Genoarchitecture and input-output organization of the mouse basal ganglia and thalamic parafascicular nucleus.
The 17 matches
- [1] § Methods › ScRNA-seq of the basal ganglia and thalamic PF nucleus ↔ scripts/make_fineres_hist_ai21_cpq.py, lines 76–122 · score 1.00 · LDT PCG CS, Gata3 Lhx1 Gaba, NDB SI MA, STRv Lhx8 Gaba, ZI Pax6 Gaba, STN PSTN Pitx2
- [2] § Results › Diverse spatial patterns of t-types in the basal ganglia and PF nucleus ↔ scripts/make_fineres_hist_ai21_cpq.py, lines 76–122 · score 1.00 · NDB SI MA, STRv Lhx8 Gaba, ZI Pax6 Gaba, STN PSTN Pitx2, GPi Tbr1 Cngb3, GPe SI Sox6
- [3] § Results › Delineation of subdivisions of the basal ganglia and PF nucleus ↔ scripts/Fig2.py, lines 19–49 · score 0.76 · CPiv, CPvm, CPdm, Astn2, Calb2, Fos
- [4] § Results › Diverse spatial patterns of t-types in the basal ganglia and PF nucleus ↔ scripts/make_fineres_hist_ai21_cpq.py, lines 174–261 · score 0.70 · D1 Sema5a Gaba, D2 Gaba, subclasses, MERFISH, CP
- [5] § Results › Diverse spatial patterns of t-types in the basal ganglia and PF nucleus ↔ scripts/spatial_pattern_figures.ipynb, lines 356–368 · score 0.69 · patchy lateral, anterior medial, anterior lateral, central medial, CP
- [6] § Methods › Quantification of anterograde projections ↔ scripts/Fig3b_projection_summary_stats_multicore.py, lines 79–132 · score 0.64 · image volumes, anterograde projections, Projection density, hemisphere, contralateral, ipsilateral
- [7] § Methods › Quantification of single-neuron projections ↔ scripts/swc_plot_terminals.ipynb, lines 24–102 · score 0.62 · leaf nodes, graph tree, SWC, terminals, neuron
- [8] § Methods › Curation of fully reconstructed single neurons ↔ scripts/_old/swc_plot_projection_bymodule.py, lines 64–68 · score 0.61 · ORBvl, ORBm, ORBl, ACAv, ILA, ACAd
- [9] § Results › Delineation of subdivisions of the basal ganglia and PF nucleus ↔ scripts/_old/plot_subcortical_overlap_heatmap.py, lines 97–129 · score 0.59 · Dice coefficients, CPiv, CPdm, injection site, overlap, CPp
- [10] § Methods › Flatmap of the isocortex ↔ scripts/Fig3d_cortex_flatmap.py, lines 1–13 · score 0.59 · anterograde injections, soma locations, flatmap, cortex, retrogradely, cortical
- [11] § Methods › Quantification of anterograde projections ↔ scripts/Fig3g_anterograde_overlap.py, lines 122–141 · score 0.58 · injected hemisphere, anterograde projections, quantify, masked, volumes, injections
- [12] § Results › Cortical cell-type-specific, single-neuron projections in the subdivisions of the basal ganglia ↔ scripts/Fig2.py, lines 19–49 · score 0.55 · CPiv, CPvm, CPdm, Aggregated, flipped, CPp
- [13] § Methods › MERFISH data and its registration to CCFv3 ↔ scripts/spatial_pattern_figures.ipynb, lines 356–368 · score 0.53 · anterior lateral, central medial, patchy, CP
- [14] § Results › Cortical and subcortical module-specific and cell-type-specific projections in the basal ganglia and PF nucleus ↔ scripts/Fig5_plot_retrograde.py, lines 198–220 · score 0.52 · CPiv, CPvm, CPdm, ipsilateral, CPp, CPl
