Flores-Lagunes L, Del Pozo-Yauner L, Carrillo-Sanchez K, Molina-Garay C, Jimenez-Olivares M, Garcia-Solorio J, Rodriguez Corona U, Herrera GA, Ricardez-Marcial E, Alaez-Verson C. First family with Perry syndrome from Mexico. Biomed Rep. 2024 Aug; 21(2):120.

Arrieta O, Caballe-Perez E, Hernandez-Pedro N, Romero-Nunez E, Lucio-Lozada J, Castillo-Ruiz C, Acevedo-Castillo K, Maria Alvarez-Gomez R, Molina-Garay C, Jimenez-Olivares M, Carrillo-Sanchez K, Cristina Mendoza-Caamal E, Cardona AF, Remon J, Alaez-Verson C. Prevalence of pathogenic or likely pathogenic germline variants in cancer predisposition genes among selected patients with lung adenocarcinoma: The GERMLUNG study. Lung Cancer. 2024 Aug; 194:107864.

Garcia-Solorio J, Martinez-Villegas O, Rodriguez-Corona U, Molina-Garay C, Jimenez-Olivares M, Carrillo-Sanchez K, Mendoza-Caamal EC, Munoz-Rivas A, Villegas-Torres BE, Cervera A, Flores-Lagunes LL, Alaez-Verson C. Case report: A familial B-acute lymphoblastic leukemia associated with a new germline pathogenic variant in PAX5. The first report in Mexico. Front Oncol. 2024; 14:1355335.

Barbosa-Amezcua M, Cuevas-Cordoba B, Fresno C, Haase-Hernandez JI, Carrillo-Sanchez K, Mata-Rocha M, Munoz-Torrico M, Backer C, Gonzalez-Covarrubias V, Alaez-Verson C, Soberon X. Rapid Identification of Drug Resistance and Phylogeny in M. tuberculosis, Directly from Sputum Samples. Microbiol Spectr. 2022 Sep 14; :e0125222.

Takada LT, Alaez-Verson C, Burgute BD, Nitrini R, Sosa AL, Castilhos RM, Chaves MF, Longoria EM, Carrillo-Sanchez K, Brucki SMD, Molina C, Olivares MJ, Ziegemeier E, Petranek J, Goate AM, Cruchaga C, Renton AE, Fernandez MV, Day GS, McDade E, Bateman RJ, Karch CM, Llibre-Guerra JJ. Discovery and validation of dominantly inherited Alzheimer's disease mutations in populations from Latin America. Alzheimers Res Ther. 2022 Aug 5; 14(1):108.

Molina Garay C, Carrillo Sanchez K, Jimenez Olivares M, Munoz Rivas A, Villegas Torres BE, Flores Aguilar H, Nunez Enriquez JC, Jimenez Hernandez E, Bekker Mendez VC, Torres Nava JR, Flores Lujano J, Martin Trejo JA, Mata Rocha M, Medina Sanson A, Espinoza Hernandez LE, Penaloza Gonzalez JG, Espinosa Elizondo RM, Flores Villegas LV, Amador Sanchez R, Perez Saldivar ML, Sepulveda Robles OA, Rosas Vargas H, Jimenez Morales S, Galindo Delgado P, Mejia Arangure JM, Alaez Verson C. Mutational Landscape of CEBPA in Mexican Pediatric Acute Myeloid Leukemia Patients: Prognostic Implications. Front Pediatr. 2022; 10:899742.

Fernandez-Hernandez L, Reyna-Fabian ME, Alcantara-Ortigoza MA, Alaez-Verson C, Carrillo-Sanchez K, Gonzalez-Del Angel A. Unusual Clinical Manifestations in a Mexican Patient with Sanfilippo B Syndrome. Diagnostics (Basel). 2022 May 19; 12(5):.

