Mouse white matter matters: cortical origins and spatial organization of mouse white matter tracts.
The 5 matches
- [1] § Materials and methods ↔ Projection_Density_Filtered_AllenSDK_Pipeline.ipynb, lines 257 to 291 · score 1.00 · SSP tr, SSP un, SSp bfd, SSp ul, AUDpo, ORBvl · Report a mismatch
- [2] § Materials and methods ↔ AllenSDK_Pipeline.ipynb, lines 107 to 135 · score 1.00 · SSP tr, SSP un, SSp bfd, SSp ul, AUDpo, ORBvl · Report a mismatch
- [3] § Results ↔ Projection_Density_Filtered_AllenSDK_Pipeline.ipynb, lines 257 to 291 · score 0.99 · SSp ll, SSp bfd, SSp tr, SSp ul, SSp un, AUDpo · Report a mismatch
- [4] § Results ↔ AllenSDK_Pipeline.ipynb, lines 107 to 135 · score 0.99 · SSp ll, SSp bfd, SSp tr, SSp ul, SSp un, AUDpo · Report a mismatch
- [5] § Materials and methods ↔ Projection_Density_Filtered_AllenSDK_Pipeline.ipynb, lines 61 to 106 · score 0.89 · projection signal, weighted center, injection centroids, projection densities, injection density, mass · Report a mismatch
Paper
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The authors' code
Jupyter notebook · 572 lines · 19 KB · no license · 3 matches
- # %%
- # imports
- import numpy as np
- import pandas as pd
- import matplotlib.pyplot as plt
- from allensdk.core.mouse_connectivity_cache import MouseConnectivityCache
- from mpl_toolkits.mplot3d import Axes3D
- from sklearn.linear_model import LinearRegression
- from scipy.stats import linregress
- import statsmodels.api as sm
- from tqdm import tqdm
- import time
- from matplotlib.patches import Patch
- # %%
- # config
- voxel_size_um = 25 # um per voxel 25um
- min_mean_bundle_density = 1e-4
- # structures
- isocortex_id = 315
- bundle_ids = [884] # replace with any fiber tract ids
- # hemisphere: right, left, or None
- hemisphere = "right"
- # cache and structure tree from allensdk
- mcc = MouseConnectivityCache()
- st = mcc.get_structure_tree()
- # %%
- # experiments
- print("loading isocortex non-cre injection experiments")
- exps = mcc.get_experiments(cre=False, injection_structure_ids=[isocortex_id])
- experiment_ids = [e["id"] for e in exps]
- print(f"using {len(experiment_ids)} isocortex experiments")
- # %%
- # build bundle mask
- mask_union = None
- for sid in bundle_ids:
- m, _ = mcc.get_structure_mask(sid)
- mask_union = m.astype(bool) if mask_union is None else (mask_union | m.astype(bool))
- if mask_union is None:
- raise RuntimeError("no structure masks were built (check bundle_ids).")
- # restrict to one hemisphere
- if hemisphere in ("right", "left"):
- mid = mask_union.shape[2] // 2
- if hemisphere == "right":
- mask_union[:, :, :mid] = False
- else:
- mask_union[:, :, mid:] = False
- # precompute voxel indices
- mx, my, mz = np.where(mask_union)
- mask_index_tuple = (mx, my, mz)
- print(f"mask ready: {mx.size:,} voxels ({hemisphere or 'both'} hemisphere)")
- # %%
- # HELPERS
- # density volumes are 3d arrays where each allensdk voxel stores the fraction of the
- # voxel filled by signal. Density values are between 0 and 1
- # as written in the allen dev docs:
- # projection density= sum of detected projection pixels / sum of all pixels in voxel
- # injection_density= density of detected projection pixels within the
- # manually annotated injection site
- # this gets the projection crossing coordinates within mask using density values
- def weighted_centroid_from_density(density_vol, idx_tuple, voxel_size_um):
- w = density_vol[idx_tuple] # get projection density values inside your mask
- pos = w > 0 # keep only voxels with nonzero density
- if not np.any(pos): # if no signal at all, return None
- return None
- x = idx_tuple[0][pos] # x voxel indices of nonzero voxels
- y = idx_tuple[1][pos] # y voxel indices
- z = idx_tuple[2][pos] # z voxel indices
- w = w[pos].astype(np.float32) # weights = projection density values
