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01.
arXiv (CS.CV) 2026-06-25

Generalised Medical Phrase Grounding

Medical phrase grounding (MPG) maps textual descriptions of radiological findings to corresponding image regions. These grounded reports are easier to interpret, especially for non-experts. Existing MPG systems mostly follow the referring expression comprehension (REC) paradigm and return exactly one bounding box per phrase. Real reports often violate this assumption. They contain multi-region findings, non-diagnostic text, and non-groundable phrases, such as negations or descriptions of normal anatomy. Motivated by this, we reformulate the task as generalised medical phrase grounding (GMPG), where each sentence is mapped to zero, one, or multiple scored regions. To realise this formulation, we introduce the first GMPG model: MedGrounder. We adopted a two-stage training regime: pre-training on report sentence–anatomy box alignment datasets and fine-tuning on report sentence–human annotated box datasets. Experiments on PadChest-GR and MS-CXR show that MedGrounder achieves strong zero-shot transfer and outperforms REC-style and grounded report generation baselines on multi-region and non-groundable phrases, while using far fewer human box annotations. Finally, we show that MedGrounder can be composed with existing report generators to produce grounded reports without retraining the generator.

02.
medRxiv (Medicine) 2026-06-25

Longitudinal Bundibugyo Virus Glycoprotein Seroreactivity Following rVSVΔG-ZEBOV-GP Vaccination in Outbreak-Affected Populations of the Democratic Republic of the Congo

Background: There are currently no vaccines approved for the prevention or treatment of Orthoebolavirus bundibugyoense (Bundibugyo virus; BDBV). The recombinant vesicular stomatitis virus- Zaire ebolavirus glycoprotein vaccine (rVSV-ZEBOV-GP; ERVEBO) has been widely deployed during Ebola virus disease (EVD) outbreaks caused by Orthoebolavirus zairense (Ebola virus; EBOV). Given the lack of vaccines and medical countermeasures we evaluated development of antibodies to Bundibugyo glycoprotein (GP) following rVSV-ZEBOV-GP vaccination in two EVD outbreak-affected populations in the Democratic Republic of the Congo (DRC). Methods: Between 2018 and 2023, serum samples were collected from vaccine recipients in Mbandaka, Equateur Province (n=482 at baseline), and Beni, North Kivu Province (n=599 at baseline). Antibody reactivity was assessed using a multiplex pan-filovirus immunoassay. We evaluated longitudinal trends in BDBV GP seroreactivity across follow-up visits extending to approximately five years after vaccination. Findings: We collected 2552 samples from 482 participants in Mbandaka and 3297 samples from 599 participants in Beni. BDBV GP responses diverged by location. Baseline BDBV GP seroreactivity differed between sites, with 3.3% of participants reactive in Mbandaka and 10.4% in Beni. In Mbandaka, BDBV GP titers remained unchanged through 6 months post-vaccination but increased markedly between 2.5 and 3.5 years (mean MFI 1,238 to 4,845; p

03.
bioRxiv (Bioinfo) 2026-06-11

VFUSE: Virulent Feature Understanding with Sparse autoEncoders

Generative models have shown remarkable progress in a variety of domains such as protein design, but such power enables the opaque generation of hazardous proteins. In this work, we introduce VFUSE (Virulent Feature Understanding with Sparse autoEncoders), a mechanistic interpretability approach that trains SAEs on diffusion-transformer activations to audit protein models for hazard-aware features. We apply VFUSE to RoseTTAFold3 and RFDiffusion3, popular open-weight models for protein folding and synthesis. We find that for certain blocks, linear probes detect hazardous designs significantly better when fit in the SAE latent space over the original model's representations: improving interpretability without sacrificing model performance. Furthermore, we identify monosemantic features from the SAE that fire only on hazardous designs at up to AUROC 0.84 (q < 10-13).

04.
medRxiv (Medicine) 2026-06-16

Reliability and construct validity of the Technology Device Interference Scale in a sample of children and parents

There is increasing interest in parent-child technoference: the interference with personal interactions caused by technology devices. This study examined the reliability and construct validity of the Technology Device Interference Scale (TDIS) to measure technoference in a sample of Canadian parents and children. Parents (n=883) and children (n=376) were recruited from clinical and community settings and completed the TDIS for their own and family member technoference over three timepoints (T1=2023, T2=2024, T3=2025). TDIS internal consistency, test-retest reliability, and construct validity were assessed using Cronbachs alpha, intraclass correlation coefficient, and confirmatory factor analysis, respectively. The TDIS showed good internal consistency and adequate to good construct validity when used by children to report on their own technoference (all >.70; CFI>.95, TLI>.95, RMSEA.70; CFI>.95, TLI>.90, RMSEA[&le;].11). The TDIS had low to acceptable internal consistency and poor model fit for parent report of their own technoference ( range: .63 - .66; CFI