V Brabec

796 citations

36 papers · 610 · h-index 12

Impact in

Genetics top 5%
- Hemoglobinopathies and Related Disorders
Physiology top 5%
- Erythrocyte Function and Pathophysiology

Papers in

Physiology 23
- Erythrocyte Function and Pathophysiology 23
Genetics 13
- Hemoglobinopathies and Related Disorders 13

Co-authors: J Palek (15 shared papers)Petr Jarolı́m (9 shared papers)HL Rubin (4 shared papers)L Chrobák (4 shared papers)SK Ballas (3 shared papers)Carlo Brugnara (2 shared papers)Hillard Rubin (2 shared papers)J. G. Murray (2 shared papers)
Journals: Blood (7 papers)Annals of Hematology (4 papers)Clinica Chimica Acta (4 papers)Journal of Clinical Investigation (2 papers)British Journal of Haematology (2 papers)
Partner nations: Czechia United States Poland

In The Last Decade

V Brabec

33 papers receiving 586 citations

Peers

Countries citing papers authored by V Brabec

Since Specialization

Citations

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

Fields of papers citing papers by V Brabec

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside V Brabec, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with V Brabec Line = papers co-authored together V Brabec links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 36 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency Blood ·Petr Jarolı́m, J. G. Murray, HL Rubin, WM Taylor, JT Prchal, SK Ballas, LM Snyder, L Chrobák, WD Melrose, V Brabec, J Palek	1996	100
2	Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE). Journal of Clinical Investigation ·Petr Jarolı́m, Hillard Rubin, S C Liu, Michael Cho, V Brabec, Laura H. Derick, S J Yi, Sara Teresinha Olalla Saad, Seth L. Alper, Carlo Brugnara	1994	82
3	Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosis Blood ·Petr Jarolı́m, HL Rubin, V Brabec, L Chrobák, А. В. Золотарев, S L Alper, Carlo Brugnara, Hynek Wichterle, J Palek	1995	73
4	Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency. Blood ·Hani Hassoun, John Vassiliadis, James Murray, Pål R. Njølstad, John Rogus, SK Ballas, Frederick L. Schaffer, Petr Jarolı́m, V Brabec, J Palek	1997	60
5	Mutations in the pyruvate kinase L gene in patients with hereditary hemolytic anemia Blood ·Cornelia Lenzner, Peter Nürnberg, BJ Thiele, André Reis, V Brabec, A Sakalová, G Jacobasch	1994	47
6	Molecular characterization of β-thalassemia in Czechoslovakia Human Genetics ·Karel Indrák, V Brabec, Jarmila Indráková, L Chrobák, A Sakalová, Marie Jarošová, Jaroslav Čermák, You-Jun Fei, F. Kutlar, Yuan-chao Gu, E. Baysal, Titus H.J. Huisman	1992	44
7	Incomplete distal renal tubular acidosis coinherited with a mutation in the band 3 (AE1) gene Nephrology Dialysis Transplantation ·Romana Ryšavá, Vladimı́r Tesař, M Jirsa, V Brabec, Petr Jarolı́m	1997	38
8	A nonsense mutation 1669Glu-->Ter within the regulatory domain of human erythroid ankyrin leads to a selective deficiency of the major ankyrin isoform (band 2.1) and a phenotype of autosomal dominant hereditary spherocytosis. Journal of Clinical Investigation ·Petr Jarolı́m, Hillard Rubin, V Brabec, J Palek	1995	29
9	Comparison of the ankyrin (AC)n microsatellites in genomic DNA and mRNA reveals absence of one ankyrin mRNA allele in 20% of patients with hereditary spherocytosis Blood ·P Jarolim, HL Rubin, V Brabec, J Palek	1995	24
10	2,3‐Diphosphoglycerate Metabolism in Hereditary Spherocytosis British Journal of Haematology ·J Palek, L Mircevová, V Brabec	1969	18
11	Adenosintriphosphatase activity in hereditary spherocytosis Annals of Hematology ·L Mircevová, V Brabec, J Palek	1967	11
12	Serum ferritin in patients with various haemolytic disorders. PubMed ·V Brabec, Jaroslav Čermák, V Sebestík	1990	11
13	Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency Blood ·Petr Jarolı́m, J. G. Murray, HL Rubin, WM Taylor, JT Prchal, SK Ballas, LM Snyder, L Chrobák, WD Melrose, V Brabec, J Palek	1996	9
14	Red cell, plasma and whole blood volumes in organs of normal and hypersplenic rats Annals of Hematology ·V Sebestík, V Brabec, Jaroslav Jelı́nek, O. Hlavatá	1974	9
15	Red Cell Lipids in Autoimmune Hemolytic Anemia Blood ·V Brabec, Č Michalec, J Palek, M Kout	1969	7
16	Germline Editing of Drosophila Using CRISPR-Cas9-Based Cytosine and Adenine Base Editors The CRISPR Journal ·Nirav Thakkar, (unknown), V Brabec, David Doležel	2023	6
17	Red cell carbohydrate metabolism in primary refractory anemias Clinica Chimica Acta ·J Palek, V Brabec, L Mircevová, V. Volek, B Friedmann	1967	5
18	The Effect of Anti A Antibody on Red Cell Organic Phosphates and Adenosine Triphosphatase Activity in vitro Scandinavian Journal of Haematology ·J Palek, L Mircevová, V Brabec, Brfzřich Friedmann, A Májský	1968	4
19	Pyruvate kinase-deficiency anemia: Membrane approach Biochemical Medicine and Metabolic Biology ·Tomáš Mařík, V Brabec, Millan Kodíček, Petr Jarolı́m	1988	4
20	A Czechoslovakian teenager with Hb E-β∘-thalassemia [IVS-I-1 (G → A)] complicated by the presence of an α-globin gene triplication Annals of Hematology ·Karel Indrák, Y. J. Fei, H. W. Li, E. Baysal, V Brabec, H Fořtová, Jaroslav Čermák, T. H. J. Huisman	1991	4

About V Brabec

V Brabec is a scholar working on Physiology, Genetics, Hematology, Pediatrics, Perinatology and Child Health and Surgery, having authored 36 papers that have together received 610 indexed citations. Recurring topics across this work include Erythrocyte Function and Pathophysiology (23 papers), Hemoglobinopathies and Related Disorders (13 papers), Neonatal Health and Biochemistry (7 papers), Blood properties and coagulation (7 papers), Blood groups and transfusion (6 papers), Pancreatic function and diabetes (5 papers), Diet, Metabolism, and Disease (4 papers) and Iron Metabolism and Disorders (4 papers). The work is most often cited by research in Genetics (175 citations), Physiology (424 citations), Hematology (127 citations), Pediatrics, Perinatology and Child Health (140 citations) and Pulmonary and Respiratory Medicine (169 citations). V Brabec has collaborated with scholars based in Czechia, United States and Poland. Frequent co-authors include J Palek, Petr Jarolı́m, HL Rubin, L Chrobák, SK Ballas, Carlo Brugnara, Hillard Rubin, J. G. Murray, JT Prchal and Laura H. Derick. Their work appears in journals such as Blood, Annals of Hematology, Clinica Chimica Acta, Journal of Clinical Investigation and British Journal of Haematology.

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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