Leopoldo A. Montano-Garcia

Mexico City, DIF, Mexico

Last Updated: 09/26/2026

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Found 9 publications

Single-nucleus and spatial landscape of the sub-ventricular zone in human glioblastoma.

Single-nucleus and spatial landscape of the sub-ventricular zone in human glioblastoma.

Journal: Cell reports

Published: June 05, 2024

Dissecting Intra-tumor Heterogeneity in the Glioblastoma Microenvironment Using Fluorescence-Guided Multiple Sampling.

Dissecting Intra-tumor Heterogeneity in the Glioblastoma Microenvironment Using Fluorescence-Guided Multiple Sampling.

Journal: Molecular cancer research : MCR

Published: January 23, 2023

AUTOSOMAL DOMINANT MÜLLER CELL SHEEN DYSTROPHY: Clinical, Histopathologic, and Genetic Assessment in an Extended Family With Long Follow-Up.

AUTOSOMAL DOMINANT MÜLLER CELL SHEEN DYSTROPHY: Clinical, Histopathologic, and Genetic Assessment in an Extended Family With Long Follow-Up.

Journal: Retina (Philadelphia, Pa.)

Published: February 07, 2022

Clinical, histopathological, and in silico pathogenicity analyses in a pedigree with familial amyloidosis of the Finnish type (Meretoja syndrome) caused by a novel gelsolin mutation.

Clinical, histopathological, and in silico pathogenicity analyses in a pedigree with familial amyloidosis of the Finnish type (Meretoja syndrome) caused by a novel gelsolin mutation.

Journal: Molecular vision

Published: February 19, 2020

Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next-generation sequencing.

Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next-generation sequencing.

Journal: Molecular genetics & genomic medicine

Published: September 07, 2019

A recurrent de novo mutation in ATP1A3 gene in a Mexican patient with alternating hemiplegia of childhood detected by massively parallel sequencing.

A recurrent de novo mutation in ATP1A3 gene in a Mexican patient with alternating hemiplegia of childhood detected by massively parallel sequencing.

Journal: Boletin medico del Hospital Infantil de Mexico

Published: January 19, 2019

Identification of novel pathogenic variants and novel gene-phenotype correlations in Mexican subjects with microphthalmia and/or anophthalmia by next-generation sequencing.

Identification of novel pathogenic variants and novel gene-phenotype correlations in Mexican subjects with microphthalmia and/or anophthalmia by next-generation sequencing.

Journal: Journal of human genetics

Published: May 29, 2018

Next generation sequencing-based molecular diagnosis in familial congenital cataract expands the mutational spectrum in known congenital cataract genes.

Next generation sequencing-based molecular diagnosis in familial congenital cataract expands the mutational spectrum in known congenital cataract genes.

Journal: American journal of medical genetics. Part A

Published: February 09, 2018

The clinical implications of molecular monitoring and analyses of inherited retinal diseases.

The clinical implications of molecular monitoring and analyses of inherited retinal diseases.

Journal: Expert review of molecular diagnostics

Published: September 26, 2017

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Last Updated: 09/26/2026