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Omics-based biomarkers: current status and potential use in the clinic

Boletín Médico del Hospital Infantil de México, 2017-05, Vol.74 (3), p.219-226

2017

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Severe congenital neutropenia due to G6PC3 deficiency: Case series of five patients and literature review

Scandinavian journal of immunology, 2022-04, Vol.95 (4), p.e13136-n/a

2022

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Classic infantile‐onset Pompe disease with histopathological neurologic findings linked to a novel GAA gene 4 bp deletion: A case study

Molecular genetics & genomic medicine, 2022-07, Vol.10 (7), p.e1957-n/a

2022

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Multiple mechanisms contribute to leakiness of a frameshift mutation in canine cone-rod dystrophy

PloS one, 2012-12, Vol.7 (12), p.e51598-e51598

2012

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High penetrance of EDA pathogenic variants in Mexican female carriers with hypohidrotic ectodermal dysplasia

Dermatologica Sinica, 2020-07, Vol.38 (3), p.172-175

2020

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Exploring single nucleotide polymorphisms previously related to obesity and metabolic traits in pediatric-onset type 2 diabetes

Acta diabetologica, 2017-07, Vol.54 (7), p.653-662

2017

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Disruption of chromosome 11 in canine fibrosarcomas highlights an unusual variability of CDKN2B in dogs

BMC veterinary research, 2009-07, Vol.5 (1), p.27-27

2009

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A single drug-resistance mutation in HSV-1 UL52 primase points to a difference between two helicase–primase inhibitors in their mode of interaction with the antiviral target

Journal of antimicrobial chemotherapy, 2008-05, Vol.61 (5), p.1044-1047

2008

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The Finnish lapphund retinal atrophy locus maps to the centromeric region of CFA9

BMC veterinary research, 2007-07, Vol.3 (1), p.14-14

2007

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Phenotypic variation and genotype-phenotype discordance in canine cone-rod dystrophy with an RPGRIP1 mutation

Molecular vision, 2009-11, Vol.15, p.2287-2305

2009

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DLA class II alleles and haplotypes are associated with risk for and protection from chronic hepatitis in the English Springer spaniel

PloS one, 2012-08, Vol.7 (8), p.e42584-e42584

2012

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Genetic structure of three Native Mexican communities based on mtDNA haplogroups, and ABO and Rh blood group systems

Revista de investigacion clinica, 2011-11, Vol.63 (6), p.614-620

2011

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Identification of human miR‐1839‐5p by small RNA‐seq, a miRNA enriched in neoplastic tissues

The journal of gene medicine, 2019-10, Vol.21 (10), p.e3117-n/a

2019

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Female child with Fabry disease and two other genetic diseases, spherocytosis, and congenital hypothyroidism, A case report

Molecular genetics and metabolism, 2021-02, Vol.132 (2), p.S24-S24

2021

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A novel nonsense variant associated with Danon disease in a pediatric male: A case report

Molecular genetics and metabolism, 2021-02, Vol.132 (2), p.S23

2021

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A novel nonsense LAMP2 variant associated with Danon disease in a pediatric male: A case report

Molecular genetics and metabolism, 2021-02, Vol.132 (2), p.S23-S23

2021

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Fenotipo de miopatía congénita central core autosómica dominante con alteraciones del gen RYR1. A propósito de un caso clínico

Acta pediátrica de México, 2023-02, Vol.43 (6), p.353-357

2023

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Omics-based biomarkers: current status and potential use in the clinic

Boletín Médico Del Hospital Infantil de México (English Edition), 2017-05, Vol.74 (3), p.219-226

2017

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Molecular genetics of canine progressive retinal atrophy

Aguirre Hernández, Jesús

2003

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Extended Microsatellite Set for Linkage Mapping in the Domestic Dog

The Journal of heredity, 2007-05, Vol.98 (3), p.221-231

2007

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Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping

PLoS genetics, 2011-10, Vol.7 (10), p.e1002316-e1002316

2011

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Importancia del diagnóstico de mutaciones en el gen de la conexina 26 en el manejo integral de la sordera congénita no sindrómica

Boletín médico del Hospital Infantil de México, 2013-04, Vol.70 (2), p.89-97

2013

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Stabilization of Affine Systems with Polytopic Control Value Sets

Journal of dynamical and control systems, 2023-10, Vol.29 (4), p.1929-1941

2023

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Geometry and dynamics of the Schur–Cohn stability algorithm for one variable polynomials

Mathematics of control, signals, and systems, 2019-12, Vol.31 (4), p.545-587

2019

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Global product structure for a space of special matrices

Boletín de la Sociedad Matemática Mexicana, 2019-03, Vol.25 (1), p.77-85

2019

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Omics-based biomarkers: current status and potential use in the clinic

Severe congenital neutropenia due to G6PC3 deficiency: Case series of five patients and literature review

Classic infantile‐onset Pompe disease with histopathological neurologic findings linked to a novel GAA gene 4 bp deletion: A case study

Multiple mechanisms contribute to leakiness of a frameshift mutation in canine cone-rod dystrophy

High penetrance of EDA pathogenic variants in Mexican female carriers with hypohidrotic ectodermal dysplasia

Exploring single nucleotide polymorphisms previously related to obesity and metabolic traits in pediatric-onset type 2 diabetes

Disruption of chromosome 11 in canine fibrosarcomas highlights an unusual variability of CDKN2B in dogs

A single drug-resistance mutation in HSV-1 UL52 primase points to a difference between two helicase–primase inhibitors in their mode of interaction with the antiviral target

The Finnish lapphund retinal atrophy locus maps to the centromeric region of CFA9

Phenotypic variation and genotype-phenotype discordance in canine cone-rod dystrophy with an RPGRIP1 mutation

DLA class II alleles and haplotypes are associated with risk for and protection from chronic hepatitis in the English Springer spaniel

Genetic structure of three Native Mexican communities based on mtDNA haplogroups, and ABO and Rh blood group systems

Identification of human miR‐1839‐5p by small RNA‐seq, a miRNA enriched in neoplastic tissues

Female child with Fabry disease and two other genetic diseases, spherocytosis, and congenital hypothyroidism, A case report

A novel nonsense variant associated with Danon disease in a pediatric male: A case report

A novel nonsense LAMP2 variant associated with Danon disease in a pediatric male: A case report

Fenotipo de miopatía congénita central core autosómica dominante con alteraciones del gen RYR1. A propósito de un caso clínico

Omics-based biomarkers: current status and potential use in the clinic

Molecular genetics of canine progressive retinal atrophy

Extended Microsatellite Set for Linkage Mapping in the Domestic Dog

Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping

Importancia del diagnóstico de mutaciones en el gen de la conexina 26 en el manejo integral de la sordera congénita no sindrómica

Stabilization of Affine Systems with Polytopic Control Value Sets

Geometry and dynamics of the Schur–Cohn stability algorithm for one variable polynomials

Global product structure for a space of special matrices

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