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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.
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.
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
ALG9 Mutation Carriers Develop Kidney and Liver Cysts.
Besse W, Chang AR, Luo JZ, Triffo WJ, Moore BS, Gulati A, Hartzel DN, Mane S; Regeneron Genetics Center; Torres VE, Somlo S, Mirshahi T. Besse W, et al. Among authors: hartzel dn. J Am Soc Nephrol. 2019 Nov;30(11):2091-2102. doi: 10.1681/ASN.2019030298. Epub 2019 Aug 8. J Am Soc Nephrol. 2019. PMID: 31395617 Free PMC article.
Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants.
Haggerty CM, Damrauer SM, Levin MG, Birtwell D, Carey DJ, Golden AM, Hartzel DN, Hu Y, Judy R, Kelly MA, Kember RL, Lester Kirchner H, Leader JB, Liang L, McDermott-Roe C, Babu A, Morley M, Nealy Z, Person TN, Pulenthiran A, Small A, Smelser DT, Stahl RC, Sturm AC, Williams H, Baras A, Margulies KB, Cappola TP, Dewey FE, Verma A, Zhang X, Correa A, Hall ME, Wilson JG, Ritchie MD, Rader DJ, Murray MF, Fornwalt BK, Arany Z. Haggerty CM, et al. Among authors: hartzel dn. Circulation. 2019 Jul 2;140(1):42-54. doi: 10.1161/CIRCULATIONAHA.119.039573. Epub 2019 Jun 20. Circulation. 2019. PMID: 31216868 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.
A Machine Learning Approach to Management of Heart Failure Populations.
Jing L, Ulloa Cerna AE, Good CW, Sauers NM, Schneider G, Hartzel DN, Leader JB, Kirchner HL, Hu Y, Riviello DM, Stough JV, Gazes S, Haggerty A, Raghunath S, Carry BJ, Haggerty CM, Fornwalt BK. Jing L, et al. Among authors: hartzel dn. JACC Heart Fail. 2020 Jul;8(7):578-587. doi: 10.1016/j.jchf.2020.01.012. Epub 2020 May 6. JACC Heart Fail. 2020. PMID: 32387064 Free 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.
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.
Prediction of mortality from 12-lead electrocardiogram voltage data using a deep neural network.
Raghunath S, Ulloa Cerna AE, Jing L, vanMaanen DP, Stough J, Hartzel DN, Leader JB, Kirchner HL, Stumpe MC, Hafez A, Nemani A, Carbonati T, Johnson KW, Young K, Good CW, Pfeifer JM, Patel AA, Delisle BP, Alsaid A, Beer D, Haggerty CM, Fornwalt BK. Raghunath S, et al. Among authors: hartzel dn. Nat Med. 2020 Jun;26(6):886-891. doi: 10.1038/s41591-020-0870-z. Epub 2020 May 11. Nat Med. 2020. PMID: 32393799
31 results