landmark_embedding, ~] = cmdscale(landmark_distmatrix, dim);
- % Calculate the pseudo-inverse of the landmark embedding
- l_sharp = pinv(landmark_embedding);
- % Calculate squared distances for non-landmark points
- landmark_to_other_distmatrix = distmatrix(1:n_landmarks, n_landmarks + 1:end);
- landmark_to_other_distmatrix_sq = landmark_to_other_distmatrix.^2;
- % Calculate delta_mu (mean squared distance) for landmarks
- delta_mu = mean(landmark_distmatrix_sq, 2);
- % Calculate embedding for non-landmark points using the landmark MDS
- % embedding
- other_embedding = 1/2 * l_sharp * ...
- (repmat(delta_mu, 1, size(landmark_to_other_distmatrix, 2)) - ...
- landmark_to_other_distmatrix_sq);
- % Concatenate landmark and non-landmark embeddings
- ret = vertcat(landmark_embedding, other_embedding');
- end
get_embedding.m at commit 2814aee, no license · at the source
Overview
- Department of Psychiatry, Yale School of Medicine, New Haven, CT, United States
- Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT, United States
- Institute of Behavioral Sciences, Feinstein Institutes for Medical Research, Manhasset, NY, United States
- Department of Psychiatry, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Uniondale, Hempstead, NY, United States
- Department of Biostatistics, Yale School of Public Health, Yale University, New Haven, CT, United States
- Department of Psychiatry, Brain Health Institute, Rutgers University, Piscataway, NJ, United States
- Child Study Center, Yale School of Medicine, New Haven, CT, United States
Abstract
Popular methods for analyzing the brain’s functional connectome examine statistical associations between pairs of atlas-defined brain regions, viewing the strength of these links as independent values. However, edges within a standard connectivity matrix, that is, correlations between individual regions or nodes, are not independent. They are part of an interconnected system. Here, we propose that consideration of both independent, linear relationships (as in standard approaches such as linear kernel ridge regression and connectome-based predictive modeling) and higher order statistical associations—such as tertiary interactions between matrix components and global features of the matrix space—will enhance identification of meaningful individual differences. To test this, we adopt a geometrically grounded measure of similarity that accounts for higher-order local statistical relationships and global interactions, the Wasserstein metric. Results indicate that considering connectivity matrices as representations of their associated Gaussian distributions significantly improves identification of individuals based on their connectivity matrices (aka, “fingerprinting”). We further show that when incorporated into our novel pipeline, “connectome-regression in any metric (CRAM)” the Wasserstein and (the CRAM pipeline itself) improve prediction of individual differences in phenotypes such as fluid intelligence and openness to experience. Thus, both pairwise local and global brain connectivity properties encode for meaningful individual differences that relate to phenotypic expressions and should be considered in brain–behavior predictive models.
Reproduced under the paper's license (CC BY), from the paper cited above.
Repository
Its files are read in the Code ↔ Paper reader above, with 1 match between paragraphs and lines of code.
YaleYipLab/CRAM
2814aee2656884776248bfb854e9a94db7b5bbcf, 7 August 2025Availability: 1 check, the latest on 27 September 2026: the link answers
- 27 September 2026: the link answers
15 files
- CRAM.m, MATLAB, 193 lines
- cpm_check_errors.m, MATLAB, 73 lines
- cpm_cv.m, MATLAB, 52 lines
- cpm_main.m, MATLAB, 67 lines
- cpm_test.m, MATLAB, 14 lines
- cpm_train.m, MATLAB, 40 lines
- cram_data.m, MATLAB, 76 lines
- ensure_distmatrix.m, MATLAB, 142 lines
- ensure_fisher_transform.
m , MATLAB, 22 lines - get_all_preds.m, MATLAB, 55 lines
- get_embedding.m, MATLAB, 38 lines, 1 match
- metric.m, MATLAB, 16 lines
- permutation_tests.m, MATLAB, 128 lines
- rsqrtm.m, MATLAB, 14 lines
- readme.md, Text, 41 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;
- 14 scripts, each with its path and the digest of its content;
- 1 match 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
No dataset and no data link were found in the paper.
Data and Code Availability
The scripts for running the analyses conducted in the study are available at https://
Reproduced under the paper's license (CC BY), from the paper cited above.
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, 27 September 2026: the first record
Recorded: type, language, journal, volume, pages, dates, 9 authors, 5 keywords, 4 funders, 44 references.
