The hippocampus becomes topographically and functionally specialized along the longitudinal axis with development.
The 13 matches · 1 of them tie a paragraph to a whole file, not to given lines: a weak match, whose lines are not tinted
- [1] § Methods › Precision mapping of hippocampal functional systems ↔ hipp_mapping/mapping.py, lines 69–134 · score 0.82 · trilinear interpolation, metric smoothing, surface mapping, BOLD signals, wb_command, fwhm
- [2] § Methods › Precision mapping of hippocampal functional systems ↔ hipp_mapping/main.py, lines 8–28 · score 0.66 · mid thickness surface, wb_command, fwhm, volume, kernel, BOLD signals
- [3] § Methods › Neocortical connectivity of the posterior hippocampus ↔ manuscript_analyses.ipynb, lines 193–248 · score 0.65 · odds ratios, logistic regression, classify, coefficients, cluster, anterior
- [4] § Results › Neocortical connectivity differs between functional systems along the hippocampal long axis ↔ manuscript_analyses.ipynb, lines 135–189 · score 0.65 · default_c, default_b, control_c, salience, FC, parietal
- [5] § Methods › Quantifying topographic and functional specialization ↔ feature_extraction/sharpness.py, the whole file · a weak match · score 0.64 · border vertex, boundary sharpness, BOLD signal, Cohen, correlating
- [6] § Methods › Neocortical connectivity of the posterior hippocampus ↔ manuscript_analyses.ipynb, lines 292–315 · score 0.64 · Picture Sequence, control_c, ROI, age adjusted, Pm, RSC
- [7] § Methods › Precision mapping of hippocampal functional systems ↔ cortex_mapping/mapping.py, lines 80–173 · score 0.60 · template matching, precision mapping, vector, matrix, profile, vertex
- [8] § Results › Neocortical connectivity differs between functional systems along the hippocampal long axis ↔ manuscript_analyses.ipynb, lines 193–248 · score 0.56 · odds ratio, logistic regression, classifiers, anterior, body, network
- [9] § Results › Precision-functional mapping of the long-axis systems of the hippocampus ↔ hipp_mapping/mapping.py, lines 69–134 · score 0.56 · trilinear interpolation, Hippocampal vertices, BOLD signal, profile, hippocampal system, template
- [10] § Methods › Sensitivity analyses ↔ manuscript_analyses.ipynb, lines 114–132 · score 0.56 · predicting age, body segregation, surface area, regression, anterior, posterior
- [11] § Results › The posterior hippocampal system becomes functionally specialized with development ↔ manuscript_analyses.ipynb, lines 114–132 · score 0.54 · linear regression predicting, surface area, sharpness, segregation, age, posterior
- [12] § Results › Posterior hippocampal system shows increased connectivity to the control-c/medial parietal network with age and memory ↔ manuscript_analyses.ipynb, lines 252–269 · score 0.51 · Picture Sequence, control_c, age adjusted, NIH, raw, memory
- [13] § Methods › Neocortical connectivity of the posterior hippocampus ↔ cortex_mapping/mapping.py, lines 80–173 · score 0.51 · template matching, Dice, thresholded, profile, signal, cortex
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
Jupyter notebook · 414 lines · 12 KB · no license · 7 matches
- # %%
- import json
- import warnings
- import numpy as np
- import pandas as pd
- import pingouin as pg
- import seaborn as sns
- import matplotlib.pyplot as plt
- %config InlineBackend.figure_format='retina'
- warnings.filterwarnings('ignore')
- # Load cluster colors for anterior, body, and posterior.
- with open('cluster_colors.json', 'r') as f:
- cluster_colors = {int(k): tuple(v) for k, v in json.load(f).items()}
- # Load data.
- df = pd.read_csv('supplementary_data.csv')
- display(df,df.columns)
- # %%
- # Plot changes in surface area with age.
