ISABEL CRISTINA IBARRA GONZALEZ



DATOS GENERALES
Nombre completo   ISABEL CRISTINA IBARRA GONZALEZ
Máximo nivel de estudios   MAESTRÍA
Antigüedad académica en la UNAM   31 años
NOMBRAMIENTOS
Vigente   TECNICO ACADEMICO TITULAR B TC Definitivo
Instituto de Investigaciones Biomédicas
Desde 16-10-2009
TECNICO ACADEMICO TITULAR A TC Definitivo
Instituto de Investigaciones Biomédicas
Desde 01-01-2008 (fecha inicial de registros en el SIIA) hasta 15-10-2009
ESTIMULOS, PROGRAMAS, PREMIOS Y RECONOCIMIENTOS
* SNI II2020 - VIGENTE
* SNI I2013 - 2019
* PRIDE D2012 - 2024

INFORMACIÓN DE PUBLICACIONES
Firmas  
Cristina Ibarra-Gonzalez, Isabel Ibarra I. Ibarra, I Ibarra-González I. Ibarra-González I.C. IbarraGonzalez, I
Ibarra-Gonzalez, I Ibarra-Gonzalez, I. Ibarra-Gonzalez, IC Ibarra-Gonzalez, Isabel
ID's SCOPUS  
57219402174
ORCID's  
0000-0001-8693-8531
Áreas de conocimiento  
Allergy Biochemistry and molecular biology Biology Clinical neurology Chemistry, medicinal
Endocrinology and metabolism Gastroenterology and hepatology Genetics & heredity Genetics and heredity Immunology
Infectious diseases Jcs 2008 Medical laboratory technology Medicine, general and internal Medicine, research & experimental
Medicine, research and experimental Microbiology Multidisciplinary sciences Nutrition and dietetics Obstetrics and gynecology
Pathology Pediatrics Peripheral vascular disease Psychology, developmental Public, environmental & occupational health
Public, environmental and occupational health Agricultural and biological sciences (miscellaneous) Biochemistry Clinical biochemistry Developmental and educational psychology
Endocrinology, diabetes and metabolism Food science Genetics Health Policy Hepatology
Immunology and allergy Infectious diseases Internal medicine Medicine (miscellaneous) Microbiology (medical)
Molecular medicine Multidisciplinary Nutrition and dietetics Obstetrics and Gynecology Pediatrics, Perinatology and Child Health
Pharmacology Pharmacology (medical) Public health, environmental and occupational health Spectroscopy
Coautorías con entidades de la UNAM  
  • Instituto de Investigaciones Biomédicas
  • Instituto de Química
  • Instituto de Fisiología Celular
  • Instituto de Biotecnología
  • Facultad de Ciencias
  • Facultad de Medicina
  • Facultad de Química
  • Escuela Nacional de Enfermería y Obstetricia
  • Coordinación de Estudios de Posgrado
Revistas en las que ha publicado  (52):
  1. ACTA DIABETOLOGICA, Italia (2018)
  2. ACTA PEDIATRICA DE MEXICO, México (2015, 2017, 2018, 2020, 2021, 2022, 2023)
  3. Advances in Experimental Medicine and Biology, Suiza (2017)
  4. ALLERGOLOGIA ET IMMUNOPATHOLOGIA, España (2021)
  5. ANALES DE PEDIATRIA, España (2014)
  6. Annals Of Hepatology, México (2014)
  7. Biomolecules, Suiza (2020)
  8. BMJ-BRITISH MEDICAL JOURNAL, Reino Unido (2011)
  9. BRAIN & DEVELOPMENT, Países Bajos (2018)
  10. CEREBROVASC DIS, Estados Unidos America (2010)
  11. CLINICA CHIMICA ACTA, Países Bajos (2018, 2020)
  12. CLINICAL BIOCHEMISTRY, Canada (2010, 2022)
  13. CLINICAL GENETICS, Estados Unidos America (2015)
  14. Clinical Nutrition Espen, Países Bajos (2021)
  15. CURRENT MEDICINAL CHEMISTRY, (2012)
  16. Children-Basel, Suiza (2023)
  17. DIABETOLOGY & METABOLIC SYNDROME, Brasil (2023)
  18. EARLY HUMAN DEVELOPMENT, Irlanda (2012)
  19. FASEB JOURNAL, Estados Unidos America (2014, 2015, 2017)
  20. Food and Nutritional Components in Focus, Reino Unido (2013)
  21. Frontiers in Genetics, Suiza (2022)
  22. FRONTIERS IN IMMUNOLOGY, Suiza (2022)
  23. GACETA MEDICA DE MEXICO, México (2007)
  24. GENES, Suiza (2021)
  25. GENETICS IN MEDICINE, Estados Unidos America (2011)
  26. Gut Microbes, Estados Unidos America (2020)
