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F. Perea · SciRah

Researcher profile · Semantic Scholar

F. Perea

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F. Perea — researcher profile on SciRah

h-index: 12
Works: 48
Citations: 416

Most-cited papers

Thalidomide therapy in a patient with thalassemia major.
L. Aguilar-López, J. L. Delgado-Lamas, B. Rubio-Jurado, F. Perea +1 more
2008Blood Cells, Molecules & Diseases44 citations
Semantic Scholar
Hb D-Los Angeles associated with Hb S or beta-thalassemia in four Mexican Mestizo families.
F. Perea, M. Casas-Castañeda, A. Villalobos-Arámbula, H. Barajas +4 more
1999Hemoglobin40 citations
Semantic Scholar
Polymorphisms in candidate genes for type 2 diabetes mellitus in a Mexican population with metabolic syndrome findings.
J. Sánchez-Corona, S. Flores-Martínez, M. Machorro-Lazo, C. Galaviz-Hernández +10 more
2004Diabetes Research and Clinical Practice37 citations
Semantic Scholar
Analysis of βS and βA Genes in a Mexican Population with African Roots
M. Magaña, Zoyla Ongay, J. Tagle, Gilberto Bentura +5 more
200232 citations
Semantic Scholar
Centromere–telomere (12;8p) fusion, telomeric 12q translocation, and i(12p) trisomy 1
H. Rivera, A. I. Vásquez, F. Perea
1999Clinical Genetics32 citations
Semantic Scholar
Red cell membrane protein deficiencies in Mexican patients with hereditary spherocytosis.
J. Sánchez-López, A. L. Camacho, M. Magaña, B. Ibarra +1 more
2003Blood Cells, Molecules & Diseases27 citations
Semantic Scholar
β‐globin gene cluster haplotypes in sickle cell patients from Panamá
I. Rusanova, Gladys Cossio, B. Moreno, F. Perea +4 more
2011American Journal of Human Biology18 citations
Semantic Scholar
β-Thalassemia and βA globin gene haplotypes in Mexican mestizos
A. Villalobos-Arámbula, R. Bustos, M. Casas-Castañeda, E. Gutiérrez +3 more
1997Human Genetics17 citations
Semantic Scholar
Prevalence of −α3.7 and αααanti3.7 alleles in sickle cell trait and β-thalassemia patients in Mexico
María Paulina Nava, B. Ibarra, M. Magaña, María de la Luz Estela Uscanga Chávez +1 more
200616 citations
Semantic Scholar
Molecular spectrum of β-thalassemia in the Mexican population
F. Perea, M. Magaña, Jośe G. Cobían, J. Sánchez-López +5 more
200415 citations
Semantic Scholar
Analysis of the SLC4A1 gene in three Mexican patients with hereditary spherocytosis: Report of a novel mutation
J. Sánchez-López, A. L. Camacho-Torres, B. Ibarra, Jesús A. Tintos +1 more
2009Genetics and Molecular Biology13 citations Open access
Semantic Scholar
βA globin gene haplotypes in Mexican Huichols: Genetic relatedness to other populations
A. Villalobos-Arámbula, F. Rivas, L. Sandoval, F. Perea +3 more
2000American Journal of Human Biology13 citations
Semantic Scholar
Analysis of betaS and betaA genes in a Mexican population with African roots.
M. Magaña, Zoyla Ongay, J. Tagle, Gilberto Bentura +5 more
2002Blood Cells, Molecules & Diseases11 citations
Semantic Scholar
Alpha-thalassemia in a selected population of Mexico.
M. Casas-Castañeda, I. Hernández-Lugo, O. Torres, H. Barajas +6 more
1998Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion11 citations
Semantic Scholar
HLA-DQB1, -DQA1, -DRB1 linkage disequilibrium and haplotype diversity in a Mestizo population from Guadalajara, Mexico.
L. M. Cortes, L. M. Baltazar, F. Perea, M. P. Gallegos-Arreola +8 more
