Publications
1181 results found
Talbot F, Feetham CH, Mokrosinski J, et al., 2023, A rare human variant that disrupts GPR10 signalling causes weight gain in mice, NATURE COMMUNICATIONS, Vol: 14
Bonnefond A, Unnikrishnan R, Doria A, et al., 2023, Monogenic diabetes, NATURE REVIEWS DISEASE PRIMERS, Vol: 9, ISSN: 2056-676X
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- Citations: 3
Kahoul Y, Yao X, Oger F, et al., 2023, Knocking Down <i>CDKN2A</i> in 3D hiPSC-Derived Brown Adipose Progenitors Potentiates Differentiation, Oxidative Metabolism and Browning Process, CELLS, Vol: 12
Folon L, Baron M, Toussaint B, et al., 2023, Contribution of heterozygous <i>PCSK1</i> variants to obesity and implications for precision medicine: a case-control study, LANCET DIABETES & ENDOCRINOLOGY, Vol: 11, Pages: 182-190, ISSN: 2213-8587
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- Citations: 3
Allesoe RL, Lundgaard AT, Medina RH, et al., 2023, Discovery of drug-omics associations in type 2 diabetes with generative deep-learning models, NATURE BIOTECHNOLOGY, Vol: 41, Pages: 399-+, ISSN: 1087-0156
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- Citations: 7
Delannoy CP, Heuson E, Herledan A, et al., 2023, High-Throughput Quantitative Screening of Glucose-Stimulated Insulin Secretion and Insulin Content Using Automated MALDI-TOF Mass Spectrometry, CELLS, Vol: 12
Saeed S, Manzoor J, Khanam R, et al., 2023, High Mortality and Morbidity of Leptin Signalling Deficiency - A Consanguineous Population, Publisher: KARGER, ISSN: 0250-6807
Froguel P, Bonnefond A, 2023, Advances and promises of personalized precision medicine for metabolic diseases: Precision metabolic medicine, BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE, Vol: 207, Pages: 199-203, ISSN: 0001-4079
Froguel P, Ning L, Boissel M, et al., 2023, centric Analysis Revealed a Novel Cause of Syndromic Obesity in Severely Obese Consanguineous Families, Publisher: KARGER, ISSN: 0250-6807
Dawed AY, Mari A, Brown A, et al., 2023, Pharmacogenomics of GLP-1 receptor agonists: a genome-wide analysis of observational data and large randomised controlled trials, LANCET DIABETES & ENDOCRINOLOGY, Vol: 11, Pages: 33-41, ISSN: 2213-8587
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- Citations: 9
Froguel P, Bonnefond A, 2022, The discovery of human agouti-induced obesity and its implication for genetic diagnosis, NATURE METABOLISM, Vol: 4, Pages: 1614-1615
Corniere N, Thomson RB, Thauvin S, et al., 2022, Dominant negative mutation in oxalate transporter <i>SLC26A6</i> associated with enteric hyperoxaluria and nephrolithiasis, JOURNAL OF MEDICAL GENETICS, Vol: 59, Pages: 1035-1043, ISSN: 0022-2593
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- Citations: 5
Pupko I, Demirkan A, Zudina L, et al., 2022, Multi-phenotype GWAS Uncovers Shared Genetic Loci between Type 2 Diabetes, BMI, Colorectal, Pancreatic, Breast and Prostate Cancers, Annual Meeting of the International-Genetic-Epidemiology-Society (IGES), Publisher: WILEY, Pages: 525-526, ISSN: 0741-0395
Pervjakova N, Moen G-H, Borges M-C, et al., 2022, Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes, HUMAN MOLECULAR GENETICS, Vol: 31, Pages: 3377-3391, ISSN: 0964-6906
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- Citations: 18
Young WJ, Lahrouchi N, Isaacs A, et al., 2022, Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways, NATURE COMMUNICATIONS, Vol: 13
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- Citations: 5
