Andrew D. Laurie

Christchurch, CAN, New Zealand

Last Updated: 09/26/2026

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Found 11 publications

Association of Clinical Characteristics With Familial Hypercholesterolaemia Variants in a Lipid Clinic Setting: A Case-Control Study.

Association of Clinical Characteristics With Familial Hypercholesterolaemia Variants in a Lipid Clinic Setting: A Case-Control Study.

Journal: Journal of lipid and atherosclerosis

Published: July 02, 2023

Mutation of the -RPVR- Propeptide Motif at C-Terminal of the Aα Chain Is Associated with Decreased Fibrinogen Expression.

Mutation of the -RPVR- Propeptide Motif at C-Terminal of the Aα Chain Is Associated with Decreased Fibrinogen Expression.

Journal: Thrombosis and haemostasis

Published: January 09, 2018

Hypofibrinogenaemia associated with novel Aα126Val→Asp mutation in the fibrinogen coiled coil.

Hypofibrinogenaemia associated with novel Aα126Val→Asp mutation in the fibrinogen coiled coil.

Journal: Thrombosis and haemostasis

Published: April 20, 2017

A novel frameshift mutation in the lipoprotein lipase gene is rescued by alternative messenger RNA splicing.

A novel frameshift mutation in the lipoprotein lipase gene is rescued by alternative messenger RNA splicing.

Journal: Journal of clinical lipidology

Published: January 06, 2017

Novel FGB mutation Bβ240Cys→Arg confirms importance of the Bβ211-240 disulphide for plasma expression of fibrinogen.

Novel FGB mutation Bβ240Cys→Arg confirms importance of the Bβ211-240 disulphide for plasma expression of fibrinogen.

Journal: Thrombosis research

Published: July 21, 2016

Exon skipping and aberrant signal peptide cleavage produce novel fibrinogen with an Aα chain lacking the first 42 residues.

Exon skipping and aberrant signal peptide cleavage produce novel fibrinogen with an Aα chain lacking the first 42 residues.

Journal: Thrombosis and haemostasis

Published: March 09, 2016

Hypofibrinogenaemia with novel mutations (γ228Leu→Leu and γ229Gly→Glu) at neighbouring codons; allelic phase and expression level.

Hypofibrinogenaemia with novel mutations (γ228Leu→Leu and γ229Gly→Glu) at neighbouring codons; allelic phase and expression level.

Journal: Thrombosis and haemostasis

Published: February 01, 2016

Novel fibrinogen mutations (Aα17Gly→Cys and Aα381Ser→Phe) occurring with a 312Thr→Ala polymorphism: allelic phase assigned by direct mass measurement.

Novel fibrinogen mutations (Aα17Gly→Cys and Aα381Ser→Phe) occurring with a 312Thr→Ala polymorphism: allelic phase assigned by direct mass measurement.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis

Published: June 18, 2015

Novel FGG variant (γ339C→S) confirms importance of the γ326-339 disulphide bond for plasma expression of newly synthesised fibrinogen.

Novel FGG variant (γ339C→S) confirms importance of the γ326-339 disulphide bond for plasma expression of newly synthesised fibrinogen.

Journal: Thrombosis and haemostasis

Published: October 12, 2014

Functionally compromised FGG variant (γ320Asp→Glu) expressed at low level in plasma fibrinogen.

Functionally compromised FGG variant (γ320Asp→Glu) expressed at low level in plasma fibrinogen.

Journal: Thrombosis research

Published: May 02, 2014

Severe FX deficiency caused by a homozygous double deletion involving F10 and PROZ genes.

Severe FX deficiency caused by a homozygous double deletion involving F10 and PROZ genes.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: June 24, 2013

Showing 1-11 of 11

Last Updated: 09/26/2026