| 1 | A predictive model for neoadjuvant therapy response in breast cancer | Coautor: Ibarra-González I., Nambo-Venegas R., Enríquez-Cárcamo V.I., Vela-Amieva M., et al. | 2025 | Metabolomics | WoS-id: 001427944800001
Scopus-id: 2-s2.0-85218488483
| 2 | 2 |
| 2 | Insomnia, Cognitive Impairment, or a Combination of Both, Alter Lipid Metabolism Due to Changes in Acylcarnitine Concentration in Older Persons | Coautor: Ibarra-González I., Castillo-Vazquez S.K., Palacios-González B., Vela-Amieva M., et al. | 2025 | Metabolites | WoS-id: 001516033300001
Scopus-id: 2-s2.0-105008942770
| 2 | 2 |
| 3 | Arginase deficiency in Mexico: Insights from the experience of a metabolic reference center | Coautor: Ibarra-González I., Vela-Amieva M., Fernández-Lainez C., Guillén-López S., et al. | 2025 | Molecular Genetics and Metabolism Reports | WoS-id: 001523349200002
Scopus-id: 2-s2.0-105008986736
| 0 | 0 |
| 4 | Gut microbiota changes in postmenopausal women with low bone density linked to serum amino acid metabolism | Coautor: Ibarra-González, I, Becerra-Cervera, A, Jiménez-Ortega, RF, Aparicio-Bautista, DI, et al. | 2025 | FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY | WoS-id: 001534030300001
Scopus-id: 2-s2.0-105011351117
| 1 | 1 |
| 5 | Biparental and Androgenetic Somatic Mosaicism with Presentation of Non-Syndromic Severe Neonatal Hyperinsulinemia | Coautor: Ibarra-González I., Alcántara-Ortigoza M.A., Vela-Amieva M., González-del Angel A., et al. | 2025 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | WoS-id: 001559702800001
Scopus-id: 2-s2.0-105014348926
| 0 | 0 |
| 6 | Hypogammaglobulinemia Class G Is Present in Compensated and Decompensated Patients with Propionate Defects, Independent of Their Nutritional Status | Coautor: Ibarra-González I., López-Mejía L.A., Vela-Amieva M., Guillén-López S., et al. | 2024 | Nutrients | WoS-id: 001246771800001
Scopus-id: 2-s2.0-85196589616
| 2 | 2 |
| 7 | Comparison of nutritional status and metabolic control in PKU infants with breastmilk vs infant formula in Mexico | Coautor: Ibarra-González, I, Guillén-López, S, López-Mejía, L, Vela-Amieva, M, et al. | 2024 | MOLECULAR GENETICS AND METABOLISM | WoS-id: 001282724000015
| 1 | 0 |
| 8 | Concordance Between Biochemical and Molecular Diagnosis Obtained by WES in Mexican Patients with Inborn Errors of Intermediary Metabolism: Utility for Therapeutic Management | Coautor: Ibarra-González, I, Vela-Amieva, M, Alcántara-Ortigoza, MA, González-del Angel, A, et al. | 2024 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | WoS-id: 001351261400001
Scopus-id: 2-s2.0-85208564008
| 1 | 1 |
| 9 | The BMI Z-Score and Protein Energy Ratio in Early- and Late-Diagnosed PKU Patients from a Single Reference Center in Mexico | Coautor: Ibarra-Gonzalez, Isabel, Lopez-Mejia, Lizbeth Alejandra, Fernandez-Lainez, Cynthia, Vela-Amieva, Marcela, et al. | 2023 | Nutrients | WoS-id: 000940997200001
Scopus-id: 2-s2.0-85148905619
| 2 | 2 |
| 10 | Biochemical goals at follow-up and dosage of the main drugs for inborn errors of intermediary metabolism | Coautor: Ibarra-Gonzalez, Isabel, Lopez-Mejia, Lizbeth, Guillen-Lopez, Sara, Carrillo-Nieto, Rosa Itzel, et al. | 2023 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000951351000007
Scopus-id: 2-s2.0-85150717835
| 0 | 1 |
| 11 | An early prediction model for gestational diabetes mellitus based on metabolomic biomarkers | Coautor: Ibarra-González I., Razo-Azamar M., Nambo-Venegas R., Meraz-Cruz N., et al. | 2023 | DIABETOLOGY & METABOLIC SYNDROME | WoS-id: 001000375200003
Scopus-id: 2-s2.0-85160911711
| 16 | 18 |
