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Author Details

Andrew D Paterson
The Hospital for Sick Children
1991
325
69
PMIDPaper TitleJournal TitlePublished Year
37939167Erythritol as a Potential Causal Contributor to Cardiometabolic Disease: A Mendelian Randomization Study.Diabetes2024
38073250Comprehensive whole-genome analyses of the UK Biobank reveal significant sex differences in both genotype missingness and allele frequency on the X chromosome.Hum Mol Genet2024
36126820Role of 19 SNPs in 10 genes with type 2 diabetes in the Pakistani population.Gene2023
37733810The effect of ascertainment on penetrance estimates for rare variants: Implications for establishing pathogenicity and for genetic counselling.PLoS One2023
38095926From black and white to fifty shades of grey.Blood2023
37494403Genetics of cannabis use in opioid use disorder: A genome-wide association and polygenic risk score study.PLoS One2023
37867527Beyond apples and pears: sex-specific genetics of body fat percentage.Front Endocrinol (Lausanne)2023
37008938Investigating the association between fasting insulin, erythrocytosis and HbA1c through Mendelian randomization and observational analyses.Front Endocrinol (Lausanne)2023
37369448Characterization of direct and/or indirect genetic associations for multiple traits in longitudinal studies of disease progression.Genetics2023
37267899eXclusionarY: 10 years later, where are the sex chromosomes in GWASs?Am J Hum Genet2023
37200064Erratum. Association Between Obesity and Chronic Kidney Disease: Multivariable Mendelian Randomization Analysis and Observational Data From a Bariatric Surgery Cohort. Diabetes 2023;72:496-510.Diabetes2023
37131148HostSeq: a Canadian whole genome sequencing and clinical data resource.BMC Genom Data2023
37263307Gut Microbiome Composition Is Associated With Future Onset of Crohn's Disease in Healthy First-Degree Relatives.Gastroenterology2023
36651668Genetics of osteonecrosis in children and adults with systemic lupus erythematosus.Rheumatology (Oxford)2023
36916720Genetics of longitudinal kidney function in children and adults with systemic lupus erythematosus.Rheumatology (Oxford)2023
36657976Association Between Obesity and Chronic Kidney Disease: Multivariable Mendelian Randomization Analysis and Observational Data From a Bariatric Surgery Cohort.Diabetes2023
33257509Linkage analysis identifies an isolated strabismus locus at 14q12 overlapping with FOXG1 syndrome region.J Med Genet2022
35474271GWAS of Hematuria.Clin J Am Soc Nephrol2022
35643175Mediterranean-Like Dietary Pattern Associations With Gut Microbiome Composition and Subclinical Gastrointestinal Inflammation.Gastroenterology2022
35639794Major sex differences in allele frequencies for X chromosomal variants in both the 1000 Genomes Project and gnomAD.PLoS Genet2022
35750789Integrating variant functional annotation scores have varied abilities to improve power of genome-wide association studies.Sci Rep2022
35748295Insulin Response to Oral Glucose and Cardiometabolic Disease: A Mendelian Randomization Study to Assess Potential Causality.Diabetes2022
36536295Genome-wide association study identifies novel loci associated with skin autofluorescence in individuals without diabetes.BMC Genomics2022
33635378Population-based studies reveal an additive role of type IV collagen variants in hematuria and albuminuria.Pediatr Nephrol2022
35273064Cohort profile: genomic data for 26 622 individuals from the Canadian Longitudinal Study on Aging (CLSA).BMJ Open2022
33283425Genetically determined lean mass and dietary response.Diabetes Obes Metab2021
33883194Genetic Risk Factors for CVD in Type 1 Diabetes: The DCCT/EDIC Study.Diabetes Care2021
33602752Patients with Protein-Truncating <i>PKD1</i> Mutations and Mild ADPKD.Clin J Am Soc Nephrol2021
33851121Type IV Collagen Variants in CKD: Performance of Computational Predictions for Identifying Pathogenic Variants.Kidney Med2021
33568380Protocol for a randomised trial evaluating a preconception-early childhood telephone-based intervention with tailored e-health resources for women and their partners to optimise growth and development among children in Canada: a Healthy Life Trajectory Initiative (HeLTI Canada).BMJ Open2021
33731350Nuclear genome-wide associations with mitochondrial heteroplasmy.Sci Adv2021
33529168Residual β cell function in long-term type 1 diabetes associates with reduced incidence of hypoglycemia.J Clin Invest2021
33632724Risk Factors for Longitudinal Resting Heart Rate and Its Associations With Cardiovascular Outcomes in the DCCT/EDIC Study.Diabetes Care2021
