Thérèse Cynober

2.2k total citations
44 papers, 1.5k citations indexed

About

Thérèse Cynober is a scholar working on Physiology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Thérèse Cynober has authored 44 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Physiology, 17 papers in Pulmonary and Respiratory Medicine and 16 papers in Genetics. Recurrent topics in Thérèse Cynober's work include Erythrocyte Function and Pathophysiology (35 papers), Blood properties and coagulation (16 papers) and Hemoglobinopathies and Related Disorders (16 papers). Thérèse Cynober is often cited by papers focused on Erythrocyte Function and Pathophysiology (35 papers), Blood properties and coagulation (16 papers) and Hemoglobinopathies and Related Disorders (16 papers). Thérèse Cynober collaborates with scholars based in France, United States and United Kingdom. Thérèse Cynober's co-authors include Gil Tchernia, Narla Mohandas, Henri Wajcman, David Chalmers, Hélène Lapillonne, Luc Douay, Marie‐Catherine Giarratana, Michael C. Marden, Ladan Kobari and Laurent Kiger and has published in prestigious journals such as Journal of Clinical Investigation, Blood and Nature Biotechnology.

In The Last Decade

Thérèse Cynober

44 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thérèse Cynober France 20 967 583 481 397 387 44 1.5k
Giovanna Graziadei Italy 20 302 0.3× 736 1.3× 628 1.3× 140 0.4× 176 0.5× 82 1.2k
E. A. Rachmilewitz Israel 20 227 0.2× 1.0k 1.8× 934 1.9× 111 0.3× 183 0.5× 47 1.4k
P Fessas Greece 21 177 0.2× 543 0.9× 369 0.8× 89 0.2× 301 0.8× 66 1.1k
Anna Zaninoni Italy 20 577 0.6× 349 0.6× 595 1.2× 146 0.4× 93 0.2× 59 1.0k
Judith Behrens United Kingdom 10 175 0.2× 219 0.4× 752 1.6× 129 0.3× 138 0.4× 18 1.1k
Dipika Mohanty India 22 115 0.1× 664 1.1× 885 1.8× 152 0.4× 328 0.8× 90 1.4k
P Stammler Switzerland 12 450 0.5× 99 0.2× 268 0.6× 139 0.4× 112 0.3× 20 837
EN Dessypris United States 19 420 0.4× 357 0.6× 779 1.6× 81 0.2× 75 0.2× 32 1.3k
N Jamal Canada 17 183 0.2× 237 0.4× 607 1.3× 136 0.3× 58 0.1× 35 1.3k
Mouhab Ayas Saudi Arabia 21 118 0.1× 251 0.4× 756 1.6× 126 0.3× 200 0.5× 92 1.3k