- for idx, pos in enumerate(['ant','body','post']):
- stats = pg.corr(df['age'], df[f'{pos}_mm'])
- r = stats['r'].values[0]
- p = stats['p-val'].values[0]
- display(stats)
- fig, ax = plt.subplots(figsize=(4.5,3.5))
- if p < .05:
- sns.regplot(x=df['age'], y=df[f'{pos}_mm'], color=cluster_colors[idx+1])
- sns.regplot(x=df['age'], y=df[f'{pos}_mm'], color=cluster_colors[idx+1], scatter_kws={'s':0})
- ax.text(16.5,25,f'$r$={r:.2f}, $p$={p:1.0e}')
- else:
- sns.regplot(x=df['age'], y=df[f'{pos}_mm'], color=cluster_colors[idx+1],fit_reg=False)
- ax.text(20,25,f'$ns$')
- sns.despine()
- ax.grid(linestyle='--', alpha=.25, axis='y')
- ax.set_ylabel('Surface area [mm$^2$]')
- ax.set_xlabel('Age')
- ax.set_xticks([6,10,14,18,22])
- ax.set_ylim([0, 1350])
- plt.tight_layout()
- plt.savefig(f'extra/{pos}_surface_area_mm.svg')
- plt.show()
- # %%
- # Plot changes in boundary-sharpness segregation with age.
- for idx, pos in enumerate(['ant','body','post']):
- print(pos)
- stats = pg.corr(df['age'], df[f'{pos}_sharpness'])
- r = stats['r'].values[0]
- p = stats['p-val'].values[0]
- display(stats)
- fig, ax = plt.subplots(figsize=(4.5,3.5))
- # Add regression line to significant effects.
- if p < .05:
- sns.regplot(x=df['age'], y=df[f'{pos}_sharpness'], color=cluster_colors[idx+1])
- sns.regplot(x=df['age'], y=df[f'{pos}_sharpness'], color=cluster_colors[idx+1], scatter_kws={'s':0})
- ax.text(.65,.025,f'$r$={r:.2f}, $p$={p:1.0e}', transform=ax.transAxes)
- else:
- sns.regplot(x=df['age'], y=df[f'{pos}_sharpness'], color=cluster_colors[idx+1],fit_reg=False)
- ax.text(.9,.025,f'$ns$', transform=ax.transAxes)
- sns.despine()
- ax.grid(linestyle='--', alpha=.25, axis='y')
- ax.set_ylabel('Boundary sharpness [$d$]')
- ax.set_xlabel('Age')
- ax.set_xticks([6,10,14,18,22])
- plt.tight_layout()
- plt.savefig(f'extra/{pos}_sharpness.svg')
- plt.show()
- # %%
- # Plot changes in segregation with age.
- for idx, pos in enumerate(['ant','body','post']):
- stats = pg.corr(df['age'], df[f'{pos}_segregation'])
- r = stats['r'].values[0]
- p = stats['p-val'].values[0]
- display(stats)
- fig, ax = plt.subplots(figsize=(4.5,3.5))
- if p < .05:
- sns.regplot(x=df['age'], y=df[f'{pos}_segregation'], color=cluster_colors[idx+1])
- sns.regplot(x=df['age'], y=df[f'{pos}_segregation'], color=cluster_colors[idx+1], scatter_kws={'s':0})
- ax.text(.65,.025,f'$r$={r:.2f}, $p$={p:1.0e}', transform=ax.transAxes)
- else:
- sns.regplot(x=df['age'], y=df[f'{pos}_segregation'], color=cluster_colors[idx+1],fit_reg=False)
- ax.text(.9,.025,f'$ns$', transform=ax.transAxes)
- sns.despine()
- ax.grid(linestyle='--', alpha=.25, axis='y')
- ax.set_ylabel('Segregation [$d$]')
- ax.set_xlabel('Age')
- ax.set_xticks([6,10,14,18,22])
- plt.tight_layout()
- plt.savefig(f'extra/{pos}_segregation.svg')
- plt.show()
- # %%
- # Plot correlation between segregation and surface area.