| 12 | A Review of Disparities and Unmet Newborn Screening Needs over 33 Years in a Cohort of Mexican Patients with Inborn Errors of Intermediary Metabolism | 1ᵉʳ autor: Ibarra-Gonzalez, I, Fernandez-Lainez, C, Vela-Amieva, M, Guillen-Lopez, S, et al. | 2023 | International Journal of Neonatal Screening | WoS-id: 001130556600001
Scopus-id: 2-s2.0-85180450425
| 11 | 10 |
| 13 | In Silico Structural Protein Evaluation of the Phenylalanine Hydroxylase p.(Tyr77His) Variant Associated with Benign Hyperphenylalaninemia as Identified through Mexican Newborn Screening | Coautor: Ibarra-González I., Vela-Amieva M., Alcántara-Ortigoza M.A., González-del Angel A., et al. | 2023 | Children-Basel | WoS-id: 001132822500001
Scopus-id: 2-s2.0-85180716992
| 0 | 0 |
| 14 | Homocystinuria: clinical characteristics of a cohort and care guidelines | Coautor: Ibarra-Gonzalez, Isabel, Guillen-Lopez, Sara, Vela-Amieva, Marcela, Fernandez-Lainez, Cynthia, et al. | 2022 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000760274500006
Scopus-id: 2-s2.0-85131104508
| 0 | 0 |
| 15 | A Longitudinal1 H NMR-Based Metabolic Profile Analysis of Urine from Hospitalized Premature Newborns Receiving Enteral and Parenteral Nutrition | Coautor: Ibarra-González I., Esturau-Escofet N., Rodríguez De San Miguel E., Vela-Amieva M., et al. | 2022 | Metabolites | WoS-id: 000778260100001
Scopus-id: 2-s2.0-85127594560
| 5 | 4 |
| 16 | Targeted Metabolomics Revealed a Sex-Dependent Signature for Metabolic Syndrome in the Mexican Population | Coautor: Ibarra-Gonzalez, Isabel, Palacios-Gonzalez, Berenice, Leon-Reyes, Guadalupe, Rivera-Paredez, Berenice, et al. | 2022 | Nutrients | WoS-id: 000857664600001
Scopus-id: 2-s2.0-85138686604
| 5 | 6 |
| 17 | Update for the diagnosis and treatment of acute hyperammonemia in patients with inborn errors of metabolism | Coautor: Ibarra-Gonzalez, Isabel, Lopez-Mejia, Lizbeth, Francisco-Revilla Estivill, Nuria, Guillen-Lopez, Sara, et al. | 2022 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000868601500005
Scopus-id: 2-s2.0-85144435373
| 1 | 1 |
| 18 | Genotypic spectrum underlying tetrahydrobiopterin metabolism defects: Experience in a single Mexican reference center | Coautor: Ibarra-Gonzalez, I., Vela-Amieva, M., Alcantara-Ortigoza, M. A., Gonzalez-Del Angel, A., et al. | 2022 | Frontiers in Genetics | WoS-id: 000877139800001
Scopus-id: 2-s2.0-85140641039
| 5 | 5 |
| 19 | Metabolic Reprogramming in SARS-CoV-2 Infection Impacts the Outcome of COVID-19 Patients | 2ᵒ autor: Ibarra-Gonzalez, Isabel, Martinez-Gomez, Laura E., Fernandez-Lainez, Cynthia, Tusie, Teresa, et al. | 2022 | FRONTIERS IN IMMUNOLOGY | WoS-id: 000880077100001
Scopus-id: 2-s2.0-85141374972
| 25 | 26 |
| 20 | Functional characterization of the p.(Gln195His) or Tainan and novel p.(Ser184Cys) or Toluca glucose-6-phosphate dehydrogenase (G6PD) gene natural variants identified through Mexican newborn screening for glucose-6-phosphate dehydrogenase deficiency | Coautor: Ibarra-González I., Alcántara-Ortigoza M.A., Hernández-Ochoa B., González-del Angel A., et al. | 2022 | CLINICAL BIOCHEMISTRY | WoS-id: 000898934500010
Scopus-id: 2-s2.0-85138041723
| 7 | 6 |
| 21 | Brief Report: Delayed Diagnosis of Treatable Inborn Errors of Metabolism in Children with Autism and Other Neurodevelopmental Disorders | 2ᵒ autor: Ibarra-González I., Márquez-Caraveo M.E., Rodríguez-Valentín R., Ramírez-García M.Á., et al. | 2021 | JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS | WoS-id: 000565469800002
Scopus-id: 2-s2.0-85090187864
| 9 | 9 |