  27. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, Suiza (2024)
  28. International Journal of Neonatal Screening, Suiza (2023)
  29. J CHILD NEUROL, Estados Unidos America (2011)
  30. JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, Estados Unidos America (2010)
  31. JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, Estados Unidos America (2021)
  32. Journal of Inborn Errors of Metabolism and Screening, Estados Unidos America (2021)
  33. JOURNAL OF MEDICAL SCREENING, Reino Unido (2011, 2018)
  34. Metabolites, Suiza (2021, 2022)
  35. Metabolomics, Estados Unidos America (2025)
  36. Microorganisms, Suiza (2020)
  37. Molecular Genetics & Genomic Medicine, Estados Unidos America (2019)
  38. MOLECULAR GENETICS AND METABOLISM, Estados Unidos America (1999, 2009, 2011, 2012, 2013, 2014, 2015, 2024)
  39. MOLECULAR MEDICINE, Estados Unidos America (2021)
  40. Neuropathology, Estados Unidos America (2017)
  41. NUTRICION HOSPITALARIA, España (2015)
  42. Nutrients, Suiza (2022, 2023, 2024)
  43. ORPHANET JOURNAL OF RARE DISEASES, Reino Unido (2021)
  44. PEDIATRIC OBESITY, Reino Unido (2018)
  45. PEDIATRIC RESEARCH, Estados Unidos America (1998)
  46. PLOS ONE, Estados Unidos America (2018, 2020)
  47. REPRODUCTIVE SCIENCES, Estados Unidos America (2014, 2015)
  48. Revista Chilena de Nutricion, Chile (2020)
  49. REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION, México (2012)
  50. SAGE Open Medicine, Estados Unidos America (2020)
  51. SALUD PUBLICA DE MEXICO, México (2017)
  52. SCIENTIFIC REPORTS, Reino Unido (2017)


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Documentos indexados (WoS y Scopus)

# Título del documento Autores Año Revista Fuente Citas WoS Citas Scopus
1A predictive model for neoadjuvant therapy response in breast cancerCoautor: Ibarra-González I., Nambo-Venegas R., Enríquez-Cárcamo V.I., Vela-Amieva M., et al.2025MetabolomicsWoS-id: 001427944800001
Scopus-id: 2-s2.0-85218488483
11
2Hypogammaglobulinemia Class G Is Present in Compensated and Decompensated Patients with Propionate Defects, Independent of Their Nutritional StatusCoautor: Ibarra-González I., López-Mejía L.A., Vela-Amieva M., Guillén-López S., et al.2024NutrientsWoS-id: 001246771800001
Scopus-id: 2-s2.0-85196589616
11
3Comparison of nutritional status and metabolic control in PKU infants with breastmilk vs infant formula in MexicoCoautor: Ibarra-González, I, Guillén-López, S, López-Mejía, L, Vela-Amieva, M, et al.2024MOLECULAR GENETICS AND METABOLISMWoS-id: 001282724000015
10
4Concordance Between Biochemical and Molecular Diagnosis Obtained by WES in Mexican Patients with Inborn Errors of Intermediary Metabolism: Utility for Therapeutic ManagementCoautor: Ibarra-González, I, Vela-Amieva, M, Alcántara-Ortigoza, MA, González-del Angel, A, et al.2024INTERNATIONAL JOURNAL OF MOLECULAR SCIENCESWoS-id: 001351261400001
Scopus-id: 2-s2.0-85208564008
00
5The BMI Z-Score and Protein Energy Ratio in Early- and Late-Diagnosed PKU Patients from a Single Reference Center in MexicoCoautor: Ibarra-Gonzalez, Isabel, Lopez-Mejia, Lizbeth Alejandra, Fernandez-Lainez, Cynthia, Vela-Amieva, Marcela, et al.2023NutrientsWoS-id: 000940997200001
Scopus-id: 2-s2.0-85148905619
11
6Biochemical goals at follow-up and dosage of the main drugs for inborn errors of intermediary metabolismCoautor: Ibarra-Gonzalez, Isabel, Lopez-Mejia, Lizbeth, Guillen-Lopez, Sara, Carrillo-Nieto, Rosa Itzel, et al.2023ACTA PEDIATRICA DE MEXICOWoS-id: 000951351000007
Scopus-id: 2-s2.0-85150717835
01
7An early prediction model for gestational diabetes mellitus based on metabolomic biomarkersCoautor: Ibarra-González I., Razo-Azamar M., Nambo-Venegas R., Meraz-Cruz N., et al.2023DIABETOLOGY & METABOLIC SYNDROMEWoS-id: 001000375200003