- fig ,ax = plt.subplots(figsize=(6,4))
- sns.regplot(x=df['ant_mm'], y=df['ant_segregation'], scatter_kws={'s':5}, color=cluster_colors[1])
- sns.regplot(x=df['body_mm'], y=df['body_segregation'], scatter_kws={'s':5}, color=cluster_colors[2])
- sns.regplot(x=df['post_mm'], y=df['post_segregation'], scatter_kws={'s':5}, color=cluster_colors[3])
- sns.despine()
- ax.grid(linestyle='--', alpha=.25)
- ax.set_xlabel('Surface area [mm$^2$]')
- ax.set_ylabel('Segregation [$d$]')
- ax.legend(['_','anterior','_','_','body','_','_','posterior'], frameon=False)
- plt.show()
- lm = pg.linear_regression(X=df[['post_mm','post_sharpness','post_segregation']], y=df['age'])
- print('Linear regression predicting age:')
- display(lm)
- # %%
- networks = {
- 1:'visual_a',
- 2:'visual_b',
- 3:'somatomotor_a',
- 4:'somatomotor_b',
- 5:'dorsal_attention_a',
- 6:'dorsal_attention_b',
- 7:'ventral_attention',
- 8:'salience',
- 9:'limbic_a',
- 10:'limbic_b',
- 11:'control_c',
- 12:'control_a',
- 13:'control_b',
- 14:'temporal_parietal',
- 15:'default_c',
- 16:'default_a',
- 17:'default_b'
- }
- network_labels = np.array(list(networks.values()))
- def cohens_d(x):
- d = (np.mean(x) - 0) / np.std(x, ddof=1)
- return np.abs(d)
- for idx, pos in enumerate(['ant','body','post']):
- fig, ax = plt.subplots(figsize=(3.25, 4))
- network_fc = np.array([df[f'{pos}_{network}_FC'].mean() for network in network_labels])
- network_fc_err = np.array([df[f'{pos}_{network}_FC'].std() for network in network_labels])
- eff_size = np.array([cohens_d(df[f'{pos}_{network}_FC']) for network in network_labels])[np.argsort(network_fc)]
- bars = ax.barh(
- width=network_fc[np.argsort(network_fc)],
- y=network_labels[np.argsort(network_fc)],
- color=cluster_colors[idx+1], xerr=network_fc_err[np.argsort(network_fc)]
- )
- yticks = ax.get_yticklabels()
- for idx, bar in enumerate(bars):
- if eff_size[idx] < 1.5: bar.set_alpha(.25)
- if eff_size[idx] >= 1.5: yticks[idx].set_fontweight('bold')
- ax.set_xlim([-1.65,1.65])
- ax.set_xlabel('$z$ score')
- ax.axvline(0, color='k')
- sns.despine()
- ax.grid(axis='y', linestyle='--', alpha=.2)
- plt.tight_layout()
- plt.savefig(f'extra/{pos}_network_barplot.svg')
- # %%
- from sklearn.utils import resample
- from sklearn.linear_model import LogisticRegression
- from sklearn.multiclass import OneVsRestClassifier
- # Convert dataframe to long-form for one-versus-rest classification.
- df_long = df.melt(id_vars='id', var_name='feature', value_name='value')
- df_long[['class', 'sub_feature']] = df_long['feature'].str.extract(r'^(ant|body|post)_(.+)$')
- df_long = df_long.drop_duplicates(subset=['id', 'class', 'sub_feature'])
- df_wide = df_long.pivot(index=['id', 'class'], columns='sub_feature', values='value').reset_index()
- df_wide = df_wide[df_wide['class'].isin(['ant','body','post'])]
- features = [f'{label}_FC' for label in network_labels]
- X = df_wide[features].to_numpy()
- y = df_wide['class']
- # Fit base classifier for coefficients.
- clf = OneVsRestClassifier(LogisticRegression(penalty='l2', solver='liblinear'))
- clf.fit(X, y)
- coefs = np.vstack([est.coef_ for est in clf.estimators_])
- titles = ['anterior','body','posterior']
- for idx, pos in enumerate(['ant','body','post']):
- coef = clf.estimators_[idx].coef_[0]
- odds_ratios = np.exp(coef)
- odds_ratios_sorted = odds_ratios[np.argsort(odds_ratios)]
- network_labels_sorted = network_labels[np.argsort(odds_ratios)]
- fig, ax = plt.subplots(figsize=(3, 4))
- bars = ax.barh(
- width=odds_ratios_sorted,
- y=network_labels_sorted,
- color=cluster_colors[idx+1]
- )
- yticks = ax.get_yticklabels()
- for bar_idx, bar in enumerate(bars):
- if odds_ratios_sorted[bar_idx] < 10: bar.set_alpha(.15)
- if odds_ratios_sorted[bar_idx] > 10: yticks[bar_idx].set_fontweight('bold')
- ax.set_xlim([0,15])
- ax.set_xlabel('Odds-ratio')
- ax.axvline(0, color='k', alpha=.75)
- sns.despine()
- ax.grid(axis='y', linestyle='--', alpha=.2)
- plt.tight_layout()
- plt.savefig(f'extra/{pos}_network_barplot.svg')
- print(titles[idx])
- display(dict(zip(network_labels_sorted,odds_ratios_sorted)))
- # %%
- # Plot changes in connectivity of posterior_hipp – control_c network with age and memory.
