Amanda Hooper

Professor

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

    6009 Perth

    Australia

  • 1339 Citations
  • 21 h-Index
20022019
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Research Output 2002 2019

2019
Hyperlipoproteinemia Type II
Coronary Artery Disease
Life Style
Atherosclerosis
Coronary Vessels
2 Citations (Scopus)
Hyperlipoproteinemia Type II
Lipoprotein(a)
LDL Cholesterol
Cholesterol
Lipids

Lipids and cardiovascular disease

Burnett, J. R., Hooper, A. J. & Hegele, R. A., Feb 2019, In : Pathology. 51, 2, p. 129-130 2 p.

Research output: Contribution to journalEditorial

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
10 Citations (Scopus)
222 Downloads (Pure)
Open Access
File
Hyperlipoproteinemia Type II
Lipids
Mutation
Early Diagnosis
Xanthomatosis
9 Citations (Scopus)

ClinVar database of global familial hypercholesterolemia-associated DNA variants

on behalf of the ClinGen FH Variant Curation Expert Panel, 1 Nov 2018, In : Human Mutation. 39, 11, p. 1631-1640 10 p.

Research output: Contribution to journalArticle

Hyperlipoproteinemia Type II
Databases
DNA
Information Dissemination
Patient Care
2 Citations (Scopus)

Heterozygous familial hypercholesterolaemia in specialist centres in South Africa, Australia and Brazil: Importance of early detection and lifestyle advice

Pang, J., David Marais, A., Blom, D. J., Brice, B. C., Silva, P. R., Jannes, C. E., Pereira, A. C., Hooper, A. J., Ray, K. K., Santos, R. D. & Watts, G. F., Oct 2018, In : Atherosclerosis. 277, p. 470-476 7 p.

Research output: Contribution to journalArticle

South Australia
Hyperlipoproteinemia Type II
South Africa
Brazil
Life Style
3 Citations (Scopus)

Homozygous familial hypercholesterolaemia in Vietnam: Case series, genetics and cascade testing of families

Truong, T. H., Kim, N. T., Nguyen, M. N. T., Pang, J., Hooper, A. J., Watts, G. F. & Do, D. L., Oct 2018, In : Atherosclerosis. 277, p. 392-398 7 p.

Research output: Contribution to journalArticle

Hyperlipoproteinemia Type II
Vietnam
Genetic Testing
LDL Receptors
Mutation
5 Citations (Scopus)
Hyperlipoproteinemia Type II
Genetic Testing
LDL Cholesterol
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Costs and Cost Analysis
2 Citations (Scopus)

PCSK9 - A journey to cardiovascular outcomes

Burnett, J. & Hooper, A., 29 Nov 2018, In : The New England Journal of Medicine. 379, 22, p. 2161-2162

Research output: Contribution to journalEditorial

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
2017

Clinical utility gene card for: Tangier disease

Hooper, A. J., McCormick, S. P. A., Hegele, R. A. & Burnett, J. R., 1 Jun 2017, In : European Journal of Human Genetics. 25, 7

Research output: Contribution to journalArticle

2 Citations (Scopus)

Clinical utility gene card for: Sitosterolaemia

Hooper, A. J., Bell, D. A., Hegele, R. A. & Burnett, J. R., 1 Apr 2017, In : European Journal of Human Genetics. 25, 4, p. e1-e3

Research output: Contribution to journalArticle

Isolated brachydactyly type e and idiopathic pancreatitis in a patient presenting to a lipid disorders clinic

Page, M. M., Hooper, A. J., Glendenning, P. & Burnett, J. R., 1 Jan 2017, In : BMJ Case Reports. 2017, 218825.

Research output: Contribution to journalArticle

Brachydactyly
Metacarpal Bones
Genetic Testing
Pancreatitis
Hand Joints

Lipoprotein Lipase Deficiency in an Infant With Chylomicronemia, Hepatomegaly, and Lipemia Retinalis

Vidanapathirana, D. M., Rodrigo, T., Waidyanatha, S., Jasinge, E., Hooper, A. J. & Burnett, J. R., 2017, In : Global Pediatric Health. 4, p. 1-4

Research output: Contribution to journalArticle

Open Access

Systematic Screening for Familial Hypercholesterolaemia and Elevated Lp (a) in Families

Ellis, K. L., Pang, J., Bell, D. A., Hooper, A. J., Burnett, J. R. & Watts, G. F., 2017, In : Heart, Lung and Circulation. 26, Supp. 2, p. S121-S122

Research output: Contribution to journalAbstract/Meeting Abstract

2016

Abetalipoproteinaemia and hereditary hypobetalipoproteinaemia

Hooper, A. & Burnett, J., 2016, A Clinical Guide to Inherited Metabolic Diseases in Adults. Hollak, CEM., Lachmann, R. & Sedel, F. (eds.). Oxford University Press, p. 225-228

