Concepedia

Author

M T Tusié-Luna

Cornell University

Also Known As

M T Tusie-Luna, M T Tusié-Luna, M. T. Tusié-Luna, M. T. Tusié‐Luna, M. Teresa Tusié-Luna, Maria-Teresa Tusie-Luna

12

Publications

1.5K

Citations

9

H-Index

36

Concepts

All Affiliations

Cornell UniversityUniversidad Nacional Autónoma de MéxicoInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán
MT

About

M T Tusié-Luna is an author at Cornell University specializing in medicine, inherited metabolic disease, and clinical genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

4

4

748

2

Public Health

2

2

122

3

Health Sciences

1

1

14

4

Natural Sciences

1

1

121

5

Clinical Nutrition

1

1

14

M T Tusié-Luna

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9

Publications

1.5K

Citations

9

H-Index

YearCitations

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

Phyllis Speiser, Jakob Dupont, Dongjian Zhu,

Journal of Clinical Investigation

1992

580

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

Kathleen M. Curnow, M T Tusié-Luna, Leigh Pascoe,

Molecular Endocrinology

1991

357

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

M T Tusié-Luna, Paula Traktman, Perrin C. White

Journal of Biological Chemistry

1990

259

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

Arno Helmberg, M T Tusié-Luna, M. Tabarelli,

Molecular Endocrinology

1992

121

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

José C. Florez, Alkes L. Price, Desmond Campbell,

Diabetologia

2009

108

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

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

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

Adriana Huertas‐Vázquez, Juan P. del Rincón, Samuel Canizales‐Quinteros,

Annals of Human Genetics

2004

28

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

Emilio García García, M De la Llata-Romero, Martha Kaufer‐Horwitz,

PubMed

2009

14

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