C. Galaviz-Hernández

C. López-Camarillo, L. Marchat, A. Zamorano-Carrillo, 2014, Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences.

Genomic Instability Decreases in HIV Patient by Complementary Therapy with Rosmarinus officinalis Extracts.

M. Sosa-Macías, C. Galaviz-Hernández, B. Lazalde-Ramos, 2020, Journal of medicinal food.

The D543N polymorphism of the SLC11A1/NRAMP1 gene is associated with treatment failure in male patients with pulmonary tuberculosis

Antonio Martínez, M. Sosa-Macías, C. Galaviz-Hernández, 2015, Drug metabolism and personalized therapy.

Influence of CYP1A1*2C on high triglyceride levels in female Mexican indigenous Tarahumaras.

J. Salas-Pacheco, C. E. Bailón-Soto, M. Sosa-Macías, 2014, Archives of medical research.

Transcriptomic Profiling of Adipose Tissue in Obese Women in Response to Acupuncture Catgut Embedding Therapy with Moxibustion.

C. Pérez-Plasencia, C. López-Camarillo, L. Marchat, 2016, Journal of alternative and complementary medicine.

Syncytiotrophoblast stress in early onset preeclampsia: The issues perpetuating the syndrome.

M. Sosa-Macías, C. Galaviz-Hernández, J. Gutiérrez, 2021, Placenta.

Placental SLC38A4 gene polymorphisms 1304 G > A and 292 C > T, and their association with glucose > 95 mg/dl in normal weight full-term healthy newborns.

M. Rodríguez-Moran, F. Guerrero‐Romero, M. Sosa-Macías, 2021, Boletin medico del Hospital Infantil de Mexico.

Comparative expression profiles for KiSS-1 and REN genes in preeclamptic and healthy placental tissues.

L. Marchat, J. Salas-Pacheco, I. Chairez-hernández, 2011, European journal of obstetrics, gynecology, and reproductive biology.

Population genetics of PDE4B (phosphodiesterase‐4B) in neglected Native Americans: Implications for cancer pharmacogenetics

T. O’Connor, J. Mill, R. Gilman, 2022, Clinical and translational science.

Genetic Polymorphisms Associated to Folate Transport as Predictors of Increased Risk for Acute Lymphoblastic Leukemia in Mexican Children

L. Quiñones, M. Sosa-Macías, C. Galaviz-Hernández, 2016, Front. Pharmacol..

A shortened treatment with rosemary tea (rosmarinus officinalis) instead of glucose in patients with diabetes mellitus type 2 (TSD).

M. Sosa-Macías, C. Galaviz-Hernández, B. Lazalde-Ramos, 2019, Journal of population therapeutics and clinical pharmacology = Journal de la therapeutique des populations et de la pharamcologie clinique.

Paternal Determinants in Preeclampsia

J. García-Ortiz, E. Terán, M. Sosa-Macías, 2019, Front. Physiol..

The paternal polymorphism rs5370 in the EDN1 gene decreases the risk of preeclampsia.

E. Arámbula-Meraz, M. Sosa-Macías, C. Galaviz-Hernández, 2016, Pregnancy hypertension.

Involvement of MTHFR and TPMT genes in susceptibility to childhood acute lymphoblastic leukemia (ALL) in Mexicans

J. Salas-Pacheco, C. E. Bailón-Soto, M. Sosa-Macías, 2016, Drug metabolism and personalized therapy.

Glucose-6-phosphate dehydrogenase deficiency in northern Mexico and description of a novel mutation

H. Rangel-Villalobos, E. Arámbula-Meraz, N. García-Magallanes, 2014, Journal of Genetics.

Predictive model for pregnancy- induced hypertension in mexican women

I. Osuna‐Ramírez, M. Sosa-Macías, C. Galaviz-Hernández, 2021 .

The genomic landscape of Mexican Indigenous populations brings insights into the peopling of the Americas

Deborah A. Bolnick, A. Kostic, Federico Sánchez-Quinto, 2021, Nature Communications.

Unraveling Signatures of Local Adaptation among Indigenous Groups from Mexico

Deborah A. Bolnick, A. Kostic, H. Rangel-Villalobos, 2022, Genes.

Association of ABCB1, ABCC5 and xanthine oxidase genetic polymorphisms with methotrexate adverse reactions in Mexican pediatric patients with ALL

I. Chairez-hernández, M. Sosa-Macías, C. Galaviz-Hernández, 2015, Drug metabolism and personalized therapy.

Pharmacogenetics and ethnicity: relevance for clinical implementation, clinical trials, pharmacovigilance and drug regulation in Latin America.

E. Tarazona-Santos, A. Llerena, E. Terán, 2016, Pharmacogenomics.

Influence of admixture components on CYP2C9*2 allele frequency in eight indigenous populations from Northwest Mexico

J. Licinio, H. Rangel-Villalobos, A. Llerena, 2013, The Pharmacogenomics Journal.

Micronuclei and nuclear anomalies in Mexico's indigenous population.

M. Sosa-Macías, C. Galaviz-Hernández, B. Lazalde-Ramos, 2017, Salud publica de Mexico.

SLC41A1 is the only magnesium responsive gene significantly overexpressed in placentas of preeclamptic women

M. Rodríguez-Moran, F. Guerrero‐Romero, J. Vormann, 2013, Hypertension in pregnancy.

Morbidity and mortality from cancer: experience of the State Center of Cancer from the SSA of Durango State, Mexico

M. Sosa-Macías, C. Galaviz-Hernández, V. Loera-Castañeda, 2010 .

Glucose-6-phosphate dehydrogenase deficiency in northern Mexico and description of a novel mutation

H. Rangel-Villalobos, E. Arámbula-Meraz, N. García-Magallanes, 2014, Journal of Genetics.

CYP2D6 gene polymorphisms and predicted phenotypes in eight indigenous groups from northwestern Mexico.