Research output: Chapter in Book/Conference paperChapter

8 Citations (Scopus)
Cholesterol Ester Transfer Proteins
Dyslipidemias
LDL Cholesterol
HDL Cholesterol
Hydroxymethylglutaryl-CoA Reductase Inhibitors
18 Citations (Scopus)
Familial Combined Hyperlipidemia
Hyperlipoproteinemia Type II
Lipoprotein(a)
Coronary Artery Disease
Mutation
2 Citations (Scopus)

Interpretative comments specifically suggesting specialist referral increase the detection of familial hypercholesterolaemia

Bender, R., Edwards, G., Mcmahon, J., Hooper, A., Watts, G., Burnett, J. & Bell, D., 2016, In : Pathology. 48, 5, p. 463-466

Research output: Contribution to journalArticle

Hyperlipoproteinemia Type II
Telefacsimile
LDL Cholesterol
Referral and Consultation
Genetic Testing
1 Citation (Scopus)
161 Downloads (Pure)

Lipoprotein metabolism in an apoB-80 familial hypobetalipoproteinemia heterozygote

Hooper, A., Robertson, K., Champain, D., Hua, J., Song, S., Parhofer, K. G., Barrett, H., Van Bockxmeer, F. & Burnett, J., Jun 2016, In : Clinical Biochemistry. 49, 9, p. 720-722

Research output: Contribution to journalArticle

Open Access
File
Hypobetalipoproteinemias
Apolipoproteins B
Heterozygote
Metabolism
Lipoproteins
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
2 Citations (Scopus)

Novel APOB missense variants, A224T and V925L, in black South African Woman with marked hypocholesterolemia

Miller, S. A., Hooper, A. J., Mantiri, G., Marais, D., Tanyanyiwa, DM., McKnight, J. & Burnett, J. R., 2016, In : Journal of Clinical Lipidology. 10, 3, p. 604-609 6 p.

Research output: Contribution to journalArticle

19 Citations (Scopus)
Apolipoproteins B
Cardiovascular Diseases
Familial Combined Hyperlipidemia
Hyperlipoproteinemia Type II
Lipoprotein(a)
2015
5 Citations (Scopus)

Clinical utility gene card for: Abetalipoproteinaemia - Update 2014

Burnett, J., Bell, D., Hooper, A. & Hegele, R. A., 2015, In : European Journal of Human Genetics. 23, 6, p. e1-e3

Research output: Contribution to journalArticle

13 Citations (Scopus)

Clinical utility gene card for: Familial hypobetalipoproteinaemia (APOB) - Update 2014

Burnett, J., Bell, D., Hooper, A. & Hegele, R. A., 2015, In : European Journal of Human Genetics. 23, 6, p. e1-e3

Research output: Contribution to journalArticle

33 Citations (Scopus)
127 Downloads (Pure)
Open Access
File
Abetalipoproteinemia
Apolipoproteins B
Chylomicrons
Lipoproteins
Therapeutics
33 Citations (Scopus)
Hyperlipoproteinemia Type II
Genetic Testing
LDL Cholesterol
Coronary Artery Disease
Christianity
35 Citations (Scopus)
Hyperlipoproteinemia Type II
Lipoprotein(a)
Renal Insufficiency
Coronary Artery Disease
Hypertension

Genetic abetalipoproteinaemia and hypobetalipoproteinaemia

Burnett, J. & Hooper, A., 2015, Contemporary Endocrinology. Garg, A. (ed.). Humana Press, Vol. 1. p. 251-266

Research output: Chapter in Book/Conference paperChapter

5 Citations (Scopus)
98 Downloads (Pure)

Lipoprotein Metabolism in APOB L343V Familial Hypobetalipoproteinemia.

Hooper, A., Heeks, L., Robertson, K., Champain, D., Hua, J., Song, S., Parhofer, P., Barrett, H., Van Bockxmeer, F. & Burnett, J., Nov 2015, In : Journal of Clinical Endocrinology and Metabolism. 100, 11, p. E1484-E1490 7 p.

Research output: Contribution to journalArticle

Open Access
File
Hypobetalipoproteinemias
Apolipoproteins B
Metabolism
Lipoproteins
Triglycerides
2 Citations (Scopus)

Plasma cholesterol in adults with phenylketonuria

Williams, R. A., Hooper, A., Bell, D., Mamotte, C. D. S. & Burnett, J., 2015, In : Pathology. 47, 2, p. 134-137

Research output: Contribution to journalArticle

Phenylketonurias
Cholesterol
Phenylalanine
LDL Cholesterol
Body Mass Index

Sorting the wheat from the chaff in familial hypercholesterolemia

Hooper, A. J. & Watts, G. F., Jan 2015, In : Clinical Chemistry. 61, 1, p. 6-8 3 p.

