The Monitor Project: Stellar rotation at 13~Myr: I. A photometric monitoring survey of the young open cluster h~Per by Moraux, E, Artemenko, S, Bouvier, J, Irwin, J, Ibrahimov, M, Magakian, T, Grankin, K, Nikogossian, E, Cardoso, C, Hodgkin, S, Aigrain, S, Movsessian, T

Sudden spleen rupture in a Plasmodium vivax-infected patient undergoing malaria treatment by Aleix Elizalde-Torrent, Fernando Val, Ingrid Cardoso C. Azevedo, Wuelton M. Monteiro, Luiz C. L. Ferreira, Carmen Fernández-Becerra, Hernando A. del Portillo, Marcus V. G. Lacerda

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A novel strategy combining array-CGH, whole-exome sequencing and in utero electroporation in rodents to identify causative genes for brain malformations by Conti, V, Carabalona, A, Pallesi-Pocachard, E, Leventer, R, Schaller, F, Parrini, E, Deparis, A, Watrin, F, Buhler, E, Novara, F, Lise, S, Pagnamenta, A, Kini, U, Taylor, J, Zuffardi, O, Represa, A, Keays, D, Guerrini, R, Falace, A, Cardoso, C

Patients’ and physicians’ preferences for type 2 diabetes mellitus treatments in Spain and Portugal: a discrete choice experiment by Morillas C, Feliciano R, Catalina PF, Ponte C, Botella M, Rodrigues J, Esmatjes E, Lafita J, Lizán L, Llorente I, Morales C, Navarro-Pérez J, Orozco-Beltran D, Paz S, Ramirez de Arellano A, Cardoso C, Tribaldos Causadias M

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Short report: Early genomic detection of SARS-CoV-2 P.1 variant in Northeast Brazil by Tosta, S, Giovanetti, M, Brandão Nardy, V, Kelly Astete Gómez, M, Gomes Lima, J, Wanderley Cardoso, C, Oliveira Silva, T, Reboredo de Oliveira da Silva, L, São Pedro Leal de Souza, M, Presta Dia, PH, Fonseca, V, de Oliveira, T, Lourenco, JM, Carlos Junior Alcantara, L, Pereira, F, Leal, A

Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene. by Conti, V, Carabalona, A, Pallesi-Pocachard, E, Parrini, E, Leventer, R, Buhler, E, McGillivray, G, Michel, F, Striano, P, Mei, D, Watrin, F, Lise, S, Pagnamenta, A, Taylor, J, Kini, U, Clayton-Smith, J, Novara, F, Zuffardi, O, Dobyns, W, Scheffer, I, Robertson, S, Berkovic, S, Represa, A, Keays, D, Cardoso, C

Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria. by Jaglin, X, Poirier, K, Saillour, Y, Buhler, E, Tian, G, Bahi-Buisson, N, Fallet-Bianco, C, Phan-Dinh-Tuy, F, Kong, X, Bomont, P, Castelnau-Ptakhine, L, Odent, S, Loget, P, Kossorotoff, M, Snoeck, I, Plessis, G, Parent, P, Beldjord, C, Cardoso, C, Represa, A, Flint, J, Keays, D, Cowan, N, Chelly, J