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Page 1
The general fault in our fault lines.
Ruggeri K, Većkalov B, Bojanić L, Andersen TL, Ashcroft-Jones S, Ayacaxli N, Barea-Arroyo P, Berge ML, Bjørndal LD, Bursalıoğlu A, Bühler V, Čadek M, Çetinçelik M, Clay G, Cortijos-Bernabeu A, Damnjanović K, Dugue TM, Esberg M, Esteban-Serna C, Felder EN, Friedemann M, Frontera-Villanueva DI, Gale P, Garcia-Garzon E, Geiger SJ, George L, Girardello A, Gracheva A, Gracheva A, Guillory M, Hecht M, Herte K, Hubená B, Ingalls W, Jakob L, Janssens M, Jarke H, Kácha O, Kalinova KN, Karakasheva R, Khorrami PR, Lep Ž, Lins S, Lofthus IS, Mamede S, Mareva S, Mascarenhas MF, McGill L, Morales-Izquierdo S, Moltrecht B, Mueller TS, Musetti M, Nelsson J, Otto T, Paul AF, Pavlović I, Petrović MB, Popović D, Prinz GM, Razum J, Sakelariev I, Samuels V, Sanguino I, Say N, Schuck J, Soysal I, Todsen AL, Tünte MR, Vdovic M, Vintr J, Vovko M, Vranka MA, Wagner L, Wilkins L, Willems M, Wisdom E, Yosifova A, Zeng S, Ahmed MA, Dwarkanath T, Cikara M, Lees J, Folke T. Ruggeri K, et al. Among authors: willems m. Nat Hum Behav. 2021 Oct;5(10):1369-1380. doi: 10.1038/s41562-021-01092-x. Epub 2021 Apr 22. Nat Hum Behav. 2021. PMID: 33888880
Abnormal Immune Profile in Individuals with Kabuki Syndrome.
Comel M, Saad N, Sil D, Apparailly F, Willems M, Djouad F, Andrau JC, Lozano C, Genevieve D. Comel M, et al. Among authors: willems m. J Clin Immunol. 2024 Sep 12;45(1):7. doi: 10.1007/s10875-024-01796-5. J Clin Immunol. 2024. PMID: 39264387
Discovery of DNA methylation signature in the peripheral blood of individuals with history of antenatal exposure to valproic acid.
Haghshenas S, Putoux A, Reilly J, Levy MA, Relator R, Ghosh S, Kerkhof J, McConkey H, Edery P, Lesca G, Besson A, Coubes C, Willems M, Ruiz-Pallares N, Barat-Houari M, Tizzano EF, Valenzuela I, Sabbagh Q, Clayton-Smith J, Jackson A, O'Sullivan J, Bromley R, Banka S, Genevieve D, Sadikovic B. Haghshenas S, et al. Among authors: willems m. Genet Med. 2024 Jul 31;26(10):101226. doi: 10.1016/j.gim.2024.101226. Online ahead of print. Genet Med. 2024. PMID: 39097820
Expanding the genetic and clinical spectrum of Tatton-Brown-Rahman syndrome in a series of 24 French patients.
Thomas H, Alix T, Renard É, Renaud M, Wourms J, Zuily S, Leheup B, Geneviève D, Dreumont N, Schmitt E, Bronner M, Muller M, Divoux M, Wandzel M, Ravel JM, Dexheimer M, Becker A, Roth V, Willems M, Coubes C, Vieville G, Devillard F, Schaefer É, Baer S, Piton A, Gérard B, Vincent M, Nizon M, Cogné B, Ruaud L, Couque N, Putoux A, Edery P, Lesca G, Chatron N, Till M, Faivre L, Tran-Mau-Them F, Alessandri JL, Lebrun M, Quélin C, Odent S, Dubourg C, David V, Faoucher M, Mignot C, Keren B, Pisan É, Afenjar A, Julia S, Bieth É, Banneau G, Goldenberg A, Husson T, Campion D, Lecoquierre F, Nicolas G, Charbonnier C, De Saint Martin A, Naudion S, Degoutin M, Rondeau S, Michot C, Cormier-Daire V, Oussalah A, Pourié C, Lambert L, Bonnet C. Thomas H, et al. Among authors: willems m. J Med Genet. 2024 Aug 29;61(9):878-885. doi: 10.1136/jmg-2024-110031. J Med Genet. 2024. PMID: 38937076
454 results