| 22 | Abnormalities in subsets of B and T cells in Mexican patients with inborn errors of propionate metabolism: observations from a single-center case series | Coautor: Ibarra-Gonzalez, I., Medina-Torrez, E. A., Vela-Amieva, M., Galindo-Campos, L., et al. | 2021 | ALLERGOLOGIA ET IMMUNOPATHOLOGIA | WoS-id: 000619192200014
Scopus-id: 2-s2.0-85101248688
| 5 | 4 |
| 23 | Genetic spectrum and clinical early natural history of glucose-6-phosphate dehydrogenase deficiency in Mexican children detected through newborn screening | Coautor: Ibarra-González I., Vela-Amieva M., Alcántara-Ortigoza M.A., González-del Angel A., et al. | 2021 | ORPHANET JOURNAL OF RARE DISEASES | WoS-id: 000622331000001
Scopus-id: 2-s2.0-85101749732
| 8 | 7 |
| 24 | Metabolic flexibility during normal pregnancy allows appropriate adaptation during gestation independently of BMI | Coautor: Ibarra-Gonzalez, Isabel, Delgadillo-Velazquez, Jaime A., Nambo-Venegas, Rafael, Patino, Nayelli, et al. | 2021 | Clinical Nutrition Espen | WoS-id: 000678558000032
Scopus-id: 2-s2.0-85108856650
| 0 | 0 |
| 25 | A higher bacterial inward BCAA transport driven by Faecalibacterium prausnitzii is associated with lower serum levels of BCAA in early adolescents | Coautor: Ibarra-Gonzalez, Isabel, Moran-Ramos, Sofia, Macias-Kauffer, Luis, Lopez-Contreras, Blanca E., et al. | 2021 | MOLECULAR MEDICINE | WoS-id: 000696195100001
Scopus-id: 2-s2.0-85115046999
| 20 | 19 |
| 26 | Serum metabolite profile associated with sex-dependent visceral adiposity index and low bone mineral density in a mexican population | Coautor: Ibarra-Gonzalez, Isabel, Palacios-Gonzalez, Berenice, Leon-Reyes, Guadalupe, Rivera-Paredez, Berenice, et al. | 2021 | Metabolites | WoS-id: 000701861300001
Scopus-id: 2-s2.0-85114770129
| 13 | 13 |
| 27 | An updated PAH mutational spectrum of phenylketonuria in mexican patients attending a single center: Biochemical, clinical-genotyping correlations | Coautor: Ibarra-Gonzalez, Isabel, Vela-Amieva, Marcela, Alcantara-Ortigoza, Miguel Angel, Angel A.G., et al. | 2021 | GENES | WoS-id: 000727214900001
Scopus-id: 2-s2.0-85120708050
| 8 | 7 |
| 28 | Atención de pacientes con errores innatos del metabolismo durante la pandemia de COVID-19 en México: Importancia de la telemedicina | Coautor: Ibarra-González I., Guillén-López S., López-Mejía L., Carrillo-Nieto R.I., et al. | 2021 | ACTA PEDIATRICA DE MEXICO | Scopus-id: 2-s2.0-85109697010
| 0 | 1 |
| 29 | Importance of Studying Older Siblings of Patients Identified by Newborn Screening: a Single-Center Experience in Mexico | 1ᵉʳ autor: Ibarra-González I., Fernández-Lainez C., Guillén-López S., López-Mejía L., et al. | 2021 | Journal of Inborn Errors of Metabolism and Screening | Scopus-id: 2-s2.0-85137880818
| 0 | 7 |
| 30 | Environmental and intrinsic factors shaping gut microbiota composition and diversity and its relation to metabolic health in children and early adolescents: A population-based study | Coautor: Ibarra-Gonzalez I., Moran-Ramos S., Lopez-Contreras B.E., Villarruel-Vazquez R., et al. | 2020 | Gut Microbes | WoS-id: 000509242900001
Scopus-id: 2-s2.0-85078466788
| 45 | 55 |
| 31 | Molecular analysis using targeted next generation DNA sequencing and clinical spectrum of Mexican patients with isovaleric acidemia | 1ᵉʳ autor: Ibarra-González I., Fernández-Lainez C., Guillén-López S., López-Mejía L., et al. | 2020 | CLINICA CHIMICA ACTA | WoS-id: 000512220100030
Scopus-id: 2-s2.0-85076618908
| 9 | 14 |
| 32 | Altered Plasma Acylcarnitines and Amino Acids Profile in Spinocerebellar Ataxia Type 7 | Coautor: Ibarra-González I., Nambo-Venegas R., Valdez-Vargas C., Cisneros B., et al. | 2020 | Biomolecules | WoS-id: 000529877600041
Scopus-id: 2-s2.0-85081966158
| 8 | 10 |