Gonzalez-Dominguez CA, Fiesco-Roa MO, Gomez-Carmona S, Kleinert-Altamirano API, He M, Daniel EJP, Raymond KM, Abreu-Gonzalez M, Manrique-Hernandez S, Gonzalez-Jaimes A, Salinas-Marin R, Molina-Garay C, Carrillo-Sanchez K, Jimenez-Olivares M, Munoz-Rivas A, Cruz-Munoz ME, Ruiz-Garcia M, Freeze HH, Mora-Montes HM, Alaez-Verson C, Martinez-Duncker I. Corrigendum: ALG1-CDG Caused by Non-Functional Alternative Splicing Involving a Novel Pathogenic Complex Allele. Front Genet. 2021; 12:777731.

Gonzalez-Dominguez CA, Villarroel CE, Rodriguez-Morales M, Manrique-Hernandez S, Gonzalez-Jaimes A, Olvera-Rodriguez F, Beutelspacher K, Molina-Garay C, Carrillo-Sanchez K, Jimenez-Olivares M, Munoz-Rivas A, Cruz-Munoz ME, Mora-Montes HM, Salinas-Marin R, Alaez-Verson C, Martinez-Duncker I. Non-functional alternative splicing caused by a Latino pathogenic variant in a case of PMM2-CDG. Mol Genet Metab Rep. 2021 Sep; 28:100781.

Lugo-Reyes SO, Pastor N, Gonzalez-Serrano E, Yamazaki-Nakashimada MA, Scheffler-Mendoza S, Berron-Ruiz L, Wakida G, Nunez-Nunez ME, Macias-Robles AP, Staines-Boone AT, Venegas-Montoya E, Alaez-Verson C, Molina-Garay C, Carrillo-Sanchez K, Niemela J, Rosenzweig SD, Gaytan P, Yanez JA, Martinez-Duncker I, Notarangelo LD, Espinosa-Padilla S, Cruz-Munoz ME. Clinical Manifestations, Mutational Analysis, and Immunological Phenotype in Patients with RAG1/2 Mutations: First Cases Series from Mexico and Description of Two Novel Mutations. J Clin Immunol. 2021 Aug; 41(6):1291-1302.

Llibre-Guerra JJ, Li Y, Allegri RF, Mendez PC, Surace EI, Llibre-Rodriguez JJ, Sosa AL, Alaez-Verson C, Longoria EM, Tellez A, Carrillo-Sanchez K, Sanchez V, Takada LT, Nitrini R, Ferreira-Frota NA, Benevides-Lima J, Lopera F, Ramirez L, Jimenez-Velazquez I, Schenk C, Acosta D, Behrens MI, Doering M, Ziegemeier E, Morris JC, McDade E, Bateman RJ. Dominantly inherited Alzheimer's disease in Latin America: Genetic heterogeneity and clinical phenotypes. Alzheimers Dement. 2020 Nov 23; :.

Molina Garay C, Carrillo Sanchez K, Jimenez Olivares M, Munoz Rivas A, Villegas Torres BE, Flores Aguilar H, Nunez Enriquez JC, Jimenez Hernandez E, Bekker Mendez VC, Torres Nava JR, Flores Lujano J, Martin Trejo JA, Mata Rocha M, Medina Sanson A, Espinoza Hernandez LE, Penaloza Gonzalez JG, Espinosa Elizondo RM, Flores Villegas LV, Amador Sanchez R, Perez Saldivar ML, Sepulveda Robles OA, Rosas Vargas H, Rangel Lopez A, Dominguez Lopez ML, Garcia Latorre EA, Reyes Maldonado E, Galindo Delgado P, Mejia Arangure JM, Alaez Verson C. Profiling FLT3 Mutations in Mexican Acute Myeloid Leukemia Pediatric Patients: Impact on Overall Survival. Front Pediatr. 2020; 8:586.

Gonzalez-Dominguez CA, Raya-Trigueros A, Manrique-Hernandez S, Gonzalez Jaimes A, Salinas-Marin R, Molina-Garay C, Carrillo-Sanchez K, Jimenez-Olivares M, Dehesa-Caballero C, Alaez-Verson C, Martinez-Duncker I. Identification through exome sequencing of the first PMM2-CDG individual of Mexican mestizo origin. Mol Genet Metab Rep. 2020 Dec; 25:100637.