Scopus-id: 2-s2.0-85160911711
1011
8A Review of Disparities and Unmet Newborn Screening Needs over 33 Years in a Cohort of Mexican Patients with Inborn Errors of Intermediary Metabolism1ᵉʳ autor: Ibarra-Gonzalez, I, Fernandez-Lainez, C, Vela-Amieva, M, Guillen-Lopez, S, et al.2023International Journal of Neonatal ScreeningWoS-id: 001130556600001
Scopus-id: 2-s2.0-85180450425
66
9In Silico Structural Protein Evaluation of the Phenylalanine Hydroxylase p.(Tyr77His) Variant Associated with Benign Hyperphenylalaninemia as Identified through Mexican Newborn ScreeningCoautor: Ibarra-González I., Vela-Amieva M., Alcántara-Ortigoza M.A., González-del Angel A., et al.2023Children-BaselWoS-id: 001132822500001
Scopus-id: 2-s2.0-85180716992
00
10Homocystinuria: clinical characteristics of a cohort and care guidelinesCoautor: Ibarra-Gonzalez, Isabel, Guillen-Lopez, Sara, Vela-Amieva, Marcela, Fernandez-Lainez, Cynthia, et al.2022ACTA PEDIATRICA DE MEXICOWoS-id: 000760274500006
Scopus-id: 2-s2.0-85131104508
00
11A Longitudinal1 H NMR-Based Metabolic Profile Analysis of Urine from Hospitalized Premature Newborns Receiving Enteral and Parenteral NutritionCoautor: Ibarra-González I., Esturau-Escofet N., Rodríguez De San Miguel E., Vela-Amieva M., et al.2022MetabolitesWoS-id: 000778260100001
Scopus-id: 2-s2.0-85127594560
54
12Targeted Metabolomics Revealed a Sex-Dependent Signature for Metabolic Syndrome in the Mexican PopulationCoautor: Ibarra-Gonzalez, Isabel, Palacios-Gonzalez, Berenice, Leon-Reyes, Guadalupe, Rivera-Paredez, Berenice, et al.2022NutrientsWoS-id: 000857664600001
Scopus-id: 2-s2.0-85138686604
23
13Update for the diagnosis and treatment of acute hyperammonemia in patients with inborn errors of metabolismCoautor: Ibarra-Gonzalez, Isabel, Lopez-Mejia, Lizbeth, Francisco-Revilla Estivill, Nuria, Guillen-Lopez, Sara, et al.2022ACTA PEDIATRICA DE MEXICOWoS-id: 000868601500005
Scopus-id: 2-s2.0-85144435373
11
14Genotypic spectrum underlying tetrahydrobiopterin metabolism defects: Experience in a single Mexican reference centerCoautor: Ibarra-Gonzalez, I., Vela-Amieva, M., Alcantara-Ortigoza, M. A., Gonzalez-Del Angel, A., et al.2022Frontiers in GeneticsWoS-id: 000877139800001
Scopus-id: 2-s2.0-85140641039
55
15Metabolic Reprogramming in SARS-CoV-2 Infection Impacts the Outcome of COVID-19 Patients2ᵒ autor: Ibarra-Gonzalez, Isabel, Martinez-Gomez, Laura E., Fernandez-Lainez, Cynthia, Tusie, Teresa, et al.2022FRONTIERS IN IMMUNOLOGYWoS-id: 000880077100001
Scopus-id: 2-s2.0-85141374972
2124
16Functional 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 deficiencyCoautor: Ibarra-González I., Alcántara-Ortigoza M.A., Hernández-Ochoa B., González-del Angel A., et al.2022CLINICAL BIOCHEMISTRYWoS-id: 000898934500010
Scopus-id: 2-s2.0-85138041723
55
17Brief Report: Delayed Diagnosis of Treatable Inborn Errors of Metabolism in Children with Autism and Other Neurodevelopmental Disorders2ᵒ autor: Ibarra-González I., Márquez-Caraveo M.E., Rodríguez-Valentín R., Ramírez-García M.Á., et al.2021JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERSWoS-id: 000565469800002
Scopus-id: 2-s2.0-85090187864
89
18Abnormalities in subsets of B and T cells in Mexican patients with inborn errors of propionate metabolism: observations from a single-center case seriesCoautor: Ibarra-Gonzalez, I., Medina-Torrez, E. A., Vela-Amieva, M., Galindo-Campos, L., et al.2021ALLERGOLOGIA ET IMMUNOPATHOLOGIAWoS-id: 000619192200014
Scopus-id: 2-s2.0-85101248688
43
