SkyWhal3/stxbp1-pubmed-central-fulltext
source_datasets: - PubMed Central STXBP1 PubMed Central Full-Text Dataset v2 A comprehensive collection of 31,786 full-text scientific articles from PubMed Central related to STXBP1, synaptic function, and neurological research. ๐ Version 2 Updates (December 2025) Complete re-extraction with improved HTML parsing Full main text with proper section headers Enhanced metadata extraction 99.7% figure-image matching (see companion multimodal dataset)โฆ See the full description on the dataset page: https://huggingface.co/datasets/SkyWhal3/stxbp1-pubmed-central-fulltext.
source_datasets:
- PubMed Central ---
STXBP1 PubMed Central Full-Text Dataset v2
A comprehensive collection of 31,786 full-text scientific articles from PubMed Central related to STXBP1, synaptic function, and neurological research.
๐ Version 2 Updates (December 2025)
- Complete re-extraction with improved HTML parsing
- Full main text with proper section headers
- Enhanced metadata extraction
- 99.7% figure-image matching (see companion multimodal dataset)
Dataset Overview
Schema
Usage
Load with Hugging Face Datasets
from datasets import load_dataset
dataset = load_dataset("SkyWhal3/stxbp1-pubmed-central-fulltext")
# Access the data
df = dataset['train'].to_pandas()
# Filter STXBP1-specific articles
stxbp1_articles = df[df['stxbp1_mentions'] > 0]
print(f"Found {len(stxbp1_articles)} STXBP1-related articles")Load with Pandas
import pandas as pd
df = pd.read_parquet("hf://datasets/SkyWhal3/stxbp1-pubmed-central-fulltext/stxbp1_pubmed_articles.parquet")Example Queries
# Find articles about specific topics
seizure_articles = df[df['main_text'].str.contains('seizure', case=False, na=False)]
# Get articles with most STXBP1 mentions
top_stxbp1 = df.nlargest(10, 'stxbp1_mentions')[['pmc_id', 'title', 'stxbp1_mentions']]
# Find articles by keyword in title
crispr_articles = df[df['title'].str.contains('CRISPR|gene therapy', case=False, na=False)]Related Resources
About STXBP1
STXBP1 (Syntaxin-Binding Protein 1), also known as Munc18-1, is essential for synaptic vesicle fusion and neurotransmitter release. Mutations cause STXBP1 Encephalopathy, a rare neurological disorder characterized by:
- Early-onset epilepsy
- Developmental delays
- Movement disorders
- Intellectual disability
This dataset supports AI-powered research into understanding and treating STXBP1-related conditions.
Citation
@dataset{stxbp1_fulltext_2025,
author = {SkyWhal3},
title = {STXBP1 PubMed Central Full-Text Dataset},
year = {2025},
publisher = {Hugging Face},
url = {https://huggingface.co/datasets/SkyWhal3/stxbp1-pubmed-central-fulltext}
}License
CC-BY-4.0. Source articles are from PubMed Central's Open Access subset.
Changelog
v2.0 (December 2025)
- Complete re-extraction with improved parsing
- Added section headers to main_text
- Enhanced metadata fields
- Added figure/image counts
- Added text length statistics
v1.0 (December 2025)
- Initial release
This dataset is dedicated to all children and families affected by STXBP1 Encephalopathy.