2004Tissue Antigens10 citations
Semantic Scholar
EGFR gene polymorphisms -216G>T and -191C>A are risk markers for gastric cancer in Mexican population.
J. Torres-Jasso, M. E. Marín, E. Santiago-Luna, J. C. Leoner +5 more
2015Genetics and Molecular Research8 citations Open access
Semantic Scholar
HB Fannin-Lubbock-I with A Single GGC>GAC Mutation at β119(GH2)Gly→Asp in a Homozygous Mexican Patient
B. Ibarra, E. Aizpuru, J. Sánchez-López, Karina R Morales +2 more
2009Hemoglobin6 citations
Semantic Scholar
Types and frequencies of hemoglobin disorders in the pacific coast of four states of Mexico.
Jośe G. Cobían, J. Sánchez-López, M. Magaña, M. Chávez +2 more
2009Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion6 citations
Semantic Scholar
Genetic relationship of a Mexican Afromestizo population through the analysis of the 3′ haplotype of the β globin gene in βA chromosomes
M. Magaña, F. Perea, J. González, B. Ibarra
20076 citations
Semantic Scholar
[Thalassemic alleles in Mexican mestizos].
Bertha Ibarra, F. Perea, A. Villalobos-Arámbula
1995Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion6 citations
Semantic Scholar
Prevalence of -alpha(3.7) and alpha alpha alpha(anti3.7) alleles in sickle cell trait and beta-thalassemia patients in Mexico.
María Paulina Nava, B. Ibarra, M. Magaña, María de la Luz Chávez +1 more
2006Blood Cells, Molecules & Diseases5 citations
Semantic Scholar
Haplotype analysis of the Mexican frameshift Cd 11 (−T) and −28 A→C β‐thalassemia alleles
F. Perea, M. A. Esparza, A. Villalobos-Arámbula, B. Ibarra +1 more
1996American journal of hematology/oncology5 citations
Semantic Scholar
Diversity of the 5′ β-Globin Haplotype of Four β-Thalassemia Mutations in the Mexican Population
Karina R Morales, M. Magaña, B. Ibarra, F. Perea
2009Hemoglobin4 citations
Semantic Scholar
Linkage disequilibrium between four MTTP gene polymorphisms in a Mexican population
K. E. Luévano, J. R. González, F. Perea, M. Magaña
2009Annals of Human Biology3 citations
Semantic Scholar
Genetic relationship of a Mexican Afromestizo population through the analysis of the 3' haplotype of the beta globin gene in betaA chromosomes.
M. Magaña, F. Perea, J. González, B. Ibarra
2007Blood Cells, Molecules & Diseases3 citations
Semantic Scholar
3' haplotypes of the beta-globin gene in beta(S)-chromosomes of Mexican individuals.
M. Magaña, F. Perea, Zoila Ongay, B. Ibarra
2005Blood Cells, Molecules & Diseases3 citations
Semantic Scholar
Molecular spectrum of beta-thalassemia in the Mexican population.
F. Perea, M. Magaña, Jośe G. Cobían, J. Sánchez-López +5 more
2004Blood Cells, Molecules & Diseases3 citations
Semantic Scholar
[Fetal hemoglobin and the gamma G/gamma A chain ratio in children with acute lymphoblastic leukemia L1 and L2].
A. Villalobos-Arámbula, J. C. Aguilar-Luna, A. Esparza, F. Perea +3 more
1993Sangre3 citations
Semantic Scholar
Characterization of the 5′ and 3′ Breakpoints of the Spanish (δβ)0-Thalassemia Deletion in Mexican Patients
Luis F. Guzmán, F. Perea, Karina R. Morales-González, J. Sánchez-López +3 more
2011Hemoglobin2 citations
Semantic Scholar
Hb S [β6(A3)Glu→Val, GAG>GTG] in Mexican Mestizos: Frequency and Analysis of the 5' β-Globin Haplotype
Luis F. Guzmán, F. Perea, M. Magaña, Karina R. Morales-González +2 more
2010Hemoglobin2 citations
Semantic Scholar