| 33 | Causes of hospitalizations in patients with inborn errors of intermediary metabolism: analyses of a series of cases in a third level hospital | 2ᵒ autor: Cristina Ibarra-Gonzalez, Isabel, Belmont-Martinez, Leticia, Beatriz Vela-Amieva, Marcela, Guillen-Lopez, Sara, et al. | 2020 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000545371600001
| 1 | 0 |
| 34 | Simultaneous evaluation of metabolomic and inflammatory biomarkers in children with different body mass index (BMI) and waist-to-height ratio (WHtR) | Coautor: Ibarra-González I., Chavira-Suárez E., Rosel-Pech C., Polo-Oteyza E., et al. | 2020 | PLOS ONE | WoS-id: 000565550400020
Scopus-id: 2-s2.0-85089929508
| 8 | 9 |
| 35 | Positive improvement in palatability of metabolic formula with the use of miraculin protein in patients with inborn errors of metabolism and healthy adults | Coautor: Ibarra I., López L., Vela M., Díaz L., et al. | 2020 | Revista Chilena de Nutricion | WoS-id: 000581101500011
Scopus-id: 2-s2.0-85092595396
| 1 | 2 |
| 36 | Cystathionine beta-synthase and methylenetetrahydrofolate reductase mutations in Mexican individuals with hyperhomocysteinemia | Coautor: Ibarra-Gonzalez, Isabel, Figueroa-Torres, Anahi Guadalupe, Matias-Aguilar, Lisneth Osiris, Coria-Ramirez, Erika, et al. | 2020 | SAGE Open Medicine | WoS-id: 000593613700001
Scopus-id: 2-s2.0-85147485686
| 2 | 2 |
| 37 | A multi-omic analysis for low bone mineral density in postmenopausal women suggests a relationship between diet, metabolites, and microbiota | Coautor: Ibarra-González I., Palacios-González B., Ramírez-Salazar E.G., Rivera-Paredez B., et al. | 2020 | Microorganisms | WoS-id: 000594033000001
Scopus-id: 2-s2.0-85094137495
| 40 | 42 |
| 38 | Causas de hospitalización de pacientes con errores innatos del metabolismo intermediario: Análisis de una serie de casos de un hospital de tercer nivel de atención | 2ᵒ autor: Ibarra-González I.C., Belmont-Martínez L., Vela-Amieva M.B., Guillén-López S., et al. | 2020 | ACTA PEDIATRICA DE MEXICO | Scopus-id: 2-s2.0-85093077856
| 0 | 2 |
| 39 | Mutational spectrum of Mexican patients with tyrosinemia type 1: In silico modeling and predicted pathogenic effect of a novel missense FAH variant | 1ᵉʳ autor: Ibarra-Gonzalez, Isabel, Fernandez-Lainez, Cynthia, Alcántara-Ortigoza M.A., Gonzalez-Del Angel, Ariadna, et al. | 2019 | Molecular Genetics & Genomic Medicine | WoS-id: 000488590900001
Scopus-id: 2-s2.0-85073958470
| 5 | 5 |
| 40 | Family history and obesity in youth, their effect on acylcarnitine/aminoacids metabolomics and non-alcoholic fatty liver disease (NAFLD). Structural equation modeling approach | Coautor: Ibarra-González I., Romero-Ibarguengoitia M.E., Vadillo-Ortega F., Caballero A.E., et al. | 2018 | PLOS ONE | WoS-id: 000425604300088
Scopus-id: 2-s2.0-85042319394
| 30 | 39 |
| 41 | Family history and obesity in youth, their effect on acylcarnitine/aminoacids metabolomics and non-alcoholic fatty liver disease (NAFLD). Structural equation modeling approach (vol 13, e0193138, 2018) | Coautor: Ibarra-Gonzalez, Isabel, Romero-Ibarguengoitia, Maria Elena, Vadillo-Ortega, Felipe, Caballero, Augusto Enrique, et al. | 2018 | PLOS ONE | WoS-id: 000433084300143
Scopus-id: 2-s2.0-85047445555
| 0 | 0 |
| 42 | In silico prediction of the pathogenic effect of a novel variant of BCKDHA leading to classical maple syrup urine disease identified using clinical exome sequencing | Coautor: Ibarra-González I., Fernández-Lainez C., Aláez-Verson C., Enríquez-Flores S., et al. | 2018 | CLINICA CHIMICA ACTA | WoS-id: 000438180600006
Scopus-id: 2-s2.0-85045723204
| 0 | 1 |
