B Ibarra - Concepedia

Author

B Ibarra

Mexican Social Security Institute

Also Known As

B IBARRA, B Ibarra, B. Ibarra, Bertha Ibarra, Bertha Ibarra Ibarra, Blanca Catalina Colin Ibarra

Publications

811

Citations

H-Index

Concepts

All Affiliations

Mexican Social Security Institute Universidad de Guadalajara Secretaría de Salud de Jalisco Hospital de Especialidades Augusta University

About

B Ibarra is an author at Mexican Social Security Institute specializing in medicine, genetics, and genetic variation.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	16	360
2	Public Health	5	5	85
3	Natural Sciences	3	3	78
4	Biochemistry	3	3	51
5	Health Sciences	2	2	38

B Ibarra

Publications

577

Citations

H-Index

Page 1

	Year	Citations
The C677T polymorphism of the methylenetetrahydrofolate reductase gene in Mexican mestizo neural-tube defect parents, control mestizo and native populations Ingrid-Patricia Dávalos, Norma Olivares, Marı́a-Teresa Castillo, Annales de Génétique BiologyGenetic DisorderGeneticsGenetic EpidemiologyHuman Polymorphism	2000	53
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
Genetic variation among four Mexican populations (Huichol, Purepecha, Tarahumara, and Mestizo) revealed by two VNTRs and four STRs. Héctor Rangel‐Villalobos, F. Rivas, Lucila Sandoval, PubMed GeneticsHuman PolymorphismGenetic DiversityGenotype-phenotype AssociationMolecular Ecology	2000	33
Phosphoglucomutase: Evidence for a New Locus Expressed in Human Milk José María Cantú, B Ibarra Science NutritionGenetic AnalysisCommon Pgm1BiochemistryLactation	1982	28
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
Centric fission, centromere‐telomere fusion and isochromosome formation: a possible origin of a de novo 12p trisomy Horacio Rivera, L García-Esquivel, M Jiménez-Sáinz, Clinical Genetics	1987	27
The phenotype in partial 13q trisomies, apropos of a familial (13;15)(q22;q26) translocation F. Rivas, Horacio Rivera, M. L. Plascencia, Human Genetics Developmental BiologyMendelian DisorderCytogeneticsGenetic DisorderGenetics	1984	27
Trisomy 22q12 leads to qter: "aneusomie de recombinaison" of a pericentric inversion. Cantú Jm, A Hernández, G Vaca, PubMed	1981	27
G-6-PD Guadalajara. A new mutant associated with chronic nonspherocytic hemolytic anemia G Vaca, B Ibarra, F. Romero, Human Genetics ImmunohematologyLaboratory HematologyAutoimmune DiseasePathogenesisHematology	1982	26

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