H Gautero

803 total citations
28 papers, 665 citations indexed

About

H Gautero is a scholar working on Physiology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, H Gautero has authored 28 papers receiving a total of 665 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Physiology, 18 papers in Pulmonary and Respiratory Medicine and 9 papers in Genetics. Recurrent topics in H Gautero's work include Erythrocyte Function and Pathophysiology (24 papers), Blood properties and coagulation (18 papers) and Diabetes and associated disorders (8 papers). H Gautero is often cited by papers focused on Erythrocyte Function and Pathophysiology (24 papers), Blood properties and coagulation (18 papers) and Diabetes and associated disorders (8 papers). H Gautero collaborates with scholars based in France, United States and Spain. H Gautero's co-authors include D Dhermy, Pierre Boivin, Marie‐Christine Lecomte, Odile Bournier, M Garbarz, C Galand, Carlo V. Feo, Christian Auclair, Emmanuelle Voisin and Isabelle Devaux and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Blood.

In The Last Decade

H Gautero

28 papers receiving 639 citations

Peers

H Gautero
Xiu-Bao Chang United States
Charles R. Zerez United States
Takeshi Okazaki United States
Nicola Diferrante United States
Fredrick D. Oakley United States
Constance Christian United States
H Gautero
Citations per year, relative to H Gautero H Gautero (= 1×) peers Kerstin Eisele

Countries citing papers authored by H Gautero

Since Specialization
Citations

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

Fields of papers citing papers by H Gautero

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H Gautero

This figure shows the co-authorship network connecting the top 25 collaborators of H Gautero. A scholar is included among the top collaborators of H Gautero 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 H Gautero. H Gautero 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.
Nicolas, Gaël, et al.. (1997). Method of Site-Directed Mutagenesis Using Long Primer-Unique Site Elimination and Exonuclease III. BioTechniques. 22(3). 430–434. 6 indexed citations
2.
Lecomte, Marie‐Christine, Jean-Paul Mira, Philippe Marin, et al.. (1996). Inhibition of Phospholipase D Activity by Fodrin. Journal of Biological Chemistry. 271(39). 24164–24171. 54 indexed citations
3.
Garbarz, M, Marie‐Christine Lecomte, Colette Galand, et al.. (1996). Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin. British Journal of Haematology. 95(1). 57–66. 34 indexed citations
4.
Lecomte, Marie‐Christine, et al.. (1993). Heterogeneous phosphorylation of erythrocyte spectrin β chain in intact cells. Biochemical Journal. 294(3). 841–846. 11 indexed citations
5.
Lecomte, Marie‐Christine, M Garbarz, H Gautero, et al.. (1993). Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin αI variants. British Journal of Haematology. 85(3). 584–595. 21 indexed citations
6.
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
9.
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
10.
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
12.
Garbarz, M, Bernard Grandchamp, Carlo V. Feo, et al.. (1989). Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypes. Blood. 74(3). 1126–1133. 27 indexed citations
13.
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
14.
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
15.
Dhermy, D, M Garbarz, Marie‐Christine Lecomte, et al.. (1986). Hereditary elliptocytosis: clinical, morphological and biochemical studies of 38 cases.. PubMed. 28(3). 129–40. 28 indexed citations
16.
Auclair, Christian, et al.. (1984). Superoxide dismutase, catalase, and glutathione peroxidase in red blood cells from patients with malignant diseases.. PubMed. 44(9). 4137–9. 116 indexed citations
17.
Lecomte, Marie‐Christine, D Dhermy, M Garbarz, et al.. (1984). Hereditary Elliptocytosis with a Spectrin Molecular Defect in a White Patient. Acta Haematologica. 71(4). 235–240. 25 indexed citations
18.
Dhermy, D, Marie‐Christine Lecomte, M Garbarz, et al.. (1984). Molecular Defect of Spectrin in the Family of a Child with Congenital Hemolytic Poikilocytic Anemia. Pediatric Research. 18(10). 1005–1012. 30 indexed citations
19.
Gautero, H, et al.. (1983). Impaired in vitro bactericidal power of polymorphonuclear leukocytes in patients with protein calorie malnutrition.. PubMed. 156(4). 489–92. 5 indexed citations
20.
Dhermy, D, Marie‐Christine Lecomte, M Garbarz, et al.. (1982). Spectrin beta-chain variant associated with hereditary elliptocytosis.. Journal of Clinical Investigation. 70(4). 707–715. 59 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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