- [15] § Results › Delineation of subdivisions of the basal ganglia and PF nucleus ↔ scripts/Fig4b_swc_projection_densities.py, lines 1–37 · score 0.52 · CPiv, CPvm, CPdm, density, layers, CPp
- [16] § Results › Whole-brain presynaptic inputs to different neuronal types and subdivisions of the CP ↔ scripts/Fig4_plot_swc_heatmap.py, lines 38–59 · score 0.52 · CPiv, CPvm, CPdm, Contralateral, ipsilateral, CPp
- [17] § Results › Whole-brain presynaptic inputs to different neuronal types and subdivisions of the CP ↔ scripts/Fig5_plot_retrograde.py, lines 198–220 · score 0.52 · CPiv, CPvm, CPdm, Contralateral, ipsilateral, CPp
Paper
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The authors' code
Python · 267 lines · 8.4 KB · BSD-2-Clause · 3 matches
- import h5py
- import os
- import numpy as np
- import pandas as pd
- import argschema as ags
- class MakeHistogramsForNmfParameters(ags.ArgSchema):
- structure = ags.fields.String()
- brain = ags.fields.String()
- normalize_option = ags.fields.String(default="max")
- output_file = ags.fields.OutputFile()
- MERFISH_CPQ = {
- "609882": "/path/to/mouse_609882/cirro_folder/atlas_brain_609882_AIT21.0_mouse.cpq/",
- "609889": "/path/to/mouse_609889/cirro_folder/atlas_brain_609889_AIT21.0_mouse.cpq/",
- "638850": "/path/to/mouse_638850/cirro_folder/atlas_brain_609889_AIT21.0_mouse.cpq/",
- }
- BRAIN_GRIDS = {
- "609882": {
- "x_borders": np.array([-100000, -89000, -77500, -66500, -56000, -44500, -33500, -22500, -11500, -500, 10500, 21500]),
- "y_borders": np.array([50000, 60000, 68000, 75500, 84000, 92000, 99750, 108000]),
- },
- "609889": {
- "x_borders": np.array([-100000, -89000, -77500, -66500, -56000, -44500, -33500, -22500, -11500, -500, 10500, 21500]),
- "y_borders": np.array([50000, 60000, 68000, 75500, 84000, 92000, 99750, 108000]),
- },
- "638850": {
- "x_borders": np.array([-100000, -89000, -77500, -66500, -56000, -44500, -33500, -22500, -11500, -500, 10500, 21500]) + 99000,
- "y_borders": np.array([50000, 60000, 68000, 75500, 84000, 92000, 99750, 108000]) - 48000,
- }
- }
- BIN_STEP = {
- "str-msn": 100,
- "str-int": 100,
- "gpe": 100,
- "gpi": 100,
- "stn": 50,
- "snr": 100,
- "pf": 50,
- "cp": 100,
- "vstr_ot": 100,
- }
- MIN_N_PER_TTYPE = {
- "str-msn": 1000,
- "str-int": 1000,
- "gpe": 50,
- "gpi": 50,
- "stn": 40,
- "snr": 40,
- "pf": 40,
- "cp": 50,
- "vstr_ot": 50,
- }
- STRUCT_BY_TYPES = {
- "cp": [
- "0990 STR D1 Sema5a Gaba_1",
- "0991 STR D1 Sema5a Gaba_1",
- "0950 STR D1 Gaba_3",
- "0951 STR D1 Gaba_3",
- "0952 STR D1 Gaba_3",
- "0953 STR D1 Gaba_4",
- "0954 STR D1 Gaba_4",
- "0955 STR D1 Gaba_5",
- "0956 STR D1 Gaba_5",
- "0957 STR D1 Gaba_5",
- "0960 STR D1 Gaba_7",
- "0961 STR D1 Gaba_8",
- "0966 STR D2 Gaba_1",
- "0968 STR D2 Gaba_1",
- "0970 STR D2 Gaba_1",
- "0971 STR D2 Gaba_1",
- "0972 STR D2 Gaba_2",
- "0979 STR D2 Gaba_4",
- "0980 STR D2 Gaba_4",
- "0981 STR D2 Gaba_4",
- "0982 STR D2 Gaba_4",
- "0983 STR D2 Gaba_5",
- "0987 STR D2 Gaba_6",
- "0988 STR D2 Gaba_6",
- ]
- }
- STRUCT_SUBCLASSES = {
- "str-msn": [
- 'OT D3 Folh1 Gaba',
- 'STR D1 Gaba',
