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

Year Number of Results
2002 3
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2004 5
2005 7
2006 10
2007 20
2008 6
2009 17
2010 11
2011 23
2012 13
2013 26
2014 20
2015 16
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2025 13

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375 results

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Page 1
Recognition and management of persistent chylomicronemia: A joint expert clinical consensus by the National Lipid Association and the American Society for Preventive Cardiology.
Saadatagah S, Larouche M, Naderian M, Nambi V, Brisson D, Kullo IJ, Duell PB, Michos ED, Shapiro MD, Watts GF, Gaudet D, Ballantyne CM. Saadatagah S, et al. Among authors: kullo ij. J Clin Lipidol. 2025 Mar 28:S1933-2874(25)00065-0. doi: 10.1016/j.jacl.2025.03.012. Online ahead of print. J Clin Lipidol. 2025. PMID: 40360374
Recognition and management of persistent chylomicronemia: A joint expert clinical consensus by the National Lipid Association and the American Society for Preventive Cardiology.
Saadatagah S, Larouche M, Naderian M, Nambi V, Brisson D, Kullo IJ, Duell PB, Michos ED, Shapiro MD, Watts GF, Gaudet D, Ballantyne CM. Saadatagah S, et al. Among authors: kullo ij. Am J Prev Cardiol. 2025 Mar 28;22:100978. doi: 10.1016/j.ajpc.2025.100978. eCollection 2025 Jun. Am J Prev Cardiol. 2025. PMID: 40242365 Free PMC article.
Clonal Hematopoiesis of Indeterminate Potential in Chronic Coronary Disease: A Report From the ISCHEMIA Trials Biorepository.
Muller M, Liu R, Shah F, Hu J, Held C, Kullo IJ, McManus B, Wallentin L, Newby LK, Sidhu MS, Bangalore S, Reynolds HR, Hochman JS, Maron DJ, Ruggles KV, Berger JS, Newman JD. Muller M, et al. Among authors: kullo ij. Circ Genom Precis Med. 2025 Apr 10:e004921. doi: 10.1161/CIRCGEN.124.004921. Online ahead of print. Circ Genom Precis Med. 2025. PMID: 40207358 No abstract available.
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum.
Lee DSM, Cardone KM, Zhang DY, Tsao NL, Abramowitz S, Sharma P, DePaolo JS, Conery M, Aragam KG, Biddinger K, Dilitikas O, Hoffman-Andrews L, Judy RL, Khan A, Kullo IJ, Puckelwartz MJ, Reza N, Satterfield BA, Singhal P; Penn Medicine Biobank; Arany Z, Cappola TP, Carruth ED, Day SM, Do R, Haggerty CM, Joseph J, McNally EM, Nadkarni G, Owens AT, Rader DJ, Ritchie MD, Sun YV, Voight BF, Levin MG, Damrauer SM. Lee DSM, et al. Among authors: kullo ij. Nat Genet. 2025 Apr;57(4):829-838. doi: 10.1038/s41588-025-02140-2. Epub 2025 Apr 7. Nat Genet. 2025. PMID: 40195560
Mixed-effects polygenic risk score Phenome-wide association study detects genetic correlation between colorectal cancer risk and phenotype data extracted from the electronic health record.
Rosenthal EA, Wei WQ, Luo Y, Namjou-Khales B, Schaid DJ, Esplin ED, Lape M, Kottyan L, Pacheco JAPA, Weng C, Gordon AS, Kullo IJ, Crosslin DR, Grady WM, Hsu L, Peters U, Jarvik GP. Rosenthal EA, et al. Among authors: kullo ij. medRxiv [Preprint]. 2025 Feb 28:2025.02.26.25322864. doi: 10.1101/2025.02.26.25322864. medRxiv. 2025. PMID: 40061333 Free PMC article. Preprint.
Data Sharing in the PRIMED Consortium: Design, implementation, and recommendations for future policymaking.
Smith JL, Wong Q, Hornsby W, Conomos MP, Heavner BD, Kullo IJ, Psaty BM, Rich SS, Tayo B, Natarajan P, Nelson SC; Polygenic Risk Methods in Diverse Populations (PRIMED) Consortium Data Sharing Working Group, Polygenic Risk Methods in Diverse Populations (PRIMED) Consortium. Smith JL, et al. Among authors: kullo ij. ArXiv [Preprint]. 2025 Feb 12:arXiv:2502.09351v1. ArXiv. 2025. PMID: 39990790 Free PMC article. Preprint.
Genetic risk disclosure and behavioural change: not so fast.
Naderian M, Kullo IJ. Naderian M, et al. Among authors: kullo ij. Eur J Prev Cardiol. 2025 Feb 5:zwaf014. doi: 10.1093/eurjpc/zwaf014. Online ahead of print. Eur J Prev Cardiol. 2025. PMID: 39907735 No abstract available.
375 results