1. Characterisation of the Cullin‐3 mutation that causes a severe form of familial hypertension and hyperkalaemia. Issue 10 (18th August 2015) Authors: Schumacher, Frances‐Rose; Siew, Keith; Zhang, Jinwei; Johnson, Clare; Wood, Nicola; Cleary, Sarah E; Al Maskari, Raya S; Ferryman, James T; Hardege, Iris; Yasmin; Figg, Nichola L; Enchev, Radoslav; Knebel, Axel; O'Shaughnessy, Kevin M; Kurz, Thimo Journal: EMBO molecular medicine Issue: Volume 7:Issue 10(2015:Oct.) Page Start: 1285 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Functional characterization of common BCL11B gene desert variants suggests a lymphocyte-mediated association of BCL11B with aortic stiffness. (November 2018) Authors: Maskari, Raya; Hardege, Iris; Cleary, Sarah; Figg, Nicki; Li, Ye; Siew, Keith; Khir, Ashraf; Yu, Yong; Liu, Pentao; Wilkinson, Ian; O'Shaughnessy, Kevin; Yasmin, Journal: European journal of human genetics Issue: Volume 26:Number 11(2018) Page Start: 1648 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