- 'STR D2 Gaba',
- 'STR D1 Sema5a Gaba',
- 'STR-PAL Chst9 Gaba',
- ],
- "str-int": [
- ],
- "gpe": [
- 'NDB-SI-MA-STRv Lhx8 Gaba',
- 'GPe-SI Sox6 Cyp26b1 Gaba',
- 'PAL-STR Gaba-Chol'
- ],
- "gpi": [
- 'GPi Tbr1 Cngb3 Gaba-Glut',
- 'ZI Pax6 Gaba',
- ],
- "stn": [
- 'STN-PSTN Pitx2 Glut',
- ],
- "snr": [
- 'SNr-VTA Pax5 Npas1 Gaba',
- 'SNr Six3 Gaba',
- 'LDT-PCG-CS Gata3 Lhx1 Gaba',
- ],
- "pf": [
- 'PF Fzd5 Glut',
- ]
- }
- def find_tight_borders(spatial_xy, x_borders, y_borders,
- tightness_factor=0.2, min_slice_n=250):
- tight_borders = []
- select_x = spatial_xy[:, 0]
- select_y = spatial_xy[:, 1]
- counter = 0
- for xleft, xright in zip(x_borders[:-1], x_borders[1:]):
- for ybottom, ytop in zip(y_borders[:-1], y_borders[1:]):
- in_slice_mask = ((select_x >= xleft) & (select_x < xright) & (select_y >= ybottom) & (select_y < ytop))
- ncells = np.sum(in_slice_mask)
- if ncells >= min_slice_n:
- tight_borders.append((
- np.percentile(select_x[in_slice_mask], tightness_factor),
- np.percentile(select_x[in_slice_mask], 100 - tightness_factor),
- np.percentile(select_y[in_slice_mask], tightness_factor),
- np.percentile(select_y[in_slice_mask], 100 - tightness_factor),
- ))
- counter +=1
- return tight_borders
- def create_histograms(spatial_xy, tight_borders, bin_step, types_in_list,
- cluster_labels):
- hist_by_type = {}
- for ttype in types_in_list:
- ttype_mask = cluster_labels.value == ttype
- hist_list = []
- for tb in tight_borders:
- x_edges = np.arange(tb[0], tb[1] + bin_step, bin_step)
- y_edges = np.arange(tb[2], tb[3] + bin_step, bin_step)
- hist = np.histogram2d(spatial_xy[ttype_mask, 0], spatial_xy[ttype_mask, 1],
- bins=(x_edges, y_edges),
- )
- my_hist = hist[0]
- hist_list.append(my_hist)
- hist_concat = np.hstack([h.flatten() for h in hist_list])
- # # Save to a dictionary using the t-type names as keys
- hist_by_type[ttype] = hist_concat
- return hist_by_type
- def bin_coordinates(spatial_xy, ccf_xyz, tight_borders, bin_step):
- pass
- def main(args):
- struct_key = args['structure']
- brain_name = args['brain']
- print(f"Creating histograms for structure {struct_key} with brain {brain_name}")
- data_dir = MERFISH_CPQ[brain_name]
- cluster_labels = pd.read_parquet(os.path.join(data_dir, "obs/cluster_label.parquet"))
- subclass_labels = pd.read_parquet(os.path.join(data_dir, "obs/subclass_label.parquet"))
- # Find the cells in the desired subclasses
- if struct_key in STRUCT_BY_TYPES:
- types_in_list = STRUCT_BY_TYPES[struct_key]
- mask = cluster_labels.value.isin(types_in_list)
- elif struct_key in STRUCT_SUBCLASSES:
- subclass_list = STRUCT_SUBCLASSES[struct_key]
- mask = subclass_labels.value.isin(subclass_list)
- types_in_list = np.unique(cluster_labels.loc[mask, "value"])
- elif struct_key == "vstr_ot":
- subclass_list = [
- 'OT D3 Folh1 Gaba',
- 'STR D1 Gaba',
- 'STR D2 Gaba',
- 'STR D1 Sema5a Gaba',
- ]
- mask = subclass_labels.value.isin(subclass_list)
- types_in_list = np.unique(cluster_labels.loc[mask, "value"])
- types_in_list = types_in_list[~np.in1d(types_in_list, STRUCT_BY_TYPES["cp"])]
