# | Title | Journal | Year | Citations |
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1 | Markers of bone turnover for the prediction of fracture risk and monitoring of osteoporosis treatment: a need for international reference standards | Osteoporosis International | 2011 | 893 |
2 | The C679X mutation in PCSK9 is present and lowers blood cholesterol in a Southern African population | Atherosclerosis | 2007 | 323 |
3 | International Osteoporosis Foundation and International Federation of Clinical Chemistry and Laboratory Medicine Position on bone marker standards in osteoporosis | Clinical Chemistry and Laboratory Medicine | 2011 | 274 |
4 | Lipid Disorders and Mutations in the APOB Gene | Clinical Chemistry | 2004 | 191 |
5 | Meta-Analysis of Neuropsychological Symptoms of Adolescents and Adults with PKU | Neuropsychology Review | 2007 | 162 |
6 | A Meta-Analysis of Reference Markers of Bone Turnover for Prediction of Fracture | Calcified Tissue International | 2014 | 141 |
7 | Genetic determinants of hepatic steatosis in man | Journal of Lipid Research | 2011 | 115 |
8 | Bisphosphonates: an overview with special reference to alendronate | Annals of Clinical Biochemistry | 2001 | 104 |
9 | A randomized clinical trial comparing oral alendronate and intravenous pamidronate for the treatment of Paget's disease of bone | Bone | 2004 | 83 |
10 | A Novel Nontruncating APOB Gene Mutation, R463W, Causes Familial Hypobetalipoproteinemia | Journal of Biological Chemistry | 2003 | 82 |
11 | Association between the endothelin-1 gene Lys198Asn polymorphism blood pressure and plasma endothelin-1 levels in normal and pre-eclamptic pregnancy | Journal of Hypertension | 2001 | 75 |
12 | Utility of Biochemical Markers of Bone Turnover and Bone Mineral Density in Management of Osteoporosis | Critical Reviews in Clinical Laboratory Sciences | 2008 | 69 |
13 | Issues of methodology, standardization and metabolite recognition for 25-hydroxyvitamin D when comparing the DiaSorin radioimmunoassay and the Nichols Advantage automated chemiluminescence protein-binding assay in hip fracture cases | Annals of Clinical Biochemistry | 2003 | 66 |
14 | Missense Mutations in APOB within the βα1 Domain of Human APOB-100 Result in Impaired Secretion of ApoB and ApoB-containing Lipoproteins in Familial Hypobetalipoproteinemia | Journal of Biological Chemistry | 2007 | 66 |
15 | Monitoring of intra‐operative nociception: skin conductance and surgical stress index versus stress hormone plasma levels | Anaesthesia | 2010 | 64 |
16 | Mipomersen and other therapies for the treatment of severe familial hypercholesterolemia | Vascular Health and Risk Management | 2012 | 43 |
17 | Apolipoprotein A-I-stimulated Apolipoprotein E Secretion from Human Macrophages Is Independent of Cholesterol Efflux | Journal of Biological Chemistry | 2004 | 40 |
18 | Endotoxin induced TNF and IL-10 mRNA production is higher in male than female donors: Correlation with elevated expression of TLR4 | Cellular Immunology | 2008 | 40 |
19 | B-vitamins reduce plasma levels of beta amyloid | Neurobiology of Aging | 2008 | 40 |
20 | Parathyroid Hormone Is More Stable in EDTA Plasma Than in Serum | Clinical Chemistry | 2002 | 39 |
21 | Apolipoprotein B Metabolism: Tracer Kinetics, Models, and Metabolic Studies | Critical Reviews in Clinical Laboratory Sciences | 2002 | 37 |
22 | Supplementation with mixed tocopherols increases serum and blood cell γ-tocopherol but does not alter biomarkers of platelet activation in subjects with type 2 diabetes | American Journal of Clinical Nutrition | 2006 | 37 |
23 | Calculated free and bioavailable vitamin D metabolite concentrations in vitamin D-deficient hip fracture patients after supplementation with cholecalciferol and ergocalciferol | Bone | 2013 | 36 |
