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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2005 1
2008 3
2009 4
2011 4
2012 5
2013 4
2014 2
2015 4
2016 3
2017 2
2018 12
2019 13
2020 13
2021 14
2022 15
2023 11
2024 4

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103 results

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Page 1
Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel.
Sturm AC, Knowles JW, Gidding SS, Ahmad ZS, Ahmed CD, Ballantyne CM, Baum SJ, Bourbon M, Carrié A, Cuchel M, de Ferranti SD, Defesche JC, Freiberger T, Hershberger RE, Hovingh GK, Karayan L, Kastelein JJP, Kindt I, Lane SR, Leigh SE, Linton MF, Mata P, Neal WA, Nordestgaard BG, Santos RD, Harada-Shiba M, Sijbrands EJ, Stitziel NO, Yamashita S, Wilemon KA, Ledbetter DH, Rader DJ; Convened by the Familial Hypercholesterolemia Foundation. Sturm AC, et al. J Am Coll Cardiol. 2018 Aug 7;72(6):662-680. doi: 10.1016/j.jacc.2018.05.044. J Am Coll Cardiol. 2018. PMID: 30071997 Free article. Review.
Genetic Testing for Inherited Cardiovascular Diseases: A Scientific Statement From the American Heart Association.
Musunuru K, Hershberger RE, Day SM, Klinedinst NJ, Landstrom AP, Parikh VN, Prakash S, Semsarian C, Sturm AC; American Heart Association Council on Genomic and Precision Medicine; Council on Arteriosclerosis, Thrombosis and Vascular Biology; Council on Cardiovascular and Stroke Nursing; and Council on Clinical Cardiology. Musunuru K, et al. Among authors: sturm ac. Circ Genom Precis Med. 2020 Aug;13(4):e000067. doi: 10.1161/HCG.0000000000000067. Epub 2020 Jul 23. Circ Genom Precis Med. 2020. PMID: 32698598 Free article. Review.
International Atherosclerosis Society guidance for implementing best practice in the care of familial hypercholesterolaemia.
Watts GF, Gidding SS, Hegele RA, Raal FJ, Sturm AC, Jones LK, Sarkies MN, Al-Rasadi K, Blom DJ, Daccord M, de Ferranti SD, Folco E, Libby P, Mata P, Nawawi HM, Ramaswami U, Ray KK, Stefanutti C, Yamashita S, Pang J, Thompson GR, Santos RD. Watts GF, et al. Among authors: sturm ac. Nat Rev Cardiol. 2023 Dec;20(12):845-869. doi: 10.1038/s41569-023-00892-0. Epub 2023 Jun 15. Nat Rev Cardiol. 2023. PMID: 37322181 Review.
An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome.
Adler A, Novelli V, Amin AS, Abiusi E, Care M, Nannenberg EA, Feilotter H, Amenta S, Mazza D, Bikker H, Sturm AC, Garcia J, Ackerman MJ, Hershberger RE, Perez MV, Zareba W, Ware JS, Wilde AAM, Gollob MH. Adler A, et al. Among authors: sturm ac. Circulation. 2020 Feb 11;141(6):418-428. doi: 10.1161/CIRCULATIONAHA.119.043132. Epub 2020 Jan 27. Circulation. 2020. PMID: 31983240 Free PMC article.
Heterozygous Familial Hypercholesterolemia.
Onorato A, Sturm AC. Onorato A, et al. Among authors: sturm ac. Circulation. 2016 Apr 5;133(14):e587-9. doi: 10.1161/CIRCULATIONAHA.115.020701. Circulation. 2016. PMID: 27045133 Review. No abstract available.
Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association.
Landstrom AP, Kim JJ, Gelb BD, Helm BM, Kannankeril PJ, Semsarian C, Sturm AC, Tristani-Firouzi M, Ware SM; American Heart Association Council on Genomic and Precision Medicine; Council on Lifelong Congenital Heart Disease and Heart Health in the Young; Council on Arteriosclerosis, Thrombosis and Vascular Biology; and Council on Lifestyle and Cardiometabolic Health. Landstrom AP, et al. Among authors: sturm ac. Circ Genom Precis Med. 2021 Oct;14(5):e000086. doi: 10.1161/HCG.0000000000000086. Epub 2021 Aug 20. Circ Genom Precis Med. 2021. PMID: 34412507 Free PMC article.
Digital health-enabled genomics: Opportunities and challenges.
Bombard Y, Ginsburg GS, Sturm AC, Zhou AY, Lemke AA. Bombard Y, et al. Among authors: sturm ac. Am J Hum Genet. 2022 Jul 7;109(7):1190-1198. doi: 10.1016/j.ajhg.2022.05.001. Am J Hum Genet. 2022. PMID: 35803232 Free PMC article. Review.
103 results