Author

M T Tusié-Luna

Observed names: M T Tusie-Luna, M. T. Tusié-Luna, M. T. Tusié‐Luna, M. Teresa Tusié-Luna, Maria-Teresa Tusie-Luna

Observed institutions: City Of Hope National Medical Center, Innsbruck Medical University, Universität Innsbruck, Cornell University, Charles H. Revson Foundation, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Instituto Nacional de Pediatria, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Instituto Politécnico Nacional, Universidad Nacional Autónoma de México

OpenAlex ID: A5111830795

Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

1992 · P W Speiser, J Dupont, et al. · Journal of Clinical Investigation · 570

The Product of the CYP11B2 Gene Is Required for Aldosterone Biosynthesis in the Human Adrenal Cortex

1991 · Kathleen M. Curnow, Maria-Teresa Tusie-Luna, et al. · Molecular Endocrinology · 362

Determination of functional effects of mutations in the steroid 21-hydroxylase gene (CYP21) using recombinant vaccinia virus.

1990 · M T Tusie-Luna, P Traktman, et al. · Journal of Biological Chemistry · 257

R339H and P453S: CYP21 mutations associated with nonclassic steroid 21- hydroxylase deficiency that are not apparent gene conversions

1992 · A Helmberg, M T Tusie-Luna, et al. · Molecular Endocrinology · 125

Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes

2009 · J. C. Florez, A. L. Price, et al. · Diabetologia · 104

Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: evidence of different genetic mechanisms involved in the production of the disease.

1998 · A U López-Gutiérrez, L Riba, et al. · Journal of Medical Genetics · 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

1999 · M. Natividad Lobato, M. Luisa Ordóñez-Sánchez, et al. · Human Heredity · 30

Contribution of Chromosome 1q21‐q23 to Familial Combined Hyperlipidemia in Mexican Families

2004 · A. Huertas‐Vázquez, J. P. del Rincón, et al. · Annals of Human Genetics · 27

[Obesity and metabolic syndrome as public health problem. A reflection].

2008 · E García-García, M De la Llata-Romero, et al. · PubMed · 13

HNF‐1α G574S is a functional variant with decreased transactivation activity

2006 · K. Navalón‐García, L. Mendoza‐Alcantar, et al. · Diabetic Medicine · 8

Strong Association of Socioeconomic Status and Genetic Ancestry in Latinos: Implications for Admixture Studies of Type 2 Diabetes

2011 · J. C. Florez, A. L. Price, et al. · Palgrave Macmillan US eBooks · 6

Analysis of the glucokinase gene in Mexican families displaying early-onset non-insulin-dependent diabetes mellitus including MODY families

1997 · Laura del Bosque-Plata, Eduardo García-García, et al. · American Journal of Medical Genetics · 4

Works count: 12

Citation count: 1,539

H-index: 9

I10-index: 9