K99 HG011491/HG/NHGRI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2021	1
2022	7
2023	5
2024	1

1

Family-level impact of genetic testing: integrating health economics and ethical, legal, and social implications.

Smith HS, McGuire AL, Wittenberg E, Lavelle TA. Smith HS, et al. Per Med. 2021 May;18(3):209-212. doi: 10.2217/pme-2021-0016. Epub 2021 Mar 17. Per Med. 2021. PMID: 33728981 Free PMC article.

2

A call for an integrated approach to improve efficiency, equity and sustainability in rare disease research in the United States.

Halley MC, Smith HS, Ashley EA, Goldenberg AJ, Tabor HK. Halley MC, et al. Nat Genet. 2022 Mar;54(3):219-222. doi: 10.1038/s41588-022-01027-w. Nat Genet. 2022. PMID: 35256804 Free PMC article.

3

Patient and Clinician Perceptions of Precision Cardiology Care: Findings From the HeartCare Study.

Smith HS, Sanchez CE, Maag R, Buentello A, Murdock DR, Metcalf GA, Hadley TD, Riconda DL, Boerwinkle E, Wehrens XHT, Ballantyne CM, Gibbs RA, McGuire AL, Pereira S. Smith HS, et al. Circ Genom Precis Med. 2022 Dec;15(6):e003605. doi: 10.1161/CIRCGEN.121.003605. Epub 2022 Oct 25. Circ Genom Precis Med. 2022. PMID: 36282588 Free PMC article.

4

Cost-effectiveness frameworks for comparing genome and exome sequencing versus conventional diagnostic pathways: A scoping review and recommended methods.

Ferket BS, Baldwin Z, Murali P, Pai A, Mittendorf KF, Russell HV, Chen F, Lynch FL, Lich KH, Hindorff LA, Savich R, Slavotinek A, Smith HS, Gelb BD, Veenstra DL. Ferket BS, et al. Genet Med. 2022 Oct;24(10):2014-2027. doi: 10.1016/j.gim.2022.06.004. Epub 2022 Jul 14. Genet Med. 2022. PMID: 35833928 Free PMC article. Review.

5

Parent-Reported Clinical Utility of Pediatric Genomic Sequencing.

Smith HS, Ferket BS, Gelb BD, Hindorff L, Ferar KD, Norton ME, Sahin-Hodoglugil N, Slavotinek A, Lich KH, Berg JS, Russell HV. Smith HS, et al. Pediatrics. 2023 Aug 1;152(2):e2022060318. doi: 10.1542/peds.2022-060318. Pediatrics. 2023. PMID: 37470118

6

Quality of life, illness perceptions, and parental lived experiences in TANGO2-related metabolic encephalopathy and arrhythmias.

Murali CN, Lalani SR, Azamian MS, Miyake CY, Smith HS. Murali CN, et al. Eur J Hum Genet. 2022 Sep;30(9):1044-1050. doi: 10.1038/s41431-022-01127-5. Epub 2022 Jun 13. Eur J Hum Genet. 2022. PMID: 35691983 Free PMC article.

7

Clinically Indicated Genomic Sequencing of Children in Foster Care: Legal and Ethical Issues.

Smith HS, Bonkowski ES, Hickingbotham MR, Pereira S, May T, Guerrini CJ. Smith HS, et al. J Pediatr. 2023 Nov;262:113612. doi: 10.1016/j.jpeds.2023.113612. Epub 2023 Jul 17. J Pediatr. 2023. PMID: 37468037

8

Access to clinically indicated genetic tests for pediatric patients with Medicaid: Evidence from outpatient genetics clinics in Texas.

Streff H, Uhles CL, Fisher H, Franciskovich R, Littlejohn RO, Gerard A, Hudnall J, Smith HS. Streff H, et al. Genet Med. 2023 Mar;25(3):100350. doi: 10.1016/j.gim.2022.11.018. Epub 2022 Dec 6. Genet Med. 2023. PMID: 36547467 Free article.

9

Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study.

Armstrong B, Christensen KD, Genetti CA, Parad RB, Robinson JO, Blout Zawatsky CL, Zettler B, Beggs AH, Holm IA, Green RC, McGuire AL, Smith HS, Pereira S; BabySeq Project Team. Armstrong B, et al. Front Genet. 2022 Apr 27;13:867371. doi: 10.3389/fgene.2022.867371. eCollection 2022. Front Genet. 2022. PMID: 35571041 Free PMC article.

10

Key drivers of family-level utility of pediatric genomic sequencing: a qualitative analysis to support preference research.

Smith HS, Bonkowski ES, Deloge RB, Gutierrez AM, Recinos AM, Lavelle TA, Veenstra DL, McGuire AL, Pereira S. Smith HS, et al. Eur J Hum Genet. 2023 Apr;31(4):445-452. doi: 10.1038/s41431-022-01245-0. Epub 2022 Nov 25. Eur J Hum Genet. 2023. PMID: 36434257 Free PMC article.

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