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

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Article
2019
Hyperlipoproteinemia Type II
Coronary Artery Disease
Life Style
Atherosclerosis
Coronary Vessels
2 Citations (Scopus)
Hyperlipoproteinemia Type II
Lipoprotein(a)
LDL Cholesterol
Cholesterol
Lipids
2018
10 Citations (Scopus)
217 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
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
2016
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)
157 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
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

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)
126 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
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
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
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)
239 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
29 Citations (Scopus)
279 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
2013
12 Citations (Scopus)

Detection of variations and identifying genomic breakpoints for large deletions in the LDLR by Ion Torrent semiconductor sequencing

Faiz, F., Allcock, R., Hooper, A. & Van Bockxmeer, F., 2013, In : Atherosclerosis. 230, p. 249-255

Research output: Contribution to journalArticle

26 Citations (Scopus)

Impact of interpretative commenting on lipid profiles in people at high risk of familial hypercholesterolaemia

Bell, D., Bender, R., Hooper, A., Mcmahon, J., Edwards, G., Van Bockxmeer, F., Watts, G. & Burnett, J., 2013, In : Clinica Chimica Acta. 422, p. 21-25

Research output: Contribution to journalArticle

2012
8 Citations (Scopus)

Anacetrapib, a cholesteryl ester transfer protein inhibitor

Hooper, A. & Burnett, J., 2012, In : Expert Opinion on Investigational Drugs. 21, 1, p. 103-109

Research output: Contribution to journalArticle

14 Citations (Scopus)

Clinical utility gene card for: Abetalipoproteinaemia

Burnett, J., Bell, D., Hooper, A. & Hegele, R. A., 2012, In : European Journal of Human Genetics. 20, p. 3 pp

Research output: Contribution to journalArticle

10 Citations (Scopus)

Clinical utility gene card for: Familial Hypobetalipoproteinaemia (APOB)

Burnett, J., Bell, D., Hooper, A. & Hegele, R. A., 2012, In : European Journal of Human Genetics. 20, p. 909

Research output: Contribution to journalArticle

18 Citations (Scopus)

Dalcetrapib, a cholesteryl ester transfer protein modulator

Hooper, A. & Burnett, J., 2012, In : Expert Opinion on Investigational Drugs. 21, 9, p. 1427-1432

Research output: Contribution to journalArticle

43 Citations (Scopus)

Genetic analysis of familial hypercholesterolaemia in Western Australia

Hooper, A., Nguyen, L. T., Burnett, J., Bates, T., Bell, D., Redgrave, T. G., Watts, G. & Van Bockxmeer, F., 2012, In : Atherosclerosis. 224, p. 430-4

Research output: Contribution to journalArticle

34 Citations (Scopus)
Open Access
12 Citations (Scopus)
32 Citations (Scopus)

Opportunistic screening for familial hypercholesterolaemia via a community laboratory

Bell, D., Hooper, A., Bender, R., Mcmahon, J., Edwards, G., Van Bockxmeer, F., Watts, G. & Burnett, J., 2012, In : Annals of Clinical Biochemistry. 49, p. 534-537

Research output: Contribution to journalArticle

27 Citations (Scopus)

Screening for familial hypercholesterolaemia

Bender, R., Bell, D., Hooper, A., Edwards, G., Van Bockxmeer, F., Watts, G. & Burnett, J., 2012, In : Pathology. 44, 2, p. 122-128

Research output: Contribution to journalArticle

5 Citations (Scopus)

Screening for lipid disorders

Bell, D., Hooper, A., Bender, R., Edwards, G., Van Bockxmeer, F., Watts, G. & Burnett, J., 2012, In : Pathology. 44, 2, p. 115-121

Research output: Contribution to journalArticle

2011
51 Citations (Scopus)

Familial hypercholesterolemia: Epidemiology, Neolithic origins and modern geographic distribution

Liyanage, K. E., Burnett, J., Hooper, A. & Van Bockxmeer, F., 2011, In : Critical Reviews in Clinical Laboratory Sciences. 48, p. 1-18

Research output: Contribution to journalArticle

37 Citations (Scopus)

Mipomersen, an antisense apolipoprotein B synthesis inhibitor

Bell, D., Hooper, A. & Burnett, J., 2011, In : Expert Opinion on Investigational Drugs. 20, 2, p. 265-272

Research output: Contribution to journalArticle

79 Citations (Scopus)
2009
34 Citations (Scopus)
Hyperlipoproteinemia Type I
Dependovirus
Lipoprotein Lipase
Genes
Pancreatitis