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Leopoldo A. García‐Montaño
Observed names:
García-Montaño, Leopoldo A,
Leopoldo A Garcia-Montaño,
Leopoldo A García-Montaño,
Leopoldo A. García-Montaño
Institutions:
UNM Comprehensive Cancer Center,
University of New Mexico Health Sciences Center
Observed institutions:
University of New Mexico,
Instituto Tecnológico de Oaxaca,
Tecnológico Nacional de México,
Institute of Ophthalmology,
UNM Comprehensive Cancer Center,
University of New Mexico Health Sciences Center
show all 6
ORCID:
0000-0002-2972-7823
Observed ORCID:
0000-0002-2972-7823
OpenAlex ID:
A5020908571
Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next‐generation sequencing
2019
·
Juan C. Zenteno
, Leopoldo A. García‐Montaño
, et al.
·
Molecular Genetics & Genomic Medicine
·
53
PDF
Dissecting Intra-tumor Heterogeneity in the Glioblastoma Microenvironment Using Fluorescence-Guided Multiple Sampling
2023
·
Leopoldo A. García-Montaño
, Yamhilette Licón-Muñoz
, et al.
·
Molecular Cancer Research
·
30
PDF
Next generation sequencing‐based molecular diagnosis in familial congenital cataract expands the mutational spectrum in known congenital cataract genes
2018
·
Mirena C. Astiazarán
, Leopoldo A. García‐Montaño
, et al.
·
American Journal of Medical Genetics Part A
·
28
Identification of novel pathogenic variants and novel gene-phenotype correlations in Mexican subjects with microphthalmia and/or anophthalmia by next-generation sequencing
2018
·
Diana Matías-Pérez
, Leopoldo A. García-Montaño
, et al.
·
Journal of Human Genetics
·
28
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.
2020
·
Jesus Cabral-Macias
, Leopoldo A Garcia-Montaño
, et al.
·
PubMed Central
·
15
PDF
Single-nucleus and spatial landscape of the sub-ventricular zone in human glioblastoma
2025
·
Yamhilette Licón-Muñoz
, Vanessa Avalos
, et al.
·
Cell Reports
·
12
The clinical implications of molecular monitoring and analyses of inherited retinal diseases
2017
·
Oscar F. Chacón-Camacho
, Leopoldo A. García-Montaño
, et al.
·
Expert Review of Molecular Diagnostics
·
8
Mutación de novo recurrente en el gen ATP1A3 en una paciente mexicana con hemiplejia alternante de la infancia detectada por secuenciación masiva en paralelo
2019
·
Carolina I. Galaz-Montoya
, Sofia Alcaraz-Estrada
, et al.
·
Boletín Médico del Hospital Infantil de México
·
4
PDF
AUTOSOMAL DOMINANT MÜLLER CELL SHEEN DYSTROPHY: Clinical, Histopathologic, and Genetic Assessment in an Extended Family With Long Follow-Up
2022
·
José Dalma-Weiszhausz
, Oscar Chacón-Camacho
, et al.
·
Retina
·
2
A recurrent de novo mutation in ATP1A3 gene in a Mexican patient with alternating hemiplegia of childhood detected by massively parallel sequencing
2019
·
Carolina I. Galaz-Montoya
, Sofia Alcaraz-Estrada
, et al.
·
Boletín Médico Del Hospital Infantil de México (English Edition)
·
1
PDF
Csig-28. Dissecting the Functional Impairment of Wild-type P53 in Human Glioblastoma
2024
·
Leopoldo A García-Montaño
, Yamhilette Licón Muñoz
, et al.
·
Neuro-Oncology
PDF
Abstract 544: Dissecting the functional impairment of wild-type Tp53 in human glioblastoma
2023
·
Leopoldo A. García-Montaño
, Yamhilette Licón Muñoz
, et al.
·
Cancer Research
Panel-based next generation sequencing reveals extensive locus and allelic heterogeneity underlying inherited retinal degenerations in Mexican population
2019
·
Juan Carlos Zenteno
, Leopoldo A. García‐Montaño
, et al.
·
Investigative Ophthalmology & Visual Science
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Works count:
14
Citation count:
181
H-index:
7
I10-index:
6
Year
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