| 1 | Dysgerminoma Probably Due to a Novel SOHLH1-pathogenic Variant Causing Familial Ovarian Dysgenesis | Coautor: Yokoyama, E, Villarroel, CE, Zenteno, JC, Barragán-Arévalo, T, et al. | 2024 | REPRODUCTIVE SCIENCES | WoS-id: 001177015000002
Scopus-id: 2-s2.0-85186950928
| 0 | 0 |
| 2 | Danon Disease in a 14-Year-Old: An Exclusively Cardiac Phenotype | Coautor: Yokoyama-Rebollar E., Guerra E.C., Beutelspacher-Fernandez K., Silva-Estrada J.A., et al. | 2024 | Jacc: Case Reports | Scopus-id: 2-s2.0-85204503696
| 0 | 1 |
| 3 | First Report of Mexican Patients with PACS1-Related Neurodevelopmental Disorder and Review of the PACS1-, PACS2-, and WDR37-Related Ophthalmological Manifestations | Coautor: Yokoyama-Rebollar, Emiy, Roman Corona-Rivera, Jorge, Carlos Zenteno, Juan, Gildardo Lopez-Perez, Leopoldo, et al. | 2023 | Molecular Syndromology | WoS-id: 000900501700001
Scopus-id: 2-s2.0-85145289036
| 0 | 0 |
| 4 | Frequent copy number variants in a cohort of Mexican-Mestizo individuals | Coautor: Yokoyama, Emiy, Sanchez, Silvia, Juarez, Ulises, Dominguez, Julieta, et al. | 2023 | MOLECULAR CYTOGENETICS | WoS-id: 000912415900001
Scopus-id: 2-s2.0-85146115748
| 4 | 5 |
| 5 | Improved HUMARA for the Detection of X-Linked Agammaglobulinemia Carriers | Coautor: Yokoyama-Rebollar E., Carrillo-Tapia E., Espinosa-Padilla S.E., Perez-Perez D., et al. | 2022 | GENETIC TESTING AND MOLECULAR BIOMARKERS | WoS-id: 000782154600001
Scopus-id: 2-s2.0-85129581968
| 0 | 0 |
| 6 | Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review | Coautor: Yokoyama-Rebollar, E., Martinez-Hernandez, A., Martinez-Anaya, D., Duran-McKinster, C., et al. | 2022 | BMC MEDICAL GENOMICS | WoS-id: 000877014900002
Scopus-id: 2-s2.0-85140943693
| 0 | 0 |
| 7 | Analysis of the CAG tract length in the Androgen Receptor gene in Mexican patients with nonsyndromic cryptorchidism | Coautor: Yokoyama-Rebollar, Emiy, Landero-Huerta, Daniel A., Vigueras-Villasenor, Rosa M., Taja-Chayeb, Lucia, et al. | 2021 | JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | WoS-id: 000672587100003
Scopus-id: 2-s2.0-85104378860
| 3 | 4 |
| 8 | Cryptorchidism and Testicular Tumor: Comprehensive Analysis of Common Clinical Features and Search of SNVs in the KIT and AR Genes | Coautor: Yokoyama-Rebollar E., Landero-Huerta D.A., Vigueras-Villaseñor R.M., García-Andrade F., et al. | 2020 | Frontiers In Cell And Developmental Biology | WoS-id: 000568517200001
Scopus-id: 2-s2.0-85089832457
| 9 | 9 |
| 9 | Influence of SNPs in Genes that Modulate Lung Disease Severity in a Group of Mexican Patients with Cystic Fibrosis | 1ᵉʳ autor: Yokoyama E., Chávez-Saldaña M., Orozco L., Cuevas F., et al. | 2018 | Archives Of Medical Research | WoS-id: 000445443700003
Scopus-id: 2-s2.0-85046125919
| 2 | 3 |
| 10 | Angelman Syndrome due to familial translocation: Unexpected additional results characterized by Microarray-based Comparative Genomic Hybridization | 1ᵉʳ autor: Yokoyama-Rebollar E., Ruiz-Herrera A., Lieberman-Hernández E., Del Castillo-Ruiz V., et al. | 2015 | MOLECULAR CYTOGENETICS | WoS-id: 000353104300001
Scopus-id: 2-s2.0-84949127641
| 1 | 1 |
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