Belén Bornstein

3.0k total citations · 1 hit paper
49 papers, 1.6k citations indexed

About

Belén Bornstein is a scholar working on Molecular Biology, Clinical Biochemistry and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Belén Bornstein has authored 49 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 17 papers in Clinical Biochemistry and 11 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Belén Bornstein's work include Mitochondrial Function and Pathology (24 papers), Metabolism and Genetic Disorders (17 papers) and ATP Synthase and ATPases Research (14 papers). Belén Bornstein is often cited by papers focused on Mitochondrial Function and Pathology (24 papers), Metabolism and Genetic Disorders (17 papers) and ATP Synthase and ATPases Research (14 papers). Belén Bornstein collaborates with scholars based in Spain, Israel and United States. Belén Bornstein's co-authors include Pablo García‐Pavía, Marta Cobo Marcos, Clara Salas, Luis Alonso‐Pulpón, Enrique Lara‐Pezzi, Gonzalo Guzzo-Merello, Esther González-López, F. Javier de Haro-del Moral, María Gallego‐Delgado and Carolina Casado Robles and has published in prestigious journals such as Journal of Biological Chemistry, American Journal of Clinical Nutrition and Neurology.

In The Last Decade

Belén Bornstein

49 papers receiving 1.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction

2015 735 citations Esther González-López, María Gallego‐Delgado et al. European Heart Journal profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Belén Bornstein Spain	19	1.2k	461	324	297	201	49	1.6k
Sari Kiuru‐Enari Finland	20	1.1k 0.9×	186 0.4×	266 0.8×	17 0.1×	126 0.6×	44	1.3k
Yo‐ichi Takei Japan	20	739 0.6×	32 0.1×	92 0.3×	220 0.7×	120 0.6×	70	1.3k
Noriko Makita Japan	22	671 0.5×	346 0.8×	239 0.7×	13 0.0×	376 1.9×	75	1.7k
Alda Tufró United States	22	827 0.7×	89 0.2×	618 1.9×	48 0.2×	186 0.9×	39	1.5k
Tetsuo Morioka Japan	19	495 0.4×	136 0.3×	250 0.8×	34 0.1×	39 0.2×	39	928
Laura Giardino Italy	15	654 0.5×	59 0.1×	1.0k 3.2×	22 0.1×	114 0.6×	19	1.6k
Elżbieta Ciara Poland	17	647 0.5×	48 0.1×	32 0.1×	218 0.7×	67 0.3×	88	1.1k
Sadao Hori Japan	26	450 0.4×	97 0.2×	35 0.1×	150 0.5×	24 0.1×	67	2.7k
Nathalie Gaudreault Canada	20	559 0.5×	464 1.0×	44 0.1×	23 0.1×	162 0.8×	55	1.4k
Anne-Sophie Lèbre France	18	769 0.6×	51 0.1×	35 0.1×	316 1.1×	66 0.3×	38	1.1k

Countries citing papers authored by Belén Bornstein

Since Specialization

Citations

This map shows the geographic impact of Belén Bornstein'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 Belén Bornstein with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Belén Bornstein more than expected).

Fields of papers citing papers by Belén Bornstein

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Belén Bornstein. 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 Belén Bornstein. The network helps show where Belén Bornstein may publish in the future.

Co-authorship network of co-authors of Belén Bornstein

This figure shows the co-authorship network connecting the top 25 collaborators of Belén Bornstein. A scholar is included among the top collaborators of Belén Bornstein 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 Belén Bornstein. Belén Bornstein 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

Delgado‐Alvarado, Manuel, Patricia de la Riva, Haritz Jiménez‐Urbieta, et al.. (2015). Parkinsonism, cognitive deficit and behavioural disturbance caused by a novel mutation in the polymerase gamma gene. Journal of the Neurological Sciences. 350(1-2). 93–97. 14 indexed citations

González-López, Esther, María Gallego‐Delgado, Gonzalo Guzzo-Merello, et al.. (2015). Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction. European Heart Journal. 36(38). 2585–2594. 735 indexed citations breakdown →

García‐Pavía, Pablo, María Eugenia Vázquez, Javier Segovia, et al.. (2011). Genetic Basis of End-Stage Hypertrophic Cardiomyopathy. European Journal of Heart Failure. 13(11). 1193–1201. 48 indexed citations

Gallardo, M. Esther, Pablo García‐Pavía, Rodrigo Chamorro, et al.. (2011). Mitochondrial haplogroups associated with end-stage heart failure and coronary allograft vasculopathy in heart transplant patients. European Heart Journal. 33(3). 346–353. 23 indexed citations

