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

Year Number of Results
2005 75
2006 212
2007 235
2008 352
2009 474
2010 471
2011 565
2012 721
2013 875
2014 811
2015 871
2016 764
2017 614
2018 613
2019 567
2020 566
2021 584
2022 489
2023 423
2024 100

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10,359 results

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A multivariate genome-wide association study of psycho-cardiometabolic multimorbidity.
Baltramonaityte V, Pingault JB, Cecil CAM, Choudhary P, Järvelin MR, Penninx BWJH, Felix J, Sebert S, Milaneschi Y, Walton E; EarlyCause Consortium. Baltramonaityte V, et al. PLoS Genet. 2023 Jun 30;19(6):e1010508. doi: 10.1371/journal.pgen.1010508. eCollection 2023 Jun. PLoS Genet. 2023. PMID: 37390107 Free PMC article.
Endless microbes most beautiful and most wonderful.
Barsh GS, Butler G, Copenhaver GP, Crosson S, Søgaard-Andersen L, Stukenbrock EH. Barsh GS, et al. PLoS Genet. 2023 Apr 20;19(4):e1010695. doi: 10.1371/journal.pgen.1010695. eCollection 2023 Apr. PLoS Genet. 2023. PMID: 37079624 Free PMC article. No abstract available.
Genetic regulators of sputum mucin concentration and their associations with COPD phenotypes.
Van Buren E, Radicioni G, Lester S, O'Neal WK, Dang H, Kasela S, Garudadri S, Curtis JL, Han MK, Krishnan JA, Wan ES, Silverman EK, Hastie A, Ortega VE, Lappalainen T, Nawijn MC, Berge MVD, Christenson SA, Li Y, Cho MH, Kesimer M, Kelada SNP. Van Buren E, et al. PLoS Genet. 2023 Jun 23;19(6):e1010445. doi: 10.1371/journal.pgen.1010445. eCollection 2023 Jun. PLoS Genet. 2023. PMID: 37352370 Free PMC article.
IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans.
Bakey Z, Cabrera OA, Hoefele J, Antony D, Wu K, Stuck MW, Micha D, Eguether T, Smith AO, van der Wel NN, Wagner M, Strittmatter L, Beales PL, Jonassen JA, Thiffault I, Cadieux-Dion M, Boyes L, Sharif S, Tüysüz B, Dunstheimer D, Niessen HWM, Devine W, Lo CW, Mitchison HM, Schmidts M, Pazour GJ. Bakey Z, et al. PLoS Genet. 2023 Jun 14;19(6):e1010796. doi: 10.1371/journal.pgen.1010796. eCollection 2023 Jun. PLoS Genet. 2023. PMID: 37315079 Free PMC article.
Dominant negative variants in KIF5B cause osteogenesis imperfecta via down regulation of mTOR signaling.
Marom R, Zhang B, Washington ME, Song IW, Burrage LC, Rossi VC, Berrier AS, Lindsey A, Lesinski J, Nonet ML, Chen J, Baldridge D, Silverman GA, Sutton VR, Rosenfeld JA, Tran AA, Hicks MJ, Murdock DR, Dai H, Weis M, Jhangiani SN, Muzny DM, Gibbs RA, Caswell R, Pottinger C, Cilliers D, Stals K; Undiagnosed Diseases Network; Eyre D, Krakow D, Schedl T, Pak SC, Lee BH. Marom R, et al. PLoS Genet. 2023 Nov 7;19(11):e1011005. doi: 10.1371/journal.pgen.1011005. eCollection 2023 Nov. PLoS Genet. 2023. PMID: 37934770 Free PMC article.
Opticool: Cutting-edge transgenic optical tools.
Fenelon KD, Krause J, Koromila T. Fenelon KD, et al. PLoS Genet. 2024 Mar 22;20(3):e1011208. doi: 10.1371/journal.pgen.1011208. eCollection 2024 Mar. PLoS Genet. 2024. PMID: 38517915 Free PMC article. Review.
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