Lizeth Alejandra Martínez Jacobo

  • 19 Citations
  • 3 h-Index
20132019
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  • 1 Similar Profiles
Alopecia Medicine & Life Sciences
Genes Medicine & Life Sciences
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Exome Medicine & Life Sciences
Iris Medicine & Life Sciences
Transcriptome Medicine & Life Sciences
Intellectual Disability Medicine & Life Sciences

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Research Output 2013 2019

  • 19 Citations
  • 3 h-Index
  • 6 Article
  • 3 Letter
  • 1 Literature review

A giant and atypical port-wine stain with facial deformity

Villarreal-Villarreal, C. D., Ancer-Arellano, J., Boland-Rodríguez, E., Martínez-Jacobo, L. & Ocampo-Candiani, J., 1 Jan 2019, In : JDDG - Journal of the German Society of Dermatology. 17, 1, p. 68-69 2 p.

Research output: Contribution to journalLetter

Open Access

Großes und atypisches Feuermal mit Gesichtsdeformität

Villarreal-Villarreal, C. D., Ancer-Arellano, J., Boland-Rodríguez, E., Martínez-Jacobo, L. & Ocampo-Candiani, J., 1 Jan 2019, In : JDDG - Journal of the German Society of Dermatology. 17, 1, p. 68-70 3 p.

Research output: Contribution to journalLetter

Open Access

Prostaglandins in androgenetic alopecia in 12 men and four female

Villarreal-Villarreal, C. D., Sinclair, R. D., Martínez-Jacobo, L., Garza-Rodríguez, V., Rodríguez-León, S. A., Lamadrid-Zertuche, A. C., Rodríguez-Gutierrez, R., Ortiz-Lopez, R., Rojas-Martinez, A. & Ocampo-Candiani, J., 1 Jan 2019, In : Journal of the European Academy of Dermatology and Venereology.

Research output: Contribution to journalLetter

2 Citations (Scopus)

Evaluation of the Expression of Genes Associated with Inflammation and Apoptosis in Androgenetic Alopecia by Targeted RNA-Seq

Martinez-Jacobo, L., Ancer-Arellano, C. I., Ortiz-Lopez, R., Salinas-Santander, M., Villarreal-Villarreal, C. D., Ancer-Rodriguez, J., Camacho-Zamora, B., Zomosa-Signoret, V., Medina-De La Garza, C. E., Ocampo-Candiani, J. & Rojas-Martinez, A., 1 Oct 2018, In : Skin Appendage Disorders. 4, 4, p. 268-273 6 p.

Research output: Contribution to journalArticle

Alopecia
RNA
Apoptosis
Inflammation
Gene Expression

Exome sequencing reveals three homozygous missense variants in SNRPA in two sisters with syndromic intellectual disability

Rangel-Sosa, M. M., Figuera-Villanueva, L. E., González-Ramos, I. A., Pérez-Páramo, Y. X., Martínez-Jacobo, L. A., Arnaud-López, L., Nastasi-Catanese, J. A., Rivas-Estilla, A. M., Galán-Huerta, K. A., Rojas-Martínez, A., Ortiz-López, R. & Córdova-Fletes, C., 1 Jun 2018, In : Clinical Genetics. p. 1229-1233 5 p.

Research output: Contribution to journalArticle

Exome
Intellectual Disability
Siblings
Spliceosomes
Genes