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Author Details

Jonathan Marchini
Regeneron Pharmaceuticals Inc
1997
92
59
PMIDPaper TitleJournal TitlePublished Year
36384636Universal clinical Parkinson's disease axes identify a major influence of neuroinflammation.Genome Med2022
35999217Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes.Nat Commun2022
36384636Universal clinical Parkinson's disease axes identify a major influence of neuroinflammation.Genome Med2022
36450978Common and rare variant associations with clonal haematopoiesis phenotypes.Nature2022
36450978Common and rare variant associations with clonal haematopoiesis phenotypes.Nature2022
35999217Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes.Nat Commun2022
33367483A non-linear regression method for estimation of gene-environment heritability.Bioinformatics2021
34017140Computationally efficient whole-genome regression for quantitative and binary traits.Nat Genet2021
34115965Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.Am J Hum Genet2021
33619501Genome-wide analysis in 756,646 individuals provides first genetic evidence that <i>ACE2</i> expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease.medRxiv2021
34210852Sequencing of 640,000 exomes identifies <i>GPR75</i> variants associated with protection from obesity.Science2021
33367483A non-linear regression method for estimation of gene-environment heritability.Bioinformatics2021
34580220False discovery rate control in genome-wide association studies with population structure.Proc Natl Acad Sci U S A2021
34662886Exome sequencing and analysis of 454,787 UK Biobank participants.Nature2021
33619501Genome-wide analysis in 756,646 individuals provides first genetic evidence that <i>ACE2</i> expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease.medRxiv2021
34580220False discovery rate control in genome-wide association studies with population structure.Proc Natl Acad Sci U S A2021
34662886Exome sequencing and analysis of 454,787 UK Biobank participants.Nature2021
34017140Computationally efficient whole-genome regression for quantitative and binary traits.Nat Genet2021
34210852Sequencing of 640,000 exomes identifies <i>GPR75</i> variants associated with protection from obesity.Science2021
34115965Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.Am J Hum Genet2021
32300216Retraction Note: 11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project.Sci Data2020
32300216Retraction Note: 11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project.Sci Data2020
33196638Genotype imputation using the Positional Burrows Wheeler Transform.PLoS Genet2020
33087929Exome sequencing and characterization of 49,960 individuals in the UK Biobank.Nature2020
32517579Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.Stroke2020
32888427Inferring Gene-by-Environment Interactions with a Bayesian Whole-Genome Regression Model.Am J Hum Genet2020
33087929Exome sequencing and characterization of 49,960 individuals in the UK Biobank.Nature2020
33196638Genotype imputation using the Positional Burrows Wheeler Transform.PLoS Genet2020
32888427Inferring Gene-by-Environment Interactions with a Bayesian Whole-Genome Regression Model.Am J Hum Genet2020
32517579Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.Stroke2020
30908486The Plight of Muntaser Ibrahim.PLoS Genet2019
31780650Accurate, scalable and integrative haplotype estimation.Nat Commun2019
31237565Unified single-cell analysis of testis gene regulation and pathology in five mouse strains.Elife2019
31504236Handedness, language areas and neuropsychiatric diseases: insights from brain imaging and genetics.Brain2019
30908486The Plight of Muntaser Ibrahim.PLoS Genet2019
30988526The spatial correspondence and genetic influence of interhemispheric connectivity with white matter microstructure.Nat Neurosci2019
31780650Accurate, scalable and integrative haplotype estimation.Nat Commun2019
31504236Handedness, language areas and neuropsychiatric diseases: insights from brain imaging and genetics.Brain2019
31237565Unified single-cell analysis of testis gene regulation and pathology in five mouse strains.Elife2019
30988526The spatial correspondence and genetic influence of interhemispheric connectivity with white matter microstructure.Nat Neurosci2019
29632382Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.Nat Genet2018
30305743The UK Biobank resource with deep phenotyping and genomic data.Nature2018
30305740Genome-wide association studies of brain imaging phenotypes in UK Biobank.Nature2018
30158584An imputation platform to enhance integration of rice genetic resources.Nat Commun2018
30297969Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.Nat Genet2018
29700475Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.Nat Genet2018
29632382Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.Nat Genet2018
30158584An imputation platform to enhance integration of rice genetic resources.Nat Commun2018
30297969Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.Nat Genet2018
30305743The UK Biobank resource with deep phenotyping and genomic data.Nature2018
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Collaborators

Regeneron Pharmaceuticals Inc.
Co-authored papers 18
University of Oxford
Co-authored papers 16
The University of Manchester
Co-authored papers 12
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 10
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BioMarin Pharmaceutical Inc.
Co-authored papers 10
Big Data Institute, University of Oxford
Co-authored papers 9
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University of Michigan School of Public Health ann arbor
Co-authored papers 7
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Co-authored papers 7
Institute for Community Medicine, Ernst Moritz Arndt University
Co-authored papers 7
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Regeneron Pharmaceuticals
Co-authored papers 7
Co-authored papers 7
The Wellcome Trust Sanger Institute
Co-authored papers 7
Co-authored papers 7
University of Maryland School of Medicine
Co-authored papers 7
Wellcome Sanger Institute
Co-authored papers 7
University of Michigan ann arbor
Co-authored papers 7
Medical Research Council Integrative Epidemiology Unit at the University of Bristol
Co-authored papers 7
Virginia Commonwealth University
Co-authored papers 6