19Genetic spectrum and clinical early natural history of glucose-6-phosphate dehydrogenase deficiency in Mexican children detected through newborn screeningCoautor: Ibarra-González I., Vela-Amieva M., Alcántara-Ortigoza M.A., González-del Angel A., et al.2021ORPHANET JOURNAL OF RARE DISEASESWoS-id: 000622331000001
Scopus-id: 2-s2.0-85101749732
66
20Metabolic flexibility during normal pregnancy allows appropriate adaptation during gestation independently of BMICoautor: Ibarra-Gonzalez, Isabel, Delgadillo-Velazquez, Jaime A., Nambo-Venegas, Rafael, Patino, Nayelli, et al.2021Clinical Nutrition EspenWoS-id: 000678558000032
Scopus-id: 2-s2.0-85108856650
00
21A higher bacterial inward BCAA transport driven by Faecalibacterium prausnitzii is associated with lower serum levels of BCAA in early adolescentsCoautor: Ibarra-Gonzalez, Isabel, Moran-Ramos, Sofia, Macias-Kauffer, Luis, Lopez-Contreras, Blanca E., et al.2021MOLECULAR MEDICINEWoS-id: 000696195100001
Scopus-id: 2-s2.0-85115046999
1514
22Serum metabolite profile associated with sex-dependent visceral adiposity index and low bone mineral density in a mexican populationCoautor: Ibarra-Gonzalez, Isabel, Palacios-Gonzalez, Berenice, Leon-Reyes, Guadalupe, Rivera-Paredez, Berenice, et al.2021MetabolitesWoS-id: 000701861300001
Scopus-id: 2-s2.0-85114770129
1010
23An updated PAH mutational spectrum of phenylketonuria in mexican patients attending a single center: Biochemical, clinical-genotyping correlationsCoautor: Ibarra-Gonzalez, Isabel, Vela-Amieva, Marcela, Alcantara-Ortigoza, Miguel Angel, Angel A.G., et al.2021GENESWoS-id: 000727214900001
Scopus-id: 2-s2.0-85120708050
76
24Atención de pacientes con errores innatos del metabolismo durante la pandemia de COVID-19 en México: Importancia de la telemedicinaCoautor: Ibarra-González I., Guillén-López S., López-Mejía L., Carrillo-Nieto R.I., et al.2021ACTA PEDIATRICA DE MEXICOScopus-id: 2-s2.0-85109697010
01
25Importance of Studying Older Siblings of Patients Identified by Newborn Screening: a Single-Center Experience in Mexico1ᵉʳ autor: Ibarra-González I., Fernández-Lainez C., Guillén-López S., López-Mejía L., et al.2021Journal of Inborn Errors of Metabolism and ScreeningScopus-id: 2-s2.0-85137880818
04
26Environmental and intrinsic factors shaping gut microbiota composition and diversity and its relation to metabolic health in children and early adolescents: A population-based studyCoautor: Ibarra-Gonzalez I., Moran-Ramos S., Lopez-Contreras B.E., Villarruel-Vazquez R., et al.2020Gut MicrobesWoS-id: 000509242900001
Scopus-id: 2-s2.0-85078466788
3744
27Molecular analysis using targeted next generation DNA sequencing and clinical spectrum of Mexican patients with isovaleric acidemia1ᵉʳ autor: Ibarra-González I., Fernández-Lainez C., Guillén-López S., López-Mejía L., et al.2020CLINICA CHIMICA ACTAWoS-id: 000512220100030
Scopus-id: 2-s2.0-85076618908
811
28Altered Plasma Acylcarnitines and Amino Acids Profile in Spinocerebellar Ataxia Type 7Coautor: Ibarra-González I., Nambo-Venegas R., Valdez-Vargas C., Cisneros B., et al.2020BiomoleculesWoS-id: 000529877600041
Scopus-id: 2-s2.0-85081966158
79
29Causes of hospitalizations in patients with inborn errors of intermediary metabolism: analyses of a series of cases in a third level hospital2ᵒ autor: Cristina Ibarra-Gonzalez, Isabel, Belmont-Martinez, Leticia, Beatriz Vela-Amieva, Marcela, Guillen-Lopez, Sara, et al.2020ACTA PEDIATRICA DE MEXICOWoS-id: 000545371600001
10
30Simultaneous 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.2020PLOS ONEWoS-id: 000565550400020
Scopus-id: 2-s2.0-85089929508
68
31Positive improvement in palatability of metabolic formula with the use of miraculin protein in patients with inborn errors of metabolism and healthy adultsCoautor: Ibarra I., López L., Vela M., Díaz L., et al.2020Revista Chilena de NutricionWoS-id: 000581101500011