Cite
This paper
Riley, S., Cheng, A., Wang, Y.-W., Shen, X., Dhamala, E., Zhao, Y., Holmes, A., Constable, R. T., & Yip, S. W. (2026). Is the whole more than the sum of its parts? Considering global and local features of the connectome improves prediction of individuals and phenotypes. Imaging neuroscience (Cambridge, Mass.), 4, IMAG.a.1287. https://
BibTeX
@article{riley2026whole,
author = {Riley, Steve and Cheng, Annie and Wang, Yu-Wei and Shen, Xilin and Dhamala, Elvisha and Zhao, Yize and Holmes, Avram and Constable, R. Todd and Yip, Sarah W.},
title = {{Is the whole more than the sum of its parts? Considering global and local features of the connectome improves prediction of individuals and phenotypes}},
journal = {Imaging neuroscience (Cambridge, Mass.)},
year = {2026},
month = jun,
volume = {4},
pages = {IMAG.a.1287},
publisher = {MIT Press},
issn = {2837-6056},
doi = {10.1162/
url = {https://
pmid = {42382505},
pmcid = {PMC13317015}
}
RIS
TY - JOUR
AU - Riley, Steve
AU - Cheng, Annie
AU - Wang, Yu-Wei
AU - Shen, Xilin
AU - Dhamala, Elvisha
AU - Zhao, Yize
AU - Holmes, Avram
AU - Constable, R. Todd
AU - Yip, Sarah W.
TI - Is the whole more than the sum of its parts? Considering global and local features of the connectome improves prediction of individuals and phenotypes
T2 - Imaging neuroscience (Cambridge, Mass.)
J2 - Imaging Neurosci (Camb)
PY - 2026
DA - 2026/
VL - 4
SP - IMAG.a.1287
SN - 2837-6056
PB - MIT Press
DO - 10.1162/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.1162/
"type": "article-journal",
"title": "Is the whole more than the sum of its parts? Considering global and local features of the connectome improves prediction of individuals and phenotypes",
"container-title": "Imaging neuroscience (Cambridge, Mass.)",
"author": [
{
"family": "Riley",
"given": "Steve"
},
{
"family": "Cheng",
"given": "Annie"
},
{
"family": "Wang",
"given": "Yu-Wei"
},
{
"family": "Shen",
"given": "Xilin"
},
{
"family": "Dhamala",
"given": "Elvisha"
},
{
"family": "Zhao",
"given": "Yize"
},
{
"family": "Holmes",
"given": "Avram"
},
{
"family": "Constable",
"given": "R. Todd"
},
{
"family": "Yip",
"given": "Sarah W."
}
],
"container-title-short":
"volume": "4",
"page": "IMAG.a.1287",
"DOI": "10.1162/
"PMID": "42382505",
"PMCID": "PMC13317015",
"ISSN": "2837-6056",
"publisher": "MIT Press",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
6,
29
]
]
}
}
The tracing map gets a citation of its own once an author has validated it and it has a DOI.
Similar papers
The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.
- [1] doi:10.1038/s44220-026-00623-7 [code]
- Optimizing functional connectivity scanning conditions for predicting autistic traits.Journal: Nature. Mental healthIn common: Statistics and Machine Learning Toolbox, 8 references
- [2] doi:10.7554/elife.108109 [code]
- Multimodal MRI marker of cognition explains the association between cognition and mental health in the UK Biobank.Journal: eLifeIn common: 7 references
- [3] doi:10.1038/s41562-026-02447-y [code]
- Feature selection leads to divergent neurobiological interpretations of brain-based machine learning biomarkers.Journal: Nature human behaviourIn common: Statistics and Machine Learning Toolbox, 6 references
- [4] doi:10.7554/elife.104053 [code]
- Brain cognition gaps reveal associations with dopamine and factors related to brain health through artificial intelligence prediction of functional connectome.Journal: eLifeIn common: 7 references
- [5] doi:10.1038/s41467-026-73941-0 [code]
- Using connectome-based predictive models to reveal the systems standardized tests and clinical symptoms are reflecting.Journal: Nature communicationsIn common: 7 references
- [6] doi:10.1002/brb3.71363
- Brain Functional Connectivity as a Mediator Between Hematological Metrics and Cognitive Decline in Children With Beta-thalassemia Major.Journal: Brain and behaviorIn common: 6 references
- [7] doi:10.1523/eneuro.0370-25.2026 [code]
- Pretraining for Large-Scale Functional Connectome Fingerprinting Supports Generalization and Transfer Learning in Functional Neuroimaging.Journal: eNeuroIn common: 5 references
- [8] doi:10.1038/s41386-026-02401-6 [code]
- Model-based analysis of stop-signal data reveals robust neural and clinical correlates of evidence accumulation but not inhibition.Journal: Neuropsychopharmacology : official publication of the American College of NeuropsychopharmacologyIn common: 4 references
- [9] doi:10.1038/s41467-026-73668-y [code]
- Convergent and divergent brain-cognition development in early adolescence.Journal: Nature communicationsIn common: Statistics and Machine Learning Toolbox, 3 references
- [10] doi:10.1038/s41398-026-04100-8 [code]
- Bridging molecules and connectome: network biomarkers guided by neurotransmitter architecture in major depressive disorder.Journal: Translational psychiatryIn common: 3 references
Contribute
The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.
Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.
Claim this paper
Correct its record
Say what each link of this record is, remove the ones that are not the paper's, add the ones that are missing. The correction becomes a new version of the record, in its Versions section.
Validate its tracing map
You validate the map as this page shows it: 1 repository of the authors' code, each at its verified commit and with its license, 14 scripts, and 1 match 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: sha256:44e7a21f0755c290…
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.
