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Page 1
Prediction of clinical outcomes in Crohn's disease by using confocal laser endomicroscopy: results from a prospective multicenter study.
Tontini GE, Mudter J, Vieth M, Günther C, Milani V, Atreya R, Rath T, Nägel A, Hatem G, Sturniolo GC, Vecchi M, Neurath MF, Galle PR, Buda A, Neumann H. Tontini GE, et al. Among authors: hatem g. Gastrointest Endosc. 2018 Jun;87(6):1505-1514.e3. doi: 10.1016/j.gie.2017.10.033. Epub 2017 Nov 3. Gastrointest Endosc. 2018. PMID: 29108979
Detection of a fluorescent-labeled avidin-nucleic acid nanoassembly by confocal laser endomicroscopy in the microvasculature of chronically inflamed intestinal mucosa.
Buda A, Facchin S, Dassie E, Casarin E, Jepson MA, Neumann H, Hatem G, Realdon S, D'Incà R, Sturniolo GC, Morpurgo M. Buda A, et al. Among authors: hatem g. Int J Nanomedicine. 2015 Jan 8;10:399-408. doi: 10.2147/IJN.S70153. eCollection 2015. Int J Nanomedicine. 2015. PMID: 25609952 Free PMC article.
Multi-ancestry, trans-generational GWAS meta-analysis of gestational diabetes and glycaemic traits during pregnancy reveals limited evidence of pregnancy-specific genetic effects.
Brito Nunes C, Rukins V, Cisse AH, White F, McBride N, Kuang A, Allard C, Ronkainen J, Hughes A, Elliott A, Thorleifsson G, Vaudel M, Laisk T, Gu Y, Lamri A, Chen L, Tuhkanen J, Lahti J, Calas L, Muntaner M, Karhunen V, Choi J, Heiskala A, Hatem G, Fragoso-Bargas N, Rifas-Shiman SL, Paz-Lopez G, Stinson SE, Bhowmik B, Ahlqvist E; Estonian Biobank Research Team; Genes & Health Research Team; Deleuze JF, Eriksson JG, Park J, Teo K, Räikkönen K, Stefansson K, Molina-Vega M, Subbarao P, Beaumont RN, Johansson S, Tuomi T, Hansen T, Engelbrechtsen L, Morcillo S, Oken E, Quigstad E, Birkeland KI, Vääräsmäki M, Hattersley AT, Sebert S, Hitman GA, Kwak SH, Järvelin MR, Prasad RB, Heude B, Meirhaeghe A, Bouchard L, Jacques PÉ, Laivuori H, Tan KH, Anand SS, van Heel DA, Liu S, Njølstad PR, Steinthorsdottir V, Widén E, Keikkala E, Scholtens DM, Lowe WL, Finer S, Morris AP, Mägi R, Zöllner J, Borges MC, Lawlor DA, Hivert MF, Freathy RM, Evans DM, Moen GH. Brito Nunes C, et al. Among authors: hatem g. Nat Commun. 2026 Jun 1;17(1):4726. doi: 10.1038/s41467-026-73509-y. Nat Commun. 2026. PMID: 42225636 Free PMC article.
Modeling rare coding variation on chromosome X provides insight into the genetics and differential sex prevalence of autism spectrum disorder.
Satterstrom FK, Jodeiry K, Mahjani B, Hatem G, Park SJ, Klei L, Fu JM, Wigdor EM; Autism Sequencing Consortium; Betancur C, Daly MJ, Roeder K, Devlin B, Buxbaum JD, Cutler DJ. Satterstrom FK, et al. Among authors: hatem g. medRxiv [Preprint]. 2026 May 7:2026.05.04.26352380. doi: 10.64898/2026.05.04.26352380. medRxiv. 2026. PMID: 42145590 Free PMC article. Preprint.
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