Get started
Author

Emiy Yokoyama-Rebollar

Observed names: E. Yokoyama-Rebollar, E., Yokoyama-Rebollar, Emiy Yokoyama, Emiy Yokoyama‐Rebollar, Yokoyama Rebollar, Emiy, Yokoyama-Rebollar, E.
Observed institution: Instituto Nacional de Pediatria
ORCID: 0000-0003-3150-583X
Observed ORCID: 0000-0003-3150-583X
OpenAlex ID: A5030956700
Genetic and clinical characterization of 73 Pigmentary Mosaicism patients: revealing the genetic basis of clinical manifestations
2019 · C. Salas-Labadía, S. Gómez-Carmona, et al. · Orphanet Journal of Rare Diseases · 20
PDF
Cryptorchidism and Testicular Tumor: Comprehensive Analysis of Common Clinical Features and Search of SNVs in the KIT and AR Genes
2020 · Daniel Adrian Landero-Huerta, Rosa María Vigueras-Villaseñor, et al. · Frontiers in Cell and Developmental Biology · 10
PDF
Single nucleotide polymorphisms associated with nonsyndromic cryptorchidism in Mexican patients
2017 · M. Chávez-Saldaña, R. M. Vigueras-Villaseñor, et al. · Andrologia · 8
PDF
Cytogenomic characterization of small supernumerary marker chromosomes in patients with pigmentary mosaicism
2024 · M. P. Navarrete-Meneses, I. Ochoa-Mellado, et al. · Frontiers in Genetics · 6
PDF
First Report of Mexican Patients with PACS1-Related Neurodevelopmental Disorder and Review of the PACS1-, PACS2-, and WDR37-Related Ophthalmological Manifestations
2022 · Jorge Román Corona-Rivera, Juan Carlos Zenteno, et al. · Molecular Syndromology · 5
PDF
Analysis of the CAG tract length in the Androgen Receptor gene in Mexican patients with nonsyndromic cryptorchidism
2021 · Daniel A. Landero-Huerta, Rosa M. Vigueras-Villaseñor, et al. · Journal of Pediatric Endocrinology and Metabolism · 5
Danon Disease in a 14-Year-Old
2024 · Enrique C. Guerra, Kerstin Beutelspacher-Fernandez, et al. · JACC Case Reports · 4
Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review
2022 · A. Martínez-Hernández, D. Martínez-Anaya, et al. · BMC Medical Genomics · 3
PDF
Angelman Syndrome due to familial translocation: unexpected additional results characterized by Microarray-based Comparative Genomic Hybridization
2015 · Emiy Yokoyama-Rebollar, Adriana Ruiz-Herrera, et al. · Molecular Cytogenetics · 3
PDF
Abordaje citogenético y citogenómico de pacientes con discapacidad intelectual y malformaciones congénitas
2017 · Emiy Yokoyama-Rebollar, Sara Frías, et al. · Acta Pediátrica de México · 2
PDF
Expanding the Genetic and Clinical Spectrum of GZF1 ‐Related Phenotype: A Specific Ocular and Skeletal Disorder Distinguishable From Larsen Syndrome
2026 · Emiy Yokoyama‐Rebollar, Camilo E. Villarroel, et al. · American Journal of Medical Genetics Part A · 1
The Emerging Landscape of the Inherited Bone Marrow Failure Syndromes in Mexico
2024 · Alfredo De Jesus Rodriguez Gomez, Paula Leal-Anaya, et al. · Blood
Consenso mexicano de tirosinemia tipo 1
2024 · Flora E. Zárate-Mondragón, Renata I. Alcántara-García, et al. · Boletín Médico del Hospital Infantil de México
PDF
Dysgerminoma Probably Due to a Novel SOHLH1-pathogenic Variant Causing Familial Ovarian Dysgenesis
2024 · Camilo E. Villarroel, Juan C. Zenteno, et al. · Reproductive Sciences
Kawasaki Disease Associated with SARS-CoV2 in a Pair of Triplets
2023 · Luisa Berenise Gamez-Gonzalez, Luis Xochihua-Díaz, et al. · Pediatric Allergy Immunology and Pulmonology
Improved HUMARA for the Detection of X-Linked Agammaglobulinemia Carriers
2022 · Eduardo Carrillo-Tapia, Sara E. Espinosa-Padilla, et al. · Genetic Testing and Molecular Biomarkers
Supplementary Material for: First Report of Mexican Patients with PACS1-Related Neurodevelopmental Disorder and Review of the PACS1-, PACS2-, and WDR37-Related Ophthalmological Manifestations
2022 · J.R., Corona-Rivera, J.C., Zenteno, et al. · Figshare
Works count: 20
Citation count: 67
H-index: 5
I10-index: 2
Year
Topic
Type