24 | Liver Dysfunction and Steatosis in Familial Hypobetalipoproteinemia | Clinical Chemistry | 2005 | 35 |
25 | Diagnosis of primary hyperparathyroidism: controversies, practical issues and the need for Australian guidelines | Internal Medicine Journal | 2003 | 34 |
26 | Peripheral blood film of a young male who presented with persecutory delusions and suicidal behavior, showing numerous acanthocytes | Molecular Psychiatry | 2007 | 33 |
27 | Assessment of Tocopherol Metabolism and Oxidative Stress in Familial Hypobetalipoproteinemia | Clinical Chemistry | 2006 | 31 |
28 | Medications and green urine | Internal Medicine Journal | 2006 | 30 |
29 | Violent behavior associated with hypocholesterolemia due to a novel APOB gene mutation | Molecular Psychiatry | 2007 | 27 |
30 | Screening for familial hypercholesterolaemia | Pathology | 2012 | 27 |
31 | Clinical and biochemical features, molecular diagnosis and long-term management of a case of cerebrotendinous xanthomatosis | Clinica Chimica Acta | 2001 | 26 |
32 | Preanalytical Factors in the Measurement of Intact Parathyroid Hormone with the DPC IMMULITE Assay | Clinical Chemistry | 2002 | 24 |
33 | Review of a pilot quality-assessment program for interpretative comments | Annals of Clinical Biochemistry | 2002 | 24 |
34 | High-resolution melting analysis for detection of familial ligand-defective apolipoprotein B-100 mutations | Annals of Clinical Biochemistry | 2008 | 22 |
35 | Prolonged vitamin D intoxication: presentation, pathogenesis and progress | Internal Medicine Journal | 2013 | 21 |
36 | Protein Kinase C Controls Vesicular Transport and Secretion of Apolipoprotein E from Primary Human Macrophages | Journal of Biological Chemistry | 2013 | 19 |
37 | Four novel mutations inAPOB causing heterozygous and homozygous familial hypobetalipoproteinemia | Human Mutation | 2003 | 18 |
38 | Quality of interpretative commenting on common clinical chemistry results in the Asia-Pacific region and Africa | Clinical Chemistry and Laboratory Medicine | 2009 | 18 |
39 | Vitamin D: Methods of 25 hydroxyvitamin D analysis, targeting at risk populations and selecting thresholds of treatment | Clinical Biochemistry | 2012 | 17 |
40 | Familial lipoprotein lipase deficiency caused by known (G188E) and novel (W394X) LPL gene mutations | Annals of Clinical Biochemistry | 2008 | 15 |
41 | Trimethylaminuria (fish malodour syndrome): a “benign” genetic condition with major psychosocial sequelae | Medical Journal of Australia | 2008 | 14 |
42 | Vitamin E Supplementation and Hepatic Drug Metabolism in Humans | Journal of Cardiovascular Pharmacology | 2009 | 14 |
43 | The assessment of interpretation in clinical biochemistry: a personal view | Annals of Clinical Biochemistry | 2007 | 13 |
44 | Screening for vitamin D deficiency: defining vitamin D deficiency, target thresholds of treatment and estimating the benefits of treatment | Pathology | 2012 | 12 |
45 | Recent developments in the genetics of LDL deficiency | Current Opinion in Lipidology | 2013 | 12 |
46 | Non-alcoholic steatohepatitis-related cirrhosis in a patient with APOB L343V familial hypobetalipoproteinaemia | Clinica Chimica Acta | 2013 | 11 |
47 | Vitamin D Status and Redefining Serum PTH Reference Range in the Elderly | Journal of Clinical Endocrinology and Metabolism | 2002 | 10 |
48 | Hypobetalipoproteinaemia secondary to chronic hepatitis C virus infection in a patient with familial hypercholesterolaemia | Annals of Clinical Biochemistry | 2009 | 8 |
49 | Parathyroid hormone is more stable in EDTA plasma than in serum | Clinical Chemistry | 2002 | 8 |
50 | Therapeutic considerations for postprandial dyslipidaemia | Diabetes, Obesity and Metabolism | 2001 | 7 |