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Richard I. King

Observed names: King, Richard, R I King, R King, R. King, R.I. King, Richard I King, Richard King
Observed institutions: Mater Health Services, Christchurch Hospital, Canterbury Health Laboratories, Canterbury District Health Board, Health New Zealand, University of Otago
ORCID: 0000-0002-2805-9552
Observed ORCID: 0000-0002-2805-9552
OpenAlex ID: A5102916663
Disorders of sex development: insights from targeted gene sequencing of a large international patient cohort
2016 · Stefanie Eggers, Simon Sadedin, et al. · Genome biology · 409
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Sudden Cardiac Death Due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2
2016 · Hannah Kennedy, Tobias B. Haack, et al. · The American Journal of Human Genetics · 75
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A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes
2022 · Paul Bastard, Kuang-Chih Hsiao, et al. · The Journal of Experimental Medicine · 73
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How paraproteins can affect laboratory assays: spurious results and biological effects
2010 · Richard I. King, Christopher M. Florkowski · Pathology · 65
BCS1L gene mutation presenting with GRACILE-like syndrome and complex III deficiency
2012 · Adrienne M Lynn, Richard I King, et al. · Annals of Clinical Biochemistry International Journal of Laboratory Medicine · 25
Electrolytes in sick neonates – which sodium is the right answer?
2012 · Richard I King, Richard J Mackay, et al. · Archives of Disease in Childhood Fetal & Neonatal · 25
An anomalous result from gel tubes for vitamin D
2009 · Peter A. Elder, John G. Lewis, et al. · Clinica Chimica Acta · 25
A mass-spectroscopic method for measuring des-Leu albumin — A novel marker for chronic pancreatitis
2012 · Richard D. Ireland, Stephen O. Brennan, et al. · Clinical Biochemistry · 18
What is the best predictor of the atherogenic LDL subclass phenotype ‘pattern B’ in patients with type 2 diabetes mellitus?
2011 · R I King, C M Florkowski, et al. · Annals of Clinical Biochemistry International Journal of Laboratory Medicine · 14
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β37Trp → Cys mutation leads to multiple new hemoglobin species in red cells
2011 · Stephen O. Brennan, Richard I. King, et al. · Clinical Biochemistry · 8
Grossly Elevated False-Positive High-Sensitivity Troponin I Due to Heterophilic Antimouse IgG1 Antibodies
2020 · John G Lewis, Alison J L Connolly, et al. · The Journal of Applied Laboratory Medicine · 6
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Association of Clinical Characteristics With Familial Hypercholesterolaemia Variants in a Lipid Clinic Setting: A Case-Control Study
2024 · Bobby V Li, Andrew D Laurie, et al. · Journal of Lipid and Atherosclerosis · 5
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Artefactually low creatinine by Beckman Coulter enzymatic method due to immunoglobulin M paraprotein interference
2023 · Bobby Li, Simon Thompson, et al. · Annals of Clinical Biochemistry International Journal of Laboratory Medicine · 5
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CADASIL presenting with focal and generalised epilepsy due to a novel NOTCH3 mutation
2019 · Benson S. Chen, James Cleland, et al. · Seizure · 5
Hb Westport [β121 (GH4) Glu>Asp; HBB:c.366A>C]: A novel β-globin variant interfering with HbA1c measurement
2022 · Jordyn A. Moore, Bobby V. Li, et al. · Clinical Biochemistry · 4
062 Cadasil presenting with focal and generalised epilepsy due to a novel NOTCH3 mutation
2018 · Benson S Chen, James C Cleland, et al. · Journal of Neurology Neurosurgery & Psychiatry · 3
Direct analysis of VLDL by TOF-MS allows rapid definition of Apo E genotypes and facilitates characterisation of post translational changes
2016 · Richard I. King, Stephen O. Brennan · Clinica Chimica Acta · 2
Homozygous familial hypercholesterolaemia and treatment by LDL apheresis.
2010 · Richard I King, Russell S Scott, et al. · PubMed · 2
Comparison of p50 determination by siemens and radiometer blood gas analysers with tonometry
2010 · R.I. King, P.M. George, et al. · Pathology · 2
Hemoglobin C--G-Georgia double heterozygosity: a case report.
1992 · S Reynolds, C Miller, et al. · PubMed · 2
Familial pseudohyperkalaemia: An unusual cause of artefactual hyperkalaemia
2026 · Megan Rodney, Kelly Rankin, et al. · Annals of Clinical Biochemistry International Journal of Laboratory Medicine · 1
Implementing genomic medicine in New Zealand
2024 · Richard I. King · Journal of the Royal Society of New Zealand · 1
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Genetic testing for familial hyperaldosteronism type 1 in Aotearoa/New Zealand
2024 · Marianne S. Elston, Jade A. U. Tamatea, et al. · Internal Medicine Journal · 1
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Aspartate aminotransferase at large—A case of disappearing macro‐aspartate aminotransferase in a child
2026 · Aaron Weston, Megan Rodney, et al. · JPGN Reports
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Prenatal presentation of isochromosome Xq with ambiguous NIPS, QF-PCR and FISH results
2026 · Deepak Subramanian, Susannah Ford, et al. · Pathology
Works count: 51
Citation count: 776
H-index: 9
I10-index: 9
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