| 1 | NEXT-GENERATION SEQUENCING IDENTIFIES A HOMOZYGOUS NONSENSE P.TYR370*MUTATION OF THE TMC6 GENE IN A MEXICAN PEDIGREE WITH EPIDERMODYSPLASIA VERRUCIFORMIS | 2ᵒ autor: Santillan-Hernandez, Yuritzi, Lopez-Ramirez, Samantha, Carrasco-Gerard, Eugenio, Rodas-Serrano, Agustin, et al. | 2021 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000662714800001
| 2 | 0 |
| 2 | Are there biosimilar orphan drugs for gaucher disease? an overview in mexico | Coautor: Santillán-Hernández Y., Hernández G.C., Carbajal-Rodríguez L., Cerón-Rodríguez M., et al. | 2019 | GaBI Journal | WoS-id: 000518800900003
Scopus-id: 2-s2.0-85099632082
| 3 | 3 |
| 3 | Síndrome de Sjögren-Larsson: Reporte de caso pediátrico | Coautor: Santillán-Hernández Y., García-Ortiz L., Gómez-López R., Rivera-Pedroza C.I., et al. | 2018 | ARCHIVOS ARGENTINOS DE PEDIATRIA | WoS-id: 000451462900024
Scopus-id: 2-s2.0-85056722135
| 0 | 0 |
| 4 | Mexican consensus on lysosomal acid lipase deficiency diagnosis | Coautor: Santillán-Hernández Y., Vázquez-Frias R., García-Ortiz J.E., Valencia-Mayoral P.F., et al. | 2018 | REVISTA DE GASTROENTEROLOGIA DE MEXICO | Scopus-id: 2-s2.0-85039154718
| 0 | 2 |
| 5 | A rapidly progressive defective spermatogenesis in a Mexican family affected by spino-bulbar muscular atrophy | Coautor: Santillan-Hernandez, Yuritzi, Eduardo Pina-Aguilar, Raul, Angel Regalado-Hernandez, Miguel, Daniel Moreno-Garcia, Jesus, et al. | 2016 | SYSTEMS BIOLOGY IN REPRODUCTIVE MEDICINE | WoS-id: 000371929400007
Scopus-id: 2-s2.0-84960475009
| 1 | 1 |
| 6 | Novel LIPA mutations in Mexican siblings with lysosomal acid lipase deficiency | 1ᵉʳ autor: Santillán-Hernández Y., Almanza-Miranda E., Xin W.W., Goss K., et al. | 2015 | WORLD JOURNAL OF GASTROENTEROLOGY | WoS-id: 000348419400031
Scopus-id: 2-s2.0-84921479779
| 12 | 15 |
| 7 | Mucopolysaccharidosis type II in a female carrying a heterozygous stop mutation of the iduronate-2-sulfatase gene and showing a skewed X chromosome inactivation | Coautor: Santillán-Hernández Y., Pina-Aguilar, RE, Zaragoza-Arévalo G.R., Rau I., et al. | 2013 | EUROPEAN JOURNAL OF MEDICAL GENETICS | WoS-id: 000324892400007
Scopus-id: 2-s2.0-84874314465
| 16 | 18 |
| 8 | Genetic variants associated with male infertility in Mexican patients [Variantes genéticas asociadas con infertilidad masculina en pacientes mexicanos] | Coautor: Santillán-Hernández Y., Piña-Aguilar R.E., Chima-Galán M.C., Yerena-de-Vega M.C.A., et al. | 2013 | Ginecología Y Obstetricia De México | Scopus-id: 2-s2.0-84878078588
| 0 | 0 |
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