Scopus-id: 2-s2.0-85092595396
12
32Cystathionine beta-synthase and methylenetetrahydrofolate reductase mutations in Mexican individuals with hyperhomocysteinemiaCoautor: Ibarra-Gonzalez, Isabel, Figueroa-Torres, Anahi Guadalupe, Matias-Aguilar, Lisneth Osiris, Coria-Ramirez, Erika, et al.2020SAGE Open MedicineWoS-id: 000593613700001
Scopus-id: 2-s2.0-85147485686
11
33A multi-omic analysis for low bone mineral density in postmenopausal women suggests a relationship between diet, metabolites, and microbiotaCoautor: Ibarra-González I., Palacios-González B., Ramírez-Salazar E.G., Rivera-Paredez B., et al.2020MicroorganismsWoS-id: 000594033000001
Scopus-id: 2-s2.0-85094137495
3536
34Causas de hospitalización de pacientes con errores innatos del metabolismo intermediario: Análisis de una serie de casos de un hospital de tercer nivel de atención2ᵒ autor: Ibarra-González I.C., Belmont-Martínez L., Vela-Amieva M.B., Guillén-López S., et al.2020ACTA PEDIATRICA DE MEXICOScopus-id: 2-s2.0-85093077856
02
35Mutational spectrum of Mexican patients with tyrosinemia type 1: In silico modeling and predicted pathogenic effect of a novel missense FAH variant1ᵉʳ autor: Ibarra-Gonzalez, Isabel, Fernandez-Lainez, Cynthia, Alcántara-Ortigoza M.A., Gonzalez-Del Angel, Ariadna, et al.2019Molecular Genetics & Genomic MedicineWoS-id: 000488590900001
Scopus-id: 2-s2.0-85073958470
55
36Family history and obesity in youth, their effect on acylcarnitine/aminoacids metabolomics and non-alcoholic fatty liver disease (NAFLD). Structural equation modeling approachCoautor: Ibarra-González I., Romero-Ibarguengoitia M.E., Vadillo-Ortega F., Caballero A.E., et al.2018PLOS ONEWoS-id: 000425604300088
Scopus-id: 2-s2.0-85042319394
2735
37Family 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.2018PLOS ONEWoS-id: 000433084300143
Scopus-id: 2-s2.0-85047445555
00
38In silico prediction of the pathogenic effect of a novel variant of BCKDHA leading to classical maple syrup urine disease identified using clinical exome sequencingCoautor: Ibarra-González I., Fernández-Lainez C., Aláez-Verson C., Enríquez-Flores S., et al.2018CLINICA CHIMICA ACTAWoS-id: 000438180600006
Scopus-id: 2-s2.0-85045723204
01
39Composition of gut microbiota in obese and normal-weight Mexican school-age children and its association with metabolic traitsCoautor: Ibarra-Gonzalez, I., Lopez-Contreras, B. E., Moran-Ramos, S., Villarruel-Vazquez, R., et al.2018PEDIATRIC OBESITYWoS-id: 000439166300007
Scopus-id: 2-s2.0-85037610810
7377
40Mutational spectrum of PTS gene and in silico pathological assessment of a novel variant in Mexico2ᵒ autor: Ibarra-González I., Fernández-Lainez C., Alcántara-Ortigoza M., Fernández-Hernández L., et al.2018BRAIN & DEVELOPMENTWoS-id: 000440117700002
Scopus-id: 2-s2.0-85045936112
55
41Newborn cystic fibrosis screening in southeastern Mexico: Birth prevalence and novel CFTR gene variants1ᵉʳ autor: Ibarra-Gonzalez, Isabel, Campos-Garcia, Felix-Julian, del Alba Herrera-Perez, Luz, Martinez-Cruz, Patricia, et al.2018JOURNAL OF MEDICAL SCREENINGWoS-id: 000441404900003
Scopus-id: 2-s2.0-85055691032
910
42Optimization of kidney dysfunction prediction in diabetic kidney disease using targeted metabolomics1ᵉʳ autor: Ibarra-Gonzalez, Isabel, Cruz-Bautista, Ivette, Yaxmehen Bello-Chavolla, Omar, Vela-Amieva, Marcela, et al.2018ACTA DIABETOLOGICAWoS-id: 000446498100008
Scopus-id: 2-s2.0-85052814148
1820
43Relevant aspects of the congenital adrenal hyperplasia newborn screeningCoautor: Ibarra-Gonzalez, Isabel, Angelica Hinojosa-Trejo, Mirna, Lissete Arguinzoniz-Valenzuela, Sletza, del Alba Herrera-Perez, Luz, et al.2018ACTA PEDIATRICA DE MEXICOWoS-id: 000450874800002
