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Sarah E. Cleary - Publications

Affiliations: 
2010- Medicine University of Cambridge, Cambridge, England, United Kingdom 
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7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Maskari RA, Hardege I, Cleary S, Figg N, Li Y, Siew K, Khir A, Yu Y, Liu P, Wilkinson I, O'Shaughnessy K, Yasmin. Functional characterization of common BCL11B gene desert variants suggests a lymphocyte-mediated association of BCL11B with aortic stiffness. European Journal of Human Genetics : Ejhg. 26: 1648-1657. PMID 30089823 DOI: 10.1038/s41431-018-0226-z  0.594
2018 Yasmin, Maskari RA, McEniery CM, Cleary SE, Li Y, Siew K, Figg NL, Khir AW, Cockcroft JR, Wilkinson IB, O'Shaughnessy KM. The matrix proteins aggrecan and fibulin-1 play a key role in determining aortic stiffness. Scientific Reports. 8: 8550. PMID 29867203 DOI: 10.1038/s41598-018-25851-5  0.587
2016 Al Maskari R, Yasmin, Cleary S, Figg N, Mehta S, Rassl D, Wilkinson I, O'Shaughnessy KM. A missense TGFB2 variant p.(Arg320Cys) causes a paradoxical and striking increase in aortic TGFB1/2 expression. European Journal of Human Genetics : Ejhg. PMID 27782106 DOI: 10.1038/Ejhg.2016.143  0.581
2015 Schumacher FR, Siew K, Zhang J, Johnson C, Wood N, Cleary SE, Al Maskari RS, Ferryman JT, Hardege I, Yasmin, Figg NL, Enchev R, Knebel A, O'Shaughnessy KM, Kurz T. Characterisation of the Cullin-3 mutation that causes a severe form of familial hypertension and hyperkalaemia. Embo Molecular Medicine. 7: 1285-306. PMID 26286618 DOI: 10.15252/emmm.201505444  0.521
2015 Connolly* K, Maki-Petaja K, Ribey E, Ooi CY, Cleary S, Wilkinson I. P8.13 THE ROLE OF HYALURONAN IN AORTIC STIFFENING IN PATIENTS WITH RHEUMATOID ARTHRITIS Artery Research. 12: 37. DOI: 10.1016/J.Artres.2015.10.335  0.314
2014 Maskari RA, Cleary S, Li Y, Khir A, Mitchell G, Wilkinson I, O'Shaughnessy K, Yasmin. Genetic variations on chromosome 14 influence BCL11B gene expression levels and aortic stiffness Artery Research. 8: 126-127. DOI: 10.1016/J.Artres.2014.09.070  0.56
2014 Yasmin, McEniery C, Cleary S, Lam B, Kuper H, Endo Y, Kinra S, Chen D, Chandak G, Deanfield J, Lawlor D, Cockcroft J, Wilkinson I, O'Shaughnessy K. Genome wide association scan identifies loci for arterial stiffness in young healthy adults Artery Research. 8: 122. DOI: 10.1016/J.Artres.2014.09.050  0.522
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