- # weighted average voxel index + converted to um
- vx = float(np.average(x, weights=w)) * voxel_size_um
- vy = float(np.average(y, weights=w)) * voxel_size_um
- vz = float(np.average(z, weights=w)) * voxel_size_um
- return vx, vy, vz
- #finds the center of mass of the projection signal within wm mask
- # weights projection densities so that brighter voxels influence the centroid more
- # this gets the injection site centroid based on all nonzero voxels in injection volume
- def weighted_centroid_from_binary(density_vol, voxel_size_um):
- pos = density_vol > 0 # find voxels with injection signal
- if not np.any(pos): # if no injection voxels, return None
- return None
- x, y, z = np.where(pos) # voxel coordinates of injection
- w = density_vol[pos].astype(np.float32) # injection densities as weights
- # weighted centroid
- vx = float(np.average(x, weights=w)) * voxel_size_um
- vy = float(np.average(y, weights=w)) * voxel_size_um
- vz = float(np.average(z, weights=w)) * voxel_size_um
- return vx, vy, vz
- # finds the weighted center of the injection site
- # weighs injection densitites so that denser parts of the injection count more
- # outputs injection centroid
- # %%
- # main loop
- inj_x, inj_y, inj_z = {}, {}, {}
- proj_x, proj_y, proj_z = {}, {}, {}
- t0 = time.time()
- for eid in tqdm(experiment_ids, desc="processing experiments"):
- try:
- proj_vol, _ = mcc.get_projection_density(eid) # 3d projection density volume
- inj_vol, _ = mcc.get_injection_density(eid) # 3d injection density volume
- # projection densities inside WM mask (after hemisphere filtering)
- wm_densities = proj_vol[mask_index_tuple].astype(np.float32)
- # drop NaNs
- wm_densities = wm_densities[~np.isnan(wm_densities)]
- # skip if no valid voxels in the bundle
- if wm_densities.size == 0:
- continue
- # mean projection density through the WM structure
- bundle_mean = float(np.mean(wm_densities))
- # filter: require mean density >= threshold
- if bundle_mean < min_mean_bundle_density:
- continue
- # centroids only for experiments that passed the filter
- proj_centroid = weighted_centroid_from_density(
- proj_vol, mask_index_tuple, voxel_size_um
- )
- if proj_centroid is None:
- continue
- px, py, pz = proj_centroid
- proj_x[eid], proj_y[eid], proj_z[eid] = px, py, pz
- inj_centroid = weighted_centroid_from_binary(inj_vol, voxel_size_um)
- if inj_centroid is None:
- continue
- ix, iy, iz = inj_centroid
- inj_x[eid], inj_y[eid], inj_z[eid] = ix, iy, iz
- except Exception as e:
- print(f"{eid}: {e}")
- elapsed = time.time() - t0
- print(f"\n total processing time: {elapsed:.2f} s")
- # how many experiments were kept?
- kept_ids = sorted(proj_x.keys())
- print(f"kept {len(kept_ids)} / {len(experiment_ids)} experiments "
- f"(mean WM density ≥ {min_mean_bundle_density})")
- print("first few kept IDs + means:")
- for eid in kept_ids[:10]:
- # recompute just for display
- proj_vol, _ = mcc.get_projection_density(eid)
- wm = proj_vol[mask_index_tuple].astype(np.float32)
- wm = wm[~np.isnan(wm)]
- print(eid, np.mean(wm))
- # %%
- # dataframe + correlation
- common_ids = sorted(set(inj_x) & set(proj_x))
- df = pd.DataFrame({
- "injection_x": [inj_x[e] for e in common_ids],
- "injection_y": [inj_y[e] for e in common_ids],
- "injection_z": [inj_z[e] for e in common_ids],
- "projection_x": [proj_x[e] for e in common_ids],
- "projection_y": [proj_y[e] for e in common_ids],
- "projection_z": [proj_z[e] for e in common_ids],
- }, index=common_ids)
- print(f"final n = {len(df)} rows")
- print("\ncorrelation matrix (injection → projection):")
- print(df.corr(numeric_only=True))
- # %%
- import pandas as pd
- import numpy as np
- from statsmodels.stats.outliers_influence import variance_inflation_factor
- def compute_vif(df, predictors):