García‐Pavía, Pablo, Petros Syrris, Clara Salas, et al.. (2011). Desmosomal protein gene mutations in patients with idiopathic dilated cardiomyopathy undergoing cardiac transplantation: a clinicopathological study. Heart. 97(21). 1744–1752. 63 indexed citations

Bornstein, Belén, Estela Área-Gómez, Kevin M. Flanigan, et al.. (2008). Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene. Neuromuscular Disorders. 18(6). 453–459. 65 indexed citations

Montero, Raquel, José A. Sánchez‐Alcázar, Paz Briones, et al.. (2008). Coenzyme Q10 deficiency associated with a mitochondrial DNA depletion syndrome: A case report. Clinical Biochemistry. 42(7-8). 742–745. 21 indexed citations

González‐Vioque, Emiliano, Alberto Blázquez, Daniel Fernández-Moreira, et al.. (2006). Association of Novel POLGMutations and Multiple Mitochondrial DNA Deletions With Variable Clinical Phenotypes in a Spanish Population. Archives of Neurology. 63(1). 107–107. 45 indexed citations

Talamillo, Ana, Miguel Ángel Fernández‐Moreno, Francisco Martı́nez-Azorı́n, et al.. (2004). Expression of the Drosophila melanogaster ATP synthase α subunit gene is regulated by a transcriptional element containing GAF and Adf‐1 binding sites. European Journal of Biochemistry. 271(20). 4003–4013. 7 indexed citations

10.

Ser, Teodoro del, et al.. (2003). Apolipoprotein E, angiotensin-converting enzyme and α-1-antichymotrypsin genotypes are not associated with post-stroke dementia. Journal of the Neurological Sciences. 210(1-2). 77–82. 26 indexed citations

11.

Bornstein, Belén, Miguel Ángel Fernández‐Moreno, Yolanda Campos, et al.. (2002). The A8296G mtDNA mutation associated with several mitochondrial diseases does not cause mitochondrial dysfunction in cybrid cell lines. Human Mutation. 19(3). 234–239. 14 indexed citations

12.

Ser, Teodoro del, Belén Bornstein, Raquel Barba, & Carlos Cemillán. (2001). Relationship of angiotensin converting enzyme genotype with serum triglyceride concentration in stroke patients. Neuroscience Letters. 316(1). 21–24. 12 indexed citations

13.

Fernández‐Moreno, Miguel Ángel, Belén Bornstein, Yolanda Campos, Joaquı́n Arenas, & Rafael Garesse. (2000). The Pathogenic Role of Point Mutations Affecting the Translational Initiation Codon of Mitochondrial Genes. Molecular Genetics and Metabolism. 70(3). 238–240. 6 indexed citations

14.

Fernández‐Moreno, Miguel Ángel, Belén Bornstein, Nathalie Petit, & Rafael Garesse. (2000). The Pathophysiology of Mitochondrial Biogenesis: Towards Four Decades of Mitochondrial DNA Research. Molecular Genetics and Metabolism. 71(3). 481–495. 14 indexed citations

15.

Fernández‐Moreno, Miguel Ángel, et al.. (1999). Structure and Regulated Expression of the δ-Aminolevulinate Synthase Gene from Drosophila melanogaster. Journal of Biological Chemistry. 274(52). 37321–37328. 29 indexed citations

16.

Pérez‐García, Rafael, et al.. (1998). Effects of L-carnitine on erythrocyte acyl-CoA, free CoA, and glycerophospholipid acyltransferase in uremia. American Journal of Clinical Nutrition. 67(3). 386–390. 15 indexed citations

17.

Bornstein, Belén, et al.. (1998). Mitochondrial gene expression and respiratory enzyme activities in cardiac diseases. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1406(1). 85–90. 18 indexed citations

18.

Bornstein, Belén, et al.. (1998). Estudios de patogenicidad y caracterización del fenotipo molecular provocado por mutaciones en el ADN mitocondrial humano. Revista de Neurología. 26(S1). 36–36. 1 indexed citations

19.

Bornstein, Belén, Joaquı́n Arenas, J.M. Morales, et al.. (1996). Cyclosporine Nephrotoxicity and Rejection Crisis: Diagnosis by Urinary Enzyme Excretion. The Nephron journals/Nephron journals. 72(3). 402–406. 11 indexed citations

20.

Arenas, Joaquı́n, JoAl Mayor, F.-Javier Gella, et al.. (1988). Arylsulfatase A in urine of patients with urothelial tumors. Clinical Biochemistry. 21(1). 73–77. 3 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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