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Familial communication and cascade testing following elective genomic testing.
J Genet Couns. 2025 Feb;34(1):e1907. doi: 10.1002/jgc4.1907. Epub 2024 May 16.
J Genet Couns. 2025.
PMID: 38757439
Perspectives of Rare Disease Experts on Newborn Genome Sequencing.
Gold NB, Adelson SM, Shah N, Williams S, Bick SL, Zoltick ES, Gold JI, Strong A, Ganetzky R, Roberts AE, Walker M, Holtz AM, Sankaran VG, Delmonte O, Tan W, Holm IA, Thiagarajah JR, Kamihara J, Comander J, Place E, Wiggs J, Green RC.
Gold NB, et al. Among authors: adelson sm.
JAMA Netw Open. 2023 May 1;6(5):e2312231. doi: 10.1001/jamanetworkopen.2023.12231.
JAMA Netw Open. 2023.
PMID: 37155167
Free PMC article.
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Data-driven prioritization of genetic disorders for global genomic newborn screening programs.
Minten T, Gold NB, Bick S, Adelson S, Gehlenborg N, Amendola LM, Boemer F, Coffey AJ, Encina N, Ferlini A, Kirschner J, Russell BE, Servais L, Sund KL, Taft RJ, Tsipouras P, Zouk H; ICoNS Gene List Contributors; Bick D, Green RC; International Consortium on Newborn Sequencing (ICoNS).
Minten T, et al.
medRxiv [Preprint]. 2024 Sep 16:2024.03.24.24304797. doi: 10.1101/2024.03.24.24304797.
medRxiv. 2024.
PMID: 38585998
Free PMC article.
Preprint.
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