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Diabetes|January 21, 2022
Rare Variant Analysis of Obesity-Associated Genes in Young Adults With Severe Obesity From a Consanguineous Population of PakistanSadia Saeed, Qasim M Janjua, Attiya Haseeb, et al.Orphanet Journal of Rare Diseases|March 1, 2022
Compound genetic etiology in a patient with a syndrome including diabetes, intellectual deficiency and distichiasisLauriane Le Collen, Brigitte Delemer, Marta Spodenkiewicz, et al.The Lancet. Diabetes & Endocrinology|February 23, 2023
Contribution of heterozygous PCSK1 variants to obesity and implications for precision medicine: a case-control studyLise Folon, Morgane Baron, Bénédicte Toussaint, et al.Journal of Medical Genetics|February 4, 2022
Dominant negative mutation in oxalate transporter <i>SLC26A6</i> associated with enteric hyperoxaluria and nephrolithiasisNicolas Cornière, R Brent Thomson, Stéphanie Thauvin, et al.Diabetes|May 1, 2020
Genetic Causes of Severe Childhood Obesity: A Remarkably High Prevalence in an Inbred Population of PakistanSadia Saeed, Muhammad Arslan, Jaida Manzoor, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 24, 2023
Heterozygous pathogenic variants in POMC are not responsible for monogenic obesity: Implication for MC4R agonist useLauriane Le Collen, Brigitte Delemer, Christine Poitou, et al.Nature Communications|May 19, 2026
Western diet-induced MASH in PWK/PhJ mice identifies disruptions in amino acid and sphingolipid metabolism contributing to cardiac dysfunctionSandra Rodríguez-López, Miguel Pérez-Rodríguez, Alaa Badreddine, et al.Iscience|July 27, 2023
Pharmacological HDAC inhibition impairs pancreatic β-cell function through an epigenome-wide reprogrammingFrédérik Oger, Maeva Moreno, Mehdi Derhourhi, et al.Diabetes|April 21, 2023
Biallelic Mutations in P4HTM Cause Syndromic ObesitySadia Saeed, Lijiao Ning, Alaa Badreddine, et al.Nature Communications|August 5, 2024
Functional genetics reveals the contribution of delta opioid receptor to type 2 diabetes and beta-cell functionSarah Meulebrouck, Judith Merrheim, Gurvan Queniat, et al.Pageof 1