34565340LAMA2 and LOXL4 are candidate FSGS genes.BMC Nephrol2021
34293299Anti-Microbial Antibody Response is Associated With Future Onset of Crohn's Disease Independent of Biomarkers of Altered Gut Barrier Function, Subclinical Inflammation, and Genetic Risk.Gastroenterology2021
34261756Association of Coding Variants in Hydroxysteroid 17-beta Dehydrogenase 14 (<i>HSD17B14</i>) with Reduced Progression to End Stage Kidney Disease in Type 1 Diabetes.J Am Soc Nephrol2021
33435948Skin autofluorescence predicts new cardiovascular disease and mortality in people with type 2 diabetes.BMC Endocr Disord2021
33462485Large-scale association analyses identify host factors influencing human gut microbiome composition.Nat Genet2021
31236574Association of systemic lupus erythematosus (SLE) genetic susceptibility loci with lupus nephritis in childhood-onset and adult-onset SLE.Rheumatology (Oxford)2020
32086293Erratum. Evaluation of the Genetic Association Between Adult Obesity and Neuropsychiatric Disease. Diabetes 2019;68:2235-2246.Diabetes2020
32084423Prevalence and Clinical Features of Inflammatory Bowel Diseases Associated With Monogenic Variants, Identified by Whole-Exome Sequencing in 1000 Children at a Single Center.Gastroenterology2020
33059653Associations of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn's disease subjects.BMC Med Genet2020
33371892Statistical power in COVID-19 case-control host genomic study design.Genome Med2020
33277529COG5 variants lead to complex early onset retinal degeneration, upregulation of PERK and DNA damage.Sci Rep2020
32663239Enhancer-gene rewiring in the pathogenesis of Quebec platelet disorder.Blood2020
32685888Bleeding risks for uncharacterized platelet function disorders.Res Pract Thromb Haemost2020
32936915Genome-Wide Association for HbA1c in Malay Identified Deletion on SLC4A1 that Influences HbA1c Independent of Glycemia.J Clin Endocrinol Metab2020
32694834DNA methylation mediates development of HbA1c-associated complications in type 1 diabetes.Nat Metab2020
32449747TaxoNN: ensemble of neural networks on stratified microbiome data for disease prediction.Bioinformatics2020
32372567Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees.Am J Med Genet B Neuropsychiatr Genet2020
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Collaborators

Arturas Petronis
The Campbell Family Mental Health Research Institute
Co-authored papers 21
Stephen W Scherer
The Hospital for Sick Children
Co-authored papers 20
Peter Szatmari
Hospital for Sick Children, University of Toronto
Co-authored papers 18
James L Kennedy
Institute of Medical Sciences, University of Toronto
Co-authored papers 18
Cornelia M van Duijn
University of Oxford
Co-authored papers 17
Wei Xu
Princess Margaret Cancer Centre
Co-authored papers 15
Ronald Klein
University of Wisconsin School of Medicine and Public Health
Co-authored papers 14
Norman F Boyd
Co-authored papers 13
Daryl Waggott
Ontario Institute for Cancer Research
Co-authored papers 12
Veronica J Vieland
The Ohio State University
Co-authored papers 12
Peter St George-Hyslop
Cambridge Institute for Medical Research, University of Cambridge
Co-authored papers 11
Johanna M Rommens
The Hospital for Sick Children
Co-authored papers 10
Mark S Silverberg
Co-authored papers 10
Ann Thompson
McMaster University
Co-authored papers 10
Tien Yin Wong
Tsinghua University
Co-authored papers 10
Christian R Marshall
Co-authored papers 9
Bridget A Fernandez
Memorial University of Newfoundland
Co-authored papers 9
Andr?? G Uitterlinden
Erasmus University Medical Center
Co-authored papers 9
Ozren Polasek
Co-authored papers 8
Osvaldo Espin-Garcia
Princess Margaret Cancer Centre, University Health Network
Co-authored papers 8
James S Sutcliffe
Vanderbilt Genetics Institute, Vanderbilt University
Co-authored papers 8
John R McLaughlin
University of Toronto Dalla Lana School of Public Health
Co-authored papers 8
George Davey Smith
University of Bristol
Co-authored papers 8
Albert Hofman
Harvard T.H. Chan School of Public Health
Co-authored papers 8
Caroline C W Klaver
Erasmus Medical Center
Co-authored papers 8
Fernando Rivadeneira
University Medical Center Rotterdam
Co-authored papers 8
Per-Henrik Groop
Folkhalsan Institute of Genetics, Folkhalsan Research Center
Co-authored papers 8
Paul N Baird
The University of Melbourne
Co-authored papers 7
Johannes R Vingerling
Erasmus University Medical Center
Co-authored papers 7
David Moher
University of Ottawa
Co-authored papers 7
Release 1.2