Ma. Luisa Ordóñez-Sánchez

Author

Also Known As

M L Ordoñez-Sánchez, M. L. Ordoñez-Sánchez, M. Luisa Ordóñez-Sánchez, Ma Luisa Ordoñez-Sánchez, Ma. Luisa Ordóñez-Sánchez

Publications

171

Citations

H-Index

Concepts

All Affiliations

Universidad Nacional Autónoma de México Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán Mexican Social Security Institute Universidad Autónoma Metropolitana

About

Ma. Luisa Ordóñez-Sánchez is an author at Universidad Nacional Autónoma de México specializing in genetics, medicine, and inherited metabolic disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	65
2	Public Health	1	1	11
3	Diabetes	1	1	11
4	Epidemiology	1	1	11
5	Molecular Genetics	1	1	33

Ma. Luisa Ordóñez-Sánchez

Publications

171

Citations

H-Index

Page 1

	Year	Citations
Early-Onset Type 2 Diabetes: Metabolic and Genetic Characterization in the Mexican Population<sup>1</sup> Carlos A. Aguilar‐Salinas, Eduardo Reyes-Rodríguez, Ma. Luisa Ordóñez-Sánchez, The Journal of Clinical Endocrinology & Metabolism	2001	51
Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: evidence of different genetic mechanisms involved in the production of the disease. Antonio Ulises López-Gutierrez, Laura Riba, Ma. Luisa Ordóñez-Sánchez, Journal of Medical Genetics GeneticsMexican FamiliesPathologyMolecular GeneticsEpigenetics	1998	33
Mutation Analysis in Patients with Congenital Adrenal Hyperplasia in the Spanish Population: Identification of Putative Novel Steroid 21-Hydroxylase Deficiency Alleles Associated with the Classic Form of the Disease Mark N. Lobato, Ma. Luisa Ordóñez-Sánchez, M T Tusié-Luna, Human Heredity	1999	30
The SLC16A11 risk haplotype is associated with decreased insulin action, higher transaminases and large-size adipocytes Paloma Almeda‐Valdés, Donají Gómez‐Velasco, Olimpia Arellano Campos, European Journal of Endocrinology	2018	25
Low frequency of deletion alleles in patients with steroid 21-hydroxylase deficiency in a Mexican population Marı́a Teresa Tusié-Luna, Salvador Ramı́rez-Jiménez, Ma. Luisa Ordóñez-Sánchez, Human Genetics Mexican PopulationMendelian DisorderGenetic DisorderGeneticsInherited Metabolic Disease	1996	21
R230C but not − 565C/T variant of the ABCA1 gene is associated with type 2 diabetes in Mexicans through an effect on lowering HDL-cholesterol levels Ana Ochoa-Guzmán, Hortensia Moreno-Macías, D. Guillén-Quintero, Journal of Endocrinological Investigation Genetic DeterminantDiabetes EpidemiologyCardiovascular DiseaseGeneticsDiabetes	2020	11

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