E. Mendoza-Caamal

发表

Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

Tanya M. Teslovich, Anne W. Ndungu, Anthony J. Payne, 2019, Nature.

Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

Tanya M. Teslovich, Anne W. Ndungu, Anthony J. Payne, 2018, bioRxiv.

Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population.

Amy L. Williams, T. Fennell, S. Gabriel, 2014, JAMA.

Correction: ERBIN deficiency links STAT3 and TGF-β pathway defects with atopy in humans

J. Hughes, J. McElwee, J. Lyons, 2017, The Journal of experimental medicine.

ERBIN deficiency links STAT3 and TGF-β pathway defects with atopy in humans

J. Hughes, J. McElwee, Yuan Zhang, 2017, The Journal of experimental medicine.

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

Y. J. Kim, Kristin A. Maloney, C. Gieger, 2020, Nature Communications.

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

L. Orozco, H. García-Ortiz, A. Martinez-Hernandez, 2022, Frontiers in Genetics.

Two novel variants in DYRK1B causative of AOMS3: expanding the clinical spectrum

C. Aguilar-Salinas, L. Orozco, I. Ilizaliturri-Flores, 2020, Orphanet Journal of Rare Diseases.

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.

Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico

Tanya M. Teslovich, Amy L. Williams, Ian C. Smith, 2013, Nature.

Unraveling Signatures of Local Adaptation among Indigenous Groups from Mexico

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

Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes

Dajiang J. Liu, Ryan W. Kim, May E. Montasser, 2021, The American Journal of Human Genetics.

Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes

Dajiang J. Liu, Ryan W. Kim, May E. Montasser, 2020, bioRxiv.

A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes

Rachel G Liao, J. Lane, C. Hartl, 2017, Diabetes.

Genomics of a pediatric ovarian fibrosarcoma. Association with the DICER1 syndrome

J. Meléndez-Zajgla, V. Maldonado, Nayeli Belem Gabiño, 2018, Scientific Reports.

Metabolic syndrome in indigenous communities in Mexico: a descriptive and cross-sectional study

L. Orozco, H. García-Ortiz, A. Martinez-Hernandez, 2020, BMC Public Health.

Genetic variability of five ADRB2 polymorphisms among Mexican Amerindian ethnicities and the Mestizo population

L. Orozco, H. García-Ortiz, A. Martinez-Hernandez, 2019, PloS one.

The genetic era of childhood cancer: Identification of high‐risk patients and germline sequencing approaches

J. Meléndez-Zajgla, E. Mendoza-Caamal, M. Zapata-Tárres, 2023, Annals of human genetics.

Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms

Nicholette D. Palmer, Yan V. Sun, M. Fornage, 2017, Cell.

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

L. Orozco, H. García-Ortiz, A. Martinez-Hernandez, 2021, Adipocyte.

Next-generation sequencing for identifying a novel/de novo pathogenic variant in a Mexican patient with cystic fibrosis: a case report

L. Orozco, H. García-Ortiz, A. Martinez-Hernandez, 2019, BMC Medical Genomics.

Gene variants in AKT1, GCKR and SOCS3 are differentially associated with metabolic traits in Mexican Amerindians and Mestizos.

L. Orozco, H. García-Ortiz, A. Martinez-Hernandez, 2018, Gene.

Next-generation sequencing for identifying a novel/de novo pathogenic variant in a Mexican patient with cystic fibrosis: a case report

L. Orozco, H. García-Ortiz, A. Martinez-Hernandez, 2019, BMC Medical Genomics.

Genomics of a pediatric ovarian fibrosarcoma. Association with the DICER1 syndrome

J. Meléndez-Zajgla, V. Maldonado, Nayeli Belem Gabiño, 2018, Scientific Reports.

Genetic Distribution of Five Spinocerebellar Ataxia Microsatellite Loci in Mexican Native American Populations and Its Impact on Contemporary Mestizo Populations

L. Orozco, L. Velázquez-Pérez, B. Cisneros, 2022, Genes.

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.

Heterogenous Distribution of MTHFR Gene Variants among Mestizos and Diverse Amerindian Groups from Mexico

J. Fernández-López, L. Orozco, H. García-Ortiz, 2016, PloS one.

Gene variants in AKT1, GCKR and SOCS3 are differentially associated with metabolic traits in Mexican Amerindians and Mestizos.

L. Orozco, H. García-Ortiz, A. Martinez-Hernandez, 2018, Gene.

Origin of the myotonic dystrophy type 1 mutation in Mexican population and influence of Amerindian ancestry on CTG repeat allelic distribution

O. Hernández-Hernández, E. Mendoza-Caamal, Y. Tapia-Guerrero, 2017, Neuromuscular Disorders.

IKZF1plus is a frequent biomarker of adverse prognosis in Mexican pediatric patients with B-acute lymphoblastic leukemia

J. Mejía-Aranguré, E. Mendoza-Caamal, S. Jiménez-Morales, 2024, Frontiers in oncology.

Effect of the Complex Allele p.[Ile148Thr;Ile1023_Val1024del] in Cystic Fibrosis and Tracing of a Founder Effect in Mexican Families

H. García-Ortiz, A. Martinez-Hernandez, F. Barajas-Olmos, 2024, Life.

Exome Sequence Data of Eight SLC Transporters Reveal That SLC22A1 and SLC22A3 Variants Alter Metformin Pharmacokinetics and Glycemic Control

H. García-Ortiz, A. Martinez-Hernandez, F. Barajas-Olmos, 2024, Pharmaceuticals.