| 43 | Composition of gut microbiota in obese and normal-weight Mexican school-age children and its association with metabolic traits | Coautor: Ibarra-Gonzalez, I., Lopez-Contreras, B. E., Moran-Ramos, S., Villarruel-Vazquez, R., et al. | 2018 | PEDIATRIC OBESITY | WoS-id: 000439166300007
Scopus-id: 2-s2.0-85037610810
| 80 | 83 |
| 44 | Mutational spectrum of PTS gene and in silico pathological assessment of a novel variant in Mexico | 2ᵒ autor: Ibarra-González I., Fernández-Lainez C., Alcántara-Ortigoza M., Fernández-Hernández L., et al. | 2018 | BRAIN & DEVELOPMENT | WoS-id: 000440117700002
Scopus-id: 2-s2.0-85045936112
| 5 | 5 |
| 45 | Newborn cystic fibrosis screening in southeastern Mexico: Birth prevalence and novel CFTR gene variants | 1ᵉʳ autor: Ibarra-Gonzalez, Isabel, Campos-Garcia, Felix-Julian, del Alba Herrera-Perez, Luz, Martinez-Cruz, Patricia, et al. | 2018 | JOURNAL OF MEDICAL SCREENING | WoS-id: 000441404900003
Scopus-id: 2-s2.0-85055691032
| 9 | 10 |
| 46 | Optimization of kidney dysfunction prediction in diabetic kidney disease using targeted metabolomics | 1ᵉʳ autor: Ibarra-Gonzalez, Isabel, Cruz-Bautista, Ivette, Yaxmehen Bello-Chavolla, Omar, Vela-Amieva, Marcela, et al. | 2018 | ACTA DIABETOLOGICA | WoS-id: 000446498100008
Scopus-id: 2-s2.0-85052814148
| 22 | 25 |
| 47 | Relevant aspects of the congenital adrenal hyperplasia newborn screening | Coautor: Ibarra-Gonzalez, Isabel, Angelica Hinojosa-Trejo, Mirna, Lissete Arguinzoniz-Valenzuela, Sletza, del Alba Herrera-Perez, Luz, et al. | 2018 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000450874800002
Scopus-id: 2-s2.0-85115910647
| 0 | 2 |
| 48 | Epidemiology of phenylketonuria obtained through neonatal screening | 2ᵒ autor: Ibarra-Gonzalez, Isabel, Vela-Amieva, Marcela, del Alba Herrera-Perez, Luz, Caamal-Parra, Guillermo, et al. | 2018 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000450874800003
Scopus-id: 2-s2.0-85115985282
| 1 | 6 |
| 49 | Challenges and opportunities in the implementation of the neonatal screening for cystic fibrosis | 1ᵉʳ autor: Ibarra-Gonzalez, Isabel, Gutierrez-Morales, Gabriel, Vela-Amieva, Marcela, Ariel Castillo-Mogel, Jose, et al. | 2018 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000450874800004
Scopus-id: 2-s2.0-85115973420
| 0 | 1 |
| 50 | Glucose-6-phosphate dehydrogenase values and their impact on the number of suspected neonatal screening | Coautor: Ibarra-Gonzalez, Isabel, Maldonado-Silva, Karla, Angelica Hinojosa-Trejo, Mirna, Vela-Amieva, Marcela, et al. | 2018 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000450874800005
Scopus-id: 2-s2.0-85101753357
| 0 | 4 |
| 51 | Congenital hypothyroidism birth prevalence | Coautor: Ibarra-Gonzalez, Isabel, Angelica Hinojosa-Trejo, Mirna, Vela-Amieva, Marcela, de Cosio-Farias, Ana Paola, et al. | 2018 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000450874800010
Scopus-id: 2-s2.0-85112698706
| 2 | 8 |
| 52 | Serum Branched Chain and Aromatic Amino Acids Are Associated to Overweight, Obesity and Metabolic Alterations in School-Aged | Coautor: Ibarra-Gonzalez, Isabel, Ocampo-Medina, Elvira, Moran-Ramos, Sofia, Macias-Kauffer, Luis, et al. | 2017 | FASEB JOURNAL | WoS-id: 000405461405448
| 0 | 0 |
| 53 | An Amino Acid Signature Associated with Obesity Predicts 2-Year Risk of Hypertriglyceridemia in School-Age Children | Coautor: Ibarra-Gonzalez, Isabel, Moran-Ramos, Sofia, Ocampo-Medina, Elvira, Gutierrez-Aguilar, Ruth, et al. | 2017 | SCIENTIFIC REPORTS | WoS-id: 000405676800005
Scopus-id: 2-s2.0-85025172638
| 46 | 51 |
