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

Year Number of Results
2006 2
2007 3
2008 1
2009 2
2010 1
2011 6
2012 2
2013 2
2014 4
2015 2
2016 2
2017 5
2018 5
2019 5
2020 11
2021 16
2022 15
2023 16
2024 14
2025 11

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114 results

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Page 1
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: landstrom ap. 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.
Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource.
Koch RL, Soler-Alfonso C, Kiely BT, Asai A, Smith AL, Bali DS, Kang PB, Landstrom AP, Akman HO, Burrow TA, Orthmann-Murphy JL, Goldman DS, Pendyal S, El-Gharbawy AH, Austin SL, Case LE, Schiffmann R, Hirano M, Kishnani PS. Koch RL, et al. Among authors: landstrom ap. Mol Genet Metab. 2023 Mar;138(3):107525. doi: 10.1016/j.ymgme.2023.107525. Epub 2023 Jan 25. Mol Genet Metab. 2023. PMID: 36796138 Review.
Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort.
Meester JAN, Peeters S, Van Den Heuvel L, Vandeweyer G, Fransen E, Cappella E, Dietz HC, Forbus G, Gelb BD, Goldmuntz E, Hoskoppal A, Landstrom AP, Lee T, Mital S, Morris S, Olson AK, Renard M, Roden DM, Singh MN, Selamet Tierney ES, Tretter JT, Van Driest SL, Willing M, Verstraeten A, Van Laer L, Lacro RV, Loeys BL. Meester JAN, et al. Among authors: landstrom ap. Genet Med. 2022 May;24(5):1045-1053. doi: 10.1016/j.gim.2021.12.015. Epub 2022 Jan 17. Genet Med. 2022. PMID: 35058154 Free PMC article.
ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel: Reappraisal of Genes associated with Hypertrophic Cardiomyopathy.
Hespe S, Waddell A, Asatryan B, Owens E, Thaxton C, Adduru ML, Anderson K, Brown EE, Hoffman-Andrews L, Jordan E, Josephs K, Mayers M, Peters S, Stafford F, Bagnall RD, Bronicki L, Callewaert B, Chahal CAA, James CA, Jarinova O, Landstrom AP, McNally EM, Murray B, Muiño-Mosquera L, Parikh V, Reuter C, Walsh R, Wayburn B, Ware JS, Ingles J. Hespe S, et al. Among authors: landstrom ap. medRxiv [Preprint]. 2024 Jul 31:2024.07.29.24311195. doi: 10.1101/2024.07.29.24311195. medRxiv. 2024. Update in: J Am Coll Cardiol. 2025 Feb 25;85(7):727-740. doi: 10.1016/j.jacc.2024.12.010. PMID: 39132495 Free PMC article. Updated. Preprint.
Calcium Signaling and Cardiac Arrhythmias.
Landstrom AP, Dobrev D, Wehrens XHT. Landstrom AP, et al. Circ Res. 2017 Jun 9;120(12):1969-1993. doi: 10.1161/CIRCRESAHA.117.310083. Circ Res. 2017. PMID: 28596175 Free PMC article. Review.
TAX1BP3 Causes TRPV4-Mediated Autosomal Recessive Arrhythmogenic Cardiomyopathy.
Perelli RM, Dewars ER, Cope H, Behura AS, Ponek AQ, Sala AM, Zhang Z, Muralidharan P, Moya-Mendez ME, Berkman A, Monaco GG, Sullivan MC, Ezekian JE, Yang Q, Sun B, Kurzlechner LM, Asokan T, Breglio AM, Campbell MJ, Spector ZZ, Rehder CW; Undiagnosed Diseases Network; Tang PC, James CA, Calkins H, Shashi V, Landstrom AP. Perelli RM, et al. Among authors: landstrom ap. Circ Res. 2025 Mar 28;136(7):667-684. doi: 10.1161/CIRCRESAHA.124.325180. Epub 2025 Feb 18. Circ Res. 2025. PMID: 39963794 Free article.
114 results