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Vaccines|December 23, 2022
Determinants of the Level of Anti-SARS-CoV-2 IgG ANTibodiEs after Vaccination (DANTE-SIRIO 7) Study in a Large Cohort of Healthcare WorkersMagdalena Krintus, Maciej Piasecki, Piotr Lackowski, et al.
Mechanisms of Ageing and Development|October 27, 2007
Interaction of human SUV3 RNA/DNA helicase with BLM helicase; loss of the SUV3 gene results in mouse embryonic lethalityMandy Pereira, Penelope Mason, Roman J Szczesny, et al.
Journal of Medical Internet Research|March 27, 2024
Effectiveness of the Minder Mobile Mental Health and Substance Use Intervention for University Students: Randomized Controlled TrialMelissa Vereschagin, Angel Y Wang, Chris G Richardson, et al.
Current Medical Research and Opinion|May 30, 2024
Real-world service costs for neovascular-AMD clinics in the United Kingdom: structured literature review and scenario analysisSobha Sivaprasad, Clare Bailey, Louise Downey, et al.
American Journal of Medical Genetics. Part A|October 10, 2020
Exome sequencing identifies novel missense and deletion variants in RTN4IP1 associated with optic atrophy, global developmental delay, epilepsy, ataxia, and choreoathetosisAlissa M D'Gama, Eleina England, Jill A Madden, et al.
European Journal of Human Genetics : EJHG|June 13, 2019
A retrospective analysis of the prevalence of imprinting disorders in Estonia from 1998 to 2016Maria Yakoreva, Tiina Kahre, Riina Žordania, et al.
Journal of the American Heart Association|November 12, 2025
Differential Performance of Polygenic Score for Coronary Artery Disease Based on Coronary Artery Calcium Between Men Living With and Without HIVGenevieve Wojcik, Marios Arvanitis, Sabina Haberlen, et al.
International Journal of Radiation Biology|March 9, 2026
Chromosomal damage in breast cancer patients undergoing different radiotherapy schemesRenu Dayal, Lama Ramadan, Liv Veldeman, et al.
Annals of Neurology|September 8, 2022
De Novo Missense Variants in SLC32A1 Cause a Developmental and Epileptic Encephalopathy Due to Impaired GABAergic NeurotransmissionKonrad Platzer, Heinrich Sticht, Caleb Bupp, et al.
Molecular Medicine (Cambridge, Mass.)|May 24, 2013
Genetic markers of a Munc13 protein family member, BAIAP3, are gender specifically associated with anxiety and benzodiazepine abuse in mice and humansSonja M Wojcik, Martesa Tantra, Beata Stepniak, et al.
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