Folon L, Baron M, Derhourhi M, et al., 2022, Impact of rare heterozygous mutations of PCSK1 on obesity: implication for treatment with MC4R agonists, Publisher: SPRINGER, Pages: S33-S34, ISSN: 0012-186X
Hu M, Kim I, Canouil M, et al., 2022, Impact of type 2 diabetes-associated variants at the SLC30A8 locus on transcriptional activity and function of human b cells and super-enhancer at SLC30A8 gene locus, 58th Annual Meeting of the European-Association-for-the-Study-of-Diabetes (EASD), Publisher: SPRINGER, Pages: S141-S141, ISSN: 0012-186X
Dance A, Derhourhi M, Canouil M, et al., 2022, Role of GWAS associated purinergic receptor P2RY1 gene in insulin secretion and the impact of rare variants on type 2 diabetes risk, Publisher: SPRINGER, Pages: S155-S155, ISSN: 0012-186X
Orioli L, Canouil M, Sawadogo K, et al., 2022, Identification of myokines potentially involved in the improvement of glucose homeostasis after bariatric surgery, 58th Annual Meeting of the European-Association-for-the-Study-of-Diabetes (EASD), Publisher: SPRINGER, Pages: S239-S239, ISSN: 0012-186X
Kahoul Y, Montaigne J, Caron E, et al., 2022, The adipocyte-specific deletion of the tumor suppressor gene CDKN2a improves glucose tolerance in high-fat diet-fed mice, 58th Annual Meeting of the European-Association-for-the-Study-of-Diabetes (EASD), Publisher: SPRINGER, Pages: S271-S271, ISSN: 0012-186X
Saeed S, Manzoor J, Khanam R, et al., 2022, Natural History of LEP, LEPR and MC4R Deficiencies - A Population-Based Study, Publisher: KARGER, Pages: 35-36, ISSN: 1663-2818
Zaibi NS, Montaigne J, Devos C, et al., 2022, Metabolic acidosis in mice increases glucose tolerance by decreasing hepatic gluconeogenesis and proximal tubule glucose reabsorption, Publisher: WILEY, Pages: 339-339, ISSN: 1748-1708
Meulebrouck S, Canouil M, Derhourhi M, et al., 2022, The impact of rare pathogenic variants of GLIS3 on type 2 diabetes, 58th Annual Meeting of the European-Association-for-the-Study-of-Diabetes (EASD), Publisher: SPRINGER, Pages: S37-S37, ISSN: 0012-186X
Bourouh C, Courty E, Rolland L, et al., 2022, The transcription factor E2F1 controls the GLP-1 receptor pathway in pancreatic β cells, CELL REPORTS, Vol: 40, ISSN: 2211-1247
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- Citations: 3
Lemaitre M, Douillard C, Froguel P, et al., 2022, Management of pregnancy in a patient with congenital hyperinsulinism treated with association of diazoxide/calcium channel blocker, ACTA DIABETOLOGICA, Vol: 59, Pages: 1117-1120, ISSN: 0940-5429
Pelletier A, Carrier A, Zhao Y, et al., 2022, Epigenetic and Transcriptomic Programming of HSC Quiescence Signaling in Large for Gestational Age Neonates, INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, Vol: 23
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- Citations: 1
Khamis A, Ning L, Balkau B, et al., 2022, Epigenetic changes associated with hyperglycaemia exposure in the longitudinal DESIR cohort, DIABETES & METABOLISM, Vol: 48, ISSN: 1262-3636
Mahajan A, Spracklen CN, Zhang W, et al., 2022, Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation, NATURE GENETICS, Vol: 54, Pages: 560-+, ISSN: 1061-4036
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- Citations: 82
Balkhiyarova Z, Demirkan A, Pupko I, et al., 2022, Blood metabolite levels have shared genetic effects and affect risk of breast and colorectal cancer, Publisher: KARGER, Pages: 33-33, ISSN: 0001-5652
Pupko I, Demirkan A, Zudina L, et al., 2022, Multi-phenotype GWAS uncovers shared genetic loci between type 2 diabetes, BMI, colorectal, pancreatic, breast and prostate cancers, Publisher: KARGER, Pages: 35-35, ISSN: 0001-5652
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