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Page 1
Nuclear Charge Radii of Silicon Isotopes.
König K, Berengut JC, Borschevsky A, Brinson A, Brown BA, Dockery A, Elhatisari S, Eliav E, Ruiz RFG, Holt JD, Hu BS, Karthein J, Lee D, Ma YZ, Meißner UG, Minamisono K, Oleynichenko AV, Pineda SV, Prosnyak SD, Reitsma ML, Skripnikov LV, Vernon A, Zaitsevskii A. König K, et al. Among authors: dockery a. Phys Rev Lett. 2024 Apr 19;132(16):162502. doi: 10.1103/PhysRevLett.132.162502. Phys Rev Lett. 2024. PMID: 38701465
Precision Mass Measurement of the Proton Dripline Halo Candidate ^{22}Al.
Campbell SE, Bollen G, Brown BA, Dockery A, Ireland CM, Minamisono K, Puentes D, Rickey BJ, Ringle R, Yandow IT, Fossez K, Ortiz-Cortes A, Schwarz S, Sumithrarachchi CS, Villari ACC. Campbell SE, et al. Among authors: dockery a. Phys Rev Lett. 2024 Apr 12;132(15):152501. doi: 10.1103/PhysRevLett.132.152501. Phys Rev Lett. 2024. PMID: 38683002
Representation of Women Among Individuals With Mild Variants in ABCA4-Associated Retinopathy: A Meta-Analysis.
Cornelis SS, IntHout J, Runhart EH, Grunewald O, Lin S, Corradi Z, Khan M, Hitti-Malin RJ, Whelan L, Farrar GJ, Sharon D, van den Born LI, Arno G, Simcoe M, Michaelides M, Webster AR, Roosing S, Mahroo OA, Dhaenens CM, Cremers FPM; Study Group. Cornelis SS, et al. JAMA Ophthalmol. 2024 May 1;142(5):463-471. doi: 10.1001/jamaophthalmol.2024.0660. JAMA Ophthalmol. 2024. PMID: 38602673
Variant reclassification and clinical implications.
Walsh N, Cooper A, Dockery A, O'Byrne JJ. Walsh N, et al. Among authors: dockery a. J Med Genet. 2024 Feb 21;61(3):207-211. doi: 10.1136/jmg-2023-109488. J Med Genet. 2024. PMID: 38296635 Free article. Review.
Usher Syndrome on the Island of Ireland: A Genotype-Phenotype Review.
Stephenson KAJ, Whelan L, Zhu J, Dockery A, Wynne NC, Cairns RM, Kirk C, Turner J, Duignan ES, O'Byrne JJ, Silvestri G, Kenna PF, Farrar GJ, Keegan DJ. Stephenson KAJ, et al. Among authors: dockery a. Invest Ophthalmol Vis Sci. 2023 Jul 3;64(10):23. doi: 10.1167/iovs.64.10.23. Invest Ophthalmol Vis Sci. 2023. PMID: 37466950 Free PMC article.
Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction.
Reurink J, Weisschuh N, Garanto A, Dockery A, van den Born LI, Fajardy I, Haer-Wigman L, Kohl S, Wissinger B, Farrar GJ, Ben-Yosef T, Pfiffner FK, Berger W, Weener ME, Dudakova L, Liskova P, Sharon D, Salameh M, Offenheim A, Heon E, Girotto G, Gasparini P, Morgan A, Bergen AA, Ten Brink JB, Klaver CCW, Tranebjærg L, Rendtorff ND, Vermeer S, Smits JJ, Pennings RJE, Aben M, Oostrik J, Astuti GDN, Corominas Galbany J, Kroes HY, Phan M, van Zelst-Stams WAG, Thiadens AAHJ, Verheij JBGM, van Schooneveld MJ, de Bruijn SE, Li CHZ, Hoyng CB, Gilissen C, Vissers LELM, Cremers FPM, Kremer H, van Wijk E, Roosing S. Reurink J, et al. Among authors: dockery a. HGG Adv. 2023 Jan 18;4(2):100181. doi: 10.1016/j.xhgg.2023.100181. eCollection 2023 Apr 13. HGG Adv. 2023. PMID: 36785559 Free PMC article.
33 results