Author details

Full Name

AngÃ©lica MartÃnez-HernÃ¡ndez

Affiliation

ORCID

Career Start Year

2011

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36862244	The role of single nucleotide variant rs3819817 of the Histidine Ammonia-Lyase gene and 25-Hydroxyvitamin D on bone mineral density, adiposity markers, and skin pigmentation, in Mexican population.		2023
35802478	Brain radiotoxicity-related 15CAcBRT gene expression signature predicts survival prognosis of glioblastoma patients.	Neuro-Oncology	2023
37627507	Total Antioxidant Capacity in Obese and Non-Obese Subjects and Its Association with Anthropo-Metabolic Markers: Systematic Review and Meta-Analysis.		2023
36968598	Single nucleotide variants in microRNA biosynthesis genes in Mexican individuals.		2023
37144655	DNA Methylation Remodeling after Bariatric Surgery Correlates with Clinical Parameters.		2023
36631885	Frequent copy number variants in a cohort of Mexican-Mestizo individuals.		2023
36535927	DNA methylation and gene expression analysis in adipose tissue to identify new loci associated with T2D development in obesity.		2022
35669185	Exome Sequencing Data Analysis and a Case-Control Study in Mexican Population Reveals Lipid Trait Associations of New and Known Genetic Variants in Dyslipidemia-Associated Loci.	Frontiers in Genetics	2022
36445929	Kazak mitochondrial genomes provide insights into the human population history of Central Eurasia.	PLoS One	2022
36316743	Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review.	BMC Medical Genomics	2022
36714151	Ancestry-dependent genetic structure of the Xq28 risk haplotype in the Mexican population and its association with childhood-onset systemic lupus erythematosus.		2022
36553518	Unraveling Signatures of Local Adaptation among Indigenous Groups from Mexico.		2022
34642312	The genomic landscape of Mexican Indigenous populations brings insights into the peopling of the Americas.	Nature Communications	2021
34108472	Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.	Nat Commun	2021
34193236	Two novel variants in DYRK1B causative of AOMS3: expanding the clinical spectrum.	Orphanet Journal of Rare Diseases	2021
33981035	Reconstruction of ancient microbial genomes from the human gut.	Nature	2021
34388523	The L125F MATE1 variant enriched in populations of Amerindian origin is associated with increased plasma levels of metformin and lactate.		2021
34699309	Alterations of DNA methylation during adipogenesis differentiation of mesenchymal stem cells isolated from adipose tissue of patients with obesity is associated with type 2 diabetes.	Adipocyte	2021
32272872	Towards precision medicine: defining and characterizing adipose tissue dysfunction to identify early immunometabolic risk in symptom-free adults from the GEMM family study.	Adipocyte	2020
31907821	Association between vitamin D deficiency and common variants of Vitamin D binding protein gene among Mexican Mestizo and indigenous postmenopausal women.	Journal of Endocrinological Investigation	2020
32183766	Metabolic syndrome in indigenous communities in Mexico: a descriptive and cross-sectional study.	BMC Public Health	2020
31118044	Next-generation sequencing for identifying a novel/de novo pathogenic variant in a Mexican patient with cystic fibrosis: a case report.	BMC Medical Genomics	2019
31649539	Variation in Actionable Pharmacogenetic Markers in Natives and Mestizos From Mexico.	Frontiers in Pharmacology	2019
31790415	Genetic variability of five ADRB2 polymorphisms among Mexican Amerindian ethnicities and the Mestizo population.	PLoS ONE	2019
31557780	Association between APOE polymorphisms and lipid profile in Mexican Amerindian population.	Molecular genetics & genomic medicine	2019
30010053	A homozygous CEP57 c.915_925dupCAATGTTCAGC mutation in a patient with mosaic variegated aneuploidy syndrome with rhizomelic shortening in the upper and lower limbs and a narrow thorax.	European Journal of Medical Genetics	2019
30808941	Influence of obesity, parental history of diabetes, and genes in type 2 diabetes: A case-control study.	Scientific Reports	2019
31434951	Catalytically Impaired TYK2 Variants are Protective Against Childhood- and Adult-Onset Systemic Lupus Erythematosus in Mexicans.	Scientific Reports	2019
31118516	Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.	Nature	2019
29466957	Altered DNA methylation in liver and adipose tissues derived from individuals with obesity and type 2 diabetes.	BMC Medical Genetics	2018
30400254	Deep Multi-OMICs and Multi-Tissue Characterization in a Pre- and Postprandial State in Human Volunteers: The GEMM Family Study Research Design.	Genes (Basel)	2018
30150596	Association between Vitamin D Deficiency and Single Nucleotide Polymorphisms in the Vitamin D Receptor and GC Genes and Analysis of Their Distribution in Mexican Postmenopausal Women.	Nutrients	2018
30464349	[Programa de detecciÃ³n del alelo APOE-E4 en adultos mayores mexicanos con deterioro cognitivo].	Gaceta Medica de Mexico	2018
30176313	Gene variants in AKT1, GCKR and SOCS3 are differentially associated with metabolic traits in Mexican Amerindians and Mestizos.	Gene	2018
29111561	GSTT1 and GSTM1 null variants in Mestizo and Amerindian populations from northwestern Mexico and a literature review.	Genetics and Molecular Biology	2017
28838971	A Loss-of-Function Splice Acceptor Variant in <i>IGF2</i> Is Protective for Type 2 Diabetes.	Diabetes	2017
29044207	Demographic history and biologically relevant genetic variation of Native Mexicans inferred from whole-genome sequencing.	Nature Communications	2017
27649570	Heterogenous Distribution of MTHFR Gene Variants among Mestizos and Diverse Amerindian Groups from Mexico.	PLoS ONE	2016
27221928	The rs61764370 Functional Variant in the KRAS Oncogene is Associated with Chronic Myeloid Leukemia Risk in Women.		2016
26148929	Circulating levels of miR-150 are associated with poorer outcomes of A/H1N1 infection.	Experimental and Molecular Pathology	2015
25933176	Association of HMOX1 and NQO1 Polymorphisms with Metabolic Syndrome Components.	PLoS ONE	2015
26039680	NFE2L2 Gene Variants and Arsenic Susceptibility: A Lymphoblastoid Model.	Journal of Toxicology and Environmental Health - Part A: Current Issues	2015
24516582	The NRF2-KEAP1 pathway is an early responsive gene network in arsenic exposed lymphoblastoid cells.	PLoS ONE	2014
24915262	Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population.	JAMA	2014
24118457	Small MAF genes variants and chronic myeloid leukemia.	European Journal of Haematology	2014
22338608	HMOX1 promoter (GT)n polymorphim is associated with childhood-onset systemic lupus erythematosus but not with juvenile rheumatoid arthritis in a Mexican population.	Clinical and Experimental Rheumatology	2012
22364041	NFE2L2 gene variants and susceptibility to childhood-onset asthma.	Revista de Investigacion Clinica	2011