Adam D. Mcintyre

London, ON, Canada

Last Updated: 09/26/2026

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Found 71 publications

Impact of Genetic Testing in Endocrinology Practice: A Single-Center Experience Focused on Lipid and Monogenic Diabetes Disorders.

Impact of Genetic Testing in Endocrinology Practice: A Single-Center Experience Focused on Lipid and Monogenic Diabetes Disorders.

Journal: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists

Published: December 03, 2025

Spectrum of DNA Variants in Southwestern Ontario Patients with Familial Hypercholesterolemia.

Spectrum of DNA Variants in Southwestern Ontario Patients with Familial Hypercholesterolemia.

Journal: CJC open

Published: July 27, 2025

Genetic testing in kidney transplantation and living kidney donor risk assessment.

Genetic testing in kidney transplantation and living kidney donor risk assessment.

Journal: Kidney international

Published: June 26, 2025

Heterozygous pathogenic PPARG variants in patients with severe hypertriglyceridemia.

Heterozygous pathogenic PPARG variants in patients with severe hypertriglyceridemia.

Journal: Journal of clinical lipidology

Published: April 22, 2025

Genetic Testing in Adults over 50 Years with Chronic Kidney Disease: Diagnostic Yield and Clinical Implications in a Specialized Kidney Genetics Clinic.

Genetic Testing in Adults over 50 Years with Chronic Kidney Disease: Diagnostic Yield and Clinical Implications in a Specialized Kidney Genetics Clinic.

Journal: Genes

Published: February 20, 2025

Lipoprotein Lipase: Structure, Function, and Genetic Variation.

Lipoprotein Lipase: Structure, Function, and Genetic Variation.

Journal: Genes

Published: December 15, 2024

Reduced lipoprotein (a) in patients with severe hypertriglyceridaemia.

Reduced lipoprotein (a) in patients with severe hypertriglyceridaemia.

Journal: The Journal of international medical research

Published: October 14, 2024

Phenotype in Individuals with Heterozygous Rare Variants in LIPC Encoding Hepatic Lipase.

Phenotype in Individuals with Heterozygous Rare Variants in LIPC Encoding Hepatic Lipase.

Journal: International journal of molecular sciences

Published: September 29, 2024

Comparison of Patients With Familial Chylomicronemia Syndrome and Multifactorial Chylomicronemia Syndrome.

Comparison of Patients With Familial Chylomicronemia Syndrome and Multifactorial Chylomicronemia Syndrome.

Journal: The Journal of clinical endocrinology and metabolism

Published: July 02, 2024

Implementation of a Kidney Genetic Service Into the Diagnostic Pathway for Patients With Chronic Kidney Disease in Canada.

Implementation of a Kidney Genetic Service Into the Diagnostic Pathway for Patients With Chronic Kidney Disease in Canada.

Journal: Kidney international reports

Published: May 08, 2024

Rapid DNA Diagnosis of Familial Hypercholesterolemia Due to the LDLR 15.8-Kilobase Deletion.

Rapid DNA Diagnosis of Familial Hypercholesterolemia Due to the LDLR 15.8-Kilobase Deletion.

Journal: CJC open

Published: April 16, 2024

Vascular calcification in chronic kidney disease associated with pathogenic variants in ABCC6.

Vascular calcification in chronic kidney disease associated with pathogenic variants in ABCC6.

Journal: Gene

Published: April 11, 2024

Showing 1-12 of 71

Last Updated: 09/26/2026