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Automated AI based identification of autism spectrum disorder from home videos
npj Digital Medicine, Published online: 10 October 2025; doi:10.1038/s41746-025-01993-5
Automated AI based identification of autism spectrum disorder from home videosA human pan-disease blood atlas of the circulating proteome
Opinion: STAT+: 5 things to consider to bring ambient digital scribes to clinical research
About a year ago, I logged into MyChart the day before my annual wellness visit and saw a new consent form. My doctor wanted to record our visit so artificial intelligence could create notes and update my medical record. I agreed. Just hours after my visit ended, a comprehensive, accurate visit summary appeared in MyChart.
As a career clinical trialist, I immediately wondered: What if this tool were used for trial visits? Could it enable a breakthrough in research or patient engagement? How will clinical research adapt to what could be a “new normal” in medical documentation?
Driven by a crisis of clinician burnout, ambient digital scribes (ADS) like the one my doctor used are being rapidly adopted. Studies suggest these digital scribes can reduce documentation burden, improve clinician efficiency, and potentially enhance the patient experience. By digitizing conversations in real time, these scribes open possibilities beyond routine care, particularly in clinical research and trials.
Continue to STAT+ to read the full story…


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Systematic review: digital biomarkers of fatigue in chronic diseases
npj Digital Medicine, Published online: 08 October 2025; doi:10.1038/s41746-025-01939-x
Systematic review: digital biomarkers of fatigue in chronic diseasesDigital twin models for predicting venetoclax and azacitidine-induced neutropenia in patients with acute myeloid leukemia
npj Digital Medicine, Published online: 06 October 2025; doi:10.1038/s41746-025-01978-4
Digital twin models for predicting venetoclax and azacitidine-induced neutropenia in patients with acute myeloid leukemiaEfficient and accurate search in petabase-scale sequence repositories
Nature, Published online: 08 October 2025; doi:10.1038/s41586-025-09603-w
MetaGraph enables scalable indexing of large sets of DNA, RNA or protein sequences using annotated de Bruijn graphs.Chemistry Nobel for scientists who developed massively porous ‘super sponge’ materials
Nature, Published online: 08 October 2025; doi:10.1038/d41586-025-03195-1
Susumu Kitagawa, Richard Robson and Omar Yaghi pioneered the creation of metal–organic frameworks, which can capture and store molecules such as carbon dioxide.These immune cells won Nobel fame — can they solve autoimmune disease?
Nature, Published online: 07 October 2025; doi:10.1038/d41586-025-03287-y
Regulatory T cells, which help to dampen inflammation, are being used in clinical trials against ailments such as rheumatoid arthritis.Stop treating code like an afterthought: record, share and value it
Nature, Published online: 07 October 2025; doi:10.1038/d41586-025-03196-0
Scientists, research institutions, funders, libraries and publishers must all improve software practices.HALO: hierarchical causal modeling for single cell multi-omics data
Nat Commun. 2025 Oct 7;16(1):8892. doi: 10.1038/s41467-025-63921-1.
ABSTRACT
Though open chromatin may promote active transcription, gene expression responses may not be directly coordinated with changes in chromatin accessibility. Most existing methods for single-cell multi-omics data focus only on learning stationary, shared information among these modalities, overlooking modality-specific information delineating cellular states and dynamics resulting from causal relations among modalities. To address this, the epigenome-transcriptome relationship can be characterized in relation to time as coupled (changing dependently) or decoupled (changing independently). We propose the framework HALO, adopting a causal approach to model these temporal causal relations on two levels. On the representation level, HALO factorizes these two modalities into both coupled and decoupled latent representations, revealing their dynamic interplay. On the individual gene level, HALO matches gene-peak pairs and characterizes their changes over time. HALO discovers analogous biological functions between modalities, distinguishes epigenetic factors for lineage specification, and identifies temporal cis-regulation interactions relevant to cellular differentiation and human diseases.
PMID:41057364 | PMC:PMC12504611 | DOI:10.1038/s41467-025-63921-1
Pathobiology and Genetics
Pneumologie. 2025 Oct;79(10):701-711. doi: 10.1055/a-2625-4648. Epub 2025 Oct 6.
ABSTRACT
Genetics and pathobiology were addressed at the 7th World Symposium on Pulmonary Hypertension in Task Forces 2 and 3. The Genetics Task Force also focused on precision medicine approaches, and the Pathobiology working group concentrated heavily on new omics technologies. Therefore, the following not only summarises the current state of knowledge on genetics, genetic testing methods, and molecular pathophysiological changes, but also places it in context and critically discusses it. In addition, the importance of national and international biobanks and cohorts, as well as the active involvement of patients and families, is emphasized.
