Skip to Main Content

Author Details

Emmanouil T Dermitzakis
University of Geneva
1998
232
88
PMIDPaper TitleJournal TitlePublished Year
36717752Integrated multi-omics reveals anaplerotic rewiring in methylmalonyl-CoA mutase deficiency.Nat Metab2023
37604891Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits.Nat Commun2023
37550624Proteomic analysis of 92 circulating proteins and their effects in cardiometabolic diseases.Clin Proteomics2023
36717752Integrated multi-omics reveals anaplerotic rewiring in methylmalonyl-CoA mutase deficiency.Nat Metab2023
37130959Author Correction: Discovery of drug-omics associations in type 2 diabetes with generative deep-learning models.Nat Biotechnol2023
36696913Multiallelic Copy Number Variation in ORM1 is Associated with Plasma Cell-Free DNA Levels as an Intermediate Phenotype for Venous Thromboembolism.Thromb Haemost2023
37049597Impact of Christian Orthodox Church Fasting on Metabolic Syndrome Components in Adults Aged 18-49 Years.Nutrients2023
37299441The Interplay between Metabolic Syndrome and Religious Fasting in Postmenopausal Women.Nutrients2023
37299432Nutrient Intake and Risk Factors for Metabolic Syndrome in Christian Orthodox Church Religious Fasters.Nutrients2023
37543566Identifying novel regulatory effects for clinically relevant genes through the study of the Greek population.BMC Genomics2023
36977773Genetic variation in cis-regulatory domains suggests cell type-specific regulatory mechanisms in immunity.Commun Biol2023
37550624Proteomic analysis of 92 circulating proteins and their effects in cardiometabolic diseases.Clin Proteomics2023
37543566Identifying novel regulatory effects for clinically relevant genes through the study of the Greek population.BMC Genomics2023
37604891Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits.Nat Commun2023
37049597Impact of Christian Orthodox Church Fasting on Metabolic Syndrome Components in Adults Aged 18-49 Years.Nutrients2023
36977773Genetic variation in cis-regulatory domains suggests cell type-specific regulatory mechanisms in immunity.Commun Biol2023
37299441The Interplay between Metabolic Syndrome and Religious Fasting in Postmenopausal Women.Nutrients2023
37299432Nutrient Intake and Risk Factors for Metabolic Syndrome in Christian Orthodox Church Religious Fasters.Nutrients2023
37130959Author Correction: Discovery of drug-omics associations in type 2 diabetes with generative deep-learning models.Nat Biotechnol2023
36696913Multiallelic Copy Number Variation in ORM1 is Associated with Plasma Cell-Free DNA Levels as an Intermediate Phenotype for Venous Thromboembolism.Thromb Haemost2023
35106505Four groups of type 2 diabetes contribute to the etiological and clinical heterogeneity in newly diagnosed individuals: An IMI DIRECT study.Cell Rep Med2022
35906002Cross-species transcriptome analysis for early detection and specific therapeutic targeting of human lupus nephritis.Ann Rheum Dis2022
35387486Genetic Landscape of the ACE2 Coronavirus Receptor.Circulation2022
36216966An anti-influenza combined therapy assessed by single cell RNA-sequencing.Commun Biol2022
35666741Regulation of HLA class I expression by non-coding gene variations.PLoS Genet2022
36114277Leveraging interindividual variability of regulatory activity for refining genetic regulation of gene expression in schizophrenia.Mol Psychiatry2022
35272364Integrated GWAS and Gene Expression Suggest ORM1 as a Potential Regulator of Plasma Levels of Cell-Free DNA and Thrombosis Risk.Thromb Haemost2022
352454732021 Curt Stern Award: Studying the biology of "junk".Am J Hum Genet2022
35106505Four groups of type 2 diabetes contribute to the etiological and clinical heterogeneity in newly diagnosed individuals: An IMI DIRECT study.Cell Rep Med2022
35666741Regulation of HLA class I expression by non-coding gene variations.PLoS Genet2022
35387486Genetic Landscape of the ACE2 Coronavirus Receptor.Circulation2022
35906002Cross-species transcriptome analysis for early detection and specific therapeutic targeting of human lupus nephritis.Ann Rheum Dis2022
36216966An anti-influenza combined therapy assessed by single cell RNA-sequencing.Commun Biol2022
36114277Leveraging interindividual variability of regulatory activity for refining genetic regulation of gene expression in schizophrenia.Mol Psychiatry2022
352454732021 Curt Stern Award: Studying the biology of "junk".Am J Hum Genet2022
35272364Integrated GWAS and Gene Expression Suggest ORM1 as a Potential Regulator of Plasma Levels of Cell-Free DNA and Thrombosis Risk.Thromb Haemost2022
32564428Genomic profiling of late-onset basal cell carcinomas from two brothers with nevoid basal cell carcinoma syndrome.J Eur Acad Dermatol Venereol2021
33749946Single-cell transcriptomics reveal temporal dynamics of critical regulators of germ cell fate during mouse sex determination.FASEB J2021
33542415Gene regulation contributes to explain the impact of early life socioeconomic disadvantage on adult inflammatory levels in two cohort studies.Sci Rep2021
34233929Profiles of Glucose Metabolism in Different Prediabetes Phenotypes, Classified by Fasting Glycemia, 2-Hour OGTT, Glycated Hemoglobin, and 1-Hour OGTT: An IMI DIRECT Study.Diabetes2021
33671993The Christian Orthodox Church Fasting Diet Is Associated with Lower Levels of Depression and Anxiety and a Better Cognitive Performance in Middle Life.Nutrients2021
34262907Specific Transcriptomic Signatures and Dual Regulation of Steroidogenesis Between Fetal and Adult Mouse Leydig Cells.Front Cell Dev Biol2021
33558525Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
34330988Rates of SARS-CoV-2 transmission and vaccination impact the fate of vaccine-resistant strains.Sci Rep2021
33351229Ether lipids, sphingolipids and toxic 1-deoxyceramides as hallmarks for lean and obese type 2 diabetic patients.Acta Physiol (Oxf)2021
33184701Correction to: The role of physical activity in metabolic homeostasis before and after the onset of type 2 diabetes: an IMI DIRECT study.Diabetologia2021
32728807Overview of PAX gene family: analysis of human tissue-specific variant expression and involvement in human disease.Hum Genet2021
32564428Genomic profiling of late-onset basal cell carcinomas from two brothers with nevoid basal cell carcinoma syndrome.J Eur Acad Dermatol Venereol2021
33402679Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
33323478Processes Underlying Glycemic Deterioration in Type 2 Diabetes: An IMI DIRECT Study.Diabetes Care2021
  • 1 - 50 of 464

