Publications by authors named "Silvia Jiménez-Morales"

37Publications

Genotype-Environment Interaction Analysis of NQO1, CYP2E1, and NAT2 Polymorphisms and the Risk of Childhood Acute Lymphoblastic Leukemia: A Report From the Mexican Interinstitutional Group for the Identification of the Causes of Childhood Leukemia.

Front Oncol 2020 21;10:571869. Epub 2020 Sep 21.

Laboratorio de Genómica del Cáncer, Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City, Mexico.

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http://dx.doi.org/10.3389/fonc.2020.571869DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7537417PMC
September 2020

Maternal and paternal ages at conception of index child and risk of childhood acute leukaemia: A multicentre case-control study in Greater Mexico City.

Cancer Epidemiol 2020 Aug 19;67:101731. Epub 2020 May 19.

Coordinación de Investigación en Salud, CMN "Siglo XXI", IMSS. Av. Cuauhtemoc 330, Delegación Cuauhtémoc, Mexico City, 06720, Mexico; Unidad de Investigación Médica en Epidemiología Clínica, Unidad Médica de AltaEspecialidad (UMAE) Hospital de Pediatría, Centro Médico Nacional (CMN) "Siglo XXI", Instituto Mexicano del Seguro Social (IMSS). Av. Cuauhtemoc 330, Delegación Cuauhtémoc, Mexico City, 06720, Mexico; Laboratorio de Biología Molecular de las Leucemias, Unidad de Investigación en Genética Humana, UMAE, Hospital de Pediatría, CMN "Siglo XXI", IMSS. Av. Cuauhtemoc 330, Delegación Cuauhtémoc, Mexico City, 06720, Mexico. Electronic address:

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http://dx.doi.org/10.1016/j.canep.2020.101731DOI Listing
August 2020

The NR3C1 gene expression is a potential surrogate biomarker for risk and diagnosis of posttraumatic stress disorder.

Psychiatry Res 2020 02 16;284:112797. Epub 2020 Jan 16.

Laboratorio de Genética de la Licenciatura en Ciencia Forense, Facultad de Medicina, Universidad Nacional Autónoma de México, México. Electronic address:

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http://dx.doi.org/10.1016/j.psychres.2020.112797DOI Listing
February 2020

Long Non-Coding RNA and Acute Leukemia.

Int J Mol Sci 2019 Feb 9;20(3). Epub 2019 Feb 9.

Laboratorio de Genómica del Cáncer, Instituto Nacional de Medicina Genómica, Mexico City 14610, Mexico.

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http://dx.doi.org/10.3390/ijms20030735DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387068PMC
February 2019

An association study in PTPN22 suggests that is a risk factor to Takayasu's arteritis.

Inflamm Res 2019 Mar 23;68(3):195-201. Epub 2018 Nov 23.

Unidad de Investigación en Enfermedades Metabólicas y Endócrinas, Hospital Juárez de México, Av. Instituto Politécnico Nacional No. 5160, Delegación Gustavo A. Madero, C.P. 07760, Mexico City, DF, Mexico.

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http://dx.doi.org/10.1007/s00011-018-1204-1DOI Listing
March 2019

Overview of mitochondrial germline variants and mutations in human disease: Focus on breast cancer (Review).

Int J Oncol 2018 Sep 4;53(3):923-936. Epub 2018 Jul 4.

Laboratory of Cancer Genomics, National Institute of Genomic Medicine, 14610 Mexico City, Mexico.

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http://dx.doi.org/10.3892/ijo.2018.4468DOI Listing
September 2018

A greater birthweight increases the risk of acute leukemias in Mexican children-experience from the Mexican Interinstitutional Group for the Identification of the Causes of Childhood Leukemia (MIGICCL).

Cancer Med 2018 04 13;7(4):1528-1536. Epub 2018 Mar 13.

Health Research Coordination, Instituto Mexicano del Seguro Social (IMSS), Mexico City, Mexico.

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http://doi.wiley.com/10.1002/cam4.1414
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http://dx.doi.org/10.1002/cam4.1414DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5911591PMC
April 2018

[Acute lymphoblastic leukemia: a genomic perspective].

Bol Med Hosp Infant Mex 2017 Jan - Feb;74(1):13-26. Epub 2017 Jan 27.

Unidad de Investigación en Enfermedades Metabólicas y Endocrinas, Hospital Juárez de México, Ciudad de México, México.

