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764 results

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Page 1
Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery: a multi-ancestry study in 10 960 individuals from 9 biobanks.
German J, Cordioli M, Tozzo V, Urbut S, Arumäe K, Smit RAJ, Lee J, Li JH, Janucik A, Ding Y, Akinkuolie A, Heyne H, Eoli A, Saad C, Al-Sarraj Y, Abdel-Latif R, Barry A, Wang Z; Estonian Biobank research team; Natarajan P, Ripatti S, Philippakis A, Szczerbinski L, Pasaniuc B, Mbarek H, Loos RJF, Vainik U, Ganna A. German J, et al. Among authors: natarajan p. medRxiv [Preprint]. 2024 Sep 12:2024.09.11.24313458. doi: 10.1101/2024.09.11.24313458. medRxiv. 2024. PMID: 39314946 Free PMC article. Preprint.
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.
Wang Y, Selvaraj MS, Li X, Li Z, Holdcraft JA, Arnett DK, Bis JC, Blangero J, Boerwinkle E, Bowden DW, Cade BE, Carlson JC, Carson AP, Chen YI, Curran JE, de Vries PS, Dutcher SK, Ellinor PT, Floyd JS, Fornage M, Freedman BI, Gabriel S, Germer S, Gibbs RA, Guo X, He J, Heard-Costa N, Hildalgo B, Hou L, Irvin MR, Joehanes R, Kaplan RC, Kardia SL, Kelly TN, Kim R, Kooperberg C, Kral BG, Levy D, Li C, Liu C, Lloyd-Jone D, Loos RJ, Mahaney MC, Martin LW, Mathias RA, Minster RL, Mitchell BD, Montasser ME, Morrison AC, Murabito JM, Naseri T, O'Connell JR, Palmer ND, Preuss MH, Psaty BM, Raffield LM, Rao DC, Redline S, Reiner AP, Rich SS, Ruepena MS, Sheu WH, Smith JA, Smith A, Tiwari HK, Tsai MY, Viaud-Martinez KA, Wang Z, Yanek LR, Zhao W; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium; Rotter JI, Lin X, Natarajan P, Peloso GM. Wang Y, et al. Among authors: natarajan p. medRxiv [Preprint]. 2023 Jun 29:2023.06.28.23291966. doi: 10.1101/2023.06.28.23291966. medRxiv. 2023. Update in: Am J Hum Genet. 2023 Oct 5;110(10):1704-1717. doi: 10.1016/j.ajhg.2023.09.003 PMID: 37425772 Free PMC article. Updated. Preprint.
Decoding Genetics, Ancestry, and Geospatial Context for Precision Health.
Koyama S, Wang Y, Paruchuri K, Uddin MM, Cho SMJ, Urbut SM, Haidermota S, Hornsby WE, Green RC, Daly MJ, Neale BM, Ellinor PT, Smoller JW, Lebo MS, Karlson EW, Martin AR, Natarajan P. Koyama S, et al. Among authors: natarajan p. medRxiv [Preprint]. 2023 Oct 25:2023.10.24.23297096. doi: 10.1101/2023.10.24.23297096. medRxiv. 2023. PMID: 37961173 Free PMC article. Preprint.
MSGene: Derivation and validation of a multistate model for lifetime risk of coronary artery disease using genetic risk and the electronic health record.
Urbut SM, Yeung MW, Khurshid S, Cho SMJ, Schuermans A, German J, Taraszka K, Fahed AC, Ellinor P, Trinquart L, Parmigiani G, Gusev A, Natarajan P. Urbut SM, et al. Among authors: natarajan p. medRxiv [Preprint]. 2023 Nov 8:2023.11.08.23298229. doi: 10.1101/2023.11.08.23298229. medRxiv. 2023. Update in: Nat Commun. 2024 Jun 7;15(1):4884. doi: 10.1038/s41467-024-49296-9 PMID: 37986972 Free PMC article. Updated. Preprint.
Deep learning-derived splenic radiomics, genomics, and coronary artery disease.
Kamineni M, Raghu V, Truong B, Alaa A, Schuermans A, Friedman S, Reeder C, Bhattacharya R, Libby P, Ellinor PT, Maddah M, Philippakis A, Hornsby W, Yu Z, Natarajan P. Kamineni M, et al. Among authors: natarajan p. medRxiv [Preprint]. 2024 Aug 20:2024.08.16.24312129. doi: 10.1101/2024.08.16.24312129. medRxiv. 2024. PMID: 39185532 Free PMC article. Preprint.
The PRIMED Consortium: Reducing disparities in polygenic risk assessment.
Kullo IJ, Conomos MP, Nelson SC, Adebamowo SN, Choudhury A, Conti D, Fullerton SM, Gogarten SM, Heavner B, Hornsby WE, Kenny EE, Khan A, Khera AV, Li Y, Martin I, Mercader JM, Ng M, Raffield LM, Reiner A, Rowley R, Schaid D, Stilp A, Wiley K, Wilson R, Witte JS, Natarajan P; Polygenic Risk Methods in Diverse Populations (PRIMED) Consortium. Kullo IJ, et al. Among authors: natarajan p. Am J Hum Genet. 2024 Dec 5;111(12):2594-2606. doi: 10.1016/j.ajhg.2024.10.010. Epub 2024 Nov 18. Am J Hum Genet. 2024. PMID: 39561770 Free PMC article.
764 results