Publications: Dr Fu Liang Ng
Evangelou E, Warren HR, Mosen-Ansorena D, Mifsud B, Pazoki R, Gao H, Ntritsos G, Dimou N et al.(2018).
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nat Genet
vol. 50,
(12)
1755-1755.
Evangelou E, Warren HR, Mosen-Ansorena D, Mifsud B, Pazoki R, Gao H, Ntritsos G, Dimou N et al.(2018).
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nat Genet
vol. 50,
(10)
1412-1425.
Ng FL, Warren HR, Caulfield MJ(2018).
Hypertension genomics and cardiovascular prevention. Ann Transl Med
vol. 6,
(15)
291-291.
Saxena M, Shour T, Shah M, Wolff CB, Julu POO, Kapil V, Collier DJ, Ng FL et al.(2018).
Attenuation of Splanchnic Autotransfusion Following Noninvasive Ultrasound Renal Denervation: A Novel Marker of Procedural Success. J Am Heart Assoc
vol. 7,
(12)
Ren M, Ng FL, Warren HR, Witkowska K, Baron M, Jia Z, Cabrera C, Zhang R et al.(2018).
The biological impact of blood pressure-associated genetic variants in the natriuretic peptide receptor C gene on human vascular smooth muscle. Hum Mol Genet
vol. 27,
(1)
199-210.
Ng FL, Boedtkjer E, Witkowska K, Ren M, Zhang R, Tucker A, Aalkjær C, Caulfield MJ et al.(2017).
Increased NBCn1 expression, Na+/HCO3- co-transport and intracellular pH in human vascular smooth muscle cells with a risk allele for hypertension. Hum Mol Genet
Floyd CN, Adeel MY, Wolff CB, Julu P, Shah M, Collier DJ, Saxena M, Brier T et al.(2016).
First-in-man treatment of severe blood pressure variability with baroreflex activation therapy. International Journal of Cardiology
vol. 220,
Article C,
577-579.
Ng FL, Saxena M, Mahfoud F, Pathak A, Lobo MD(2016).
Device-based Therapy for Hypertension. Curr Hypertens Rep
vol. 18,
(8)
61-61.
Zhang R, Witkowska K, Afonso Guerra-Assunção J, Ren M, Ng FL, Mauro C, Tucker AT, Caulfield MJ et al.(2016).
A blood pressure-associated variant of the SLC39A8 gene influences cellular cadmium accumulation and toxicity. Hum Mol Genet
vol. 25,
(18)
4117-4126.
Yang W, Ng FL, Chan K, Pu X, Poston RN, Ren M, An W, Zhang R et al.(2016).
Coronary-Heart-Disease-Associated Genetic Variant at the COL4A1/COL4A2 Locus Affects COL4A1/COL4A2 Expression, Vascular Cell Survival, Atherosclerotic Plaque Stability and Risk of Myocardial Infarction. PLoS Genetics
vol. 12,
(7)
e1006127-e1006127.
Cabrera CP, Ng FL, Warren HR, Barnes MR, Munroe PB, Caulfield MJ(2015).
Exploring hypertension genome-wide association studies findings and impact on pathophysiology, pathways, and pharmacogenetics. Wiley Interdiscip Rev Syst Biol Med
vol. 7,
(2)
73-90.
Robinson PJ, Ng FL, Lobo MD, Akker S, Drake WM, Cavlan D, Caulfield MJ(2013).
Phaeochromocytoma-paraganglioma syndrome presenting as a para-renal mass: A case report. JOURNAL OF HUMAN HYPERTENSION
vol. 27,
(10)
654-655.
Huang C, Ng F, Kapil V, Caulfield M, Lobo M(2013).
Prognostic significance of short term blood pressure variability in a tertiary referral centre population. JOURNAL OF HUMAN HYPERTENSION
vol. 27,
(10)
651-651.
Rajoo SG, Ng FL, Lobo M(2013).
e-Learning to facilitate preparation for prescribing skills assessment. MEDICAL EDUCATION
vol. 47,
(5)
520-520.
Pu X, Xiao Q, Kiechl S, Chan K, Ng FL, Gor S, Poston RN, Fang C et al.(2013).
ADAMTS7 cleavage and vascular smooth muscle cell migration is affected by a coronary-artery-disease-associated variant. American Journal of Human Genetics
vol. 92,
(3)
366-374.
Pu X, Xiao Q, Kiechl S, Chan K, Ng FL, Gor S, Poston RN, Fang C et al.(2013).
ADAMTS7 cleavage and vascular smooth muscle cell migration is affected by a coronary-artery-disease-associated variant. Am J Hum Genet
vol. 92,
(3)
366-374.
Lidder S, Ng FL, Gulati R, Whitehand A, Perry L, Lobo M(2012).
Can renin measurement be extended to primary care to inform the stratified medicines approach to hypertension therapy?. JOURNAL OF HUMAN HYPERTENSION
vol. 26,
(10)
624-625.
Chan K, Ng FL, Saxena M, Collier D, Matson M, Jain A, Caulfield M, Lobo M(2012).
Renal denervation in resistant hypertension-a prospective case series. JOURNAL OF HUMAN HYPERTENSION
vol. 26,
(10)
631-631.
Motterle A, Pu X, Wood H, Xiao Q, Gor S, Ng FL, Chan K, Cross F et al.(2012).
Functional analyses of coronary artery disease associated variation on chromosome 9p21 in vascular smooth muscle cells. Hum Mol Genet
vol. 21,
(18)
4021-4029.
Patel S, Ng FL, Uddin I, Caulfield MJ, Lobo MD(2011).
Plasma renin activity in the South Asian population-an intermediate group. J HUM HYPERTENS
vol. 25,
(10)
631-631.
Patel S, Ng FL, Uddin I, Caulfield MJ, Lobo MD(2011).
Salt intake in hypertensive patients with at or above-target blood pressures. J HUM HYPERTENS
vol. 25,
(10)
632-632.
Ng FL, Davis AJ, Jepps TA, Harhun MI, Yeung SY, Wan A, Reddy M, Melville D et al.(2011).
Expression and function of the K+ channel KCNQ genes in human arteries. Br J Pharmacol
vol. 162,
(1)
42-53.
Ng FL, Holt DW, Chang RWS, Macphee IAM(2010).
Black renal transplant recipients have poorer long-term graft survival than CYP3A5 expressers from other ethnic groups. Nephrol Dial Transplant
vol. 25,
(2)
628-634.
Ng FL, Holt DW, MacPhee IAM(2007).
Pharmacogenetics as a tool for optimising drug therapy in solid-organ transplantation. Expert Opin Pharmacother
vol. 8,
(13)
2045-2058.