- X = df[predictors].dropna().astype(float).values
- X_ = np.column_stack([np.ones(X.shape[0]), X])
- vif_vals = [variance_inflation_factor(X_, i) for i in range(1, X_.shape[1])]
- vif_table = pd.DataFrame({
- "predictor": predictors,
- "VIF": vif_vals
- })
- def interpret(v):
- if v < 2:
- return "low collinearity"
- elif v < 5:
- return "moderate collinearity"
- elif v < 10:
- return "high collinearity"
- else:
- return "severe collinearity"
- vif_table["interpretation"] = vif_table["VIF"].apply(interpret)
- return vif_table
- predictors = ['injection_x','injection_y','injection_z']
- vif_table = compute_vif(df, predictors)
- print(vif_table)
- # %%
- # Lasso regression
- # %%
- # attach region labels to df using experiment injection structure acronyms
- # build: exp_id to injection structure acronym
- exp_struct_acro = {}
- for e in exps:
- try:
- s = st.get_structures_by_id([e['structure_id']])[0]
- exp_struct_acro[e['id']] = s['acronym']
- except Exception:
- pass
- # keep only rows present in df.index
- df_regions = df.copy()
- df_regions['region'] = [get_region_group(exp_struct_acro.get(eid, None)) for eid in df_regions.index]
- df_regions = df_regions[df_regions['region'].notna()]
- print(f"region-labeled n = {len(df_regions)} (dropped unlabeled)")
- # %%
- # modeling helpers
- predictor_cols = ['injection_x', 'injection_y', 'injection_z']
- axis_map = {'x': 'projection_x', 'y': 'projection_y', 'z': 'projection_z'}
- axis_label = {'x': 'A-P', 'y': 'D-V', 'z': 'M-L'}
- def fit_models(df_in: pd.DataFrame):
- x = sm.add_constant(df_in[predictor_cols])
- models = {}
- for ax, ycol in axis_map.items():
- y = df_in[ycol]
- models[ax] = sm.OLS(y, x).fit()
- return models
- models = fit_models(df_regions)
- # %%
- print("Experiments with NaN projection centroids:",
- sum(np.isnan(list(proj_x.values()))))
- print("Experiments used in regression dataframe:", len(df))
- # %%
- # Color palette
- region_colors = {
- 'Prefrontal': {'acronyms': {'ACAd','ACAv','FRP','ILA','ORBl','ORBvl','PL'},
- 'color': [0.97, 0.83, 0.34]},
- 'Insula': {'acronyms': {'AId','GU','VISC'},
- 'color': [1.00, 0.62, 0.23]},
- 'Motor': {'acronyms': {'MOp','MOs'},
- 'color': [0.40, 0.76, 0.40]},
- 'Somatosensory': {'acronyms': {'SSp-bfd','SSp-ll','SSp-m','SSp-n','SSp-tr','SSp-ul','SSp-un','SSs'},
- 'color': [0.85, 0.19, 0.20]},
- 'Temporal': {'acronyms': {'ECT','AUDd','AUDp','AUDpo','AUDv'},
- 'color': [1.00, 0.45, 0.71]},
- 'Retrosplenial': {'acronyms': {'RSPagl','RSPd','RSPv'},
- 'color': [0.78, 0.00, 1.00]},
- 'Visual': {'acronyms': {'VISp','VISal','VISam','VISl','VISpm','VISpor','VISpl','VISli'},
- 'color': [0.00, 0.55, 1.00]}
- }
- legend_order = ["Prefrontal", "Insula", "Motor",
- "Somatosensory", "Temporal", "Retrosplenial", "Visual"]
- # Convert RGB to hex
- def rgb_to_hex(rgb):
- r, g, b = (int(255*c) for c in rgb)
- return f"#{r:02x}{g:02x}{b:02x}"
- group_color_hex = {k: rgb_to_hex(v['color']) for k, v in region_colors.items()}
- # Helper to get region group by acronym
- def get_region_group(acronym: str):
- for group, props in region_colors.items():
- if acronym in props['acronyms']:
- return group
- return None
- # %%
- # lasso imports
- import numpy as np
- import matplotlib.pyplot as plt
- from sklearn.preprocessing import StandardScaler
- from sklearn.linear_model import LassoCV
- from sklearn.metrics import r2_score
- from matplotlib.patches import Patch
- # %%
- # axis labels and column mappings
- axis_label = {'x': 'A-P', 'y': 'D-V', 'z': 'M-L'}
- predictors = [
- 'injection_x',
- 'injection_y',
- 'injection_z'
- ]
- axis_to_ycol = {
- 'x': 'projection_x',
- 'y': 'projection_y',
- 'z': 'projection_z'
- }
- # %%
- def fit_lasso_models(df, axes=('x', 'y', 'z'), cv=5, alphas=None, random_state=0):
- """
- Fit one LassoCV model per projection axis on standardized predictors.
