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Results by year

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

Year Number of Results
2011 3
2012 6
2013 3
2014 1
2015 3
2016 4
2017 6
2018 2
2019 4
2020 6
2021 8
2022 9
2023 5
2024 5
2025 5
2026 0

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Cited In for PMID: 22072978

61 results

Results by year

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Page 1
Myocardial reprogramming by HMGN1 underlies heart defects in trisomy 21.
Ranade SS, Li F, Whalen S, Pelonero A, Ye L, Huang Y, Brand A, Nishino T, Mital R, Boileau RM, Koback F, Padmanabhan A, Yu V, Cimarosti B, Presas-Ramos D, Merriman AF, Wallace LG, Nguyen A, Poulis N, Costa MW, Gifford CA, Pollard KS, Srivastava D. Ranade SS, et al. Nature. 2025 Nov;647(8091):979-987. doi: 10.1038/s41586-025-09593-9. Epub 2025 Oct 22. Nature. 2025. PMID: 41125893 Free PMC article.
Rare genomic copy number variants implicate new candidate genes for bicuspid aortic valve.
Carlisle SG, Albasha H, Michelena HI, Sabate-Rotes A, Bianco L, De Backer J, Mosquera LM, Yetman AT, Bissell MM, Andreassi MG, Foffa I, Hui DS, Caffarelli A, Kim YY, Guo D, Citro R, De Marco M, Tretter JT, McBride KL, Milewicz DM, Body SC, Prakash SK; EBAV Investigators; BAVCon Investigators. Carlisle SG, et al. PLoS One. 2024 Sep 6;19(9):e0304514. doi: 10.1371/journal.pone.0304514. eCollection 2024. PLoS One. 2024. PMID: 39240962 Free PMC article.
Increased endothelial sclerostin caused by elevated DSCAM mediates multiple trisomy 21 phenotypes.
McKean DM, Zhang Q, Narayan P, Morton SU, Strohmenger V, Tang VT, McAllister S, Sharma A, Quiat D, Reichart D, DeLaughter DM, Wakimoto H, Gorham JM, Brown K, McDonough B, Willcox JA, Jang MY, DePalma SR, Ward T; Pediatric Cardiac Genomics Consortium Investigators; Kim R, Cleveland JD, Seidman JG, Seidman CE. McKean DM, et al. J Clin Invest. 2024 Jun 3;134(11):e167811. doi: 10.1172/JCI167811. J Clin Invest. 2024. PMID: 38828726 Free PMC article.
61 results