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Adam D. McIntyre

University of Western Ontario
Robarts Research Institute

97

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1877

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Enrichment of loss-of-function and copy number variants in ventricular cardiomyopathy genes in 'lone' atrial fibrillation

2021 Europace
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Evaluating Polygenic Risk Scores in “Lone” Atrial Fibrillation

2021
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The Lipid Profile of Individuals With the APOE c.T137C:p.L46P Mutation

2021 Canadian Journal of Diabetes
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Role of Common Genetic Variation in Lone Atrial Fibrillation.

2021
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Evidence of synergism among three genetic variants in a patient with LMNA-related lipodystrophy and amyotrophic lateral sclerosis leading to a remarkable nuclear phenotype.

2021 Molecular and Cellular Biochemistry
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Clinical and Mutation Spectra of Cockayne Syndrome in India.

2021 Neurology India
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Contribution of rare variant associations to neurodegenerative disease presentation.

2021 npj Genomic Medicine
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Abetalipoproteinemia Due to a Novel Splicing Variant in MTTP in 3 Siblings.

2021 Journal of investigative medicine high impact case reports
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Prevalence of severe hypertriglyceridemia and pancreatitis in familial partial lipodystrophy type 2

2021 Journal of Clinical Lipidology
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Neurobiology of Aging Association of apolipoprotein E variation with cognitive impairment across multiple neurodegenerative diagnoses.

2021 Neurobiology of Aging
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