PMID:41052524 | DOI:10.1055/a-2625-4648
The Potential of AI in Nursing Care: Multicenter Evaluation in Fall Risk Assessment
Quality of Cancer-Related Information on New Media (2014-2023): Systematic Review and Meta-Analysis
Evaluating Large Language Models and Retrieval-Augmented Generation Enhancement for Delivering Guideline-Adherent Nutrition Information for Cardiovascular Disease Prevention: Cross-Sectional Study
The Role of Data in Public Health and Health Innovation: Perspectives on Social Determinants of Health, Community-Based Data Approaches, and AI
Generative artificial intelligence in medicine
Nature Medicine, Published online: 06 October 2025; doi:10.1038/s41591-025-03983-2
This Review summarizes recent technical advancements in generative AI, outlines how new models might improve healthcare and discusses validation approaches—using lessons from recent successes and failures in the field.Single-cell and multi-omics analysis identifies TRIM9 as a key ubiquitination regulator in pancreatic cancer
Front Immunol. 2025 Sep 19;16:1631708. doi: 10.3389/fimmu.2025.1631708. eCollection 2025.
ABSTRACT
This study investigates the role of ubiquitination-related genes in pancreatic cancer (PC) using single-cell RNA sequencing (scRNA-seq), spatial transcriptomics, and multi-omics approaches. scRNA-seq data (GSE155698) from PC samples identified 12 cell types, with endothelial cells exhibiting high ubiquitination scores (High_ubiquitin-Endo) and enriched interactions with fibroblasts/macrophages via WNT, NOTCH, and integrin pathways. Spatial transcriptomics (GSE235315) validated cell-type localization. Mendelian randomization (SMR) analysis prioritized TRIM9 as a PC-protective gene, downregulated in tumors and correlated with better survival. WGCNA revealed TRIM9-co-expressed modules linked to prognosis. A machine learning-based prognostic model (CoxBoost+RSF) integrating seven genes (TSPAN6, TSC1, RNF167, PBXIP1, LRRC49, KATNAL2, IGF2BP2) stratified patients into high/low-risk groups with distinct survival, mutation burdens, and immune infiltration. TRIM9 overexpression suppressed PC cell proliferation/migration in vitro, while knockdown enhanced malignancy. Mechanistically, TRIM9 promoted K11-linked ubiquitination and proteasomal degradation of HNRNPU, dependent on its RING domain. In vivo, TRIM9 overexpression reduced tumor growth, rescued by HNRNPU co-expression. Integrated analyses highlight TRIM9 as a tumor suppressor and prognostic biomarker, mediated via ubiquitination-dependent regulation of HNRNPU stability. This work provides insights into ubiquitination-driven PC pathogenesis and therapeutic targeting.
PMID:41050689 | PMC:PMC12491318 | DOI:10.3389/fimmu.2025.1631708
A computational medicine framework integrating multi-omics, systems biology, and artificial neural networks for Alzheimer's disease therapeutic discovery
Acta Pharm Sin B. 2025 Sep;15(9):4411-4426. doi: 10.1016/j.apsb.2025.07.018. Epub 2025 Jul 16.
ABSTRACT
The translation of genetic findings from genome-wide association studies into actionable therapeutics persists as a critical challenge in Alzheimer's disease (AD) research. Here, we present PI4AD, a computational medicine framework that integrates multi-omics data, systems biology, and artificial neural networks for therapeutic discovery. This framework leverages multi-omic and network evidence to deliver three core functionalities: clinical target prioritisation; self-organising prioritisation map construction, distinguishing AD-specific targets from those linked to neuropsychiatric disorders; and pathway crosstalk-informed therapeutic discovery. PI4AD successfully recovers clinically validated targets like APP and ESR1, confirming its prioritisation efficacy. Its artificial neural network component identifies disease-specific molecular signatures, while pathway crosstalk analysis reveals critical nodal genes (e.g., HRAS and MAPK1), drug repurposing candidates, and clinically relevant network modules. By validating targets, elucidating disease-specific therapeutic potentials, and exploring crosstalk mechanisms, PI4AD bridges genetic insights with pathway-level biology, establishing a systems genetics foundation for rational therapeutic development. Importantly, its emphasis on Ras-centred pathways-implicated in synaptic dysfunction and neuroinflammation-provides a strategy to disrupt AD progression, complementing conventional amyloid/tau-focused paradigms, with the future potential to redefine treatment strategies in conjunction with mRNA therapeutics and thereby advance translational medicine in neurodegeneration.
PMID:41049755 | PMC:PMC12491700 | DOI:10.1016/j.apsb.2025.07.018