Countries citing papers authored by Thérèse Cynober

Since Specialization
Citations

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

Fields of papers citing papers by Thérèse Cynober

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thérèse Cynober

This figure shows the co-authorship network connecting the top 25 collaborators of Thérèse Cynober. A scholar is included among the top collaborators of Thérèse Cynober 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 Thérèse Cynober. Thérèse Cynober 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.
Talbot, Hugues, et al.. (2013). Comparison between a Camera and a Four Quadrant Detector, in the Measurement of Red Blood Cell Deformability as a Function of Osmolality. HAL (Le Centre pour la Communication Scientifique Directe). 1 indexed citations
2.
Shet, Arun S., Thomas J. Hoffmann, Markéta Jiroušková, et al.. (2008). Morphological and functional platelet abnormalities in Berkeley sickle cell mice. Blood Cells Molecules and Diseases. 41(1). 109–118. 17 indexed citations
3.
Alanio, Cécile, Pierre–Olivier Schischmanoff, Madeleine Fénéant‐Thibault, et al.. (2007). Association between myeloid malignancies and acquired deficit in protein 4.1R: A retrospective analysis of six patients. American Journal of Hematology. 83(4). 275–278. 13 indexed citations
4.
Driss, F., G. Tertian, Laurent Becquemont, et al.. (2007). Prise en charge des grossesses à risque chez les femmes drépanocytaires : intérêt d’une stratégie préventive par des transfusions de globules rouges ou des échanges érythrocytaires automatisés. Transfusion Clinique et Biologique. 14(4). 386–392. 14 indexed citations
5.
Beaurain, Geneviève, Flavie Mathieu, B. Fiquet, et al.. (2006). Dehydrated hereditary stomatocytosis mimicking familial hyperkalaemic hypertension: clinical and genetic investigation. European Journal Of Haematology. 78(3). 253–259. 7 indexed citations
6.
Bader‐Meunier, Brigitte, et al.. (2006). Infantile pyknocytosis: a cause of haemolytic anaemia of the newborn. British Journal of Haematology. 133(4). 439–442. 21 indexed citations
7.
Cynober, Thérèse, Gordon W. Stewart, Bernard Grandchamp, et al.. (2006). Mild dehydrated hereditary stomatocytosis revealed by marked hepatosiderosis. Clinical & Laboratory Haematology. 28(4). 270–274. 25 indexed citations
8.
Bader‐Meunier, Brigitte, Guy Leverger, Gil Tchernia, et al.. (2005). Clinical and Laboratory Manifestations of Congenital Dyserythropoietic Anemia Type I in a Cohort of French Children. Journal of Pediatric Hematology/Oncology. 27(8). 416–419. 9 indexed citations
9.
Delaunay, J., Alexis Proust, Pierre Olivier Schischmanoff, et al.. (2004). Different impacts of alleles αLEPRA and αLELY as assessed versus a novel, virtually null allele of the SPTA1 gene in trans. British Journal of Haematology. 127(1). 118–122. 32 indexed citations
10.
Tchernia, Gil, et al.. (2004). Congenital dyserythropoietic anemias. The Hematology Journal. 5. S191–S194. 2 indexed citations
11.
Fricke, B., C. D. L. Reid, A Robert, et al.. (2004). Four new cases of stomatin‐deficient hereditary stomatocytosis syndrome: association of the stomatin‐deficient cryohydrocytosis variant with neurological dysfunction. British Journal of Haematology. 125(6). 796–803. 33 indexed citations
12.
Jaïs, Xavier, Stephen J. Till, Thérèse Cynober, et al.. (2003). An Extreme Consequence of Splenectomy in Dehydrated Hereditary Stomatocytosis: Gradual Thrombo‐embolic Pulmonary Hypertension and Lung–Heart Transplantation. Hemoglobin. 27(3). 139–147. 48 indexed citations
13.
Grootenboer‐Mignot, S., Aurore Crétien, Ingrid Laurendeau, et al.. (2003). Sub‐lethal hydrops as a manifestation of dehydrated hereditary stomatocytosis in two consecutive pregnancies. Prenatal Diagnosis. 23(5). 380–384. 19 indexed citations
14.
Costa, Lydie Da, Narla Mohandas, Martin Sorette, et al.. (2001). Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia. Blood. 98(10). 2894–2899. 65 indexed citations
15.
Morlé, Laurette, H U Lutz, P Stammler, et al.. (2000). Heavy transfusions and presence of an anti-protein 4.2 antibody in 4. 2(-) hereditary spherocytosis (949delG).. PubMed. 85(1). 19–24. 14 indexed citations
16.
Delhommeau, François, Thérèse Cynober, Pierre Olivier Schischmanoff, et al.. (2000). Natural history of hereditary spherocytosis during the first year of life. Blood. 95(2). 393–397. 60 indexed citations
17.
Cynober, Thérèse, Brigitte Bader‐Meunier, Frédéric Gauthier, et al.. (1997). Sphérocytose héréditaire. Évolution et intérêt de la splénectomie subtotale. Archives de Pédiatrie. 4(6). 515–520. 7 indexed citations
18.
Franceschi, Lucia De, D. Bachir, Frédéric Galactéros, et al.. (1997). Oral magnesium supplements reduce erythrocyte dehydration in patients with sickle cell disease.. Journal of Clinical Investigation. 100(7). 1847–1852. 136 indexed citations
19.
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
20.
Cynober, Thérèse, Narla Mohandas, & Gil Tchernia. (1996). Red cell abnormalities in hereditary spherocytosis: Relevance to diagnosis and understanding of the variable expression of clinical severity. Journal of Laboratory and Clinical Medicine. 128(3). 259–269. 94 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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