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Systems medicine and integrated care to combat chronic noncommunicable diseases.
Bousquet J, Anto JM, Sterk PJ, Adcock IM, Chung KF, Roca J, Agusti A, Brightling C, Cambon-Thomsen A, Cesario A, Abdelhak S, Antonarakis SE, Avignon A, Ballabio A, Baraldi E, Baranov A, Bieber T, Bockaert J, Brahmachari S, Brambilla C, Bringer J, Dauzat M, Ernberg I, Fabbri L, Froguel P, Galas D, Gojobori T, Hunter P, Jorgensen C, Kauffmann F, Kourilsky P, Kowalski ML, Lancet D, Pen CL, Mallet J, Mayosi B, Mercier J, Metspalu A, Nadeau JH, Ninot G, Noble D, Oztürk M, Palkonen S, Préfaut C, Rabe K, Renard E, Roberts RG, Samolinski B, Schünemann HJ, Simon HU, Soares MB, Superti-Furga G, Tegner J, Verjovski-Almeida S, Wellstead P, Wolkenhauer O, Wouters E, Balling R, Brookes AJ, Charron D, Pison C, Chen Z, Hood L, Auffray C. Bousquet J, et al. Among authors: abdelhak s. Genome Med. 2011 Jul 6;3(7):43. doi: 10.1186/gm259. Genome Med. 2011. PMID: 21745417 Free PMC article.
Fine-scale haplotype mapping of MUT, AACS, SLC6A15 and PRKCA genes indicates association with insulin resistance of metabolic syndrome and relationship with branched chain amino acid metabolism or regulation.
Haydar S, Grigorescu F, Vintilă M, Cogne Y, Lautier C, Tutuncu Y, Brun JF, Robine JM, Pugeat M, Normand C, Poucheret P, Gheorghiu ML, Georgescu C, Badiu C, Băculescu N, Renard E, Ylli D, Badiou S, Sutra T, Cristol JP, Mercier J, Gomis R, Macias JM, Litvinov S, Khusnutdinova E, Poiana C, Pasquali R, Lauro D, Sesti G, Prudente S, Trischitta V, Tsatsoulis A, Abdelhak S, Barakat A, Zenati A, Ylli A, Satman I, Kanninen T, Rinato Y, Missoni S. Haydar S, et al. Among authors: abdelhak s. PLoS One. 2019 Mar 26;14(3):e0214122. doi: 10.1371/journal.pone.0214122. eCollection 2019. PLoS One. 2019. PMID: 30913280 Free PMC article. Clinical Trial.
Branched-Chain Amino Acid Database Integrated in MEDIPAD Software as a Tool for Nutritional Investigation of Mediterranean Populations.
Haydar S, Paillot T, Fagot C, Cogne Y, Fountas A, Tutuncu Y, Vintila M, Tsatsoulis A, Thanh Chi P, Garandeau P, Chetea D, Badiu C, Gheorghiu M, Ylli D, Lautier C, Jarec M, Monnier L, Normand C, Šarac J, Barakat A, Missoni S, Pugeat M, Poucheret P, Hanzu F, Gomis R, Macias JM, Litvinov S, Khusnutdinova E, Poiana C, Pasquali R, Lauro D, Sesti G, Trischitta V, Abdelhak S, Zenati A, Ylli A, Satman I, Kanninen T, Rinato Y, Grigorescu F. Haydar S, et al. Among authors: abdelhak s. Nutrients. 2018 Oct 1;10(10):1392. doi: 10.3390/nu10101392. Nutrients. 2018. PMID: 30275383 Free PMC article.
Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population.
Kefi R, Hechmi M, Dallali H, Elouej S, Jmel H, Halima YB, Nagara M, Chargui M, Fadhel SB, Romdhane S, Kamoun I, Turki Z, Abid A, Bahri S, Bahlous A, Gomis R, Baraket A, Grigorescu F, Normand C, Jamoussi H, Abdelhak S. Kefi R, et al. Among authors: abdelhak s. Ann Endocrinol (Paris). 2017 Jul;78(3):146-155. doi: 10.1016/j.ando.2017.01.005. Epub 2017 Jun 16. Ann Endocrinol (Paris). 2017. PMID: 28624160
Association of rs9939609 Polymorphism with Metabolic Parameters and FTO Risk Haplotype Among Tunisian Metabolic Syndrome.
Elouej S, Belfki-Benali H, Nagara M, Lasram K, Attaoua R, Sallem OK, Kamoun I, Chargui M, Romdhane L, Jamoussi H, Turki Z, Abid A, Ben Slama C, Bahri S, Abdelhak S, Grigorescu F, Ben Romdhane H, Kefi R. Elouej S, et al. Among authors: abdelhak s. Metab Syndr Relat Disord. 2016 Mar;14(2):121-8. doi: 10.1089/met.2015.0090. Epub 2016 Jan 7. Metab Syndr Relat Disord. 2016. PMID: 26741700
Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing.
Dallali H, Pezzilli S, Hechmi M, Sallem OK, Elouej S, Jmel H, Ben Halima Y, Chargui M, Gharbi M, Mercuri L, Alberico F, Mazza T, Bahlous A, Ben Ahmed M, Jamoussi H, Abid A, Trischitta V, Abdelhak S, Prudente S, Kefi R. Dallali H, et al. Among authors: abdelhak s. Acta Diabetol. 2019 May;56(5):515-523. doi: 10.1007/s00592-018-01283-5. Epub 2019 Jan 17. Acta Diabetol. 2019. PMID: 30656436
245 results