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Year Number of Results
2017 2
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2019 4
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2025 6

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Page 1
Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes.
Ingles J, Goldstein J, Thaxton C, Caleshu C, Corty EW, Crowley SB, Dougherty K, Harrison SM, McGlaughon J, Milko LV, Morales A, Seifert BA, Strande N, Thomson K, Peter van Tintelen J, Wallace K, Walsh R, Wells Q, Whiffin N, Witkowski L, Semsarian C, Ware JS, Hershberger RE, Funke B. Ingles J, et al. Among authors: milko lv. Circ Genom Precis Med. 2019 Feb;12(2):e002460. doi: 10.1161/CIRCGEN.119.002460. Circ Genom Precis Med. 2019. PMID: 30681346 Free PMC article.
Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource.
Strande NT, Riggs ER, Buchanan AH, Ceyhan-Birsoy O, DiStefano M, Dwight SS, Goldstein J, Ghosh R, Seifert BA, Sneddon TP, Wright MW, Milko LV, Cherry JM, Giovanni MA, Murray MF, O'Daniel JM, Ramos EM, Santani AB, Scott AF, Plon SE, Rehm HL, Martin CL, Berg JS. Strande NT, et al. Among authors: milko lv. Am J Hum Genet. 2017 Jun 1;100(6):895-906. doi: 10.1016/j.ajhg.2017.04.015. Epub 2017 May 25. Am J Hum Genet. 2017. PMID: 28552198 Free PMC article.
Direct-to-Consumer Genetic Testing.
O'Daniel JM, Kobelka C, Foss K, Foreman AKM, Milko LV. O'Daniel JM, et al. Among authors: milko lv. NEJM Evid. 2025 Nov;4(11):EVIDra2400455. doi: 10.1056/EVIDra2400455. Epub 2025 Oct 28. NEJM Evid. 2025. PMID: 41147825 Review.
Feasibility and clinical utility of expanded genomic newborn screening in the Early Check program.
Cope HL, Jalazo ER, Berg JS, Sullivan JA, Kucera KS, Shone SM, Frawley HE, Gwaltney AY, Forsythe AN, Migliore BA, Wright B, Moultrie RR, Milko LV, Zimmerman RS, Kruszka P, Suchy SF, Begtrup A, Langley KG, Monaghan KG, Kraczkowski C, Guenzel AJ, McWalter K, Hruska KS, Bailey DB Jr, Wheeler AC, Raspa M, Powell CM, Peay HL; Early Check Program. Cope HL, et al. Among authors: milko lv. Nat Med. 2025 Nov;31(11):3762-3771. doi: 10.1038/s41591-025-03945-8. Epub 2025 Sep 5. Nat Med. 2025. PMID: 40913169 Free PMC article.
A systematic framework for selecting gene-condition pairs for inclusion in newborn sequencing panels: Early Check implementation.
Cope HL, Milko LV, Jalazo ER, Crissman BG, Foreman AKM, Powell BC, deJong NA, Hunter JE, Boyea BL, Forsythe AN, Wheeler AC, Zimmerman RS, Suchy SF, Begtrup A, Langley KG, Monaghan KG, Kraczkowski C, Hruska KS, Kruszka P, Kucera KS, Berg JS, Powell CM, Peay HL. Cope HL, et al. Among authors: milko lv. Genet Med. 2024 Dec;26(12):101290. doi: 10.1016/j.gim.2024.101290. Epub 2024 Oct 5. Genet Med. 2024. PMID: 39375994 Free PMC article.
Extending an Antiracism Lens to the Implementation of Precision Public Health Interventions.
Allen CG, Olstad DL, Kahkoska AR, Guan Y, Ramos PS, Steinberg J, Staras SAS, Lumpkins CY, Milko LV, Turbitt E, Rahm AK, Saylor KW, Best S, Hatch A, Santangelo I, Roberts MC. Allen CG, et al. Among authors: milko lv. Am J Public Health. 2023 Nov;113(11):1210-1218. doi: 10.2105/AJPH.2023.307386. Epub 2023 Aug 31. Am J Public Health. 2023. PMID: 37651661 Free PMC article.
Newborn Sequencing in Genomic Medicine and Public Health.
Berg JS, Agrawal PB, Bailey DB Jr, Beggs AH, Brenner SE, Brower AM, Cakici JA, Ceyhan-Birsoy O, Chan K, Chen F, Currier RJ, Dukhovny D, Green RC, Harris-Wai J, Holm IA, Iglesias B, Joseph G, Kingsmore SF, Koenig BA, Kwok PY, Lantos J, Leeder SJ, Lewis MA, McGuire AL, Milko LV, Mooney SD, Parad RB, Pereira S, Petrikin J, Powell BC, Powell CM, Puck JM, Rehm HL, Risch N, Roche M, Shieh JT, Veeraraghavan N, Watson MS, Willig L, Yu TW, Urv T, Wise AL. Berg JS, et al. Among authors: milko lv. Pediatrics. 2017 Feb;139(2):e20162252. doi: 10.1542/peds.2016-2252. Epub 2017 Jan 17. Pediatrics. 2017. PMID: 28096516 Free PMC article. Clinical Trial.
29 results