Amanda Hooper

Professor

  • The University of Western Australia (M510), 35 Stirling Highway,

    6009 Perth

    Australia

  • 1342 Citations
  • 21 h-Index
20022019
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Research Output 2002 2019

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Review article
2019
5 Citations (Scopus)

Non-HDL-cholesterol and apolipoprotein B compared with LDL-cholesterol in atherosclerotic cardiovascular disease risk assessment

Carr, S. S., Hooper, A. J., Sullivan, D. R. & Burnett, J. R., 1 Feb 2019, In : Pathology. 51, 2, p. 148-154 7 p.

Research output: Contribution to journalReview article

Apolipoproteins B
LDL Cholesterol
Cardiovascular Diseases
Lipoproteins
LDL Lipoproteins
2 Citations (Scopus)

Update on the diagnosis, treatment and management of rare genetic lipid disorders

Ng, D. M., Burnett, J. R., Bell, D. A., Hegele, R. A. & Hooper, A. J., Feb 2019, In : Pathology. 51, 2, p. 193-201 9 p.

Research output: Contribution to journalReview article

2018
2 Citations (Scopus)
Hyperlipoproteinemia Type II
Genetic Testing
High-Throughput Nucleotide Sequencing
Genomics
Hypercholesterolemia
9 Citations (Scopus)

The role of patient registries for rare genetic lipid disorders

Ng, D., Hooper, A., Bellgard, M. & Burnett, J., Apr 2018, In : Current Opinion in Lipidology. 29, 2, p. 156-162

Research output: Contribution to journalReview article

Inborn Genetic Diseases
Registries
Hyperlipoproteinemia Type I
Lipids
Rare Diseases
2016
4 Citations (Scopus)

Management of familial hypercholesterolemia in Hong Kong

Hu, M., Hooper, A. J., van Bockxmeer, F. M., Watts, G. F., Chan, J. C. N. & Tomlinson, B., 2016, In : Journal of Atherosclerosis and Thrombosis. 23, 5, p. 520-531 12 p.

Research output: Contribution to journalReview article

Hyperlipoproteinemia Type II
Hong Kong
LDL Cholesterol
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Coronary Disease
19 Citations (Scopus)
Apolipoproteins B
Cardiovascular Diseases
Familial Combined Hyperlipidemia
Hyperlipoproteinemia Type II
Lipoprotein(a)
2014
1 Citation (Scopus)

Genetic screening to improve the diagnosis of familial hypercholesterolemia

Faiz, F., Nguyễn, L. T. H., Van Bockxmeer, F. & Hooper, A., 2014, In : Clinical Lipidology. 9, 5, p. 523-532

Research output: Contribution to journalReview article

Hyperlipoproteinemia Type II
Genetic Testing
Mutation
Multifactorial Inheritance
Genes
2013
32 Citations (Scopus)

Anti-PCSK9 therapies for the treatment of hypercholesterolemia

Hooper, A. & Burnett, J., 2013, In : Expert Opinion on Biological Therapy. 13, 3, p. 429-435

Research output: Contribution to journalReview article

7 Citations (Scopus)

Non-alcoholic steatohepatitis-related cirrhosis in a patient with APOB L343V familial hypobetalipoproteinaemia

Heeks, L. V., Hooper, A., Adams, L., Robbins, P., Barrett, H., Van Bockxmeer, F. & Burnett, J., 2013, In : Clinica Chimica Acta. 421, 5, p. 121-125

Research output: Contribution to journalReview article

8 Citations (Scopus)
174 Downloads (Pure)

Recent developments in the genetics of LDL deficiency

Hooper, A. & Burnett, J., 2013, In : Current Opinion in Lipidology. 24, p. 111-115

Research output: Contribution to journalReview article

Open Access
File
2010

Extreme hyperalphalipoproteinaemia in a patient with a solitary paraspinal lipoma

Musaad, S., Robertson, K., Clarke, M., Hooper, A. J., French, G., Chiu, W. & Burnett, J., 2010, In : Annals of Clinical Biochemistry. 47, p. 90-93

Research output: Contribution to journalReview article

Open Access

Fatty infiltration of the liver in a case of hypobetalipoproteinaemia with a novel mutation in the APOB gene

Florkowski, C., Hedley, J., Bickley, V., Hooper, A., Burnett, J. & George, P., 2010, In : The New Zealand Medical Journal. 123, 1310, p. 98-100

Research output: Contribution to journalReview article

2 Citations (Scopus)

Pancreatitis in a Child with Lipemia Due to Novel Lipoprotein Lipase Mutations

Gupta, N., Moore, D., Hooper, A., Burnett, J. & Metz, M., 2010, In : Journal of Pediatric Gastroenterology and Nutrition. 50, 4, p. 1-3

Research output: Contribution to journalReview article

2009
5 Citations (Scopus)

Hypobetalipoproteinaemia secondary to chronic hepatitis C virus infection in a patient with familial hypercholesterolaemia

Bima, A. I., Hooper, A., Van Bockxmeer, F. & Burnett, J., 2009, In : Annals of Clinical Biochemistry. 46, p. 420-22

Research output: Contribution to journalReview article

2008
14 Citations (Scopus)

A novel missense LIPA gene mutation, N98S in a patient with cholesteryl ester storage disease

Hooper, A., Tran, H. A., Formby, M. R. & Burnett, J., 2008, In : Clinica Chimica Acta. 398, p. 152-54

Research output: Contribution to journalReview article

Cholesterol Ester Storage Disease
Sterol Esterase
Cholesterol Esters
Genes
Exons
5 Citations (Scopus)

Familial hypobetalipoproteinemia in a Turkish family with hereditary spastic paraplegia

Hooper, A., Akinci, B., Comlekci, A. & Burnett, J., 2008, In : Clinica Chimica Acta. 390, p. 152-55

Research output: Contribution to journalReview article

Hypobetalipoproteinemias
Hereditary Spastic Paraplegia
Apolipoproteins B
Hypobetalipoproteinemia, Familial, Apolipoprotein B
LDL Cholesterol
12 Citations (Scopus)

Familial lipoprotein lipase deficiency caused by known (G188E) and novel (W394X) LPL gene mutations

Hooper, A., Crawford, G. M., Brisbane, J. M., Robertson, K., Watts, G., Van Bockxmeer, F. & Burnett, J., 2008, In : Annals of Clinical Biochemistry. 45, p. 102-105

Research output: Contribution to journalReview article

Hyperlipoproteinemia Type I
Lipoprotein Lipase
Genes
Mutation
Triglycerides