Francisco J. Perea - Concepedia

Author

Francisco J. Perea

Also Known As

Bertha Ibarra Cortés, Díaz, Francisco Javier Perea, F J Perea, F J Perea-Díaz, F Javier Perea, F Perea, F. J. Perea, F. J. Perea‐Díaz, F. Javier Perea, F.J Perea

Publications

505

Citations

H-Index

Concepts

All Affiliations

Universidad de Guadalajara Mexican Social Security Institute Secretaría de Salud de Jalisco

About

Francisco J. Perea is an author at Universidad de Guadalajara specializing in genetics, medicine, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	195
2	Public Health	3	3	59
3	Biology	3	3	62
4	Natural Sciences	2	2	45
5	Cell Biology	2	2	87

Francisco J. Perea

Publications

333

Citations

H-Index

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	Year	Citations
Centromere–telomere (12;8p) fusion, telomeric 12q translocation, and i(12p) trisomy 1 Horacio Rivera, Ana Isabel Vásquez, Francisco J. Perea Clinical Genetics CytogeneticsGeneticsMolecular BiologyMolecular GeneticsEpigenetics	1999	65
Association analysis of vitamin D receptor gene polymorphisms and bone mineral density in postmenopausal Mexican-Mestizo women Anahí González‐Mercado, Josefina Yoaly Sánchez-López, José Ángel Regla-Nava, Genetics and Molecular Research	2013	37
Analysis of βS and βA Genes in a Mexican Population with African Roots Marı́a Teresa Magaña, Zoyla Ongay, Juan Tagle, Blood Cells Molecules and Diseases BiologyGenetic DiversityMexican PopulationMolecular EcologyβA Genes	2002	34
Polymorphisms in candidate genes for type 2 diabetes mellitus in a Mexican population with metabolic syndrome findings José Sánchez‐Corona, Maria-Victoria Machorro-Lazo, Carlos Galaviz‐Hernández, Diabetes Research and Clinical Practice ObesityMetabolic SyndromeCandidate GenesMexican PopulationGenetic Determinant	2003	31
Hb D-Los Angeles Associated with Hb S or β-Thalassemia in Four Mexican Mestizo Families Francisco J. Perea, Maricela Casas-Castañeda, Alma Rosa Villalobos-Arámbula, Hemoglobin	1999	27
Autosomal dominant early onset Alzheimer's disease in the Mexican state of Jalisco: High frequency of the mutation <scp><i>PSEN1</i></scp> c.<scp>1292C</scp>>A and phenotypic profile of patients Sofía Dumois‐Petersen, Martha Patricia Gallegos‐Arreola, María Teresa Magaña‐Torres, American Journal of Medical Genetics Part C Seminars in Medical Genetics	2020	25
Red cell membrane protein deficiencies in Mexican patients with hereditary spherocytosis Josefina Yoaly Sánchez-López, Ana L Camacho, Marı́a Teresa Magaña, Blood Cells Molecules and Diseases GeneticsMexican PatientsPathologyMedicineCell Biology	2003	22
β-Thalassemia and β A globin gene haplotypes in Mexican mestizos Alma Rosa Villalobos-Arámbula, Rocío Bustos, Maricela Casas-Castañeda, Human Genetics BiologyMedicineGeneticsHematologyMolecular Genetics	1997	17
β‐globin gene cluster haplotypes in sickle cell patients from Panamá Iryna Rusanova, Gladys Cossio, Bélgica Moreno, American Journal of Human Biology	2011	16
Molecular spectrum of β-thalassemia in the Mexican population Francisco J. Perea, Marı́a Teresa Magaña, José G. Cobián, Blood Cells Molecules and Diseases Genetic DisorderMedicineGeneticsHematologyGenetic Epidemiology	2004	15

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