| Mitosis is a source of potential markers for screening and survival and therapeutic targets in cervical cancer AM Espinosa, A Alfaro, E Roman-Basaure, M Guardado-Estrada, Í Palma, ... PloS one 8 (2), e55975, 2013 | 148 | 2013 |
| BCR/ABL p210, p190 and p230 fusion genes in 250 Mexican patients with chronic myeloid leukaemia (CML) RM Arana‐Trejo, ER Sanchez, G Ignacio‐Ibarra, EB De La Fuente, ... Clinical & Laboratory Haematology 24 (3), 145-150, 2002 | 91 | 2002 |
| Amplified genes may be overexpressed, unchanged, or downregulated in cervical cancer cell lines O Vazquez-Mena, I Medina-Martinez, E Juárez-Torres, V Barrón, ... PloS one 7 (3), e32667, 2012 | 63 | 2012 |
| The Amerindian mtDNA haplogroup B2 enhances the risk of HPV for cervical cancer: de-regulation of mitochondrial genes may be involved M Guardado-Estrada, I Medina-Martínez, E Juárez-Torres, ... Journal of human genetics 57 (4), 269-276, 2012 | 59 | 2012 |
| A Boolean network model of human gonadal sex determination O Ríos, S Frias, A Rodríguez, S Kofman, H Merchant, L Torres, ... Theoretical Biology and Medical Modelling 12, 1-18, 2015 | 56 | 2015 |
| Impact of gene dosage on gene expression, biological processes and survival in cervical cancer: a genome-wide follow-up study I Medina-Martinez, V Barron, E Roman-Bassaure, E Juarez-Torres, ... PLoS One 9 (5), e97842, 2014 | 52 | 2014 |
| Pattern of deletions of the dystrophin gene in Mexican Duchenne/Becker muscular dystrophy patients: the use of new designed primers for the analysis of the major deletion “hot … R Coral‐Vázquez, D Arenas, B Cisneros, L Peñaloza, F Salamanca, ... American journal of medical genetics 70 (3), 240-246, 1997 | 38 | 1997 |
| CDKN3 mRNA as a Biomarker for Survival and Therapeutic Target in Cervical Cancer EV Barrón, E Roman-Bassaure, AL Sánchez-Sandoval, AM Espinosa, ... PloS one 10 (9), e0137397, 2015 | 35 | 2015 |
| Clinical and endocrine spectrum in patients with the 45, X/46, XY karyotype S Kofman, G Pérez-Palacios, M Medina, N Escobar, M García, L Ruz, ... Human Genetics 58, 373-376, 1981 | 27 | 1981 |
| Genetic features of Mexican women predisposing to cancer of the uterine cervix B Silva, G Vargas-Alarcón, J Zúñiga-Ramos, TS Rodríguez-Reyna, ... Human pathology 30 (6), 626-628, 1999 | 22 | 1999 |
| A t (1; 22)(p13; q13) in four children with acute megakaryoblastic leukemia (M7), two with Down syndrome RMA Trejo, RP Aguilera, S Nieto, S Kofman Cancer genetics and cytogenetics 120 (2), 160-162, 2000 | 21 | 2000 |
| Characterization of a group unrelated patients with arthrogryposis multiplex congenita M Valdés-Flores, L Casas-Avila, E Hernández-Zamora, S Kofman, ... Jornal de Pediatria 92, 58-64, 2016 | 19 | 2016 |
| Analysis of dystrophin gene deletions in patients from the Mexican population with Duchenne/Becker muscular dystrophy. R Coral-Vázquez, D Arenas, B Cisneros, L Peñaloza, S Kofman, ... Archives of medical research 24 (1), 1-6, 1993 | 18 | 1993 |
| 19q13.11 microdeletion concomitant with ins(2;19)(p25.3;q13.1q13.4)dn in a boy: potential role of UBA2 in the associated phenotype C Venegas-Vega, K Nieto-Martínez, A Martínez-Herrera, ... Molecular Cytogenetics 7, 1-7, 2014 | 16 | 2014 |
| A de novo phe67leu mutation in the SRY gene in a patient with complete 46,XY gonadal dysgenesis JC Zenteno, S Carranza-Lira, AL Jimenez, S Kofman Journal of endocrinological investigation 26, 1117-1119, 2003 | 11 | 2003 |
| Carrier detection in Duchenne and Becker muscular dystrophy using dinucleotide repeat polymorphisms. A study in Mexican families. D Arenas, R Coral, B Cisneros, L Peñaloza, F Salamanca, S Kofman, ... Archives of medical research 27 (2), 151-156, 1996 | 11 | 1996 |
| Nance–Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature L Gómez-Laguna, A Martínez-Herrera, AP Reyes-de la Rosa, ... Ophthalmic Genetics 39 (1), 56-62, 2018 | 8 | 2018 |
| Sex reversal in humans: The XX Male Syndrome and related disorders G Pérez-Palacios, S Kofman, JP Méndez, A Ulloa-Aguirre Textbook of intersexual states. Barcelona, Spain: Doyma 269, 1994 | 8 | 1994 |
| Diagnosis of familial Wolf-Hirschhorn syndrome due to a paternal cryptic chromosomal rearrangement by conventional and molecular cytogenetic techniques CA Venegas-Vega, F Fernández-Ramírez, LM Zepeda, K Nieto-Martínez, ... BioMed Research International 2013, 2013 | 7 | 2013 |
| Defectos congénitos en el Hospital General de México. Frecuencia observada durante 10 años mediante el RYVEMCE JM Valdés M, ME Blanco A, S Kofman, O Mutchinick Rev. méd. Hosp. Gen. Méx, 181-7, 1997 | 7 | 1997 |
