| DEB test for Fanconi anemia detection in patients with atypical phenotypes. C Esmer, S Sánchez, S Ramos, B Molina, S Frias, A Carnevale American journal of Medical Genetics., 35-39., 2004 | 75 | 2004 |
| Nonclonal chromosome aberrations and genome chaos in somatic and germ cells from patients and survivors of hodgkin lymphoma S Frias, S Ramos, C Salas, B Molina, S Sánchez, R Rivera-Luna Genes 10 (1), 37, 2019 | 27 | 2019 |
| RAD50 targeting impairs DNA damage response and sensitizes human breast cancer cells to cisplatin therapy A Flores-Pérez, LE Rafaelli, N Ramírez-Torres, E aréchaga-Ocampo, ... cancer Biology & Therapy 15 (6), 1–12, 2014 | 27 | 2014 |
| Trisomy of the short arm of chromosome 5 due to a de novo inversion and duplication (5)(p15.3 p13.3). M Cervera, S Sánchez, B Molina, MA Alcántara, V del Castillo, ... American Journal of Medical Genetics., 381-385., 2005 | 27 | 2005 |
| Persistent Genomic Instability in Peripheral Blood Lymphocytes From Hodgkin Lymphoma Survivors C Salas, A Niembro, V Lozano, E Gallardo, B Molina, S Sánchez, ... Environmental and Molecular Mutagenesis, 271-280, 2012 | 25 | 2012 |
| Significant transcriptional changes in 15q duplication but not Angelman syndrome deletion stem cell-derived neurons. N Urraca, K Hope A, K Victor T, G Belgard, R Memon, S Goorha, C Valdez, ... Molecular Autism, 6, 2018 | 23 | 2018 |
| Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics E Yokoyama, V Del Castillo, S Sánchez, S Ramos, B Molina, L Torres, ... Molecular Cytogenetics 11, 1-8, 2018 | 10 | 2018 |
| Inhibition of TGFβ1 and TGFβ3 promotes hematopoiesis in Fanconi anemia A Rodríguez, C Yang, E Furutani, BG de Teresa, M Velázquez, J Filiatrault, ... Experimental hematology 93, 70-84. e4, 2021 | 9 | 2021 |
| Acrocentric cryptic translocation associated with nondisjunction of chromosome 21. S Ramos, MA Alcántara, B Molina, V del Castillo, S Sánchez, S Frias American Journal of Medical Genetics 146 (A1), 97-102, 2008 | 9 | 2008 |
| Frequent copy number variants in a cohort of Mexican-Mestizo individuals S Sánchez, U Juárez, J Domínguez, B Molina, R Barrientos, ... Molecular Cytogenetics 16 (1), 2, 2023 | 5 | 2023 |
| Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes R Barrientos-Rios, S Frias, JA Velázquez-Aragón, CE Villaroel, ... Gynecological Endocrinology, 2019 | 5 | 2019 |
| 7p15 deletion as the cause of hand-foot- genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype. E Yokoyama, DL Smith-Pellegrin, S Sánchez, B Molina, A Rodríguez, ... Molecular Cytogenetics, 42, 2017 | 4 | 2017 |
| Angelman Syndrome due to familial translocation: unexpected additional results characterized by Microarray-based Comparative Genomic Hybridization E Yokoyama-Rebollar, A Ruiz-Herrera, E Lieberman-Hernández, ... Molecular Cytogenetics : 10.1186/s13039-015-0127-6. eCollection 2015. 8 (27), 8, 2015 | 4 | 2015 |
| 5q34q35.3 duplication involving the NSD1 gene: region defined by microarray CGH. A case report AR Vázquez-del Campo, L Torres-Maldonado, S Sánchez-Sandoval, ... Acta Pediátrica de México 37 (5), 271-281, 2016 | 2* | 2016 |
| Interstitial Deletion of 2q24.2: Further Delineation of an Emerging Syndrome Associated With Intellectual Disability, Severe Hypotonia and Moderate Intrauterine Growth Restriction Emiy Yokoyama,Camilo E. Villarroel, Victoria Del Castillo, Leda Torres ... Am J Med Genet: 164 (Part A), 824–827, 2014 | 2* | 2014 |
| Unravelling complex mosaicism of sex chromosomes in a patient with primary amenorrhea through cytogenetic analysis on urothelial cells R Sevilla-Montoya, M de Jesus Zavaleta-Abreu, G Queipo, S Sanchez, ... Taiwanese Journal of Obstetrics and Gynecology 60 (3), 526-529, 2021 | 1 | 2021 |
| Variabilidad clínica citogenética en doce familias mexicanas con anemia de Fanconi y su relación con el grupo de complementación al que pertenecen MC Esmer Sánchez, A Carnevale Cantoni, B Molina Alvarez, ... Rev. invest. clín, 273-83, 1999 | 1 | 1999 |
| Translational Medicine Copy Number Variants CNV in the Regulatory Region of SHOX Gene and Bone Modeling in Girls with Turner Syndrome 45X TS45X Preliminary Results A Gonzalez, R Rios, S Vazquez, J Velazquez, C Villarroel, S Sanchez, ... HORMONE RESEARCH IN PAEDIATRICS 90, 25-25, 2018 | | 2018 |
| In Search of Candidate Genes Genotype Phenotype Correlation: Role of Klotho Polymorphisms and Vitamin D Receptor in Bone Mineral Density in Mexican Children and Adolescents … A León, R Ríos, S Vázquez, J Velázquez, C Villarroel, S Sánchez, ... Hormone Research in Paediatrics 90, 1-1, 2018 | | 2018 |
| ANEXO III Citogenética molecular Sara Frías, Sandra Ramos, Silvia Sánchez Genética Clínica, 141-146, 2012 | | 2012 |
