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Page 1
Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome.
Courraud J, Engel C, Quartier A, Drouot N, Houessou U, Plassard D, Sorlin A, Brischoux-Boucher E, Gouy E, Van Maldergem L, Rossi M, Lesca G, Edery P, Putoux A, Bilan F, Gilbert-Dussardier B, Atallah I, Kalscheuer VM, Mandel JL, Piton A. Courraud J, et al. Mol Psychiatry. 2024 Feb;29(2):287-296. doi: 10.1038/s41380-023-02323-5. Epub 2023 Nov 29. Mol Psychiatry. 2024. PMID: 38030819
Effects of Long-Term Storage on the Biobanked Neonatal Dried Blood Spot Metabolome.
Ottosson F, Russo F, Abrahamsson A, MacSween N, Courraud J, Nielsen ZK, Hougaard DM, Cohen AS, Ernst M. Ottosson F, et al. Among authors: courraud j. J Am Soc Mass Spectrom. 2023 Apr 5;34(4):685-694. doi: 10.1021/jasms.2c00358. Epub 2023 Mar 13. J Am Soc Mass Spectrom. 2023. PMID: 36913955 Free PMC article.
Multi-omics to predict changes during cold pressor test.
Kogelman LJA, Ernst M, Falkenberg K, Mazzoni G, Courraud J, Lundgren LP, Laursen SS, Cohen A, Olesen J, Hansen TF. Kogelman LJA, et al. Among authors: courraud j. BMC Genomics. 2022 Nov 19;23(1):759. doi: 10.1186/s12864-022-08981-z. BMC Genomics. 2022. PMID: 36402977 Free PMC article.
Neonatal metabolome of caesarean section and risk of childhood asthma.
Gürdeniz G, Ernst M, Rago D, Kim M, Courraud J, Stokholm J, Bønnelykke K, Björkbom A, Trivedi U, Sørensen SJ, Brix S, Hougaard D, Rasmussen M, Cohen AS, Bisgaard H, Chawes B. Gürdeniz G, et al. Among authors: courraud j. Eur Respir J. 2022 Jun 23;59(6):2102406. doi: 10.1183/13993003.02406-2021. Print 2022 Jun. Eur Respir J. 2022. PMID: 34887324 Free article.
Genetic regulation of spermine oxidase activity and cancer risk: a Mendelian randomization study.
Fadista J, Yakimov V, Võsa U, Hansen CS, Kasela S, Skotte L, Geller F, Courraud J, Esko T, Kukuškina V, Buil A, Melbye M, Werge TM, Hougaard DM, Milani L, Bybjerg-Grauholm J, Cohen AS, Feenstra B. Fadista J, et al. Among authors: courraud j. Sci Rep. 2021 Aug 31;11(1):17463. doi: 10.1038/s41598-021-97069-x. Sci Rep. 2021. PMID: 34465810 Free PMC article.
Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder.
Courraud J, Chater-Diehl E, Durand B, Vincent M, Del Mar Muniz Moreno M, Boujelbene I, Drouot N, Genschik L, Schaefer E, Nizon M, Gerard B, Abramowicz M, Cogné B, Bronicki L, Burglen L, Barth M, Charles P, Colin E, Coubes C, David A, Delobel B, Demurger F, Passemard S, Denommé AS, Faivre L, Feger C, Fradin M, Francannet C, Genevieve D, Goldenberg A, Guerrot AM, Isidor B, Johannesen KM, Keren B, Kibæk M, Kuentz P, Mathieu-Dramard M, Demeer B, Metreau J, Steensbjerre Møller R, Moutton S, Pasquier L, Pilekær Sørensen K, Perrin L, Renaud M, Saugier P, Rio M, Svane J, Thevenon J, Tran Mau Them F, Tronhjem CE, Vitobello A, Layet V, Auvin S, Khachnaoui K, Birling MC, Drunat S, Bayat A, Dubourg C, El Chehadeh S, Fagerberg C, Mignot C, Guipponi M, Bienvenu T, Herault Y, Thompson J, Willems M, Mandel JL, Weksberg R, Piton A. Courraud J, et al. Genet Med. 2021 Nov;23(11):2150-2159. doi: 10.1038/s41436-021-01263-1. Epub 2021 Aug 3. Genet Med. 2021. PMID: 34345024 Free article.
30 results