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Author Details

John Brent Richards
Lady Davis Institute for Medical Research, Jewish General Hospital
1998
217
65
PMIDPaper TitleJournal TitlePublished Year
36528344Mendelian randomisation and vitamin D: the importance of model assumptions.Lancet Diabetes Endocrinol2023
37830501Identifying Rare Genetic Determinants for Improved Polygenic Risk Prediction of Bone Mineral Density and Fracture Risk.J Bone Miner Res2023
37579195Leveraging osteoclast genetic regulatory data to identify genes with a role in osteoarthritis.Genetics2023
37612393From target discovery to clinical drug development with human genetics.Nature2023
37348500Integrating genetics and metabolomics from multi-ethnic and multi-fluid data reveals putative mechanisms for age-related macular degeneration.Cell Rep Med2023
37402774Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis.Commun Biol2023
36773317Increasing serum iron levels and their role in the risk of infectious diseases: a Mendelian randomization approach.Int J Epidemiol2023
36635386Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases.Nat Genet2023
37069249Circulating proteins to predict COVID-19 severity.Sci Rep2023
37009933Predicting ExWAS findings from GWAS data: a shorter path to causal genes.Hum Genet2023
36805566Proteome-wide Mendelian randomization implicates nephronectin as an actionable mediator of the effect of obesity on COVID-19 severity.Nat Metab2023
37308534Proteomic characterization of acute kidney injury in patients hospitalized with SARS-CoV2 infection.Commun Med (Lond)2023
36993735Proteomic Characterization of Acute Kidney Injury in Patients Hospitalized with SARS-CoV2 Infection.Res Sq2023
37368847Dose-dependent Association of Alcohol Consumption With Obesity and Type 2 Diabetes: Mendelian Randomization Analyses.J Clin Endocrinol Metab2023
36528344Mendelian randomisation and vitamin D: the importance of model assumptions.Lancet Diabetes Endocrinol2023
37612393From target discovery to clinical drug development with human genetics.Nature2023
37579195Leveraging osteoclast genetic regulatory data to identify genes with a role in osteoarthritis.Genetics2023
37830501Identifying Rare Genetic Determinants for Improved Polygenic Risk Prediction of Bone Mineral Density and Fracture Risk.J Bone Miner Res2023
36993735Proteomic Characterization of Acute Kidney Injury in Patients Hospitalized with SARS-CoV2 Infection.Res Sq2023
37348500Integrating genetics and metabolomics from multi-ethnic and multi-fluid data reveals putative mechanisms for age-related macular degeneration.Cell Rep Med2023
37308534Proteomic characterization of acute kidney injury in patients hospitalized with SARS-CoV2 infection.Commun Med (Lond)2023
37009933Predicting ExWAS findings from GWAS data: a shorter path to causal genes.Hum Genet2023
37402774Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis.Commun Biol2023
37368847Dose-dependent Association of Alcohol Consumption With Obesity and Type 2 Diabetes: Mendelian Randomization Analyses.J Clin Endocrinol Metab2023
37069249Circulating proteins to predict COVID-19 severity.Sci Rep2023
36805566Proteome-wide Mendelian randomization implicates nephronectin as an actionable mediator of the effect of obesity on COVID-19 severity.Nat Metab2023
36773317Increasing serum iron levels and their role in the risk of infectious diseases: a Mendelian randomization approach.Int J Epidemiol2023
36635386Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases.Nat Genet2023
34172473Genetically increased circulating FUT3 level leads to reduced risk of idiopathic pulmonary fibrosis: a Mendelian randomisation study.Eur Respir J2022
36250789Genetic determinants of polygenic prediction accuracy within a population.Genetics2022
35460399Polygenic risk score as a possible tool for identifying familial monogenic causes of complex diseases.Genet Med2022
35970849ELF5 is a potential respiratory epithelial cell-specific risk gene for severe COVID-19.Nat Commun2022
35710731Capturing additional genetic risk from family history for improved polygenic risk prediction.Commun Biol2022
