Mariana Elizabeth Herrera García

Ibis Menéndez, Claudia Carranza, Mariana Herrera, Nely Marroquín, Joseph Foster II, Filiz Basak Cengiz, Guney Bademci, Mustafa Tekin. (2017). Dominant deafness-onychodystrophy síndrome caused by an ATP6V1B2 mutation. Clin Case Rep. 8;5(4):376-379. doi: 10.1002/ccr3.761

Denise Yan, Demet Tekin, Guney Bademci, Joseph Foster II, Basak Cengiz, Abhiraami Kannan Sundhari, Shengru Guo, Rahul Mittal, Bing Zou, Mhamed Grati, Rosemary I. Kabahuma, Mohan Kameswaran, Taye J. Lasisi, Waheed A. Adedeji, Akeem O. Lasisi, Ibis Menendez, Mariana Herrera, Claudia Carranza, Reza Maroofian, Andrew H. Crosby, Mariem Bensaid, Saber Masmoudi, Mahdiyeh Behnam, Majid Mojarrad, Yong Feng, Duygu Duman, Alex M. Mawla, Alex S. Nord, Susan H. Blanton, Xue Z. Liu & Mustafa Tekin. (2016). Spectrum of DNA variants for non syndromic deafness in a large cohort from multiple continents. Human genetics, 135(8), 953-961. http://dx.doi.org/10.1007/s00439-016-1697-z

Claudia Carranza, Vanessa Zamora, Mariana Herrera, Luisa Rosales, Mauricio Villlegas, Mariela Guerra, Nancy Escobar, Nely Marroquín, Claudia Osorio, Darwin Alvarez, Luis Alvarez. (2016). High frequency of MTHFR, MTR and TC2 gene polymorphisms in Guatemalan Children with ALL. Clinical Lymphoma, Myeloma & Leukemia. Volume 16, supplement 2.

Carranza, C., Menéndez, I., Herrera, M., Castellanos, P., Maldonado, F., Rosales, L., Escobar, N., Guerra, M., Alvarez, D., Foster, J., Guo, S., Blanton, Sh., Bademeci, G. & Tekin, M. (2015). A mayan founder mutation is a common cause of deafness in Guatemala. Journal of Genetics and Genome Research.

Nancy Escobar, Mariana Herrera, Luisa Rosales, Silvana Torselli, Julio Cáceres, Mauricio Villegas, Mariela Guerra, Nely Marroquín, Claudia Osorio, Vanessa Zamora, Darwin Alvarez, Luis Alvarez, Claudia Carranza. (2016). Detection of BCR-ABL kinase domain mutations in Chronic Myeloid Leukemia Patients. Clinical Lymphoma, Myeloma & Leukemia. Volume 16, supplement 2.

Claudia Carranza, Luisa Rosales, Nancy Escobar, Claudia Osorio, Nely Marroquín, Federico Antillón, Mariela Guerra, Mariana Herrera, Mauricio Villegas, Nancy Zamora, Silvana Torselli, Darwin Alvarez, Luis Alvarez. (2015). Genetic Alterations in Guatemalan acute myeloid leukemia patients. Clinical Lymphoma, Myeloma & Leukemia. Volume 15, supplement 2.

Mariela Guerra, Mariana Herrera, Luisa Rosales, Mauricio Villegas, Claudia Osorio, Nely Marrquín, Darwin Alvarez, Nancy Escobar, Nancy Zamora, Silvana Torselli, Luis Alvarez, Claudia Carranza. (2015). Genetic Characterization of myeloproliferative neoplasms in Guatemala. Clinical Lymphoma, Myeloma & Leukemia. Volume 15, supplement 2.

Carranza C, Tinti D, Herrera M, Rosales L, Villegas M, et al. (2014) Detection of JAK2 V617f Mutation, Secondary to the Presence of BCR-ABL1Translocation in a Patient with Chronic Myeloid Leukemia: Report of a Case and Review of the Literature. Int J Genomic Med 2: 116. doi: 10.4172/2332-0672.1000116

García, M. L., Herrera, M., Pérez, A., Castillo, L. y Kestler, R. (2013). Seroprevalencia de la leptospirosis humana en un asentamiento del área urbana de la ciudad de Guatemala. Revista Cubana de Medicina Tropical. Volumen 65 (2), 2013.