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The MEG3-miRNA regulatory axis could potentially modulate response to biological therapies in psoriatic arthritis.

Pharmacological reports : PR·2026

ExposoGenomics: integrating genome and exposome as jointly dynamic systems for causal discovery and precision health.

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Frailty in elderly with a rare genetic disease: a geriatric score analysis in C1 inhibitor Hereditary Angioedema.

Frontiers in medicine·2026

Cost-effectiveness analysis of lorlatinib as first-line treatment for anaplastic lymphoma kinase (ALK)-positive non-small cell lung cancer in Italy.

Journal of medical economics·2026

Cost-Effectiveness of Elranatamab Versus Teclistamab for the Management of Patients with Triple-Class Exposed Relapsed/Refractory Multiple Myeloma in Italy.

Cancers·2026

Pharmacogenetic testing in Italy: results of a nationwide survey by the Joint Working Group for the pharmacogenetics implementation in Italy.

European journal of human genetics : EJHG·2026

Rapid Genome Sequencing Identifies Treatable Conditions in Non-Intensive Care Unit Hospitalized Children.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Transmission ratio distortion of NF1 mutant alleles in familial Neurofibromatosis type 1.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

The Patient-reported Genetic testing Utility InDEx (P-GUIDE): A novel measure of personal utility.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Retrospective Study of Foramen Magnum Development in Patients with Achondroplasia Starting Vosoritide Before Age Three.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Familial Risk Stratification Across Cancer Syndromes Using Fam3PRO.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Indigenous perspectives on biobanking, specimen storage, and data governance: A scoping review.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Whole exome sequencing identifies three novel variants and establishes the molecular diagnosis of ATP6V0A4-related distal renal tubular acidosis in a lebanese infant.

Molecular biology reports·2026

Anesthetic Management of a Pediatric Patient With Carnitine Deficiency: A Case Report.

A&A practice·2026

The importance of early diagnosis of congenital torticollis: a five-year retrospective study at a tertiary centre.

Medicinski glasnik : official publication of the Medical Association of Zenica-Doboj Canton, Bosnia and Herzegovina·2026

Post-surgical Pyoderma Gangrenosum Following Elective Aesthetic Procedures: A Case Series of 10 Patients and a Multidisciplinary Treatment Approach.

Indian journal of plastic surgery : official publication of the Association of Plastic Surgeons of India·2026

Optimized ensemble learning framework for neonatal asphyxia prediction using perinatal clinical features.

Frontiers in public health·2026

Systemic immune-inflammation index as a risk factor for acute kidney injury in patients with neonatal jaundice.

Translational pediatrics·2026

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Neonatal screening, clinical features and genetic testing for galactosemia

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Neonatal screening, clinical features and genetic testing for galactosemia

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