A Frameshift at Codons 77/78 (–C): A Novel β‐Thalassemia Mutation
F. Perea, M. Magaña, M. A. Esparza, B. Ibarra
20042 citations
Semantic Scholar
Hb Lepore Washington-Boston in two Mexican mestizo families.
B. Ibarra, M. Casas-Castañeda, A. Villalobos-Arámbula, G. Zamudio +8 more
1997Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion2 citations
Semantic Scholar
Screening for thermostability and electrophoretic red blood cell sorbitol dehydrogenase (E.C.1.1.1.14) variants.
B. Ibarra, G. Vaca, F. Perea, M. Rábago +3 more
1989Annales de Genetique2 citations
Semantic Scholar
Electrophoretic pattern of sorbitol dehydrogenase (E.C.1.1.1.14) in human seminal plasma and spermatozoa.
F. Perea, G. Vaca, C. Alvarez, J. Cantú +1 more
1989Annales de Genetique2 citations
Semantic Scholar
DIVERSITY OF THE 5 ¢ b-GLOBIN HAPLOTYPE OF FOUR b-THALASSEMIA MUTATIONS IN THE MEXICAN POPULATION β-Thalassemia Haplotypes in Mexico
Karina R Morales, M. Magaña, B. Ibarra, F. Perea
20091 citations
Semantic Scholar
Hemoglobin D-Los Angeles (Btha 121 Glu-Gln) in a mexican family
A. R. Cabrera, L. Holley, D. Elam, F. Kutlar +6 more
20041 citations
Semantic Scholar
Analysis of HLA DQA1 and DQB1 alleles and glycated hemoglobin in healthy Mexican mestizo individuals from families with type 1 diabetes mellitus
R. M. Hermosillo-Bañuelos, C. Ramos, F. Perea, F. Rivas +4 more
20031 citations
Semantic Scholar
Hb COLIMA [β49(CD8)Ser→Cys]: A NEW HEMOGLOBIN VARIANT
Jośe G. Cobían, Maria-Teresa Magan ̃a, F. Perea, B. Ibarra
20021 citations
Semantic Scholar
Hb Colima [beta 49(CD8)Ser-->Cys]: a new hemoglobin variant.
Jośe G. Cobían, M. Magaña, F. Perea, B. Ibarra
2002Hemoglobin1 citations
Semantic Scholar
The Hb Tarrant [alpha126(H9)Asp-->Asn]] mutation is localized in the alpha2-globin gene.
F. Perea, G. Zamudio, L. Meillon, B. Ibarra
1999Hemoglobin1 citations
Semantic Scholar
Beta-thalassemia and beta[A] globin gene haplotypes in Mexican mestizos.
A. Villalobos-Arámbula, R. Bustos, M. Casas-Castañeda, E. Gutiérrez +3 more
1997Human Genetics1 citations
Semantic Scholar
beta haplotypes of three Mexican Mestizo families with Spanish (delta beta)o-thalassemia.
A. Villalobos-Arámbula, R. Bustos, F. Perea, B. Ibarra +4 more
1996Hemoglobin1 citations
Semantic Scholar
Wayward effect of polymorphism (TA)8 in the promoter region of UGT1A1 gene in a Mexican family.
JA Tintos-Hernández, F. Perea, B. Ibarra, LE Figuera
2012West Indian medical journal0 citations
Semantic Scholar
H-hemoglobin: A case report identified at Monterrey, Nuevo Leon
Guillermo J. Ruiz Delgado, E. Garza, B. Ibarra, F. Perea +1 more
20080 citations
Semantic Scholar
A frameshift at codons 77/78 (-C): a novel beta-thalassemia mutation.
F. Perea, M. Magaña, M. A. Esparza, B. Ibarra
2004Hemoglobin0 citations
Semantic Scholar
Analysis of HLA DQA 1 and DQB 1 alleles and glycated hemoglobin in healthy Mexican mestizo individuals from families with type 1 diabetes mellitus
R. M. Hermosillo-Bañuelos, C. Ramos, F. Perea, F. Rivas +5 more
20030 citations
Semantic Scholar
Reply to “frameshift Cd 11 (‐T) β‐thalassemia mutation”
B. Ibarra, A. Villalobos-Arámbula, F. Perea
19970 citations Open access
Semantic Scholar
[Molecular aspects of alpha dn beta thalassemias].
B. Ibarra, F. Perea, A. Hernández-Córdova
1990Archivos de investigacion medica0 citations
Semantic Scholar

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