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Bioinformatic Analysis of Gene Variants from Gastroschisis Recurrence Identifies Multiple Novel Pathogenetic Pathways: Implication for the Closure of the Ventral Body Wall

International journal of molecular sciences, 2019-05, Vol.20 (9), p.2295

2019

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An Autosomal Recessive Syndrome of Joint Contractures, Muscular Atrophy, Microcytic Anemia, and Panniculitis-Associated Lipodystrophy

The journal of clinical endocrinology and metabolism, 2010-09, Vol.95 (9), p.E58-E63

2010

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Mitochondrial dysfunction: The pathological link between psoriasis and insulin resistance?

Journal of the European Academy of Dermatology and Venereology, 2023-02, Vol.37 (2), p.340-347

2023

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PSMB8 Encoding the β5i Proteasome Subunit Is Mutated in Joint Contractures, Muscle Atrophy, Microcytic Anemia, and Panniculitis-Induced Lipodystrophy Syndrome

American journal of human genetics, 2010-12, Vol.87 (6), p.866-872

2010

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PSMB8 Encoding the beta 5i Proteasome Subunit Is Mutated in Joint Contractures, Muscle Atrophy, Microcytic Anemia, and Panniculitis-Induced Lipodystrophy Syndrome

American journal of human genetics, 2010-12, Vol.87 (6), p.866-872

2010

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Molecular genetic diagnosis by next-generation sequencing in a cohort of Mexican patients with haemophilia and report of novel variants

Blood cells, molecules, & diseases, 2020-07, Vol.83, p.102423-102423, Article 102423

2020

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Plasma and urine metabolic profiles are reflective of altered beta-oxidation in non-diabetic obese subjects and patients with type 2 diabetes mellitus

Diabetology and metabolic syndrome, 2014-11, Vol.6 (1), p.129-129, Article 129

2014

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Evaluation of familial factors in a Mexican population-based setting with gastroschisis: Further evidence for an underlying genetic susceptibility

Journal of pediatric surgery, 2018-03, Vol.53 (3), p.521-524

2018

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Maternal Folic Acid Intake and Methylation Status of Genes Associated with Ventricular Septal Defects in Children: Case–Control Study

Nutrients, 2021-06, Vol.13 (6), p.2071

2021

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Hypospadias Prevalence and Trends in International Birth Defect Surveillance Systems, 1980–2010

European urology, 2019-10, Vol.76 (4), p.482-490

2019

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Whole exome sequencing identifies multiple novel candidate genes in familial gastroschisis

Molecular genetics & genomic medicine, 2020-05, Vol.8 (5), p.e1176-n/a

2020

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Reactivation of Elective Surgery During SARS-CoV-2 Pandemic: Pediatric Medically Necessary Time-Sensitive Score Implementation at a High-Complexity Pediatric Hospital

Journal of the American College of Surgeons, 2021-02, Vol.232 (2), p.225

2021

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The phenotype, psychotype and genotype of bruxism

Biomedical reports, 2018-03, Vol.8 (3), p.264-268

2018

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Optic nerve abnormalities in female-restricted Wieacker-Wolff syndrome by a novel variant in the ZC4H2 gene

Ophthalmic genetics, 2023-09, Vol.44 (5), p.1-468

2023

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Prevalence, Mortality, and Spatial Distribution of Gastroschisis in Mexico

Journal of pediatric & adolescent gynecology, 2018-06, Vol.31 (3), p.232-237

2018

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Diagnosis and treatment of benign adipocytic tumors in children

Pediatric surgery international, 2022-12, Vol.38 (12), p.2045-2051

2022

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Consistency and reproducibility in the platelet‐rich plasma preparation method: Mexican experience

International journal of laboratory hematology, 2019-12, Vol.41 (6), p.e148-e151

2019

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Congenital Heart Diseases: Genetic Risk Variants and Their Methylation Status

Genes, 2022-11, Vol.13 (11), p.2115

2022

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Ring 2 chromosome associated with failure to thrive, microcephaly and dysmorphic facial features

Gene, 2013-10, Vol.529 (1), p.65-68

2013

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Unconventional Secretion is a Major Contributor of Cancer Cell Line Secretomes