| 54 | Metabolic screening and metabolomics analysis in the Intellectual Developmental Disorders Mexico Study | 1ᵉʳ autor: Ibarra-González I., Rodríguez-Valentín R., Lazcano-Ponce E., Vela-Amieva M. | 2017 | SALUD PUBLICA DE MEXICO | WoS-id: 000408398400011
Scopus-id: 2-s2.0-85026203705
| 8 | 8 |
| 55 | Neurologic crises after interruption of nitisinone in a tyrosinemia patient: case report | 1ᵉʳ autor: Ibarra-Gonzalez, I., Belmont-Martinez, L., Cervantes-Bustamante, R., Zarate-Mondragon, F., et al. | 2017 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000416316200005
Scopus-id: 2-s2.0-85031927507
| 1 | 3 |
| 56 | Kernicterus in a boy with ornithine transcarbamylase deficiency: A case report | 2ᵒ autor: Ibarra-Gonzalez, Isabel, Lopez-Corella, Eduardo, Fernandez-Lainez, Cynthia, Rodriguez-Weber, Miguel A., et al. | 2017 | Neuropathology | WoS-id: 000417582900013
Scopus-id: 2-s2.0-85037617305
| 7 | 8 |
| 57 | Hepatorenal Tyrosinemia in Mexico: A Call to Action | 1ᵉʳ autor: Ibarra-Gonzalez, Isabel, Ridaura-Sanz, Cecilia, Fernandez-Lainez, Cynthia, Guillen-Lopez, Sara, et al. | 2017 | Advances in Experimental Medicine and Biology | WoS-id: 000438242100016
Scopus-id: 2-s2.0-85027298095
| 9 | 11 |
| 58 | Prospective Evaluation of Seric Acyl-Carnitine and Amino Acid Profiles in Obese Women With or Without Gestational Diabetes and Normal Pregnant Women | Coautor: Ibarra, I, AguilarLozano, AG, CeballosAngeles, A, PrunedaPadilla, Y, et al. | 2015 | REPRODUCTIVE SCIENCES | WoS-id: 000351407201186
| 0 | 0 |
| 59 | Biomarkers of Metabolic Disruption and Mitochondrial Dysfunction in Obese Pregnant Women With Non-Complicated Pregnancies | Coautor: Ibarra, I, AguilarLozano, AG, Resendiz, O, PrunedaPadilla, Y, et al. | 2015 | REPRODUCTIVE SCIENCES | WoS-id: 000351407201187
| 0 | 0 |
| 60 | Phenylalanine hydroxylase deficiency in Mexico: Genotype-phenotype correlations, BH4 responsiveness and evidence of a founder effect | Coautor: IbarraGonzalez, I, VelaAmieva, M, AbreuGonzalez, M, Gonzalezdel Angel, A, et al. | 2015 | CLINICAL GENETICS | WoS-id: 000355842300010
Scopus-id: 2-s2.0-84930415915
| 17 | 18 |
| 61 | Brain nuclear magnetic resonance in patients with late diagnosis of phenylketonuria | Coautor: Ibarra-Gonzalez, Isabel, Jimenez-Perez, Mario O., Gomez-Garza, Gilberto, Ruiz-Garcia, Matilde, et al. | 2015 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000360926600003
| 1 | 0 |
| 62 | Evaluation of seric acyl-carnitine and amino acid profiles in obese pregnant women with or without gestational diabetes. | Coautor: IbarraGonzalez, I, AguilarLozano, AG, CeballosAngeles, A, PrunedaPadilla, Y, et al. | 2015 | FASEB JOURNAL | WoS-id: 000361470502299
| 0 | 0 |
| 63 | Biotin deprivation impairs mitochondrial structure and function and has implications for inherited metabolic disorders | Coautor: Ibarra-González I., Ochoa-Ruiz E., Díaz-Ruiz R., HernandezVazquez, AD, et al. | 2015 | MOLECULAR GENETICS AND METABOLISM | WoS-id: 000364984200016
Scopus-id: 2-s2.0-84948711997
| 15 | 18 |
| 64 | Comparison of free carnitine levels with nutritional status in infantile nephropathyc cistinosis patients | 2ᵒ autor: IbarraGonzalez, I, GuillenLopez, S, Martinez, LB, JuarezCruz, MV, et al. | 2015 | NUTRICION HOSPITALARIA | WoS-id: 000367417600034
Scopus-id: 2-s2.0-84949960386
| 0 | 0 |
| 65 | Resonancia magnética nuclear de encéfalo en pacientes con fenilcetonuria diagnosticada tardíamente | Coautor: Ibarra-González I., Jiménez-Pérez M.O., Gómez-Garza G., Ruiz-García M., et al. | 2015 | ACTA PEDIATRICA DE MEXICO | Scopus-id: 2-s2.0-84930815378
| 0 | 2 |