Recommended Authors

Shanghai Institute of Nutrition and Health, Chinese Academy of Sciences
Career Start Year 2013
Number of shared co-authors 22
Wellcome Sanger Institute
Career Start Year 2010
Number of shared co-authors 29
Stanford University
Career Start Year 2010
Number of shared co-authors 13
and Blood Institute, National Institutes of Health
Career Start Year 2008
Number of shared co-authors 82
University of Copenhagen
Career Start Year 2007
Number of shared co-authors 18
Research Institute of the McGill University Health Centre
Career Start Year 2006
Number of shared co-authors 20
The Center for Functional Cancer Epigenetics, Dana Farber Cancer Institute
Career Start Year 2006
Number of shared co-authors 44
Center for Disease Neurogenomics, Icahn School of Medicine at Mount Sinai
Career Start Year 2006
Number of shared co-authors 13
The University of North Carolina at Chapel Hill
Career Start Year 2005
Number of shared co-authors 16
William Harvey Research Institute, Queen Mary University of London
Career Start Year 2004
Number of shared co-authors 10
Genome Institute of Singapore (GIS)
Career Start Year 2004
Number of shared co-authors 20
Knight Cancer Institute, Oregon Health & Science University
Career Start Year 2004
Number of shared co-authors 76
Altius Institute for Biomedical Sciences
Career Start Year 2003
Number of shared co-authors 119
Bakar Computational Health Sciences Institute, University of California san francisco
Career Start Year 2003
Number of shared co-authors 11
Department of Pediatrics and Rady's Children's Hospital, University of California
Career Start Year 2002
Number of shared co-authors 104
Harvard University, USA Broad Institute, USA Harvard Stem Cell Institute
Career Start Year 2001
Number of shared co-authors 75
Center for Spatial and Functional Genomics, Children's Hospital of Philadelphia
Career Start Year 2001
Number of shared co-authors 9
Institute for Genomic Medicine, Columbia University
Career Start Year 2001
Number of shared co-authors 1
Boston University School of Public Health
Career Start Year 2001
Number of shared co-authors 108
SickKids Research Institute
Career Start Year 2000
Number of shared co-authors 20
Center for Omics Sciences, IRCCS San Raffaele Scientific Institute
Career Start Year 2000
Number of shared co-authors 77
Institute of Genetics and Cancer, University of Edinburgh
Career Start Year 2000
Number of shared co-authors 71
University of California san francisco
Career Start Year 1998
Number of shared co-authors 17
The Hospital for Sick Children
Career Start Year 1997
Number of shared co-authors 55
Princeton University
Career Start Year 1997
Number of shared co-authors 50
Institute of Genetics and Cancer, University of Edinburgh
Career Start Year 1997
Number of shared co-authors 35
Genomics and Translational Research Center
Career Start Year 1996
Number of shared co-authors 12
Barcelona Institute of Science and Technology (BIST)
Career Start Year 1995
Number of shared co-authors 147
Institute for Genomic Medicine, Columbia University Irving Medical Center
Career Start Year 1992
Number of shared co-authors 79
University of Washington
Career Start Year 1976
Number of shared co-authors 161

Collaborators

Co-authored papers 36
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 28
Co-authored papers 27
Co-authored papers 26
Stanford University
Co-authored papers 26
Co-authored papers 25
Columbia University
Co-authored papers 24
Center for Genetic Medicine, Northwestern University Feinberg School of Medicine
Co-authored papers 24
King's College London
Co-authored papers 21
Co-authored papers 21
Co-authored papers 20
Co-authored papers 20
Co-authored papers 17
Co-authored papers 16
Co-authored papers 15
Co-authored papers 15
Co-authored papers 14
Barcelona Institute of Science and Technology
Co-authored papers 13
Co-authored papers 12
Co-authored papers 12
KTH Royal Institute of Technology
Co-authored papers 12
Novo Nordisk Foundation Center for Protein Research, University of Copenhagen
Co-authored papers 11
Co-authored papers 11
Wellcome Sanger Institute
Co-authored papers 11
Co-authored papers 10
Co-authored papers 10
Co-authored papers 10
Wellcome Sanger Institute
Co-authored papers 9
University of Cambridge
Co-authored papers 8
Co-authored papers 8