Molecular & cellular proteomics, 2013-05, Vol.12 (5), p.1046-1060

2013

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Expression profile of microRNAs in the testes of patients with Klinefelter syndrome

Scientific reports, 2020-07, Vol.10 (1), p.11470-11470, Article 11470

2020

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Whole-Exome Sequencing, Proteome Landscape, and Immune Cell Migration Patterns in a Clinical Context of Menkes Disease

Genes, 2021-05, Vol.12 (5), p.744

2021

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Familial occurrence of gastroschisis: a population-based overview on recurrence risk, sex-dependent influence, and geographical distribution

Pediatric surgery international, 2018-03, Vol.34 (3), p.277-282

2018

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Primary hypertrophic osteoarthropathy: Report of two novel genetic variants in the SLCO2A1 gene in two Mexican patients

Indian journal of dermatology, venereology, and leprology, 2018-07, Vol.84 (4), p.446-447

2018

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Genetic variants conferring susceptibility to gastroschisis: a phenomenon restricted to the interaction with the environment?

Pediatric surgery international, 2018-05, Vol.34 (5), p.505-514

2018

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Bioinformatic Analysis of Gene Variants from Gastroschisis Recurrence Identifies Multiple Novel Pathogenetic Pathways: Implication for the Closure of the Ventral Body Wall

An Autosomal Recessive Syndrome of Joint Contractures, Muscular Atrophy, Microcytic Anemia, and Panniculitis-Associated Lipodystrophy

Mitochondrial dysfunction: The pathological link between psoriasis and insulin resistance?

PSMB8 Encoding the β5i Proteasome Subunit Is Mutated in Joint Contractures, Muscle Atrophy, Microcytic Anemia, and Panniculitis-Induced Lipodystrophy Syndrome

PSMB8 Encoding the beta 5i Proteasome Subunit Is Mutated in Joint Contractures, Muscle Atrophy, Microcytic Anemia, and Panniculitis-Induced Lipodystrophy Syndrome

Molecular genetic diagnosis by next-generation sequencing in a cohort of Mexican patients with haemophilia and report of novel variants

Plasma and urine metabolic profiles are reflective of altered beta-oxidation in non-diabetic obese subjects and patients with type 2 diabetes mellitus

Evaluation of familial factors in a Mexican population-based setting with gastroschisis: Further evidence for an underlying genetic susceptibility

Maternal Folic Acid Intake and Methylation Status of Genes Associated with Ventricular Septal Defects in Children: Case–Control Study

Hypospadias Prevalence and Trends in International Birth Defect Surveillance Systems, 1980–2010

Whole exome sequencing identifies multiple novel candidate genes in familial gastroschisis

Reactivation of Elective Surgery During SARS-CoV-2 Pandemic: Pediatric Medically Necessary Time-Sensitive Score Implementation at a High-Complexity Pediatric Hospital

The phenotype, psychotype and genotype of bruxism

Optic nerve abnormalities in female-restricted Wieacker-Wolff syndrome by a novel variant in the ZC4H2 gene

Prevalence, Mortality, and Spatial Distribution of Gastroschisis in Mexico

Diagnosis and treatment of benign adipocytic tumors in children

Consistency and reproducibility in the platelet‐rich plasma preparation method: Mexican experience

Congenital Heart Diseases: Genetic Risk Variants and Their Methylation Status

Ring 2 chromosome associated with failure to thrive, microcephaly and dysmorphic facial features

Unconventional Secretion is a Major Contributor of Cancer Cell Line Secretomes

Expression profile of microRNAs in the testes of patients with Klinefelter syndrome

Whole-Exome Sequencing, Proteome Landscape, and Immune Cell Migration Patterns in a Clinical Context of Menkes Disease

Familial occurrence of gastroschisis: a population-based overview on recurrence risk, sex-dependent influence, and geographical distribution

Primary hypertrophic osteoarthropathy: Report of two novel genetic variants in the SLCO2A1 gene in two Mexican patients

Genetic variants conferring susceptibility to gastroschisis: a phenomenon restricted to the interaction with the environment?

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