Publications by authors named "Adam D McIntyre"

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Heterozygous pathogenic PPARG variants in patients with severe hypertriglyceridemia.
Shyann Hang, Jian Wang, Zahra Taboun, Adam D McIntyre, Robert A Hegele

J Clin Lipidol· September 2025

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Comparison of Patients With Familial Chylomicronemia Syndrome and Multifactorial Chylomicronemia Syndrome.
Catherine M Spagnuolo, Jian Wang, Adam D McIntyre, Brooke A Kennedy, Robert A Hegele

J Clin Endocrinol Metab· March 2025

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Genetic Testing in Adults over 50 Years with Chronic Kidney Disease: Diagnostic Yield and Clinical Implications in a Specialized Kidney Genetics Clinic.
Clara Schott, Mohammad Alajmi, Mohammad Bukhari, Sydney Relouw, Jian Wang, Adam D McIntyre

Genes (Basel)· March 2025

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Implementation of a Kidney Genetic Service Into the Diagnostic Pathway for Patients With Chronic Kidney Disease in Canada.
Clara Schott, Monica Arnaldi, Cadence Baker, Jian Wang, Adam D McIntyre

Kidney Int Rep· February 2025

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Lipoprotein Lipase: Structure, Function, and Genetic Variation.
Shehan D Perera, Jian Wang, Adam D McIntyre, Robert A Hegele

Genes (Basel)· January 2025

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Vascular calcification in chronic kidney disease associated with pathogenic variants in ABCC6.
Clara Schott, Allison A Dilliott, Jian Wang, Adam D McIntyre, Surim Son

Gene· November 2024

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Reduced lipoprotein (a) in patients with severe hypertriglyceridaemia.
Erin O Jacob, Adam D McIntyre, Jian Wang, Robert A Hegele

J Int Med Res· October 2024

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Phenotype in Individuals with Heterozygous Rare Variants in Encoding Hepatic Lipase.
Erin O Jacob, Jian Wang, Adam D McIntyre, Robert A Hegele

Int J Mol Sci· October 2024

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Rapid DNA Diagnosis of Familial Hypercholesterolemia Due to the 15.8-Kilobase Deletion.
Sanaz Lordfard, Jian Wang, Adam D McIntyre, Robert A Hegele

CJC Open· September 2024

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Combined hyperlipidemia is genetically similar to isolated hypertriglyceridemia.
Praneet K Gill, Jacqueline S Dron, Amanda J Berberich, Jian Wang, Adam D McIntyre

J Clin Lipidol· July 2024

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Ancestry-specific profiles of genetic determinants of severe hypertriglyceridemia.
Praneet K Gill, Jacqueline S Dron, Allison A Dilliott, Adam D McIntyre, Henian Cao

J Clin Lipidol· July 2024

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Interrogation of selected genes influencing serum LDL-Cholesterol levels in patients with well characterized NAFLD.
Eduardo Vilar-Gomez, Samer Gawrieh, Tiebing Liang, Adam D McIntyre, Robert A Hegele

J Clin Lipidol· July 2024

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Carotid intima-medial thickness in patients with severe hypertriglyceridemia.
Maud Ahmad, Brooke A Kennedy, Surim Son, Adam D McIntyre, Julieta Lazarte

Atheroscler Plus· June 2024

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Lipoprotein(a) in Familial Hypercholesterolemia.
Erin O Jacob, Adam D McIntyre, Jian Wang, Robert A Hegele

CJC Open· January 2024

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Variability of longitudinal triglyceride phenotype in patients heterozygous for pathogenic APOA5 variants.
Shehan D Perera, Jian Wang, Adam D McIntyre, Robert A Hegele

J Clin Lipidol· December 2023

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The longitudinal triglyceride phenotype in heterozygotes with LPL pathogenic variants.
Shehan D Perera, Jian Wang, Adam D McIntyre, Jacqueline S Dron, Robert A Hegele

J Clin Lipidol· February 2023

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Defective KIM-1 phagocytosis does not predispose to acute graft dysfunction after kidney transplantation in humans.
Rita S Suri, Ji Yun Lee, Matthew R Ban, Bradly Shrum, Elena Tutunea-Fatan, Adam D McIntyre

Kidney Int· August 2022

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Prevalence of severe hypertriglyceridemia and pancreatitis in familial partial lipodystrophy type 2.
Julieta Lazarte, Jian Wang, Adam D McIntyre, Robert A Hegele

J Clin Lipidol· March 2022

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Abetalipoproteinemia Due to a Novel Splicing Variant in in 3 Siblings.
Caitlyn Vlasschaert, Adam D McIntyre, Lauren A Thomson, Brooke A Kennedy, Suzanne Ratko

J Investig Med High Impact Case Rep· October 2021

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Association of apolipoprotein E variation with cognitive impairment across multiple neurodegenerative diagnoses.
Allison A Dilliott, Kelly M Sunderland, Paula M McLaughlin, Angela C Roberts, Emily C Evans, Adam D McIntyre

Neurobiol Aging· September 2021

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Contribution of rare variant associations to neurodegenerative disease presentation.
Allison A Dilliott, Abdalla Abdelhady, Kelly M Sunderland, Sali M K Farhan, Agessandro Abrahao, Adam D McIntyre

NPJ Genom Med· September 2021

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Enrichment of loss-of-function and copy number variants in ventricular cardiomyopathy genes in 'lone' atrial fibrillation.
Julieta Lazarte, Zachary W Laksman, Jian Wang, John F Robinson, Jacqueline S Dron, Adam D McIntyre

Europace· June 2021

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Clinical and Mutation Spectra of Cockayne Syndrome in India.
Dhanya L Narayanan, Moni Tuteja, Adam D McIntyre, Robert A Hegele, Nadege Calmels

Neurol India· June 2021

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Evaluating Polygenic Risk Scores in "Lone" Atrial Fibrillation.
Julieta Lazarte, Jacqueline S Dron, Adam D McIntyre, Allan C Skanes, Lorne J Gula

CJC Open· June 2021

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Role of Common Genetic Variation in Lone Atrial Fibrillation.
Julieta Lazarte, Jacqueline S Dron, Adam D McIntyre, Allan C Skanes, Lorne J Gula

Circ Genom Precis Med· February 2021

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