B Ibarra

812 total citations
74 papers, 628 citations indexed

About

B Ibarra is a scholar working on Genetics, Hematology and Genetics. According to data from OpenAlex, B Ibarra has authored 74 papers receiving a total of 628 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 23 papers in Hematology and 22 papers in Genetics. Recurrent topics in B Ibarra's work include Hemoglobinopathies and Related Disorders (30 papers), Iron Metabolism and Disorders (17 papers) and Erythrocyte Function and Pathophysiology (13 papers). B Ibarra is often cited by papers focused on Hemoglobinopathies and Related Disorders (30 papers), Iron Metabolism and Disorders (17 papers) and Erythrocyte Function and Pathophysiology (13 papers). B Ibarra collaborates with scholars based in Mexico, United States and United Kingdom. B Ibarra's co-authors include Francisco J. Perea, G Vaca, Horacio Rivera, J. M. Cant�, Lucila Sandoval, J. M. Cantú, José María Cantú, Alma Rosa Villalobos-Arámbula, Cantú Jm and Luis E. Figuera and has published in prestigious journals such as Science, Genomics and Human Genetics.

In The Last Decade

B Ibarra

70 papers receiving 604 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
B Ibarra Mexico	16	246	209	166	152	147	74	628
R. Öner Türkiye	14	101 0.4×	352 1.7×	305 1.8×	132 0.9×	81 0.6×	36	693
Johannes Kristian Ploos van Amstel Netherlands	13	129 0.5×	131 0.6×	118 0.7×	197 1.3×	129 0.9×	17	695
Nisha Vasavda United Kingdom	13	120 0.5×	319 1.5×	290 1.7×	130 0.9×	102 0.7×	19	575
H H Kazazian United States	8	142 0.6×	251 1.2×	204 1.2×	262 1.7×	50 0.3×	8	754
M. Furbetta Italy	15	158 0.6×	802 3.8×	583 3.5×	243 1.6×	374 2.5×	48	1.1k
Gillian R. Milner United Kingdom	12	79 0.3×	114 0.5×	209 1.3×	171 1.1×	50 0.3×	21	487
Henriette S. Andersen Denmark	19	52 0.2×	264 1.3×	275 1.7×	516 3.4×	118 0.8×	26	1.1k
Catherine Driscoll United States	12	80 0.3×	702 3.4×	615 3.7×	227 1.5×	183 1.2×	33	1.0k
María de Fátima Sonati Brazil	14	55 0.2×	537 2.6×	457 2.8×	103 0.7×	200 1.4×	83	720
Vivien Sheehan United States	15	92 0.4×	559 2.7×	432 2.6×	291 1.9×	161 1.1×	77	840

Countries citing papers authored by B Ibarra

Since Specialization

Citations

This map shows the geographic impact of B Ibarra's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by B Ibarra with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites B Ibarra more than expected).

Fields of papers citing papers by B Ibarra

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by B Ibarra. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by B Ibarra. The network helps show where B Ibarra may publish in the future.

Co-authorship network of co-authors of B Ibarra

This figure shows the co-authorship network connecting the top 25 collaborators of B Ibarra. A scholar is included among the top collaborators of B Ibarra based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with B Ibarra. B Ibarra is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Torres, Javier, et al.. (2015). EGFR gene polymorphisms -216G>T and -191C>A are risk markers for gastric cancer in Mexican population. Genetics and Molecular Research. 14(1). 1802–1807. 9 indexed citations

Regla-Nava, José Ángel, Jorge Iván Gámez-Nava, Laura González-López, et al.. (2013). Association analysis of vitamin D receptor gene polymorphisms and bone mineral density in postmenopausal Mexican-Mestizo women. Genetics and Molecular Research. 12(3). 2755–2763. 28 indexed citations

Ibarra, B, et al.. (2012). Wayward effect of polymorphism (TA)8 in the promoter region of UGT1A1 gene in a Mexican family.. PubMed. 61(1). 81–3.

