D Dhermy

2.4k total citations
102 papers, 1.9k citations indexed

About

D Dhermy is a scholar working on Physiology, Pulmonary and Respiratory Medicine and Hematology. According to data from OpenAlex, D Dhermy has authored 102 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Physiology, 55 papers in Pulmonary and Respiratory Medicine and 29 papers in Hematology. Recurrent topics in D Dhermy's work include Erythrocyte Function and Pathophysiology (76 papers), Blood properties and coagulation (53 papers) and Blood groups and transfusion (17 papers). D Dhermy is often cited by papers focused on Erythrocyte Function and Pathophysiology (76 papers), Blood properties and coagulation (53 papers) and Blood groups and transfusion (17 papers). D Dhermy collaborates with scholars based in France, United States and United Kingdom. D Dhermy's co-authors include Marie‐Christine Lecomte, Pierre Boivin, M Garbarz, Odile Bournier, H Gautero, J. Delaunay, C Galand, Gaël Nicolas, Carlo V. Feo and Yolande Kroviarski and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Blood.

In The Last Decade

D Dhermy

101 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
D Dhermy France 28 1.3k 702 576 416 407 102 1.9k
Lesley J. Bruce United Kingdom 29 1.7k 1.4× 494 0.7× 1.1k 2.0× 572 1.4× 415 1.0× 80 2.7k
Elisa Fermo Italy 25 1.2k 0.9× 401 0.6× 524 0.9× 781 1.9× 789 1.9× 93 2.0k
C Galand France 22 900 0.7× 360 0.5× 292 0.5× 161 0.4× 171 0.4× 85 1.6k
Véronique Picard France 19 502 0.4× 269 0.4× 486 0.8× 391 0.9× 180 0.4× 53 1.4k
Hitoshi Kanno Japan 24 818 0.6× 114 0.2× 528 0.9× 383 0.9× 315 0.8× 131 1.5k
Stephen T. Koury United States 20 544 0.4× 139 0.2× 643 1.1× 518 1.2× 268 0.7× 31 1.5k
Stephen O. Brennan New Zealand 26 429 0.3× 905 1.3× 814 1.4× 657 1.6× 274 0.7× 105 2.5k
C Borrone Italy 24 613 0.5× 106 0.2× 753 1.3× 109 0.3× 99 0.2× 86 1.7k
Stephen H. Robinson United States 23 302 0.2× 91 0.1× 510 0.9× 302 0.7× 243 0.6× 51 1.2k
J. M. J. M. Zijlmans Netherlands 15 852 0.7× 69 0.1× 1.0k 1.8× 325 0.8× 189 0.5× 30 2.2k

Countries citing papers authored by D Dhermy

Since Specialization
Citations

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

Fields of papers citing papers by D Dhermy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D Dhermy

This figure shows the co-authorship network connecting the top 25 collaborators of D Dhermy. A scholar is included among the top collaborators of D Dhermy 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 D Dhermy. D Dhermy 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.
Malbert-Colas, Laurence, Gaël Nicolas, Colette Galand, Marie‐Christine Lecomte, & D Dhermy. (2003). Identification of new partners of the epithelial sodium channel alpha subunit. Comptes Rendus Biologies. 326(7). 615–624. 16 indexed citations
2.
Malbert-Colas, Laurence, Michel Fay, Marcel Blot‐Chabaud, et al.. (2003). Differential expression and localisation of WWP1, a Nedd4-like protein, in epithelia. Pflügers Archiv - European Journal of Physiology. 447(1). 35–43. 12 indexed citations
3.
Dhermy, D, J Steen-Johnsen, Odile Bournier, et al.. (2000). Coinheritance of two α-spectrin gene defects in a recessive spherocytosis family. Clinical & Laboratory Haematology. 22(6). 329–336. 11 indexed citations
4.
Pérel, Yves, et al.. (1999). Portal vein thrombosis after splenectomy for hereditary stomatocytosis in childhood. European Journal of Pediatrics. 158(8). 628–630. 24 indexed citations
5.
Dhermy, D, Odile Bournier, Monique Bourgeois, & Bernard Grandchamp. (1999). The red blood cell band 3 variant (band 3Bicetrel: R490C) associated with dominant hereditary spherocytosis causes defective membrane targeting of the molecule and a dominant negative effect. Molecular Membrane Biology. 16(4). 305–312. 19 indexed citations
6.
Lecomte, Marie‐Christine, Gaël Nicolas, D Dhermy, Jennifer C. Pinder, & Walter Gratzer. (1999). Properties of normal and mutant polypeptide fragments from the dimer self-association sites of human red cell spectrin. European Biophysics Journal. 28(3). 208–215. 18 indexed citations
7.
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
8.
Boavida, Maria Guida, et al.. (1997). Isochromosome 14q in refractory anemia. Cancer Genetics and Cytogenetics. 97(2). 155–156. 11 indexed citations
9.
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
10.
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
11.
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
12.
13.
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
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.
Bertrand, Olivier, et al.. (1989). An efficient laboratory made apparatus for DNA amplification. Journal of Biochemical and Biophysical Methods. 18(3). 227–235. 1 indexed citations
16.
Dhermy, D, Jacqueline Siméon, Marie‐Paule Wautier, Pierre Boivin, & Jean‐Luc Wautier. (1987). Role of membrane sialic acid content in the adhesiveness of aged erythrocytes to human cultured endothelial cells. Biochimica et Biophysica Acta (BBA) - Biomembranes. 904(2). 201–206. 19 indexed citations
17.
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
18.
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
19.
Henin, Dolaji, et al.. (1979). [Cerebro-meningeal involvement in acute myeloblastic leukaemia and myeloproliferative syndromes in acute transformation. Cytological, histological and clinical study of 62 cases (author's transl)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 8(10). 751–4. 1 indexed citations
20.
Dhermy, D, et al.. (1977). Inhibition of the deoxyribonuclease I by actin from human erythrocytes.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 27(8). 315–7. 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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