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Year Number of Results
2007 1
2008 6
2009 8
2010 6
2011 8
2012 5
2013 5
2014 2
2015 5
2016 6
2017 2
2018 4
2019 6
2020 15
2021 12
2022 11
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2024 5

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99 results

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Page 1
[Phenylketonuria, from diet to gene therapy].
Wiedemann A, Oussalah A, Jeannesson É, Guéant JL, Feillet F. Wiedemann A, et al. Among authors: oussalah a. Med Sci (Paris). 2020 Aug-Sep;36(8-9):725-734. doi: 10.1051/medsci/2020127. Epub 2020 Aug 21. Med Sci (Paris). 2020. PMID: 32821049 Free article. Review. French.
Common genetic variation in alcohol-related hepatocellular carcinoma: a case-control genome-wide association study.
Trépo E, Caruso S, Yang J, Imbeaud S, Couchy G, Bayard Q, Letouzé E, Ganne-Carrié N, Moreno C, Oussalah A, Féray C, Blanc JF, Clément B, Hillon P, Boursier J, Paradis V, Calderaro J, Gnemmi V, Nault JC, Guéant JL, Devière J, Archambeaud I, Vitellius C, Turlin B, Bronowicki JP, Gustot T, Sutton A; GENTHEP Consortium; Ziol M, Nahon P, Zucman-Rossi J. Trépo E, et al. Among authors: oussalah a. Lancet Oncol. 2022 Jan;23(1):161-171. doi: 10.1016/S1470-2045(21)00603-3. Epub 2021 Dec 11. Lancet Oncol. 2022. PMID: 34902334 Free article.
A transgenic mice model of retinopathy of cblG-type inherited disorder of one-carbon metabolism highlights epigenome-wide alterations related to cone photoreceptor cells development and retinal metabolism.
Matmat K, Conart JB, Graindorge PH, El Kouche S, Hassan Z, Siblini Y, Umoret R, Safar R, Baspinar O, Robert A, Alberto JM, Oussalah A, Coelho D, Guéant JL, Guéant-Rodriguez RM. Matmat K, et al. Among authors: oussalah a. Clin Epigenetics. 2023 Oct 5;15(1):158. doi: 10.1186/s13148-023-01567-w. Clin Epigenetics. 2023. PMID: 37798757 Free PMC article.
Genetic Predictors of Drug Hypersensitivity.
Cornejo-Garcia JA, Oussalah A, Blanca M, Gueant-Rodriguez RM, Mayorga C, Waton J, Barbaud A, Gaeta F, Romano A, Gueant JL. Cornejo-Garcia JA, et al. Among authors: oussalah a. Curr Pharm Des. 2016;22(45):6725-6733. doi: 10.2174/1381612822666160927114941. Curr Pharm Des. 2016. PMID: 27779086 Review.
[Newborn screening of phenylketonuria in France].
Wiedemann A, Jeannesson É, Oussalah A, Guéant JL, Guéant-Rodriguez RM, Feillet F. Wiedemann A, et al. Among authors: oussalah a. Med Sci (Paris). 2021 May;37(5):468-473. doi: 10.1051/medsci/2021061. Epub 2021 May 18. Med Sci (Paris). 2021. PMID: 34003092 Free article. French.
Multiomic analysis in fibroblasts of patients with inborn errors of cobalamin metabolism reveals concordance with clinical and metabolic variability.
Wiedemann A, Oussalah A, Guéant Rodriguez RM, Jeannesson E, Mertens M, Rotaru I, Alberto JM, Baspinar O, Rashka C, Hassan Z, Siblini Y, Matmat K, Jeandel M, Chery C, Robert A, Chevreux G, Lignières L, Camadro JM, Feillet F, Coelho D, Guéant JL. Wiedemann A, et al. Among authors: oussalah a. EBioMedicine. 2024 Jan;99:104911. doi: 10.1016/j.ebiom.2023.104911. Epub 2024 Jan 1. EBioMedicine. 2024. PMID: 38168585 Free PMC article.
99 results