Scopus-id: 2-s2.0-85115910647
02
44Epidemiology of phenylketonuria obtained through neonatal screening2ᵒ autor: Ibarra-Gonzalez, Isabel, Vela-Amieva, Marcela, del Alba Herrera-Perez, Luz, Caamal-Parra, Guillermo, et al.2018ACTA PEDIATRICA DE MEXICOWoS-id: 000450874800003
Scopus-id: 2-s2.0-85115985282
15
45Challenges and opportunities in the implementation of the neonatal screening for cystic fibrosis1ᵉʳ autor: Ibarra-Gonzalez, Isabel, Gutierrez-Morales, Gabriel, Vela-Amieva, Marcela, Ariel Castillo-Mogel, Jose, et al.2018ACTA PEDIATRICA DE MEXICOWoS-id: 000450874800004
Scopus-id: 2-s2.0-85115973420
01
46Glucose-6-phosphate dehydrogenase values and their impact on the number of suspected neonatal screeningCoautor: Ibarra-Gonzalez, Isabel, Maldonado-Silva, Karla, Angelica Hinojosa-Trejo, Mirna, Vela-Amieva, Marcela, et al.2018ACTA PEDIATRICA DE MEXICOWoS-id: 000450874800005
Scopus-id: 2-s2.0-85101753357
04
47Congenital hypothyroidism birth prevalenceCoautor: Ibarra-Gonzalez, Isabel, Angelica Hinojosa-Trejo, Mirna, Vela-Amieva, Marcela, de Cosio-Farias, Ana Paola, et al.2018ACTA PEDIATRICA DE MEXICOWoS-id: 000450874800010
Scopus-id: 2-s2.0-85112698706
28
48Serum Branched Chain and Aromatic Amino Acids Are Associated to Overweight, Obesity and Metabolic Alterations in School-AgedCoautor: Ibarra-Gonzalez, Isabel, Ocampo-Medina, Elvira, Moran-Ramos, Sofia, Macias-Kauffer, Luis, et al.2017FASEB JOURNALWoS-id: 000405461405448
00
49An Amino Acid Signature Associated with Obesity Predicts 2-Year Risk of Hypertriglyceridemia in School-Age ChildrenCoautor: Ibarra-Gonzalez, Isabel, Moran-Ramos, Sofia, Ocampo-Medina, Elvira, Gutierrez-Aguilar, Ruth, et al.2017SCIENTIFIC REPORTSWoS-id: 000405676800005
Scopus-id: 2-s2.0-85025172638
4247
50Metabolic screening and metabolomics analysis in the Intellectual Developmental Disorders Mexico Study1ᵉʳ autor: Ibarra-González I., Rodríguez-Valentín R., Lazcano-Ponce E., Vela-Amieva M.2017SALUD PUBLICA DE MEXICOWoS-id: 000408398400011
Scopus-id: 2-s2.0-85026203705
88
51Neurologic crises after interruption of nitisinone in a tyrosinemia patient: case report1ᵉʳ autor: Ibarra-Gonzalez, I., Belmont-Martinez, L., Cervantes-Bustamante, R., Zarate-Mondragon, F., et al.2017ACTA PEDIATRICA DE MEXICOWoS-id: 000416316200005
Scopus-id: 2-s2.0-85031927507
12
52Kernicterus in a boy with ornithine transcarbamylase deficiency: A case report2ᵒ autor: Ibarra-Gonzalez, Isabel, Lopez-Corella, Eduardo, Fernandez-Lainez, Cynthia, Rodriguez-Weber, Miguel A., et al.2017NeuropathologyWoS-id: 000417582900013
Scopus-id: 2-s2.0-85037617305
77
53Hepatorenal Tyrosinemia in Mexico: A Call to Action1ᵉʳ autor: Ibarra-Gonzalez, Isabel, Ridaura-Sanz, Cecilia, Fernandez-Lainez, Cynthia, Guillen-Lopez, Sara, et al.2017Advances in Experimental Medicine and BiologyWoS-id: 000438242100016
Scopus-id: 2-s2.0-85027298095
810
54Prospective Evaluation of Seric Acyl-Carnitine and Amino Acid Profiles in Obese Women With or Without Gestational Diabetes and Normal Pregnant WomenCoautor: Ibarra, I, AguilarLozano, AG, CeballosAngeles, A, PrunedaPadilla, Y, et al.2015REPRODUCTIVE SCIENCESWoS-id: 000351407201186
00
55Biomarkers of Metabolic Disruption and Mitochondrial Dysfunction in Obese Pregnant Women With Non-Complicated PregnanciesCoautor: Ibarra, I, AguilarLozano, AG, Resendiz, O, PrunedaPadilla, Y, et al.2015REPRODUCTIVE SCIENCESWoS-id: 000351407201187
00
56Phenylalanine hydroxylase deficiency in Mexico: Genotype-phenotype correlations, BH4 responsiveness and evidence of a founder effectCoautor: IbarraGonzalez, I, VelaAmieva, M, AbreuGonzalez, M, Gonzalezdel Angel, A, et al.2015CLINICAL GENETICSWoS-id: 000355842300010
Scopus-id: 2-s2.0-84930415915