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http://dx.doi.org/10.1016/j.bmhimx.2016.07.007DOI Listing
April 2019

High frequency of mutant thiopurine S-methyltransferase genotypes in Mexican patients with systemic lupus erythematosus and rheumatoid arthritis.

Clin Rheumatol 2018 Apr 20;37(4):963-970. Epub 2017 Dec 20.

Unidad de Investigación en Enfermedades Endócrinas y Metabólicas, Hospital Juárez de México, Av. Instituto Politécnico Nacional No. 5160 Delegación Gustavo A. Madero, C.P. 07760, Mexico City, D.F., Mexico.

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http://dx.doi.org/10.1007/s10067-017-3955-4DOI Listing
April 2018

Mutation Screening in a Case with Cleft Lip, Hypothyroidism, and Thyroid Carcinoma: A New Syndrome?

Case Rep Genet 2017 27;2017:6390545. Epub 2017 Aug 27.

Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City, Mexico.

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http://dx.doi.org/10.1155/2017/6390545DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5591984PMC
August 2017

Genomewide admixture study in Mexican Mestizos with multiple sclerosis.

Clin Neurol Neurosurg 2015 Mar 24;130:55-60. Epub 2014 Dec 24.

National Institute of Neurology and Neurosurgery of Mexico, Insurgentes Sur #3877, Mexico City 14269, Mexico. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S03038467140047
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http://dx.doi.org/10.1016/j.clineuro.2014.11.026DOI Listing
March 2015

[Tumor necrosis factor alpha (TNF-α) in autoimmune diseases (AIDs): molecular biology and genetics].

Gac Med Mex 2014 Jul-Aug;150(4):334-44

Laboratorio de Medicina Genómica, Unidad de Investigación, Hospital Juárez de México, México, D.F.

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January 2015

Increased incidence and disparity of diagnosis of retinoblastoma patients in Guatemala.

Cancer Lett 2014 Aug 6;351(1):59-63. Epub 2014 May 6.

Stanford University, Stanford, CA 94305, USA; Unidad Nacional de Oncología Pediátrica, Guatemala City, Guatemala; Pediatric Hematology/Oncology/SCT/Cancer Bio, Stanford University School of Medicine, Stanford, CA 94305, USA.

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http://dx.doi.org/10.1016/j.canlet.2014.04.023DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4490907PMC
August 2014

CHRM2 but not CHRM1 or CHRM3 polymorphisms are associated with asthma susceptibility in Mexican patients.

Mol Biol Rep 2014 16;41(4):2109-17. Epub 2014 Jan 16.

Laboratory of Immunogenomics and Metabolic Diseases, Instituto Nacional de Medicina Genómica, SS, Periférico Sur 4809, Col. Arenal Tepepan, CP. 014610, Mexico City, Mexico.

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http://dx.doi.org/10.1007/s11033-014-3060-6DOI Listing
December 2014

Polymorphisms in metalloproteinase-9 are associated with the risk for asthma in Mexican pediatric patients.

Hum Immunol 2013 Aug 29;74(8):998-1002. Epub 2013 Apr 29.

Laboratorio de Inmunogenómica y Enfermedades Metabólicas, Instituto Nacional de Medicina Genómica, SS, Mexico City, Mexico.

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http://dx.doi.org/10.1016/j.humimm.2013.04.036DOI Listing
August 2013

[Systemic lupus erythematosus: genomics of the disease].

Gac Med Mex 2012 Jul-Aug;148(4):371-80

Laboratorio de Inmunogenómica y Enfermedades Metabólicas, Instituto Nacional de Medicina Genómica, SSA, México.

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January 2013

NFE2L2 gene variants and susceptibility to childhood-onset asthma.

Rev Invest Clin 2011 Jul-Aug;63(4):407-11

Laboratorio de Inmunogenómica y enfermedades metabólicas, Instituto Nacional de Medicina Genómica, SSA.

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April 2012

Molecular screening of the CFTR gene in Mexican patients with congenital absence of the vas deferens.

Genet Test Mol Biomarkers 2012 Apr 21;16(4):292-6. Epub 2011 Nov 21.

Genomic of Complex Diseases Laboratory, Instituto Nacional de Medicina Genómica, SS, Mexico City, Mexico.

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http://dx.doi.org/10.1089/gtmb.2011.0124DOI Listing
April 2012