Mariscal-Mendizabal LF, Sevilla-Montoya R, Martinez-Garcia AJ, Alaez-Verson C, Monroy-Munoz IE, Perez-Duran J, Ceron-Albarran JA, Carrillo-Sanchez K, Molina-Garay C, Jimenez-Olivares M, Aguinaga-Rios M. Clinical and genetic description of patients with prenatally identified cardiac tumors. Prenat Diagn. 2019 Jul 10; 39:.

Hernandez-Pedro N, Soca-Chafre G, Alaez-Verson C, Carrillo-Sanchez K, Aviles-Salas A, Vergara E, Arrieta O. Mutational profile by targeted next generation sequencing of non-small cell lung cancer in the Mexican population. Salud Publica de Mexico. 2019 May-Jun; 11(3):308-317.

Staines Boone AT, Chinn IK, Alaez-Verson C, Yamazaki-Nakashimada MA, Carrillo-Sanchez K, Garcia-Cruz MLH, Poli MC, Gonzalez Serrano ME, Medina Torres EA, Muzquiz Zermeno D, Forbes LR, Espinosa-Rosales FJ, Espinosa-Padilla SE, Orange JS, Lugo Reyes SO. Failing to Make Ends Meet: The Broad Clinical Spectrum of DNA Ligase IV Deficiency. Case Series and Review of the Literature. Front Pediatr. 2019; 6:426.

Fernandez-Lainez C, Alaez-Verson C, Ibarra-Gonzalez I, Enriquez-Flores S, Carrillo-Sanchez K, Flores-Lagunes L, Guillen-Lopez S, Belmont-Martinez L, Vela-Amieva M. In silico prediction of the pathogenic effect of a novel variant of BCKDHA leading to classical maple syrup urine disease identified using clinical exome sequencing. Clin Chim Acta. 2018 Aug; 483:33-38.

Soca-Chafre G., Hernández-Pedro N., Aviles-Salas A., Alaez Versón C., Carrillo Sánchez K., Cardona AF., Avila-Moreno F., Barrios-Bernal P., Flores-Estrada D., Arrieta O.. Targeted next generation sequencing identified a high frequency genetic mutated profile in wood smoke exposure-related lung adenocarcinoma patients. Oncotarget. 2018 2018; 9(55):None.

Ruiz-Contreras AE, Roman-Lopez TV, Caballero-Sanchez U, Rosas-Escobar CB, Ortega-Mora EI, Barrera-Tlapa MA, Romero-Hidalgo S, Carrillo-Sanchez K, Hernandez-Morales S, Vadillo-Ortega F, Gonzalez-Barrios JA, Mendez-Diaz M, Prospero-Garcia O. Because difficulty is not the same for everyone: the impact of complexity in working memory is associated with cannabinoid 1 receptor genetic variation in young adults. Memory. 2016 Apr 25; 35:1-9.

Garza-Veloz I, Martinez-Fierro ML, Jaime-Perez JC, Carrillo-Sanchez K, Ramos-Del Hoyo MG, Lugo-Trampe A, Rojas-Martinez A, Gutierrez-Aguirre CH, Gonzalez-Llano O, Salazar-Riojas R, Hidalgo-Miranda A, Gomez-Almaguer D, Ortiz-Lopez R. Identification of differentially expressed genes associated with prognosis of B acute lymphoblastic leukemia. Dis Markers. 2015; 2015:828145.

Martinez-Fierro ML, Garza-Veloz I, Carrillo-Sanchez K, Martinez-Gaytan V, Cortes-Flores R, Ochoa-Torres MA, Guerrero GG, Rodriguez-Sanchez IP, Cancela-Murrieta CO, Zamudio-Osuna M, Badillo-Almaraz JI, Castruita-De la Rosa C. Expression levels of seven candidate genes in human peripheral blood mononuclear cells and their association with preeclampsia. Hypertens Pregnancy. 2014 May; 33(2):191-203.