1516
57Brain nuclear magnetic resonance in patients with late diagnosis of phenylketonuriaCoautor: Ibarra-Gonzalez, Isabel, Jimenez-Perez, Mario O., Gomez-Garza, Gilberto, Ruiz-Garcia, Matilde, et al.2015ACTA PEDIATRICA DE MEXICOWoS-id: 000360926600003
10
58Evaluation 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.2015FASEB JOURNALWoS-id: 000361470502299
00
59Biotin deprivation impairs mitochondrial structure and function and has implications for inherited metabolic disordersCoautor: Ibarra-González I., Ochoa-Ruiz E., Díaz-Ruiz R., HernandezVazquez, AD, et al.2015MOLECULAR GENETICS AND METABOLISMWoS-id: 000364984200016
Scopus-id: 2-s2.0-84948711997
1316
60Comparison of free carnitine levels with nutritional status in infantile nephropathyc cistinosis patients2ᵒ autor: IbarraGonzalez, I, GuillenLopez, S, Martinez, LB, JuarezCruz, MV, et al.2015NUTRICION HOSPITALARIAWoS-id: 000367417600034
Scopus-id: 2-s2.0-84949960386
00
61Resonancia magnética nuclear de encéfalo en pacientes con fenilcetonuria diagnosticada tardíamenteCoautor: Ibarra-González I., Jiménez-Pérez M.O., Gómez-Garza G., Ruiz-García M., et al.2015ACTA PEDIATRICA DE MEXICOScopus-id: 2-s2.0-84930815378
02
62NEONATAL ACUTE SEVERE ONSET INBORN ERRORS OF INTERMEDIARY METABOLISM IN NEONATAL INTENSIVE CARE UNITS AND EMERGENCY WARDS IN MEXICO2ᵒ autor: Ibarra-Gonzalez, I, Vela-Amieva, M, Fernandez-Lainez, C, Belmont-Martinez, L, et al.2014MOLECULAR GENETICS AND METABOLISMWoS-id: 000332500200100
00
63Prospective Evaluation of Seric Acyl-Carnitine Profiles in Obese and Normal Pregnant Women with Non-Complicated PregnanciesCoautor: Ibarra, I, Aguilar-Lozano, AG, Pruneda, Y, Vela, M, et al.2014REPRODUCTIVE SCIENCESWoS-id: 000333813002245
00
64Longitudinal 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.2014REPRODUCTIVE SCIENCESWoS-id: 000333813002246
00
65Characterization of inborn errors of intermediary metabolism in mexican patients1ᵉʳ autor: Ibarra-González I., Fernández-Lainez C., Belmont-Martínez L., Guillén-López S., et al.2014ANALES DE PEDIATRIAWoS-id: 000336076600007
Scopus-id: 2-s2.0-84936772349
1211
66Tyrosinemia type I: Clinical and biochemical analysis of patients in Mexico2ᵒ autor: Ibarra-González I., Fernández-Lainez C., Belmont-Martínez L., Monroy-Santoyo S., et al.2014Annals Of HepatologyWoS-id: 000341467100013
Scopus-id: 2-s2.0-84893669123
1216
67Amino-acid seric profiles in obese and normal women with normal non-complicated pregnanciesCoautor: Ibarra-Gonzalez, I, Ceballos-Angeles, A, Pruneda-Padilla, Y, Vela-Amieva, M, et al.2014FASEB JOURNALWoS-id: 000346646702357
00
68Biotinidase 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 disorderCoautor: Ibarra-González I., Hernández-Vázquez A., Wolf B., Pindolia K., et al.2013MOLECULAR GENETICS AND METABOLISMWoS-id: 000326058000009
Scopus-id: 2-s2.0-84885422398
2123
69The Chemistry and Biochemistry of Niacin (B-3)Coautor: Ibarra-Gonzalez, Isabel, Aguilera-Mendez, Asdrubal, Fernandez-Lainez, Cynthia, Fernandez-Mejia, Cristina2013Food and Nutritional Components in FocusWoS-id: 000326647100008
00
70Higher incidence of thyroid agenesis in Mexican newborns with congenital hypothyroidism associated with birth defects2ᵒ autor: Ibarra-Gonzalez, I, Monroy-Santoyo, S, Fernandez-Lainez, C, Greenawalt-Rodriguez, S, et al.2012EARLY HUMAN DEVELOPMENTWoS-id: 000299449700012
Scopus-id: 2-s2.0-84355166724
1820
71Mutation analysis of the methylmalonyl-CoA mutase gene in ten Mexican patients with methylmalonic acidemiaCoautor: Ibarra I., Méndez S.T., Vela-Amieva M., Velázquez-Arellano A., et al.2012REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATIONWoS-id: 000309196300007
Scopus-id: 2-s2.0-84868223674
33