- Returns:
- dict: axis {
- 'scaler': StandardScaler,
- 'model': LassoCV,
- 'index': DataFrame index used for fitting
- }
- """
- models = {}
- for ax in axes:
- cols = predictors + [axis_to_ycol[ax]]
- sub = df.dropna(subset=cols).copy()
- X = sub[predictors].to_numpy(float)
- y = sub[axis_to_ycol[ax]].to_numpy(float)
- scaler = StandardScaler()
- Xz = scaler.fit_transform(X)
- lcv = LassoCV(
- cv=cv,
- alphas=alphas,
- random_state=random_state,
- max_iter=10000
- )
- lcv.fit(Xz, y)
- models[ax] = {
- 'scaler': scaler,
- 'model': lcv,
- 'index': sub.index
- }
- return models
- # %%
- def plot_axis_summary_lasso(
- models,
- df_regions,
- group_color_hex,
- legend_order,
- axis_key='x'
- ):
- """
- Two-panel summary for a single axis using LassoCV.
- Left:
- Predicted vs actual projection coordinate, colored by region.
- Right:
- Lasso coefficients (betas) on standardized predictors.
- Title reports R squared and chosen alpha.
- """
- assert axis_key in ('x', 'y', 'z')
- pack = models[axis_key]
- scaler = pack['scaler']
- lcv = pack['model']
- # align rows used by the model
- idx = pack['index']
- X = df_regions.loc[idx, predictors].to_numpy(float)
- y = df_regions.loc[idx, axis_to_ycol[axis_key]].to_numpy(float)
- Xz = scaler.transform(X)
- y_pred = lcv.predict(Xz)
- fig, (ax_scatter, ax_bar) = plt.subplots(
- nrows=1,
- ncols=2,
- figsize=(12, 5),
- gridspec_kw={'width_ratios': [1.25, 1]}
- )
- # predicted vs actual
- for region in legend_order:
- if region not in group_color_hex:
- continue
- mask = (df_regions.loc[idx, 'region'] == region).to_numpy()
- if not np.any(mask):
- continue
- ax_scatter.scatter(
- y_pred[mask],
- y[mask],
- s=70,
- edgecolor='black',
- alpha=0.85,
- color=group_color_hex[region],
- label=region
- )
- lo = float(min(y.min(), y_pred.min()))
- hi = float(max(y.max(), y_pred.max()))
- ax_scatter.plot([lo, hi], [lo, hi], 'r--', lw=2)
- pretty = axis_label[axis_key]
- r2 = r2_score(y, y_pred)
- ax_scatter.set_xlabel(f"Predicted {pretty} Projection (µm)")
- ax_scatter.set_ylabel(f"Actual {pretty} Projection (µm)")
- ax_scatter.set_title(f"{pretty} Prediction (LassoCV: R²={r2:.3f}, α={lcv.alpha_:.3g})")
- ax_scatter.grid(True, linestyle='--', alpha=0.6)
- # RIGHT: beta bars (standardized-X coefficients)
- coef = lcv.coef_ # corresponds to predictors after standardization
- label_map = {
- 'injection_x': 'A-P Injection Coordinate',
- 'injection_y': 'D-V Injection Coordinate',
- 'injection_z': 'M-L Injection Coordinate'
- }
- labels = [label_map[p] for p in predictors]
- bars = ax_bar.bar(labels, coef, color='skyblue', edgecolor='black')
- # annotate zeros and values
- rng = (max(coef.max(), 0) - min(coef.min(), 0)) or 1.0
- for b, v in zip(bars, coef):
- ytxt = (b.get_height() + 0.05*rng) if v >= 0 else (b.get_height() - 0.05*rng)
- va = 'bottom' if v >= 0 else 'top'
- ax_bar.text(b.get_x()+b.get_width()/2, ytxt, f"{v:.3f}", ha='center', va=va, fontsize=10)
- ax_bar.axhline(0, color='gray', linestyle='--', linewidth=1)
- ax_bar.set_ylabel("Lasso coefficient (β) on standardized predictors")
- ax_bar.set_title(f"Influence of Injection Coordinates\non {pretty} Projection")
- ax_bar.grid(True, axis='y', linestyle='--', alpha=0.6)
- ax_bar.tick_params(axis='x', labelrotation=20)
- plt.tight_layout()
- plt.show()
- # %%
- # fit lasso models
- lasso_models = fit_lasso_models(df_regions, cv=5)
- # plot
- plot_axis_summary_lasso(lasso_models, df_regions, group_color_hex, legend_order, axis_key='x') # A-P
