|
| 36084730 | Extended Risk of Mortality in Children with Inborn Errors of Metabolism: AÂ Longitudinal Cohort Study. | J Pediatr | 2023 |
| 37804262 | The Prevalence and Characteristics of Arrhythmic Mitral Valve Prolapse in Patients With Unexplained Cardiac Arrest. | JACC Clin Electrophysiol | 2023 |
| 37124966 | Management of Inherited Arrhythmia Syndromes: A HiRO Consensus Handbook on Process of Care. | CJC Open | 2023 |
| 36369700 | Validation of case definition algorithms for the ascertainment of congenital anomalies. | Birth Defects Res | 2023 |
| 34715283 | Return of Results Policies for Genomic Research: Current Practices and the Hearts in Rhythm Organization (HiRO) Approach. | Can J Cardiol | 2022 |
| 35352813 | Importance of genetic testing in unexplained cardiac arrest. | Eur Heart J | 2022 |
| 35404459 | Association of Birth Defects With Child Mortality Before Age 14 Years. | JAMA Netw Open | 2022 |
| 35718241 | A Call to Action: Optimizing Indigenous Cardiovascular Health in Canada. | Can J Cardiol | 2022 |
| 35659933 | Is there a way to reduce the inequity in variant interpretation on the basis of ancestry? | Am J Hum Genet | 2022 |
| 36102233 | Sex Differences and Utility of Treadmill Testing in Long-QT Syndrome. | J Am Heart Assoc | 2022 |
| 33655302 | Association of first trimester anaesthesia with risk of congenital heart defects in offspring. | Int J Epidemiol | 2022 |
| 35149971 | Implementation of the BC Congenital Anomalies Surveillance System (BCCASS). | Can J Public Health | 2022 |
| 35032083 | Cascade testing for inherited arrhythmia conditions: Experiences and attitudes of family communication approaches for a Canadian cohort. | J Genet Couns | 2022 |
| 35058604 | Observational study of birth outcomes in children with inborn errors of metabolism. | Pediatr Res | 2022 |
| 32440749 | Post-partum Primary Biliary Cholangitis Preceded by Intrahepatic Cholestasis of Pregnancy in Three First Nation Patients. | Dig Dis Sci | 2021 |
| 33742313 | Stillbirth in Canada: anachronistic definition and registration processes impede public health surveillance and clinical care. | Can J Public Health | 2021 |
| 34472132 | Time trends, geographic variation and risk factors for gastroschisis in Canada: A population-based cohort study 2006-2017. | Paediatr Perinat Epidemiol | 2021 |
| 34295859 | Association of the <i>CPT1A</i> p.P479L Metabolic Gene Variant With Childhood Respiratory and Other Infectious Illness in Nunavut. | Front Pediatr | 2021 |
| 33960826 | Variant Reinterpretation in Survivors of Cardiac Arrest With Preserved Ejection Fraction (the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry) by Clinicians and Clinical Commercial Laboratories. | Circ Genom Precis Med | 2021 |
| 32816918 | Coeliac disease and risk of birth defects in pregnancy. | Gut | 2021 |
| 31407359 | Severe maternal morbidity surveillance: Monitoring pregnant women at high risk for prolonged hospitalisation and death. | Paediatr Perinat Epidemiol | 2020 |
| 34131458 | Neonatal hypoglycemia and the CPT1A P479L variant in term newborns: A retrospective cohort study of Inuit newborns from Kivalliq Nunavut. | Paediatr Child Health | 2020 |
| 31907519 | Inflammatory Bowel Disease and Risk of Birth Defects in Offspring. | J Crohns Colitis | 2020 |
| 31994352 | Cardiac arrest in a mother and daughter and the identification of a novel RYR2 variant, predisposing to low penetrant catecholaminergic polymorphic ventricular tachycardia in a four-generation Canadian family. | Mol Genet Genomic Med | 2020 |