35708486Novel genes and sex differences in COVID-19 severity.Hum Mol Genet2022
35839461Circulating Isovalerylcarnitine and Lung Cancer Risk: Evidence from Mendelian Randomization and Prediagnostic Blood Measurements.Cancer Epidemiol Biomarkers Prev2022
35816432Colocalization of Gene Expression and DNA Methylation with Genetic Risk Variants Supports Functional Roles of <i>MUC5B</i> and <i>DSP</i> in Idiopathic Pulmonary Fibrosis.Am J Respir Crit Care Med2022
35689460Identifying Causes of Fracture Beyond Bone Mineral Density: Evidence From Human Genetics.J Bone Miner Res2022
36271419Dehydration is associated with production of organic osmolytes and predicts physical long-term symptoms after COVID-19: a multicenter cohort study.Crit Care2022
35992131Causal associations between body fat accumulation and COVID-19 severity: A Mendelian randomization study.Front Endocrinol (Lausanne)2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
36376796Correction: The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals.Clin Proteomics2022
34172473Genetically increased circulating FUT3 level leads to reduced risk of idiopathic pulmonary fibrosis: a Mendelian randomisation study.Eur Respir J2022
35273064Cohort profile: genomic data for 26 622 individuals from the Canadian Longitudinal Study on Aging (CLSA).BMJ Open2022
35234851Connecting Genomics and Proteomics to Identify Protein Biomarkers for Adult and Youth-Onset Type 2 Diabetes: A Two-Sample Mendelian Randomization Study.Diabetes2022
35194177Reply to 'The emerging evidence for non-skeletal health benefits of vitamin D supplementation in adults'.Nat Rev Endocrinol2022
35027740Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19.Nat Genet2022
35147782An effector index to predict target genes at GWAS loci.Hum Genet2022
34889978Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity.Hum Genet2022
34758976Clinically Relevant Circulating Protein Biomarkers for Type 1 Diabetes: Evidence From a Two-Sample Mendelian Randomization Study.Diabetes Care2022
34815552The health effects of vitamin D supplementation: evidence from human studies.Nat Rev Endocrinol2022
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Collaborators

Tim D Spector
King's College London
Co-authored papers 73
Vincenzo Forgetta
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Co-authored papers 60
Celia M T Greenwood
Co-authored papers 41
Fernando Rivadeneira
University Medical Center Rotterdam
Co-authored papers 36
Nicole Soranzo
Wellcome Sanger Institute
Co-authored papers 33
Nicholas J Timpson
Co-authored papers 28
Andr?? G Uitterlinden
Erasmus University Medical Center
Co-authored papers 27
Douglas P Kiel
Hinda and Arthur Marcus Institute for Aging Research
Co-authored papers 25
Guillaume Butler-Laporte
McGill University
Co-authored papers 24
George Davey Smith
University of Bristol
Co-authored papers 24
Claes Ohlsson
Center for Bone and Arthritis Research, University of Gothenburg
Co-authored papers 24
Vincent Mooser
McGill University
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David M Evans
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Co-authored papers 22
Zari Dastani
Co-authored papers 20
David Karasik
Co-authored papers 20
Albert Hofman
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Co-authored papers 19
Claudia Langenberg
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John A Morris
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Maria Carola Zillikens
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Nicholas J Wareham
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Kari Stefansson
University of Iceland
Co-authored papers 15
John R B Perry
Co-authored papers 15
Elin Grundberg
Co-authored papers 14
Mattias Lorentzon
Co-authored papers 14
Cornelia M van Duijn
University of Oxford
Co-authored papers 14
Panos Deloukas
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 13
John P Kemp
Co-authored papers 13
Ching-Ti Liu
Co-authored papers 13
Liesbeth Vandenput
Mary McKillop Institute for Health Research, Australian Catholic University
Co-authored papers 13
Gabriela L Surdulescu
Co-authored papers 13
Release 1.2