Kevin Michael O'Shaughnessy, MB, BS, DPhil
Affiliations: | University of Oxford, Oxford, United Kingdom | ||
Medicine | University of Cambridge, Cambridge, England, United Kingdom |
Area:
Hypertension, WNK pathway, Renal Physiology, Pre-eclampsia, medical genetics, arterial stiffness, Aldosterone, Conn's SyndromeWebsite:
http://emit.medschl.cam.ac.uk/people/investigators/dr-kevin-oshaughnessy/Google:
"Kevin O'Shaughnessy"Children
Sign in to add traineeSarah E. Cleary | research assistant | 2010- | Cambridge |
Iris Hardege | grad student | 2013- | Cambridge |
Raya Al Maskari | grad student | 2013- | Cambridge |
Mark Glover | grad student | 2010 | Cambridge |
Keith Siew | grad student | 2011-2019 | Cambridge |
Meena Murthy | post-doc | Cambridge |
Collaborators
Sign in to add collaboratorDario Renato Alessi | collaborator | ||
Yasmin Yasmin | collaborator | 2005- | Cambridge |
Ruth Murrell-Lagnado | collaborator | 2013- | Cambridge |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Siew K, Nestler KA, Nelson C, et al. (2024) Cosmic kidney disease: an integrated pan-omic, physiological and morphological study into spaceflight-induced renal dysfunction. Nature Communications. 15: 4923 |
Louis-Dit-Picard H, Kouranti I, Rafael C, et al. (2020) Mutations affecting the conserved acidic WNK1 motif cause inherited hyperkalemic hyperchloremic acidosis. The Journal of Clinical Investigation |
Murthy M, O'Shaughnessy KM. (2019) Modified HEK cells simulate DCT cells in their sensitivity and response to changes in extracellular K. Physiological Reports. 7: e14280 |
Sandilands AJ, O'Shaughnessy KM, Yasmin Y. (2019) 1-adrenoceptor polymorphisms and blood pressure: 49S variant increases plasma renin but not blood pressure in hypertensive patients. American Journal of Hypertension |
Maskari RA, Hardege I, Cleary S, et al. (2018) 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 |
Yasmin, Maskari RA, McEniery CM, et al. (2018) The matrix proteins aggrecan and fibulin-1 play a key role in determining aortic stiffness. Scientific Reports. 8: 8550 |
Hardege I, Long L, Al Maskari R, et al. (2017) Targeted disruption of the KCNJ5 gene in the female mouse lowers aldosterone levels. Clinical Science (London, England : 1979) |
Ware JS, Wain LV, Channavajjhala SK, et al. (2017) Phenotypic and pharmacogenetic evaluation of patients with thiazide-induced hyponatremia. The Journal of Clinical Investigation. 127: 3367-3374 |
Murthy M, Kurz T, O'Shaughnessy KM. (2016) WNK signalling pathways in blood pressure regulation. Cellular and Molecular Life Sciences : Cmls |
Al Maskari R, Yasmin, Cleary S, et al. (2016) A missense TGFB2 variant p.(Arg320Cys) causes a paradoxical and striking increase in aortic TGFB1/2 expression. European Journal of Human Genetics : Ejhg |