Ibarra, B, et al.. (2009). Analysis of linkage disequilibrium between the 5′ and 3′ haplotypes of the β-globin gene cluster in Mexican afromestizos. Blood Cells Molecules and Diseases. 44(2). 89–94. 3 indexed citations

Ibarra, B, et al.. (2009). Diversity of the 5′ β-Globin Haplotype of Four β-Thalassemia Mutations in the Mexican Population. Hemoglobin. 33(1). 66–71. 4 indexed citations

López, Karen, et al.. (2007). Genetic diversity of the IL‐4, IL‐4 receptor and IL‐13 loci in mestizos in the general population and in patients with asthma from three subpopulations in Mexico. International Journal of Immunogenetics. 34(1). 27–33. 9 indexed citations

Perea, Francisco J., et al.. (2007). Genetic relationship of a Mexican Afromestizo population through the analysis of the 3′ haplotype of the β globin gene in βA chromosomes. Blood Cells Molecules and Diseases. 39(2). 169–177. 5 indexed citations

Perea, Francisco J., et al.. (2004). Molecular spectrum of β-thalassemia in the Mexican population. Blood Cells Molecules and Diseases. 33(2). 150–152. 10 indexed citations

Perea, Francisco J., et al.. (2004). A Frameshift at Codons 77/78 (–C): A Novel β‐Thalassemia Mutation. Hemoglobin. 28(3). 261–265. 2 indexed citations

10.

Ramos, Carmen, et al.. (2003). Analysis of HLA DQA1 and DQB1 alleles and glycated hemoglobin in healthy Mexican mestizo individuals from families with type 1 diabetes mellitus. 14(3). 125–130.

11.

Ibarra, B, et al.. (2003). Red cell membrane protein deficiencies in Mexican patients with hereditary spherocytosis. Blood Cells Molecules and Diseases. 31(3). 357–359. 21 indexed citations

12.

Perea, Francisco J., et al.. (2002). Analysis of βS and βA Genes in a Mexican Population with African Roots. Blood Cells Molecules and Diseases. 28(2). 121–126. 26 indexed citations

13.

Perea, Francisco J., et al.. (1999). The Hb Tarrant [α126(H9)Asp→Asn] Mutation is Localized in the α2-Globin Gene. Hemoglobin. 23(3). 295–297.

14.

Perea, Francisco J., et al.. (1999). Hb D-Los Angeles Associated with Hb S or β-Thalassemia in Four Mexican Mestizo Families. Hemoglobin. 23(3). 231–237. 22 indexed citations

15.

Villalobos-Arámbula, Alma Rosa, et al.. (1997). β-Thalassemia and β A globin gene haplotypes in Mexican mestizos. Human Genetics. 99(4). 498–500. 15 indexed citations

16.

Villalobos-Arámbula, Alma Rosa, Francisco J. Perea, B Ibarra, et al.. (1996). β Haplotypes of Three Mexican Mestizo Famis with Spanish (δ β)^O-Thalassemia. Hemoglobin. 20(4). 439–442. 1 indexed citations

17.

Antonarakis, Stylianos E., et al.. (1991). Molecular heterogeneity of β-thalassemia in Mestizo Mexicans. Genomics. 11(2). 474–474. 12 indexed citations

18.

Ibarra, B, et al.. (1990). Hematological and biochemical studies in children with Down syndrome.. PubMed. 33(2). 84–7. 18 indexed citations

19.

Nazará, Z., et al.. (1980). Autosomal Recessive. Spondylo‐epi‐metaphyseal dysplasia (Irapa type) in a Mexican family: Delineation of the syndrome. American Journal of Medical Genetics. 5(2). 179–188. 10 indexed citations

20.

Nazará, Z., et al.. (1979). De novo partial trisomy of chromosome 18(pter yields q11:). Some observations on the phenotype mapping of chromosome 18 imbalances.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 22(3). 165–7. 5 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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