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

Year Number of Results
1972 1
1973 2
1977 1
1978 2
1980 4
1981 1
1982 3
1987 1
1988 5
1989 5
1992 1
1993 3
1994 1
1995 3
1996 1
1997 2
2001 1
2005 2
2006 2
2007 5
2008 4
2009 3
2010 8
2011 6
2012 4
2014 10
2015 8
2016 10
2017 3
2018 7
2019 10
2020 10
2021 7
2022 8
2023 6
2024 6

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143 results

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Page 1
Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.
Pierpont ME, Brueckner M, Chung WK, Garg V, Lacro RV, McGuire AL, Mital S, Priest JR, Pu WT, Roberts A, Ware SM, Gelb BD, Russell MW; American Heart Association Council on Cardiovascular Disease in the Young; Council on Cardiovascular and Stroke Nursing; and Council on Genomic and Precision Medicine. Pierpont ME, et al. Among authors: priest jr. Circulation. 2018 Nov 20;138(21):e653-e711. doi: 10.1161/CIR.0000000000000606. Circulation. 2018. PMID: 30571578 Free PMC article. Review.
Congenital heart disease risk loci identified by genome-wide association study in European patients.
Lahm H, Jia M, Dreßen M, Wirth F, Puluca N, Gilsbach R, Keavney BD, Cleuziou J, Beck N, Bondareva O, Dzilic E, Burri M, König KC, Ziegelmüller JA, Abou-Ajram C, Neb I, Zhang Z, Doppler SA, Mastantuono E, Lichtner P, Eckstein G, Hörer J, Ewert P, Priest JR, Hein L, Lange R, Meitinger T, Cordell HJ, Müller-Myhsok B, Krane M. Lahm H, et al. Among authors: priest jr. J Clin Invest. 2021 Jan 19;131(2):e141837. doi: 10.1172/JCI141837. J Clin Invest. 2021. PMID: 33201861 Free PMC article. Clinical Trial.
Targeting HDAC6 to treat heart failure with preserved ejection fraction in mice.
Ranjbarvaziri S, Zeng A, Wu I, Greer-Short A, Farshidfar F, Budan A, Xu E, Shenwai R, Kozubov M, Li C, Van Pell M, Grafton F, MacKay CE, Song X, Priest JR, Argast G, Mandegar MA, Hoey T, Yang J. Ranjbarvaziri S, et al. Among authors: priest jr. Nat Commun. 2024 Feb 26;15(1):1352. doi: 10.1038/s41467-024-45440-7. Nat Commun. 2024. PMID: 38409164 Free PMC article.
Imaging of DICER1 syndrome.
Guillerman RP, Foulkes WD, Priest JR. Guillerman RP, et al. Among authors: priest jr. Pediatr Radiol. 2019 Oct;49(11):1488-1505. doi: 10.1007/s00247-019-04429-x. Epub 2019 Oct 16. Pediatr Radiol. 2019. PMID: 31620849 Review.
DICER1 gene mutations in endocrine tumors.
Solarski M, Rotondo F, Foulkes WD, Priest JR, Syro LV, Butz H, Cusimano MD, Kovacs K. Solarski M, et al. Among authors: priest jr. Endocr Relat Cancer. 2018 Mar;25(3):R197-R208. doi: 10.1530/ERC-17-0509. Epub 2018 Jan 12. Endocr Relat Cancer. 2018. PMID: 29330195 Review.
A primer to clinical genome sequencing.
Priest JR. Priest JR. Curr Opin Pediatr. 2017 Oct;29(5):513-519. doi: 10.1097/MOP.0000000000000532. Curr Opin Pediatr. 2017. PMID: 28786837 Free PMC article. Review.
DICER1: mutations, microRNAs and mechanisms.
Foulkes WD, Priest JR, Duchaine TF. Foulkes WD, et al. Among authors: priest jr. Nat Rev Cancer. 2014 Oct;14(10):662-72. doi: 10.1038/nrc3802. Epub 2014 Sep 1. Nat Rev Cancer. 2014. PMID: 25176334 Review.
High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease.
Tcheandjieu C, Xiao K, Tejeda H, Lynch JA, Ruotsalainen S, Bellomo T, Palnati M, Judy R, Klarin D, Kember RL, Verma S; Regeneron Genetics Center; VA Million Veterans Program; FinnGen Project; Palotie A, Daly M, Ritchie M, Rader DJ, Rivas MA, Assimes T, Tsao P, Damrauer S, Priest JR. Tcheandjieu C, et al. Among authors: priest jr. Nat Genet. 2022 Jun;54(6):772-782. doi: 10.1038/s41588-022-01070-7. Epub 2022 May 30. Nat Genet. 2022. PMID: 35637384
143 results