- mask = cluster_labels.value.isin(types_in_list)
- print("Number of selected t-types:", len(types_in_list))
- print("Number of selected cells in this brain:", mask.sum())
- print("Finding ROIs")
- grid_info = BRAIN_GRIDS[brain_name]
- x_borders = grid_info['x_borders']
- y_borders = grid_info['y_borders']
- spatial_xy = pd.read_parquet(os.path.join(data_dir, "obsm/spatial_cirro.parquet"))
- tight_borders = find_tight_borders(spatial_xy.loc[mask, :].values, x_borders, y_borders)
- print(f"Identified {len(tight_borders)} ROIs")
- print("Creating histograms")
- bin_step = BIN_STEP[struct_key]
- hist_by_type = create_histograms(spatial_xy.values, tight_borders, bin_step,
- types_in_list, cluster_labels)
- print("Normalizing histograms")
- ttype_counts = np.array([h.sum() for h in hist_by_type.values()])
- ttype_order = list(hist_by_type.keys())
- min_n = MIN_N_PER_TTYPE[struct_key]
- n_with_min_cells = (ttype_counts >= min_n).sum()
- print(f"{n_with_min_cells} types have at least {min_n} cells")
- hists_as_1d_arr = np.zeros((
- n_with_min_cells,
- hist_by_type[list(hist_by_type.keys())[0]].size))
- ttype_order_min_n = np.array(ttype_order)[ttype_counts >= min_n]
- normalize_option = args['normalize_option']
- for i, t in enumerate(ttype_order_min_n):
- print(t)
- if normalize_option == 'sum':
- hists_as_1d_arr[i, :] = hist_by_type[t] / hist_by_type[t].sum()
- elif normalize_option == 'max':
- hists_as_1d_arr[i, :] = hist_by_type[t] / hist_by_type[t].max()
- elif normalize_option == 'none':
- hists_as_1d_arr[i, :] = hist_by_type[t]
- print("Saving results")
- X_input = np.asfortranarray(hists_as_1d_arr.T)
- data_f = h5py.File(args['output_file'], "w")
- dset = data_f.create_dataset("data", data=X_input)
- dset.attrs['min_n'] = min_n
- tight_borders_arr = np.array(tight_borders)
- tb_dset = data_f.create_dataset("tight_borders", data=tight_borders_arr)
- tb_dset.attrs['bin_step'] = bin_step
- dt = h5py.special_dtype(vlen=str)
- ttype_names = np.array(ttype_order_min_n, dtype=dt)
- ttypes_dset = data_f.create_dataset("ttypes", data=ttype_names)
- data_f.close()
- if __name__ == "__main__":
- module = ags.ArgSchemaParser(schema_type=MakeHistogramsForNmfParameters)
- main(module.args)
make_fineres_hist_ai21_cpq.py at commit ebc2d9b, under BSD-2-Clause · at the source
Overview
and 6 other authors
Qingming Luo4, Michael Kunst1, Cindy T. J. van Velthoven1, Zizhen Yao1, Staci A. Sorensen1, Hongkui Zeng1- Allen Institute for Brain Science,Seattle, WA USA
- School of Optometry and Ophthalmology, Wenzhou Medical University,Wenzhou, China
- HUST-Suzhou Institute for Brainsmatics, Jiangsu Industrial Technology Research Institute,Suzhou, China
- State Key Laboratory of Digital Medical Engineering, Key Laboratory of Biomedical Engineering of Hainan Province, School of Biomedical Engineering, Hainan University,Haikou, China
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.
Repository
Its files are read in the Code ↔ Paper reader above, with 17 matches between paragraphs and lines of code.
