| 1 | 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 | Coautor: Nieto-Martínez K., Gómez-Laguna L., Martínez-Herrera A., Reyes-de la Rosa A.D.P., et al. | 2018 | OPHTHALMIC GENETICS | WoS-id: 000428520500011
Scopus-id: 2-s2.0-85029587680
| 7 | 8 |
| 2 | Detection of Common Chromosomal Translocations in Small Round Blue Cell Pediatric Tumors | Coautor: Nieto-Martínez K., Ponce-Castañeda M.V., García-Chéquer A.J., Aguilar, PE, et al. | 2014 | Archives Of Medical Research | WoS-id: 000333139100006
Scopus-id: 2-s2.0-84896833378
| 3 | 4 |
| 3 | Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): Further delineation of the syndromes | Coautor: Nieto-Martínez K., Cervantes A., García-Delgado C., Fernández-Ramírez F., et al. | 2014 | BMC MEDICAL GENOMICS | WoS-id: 000342094500001
Scopus-id: 2-s2.0-84908160780
| 3 | 4 |
| 4 | 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 | 2ᵒ autor: Nieto-Martínez K., Venegas-Vega C., Martínez-Herrera A., Gómez-Laguna L., et al. | 2014 | MOLECULAR CYTOGENETICS | WoS-id: 000347350100001
Scopus-id: 2-s2.0-84989311431
| 15 | 15 |
| 5 | Diagnosis of Familial Wolf-Hirschhorn Syndrome due to a Paternal Cryptic Chromosomal Rearrangement by Conventional and Molecular Cytogenetic Techniques | Coautor: Nieto-Martínez K., Venegas-Vega C.A., Fernández-Ramírez F., Zepeda L.M., et al. | 2013 | BIOMED RESEARCH INTERNATIONAL | WoS-id: 000314934600001
Scopus-id: 2-s2.0-84874608265
| 3 | 5 |
| 6 | Amplified Genes May Be Overexpressed, Unchanged, or Downregulated in Cervical Cancer Cell Lines | Coautor: Nieto-Martínez K., Vazquez-Mena O., Medina-Martinez I., Juárez-Torres E., et al. | 2012 | PLOS ONE | WoS-id: 000303060800039
Scopus-id: 2-s2.0-84857856392
| 43 | 43 |
| 7 | Detection of Fusion Genes in Formalin-fixed Paraffin-embedded Tissue Sections of Rhabdomyosarcoma by RT-PCR and Fluorescence In Situ Hybridization in Mexican Patients | Coautor: Nieto-Martinez, K, Eguia-Aguilar, P, Ponce-Castaneda, V, Najera-Garcia, N, et al. | 2010 | Archives Of Medical Research | WoS-id: 000277930800008
Scopus-id: 2-s2.0-77952765722
| 5 | 6 |
| 8 | Mix Gonadal Dysgenesis Associated with Ring Y Chromosome Mosaics in a Phenotypic Male | 2ᵒ autor: Nieto, K, Lopez-Valdes, JA, Najera, N, Cervantes, A, et al. | 2009 | SEXUAL DEVELOPMENT | WoS-id: 000269789400001
Scopus-id: 2-s2.0-70349272265
| 4 | 7 |
| 9 | Intracranial germ cell tumors: association with Klinefelter syndrome and sex chromosome aneuploidies | Coautor: Nieto K., Queipo G., Aguirre D., Pena, YR, et al. | 2008 | CYTOGENETIC AND GENOME RESEARCH | WoS-id: 000259032000007
Scopus-id: 2-s2.0-50849108549
| 16 | 29 |
| 10 | Extragonadal germ cell tumors are often associated with Klinefelter syndrome | 2ᵒ autor: Nieto K., Aguirre D., Lazos M., Peña Y.R., et al. | 2006 | HUMAN PATHOLOGY | WoS-id: 000236727500014
Scopus-id: 2-s2.0-33645129598
| 45 | 65 |
| 11 | Distribution of Y-chromosome-bearing cells in gonadoblastoma and dysgenetic testis in 45,X/46,XY infants | 2ᵒ autor: Nieto K., Peña-Alonso R., Alvarez R., Palma I., et al. | 2005 | MODERN PATHOLOGY | WoS-id: 000227168100018
Scopus-id: 2-s2.0-15444379250
| 27 | 33 |
| 12 | Unusual mixed gonadal dysgenesis associated with Müllerian duct persistence, polygonadia, and a 45,X/46,X,idic(Y)(p) karyotype | 2ᵒ autor: Nieto K., Queipo G., Grether P., Frías S., et al. | 2005 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000230949400018
Scopus-id: 2-s2.0-23044484449
| 9 | 9 |
| 13 | 45,X/47,XXX/47,XX, del(Y)(p?)/46,XX mosaicism causing true hermaphroditism | 1ᵉʳ autor: Nieto K., Peña R., Palma I., Dorantes L.M., et al. | 2004 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000224181700017
Scopus-id: 2-s2.0-4744337724
| 5 | 5 |
ID's SCOPUS 