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Year Number of Results
2015 1
2016 2
2017 2
2018 5
2019 5
2020 7
2021 5
2022 4
2023 2
2024 0

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31 results

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Page 1
Rare coding variants in CHRNB2 reduce the likelihood of smoking.
Rajagopal VM, Watanabe K, Mbatchou J, Ayer A, Quon P, Sharma D, Kessler MD, Praveen K, Gelfman S, Parikshak N, Otto JM, Bao S, Chim SM, Pavlopoulos E, Avbersek A, Kapoor M, Chen E, Jones MB, Leblanc M, Emberson J, Collins R, Torres J, Morales PK, Tapia-Conyer R, Alegre J, Berumen J; GHS-REGN DiscovEHR collaboration; Regeneron Genetics Center; Shuldiner AR, Balasubramanian S, Abecasis GR, Kang HM, Marchini J, Stahl EA, Jorgenson E, Sanchez R, Liedtke W, Anderson M, Cantor M, Lederer D, Baras A, Coppola G. Rajagopal VM, et al. Nat Genet. 2023 Jul;55(7):1138-1148. doi: 10.1038/s41588-023-01417-8. Epub 2023 Jun 12. Nat Genet. 2023. PMID: 37308787 Free PMC article.
An ECG-based machine learning model for predicting new-onset atrial fibrillation is superior to age and clinical features in identifying patients at high stroke risk.
Raghunath S, Pfeifer JM, Kelsey CR, Nemani A, Ruhl JA, Hartzel DN, Ulloa Cerna AE, Jing L, vanMaanen DP, Leader JB, Schneider G, Morland TB, Chen R, Zimmerman N, Fornwalt BK, Haggerty CM. Raghunath S, et al. Among authors: hartzel dn. J Electrocardiol. 2023 Jan-Feb;76:61-65. doi: 10.1016/j.jelectrocard.2022.11.001. Epub 2022 Nov 8. J Electrocardiol. 2023. PMID: 36436476 Free article.
ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma.
Praveen K, Patel GC, Gurski L, Ayer AH, Persaud T, Still MD, Miloscio L, Van Zyl T, Di Gioia SA, Brumpton B, Krebs K, Åsvold BO, Chen E, Chavali VRM, Fury W, Gudiseva HV, Hyde S, Jorgenson E, Lefebvre S, Li D, Li A, Mclninch J, Patel B, Rabinowitz JS, Salowe R, Schurmann C, Seidelin AS, Stahl E, Sun D, Teslovich TM, Tybjærg-Hansen A, Willer C, Waldron S, Walley S, Yang H, Zaveri S; Regeneron Genetics Center; GHS-RGC DiscovEHR Collaboration; Estonian Biobank Research Team; Hu Y, Hveem K, Melander O, Milani L, Stender S, O'Brien JM, Jones MB, Abecasis GR, Cantor MN, Weyne J, Karalis K, Economides A, Della Gatta G, Ferreira MA, Yancopoulos GD, Baras A, Romano C, Coppola G. Praveen K, et al. Commun Biol. 2022 Oct 3;5(1):1051. doi: 10.1038/s42003-022-03932-6. Commun Biol. 2022. PMID: 36192519 Free PMC article.
Impact of a Population Genomic Screening Program on Health Behaviors Related to Familial Hypercholesterolemia Risk Reduction.
Jones LK, Chen N, Hassen DA, Betts MN, Klinger T, Hartzel DN, Veenstra DL, Spencer SJ, Snyder SR, Peterson JF, Schlieder V, Sturm AC, Gidding SS, Williams MS, Hao J. Jones LK, et al. Among authors: hartzel dn. Circ Genom Precis Med. 2022 Oct;15(5):e003549. doi: 10.1161/CIRCGEN.121.003549. Epub 2022 Jul 12. Circ Genom Precis Med. 2022. PMID: 35862023 Free PMC article.
Population-scale analysis of common and rare genetic variation associated with hearing loss in adults.
Praveen K, Dobbyn L, Gurski L, Ayer AH, Staples J, Mishra S, Bai Y, Kaufman A, Moscati A, Benner C, Chen E, Chen S, Popov A, Smith J; GHS-REGN DiscovEHR collaboration; Regeneron Genetics Center; Decibel-REGN collaboration; Melander O, Jones MB, Marchini J, Balasubramanian S, Zambrowicz B, Drummond MC, Baras A, Abecasis GR, Ferreira MA, Stahl EA, Coppola G. Praveen K, et al. Commun Biol. 2022 Jun 3;5(1):540. doi: 10.1038/s42003-022-03408-7. Commun Biol. 2022. PMID: 35661827 Free PMC article.
Predictive Accuracy of a Clinical and Genetic Risk Model for Atrial Fibrillation.
Khurshid S, Mars N, Haggerty CM, Huang Q, Weng LC, Hartzel DN; Regeneron Genetics Center; Lunetta KL, Ashburner JM, Anderson CD, Benjamin EJ, Salomaa V, Ellinor PT, Fornwalt BK, Ripatti S, Trinquart L, Lubitz SA. Khurshid S, et al. Among authors: hartzel dn. Circ Genom Precis Med. 2021 Oct;14(5):e003355. doi: 10.1161/CIRCGEN.121.003355. Epub 2021 Aug 31. Circ Genom Precis Med. 2021. PMID: 34463125 Free PMC article. Clinical Trial.
GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms.
Ward LD, Tu HC, Quenneville CB, Tsour S, Flynn-Carroll AO, Parker MM, Deaton AM, Haslett PAJ, Lotta LA, Verweij N, Ferreira MAR; Regeneron Genetics Center; Geisinger-Regeneron DiscovEHR Collaboration; Baras A, Hinkle G, Nioi P. Ward LD, et al. Nat Commun. 2021 Jul 27;12(1):4571. doi: 10.1038/s41467-021-24563-1. Nat Commun. 2021. PMID: 34315874 Free PMC article.
Deep Neural Networks Can Predict New-Onset Atrial Fibrillation From the 12-Lead ECG and Help Identify Those at Risk of Atrial Fibrillation-Related Stroke.
Raghunath S, Pfeifer JM, Ulloa-Cerna AE, Nemani A, Carbonati T, Jing L, vanMaanen DP, Hartzel DN, Ruhl JA, Lagerman BF, Rocha DB, Stoudt NJ, Schneider G, Johnson KW, Zimmerman N, Leader JB, Kirchner HL, Griessenauer CJ, Hafez A, Good CW, Fornwalt BK, Haggerty CM. Raghunath S, et al. Among authors: hartzel dn. Circulation. 2021 Mar 30;143(13):1287-1298. doi: 10.1161/CIRCULATIONAHA.120.047829. Epub 2021 Feb 16. Circulation. 2021. PMID: 33588584 Free PMC article.
Deep-learning-assisted analysis of echocardiographic videos improves predictions of all-cause mortality.
Ulloa Cerna AE, Jing L, Good CW, vanMaanen DP, Raghunath S, Suever JD, Nevius CD, Wehner GJ, Hartzel DN, Leader JB, Alsaid A, Patel AA, Kirchner HL, Pfeifer JM, Carry BJ, Pattichis MS, Haggerty CM, Fornwalt BK. Ulloa Cerna AE, et al. Among authors: hartzel dn. Nat Biomed Eng. 2021 Jun;5(6):546-554. doi: 10.1038/s41551-020-00667-9. Epub 2021 Feb 8. Nat Biomed Eng. 2021. PMID: 33558735
31 results