Ruiz-Contreras AE, Carrillo-Sanchez K, Ortega-Mora I, Barrera-Tlapa MA, Roman-Lopez TV, Rosas-Escobar CB, Flores-Barrera L, Caballero-Sanchez U, Munoz-Torres Z, Romero-Hidalgo S, Hernandez-Morales S, Gonzalez-Barrios JA, Vadillo-Ortega F, Mendez-Diaz M, Aguilar-Roblero R, Prospero-Garcia O. Performance in working memory and attentional control is associated with the rs2180619 SNP in the CNR1 gene. Genes Brain Behav. 2013 Oct 23; 13(2):173-8.

Martinez-Hernandez A, Gutierrez-Malacatt H, Carrillo-Sanchez K, Saldana-Alvarez Y, Rojas-Ochoa A, Crespo-Solis E, Aguayo-Gonzalez A, Rosas-Lopez A, Ayala-Sanchez J, Aquino-Ortega X, Orozco L, Cordova E. Small Maf Genes Variants And Chronic Myeloid Leukaemia. Eur J Haematol. 2013 Oct 14; 92(1):35-41.

Edith A Fernández-Figueroa, Claudia Rangel-Escareño, Valeria Espinosa-Mateos, Karol Carrillo-Sánchez, Norma Salaiza-Suazo, Georgina Carrada-Figueroa, Santiago March-Mifsut, Ingeborg Becker. Disease Severity In Patients Infected With Leishmania Mexicana Relates To Il-1B. PLoS Neglected Tropical Diseases. 2012; :0-0.

Ruiz-Contreras AE, Karol Carrillo-Sánchez, Gomez-Lopez N, Vadillo-Ortega F, Hernandez-Morales S, Alessandra Carnevale, Espejel-Nunez A, Mendez-Diaz M, Prospero-Garcia O. Working memory performance in young adults is associated to the AATn polymorphism of the CNR1 gene.. Behav Brain Res. 2013 Jan 1; 236(1):62-6.

Balam-Ortiz E, Esquivel-Villarreal A, Huerta-Hernandez D, Fernandez-Lopez JC, Alfaro-Ruiz L, Munoz-Monroy O, Gutierrez R, Figueroa-Genis E, Carrillo K, Elizalde A, Hidalgo A, Rodriguez M, Urushihara M, Kobori H, Jimenez-Sanchez G. Hypercontrols in genotype-phenotype analysis reveal ancestral haplotypes associated with essential hypertension. Hypertension. 2012 Apr; 59(4):847-53.

Balam-Ortiz E, Esquivel-Villarreal A, Alfaro-Ruiz L, Carrillo K, Elizalde A, Gil T, Urushihara M, Kobori H, Jimenez-Sanchez G. Variants and haplotypes in angiotensinogen gene are associated with plasmatic angiotensinogen level in Mexican population.. Am J Med Sci. 2011 Sep; 342(3):205-11.

Ruiz-Contreras AE, Delgado-Herrera M, Garcia-Vaca PA, Almeida-Rosas GA, Soria-Rodriguez G, Soriano-Bautista A, Cadena-Valencia J, Bazan-Frias JR, Gomez-Lopez N, Espejel-Nunez A, Vadillo-Ortega F, Carrillo-Sanchez K, Verdin-Reyes JC, March-Mifsut S, Mendez-Diaz M, Prospero-Garcia O. Involvement of the AATn polymorphism of the CNR1 gene in the efficiency of procedural learning in humans. Neurosci Lett. 2011 May 2; 494(3):202-6.

Contreras AV, Monge-Cazares T, Alfaro-Ruiz L, Hernandez-Morales S, Miranda-Ortiz H, Carrillo-Sanchez K, Jimenez-Sanchez G, Silva-Zolezzi I. Resequencing, haplotype construction and identification of novel variants of CYP2D6 in Mexican Mestizos. Pharmacogenomics. 2011 May; 12(5):745-56.

Escorcia M, Carrillo-Sanchez K, March-Mifsut S, Chapa J, Lucio E, Nava GM. Impact of antigenic and genetic drift on the serologic surveillance of H5N2 avian influenza viruses.. BMC Vet Res. 2010; 6:57.