- plot_axis_summary_lasso(lasso_models, df_regions, group_color_hex, legend_order, axis_key='y') # D-V
- plot_axis_summary_lasso(lasso_models, df_regions, group_color_hex, legend_order, axis_key='z') # M-L
- # %%
- # partial regression plots
- # %%
- # labels and columns
- axis_label = {'x': 'A-P', 'y': 'D-V', 'z': 'M-L'}
- predictors = ['injection_x', 'injection_y', 'injection_z']
- axis_to_ycol = {'x': 'projection_x', 'y': 'projection_y', 'z': 'projection_z'}
- def _residualize(y, X):
- """Return residuals of OLS: y ~ X (with constant)."""
- Xc = sm.add_constant(X, has_constant='add')
- model = sm.OLS(y, Xc, missing='drop').fit()
- return model.resid, model
- def partial_regression_plots(
- df_regions,
- axis_key='x',
- group_color_hex=None,
- legend_order=None,
- point_size=70,
- alpha=0.85,
- show=True
- ):
- """
- Added-variable plots for a chosen projection axis.
- Rows used: non-NA on projection axis + all three predictors.
- Returns (fig, axes, full_model) where full_model is OLS on all 3 predictors.
- """
- assert axis_key in ('x','y','z')
- ycol = axis_to_ycol[axis_key]
- # rows with complete data
- needed = predictors + [ycol]
- d = df_regions.dropna(subset=needed).copy()
- # Fit the full OLS once (y ~ X,Y,Z) for reference
- X_full = sm.add_constant(d[predictors], has_constant='add')
- full_model = sm.OLS(d[ycol], X_full).fit()
- # figure: one subplot per predictor
- fig, axes = plt.subplots(1, 3, figsize=(16, 4.8), sharey=False)
- fig.suptitle(f"Partial regression (added-variable) plots for {axis_label[axis_key]} projection", y=1.02)
- for ax, pred in zip(axes, predictors):
- others = [p for p in predictors if p != pred]
- # residualize outcome on "others", and predictor on "others"
- y_res, _ = _residualize(d[ycol].to_numpy(float), d[others].to_numpy(float))
- x_res, _ = _residualize(d[pred].to_numpy(float), d[others].to_numpy(float))
- # quick simple regression on residuals -> partial slope & p-value
- lr = linregress(x_res, y_res)
- slope, intercept, r_val, p_val = lr.slope, lr.intercept, lr.rvalue, lr.pvalue
- # scatter (by region if provided)
- if group_color_hex and 'region' in d.columns and legend_order:
- for region in legend_order:
- if region not in group_color_hex:
- continue
- m = (d['region'] == region).to_numpy()
- if not np.any(m):
- continue
- ax.scatter(
- x_res[m], y_res[m],
- s=point_size, alpha=alpha,
- color=group_color_hex[region],
- edgecolor='black', linewidths=0.5
- )
- else:
- ax.scatter(x_res, y_res, s=point_size, alpha=alpha,
- color='#4c78a8', edgecolor='black', linewidths=0.5)
- # regression line on residuals
- xx = np.linspace(x_res.min(), x_res.max(), 100)
- ax.plot(xx, intercept + slope*xx, 'r--', lw=2)
- # labels and title with stats
- nice_pred = {
- 'injection_x': 'A-P injection',
- 'injection_y': 'D-V injection',
- 'injection_z': 'M-L injection'
- }[pred]
- ax.set_xlabel(f"{nice_pred} residual (µm)")
- ax.set_ylabel(f"{axis_label[axis_key]} projection residual (µm)")
- beta_full = full_model.params[pred] # equals slope on residuals
- ax.set_title(f"{nice_pred} | others\nβ={beta_full:.3f}, R²={r_val**2:.2f}, p={p_val:.2e}")
- ax.grid(True, linestyle='--', alpha=0.5)
- # shared legend (if region colors provided)
- if group_color_hex and legend_order:
- handles = [Patch(facecolor=group_color_hex[r], edgecolor='black', label=r)
- for r in legend_order if r in group_color_hex]
- fig.legend(handles=handles, title='region', bbox_to_anchor=(1.01, 0.5), loc='center left')
- plt.tight_layout(rect=[0, 0, 0.95, 1])
- if show:
- plt.show()
- return fig, axes, full_model
- # %%
