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Molecular epidemiology identifies the expansion of the DENV2 epidemic lineage from the French Caribbean Islands to French Guiana and mainland France, 2023 to 2024.
Klitting R, Piorkowski G, Rousset D, Cabié A, Frumence E, Lagrave A, Lavergne A, Enfissi A, Dos Santos G, Fagour L, Césaire R, Jaffar-Bandjee MC, Traversier N, Gérardin P, Amaral R, Fournier L, Leon L, Dorléans F, Vincent M; arbovirus genomics diagnostic laboratories working group; Fontaine A, Failloux AB, Ayhan N, Pezzi L, Grard G, Durand GA, de Lamballerie X; Arbovirus genomics diagnostic laboratories working group members. Klitting R, et al. Among authors: vincent m. Euro Surveill. 2024 Mar;29(13):2400123. doi: 10.2807/1560-7917.ES.2024.29.13.2400123. Euro Surveill. 2024. PMID: 38551097 Free PMC article.
De novo variants predicting haploinsufficiency for DIP2C are associated with expressive speech delay.
Ha T, Morgan A, Bartos MN, Beatty K, Cogné B, Braun D, Gerber CB, Gaspar H, Kopps AM, Rieubland C, Hurst ACE, Amor DJ, Nizon M, Pasquier L, Pfundt R, Reis A, Siu VM, Tessarech M, Thompson ML, Vincent M, de Vries BBA, Walsh MB, Wechsler SB, Zweier C, Schnur RE, Guillen Sacoto MJ, Margot H, Masotto B, Palafoll MIV, Nawaz U, Voineagu I, Slavotinek A. Ha T, et al. Among authors: vincent m. Am J Med Genet A. 2024 Feb 29:e63559. doi: 10.1002/ajmg.a.63559. Online ahead of print. Am J Med Genet A. 2024. PMID: 38421105 Free article.
Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability.
Pérez Baca MDR, Jacobs EZ, Vantomme L, Leblanc P, Bogaert E, Dheedene A, De Cock L, Haghshenas S, Foroutan A, Levy MA, Kerkhof J, McConkey H, Chen CA, Batzir NA, Wang X, Palomares M, Carels M; ZFHX3 consortium; Dermaut B, Sadikovic B, Menten B, Yuan B, Vergult S, Callewaert B. Pérez Baca MDR, et al. Am J Hum Genet. 2024 Mar 7;111(3):509-528. doi: 10.1016/j.ajhg.2024.01.013. Epub 2024 Feb 26. Am J Hum Genet. 2024. PMID: 38412861
1,805 results