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Influenza Vaccine Effectiveness in European Primary Care Pediatric Practices: 2022-2024.
Lucaccioni H, Maurel M, Pérez-Gimeno G, Buda S, Sève N, Domegan L, de Lange M, Rodrigues AP, Martínez-Baz I, Hagey TS, Mlinarić I, Túri G, Lazar M, García Becerril M, Dürrwald R, Enouf V, O'Leary M, Meijer A, Guiomar R, Trobajo-Sanmartín C, Latorre-Margalef N, Ilić M, Vázquez Rincón IM, Erdwiens A, Falchi A, McKenna A, Hooiveld M, Gómez V, Castilla J, Višekruna Vučina V, Pozo F, Bacci S, Kaczmarek M, Kissling E; European primary care VE group. Lucaccioni H, et al. Among authors: o leary m. Pediatrics. 2026 May 1;157(5):e2025072907. doi: 10.1542/peds.2025-072907. Pediatrics. 2026. PMID: 41936398
De Novo Variants Associated With Autosomal Recessive Conditions: Case Series and Implications for Genetic Testing and Counseling.
Niehaus AD, Bonner DE, Carter J, Avello K, Jacob N, Neu MB, Mendez R, Qiao W, Scott SA, Levy RJ, Mattas L, Schymick J, Van Andel M, Muntoni F, Mueller J, Sarkozy A, DiTroia S, O'Leary M, Neale A, O'Donnell-Luria A, Toro C, Wolfe LA, Martinez-Agosto JA, Montgomery SB, Wheeler MT, Bernstein JA, Tise CG. Niehaus AD, et al. Among authors: o leary m. Am J Med Genet A. 2026 Apr 19. doi: 10.1002/ajmg.a.70162. Online ahead of print. Am J Med Genet A. 2026. PMID: 42002855
The Mechanics of Improving Compliance.
O'Leary MC, Schumacher JR, Mody GN. O'Leary MC, et al. JAMA Surg. 2026 Apr 15. doi: 10.1001/jamasurg.2026.0897. Online ahead of print. JAMA Surg. 2026. PMID: 41984440 No abstract available.
Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.
Rius R, Blakes AJM, Chen Y, De Jonghe J, Lecoquierre F, Dawes R, Cogne B, Kim HC, Alvi JR, Amblard F, Ansari M, Arlt A, Austin-Tse C, Baer S, Balasubramanian M, Balton EV, Barcia G, Beleza-Meireles A, Bernstein JA, Beygo J, Blanc P, Bramswig NC, Braun F, Buchzik D, Calame DG, Campbell J, Coutton C, Cunningham CA, Dargie N, Depienne C, Dipple KM, Dieux A, Dixit A, Dreyer L, Du H, El Chehadeh S, Field M, Ewans LJ, Geiger V, Gibbs RA, Glass I, Grunewald O, Gueguen P, Haack TB, Hadj Abdallah H, Harbuz R, Helbig I, Horvath J, Hustinx A, Isidor B, Jacquemont ML, Jamie F, Jeanne M, Kessler R, Klinkhammer H, Korenke GC, Kotzaeridou U, Krawitz P, Laurie S, Leventer RJ, Levy RJ, Lupski JR, Marijon P, McGinnis KE, Mendez R, Messaoud O, Nava C, Nizard M, O'Donnell-Luria A, O'Leary MC, Olivieri S, Parida A, Pehlivan D, Prentice AJ, Posey JE, Reuter CM, Satre V, Schluth-Bolard C, Smol T, Sultan T, Taylor J, Thauvin-Robinetvin C, Thevenon J, Uebergang E, Ueberberg S, Vincent-Delorme C, Wassmer E, Westwood E, Wheeler MT, Gulec EY, Vanderver A, Vossough A, Sanders SJ, Banka S, Findlay GM, MacArthur DG, Simons C, Whiffin N. Rius R, et al. Among authors: o leary mc. Nat Genet. 2026 Apr;58(4):761-773. doi: 10.1038/s41588-026-02554-6. Epub 2026 Apr 8. Nat Genet. 2026. PMID: 41951959 Free PMC article.
1,168 results