- labels = ['Picture-sequence scores [raw]','Picture-sequence scores [age-adjusted]','Age']
- for idx, feature in enumerate(['nih_picseq_raw','nih_picseq_ageadjusted','age']):
- display(pg.corr(df[feature], df['post_control_c']))
- fig, ax = plt.subplots(figsize=(4,3))
- sns.regplot(x=df[feature], y=df['post_control_c'], color=cluster_colors[3], scatter_kws={'s':20})
- sns.despine()
- ax.axhline(0, linestyle='--', color='k')
- ax.set_ylabel('$z$-score')
- ax.set_xlabel(labels[idx])
- ax.set_title(f'Connectivity with control_c', loc='left')
- ax.grid(linestyle='--', alpha=.25)
- plt.show()
- # %%
- # Plot changes in connectivity of posterior_hipp – control_c, versus-anterior/body, network with age and memory.
- labels = ['Picture-sequence scores [raw]','Picture-sequence scores [age-adjusted]','Age']
- for idx, feature in enumerate(['nih_picseq_raw','nih_picseq_ageadjusted','age']):
- display(pg.corr(df[feature], df['post_control_c_OVR']))
- fig, ax = plt.subplots(figsize=(4,3))
- sns.regplot(x=df[feature], y=df['post_control_c_OVR'], color=cluster_colors[3], scatter_kws={'s':20})
- sns.despine()
- ax.axhline(0, linestyle='--', color='k')
- ax.set_ylabel('$z$-score')
- ax.set_xlabel(labels[idx])
- ax.set_title(f'Connectivity with control_c', loc='left')
- ax.grid(linestyle='--', alpha=.25)
- plt.show()
- # %%
- labels = ['Picture-sequence scores [raw]','Picture-sequence scores [age-adjusted]','Age']
- col = (0.4627450980392157, 0.5450980392156862, 0.6862745098039216) # Yeo control_c Color.
- for roi in ['POS2','RSC','7Pm']:
- print(roi)
- for idx, feature in enumerate(['nih_picseq_raw','nih_picseq_ageadjusted','age']):
- fig, ax = plt.subplots(figsize=(4,3))
- stats = pg.corr(df[feature], df[f'post_{roi}_OVR'])
- display(stats)
- sns.regplot(x=df[feature], y=df[f'post_{roi}_OVR'], color=col, scatter_kws={'s':20})
- sns.despine()
- ax.axhline(0, linestyle='--', color='k')
- ax.set_ylabel('$z$-score')
- ax.set_xlabel(labels[idx])
- ax.grid(linestyle='--', alpha=.25)
- ax.text(.02,.075,f"$r$={stats['r'].values[0]:.2f}, $p$={stats['p-val'].values[0]:.0e}", transform=ax.transAxes)
- plt.show()
- print('Mediation analysis:')
- display(pg.mediation_analysis(data=df, x='age', m=f'post_{roi}_OVR', y='nih_picseq_ageadjusted'))
- # %%
- # Replication across sites.
- for feature in ['post_mm','post_segregation','post_sharpness']:
- print(f'Feature: {feature}')
- for site in set(df.site):
- print(f'{site}:')
- display(pg.corr(
- df[df.site == site]['age'],
- df[df.site == site][feature])
- )
- print('\n')
- for feature in ['post_control_c_OVR']:
- print(f'Feature: {feature}')
- for site in set(df.site):
- print(f'{site}:')
- print('Age:')
- display(pg.corr(
- df[df.site == site]['age'],
- df[df.site == site][feature])
- )
- print('Age-adjusted memory:')
- display(pg.corr(
- df[df.site == site]['nih_picseq_raw'],
- df[df.site == site][feature])
- )
- print('Raw-memory:')
- display(pg.corr(
- df[df.site == site]['nih_picseq_ageadjusted'],
- df[df.site == site][feature])
- )
- print('\n')
- display(pg.anova(data=df, dv='age', between='site'))
- for site in set(df.site):
- print(site)
- print(f'{df[df.site == site].age.mean():2.1f} ± {df[df.site == site].age.std():2.1f}')
- display(pg.chi2_independence(data=df, x='site', y='sex'))
- # %%
- # Replication across sites.
