Publicaciones:

2021:

González-Domínguez CA, Fiesco-Roa MO, Gómez-Carmona S, Kleinert-Altamirano API, He M, Daniel EJP, Raymond KM, Abreu-González M, Manrique-Hernández S, González-Jaimes A, Salinas-Marín R, Molina-Garay C, Carrillo-Sánchez K, Flores-Lagunes LL, Jiménez-Olivares M, Muñoz-Rivas A, Cruz-Muñoz ME, Ruíz-García M, Freeze HH, Mora-Montes HM, Alaez-Verson C and Martínez-Duncker I 2021 Corrigendum: ALG1-CDG caused by non-functional alternative splicing involving a novel pathogenic Complex Allele. Front. Genet. 12:777731.

González-Domínguez CA, Villarroel CE, Rodríguez-Morales M, Manrique-Hernández S, González-Jaimes A, Olvera-Rodriguez F, Beutelspacher K, Molina-Garay C, Carrillo-Sánchez K, Flores-Lagunes LL, Jiménez-Olivares M, Muñoz-Rivas A, Cruz-Muñoz ME, Mora-Montes HM, Salinas-Marín R, Alaez-Verson C, Martínez-Duncker I. 2021. Non-functional alternative splicing caused by a Latino pathogenic variant in a case of PMM2-CDG. Mol Genet Metab Rep. 28:100781.

Manrique-Hernández, Sandra, González-Ortiz, Rebeca, Salinas-Marín, Roberta, Asteggiano, Carla Gabriela, Martínez-Duncker, Iván. 2021. Desórdenes congénitos de la glicosilación. Glicobiología. Avances en temas prioritarios de salud. ISBN: 978-607-8784-29-5. Primera edición: UAEM.

2020:
González-Domínguez C.A., Raya-Trigueros A., Manrique-Hernández S., González Jaimes A., Salinas-Marín R., Molina-Garay C., Carrillo-Sánchez K., Flores-Lagunes L.L., Jiménez-Olivares M., Dehesa-Caballero C., Alaez-Versón C., Martínez-Duncker I. 2020. Identification through exome sequencing of the first PMM2-CDG individual of Mexican mestizo origin. Mol Genet Metab Rep 25:100637.