AllenInstitute/CP_molecular_organization
ebc2d9bfbdba4204f053112ea3671f7e11610437, 26 February 2024Availability: 1 check, the latest on 30 September 2026: the link answers
- 30 September 2026: the link answers
50 files
- scripts/
.ipynb_checkpoints/ , Jupyter, 109 linesFig6c_chord-checkpoint.i pynb - scripts/
ExtendedDataFig20_CPoutp , Python, 191 linesut_swc_quantification.py - scripts/
ExtendedDataFig20_CPoutp , Python, 118 linesuts_heatmap.py - scripts/
ExtendedDataFig20_cp_out , Python, 188 linesput_GPe_GPi_SNr_overlap. py - scripts/
Fig2.py , Python, 49 lines, 2 matches - scripts/
Fig3_Fig4_Fig5_plot_inje , Python, 320 linesction_sites.py - scripts/
Fig3b_assign_hemispheres , Python, 19 lines.py - scripts/
Fig3b_download_quantify. , Python, 117 linespy - scripts/
Fig3b_plot_quantificatio , Python, 167 linesn.py - scripts/
Fig3b_projection_summary , Python, 162 lines, 1 match_stats_multicore.py - scripts/
Fig3d_cortex_flatmap.py , Python, 159 lines, 1 match - scripts/
Fig3d_swc_plot_singleneu , Python, 71 linesron.py - scripts/
Fig3g_anterograde_overla , Python, 145 lines, 1 matchp.py - scripts/
Fig3g_plot_cortical_subc , Python, 147 linesortical_overlap_heatmap. py - scripts/
Fig3g_plot_overlap_heatm , Python, 118 linesap.py - scripts/
Fig4_calculate_swc_arbor , Python, 90 lines.py - scripts/
Fig4_plot_swc_heatmap.py , Python, 93 lines, 1 match - scripts/
Fig4_swc_size_dispersion , Python, 74 lines_scatterplot.py - scripts/
Fig4b_swc_projection_den , Python, 149 lines, 1 matchsities.py - scripts/
Fig4c_swc_celltype_assig , Python, 197 linesnment.py - scripts/
Fig4d_swc_ipsi_contra_mo , Python, 60 linesrphologies_plot.py - scripts/
Fig4e_swc_bilateral_perc , Python, 110 linesentage.py - scripts/
Fig5_plot_retrograde.py , Python, 225 lines, 2 matches - scripts/
Fig6a_summary_diagram.py , Python, 96 lines - scripts/
Fig6c_chord.ipynb , Jupyter, 109 lines - scripts/
SupplementaryTable1_Meta , Python, 62 linesdata.py - scripts/
SupplementaryTable3_assi , Python, 37 linesgn_retrograde_subdivisio n.py - scripts/
_old/ , Python, 109 linesFig2_combinatorial_bound aries.py - scripts/
_old/ , Python, 148 linesanterograde_overlap_laye rs.py - scripts/
_old/ , Python, 32 linescombine_anterograde.py - scripts/
_old/ , Python, 120 linesdownload_quantify.py - scripts/
_old/ , Python, 47 linesfilter_swcs.py - scripts/
_old/ , Python, 48 linesflip_ccf_to_QW.py - scripts/
_old/ , Python, 95 linesget_volume_from_LIMS.py - scripts/
_old/ , Python, 229 linesplot_retrograde.py - scripts/
_old/ , Python, 129 lines, 1 matchplot_subcortical_overlap _heatmap.py - scripts/
_old/ , Python, 30 linesshuffle_image.py - scripts/
_old/ , Python, 38 linesshuffle_xyz_image.py - scripts/
_old/ , Python, 69 lines, 1 matchswc_plot_projection_bymo dule.py - scripts/
_old/ , Python, 66 linesswc_termination_plot.py - scripts/
generate_dictionaries.py , Python, 142 lines - scripts/
generate_subdivision_loo , Python, 35 lineskup.py - scripts/
make_fineres_hist_ai21_c , Python, 267 lines, 3 matchespq.py - scripts/
spatial_pattern_figures. , Jupyter, 926 lines, 2 matchesipynb - scripts/
swc_plot_terminals.ipynb , Jupyter, 124 lines, 1 match - scripts/
swc_termination_point_vo , Jupyter, 123 lineslume.ipynb - src/
__init__.py , Python, 1 line - src/
swc_tools.py , Python, 128 lines - LICENSE, License, 33 lines
- README.md, Text, 19 lines
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: AllenInstitute/
CP_molecular_organizatio n
Read it in the paper: doi.org/10.1038/s41593-026-02253-9.
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;
- 48 scripts, each with its path and the digest of its content;
- 17 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: AllenInstitute/
CP_molecular_organizatio n
Read it in the paper: doi.org/10.1038/s41593-026-02253-9.
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, 30 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 26 authors, 2 keywords, 8 MeSH terms, 2 funders, 60 references, 4 RRIDs.