- for feature in ['post_mm','post_segregation','post_sharpness']:
- print(f'Feature: {feature}')
- for site in set(df.site):
- print(f'{site}:')
- display(pg.corr(
- df[df.site != site]['age'],
- df[df.site != site][feature])
- )
- print('\n')
- for feature in ['post_control_c_OVR']:
- print(f'Feature: {feature}')
- for site in set(df.site):
- print(f'{site}:')
- print('Age:')
- display(pg.corr(
- df[df.site != site]['age'],
- df[df.site != site][feature])
- )
- print('Age-adjusted memory:')
- display(pg.corr(
- df[df.site != site]['nih_picseq_raw'],
- df[df.site != site][feature])
- )
- print('Raw-memory:')
- display(pg.corr(
- df[df.site != site]['nih_picseq_ageadjusted'],
- df[df.site != site][feature])
- )
- print('\n')
- display(pg.anova(data=df, dv='age', between='site'))
- for site in set(df.site):
- print(site)
- print(f'{df[df.site != site].age.mean():2.1f} ± {df[df.site != site].age.std():2.1f}')
- display(pg.chi2_independence(data=df, x='site', y='sex'))
manuscript_analyses.ipynb at commit 5fd2858, no license · at the source
Overview
- McGill University, Department of Neurology and Neurosurgery, McGill University,Montréal, QC Canada
- Department of Statistical Methods, University of Zaragoza, C. de Pedro Cerbuna, 12,Zaragoza, Spain
Abstract
The abstract is not reproduced here: the paper's license (CC BY-NC-ND) does not allow it. Read it in the paper, at the publisher or on Europe PMC.
Repositories
Its files are read in the Code ↔ Paper reader above, with 13 matches between paragraphs and lines of code.
JonahKember/precision_mapping
0062892cd994b7397bed514d90aed83ef1d2602e, 29 January 2026Availability: 1 check, the latest on 27 September 2026: the link answers
- 27 September 2026: the link answers
17 files
- cortex_mapping/
__init__.py , Python, 1 line - cortex_mapping/
data/ , Python, 1 line__init__.py - cortex_mapping/
data/ , Python, 1 lineparcellations/ __init__.py - cortex_mapping/
main.py , Python, 32 lines - cortex_mapping/
mapping.py , Python, 173 lines, 2 matches - feature_extraction/
__init__.py , Python, 1 line - feature_extraction/
clusters.py , Python, 80 lines - feature_extraction/
connectivity.py , Python, 38 lines - feature_extraction/
parcellation_overlap.py , Python, 71 lines - feature_extraction/
pipeline.py , Python, 13 lines - feature_extraction/
sharpness.py , Python, 128 lines, 1 match - feature_extraction/
surface_area.py , Python, 30 lines - feature_extraction/
utils.py , Python, 61 lines - hipp_mapping/
main.py , Python, 32 lines, 1 match - hipp_mapping/
mapping.py , Python, 134 lines, 2 matches - setup.py, Python, 25 lines
- README.md, Text, 41 lines
Zenodo 20086215
Availability: 1 check, the latest on 27 September 2026: the link answers (HTTP 200)
- 27 September 2026: the link answers (HTTP 200)
1 file
- manuscript_analyses.ipyn
b , Jupyter, 414 lines
codeocean:7323987
Availability: 1 check, the latest on 27 September 2026: cannot be verified
- 27 September 2026: cannot be verified
jonahkember/posterior_hippocampus_development
5fd2858ca8979891216f518b45751d4517e037a0, 7 May 2026Availability: 1 check, the latest on 27 September 2026: the link answers
- 27 September 2026: the link answers
1 file
- manuscript_analyses.ipyn
b , Jupyter, 414 lines, 7 matches
Code availability statement
The paper has a code 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 the authors' code: codeocean:7323987, JonahKember/
precision_mapping , Zenodo 20086215
Read it in the paper: doi.org/10.1038/s41467-026-74572-1.
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:
- 4 repositories of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
- 18 scripts, each with its path and the digest of its content;
- 13 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
No dataset and no data link were found in the paper.
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 the authors' code: codeocean:7323987, JonahKember/
precision_mapping , Zenodo 20086215
Read it in the paper: doi.org/10.1038/s41467-026-74572-1.
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 2, 28 September 2026
- Funding: added McGill University; Canada Research Chairs; Canada First Research Excellence Fund; Natural Sciences and Engineering Research Council of Canada: RGPIN 2020, rgpin-2020-05520; Fonds de recherche du Québec – Nature et technologies: 283571
Version 1, 27 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 5 authors, 2 keywords, 11 MeSH terms, 44 references.