72Tandem Mass Spectrometry Newborn Screening for Inborn Errors of Intermediary Metabolism: Abnormal Profile InterpretationCoautor: Ibarra-Gonzalez, I, Fernandez-Lainez, C, Aguilar-Lemus, JJ, Vela-Amieva, M2012CURRENT MEDICINAL CHEMISTRYWoS-id: 000309511500011
Scopus-id: 2-s2.0-84868031084
1517
73Temporal development of genetic and metabolic effects of biotin deprivation. A search for the optimum time to study a vitamin deficiencyCoautor: Ibarra-González I., Hernández-Vázquez A., Ochoa-Ruiz E., Ortega-Cuellar D., et al.2012MOLECULAR GENETICS AND METABOLISMWoS-id: 000310720200015
Scopus-id: 2-s2.0-84867895871
68
74Correspondence 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.2011J CHILD NEUROLWoS-id: 000286834000023
Scopus-id: 2-s2.0-79551640527
00
75Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: A worldwide collaborative projectCoautor: Ibarra-Gonzalez, I, Abdenur, JE, Abdulrahman, M, Adair, O, et al.2011GENETICS IN MEDICINEWoS-id: 000287694800013
Scopus-id: 2-s2.0-79952194543
282304
76Hepatorenal tyrosinemia: The devastating natural history of the disease in Mexico2ᵒ autor: Ibarra-Gonzalez, I, Fernandez-Lainez, C, Ruiz-Gomez, M, Guillen-Lopez, S, et al.2011MOLECULAR GENETICS AND METABOLISMWoS-id: 000287773800069
00
77Effect of supplementation during pregnancy with L-arginine and antioxidant vitamins in medical food on pre-eclampsia in high risk population: randomised controlled trialCoautor: Ibarra, I, Vadillo-Ortega, F, Perichart-Perera, O, Espino, S, et al.2011BMJ-BRITISH MEDICAL JOURNALWoS-id: 000290952100004
Scopus-id: 2-s2.0-81355136042
11342
78Causes of delay in referral of patients with phenylketonuria to a specialized reference centre in Mexico2ᵒ autor: Ibarra-Gonzalez, I, Vela-Amieva, M, Fernandez-Lainez, C, Monroy-Santoyo, S, et al.2011JOURNAL OF MEDICAL SCREENINGWoS-id: 000297908900004
Scopus-id: 2-s2.0-80655139845
1013
79Clinical and biochemical characteristics of patients with urea cycle disorders in a developing country1ᵉʳ autor: Ibarra-Gonzalez, I, Fernandez-Lainez, C, Vela-Amieva, M2010CLINICAL BIOCHEMISTRYWoS-id: 000275219400019
Scopus-id: 2-s2.0-77149127415
1013
80The C677T polymorphism of the methylenetetrahydrofolate reductase gene is associated with idiopathic ischemic stroke in the young mexican-mestizo populationCoautor: Ibarra-González I., Isordia-Salas I., Barinagarrementería-Aldatz F., Leanos-Miranda, A, et al.2010CEREBROVASC DISWoS-id: 000277050000006
Scopus-id: 2-s2.0-77951831327
2428
81Effect of Highly Active Antiretroviral Therapy on Homocysteine Plasma Concentrations in HIV-1-Infected PatientsCoautor: Ibarra-Gonzalez, I, Coria-Ramirez, E, Cisneros, LN, Trevino-Perez, S, et al.2010JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMESWoS-id: 000280149000005
Scopus-id: 2-s2.0-77955012573
69
82UREA CYCLE DISORDERS: A LABORATORY APPROACH. EXPERIENCE AT A TERTIARY CARE CENTER IN A DEVELOPING COUNTRY2ᵒ autor: Ibarra-Gonzalez, IC, Vela-Amieva, MB, Fernandez-Lainez, C2009MOLECULAR GENETICS AND METABOLISMWoS-id: 000268942600611
00
83Increased 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.2007GACETA MEDICA DE MEXICOWoS-id: 000254326600005
Scopus-id: 2-s2.0-38449084779
68
84Differential effects of biotin deficiency and replenishment on rat liver pyruvate and propionyl-CoA carboxylases and on their mRNAsCoautor: Ibarra I., Rodríguez-Meléndez R., Pérez-Andrade M.E., Díaz A., et al.1999MOLECULAR GENETICS AND METABOLISMWoS-id: 000078706700003
Scopus-id: 2-s2.0-0344069769
3539
85Urinary organic acids in infant malnutrition2ᵒ autor: Ibarra I., Terán-García M., Velázquez A.1998PEDIATRIC RESEARCHWoS-id: 000075500100020
Scopus-id: 2-s2.0-0345451115
1518
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