| 1 | An Exploration of Social Cognition in Children with Different Degrees of Genetic Deletion in Williams Syndrome | Coautor: Venegas-Vega C.A., Serrano-Juárez C.A., Prieto-Corona B., Rodríguez-Camacho M., et al. | 2021 | JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS | WoS-id: 000560628200003
Scopus-id: 2-s2.0-85089605545
| 6 | 6 |
| 2 | Further definition of the proximal 19p13.3 microdeletion/microduplication syndrome and implication of PIAS4 as the major contributor | Coautor: Venegas-Vega, Carlos A., Tenorio, Jair, Nevado, Julian, Gonzalez-Meneses, Antonio, et al. | 2020 | CLINICAL GENETICS | WoS-id: 000508802600001
Scopus-id: 2-s2.0-85078660639
| 10 | 10 |
| 3 | Familial mesial temporal lobe epilepsy in Mexico: Inheritance pattern and clinical features | Coautor: Venegas-Vega C.A., Guzmán-Jiménez D.E., Campos J.B., Sánchez M.A., et al. | 2020 | EPILEPSY RESEARCH | WoS-id: 000587830900024
Scopus-id: 2-s2.0-85090991258
| 4 | 4 |
| 4 | Cognitive, Behavioral, and Adaptive Profiles in Williams Syndrome with and Without Loss of GTF2IRD2 | 2ᵒ autor: Venegas-Vega C.A., Serrano-Juárez C.A., Yáñez-Téllez M.G., Rodríguez-Camacho M., et al. | 2018 | JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY | WoS-id: 000449588200002
Scopus-id: 2-s2.0-85055617146
| 11 | 11 |
| 5 | Orquiectomía parcial en un paciente con tumor de células de Leydig asociado con síndrome de Klinefelter | Coautor: Venegas-Vega C., Cumming A., Manzanilla-García H.A., Arana-Trejo R.M., et al. | 2017 | Revista mexicana de urología (Impresa) | Scopus-id: 2-s2.0-85069187934
| 0 | 0 |
| 6 | PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndrome | Coautor: Venegas-Vega C.A., Nevado J., Rosenfeld J.A., Mena R., et al. | 2015 | EUROPEAN JOURNAL OF HUMAN GENETICS | WoS-id: 000365129700006
Scopus-id: 2-s2.0-84948711927
| 27 | 27 |
| 7 | Mutations in the Human UBR1 Gene and the Associated Phenotypic Spectrum | Coautor: Venegas-Vega C.A., Sukalo M., Fiedler A., Guzmán C., et al. | 2014 | HUMAN MUTATION | WoS-id: 000334658800003
Scopus-id: 2-s2.0-84898812128
| 29 | 36 |
| 8 | Impact of gene dosage on gene expression, biological processes and survival in cervical cancer: A genome-wide follow-up study | Coautor: Venegas-Vega C., Medina-Martinez I., Barrón V., Roman-Bassaure E., et al. | 2014 | PLOS ONE | WoS-id: 000338101500025
Scopus-id: 2-s2.0-84902302974
| 43 | 44 |
| 9 | 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 | 1ᵉʳ autor: Venegas-Vega C., Nieto-Martínez K., Martínez-Herrera A., Gómez-Laguna L., et al. | 2014 | MOLECULAR CYTOGENETICS | WoS-id: 000347350100001
Scopus-id: 2-s2.0-84989311431
| 15 | 15 |
| 10 | Diagnosis of Familial Wolf-Hirschhorn Syndrome due to a Paternal Cryptic Chromosomal Rearrangement by Conventional and Molecular Cytogenetic Techniques | 1ᵉʳ autor: Venegas-Vega C.A., Fernández-Ramírez F., Zepeda L.M., Nieto-Martínez K., et al. | 2013 | BIOMED RESEARCH INTERNATIONAL | WoS-id: 000314934600001
Scopus-id: 2-s2.0-84874608265
| 3 | 5 |
| 11 | Amplified Genes May Be Overexpressed, Unchanged, or Downregulated in Cervical Cancer Cell Lines | Coautor: Venegas-Vega C., Vazquez-Mena O., Medina-Martinez I., Juárez-Torres E., et al. | 2012 | PLOS ONE | WoS-id: 000303060800039
Scopus-id: 2-s2.0-84857856392
| 41 | 43 |
| 12 | Satoyoshi Syndrome With Unusual Skeletal Abnormalities and Parental Consanguinity | 1ᵉʳ autor: Venegas-Vega C.A., Rivera-Vega M.R., Cuevas-Covarrubias S., Orozco J., et al. | 2009 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000271587600015
Scopus-id: 2-s2.0-70449346630
| 7 | 9 |
| 13 | Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: Cytogenetic and molecular analysis with delineation of the phenotype | 2ᵒ autor: Venegas-Vega C.A., Zafra De La Rosa G., Monroy N., Contreras-Bucio G., et al. | 2005 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000230288400006
Scopus-id: 2-s2.0-22044437226
| 9 | 9 |
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