Cite
This paper
Kember, J., He, Y., Gracia-Tabuenca, Z., Barnett, A., & Chai, X. J. (2026). The hippocampus becomes topographically and functionally specialized along the longitudinal axis with development. Nature communications, 17(1), 7699. https://
BibTeX
@article{kember2026hippo
author = {Kember, Jonah and He, Ying and Gracia-Tabuenca, Zeus and Barnett, Alexander and Chai, Xiaoqian J.},
title = {{The hippocampus becomes topographically and functionally specialized along the longitudinal axis with development}},
journal = {Nature communications},
year = {2026},
month = jun,
volume = {17},
number = {1},
pages = {7699},
publisher = {Nature Publishing Group},
issn = {2041-1723},
doi = {10.1038/
url = {https://
pmid = {42315845},
pmcid = {PMC13434241}
}
RIS
TY - JOUR
AU - Kember, Jonah
AU - He, Ying
AU - Gracia-Tabuenca, Zeus
AU - Barnett, Alexander
AU - Chai, Xiaoqian J.
TI - The hippocampus becomes topographically and functionally specialized along the longitudinal axis with development
T2 - Nature communications
J2 - Nat Commun
PY - 2026
DA - 2026/
VL - 17
IS - 1
SP - 7699
SN - 2041-1723
PB - Nature Publishing Group
DO - 10.1038/
UR - https://
LA - en
ER -
CSL-JSON
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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:10.1016/j.dcn.2026.101808 [code]
- Development of functional topography of the default mode subnetworks revealed by precision mapping.Journal: Developmental cognitive neuroscienceIn common: Connectome Workbench, NiBabel, scikit-learn, 4 other tools, 7 references
- [2] doi:10.1038/s41467-026-72931-6 [code]
- Three parsimonious spatiotemporal patterns in cerebellum reveal individual traits in function and behavior.Journal: Nature communicationsIn common: Connectome Workbench, NiBabel, seaborn, 5 other tools, fMRI, 5 references
- [3] doi:10.1038/s41467-026-71270-w [code]
- Spatiotemporal dynamics of the human cortical functional hierarchy across the lifespan.Journal: Nature communicationsIn common: Connectome Workbench, NiBabel, seaborn, 5 other tools, developmental, fMRI, 4 references
- [4] doi:10.1093/psyrad/kkag013 [code]
- Convergent and divergent spatial topographies of individualized brain functional networks and their developmental origins.Journal: PsychoradiologyIn common: Connectome Workbench, scikit-learn, SciPy, 1 other tool, developmental, fMRI, 6 references
- [5] doi:10.1038/s41467-026-73668-y [code]
- Convergent and divergent brain-cognition development in early adolescence.Journal: Nature communicationsIn common: Connectome Workbench, NiBabel, seaborn, 5 other tools, fMRI, 3 references
- [6] doi:10.1162/imag.a.1262 [code]
- Frame-wise multi-echo distortion correction for superior functional MRI.Journal: Imaging neuroscience (Cambridge, Mass.)In common: Connectome Workbench, NiBabel, seaborn, 4 other tools, fMRI, 3 references
- [7] doi:10.1038/s41398-026-04025-2 [code]
- Brain energetic landscapes shape state dysregulation in major depressive disorder: a morphological network controllability perspective.Journal: Translational psychiatryIn common: Connectome Workbench, Pingouin, NiBabel, 6 other tools, 2 references
- [8] doi:10.1162/imag.a.1222 [code]
- Network-based near-scalp personalized brain stimulation targets.Journal: Imaging neuroscience (Cambridge, Mass.)In common: Connectome Workbench, NiBabel, scikit-learn, 3 other tools, 5 references
- [9] doi:10.1371/journal.pbio.3003684 [code]
- The retrieval of previously learned motor memories is facilitated by the reinstatement of default mode network manifold structures.Journal: PLoS biologyIn common: Pingouin, NiBabel, seaborn, 5 other tools, fMRI, 3 references
- [10] doi:10.21203/rs.3.rs-9326213/v1 [code]
- Multi-task fMRI outperforms resting-state fMRI for revealing task-invariant organization of the human brainJournal: Research Square (preprint)In common: Connectome Workbench, NiBabel, seaborn, 5 other tools, fMRI, 3 references
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