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 Syndrome
Website:
http://emit.medschl.cam.ac.uk/people/investigators/dr-kevin-oshaughnessy/
Google:
"Kevin O'Shaughnessy"

Children

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Sarah 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

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Dario Renato Alessi collaborator
Yasmin Yasmin collaborator 2005- Cambridge
Ruth Murrell-Lagnado collaborator 2013- Cambridge
BETA: Related publications

Publications

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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
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