- # plot
- fig, axes, full_ap = partial_regression_plots(
- df_regions,
- axis_key='x',
- group_color_hex=group_color_hex,
- legend_order=legend_order
- )
- partial_regression_plots(df_regions, axis_key='y', group_color_hex=group_color_hex, legend_order=legend_order)
- partial_regression_plots(df_regions, axis_key='z', group_color_hex=group_color_hex, legend_order=legend_order)
Projection_Density_Filtered_AllenSDK_Pipeline.ipynb at commit dfcdc36, no license · at the source
Overview
- Program in Neuroscience, Rice University,77005 Houston, TX USA
- Department of Neurosurgery, Baylor College of Medicine,S836, 1 Baylor Plaza, TX Houston, 77030 USA
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.
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sdg5-create/MouseWMMatters
dfcdc365e212e93131236e7c300e3393998791c0, 29 December 2025Availability: 1 check, the latest on 30 September 2026: the link answers
- 30 September 2026: the link answers
4 files
- AllenSDK_Pipeline.ipynb, Jupyter, 578 lines, 2 matches
- Experiment_Info.ipynb, Jupyter, 128 lines
- Projection_Density_Filte
red_AllenSDK_Pipeline.ip , Jupyter, 572 lines, 3 matchesynb - WholeBrain_Figs.ipynb, Jupyter, 96 lines
The paper's code and data availability statement is in the Data section.
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Its JSON (tracing-map.json) is deposited on Zenodo with its DOI once the map is validated.
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- it points to the authors' code: sdg5-create/
MouseWMMatters
Read it in the paper: doi.org/10.1007/s00429-026-03101-z.
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Version 1, 30 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 3 authors, 5 keywords, 8 MeSH terms, 2 funders, 60 references.
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This paper
Gordeev, S. D., Franch, M., & Heilbronner, S. R. (2026). Mouse white matter matters: cortical origins and spatial organization of mouse white matter tracts. Brain structure & function, 231(3), 46. https://
BibTeX
@article{gordeev2026mous
author = {Gordeev, Sofia D. and Franch, Melissa and Heilbronner, Sarah R.},
title = {{Mouse white matter matters: cortical origins and spatial organization of mouse white matter tracts}},
journal = {Brain structure \& function},
year = {2026},
month = mar,
volume = {231},
number = {3},
pages = {46},
publisher = {Springer Science+Business Media},
issn = {1863-2653},
doi = {10.1007/
url = {https://
pmid = {41893879},
pmcid = {PMC13031187}
}
RIS
TY - JOUR
AU - Gordeev, Sofia D.
AU - Franch, Melissa
AU - Heilbronner, Sarah R.
TI - Mouse white matter matters: cortical origins and spatial organization of mouse white matter tracts
T2 - Brain structure & function
J2 - Brain Struct Funct
PY - 2026
DA - 2026/
VL - 231
IS - 3
SP - 46
SN - 1863-2653
PB - Springer Science+Business Media
DO - 10.1007/
UR - https://
LA - en
ER -
CSL-JSON
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"given": "Sofia D."
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"given": "Melissa"
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{
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"container-title-short":
"volume": "231",
"issue": "3",
"page": "46",
"DOI": "10.1007/
"PMID": "41893879",
"PMCID": "PMC13031187",
"ISSN": "1863-2653",
"publisher": "Springer Science+Business Media",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
3,
27
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]
}
}
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