| 32068812 | Risk of Offspring Birth Defects in Women After Bariatric Surgery. | JAMA | 2020 |
| 33305225 | The Hearts in Rhythm Organization: A Canadian National Cardiogenetics Network. | CJC Open | 2020 |
| 33381478 | Barriers and Considerations for Diagnosing Rare Diseases in Indigenous Populations. | Front Pediatr | 2020 |
| 32391301 | Indigenous Genomic Databases: Pragmatic Considerations and Cultural Contexts. | Front Public Health | 2020 |
| 32329955 | Understanding the personal and community impact of long QT syndrome: A perspective from Gitxsan women. | J Genet Couns | 2020 |
| 32251390 | Rights, interests and expectations: Indigenous perspectives on unrestricted access to genomic data. | Nat Rev Genet | 2020 |
| 29327608 | Pregnancy outcomes of women with spina bifida. | Disabil Rehabil | 2019 |
| 31868600 | Explaining the variability in cardiovascular risk factors among First Nations communities in Canada: a population-based study. | Lancet Planet Health | 2019 |
| 29908350 | Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplication. | Eur J Med Genet | 2019 |
| 31504102 | Bariatric surgery and the risk of congenital anomalies in subsequent pregnancies. | Am J Clin Nutr | 2019 |
| 31387776 | Future risk of cancer in women who have children with birth defects. | Ann Epidemiol | 2019 |
| 30892943 | Genomic Research Through an Indigenous Lens: Understanding the Expectations. | Annu Rev Genomics Hum Genet | 2019 |
| 30977029 | Maternal proximity to extremely low frequency electromagnetic fields and risk of birth defects. | Eur J Epidemiol | 2019 |
| 31060985 | Severe Maternal Morbidity in Canada: Temporal Trends and Regional Variations, 2003-2016. | J Obstet Gynaecol Can | 2019 |
| 30996616 | The p.P479L variant in CPT1A is associated with infectious disease in a BC First Nation. | Paediatr Child Health | 2019 |
| 30623609 | Prepregnancy asthma and the subsequent risk of central nervous system defects in offspring. | Birth Defects Res | 2019 |
| 28676560 | Congenital microcephaly in Quebec: baseline prevalence, risk factors and outcomes in a large cohort of neonates. | Arch Dis Child Fetal Neonatal Ed | 2018 |
| 29981096 | Red blood cell folate levels in Canadian Inuit women of childbearing years: influence of food security, body mass index, smoking, education, and vitamin use. | Can J Public Health | 2018 |
| 30466855 | Early Repolarization Pattern Inheritance in the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry (CASPER). | JACC Clin Electrophysiol | 2018 |
| 29470717 | Risk of central nervous system defects in offspring of women with and without mental illness. | Arch Womens Ment Health | 2018 |
| 29606693 | Canadian Alliance for Healthy Hearts and Minds: First Nations Cohort Study Rationale and Design. | Prog Community Health Partnersh | 2018 |
| 29297981 | Primary Biliary Cholangitis in British Columbia First Nations: Clinical features and discovery of novel genetic susceptibility loci. | Liver Int | 2018 |
| 27369690 | Patient Recall, Interpretation, and Perspective of an Inconclusive Long QT Syndrome Genetic Test Result. | J Genet Couns | 2017 |
| 28196901 | Novel Variant in the <i>ANK2</i> Membrane-Binding Domain Is Associated With Ankyrin-B Syndrome and Structural Heart Disease in a First Nations Population With a High Rate of Long QT Syndrome. | Circ Cardiovasc Genet | 2017 |
| 28347582 | Cost Analysis of Patients Referred for Inherited Heart Rhythm Disorder Evaluation. | Can J Cardiol | 2017 |
| 28264985 | KCNQ1 p.L353L affects splicing and modifies the phenotype in a founder population with long QT syndrome type 1. | J Med Genet | 2017 |