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A Melanocortin-4 Receptor Agonist Induces Skin and Hair Pigmentation in Patients with Monogenic Mutations in the Leptin-Melanocortin Pathway.
Kanti V, Puder L, Jahnke I, Krabusch PM, Kottner J, Vogt A, Richter C, Andruck A, Lechner L, Poitou C, Krude H, Gottesdiener K, Clément K, Farooqi IS, Wiegand S, Kühnen P, Blume-Peytavi U. Kanti V, et al. Among authors: farooqi is. Skin Pharmacol Physiol. 2021;34(6):307-316. doi: 10.1159/000516282. Epub 2021 May 31. Skin Pharmacol Physiol. 2021. PMID: 34058738 Clinical Trial.
Efficacy and safety of setmelanotide, an MC4R agonist, in individuals with severe obesity due to LEPR or POMC deficiency: single-arm, open-label, multicentre, phase 3 trials.
Clément K, van den Akker E, Argente J, Bahm A, Chung WK, Connors H, De Waele K, Farooqi IS, Gonneau-Lejeune J, Gordon G, Kohlsdorf K, Poitou C, Puder L, Swain J, Stewart M, Yuan G, Wabitsch M, Kühnen P; Setmelanotide POMC and LEPR Phase 3 Trial Investigators. Clément K, et al. Among authors: farooqi is. Lancet Diabetes Endocrinol. 2020 Dec;8(12):960-970. doi: 10.1016/S2213-8587(20)30364-8. Epub 2020 Oct 30. Lancet Diabetes Endocrinol. 2020. PMID: 33137293 Clinical Trial.
Classification of Congenital Leptin Deficiency.
von Schnurbein J, Zorn S, Nunziata A, Brandt S, Moepps B, Funcke JB, Hussain K, Farooqi IS, Fischer-Posovszky P, Wabitsch M. von Schnurbein J, et al. Among authors: farooqi is. J Clin Endocrinol Metab. 2024 Mar 12:dgae149. doi: 10.1210/clinem/dgae149. Online ahead of print. J Clin Endocrinol Metab. 2024. PMID: 38470203
Rare Antagonistic Leptin Variants and Severe, Early-Onset Obesity.
Funcke JB, Moepps B, Roos J, von Schnurbein J, Verstraete K, Fröhlich-Reiterer E, Kohlsdorf K, Nunziata A, Brandt S, Tsirigotaki A, Dansercoer A, Suppan E, Haris B, Debatin KM, Savvides SN, Farooqi IS, Hussain K, Gierschik P, Fischer-Posovszky P, Wabitsch M. Funcke JB, et al. Among authors: farooqi is. N Engl J Med. 2023 Jun 15;388(24):2253-2261. doi: 10.1056/NEJMoa2204041. N Engl J Med. 2023. PMID: 37314706
A novel mutation in the leptin gene (W121X) in an Egyptian family.
Mazen I, Amr K, Tantawy S, Farooqi IS, El Gammal M. Mazen I, et al. Among authors: farooqi is. Mol Genet Metab Rep. 2014 Nov 11;1:474-476. doi: 10.1016/j.ymgmr.2014.10.002. eCollection 2014. Mol Genet Metab Rep. 2014. PMID: 27896126 Free PMC article.
FTO and obesity: the missing link.
Farooqi IS. Farooqi IS. Cell Metab. 2011 Jan 5;13(1):7-8. doi: 10.1016/j.cmet.2010.12.016. Cell Metab. 2011. PMID: 21195343 Free article.
Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction.
McCabe MJ, Gaston-Massuet C, Tziaferi V, Gregory LC, Alatzoglou KS, Signore M, Puelles E, Gerrelli D, Farooqi IS, Raza J, Walker J, Kavanaugh SI, Tsai PS, Pitteloud N, Martinez-Barbera JP, Dattani MT. McCabe MJ, et al. Among authors: farooqi is. J Clin Endocrinol Metab. 2011 Oct;96(10):E1709-18. doi: 10.1210/jc.2011-0454. Epub 2011 Aug 10. J Clin Endocrinol Metab. 2011. PMID: 21832120 Free PMC article.
Antidiabetic effects of IGFBP2, a leptin-regulated gene.
Hedbacker K, Birsoy K, Wysocki RW, Asilmaz E, Ahima RS, Farooqi IS, Friedman JM. Hedbacker K, et al. Among authors: farooqi is. Cell Metab. 2010 Jan;11(1):11-22. doi: 10.1016/j.cmet.2009.11.007. Cell Metab. 2010. PMID: 20074524 Free article.
229 results