| 66 | NEONATAL ACUTE SEVERE ONSET INBORN ERRORS OF INTERMEDIARY METABOLISM IN NEONATAL INTENSIVE CARE UNITS AND EMERGENCY WARDS IN MEXICO | 2ᵒ autor: Ibarra-Gonzalez, I, Vela-Amieva, M, Fernandez-Lainez, C, Belmont-Martinez, L, et al. | 2014 | MOLECULAR GENETICS AND METABOLISM | WoS-id: 000332500200100
| 0 | 0 |
| 67 | Prospective Evaluation of Seric Acyl-Carnitine Profiles in Obese and Normal Pregnant Women with Non-Complicated Pregnancies | Coautor: Ibarra, I, Aguilar-Lozano, AG, Pruneda, Y, Vela, M, et al. | 2014 | REPRODUCTIVE SCIENCES | WoS-id: 000333813002245
| 0 | 0 |
| 68 | Longitudinal Amino-Acid Seric Profiles in Obese and Normal Women with Normal Non-Complicated Pregnancies. | Coautor: Ibarra-Gonzalez, I, Pruneda-Padilla, Y, Ceballos-Angeles, A, Vela-Amieva, M, et al. | 2014 | REPRODUCTIVE SCIENCES | WoS-id: 000333813002246
| 0 | 0 |
| 69 | Characterization of inborn errors of intermediary metabolism in mexican patients | 1ᵉʳ autor: Ibarra-González I., Fernández-Lainez C., Belmont-Martínez L., Guillén-López S., et al. | 2014 | ANALES DE PEDIATRIA | WoS-id: 000336076600007
Scopus-id: 2-s2.0-84936772349
| 12 | 12 |
| 70 | Tyrosinemia type I: Clinical and biochemical analysis of patients in Mexico | 2ᵒ autor: Ibarra-González I., Fernández-Lainez C., Belmont-Martínez L., Monroy-Santoyo S., et al. | 2014 | Annals Of Hepatology | WoS-id: 000341467100013
Scopus-id: 2-s2.0-84893669123
| 13 | 18 |
| 71 | Amino-acid seric profiles in obese and normal women with normal non-complicated pregnancies | Coautor: Ibarra-Gonzalez, I, Ceballos-Angeles, A, Pruneda-Padilla, Y, Vela-Amieva, M, et al. | 2014 | FASEB JOURNAL | WoS-id: 000346646702357
| 0 | 0 |
| 72 | Biotinidase knockout mice show cellular energy deficit and altered carbon metabolism gene expression similar to that of nutritional biotin deprivation: Clues for the pathogenesis in the human inherited disorder | Coautor: Ibarra-González I., Hernández-Vázquez A., Wolf B., Pindolia K., et al. | 2013 | MOLECULAR GENETICS AND METABOLISM | WoS-id: 000326058000009
Scopus-id: 2-s2.0-84885422398
| 21 | 23 |
| 73 | The Chemistry and Biochemistry of Niacin (B-3) | Coautor: Ibarra-Gonzalez, Isabel, Aguilera-Mendez, Asdrubal, Fernandez-Lainez, Cynthia, Fernandez-Mejia, Cristina | 2013 | Food and Nutritional Components in Focus | WoS-id: 000326647100008
| 0 | 0 |
| 74 | Higher incidence of thyroid agenesis in Mexican newborns with congenital hypothyroidism associated with birth defects | 2ᵒ autor: Ibarra-Gonzalez, I, Monroy-Santoyo, S, Fernandez-Lainez, C, Greenawalt-Rodriguez, S, et al. | 2012 | EARLY HUMAN DEVELOPMENT | WoS-id: 000299449700012
Scopus-id: 2-s2.0-84355166724
| 19 | 22 |
| 75 | Mutation analysis of the methylmalonyl-CoA mutase gene in ten Mexican patients with methylmalonic acidemia | Coautor: Ibarra I., Méndez S.T., Vela-Amieva M., Velázquez-Arellano A., et al. | 2012 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000309196300007
Scopus-id: 2-s2.0-84868223674
| 3 | 3 |
| 76 | Tandem Mass Spectrometry Newborn Screening for Inborn Errors of Intermediary Metabolism: Abnormal Profile Interpretation | Coautor: Ibarra-Gonzalez, I, Fernandez-Lainez, C, Aguilar-Lemus, JJ, Vela-Amieva, M | 2012 | CURRENT MEDICINAL CHEMISTRY | WoS-id: 000309511500011
Scopus-id: 2-s2.0-84868031084
| 18 | 20 |
| 77 | Temporal development of genetic and metabolic effects of biotin deprivation. A search for the optimum time to study a vitamin deficiency | Coautor: Ibarra-González I., Hernández-Vázquez A., Ochoa-Ruiz E., Ortega-Cuellar D., et al. | 2012 | MOLECULAR GENETICS AND METABOLISM | WoS-id: 000310720200015
Scopus-id: 2-s2.0-84867895871
| 6 | 8 |