Cite
This paper
Wang, Q., Bhandiwad, A., Gouwens, N. W., Yao, S., Wang, Y., Kuang, X., Li, A., Li, X., Dalley, R., Kuo, H.-C., Lesnar, P., Xu, W., Mallory, M., Li, Y., El-Hifnawi, L., Ahmadinia, L., Ouellette, B., Kruse, L., Ng, L., . . . Zeng, H. (2026). Genoarchitecture and input-output organization of the mouse basal ganglia and thalamic parafascicular nucleus. Nature neuroscience, 29(5), 1248-1264. https://
BibTeX
@article{wang2026genoarc
author = {Wang, Quanxin and Bhandiwad, Ashwin and Gouwens, Nathan W. and Yao, Shenqin and Wang, Yun and Kuang, Xiuli and Li, Anan and Li, Xiangning and Dalley, Rachel and Kuo, Hsien-Chi and Lesnar, Phil and Xu, Wenjie and Mallory, Matt and Li, Yaoyao and El-Hifnawi, Laila and Ahmadinia, Leila and Ouellette, Ben and Kruse, Lauren and Ng, Lydia and Gong, Hui and Luo, Qingming and Kunst, Michael and van Velthoven, Cindy T. J. and Yao, Zizhen and Sorensen, Staci A. and Zeng, Hongkui},
title = {{Genoarchitecture and input-output organization of the mouse basal ganglia and thalamic parafascicular nucleus}},
journal = {Nature neuroscience},
year = {2026},
month = apr,
volume = {29},
number = {5},
pages = {1248--1264},
publisher = {Nature Portfolio},
issn = {1097-6256},
doi = {10.1038/
url = {https://
pmid = {42049879},
pmcid = {PMC13156036}
}
RIS
TY - JOUR
AU - Wang, Quanxin
AU - Bhandiwad, Ashwin
AU - Gouwens, Nathan W.
AU - Yao, Shenqin
AU - Wang, Yun
AU - Kuang, Xiuli
AU - Li, Anan
AU - Li, Xiangning
AU - Dalley, Rachel
AU - Kuo, Hsien-Chi
AU - Lesnar, Phil
AU - Xu, Wenjie
AU - Mallory, Matt
AU - Li, Yaoyao
AU - El-Hifnawi, Laila
AU - Ahmadinia, Leila
AU - Ouellette, Ben
AU - Kruse, Lauren
AU - Ng, Lydia
AU - Gong, Hui
AU - Luo, Qingming
AU - Kunst, Michael
AU - van Velthoven, Cindy T. J.
AU - Yao, Zizhen
AU - Sorensen, Staci A.
AU - Zeng, Hongkui
TI - Genoarchitecture and input-output organization of the mouse basal ganglia and thalamic parafascicular nucleus
T2 - Nature neuroscience
J2 - Nat Neurosci
PY - 2026
DA - 2026/
VL - 29
IS - 5
SP - 1248
EP - 1264
SN - 1097-6256
PB - Nature Portfolio
DO - 10.1038/
UR - https://
LA - en
ER -
CSL-JSON
{
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"container-title": "Nature neuroscience",
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{
"family": "El-Hifnawi",
"given": "Laila"
},
{
"family": "Ahmadinia",
"given": "Leila"
},
{
"family": "Ouellette",
"given": "Ben"
},
{
"family": "Kruse",
"given": "Lauren"
},
{
"family": "Ng",
"given": "Lydia"
},
{
"family": "Gong",
"given": "Hui"
},
{
"family": "Luo",
"given": "Qingming"
},
{
"family": "Kunst",
"given": "Michael"
},
{
"family": "van Velthoven",
"given": "Cindy T. J."
},
{
"family": "Yao",
"given": "Zizhen"
},
{
"family": "Sorensen",
"given": "Staci A."
},
{
"family": "Zeng",
"given": "Hongkui"
}
],
"container-title-short":
"volume": "29",
"issue": "5",
"page": "1248-1264",
"DOI": "10.1038/
"PMID": "42049879",
"PMCID": "PMC13156036",
"ISSN": "1097-6256",
"publisher": "Nature Portfolio",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
4,
28
]
]
}
}
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