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The motivation and process for developing a consortium-wide time and motion study to estimate resource implications of innovations in the use of genome sequencing to inform patient care.
Clin Transl Sci. 2024 Jan;17(1):e13635. doi: 10.1111/cts.13635. Epub 2023 Dec 8.
Clin Transl Sci. 2024.
PMID: 38064200
Free PMC article.
Review.
Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population.
Slavotinek A, Rego S, Sahin-Hodoglugil N, Kvale M, Lianoglou B, Yip T, Hoban H, Outram S, Anguiano B, Chen F, Michelson J, Cilio RM, Curry C, Gallagher RC, Gardner M, Kuperman R, Mendelsohn B, Sherr E, Shieh J, Strober J, Tam A, Tenney J, Weiss W, Whittle A, Chin G, Faubel A, Prasad H, Mavura Y, Van Ziffle J, Devine WP, Hodoglugil U, Martin PM, Sparks TN, Koenig B, Ackerman S, Risch N, Kwok PY, Norton ME.
Slavotinek A, et al. Among authors: hoban h.
NPJ Genom Med. 2023 Oct 23;8(1):34. doi: 10.1038/s41525-023-00382-9.
NPJ Genom Med. 2023.
PMID: 37872195
Free PMC article.
No abstract available.
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Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population.
Slavotinek A, Rego S, Sahin-Hodoglugil N, Kvale M, Lianoglou B, Yip T, Hoban H, Outram S, Anguiano B, Chen F, Michelson J, Cilio RM, Curry C, Gallagher RC, Gardner M, Kuperman R, Mendelsohn B, Sherr E, Shieh J, Strober J, Tam A, Tenney J, Weiss W, Whittle A, Chin G, Faubel A, Prasad H, Mavura Y, Van Ziffle J, Devine WP, Hodoglugil U, Martin PM, Sparks TN, Koenig B, Ackerman S, Risch N, Kwok PY, Norton ME.
Slavotinek A, et al. Among authors: hoban h.
NPJ Genom Med. 2023 May 26;8(1):10. doi: 10.1038/s41525-023-00353-0.
NPJ Genom Med. 2023.
PMID: 37236975
Free PMC article.
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Information-seeking preferences in diverse patients receiving a genetic testing result in the Clinical Sequencing Evidence-Generating Research (CSER) study.
Slavotinek A, Prasad H, Outram S, Scollon S, Rego S, Yip T, Hoban H, Foreman KM, Kelley W, Finnila C, Berg J, Murali P, Bonini KE, Martin LJ, Hott A.
Slavotinek A, et al. Among authors: hoban h.
Genet Med. 2023 Sep;25(9):100899. doi: 10.1016/j.gim.2023.100899. Epub 2023 May 19.
Genet Med. 2023.
PMID: 37212252
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Perspectives and preferences regarding genomic secondary findings in underrepresented prenatal and pediatric populations: A mixed-methods approach.
Rego S, Hoban H, Outram S, Zamora AN, Chen F, Sahin-Hodoglugil N, Anguiano B, Norstad M, Yip T, Lianoglou B, Sparks TN, Norton ME, Koenig BA, Slavotinek AM, Ackerman SL.
Rego S, et al. Among authors: hoban h.
Genet Med. 2022 Jun;24(6):1206-1216. doi: 10.1016/j.gim.2022.02.004. Epub 2022 Apr 8.
Genet Med. 2022.
PMID: 35396980
Free PMC article.
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Predicting genes from phenotypes using human phenotype ontology (HPO) terms.
Slavotinek A, Prasad H, Yip T, Rego S, Hoban H, Kvale M.
Slavotinek A, et al. Among authors: hoban h.
Hum Genet. 2022 Nov;141(11):1749-1760. doi: 10.1007/s00439-022-02449-6. Epub 2022 Mar 31.
Hum Genet. 2022.
PMID: 35357580
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Examining access to care in clinical genomic research and medicine: Experiences from the CSER Consortium.
Gutierrez AM, Robinson JO, Outram SM, Smith HS, Kraft SA, Donohue KE, Biesecker BB, Brothers KB, Chen F, Hailu B, Hindorff LA, Hoban H, Hsu RL, Knight SJ, Koenig BA, Lewis KL, Lich KH, O'Daniel JM, Okuyama S, Tomlinson GE, Waltz M, Wilfond BS, Ackerman SL, Majumder MA.
Gutierrez AM, et al. Among authors: hoban h.
J Clin Transl Sci. 2021 Sep 14;5(1):e193. doi: 10.1017/cts.2021.855. eCollection 2021.
J Clin Transl Sci. 2021.
PMID: 34888063
Free PMC article.
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