| 78 | Correspondence on "Experience With Hyperphenylalaninemia in a Developing Country: Unusual Clinical Manifestations and a Novel Gene Mutation" | 2ᵒ autor: Ibarra-González I., Vela-Amieva M., Fernández-Lainez C., Monroy-Santoyo S. | 2011 | J CHILD NEUROL | WoS-id: 000286834000023
Scopus-id: 2-s2.0-79551640527
| 0 | 0 |
| 79 | Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: A worldwide collaborative project | Coautor: Ibarra-Gonzalez, I, Abdenur, JE, Abdulrahman, M, Adair, O, et al. | 2011 | GENETICS IN MEDICINE | WoS-id: 000287694800013
Scopus-id: 2-s2.0-79952194543
| 288 | 317 |
| 80 | Hepatorenal tyrosinemia: The devastating natural history of the disease in Mexico | 2ᵒ autor: Ibarra-Gonzalez, I, Fernandez-Lainez, C, Ruiz-Gomez, M, Guillen-Lopez, S, et al. | 2011 | MOLECULAR GENETICS AND METABOLISM | WoS-id: 000287773800069
| 0 | 0 |
| 81 | Effect of supplementation during pregnancy with L-arginine and antioxidant vitamins in medical food on pre-eclampsia in high risk population: randomised controlled trial | Coautor: Ibarra, I, Vadillo-Ortega, F, Perichart-Perera, O, Espino, S, et al. | 2011 | BMJ-BRITISH MEDICAL JOURNAL | WoS-id: 000290952100004
Scopus-id: 2-s2.0-81355136042
| 116 | 42 |
| 82 | Causes of delay in referral of patients with phenylketonuria to a specialized reference centre in Mexico | 2ᵒ autor: Ibarra-Gonzalez, I, Vela-Amieva, M, Fernandez-Lainez, C, Monroy-Santoyo, S, et al. | 2011 | JOURNAL OF MEDICAL SCREENING | WoS-id: 000297908900004
Scopus-id: 2-s2.0-80655139845
| 10 | 13 |
| 83 | Clinical and biochemical characteristics of patients with urea cycle disorders in a developing country | 1ᵉʳ autor: Ibarra-Gonzalez, I, Fernandez-Lainez, C, Vela-Amieva, M | 2010 | CLINICAL BIOCHEMISTRY | WoS-id: 000275219400019
Scopus-id: 2-s2.0-77149127415
| 11 | 14 |
| 84 | The C677T polymorphism of the methylenetetrahydrofolate reductase gene is associated with idiopathic ischemic stroke in the young mexican-mestizo population | Coautor: Ibarra-González I., Isordia-Salas I., Barinagarrementería-Aldatz F., Leanos-Miranda, A, et al. | 2010 | CEREBROVASC DIS | WoS-id: 000277050000006
Scopus-id: 2-s2.0-77951831327
| 24 | 28 |
| 85 | Effect of Highly Active Antiretroviral Therapy on Homocysteine Plasma Concentrations in HIV-1-Infected Patients | Coautor: Ibarra-Gonzalez, I, Coria-Ramirez, E, Cisneros, LN, Trevino-Perez, S, et al. | 2010 | JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES | WoS-id: 000280149000005
Scopus-id: 2-s2.0-77955012573
| 6 | 9 |
| 86 | UREA CYCLE DISORDERS: A LABORATORY APPROACH. EXPERIENCE AT A TERTIARY CARE CENTER IN A DEVELOPING COUNTRY | 2ᵒ autor: Ibarra-Gonzalez, IC, Vela-Amieva, MB, Fernandez-Lainez, C | 2009 | MOLECULAR GENETICS AND METABOLISM | WoS-id: 000268942600611
| 0 | 0 |
| 87 | Increased mortality and disability in Mexican children with maple syrup urine disease (MSUD) [Elevada mortalidad y discapacidad en niños mexicanos con enfermedad de orina con olor a jarabe de arce (EOJA)] | 1ᵉʳ autor: Ibarra-González I., Fernández-Lainez C., Belmont-Martínez L., Vela-Amieva M. | 2007 | GACETA MEDICA DE MEXICO | WoS-id: 000254326600005
Scopus-id: 2-s2.0-38449084779
| 6 | 8 |
| 88 | Differential effects of biotin deficiency and replenishment on rat liver pyruvate and propionyl-CoA carboxylases and on their mRNAs | Coautor: Ibarra I., Rodríguez-Meléndez R., Pérez-Andrade M.E., Díaz A., et al. | 1999 | MOLECULAR GENETICS AND METABOLISM | WoS-id: 000078706700003
Scopus-id: 2-s2.0-0344069769
| 35 | 39 |
| 89 | Urinary organic acids in infant malnutrition | 2ᵒ autor: Ibarra I., Terán-García M., Velázquez A. | 1998 | PEDIATRIC RESEARCH | WoS-id: 000075500100020
Scopus-id: 2-s2.0-0345451115
| 15 | 18 |
ID's SCOPUS 
ORCID's 