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Francisco Javier Perea

Observed names: F J Perea, F J Perea-Díaz, F Javier Perea, F. J. Perea, F. J. Perea‐Díaz, F. Javier Perea, F.J Perea, F.J. Perea, F.J. Perea-Díaz, F.Javier Perea, F.Javier Perea-Dı́az, FRANCISCO JAVIER PEREA-DÍAZ, Francisco J Perea, Francisco J. Perea, Francisco J. Perea-Díaz, Francisco J. Perea‐Díaz, Francisco Javier Perea D, Francisco Javier Perea Díaz, Francisco Javier Perea-Díaz, Francisco Javier Perea‐Díaz, Francisco Perea-Díaz, Francisco Perea‑Díaz, Francisco-Javier Perea, Francisco Javier Perea‐Díaz, J. Perea-Díaz
ORCID: 0000-0003-4227-4539
Observed ORCID: 0000-0003-4227-4539
OpenAlex ID: A5073718612
Centromere–telomere (12;8p) fusion, telomeric 12q translocation, and i(12p) trisomy 1
1999 · Horacio Rivera, Ana Isabel Vásquez, et al. · Clinical Genetics · 65
Thalidomide therapy in a patient with thalassemia major
2008 · Lilia Beatriz Aguilar-Lopez, José Luis Delgado-Lamas, et al. · Blood Cells Molecules and Diseases · 41
Association analysis of vitamin D receptor gene polymorphisms and bone mineral density in postmenopausal Mexican-Mestizo women
2013 · A. González-Mercado, J.Y. Sánchez-López, et al. · Genetics and Molecular Research · 35
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Analysis of βS and βA Genes in a Mexican Population with African Roots
2002 · Marı́a Teresa Magaña, Zoyla Ongay, et al. · Blood Cells Molecules and Diseases · 34
Polymorphisms in candidate genes for type 2 diabetes mellitus in a Mexican population with metabolic syndrome findings
2003 · J Sánchez-Corona, S.E Flores-Martı́nez, et al. · Diabetes Research and Clinical Practice · 33
Hb D-Los Angeles Associated with Hb S or β-Thalassemia in Four Mexican Mestizo Families
1999 · F. J. Perea, M. Casas-castañeda, et al. · Hemoglobin · 27
Autosomal dominant early onset Alzheimer's disease in the Mexican state of Jalisco: High frequency of the mutation PSEN1 c. 1292C >A and phenotypic profile of patients
2020 · Sofia Dumois‐Petersen, Martha P. Gallegos‐Arreola, et al. · American Journal of Medical Genetics Part C Seminars in Medical Genetics · 25
Red cell membrane protein deficiencies in Mexican patients with hereditary spherocytosis
2003 · J.Yoaly Sánchez-López, Ana L Camacho, et al. · Blood Cells Molecules and Diseases · 22
β‐globin gene cluster haplotypes in sickle cell patients from Panamá
2011 · Iryna Rusanova, Gladys Cossio, et al. · American Journal of Human Biology · 18
β-Thalassemia and β A globin gene haplotypes in Mexican mestizos
1997 · Alma R. Villalobos-Arámbula, Rocío Bustos, et al. · Human Genetics · 16
Molecular spectrum of β-thalassemia in the Mexican population
2004 · F.Javier Perea, Marı́a Teresa Magaña, et al. · Blood Cells Molecules and Diseases · 14
Prevalence of −α3.7 and αααanti3.7 alleles in sickle cell trait and β-thalassemia patients in Mexico
2006 · María Paulina Nava, Bertha Ibarra, et al. · Blood Cells Molecules and Diseases · 13
HLA‐DQB1, ‐DQA1, ‐DRB1 linkage disequilibrium and haplotype diversity in a Mestizo population from Guadalajara, Mexico
2004 · L.M. Cortes, L.M. Baltazar, et al. · Tissue Antigens · 11
?A globin gene haplotypes in Mexican Huichols: Genetic relatedness to other populations
2000 · A.R. Villalobos-Ar�mbula, F. Rivas, et al. · American Journal of Human Biology · 11
Association of polymorphisms of the TNFRSF11B and TNFSF11 genes with bone mineral density in postmenopausal women from western Mexico
2019 · Anahi González-Mercado, Josefina Sánchez-López, et al. · Archives of Medical Science · 10
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Alpha-thalassemia in a selected population of Mexico.
1998 · M Casas-Castañeda, I Hernandez-Lugo, et al. · PubMed · 10
EGFR gene polymorphisms -216G>T and -191C>A are risk markers for gastric cancer in Mexican population
2015 · J.H. Torres-Jasso, M.E. Marín, et al. · Genetics and Molecular Research · 9
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Analysis of the SLC4A1 gene in three Mexican patients with hereditary spherocytosis: report of a novel mutation
2009 · Josefina Y. Sánchez-López, Ana L. Camacho-Torres, et al. · Genetics and Molecular Biology · 9
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Hb Lepore Washington-Boston in two Mexican mestizo families.
1997 · B Ibarra, M Casas-Castañeda, et al. · PubMed · 9
Three Mexican Families with β thalassemia intermedia with different molecular basis
2019 · Lourdes del Carmen Rizo de la Torre, Francisco Javier Perea Díaz, et al. · Genetics and Molecular Biology · 8
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Fetal hemoglobin regulating genetic variants identified in homozygous (HbSS) and heterozygous (HbSA) subjects from South Mexico
2022 · L C Rizo-de la Torre, F J Borrayo-López, et al. · Journal of Tropical Pediatrics · 7
Molecular analysis of complex cases of alpha‐ and beta‐thalassemia in Mexican mestizo patients with microcytosis and hypochromia reveals two novel alpha0‐thalassemia deletions ‐ ‐Mex1and ‐ ‐Mex2
2016 · E. I. de‐la‐Cruz‐Salcedo, B. Ibarra, et al. · International Journal of Laboratory Hematology · 6
Genetic relationship of a Mexican Afromestizo population through the analysis of the 3′ haplotype of the β globin gene in βA chromosomes
2007 · María Teresa Magaña, F. Javier Perea, et al. · Blood Cells Molecules and Diseases · 6
HB Fannin-Lubbock-I with A Single GGC>GAC Mutation at β119(GH2)Gly→Asp in a Homozygous Mexican Patient
2009 · Bertha Ibarra, Edna Aizpuru, et al. · Hemoglobin · 5
Diversity of the 5′ β-Globin Haplotype of Four β-Thalassemia Mutations in the Mexican Population
2009 · Karina R. Morales, Maria T. Magaña, et al. · Hemoglobin · 5
Works count: 66
Citation count: 519
H-index: 12
I10-index: 16
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