Validation of a semiconductor next‐generation sequencing assay for the clinical genetic screening of CFTR - Trujillano - 2015 - Molecular Genetics & Genomic Medicine - Wiley Online Library
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An ancient founder mutation located between ROBO1 and ROBO2 is responsible for increased microtia risk in Amerindigenous populations | PNAS
Lorena OROZCO | Senior Researcher | PhD | Instituto Nacional de Medicina Genómica, Mexico City | Medical Research | Research profile
Genotyping, sequencing and analysis of 140,000 adults from the Mexico City Prospective Study | bioRxiv
PDF) Population history and gene divergence in Native Mexicans inferred from 76 human exomes: Supplementary Figures and Tables
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Phenotypic Variability of an Inherited Pathogenic Variant in CIC Gene: A New Case Report in Two-Generation Family and Literature
Exomic variants of an elderly cohort of Brazilians in the ABraOM database - Naslavsky - 2017 - Human Mutation - Wiley Online Library
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Frontiers | Genotyping Squamous Cell Lung Carcinoma in Colombia (Geno1.1-CLICaP)
The genetic architecture of type 2 diabetes | Nature
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Genotyping, sequencing and analysis of 140,000 adults from the Mexico City Prospective Study | bioRxiv
Leveraging Big Data to Fuel Precision Health Research
Exome sequencing as the first‐tier test for pediatric respiratory diseases: A single‐center study - Hao - 2021 - Human Mutation - Wiley Online Library
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
Frontiers | Clinical and Genetic Characteristics of IKZF1 Mutation in Chinese Children With B-Cell Acute Lymphoblastic Leukemia
Geographic variation of ancestry sub-components in Latin American... | Download Scientific Diagram
Analysis of protein-coding genetic variation in 60,706 humans | Nature
A structural variation reference for medical and population genetics | Nature
Whole Genome Sequence, Variant Discovery and Annotation in Mapuche-Huilliche Native South Americans | Scientific Reports
PDF) Genotyping, sequencing and analysis of 140,000 adults from the Mexico City Prospective Study
Frontiers | Molecular identification of T-box transcription factor 6 and prognostic assessment in patients with congenital scoliosis: A single-center study
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Genotype imputation performance of three reference panels using African ancestry individuals | SpringerLink
Times since admixture estimated using GLOBETROTTER. a Top: frequency... | Download Scientific Diagram
Cancers | Free Full-Text | Comprehensive Analysis of Germline Variants in Mexican Patients with Hereditary Breast and Ovarian Cancer Susceptibility
Novel HLA-DRB1 alleles contribute risk for disease susceptibility in primary biliary cholangitis - ScienceDirect