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PNLIPRP1 Hypermethylation in Exocrine Pancreas Links Type 2 Diabetes and Cholesterol Metabolism

Diabetes (New York, N.Y.), 2024-11, Vol.73 (11), p.1908-1918

2024

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Genetics brings new insight to β-cell function

Nature metabolism, 2024-10, Vol.6 (10), p.1848-1849

2024

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Interview: Philippe Froguel

European medical journal. Diabetes, 2024-10

Froguel, Philippe

2024

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Apport des techniques de séquençage de l’ADN de nouvelle génération en pratique et en recherche médicale en France

Bulletin de l'Académie nationale de médecine, 2024-10, Vol.208 (8), p.1141-1149

2024

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Obesity: exploring its connection to brain function through genetic and genomic perspectives

Molecular psychiatry, 2024-09

2024

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Towards the recognition of oligogenic forms of type 2 diabetes

Trends in endocrinology and metabolism, 2024-07

2024

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comorbidPGS: An R Package Assessing Shared Predisposition between Phenotypes Using Polygenic Scores

Human heredity, 2024-05, Vol.89 (1), p.60-70

2024

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Multiple genetic variants at the SLC30A8 locus affect local super‐enhancer activity and influence pancreatic β‐cell survival and function

The FASEB journal, 2024-04, Vol.38 (8), p.e23610-n/a

2024

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Salvage Therapy Including Foscarnet and Ibalizumab for Multidrug-Resistant Human Immunodeficiency Virus Type 2 Infection

Clinical infectious diseases, 2024-04, Vol.78 (4), p.1005-1010

2024

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Pathogenic, Total Loss-of-Function DYRK1B Variants Cause Monogenic Obesity Associated With Type 2 Diabetes

Diabetes care, 2024-03, Vol.47 (3), p.444-451

2024

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Pathogenic monoallelic variants in GLIS3 increase type 2 diabetes risk and identify a subgroup of patients sensitive to sulfonylureas

Diabetologia, 2024-02, Vol.67 (2), p.327-332

2024

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Exploring the role of purinergic receptor P2RY1 in type 2 diabetes risk and pathophysiology: Insights from human functional genomics

Molecular metabolism (Germany), 2024-01, Vol.79

2024

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Exploring the Role of Purinergic Receptor P2RY1 in Type 2 Diabetes Risk and Pathophysiology: Insights from Human Functional Genomics

Molecular metabolism (Germany), 2024-01, Vol.79, p.101867-101867, Article 101867

2024

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Dominant PDX1 deficiency causes highly penetrant diabetes at different ages, associated with obesity and exocrine pancreatic deficiency: Lessons for precision medicine

Diabetes & metabolism, 2024-01, Vol.50 (1), p.101507-101507, Article 101507

2024

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Time-of-day-dependent variation of the human liver transcriptome and metabolome is disrupted in MASLD

JHEP reports, 2024-01, Vol.6 (1), p.100948-100948, Article 100948

2024

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Pathogenic monoallelic variants in GLIS3 increase type 2 diabetes risk and identify a subgroup of patients sensitive to sulfonylureas

Diabetologia, 2023-12, Vol.67 (2), p.327-332

2023

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Genetic variants of interferon-response factor 5 are associated with the incidence of chronic kidney disease: the D.E.S.I.R. study

Genes and immunity, 2023-12, Vol.24 (6), p.303-308

2023

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Genetic variants of interferon-response factor 5 are associated with the incidence of chronic kidney disease: the D.E.S.I.R. study

Genes and immunity, 2023-11, Vol.24 (6), p.303-308

2023

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Human GLP1R variants affecting GLP1R cell surface expression are associated with impaired glucose control and increased adiposity

Nature metabolism, 2023-10, Vol.5 (10), p.1673-1684

2023

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Advances in the integration of metabolomics and metagenomics for human gut microbiome and their clinical applications

TrAC, Trends in analytical chemistry (Regular ed.), 2023-10, Vol.167, p.117248, Article 117248

2023

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High morbidity and mortality in children with untreated congenital deficiency of leptin or its receptor

Cell reports. Medicine, 2023-09, Vol.4 (9), p.101187-101187, Article 101187

2023

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Identification of myokines susceptible to improve glucose homeostasis after bariatric surgery

European journal of endocrinology, 2023-09, Vol.189 (3), p.409-421

2023

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Bidirectional Mendelian Randomization and Multiphenotype GWAS Show Causality and Shared Pathophysiology Between Depression and Type 2 Diabetes

Diabetes care, 2023-09, Vol.46 (9), p.1707-1714

2023

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PNLIPRP1 Hypermethylation in Exocrine Pancreas Links Type 2 Diabetes and Cholesterol Metabolism

Genetics brings new insight to β-cell function

Interview: Philippe Froguel

Apport des techniques de séquençage de l’ADN de nouvelle génération en pratique et en recherche médicale en France

Obesity: exploring its connection to brain function through genetic and genomic perspectives

Towards the recognition of oligogenic forms of type 2 diabetes

comorbidPGS: An R Package Assessing Shared Predisposition between Phenotypes Using Polygenic Scores

Multiple genetic variants at the SLC30A8 locus affect local super‐enhancer activity and influence pancreatic β‐cell survival and function

Salvage Therapy Including Foscarnet and Ibalizumab for Multidrug-Resistant Human Immunodeficiency Virus Type 2 Infection

Pathogenic, Total Loss-of-Function DYRK1B Variants Cause Monogenic Obesity Associated With Type 2 Diabetes

Pathogenic monoallelic variants in GLIS3 increase type 2 diabetes risk and identify a subgroup of patients sensitive to sulfonylureas

Exploring the role of purinergic receptor P2RY1 in type 2 diabetes risk and pathophysiology: Insights from human functional genomics

Exploring the Role of Purinergic Receptor P2RY1 in Type 2 Diabetes Risk and Pathophysiology: Insights from Human Functional Genomics

Time-of-day-dependent variation of the human liver transcriptome and metabolome is disrupted in MASLD

Time-of-day-dependent variation of the human liver transcriptome and metabolome is disrupted in MASLD

Dominant PDX1 deficiency causes highly penetrant diabetes at different ages, associated with obesity and exocrine pancreatic deficiency: Lessons for precision medicine

Time-of-day-dependent variation of the human liver transcriptome and metabolome is disrupted in MASLD

Pathogenic monoallelic variants in GLIS3 increase type 2 diabetes risk and identify a subgroup of patients sensitive to sulfonylureas

Genetic variants of interferon-response factor 5 are associated with the incidence of chronic kidney disease: the D.E.S.I.R. study

Genetic variants of interferon-response factor 5 are associated with the incidence of chronic kidney disease: the D.E.S.I.R. study

Human GLP1R variants affecting GLP1R cell surface expression are associated with impaired glucose control and increased adiposity

Advances in the integration of metabolomics and metagenomics for human gut microbiome and their clinical applications

High morbidity and mortality in children with untreated congenital deficiency of leptin or its receptor

Identification of myokines susceptible to improve glucose homeostasis after bariatric surgery

Bidirectional Mendelian Randomization and Multiphenotype GWAS Show Causality and Shared Pathophysiology Between Depression and Type 2 Diabetes

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