| 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 |
0.363 |
|
| 2017 |
Hardege I, Long L, Al Maskari R, Figg N, O'Shaughnessy KM. Targeted disruption of the KCNJ5 gene in the female mouse lowers aldosterone levels. Clinical Science (London, England : 1979). PMID 29222092 DOI: 10.1042/Cs20171285 |
0.614 |
|
| 2015 |
Hardege I, Xu S, Gordon RD, Thompson AJ, Figg N, Stowasser M, Murrell-Lagnado R, O'Shaughnessy KM. Novel insertion mutation in KCNJ5 channel produces constitutive aldosterone release from H295R cells. Molecular Endocrinology (Baltimore, Md.). me20151195. PMID 26340408 DOI: 10.1210/Me.2015-1195 |
0.649 |
|
| 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 |
0.655 |
|
| 2015 |
Xu S, Hardege I, Murthy M, Gordon R, Stowasser M, OʼShaughnessy K. 9B.03: A NOVEL INSERTIONAL SOMATIC KCNJ5 MUTATION IN AN AUSTRALIAN PATIENT WITH AN ALDOSTERONE PRODUCING ADENOMA. Journal of Hypertension. 33: e120. PMID 26102711 DOI: 10.1097/01.hjh.0000467675.16684.bb |
0.546 |
|
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