| Genetic causes of severe childhood obesity: a remarkably high prevalence in an inbred population of Pakistan S Saeed, M Arslan, J Manzoor, SM Din, QM Janjua, H Ayesha, Q Ain, ... Diabetes 69 (7), 1424-1438, 2020 | 26 | 2020 |
| Contribution of heterozygous PCSK1 variants to obesity and implications for precision medicine: a case-control study L Folon, M Baron, B Toussaint, E Vaillant, M Boissel, V Scherrer, ... The Lancet Diabetes & Endocrinology 11 (3), 182-190, 2023 | 16 | 2023 |
| Rare variant analysis of obesity-associated genes in young adults with severe obesity from a consanguineous population of Pakistan S Saeed, QM Janjua, A Haseeb, R Khanam, E Durand, E Vaillant, L Ning, ... Diabetes 71 (4), 694-705, 2022 | 14 | 2022 |
| Dominant negative mutation in oxalate transporter SLC26A6 associated with enteric hyperoxaluria and nephrolithiasis N Cornière, RB Thomson, S Thauvin, BO Villoutreix, S Karp, DW Dynia, ... Journal of medical genetics 59 (11), 1035-1043, 2022 | 12 | 2022 |
| Patient-matched analysis identifies deregulated networks in prostate cancer to guide personalized therapeutic intervention A Kumar, Y Kasikci, A Badredine, K Azzag, MLQ Ranty, F Zaidi, N Aragou, ... American Journal of Cancer Research 11 (11), 5299, 2021 | 8 | 2021 |
| Heterozygous pathogenic variants in POMC are not responsible for monogenic obesity: Implication for MC4R agonist use L Le Collen, B Delemer, C Poitou, M Vaxillaire, B Toussaint, A Dechaume, ... Genetics in Medicine 25 (7), 100857, 2023 | 7 | 2023 |
| Biallelic Mutations in P4HTM Cause Syndromic Obesity S Saeed, L Ning, A Badreddine, MU Mirza, M Boissel, R Khanam, ... Diabetes 72 (9), 1228-1234, 2023 | 6 | 2023 |
| Pharmacological HDAC inhibition impairs pancreatic β-cell function through an epigenome-wide reprogramming F Oger, M Moreno, M Derhourhi, B Thiroux, L Berberian, C Bourouh, ... Iscience 26 (7), 2023 | 1 | 2023 |
| Functional genetics reveals the contribution of delta opioid receptor to type 2 diabetes and beta-cell function S Meulebrouck, J Merrheim, G Queniat, C Bourouh, M Derhourhi, ... Nature communications 15 (1), 6627, 2024 | | 2024 |
| centric Analysis Revealed a Novel Cause of Syndromic Obesity in Severely Obese Consanguineous Families P Froguel, L Ning, M Boissel, M Usman, R Khanam, J Manzoor, ... ANNALS OF NUTRITION AND METABOLISM 79 (1), 2023 | | 2023 |
| Epigenetics of PNLIPRP1 in human pancreas reveals a molecular path between type 2 diabetes and pancreatic cancer L Maurin, L Marselli, L Ning, M Boissel, R Boutry, M Suleiman, A Leloire, ... medRxiv, 2022.12. 30.22284058, 2022 | | 2022 |
| The HDAC inhibitor trichostatin A impairs pancreatic β-cell function through an epigenome-wide reprogramming F Oger, M Moreno, M Derhourhi, B Thiroux, L Berberian, C Bourouh, ... bioRxiv, 2022.12. 14.519294, 2022 | | 2022 |
| Rare variant analysis of obesity associated genes in young adults from a consanguineous population of Pakistan S Saeed, QM Janjua, A Haseeb, R Khanam, E Durand, E Vaillant, L Ninj, ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 441-441, 2022 | | 2022 |
| Compound genetic etiology in a patient with a syndrome including diabetes, intellectual deficiency and distichiasis L Le Collen, B Delemer, M Spodenkiewicz, P Cornillet Lefebvre, ... Orphanet Journal of Rare Diseases 17 (1), 86, 2022 | | 2022 |
Sadia SaeedUniversity of Cambridge, Imperial College London在 imperial.ac.uk 的电子邮件经过验证