Research output: Contribution to journalEditorial

7 Citations (Scopus)
Expert Systems
Hyperlipoproteinemia Type II
Computer Systems
Computer systems
Lipids
5 Citations (Scopus)
Hypobetalipoproteinemias
Abetalipoproteinemia
Oxidative stress
Vitamin E
Oxidative Stress
2014
2 Citations (Scopus)
Type B Niemann-Pick Disease
Genes
Lipids
Mutation
Hyperlipidemias
8 Citations (Scopus)

Clinical features and genetic analysis of three patients with severe hypertriglyceridaemia

Hooper, A., Kurtkoti, J., Hamilton-Craig, I. R. & Burnett, J., 2014, In : Annals of Clinical Biochemistry. 51, 4, p. 485-489

Research output: Contribution to journalArticle

Lipoprotein Lipase
Hypertriglyceridemia
Hyperlipoproteinemia Type I
Mutation
Genes
17 Citations (Scopus)

Detecting familial hypercholesterolaemia in the community: Impact of a telephone call from a chemical pathologist to the requesting general practitioner

Bell, D., Hooper, A., Edwards, G. A., Southwell, L., Pang, J., Van Bockxmeer, F., Watts, G. & Burnett, J., 2014, In : Atherosclerosis. 234, 2, p. 469-472

Research output: Contribution to journalArticle

Hyperlipoproteinemia Type II
Telephone
General Practitioners
Referral and Consultation
LDL Cholesterol
38 Citations (Scopus)

Elevated plasma PCSK9 level is equally detrimental for patients with nonfamilial hypercholesterolemia and heterozygous familial hypercholesterolemia, irrespective of low-density lipoprotein receptor defects

Lambert, G., Petrides, F., Chatelais, M., Blom, D. J., Choque, B., Tabet, F., Wong, G., Rye, K. A., Hooper, A., Burnett, J., Barter, P. J. & Marais, A. D., 10 Jun 2014, In : Journal of the American College of Cardiology. 63, 22, p. 2365-2373

Research output: Contribution to journalArticle

Open Access
Hyperlipoproteinemia Type II
LDL Receptors
Hypercholesterolemia
LDL Cholesterol
Fibroblasts
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
24 Citations (Scopus)
Hyperlipoproteinemia Type II
Blood Component Removal
Lipoproteins
Coronary Disease
Hypercholesterolemia

Molecular characterization of a Chinese woman homozygous for the familial hypercholesterolemia LDLR c.1474G>A (p.Asp492Asn) mutation

Faiz, F., Hu, M., Hooper, A., Tomlinson, B. T. & Van Bockxmeer, F., 2014, In : Clinical Lipidology. 9, 2, p. 163-170

Research output: Contribution to journalArticle

Hyperlipoproteinemia Type II
Hypercholesterolemia
Microsatellite Repeats
Haplotypes
Mutation
16 Citations (Scopus)
241 Downloads (Pure)

Novel missense MTTP gene mutations causing abetalipoproteinemia

Miller, S., Burnett, J., Leonis, M. A., Mcknight, C. J., Van Bockxmeer, F. & Hooper, A., Oct 2014, In : Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids. 1841, 10, p. 1548-1554

Research output: Contribution to journalArticle

Open Access
File
Abetalipoproteinemia
Mutation
Genes
Missense Mutation
Protein Disulfide-Isomerases
6 Citations (Scopus)

Quantification and genotyping of lipoprotein lipase in patients with diabetic lipaemia

Radhakutty, A., Shen, J., Hooper, A., Miller, S., Burnett, J., Mah, P. M., Burt, M. G. & Doogue, M. P., 2014, In : Diabetic Medicine. 31, 12, p. 1702-1707

Research output: Contribution to journalArticle

Lipoprotein Lipase
Diabetic Ketoacidosis
Mutation
Hyperlipoproteinemia Type I
Ketosis
8 Citations (Scopus)

Running interference to lower cholesterol

Burnett, J. & Hooper, A., 2014, In : The Lancet. 383, 9911, p. 10-12

Research output: Contribution to journalLetter

29 Citations (Scopus)
282 Downloads (Pure)

Update on primary hypobetalipoproteinemia

Hooper, A. & Burnett, J., Jul 2014, In : Current Atherosclerosis Reports. 16, 7, 7 p.

Research output: Contribution to journalArticle

Open Access
File
Hypobetalipoproteinemias
LDL Cholesterol
Exons
Abetalipoproteinemia
Angiopoietins