A. Llerena, M. Martinez-Fierro, M. Sosa-Macías, 2014, Pharmacogenomics.

Pharmacoepidemiology of psychoactive medication in adult patients in the psychiatric department of Durango General Hospital

C. Galaviz-Hernández, I. L. Asseff, V. L. Castañeda, 2011 .

The CYP2C19*2 and CYP2C19*17 Polymorphisms Influence Responses to Clozapine for the Treatment of Schizophrenia

M. Sosa-Macías, C. Galaviz-Hernández, P. C. Ghedini, 2020, Neuropsychiatric disease and treatment.

Biochemical differences in ethnic groups in Durango, Mexico.

M. Sosa-Macías, C. Galaviz-Hernández, B. Lazalde-Ramos, 2012, Ethnicity & disease.

Antiobesity and Hypoglycaemic Effects of Aqueous Extract of Ibervillea sonorae in Mice Fed a High-Fat Diet with Fructose

C. Galaviz-Hernández, N. Paniagua-Castro, G. Escalona-Cardoso, 2011, Journal of biomedicine & biotechnology.

Influence of Genetic Admixture Components on CYP3A5*3 Allele-Associated Hypertension in Amerindian Populations From Northwest Mexico

H. Rangel-Villalobos, M. Sosa-Macías, C. Galaviz-Hernández, 2020, Frontiers in Pharmacology.

Hajdu-Cheney syndrome associated with calcinosis cutis. Presentation of one case and literature review

C. Galaviz-Hernández, Martha Orozco-Quiyono, Gerardo R. Zaragoza-Arévalo, 2013 .

Effect on risk of anencephaly of gene–nutrient interactions between methylenetetrahydrofolate reductase C677T polymorphism and maternal folate, vitamin B12 and homocysteine profile

V. Borja-Aburto, M. Rodríguez-Barranco, M. Lacasaña, 2012, Public Health Nutrition.

Association of the polymorphisms 292 C>T and 1304 G>A in the SLC38A4 gene with hyperglycaemia

M. Rodríguez-Moran, F. Guerrero‐Romero, I. Chairez-hernández, 2013, Diabetes/metabolism research and reviews.

Editorial: Vascular dysfunction beyond pathological pregnancies. An international effort addressed to fill the gaps in Latin America, Volume II

A. Damiano, C. Galaviz-Hernández, C. Escudero, 2022, Frontiers in Physiology.

Editorial: Vascular Dysfunction Beyond Pathological Pregnancies. An International Effort Addressed to Fill the Gaps in Latin America

A. Damiano, C. Galaviz-Hernández, C. Escudero, 2019, Front. Physiol..

Preeclampsia association of placental nucleotide variations in eNOS, VEGFA, and FLT-1 genes in Latin American pregnant women.

A. Damiano, P. Ayala-Ramírez, M. Sosa-Macías, 2023, Placenta.

Methylenetetrahydrofolate reductase gene 677CT polymorphism and isolated congenital heart disease in a Mexican population.

H. Rangel-Villalobos, E. Arámbula-Meraz, C. Galaviz-Hernández, 2012, Revista espanola de cardiologia.

A new missense variant in RAB3GAP2 in a family with muscular dystrophy–short stature and defective autophagy: An expansion of the micro/Martsolf spectrum or a new phenotype?

J. Zenteno, C. Galaviz-Hernández, Arturo Hernández, 2022, American journal of medical genetics. Part A.

The CYP2C19*2 and CYP2C19*17 Polymorphisms In ﬂ uence Responses to Clozapine for the Treatment of Schizophrenia

M. Sosa-Macías, C. Galaviz-Hernández, P. C. Ghedini, 2020 .

Whole mitogenome analysis highlights demographic history and shared connections among distal Indigenous groups of Mexico Complete mitogenome sequencing from 60 Mexican Native American groups

S. Flores-Martínez, H. García-Ortiz, A. Martinez-Hernandez, 2023, bioRxiv.

F. Guerrero‐Romero, L. Marchat, M. Sosa-Macías, 2018, Drug metabolism and personalized therapy.

Methylenetetrahydrofolate reductase gene polymorphisms and the risk of anencephaly in Mexico.

V. Borja-Aburto, M. Lacasaña, C. Galaviz-Hernández, 2007, Molecular human reproduction.

Haplotype analysis of TGF-β1 gene in a preeclamptic population of northern Mexico.

A. Sandoval-Carrillo, J. Salas-Pacheco, C. Galaviz-Hernández, 2014, Pregnancy hypertension.

eoPred: predicting the placental phenotype of early-onset preeclampsia using public DNA methylation data

C. Galaviz-Hernández, A. Inkster, V. Yuan, 2023, Frontiers in genetics.

[Probable association between preeclampsia/eclampsia and paternal age: a pilot study].

C. Galaviz-Hernández, J. Gutiérrez-Salinas, M. D. C. Chima-Galán, 2011, Ginecologia y obstetricia de Mexico.

Forensic parameters for 15 STRs in eight Amerindian populations from the north and west of Mexico.

H. Rangel-Villalobos, J. Muñóz-Valle, V. Martínez-Sevilla, 2013, Forensic science international. Genetics.