M Garbarz

1.2k total citations
52 papers, 988 citations indexed

About

M Garbarz is a scholar working on Physiology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, M Garbarz has authored 52 papers receiving a total of 988 indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Physiology, 38 papers in Pulmonary and Respiratory Medicine and 16 papers in Genetics. Recurrent topics in M Garbarz's work include Erythrocyte Function and Pathophysiology (47 papers), Blood properties and coagulation (38 papers) and Diabetes and associated disorders (15 papers). M Garbarz is often cited by papers focused on Erythrocyte Function and Pathophysiology (47 papers), Blood properties and coagulation (38 papers) and Diabetes and associated disorders (15 papers). M Garbarz collaborates with scholars based in France, United States and Portugal. M Garbarz's co-authors include D Dhermy, Pierre Boivin, Marie‐Christine Lecomte, C Galand, Odile Bournier, H Gautero, Carlo V. Feo, William Tse, J. Delaunay and BG Forget and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Blood.

In The Last Decade

M Garbarz

51 papers receiving 954 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M Garbarz France 22 830 541 219 196 178 52 988
Laurie A. Steiner United States 15 176 0.2× 94 0.2× 451 2.1× 52 0.3× 157 0.9× 43 710
Loyda N. Vida United States 13 200 0.2× 30 0.1× 325 1.5× 86 0.4× 244 1.4× 28 642
Sandrine Hayette France 16 175 0.2× 99 0.2× 164 0.7× 26 0.1× 318 1.8× 33 696
Emilie‐Fleur Gautier France 10 201 0.2× 102 0.2× 319 1.5× 27 0.1× 118 0.7× 21 588
François Plassa France 10 64 0.1× 253 0.5× 127 0.6× 30 0.2× 178 1.0× 18 618
Wulin Aerbajinai United States 15 98 0.1× 85 0.2× 270 1.2× 49 0.3× 179 1.0× 34 630
Martin Mynarek Germany 16 76 0.1× 114 0.2× 197 0.9× 46 0.2× 307 1.7× 47 672
Yuji Miyajima Japan 14 47 0.1× 76 0.1× 132 0.6× 55 0.3× 77 0.4× 29 592
C. Naizot France 4 135 0.2× 38 0.1× 132 0.6× 27 0.1× 37 0.2× 5 482
N. Ghanem France 14 39 0.0× 125 0.2× 265 1.2× 37 0.2× 114 0.6× 46 756

Countries citing papers authored by M Garbarz

Since Specialization
Citations

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

Fields of papers citing papers by M Garbarz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M Garbarz

This figure shows the co-authorship network connecting the top 25 collaborators of M Garbarz. A scholar is included among the top collaborators of M Garbarz 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 M Garbarz. M Garbarz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Boulanger, Laurent, Denise E. Sabatino, Ellice Wong, et al.. (2002). Erythroid Expression of the Human α-Spectrin Gene Promoter Is Mediated by GATA-1- and NF-E2-binding Proteins. Journal of Biological Chemistry. 277(44). 41563–41570. 19 indexed citations
2.
Dhermy, D, et al.. (1998). Hereditary Spherocytosis with Spectrin Deficiency Related to Null Mutations of the β-Spectrin Gene. Blood Cells Molecules and Diseases. 24(2). 251–261. 10 indexed citations
3.
4.
Dhermy, D, Colette Galand, Odile Bournier, et al.. (1997). Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects. British Journal of Haematology. 98(1). 32–40. 34 indexed citations
5.
Abou‐Alfa, Ghassan K., D Dhermy, E Bursaux, et al.. (1996). A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.. Journal of Clinical Investigation. 97(2). 373–380. 31 indexed citations
6.
Maréchal, J, R Wilmotte, Akio Kanzaki, et al.. (1995). Ethnic distribution of allele aLELY, a low‐expression allele of red‐cell spectrin a‐gene. British Journal of Haematology. 90(3). 553–556. 22 indexed citations
7.
Randon, Jacques, Laurent Boulanger, J Maréchal, et al.. (1994). A variant of spectrin low‐expression allele αLELY carrying a hereditary elliptocytosis mutation in codon 28. British Journal of Haematology. 88(3). 534–540. 30 indexed citations
8.
Venezia, Nicole Dalla, R Wilmotte, Nathalie Parquet, et al.. (1993). An ?-spectrin mutation responsible for hereditary elliptocytosis associated in cis with the ?V/41 polymorphism. Human Genetics. 90(6). 641–4. 8 indexed citations
9.
Boivin, Pierre, C Galand, Isabelle Devaux, et al.. (1993). Spectrin ?IIa variant in dominant and non-dominant spherocytosis. Human Genetics. 92(2). 153–6. 13 indexed citations
10.
11.
Lecomte, Marie‐Christine, H Gautero, Odile Bournier, et al.. (1992). Elliptocytosis‐associated spectrin Rouen (β220/218) has a truncated but still phosphorylatable β chain. British Journal of Haematology. 80(2). 242–250. 13 indexed citations
12.
13.
Tse, William, Marie‐Christine Lecomte, Fernando Ferreira Costa, et al.. (1990). Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.. Journal of Clinical Investigation. 86(3). 909–916. 90 indexed citations
14.
Lecomte, Marie‐Christine, Carlo V. Feo, H Gautero, et al.. (1990). Severe recessive poikilocytic anaemia with a new spectrin α chain variant. British Journal of Haematology. 74(4). 497–507. 8 indexed citations
15.
Lecomte, Marie‐Christine, H Gautero, M Garbarz, Pierre Boivin, & D Dhermy. (1990). Abnormal tryptic peptide from the spectrin α‐chain resulting from α‐ or β‐chain mutations: two genetically distinct forms of the Sp αI/74 variant. British Journal of Haematology. 76(3). 406–413. 16 indexed citations
16.
Lecomte, Marie‐Christine, D Dhermy, M Garbarz, et al.. (1987). Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family. Human Genetics. 77(4). 329–334. 8 indexed citations
17.
Dhermy, D, Carlo V. Feo, M Garbarz, et al.. (1987). Prenatal diagnosis of hereditary elliptocytosis with molecular defect of spectrin. Prenatal Diagnosis. 7(7). 471–483. 5 indexed citations
18.
Garbarz, M, et al.. (1984). A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosis. Blood. 64(5). 1006–1015. 21 indexed citations
19.
Dhermy, D, Carlo V. Feo, M Garbarz, et al.. (1983). [Congenital hemolytic anemia with erythrocyte thermal instability and defect of spectrin tetrameric polymerization. Study of erythrocyte deformability in a new case of hereditary pyropoikilocytosis using diffraction viscosimetry].. PubMed. 25(1). 7–16. 1 indexed citations
20.
Garbarz, M, D Dhermy, Odile Bournier, Annie Bezeaud, & Pierre Boivin. (1981). Anti-spectrin in sera containing smooth muscle autoantibodies from patients with chronic active hepatitis.. PubMed. 43(1). 87–93. 9 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Laurie A. Steiner Breakdown of academic impact, for papers by Loyda N. Vida Breakdown of academic impact, for papers by Sandrine Hayette Breakdown of academic impact, for papers by Emilie‐Fleur Gautier Breakdown of academic impact, for papers by François Plassa Breakdown of academic impact, for papers by Wulin Aerbajinai Breakdown of academic impact, for papers by Martin Mynarek Breakdown of academic impact, for papers by Yuji Miyajima Breakdown of academic impact, for papers by C. Naizot Breakdown of academic impact, for papers by N. Ghanem
Rankless by CCL
2026