J. Delaunay

12.3k total citations · 1 hit paper
341 papers, 7.6k citations indexed

About

J. Delaunay is a scholar working on Physiology, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, J. Delaunay has authored 341 papers receiving a total of 7.6k indexed citations (citations by other indexed papers that have themselves been cited), including 189 papers in Physiology, 85 papers in Molecular Biology and 79 papers in Pulmonary and Respiratory Medicine. Recurrent topics in J. Delaunay's work include Erythrocyte Function and Pathophysiology (188 papers), Blood properties and coagulation (75 papers) and Hemoglobinopathies and Related Disorders (59 papers). J. Delaunay is often cited by papers focused on Erythrocyte Function and Pathophysiology (188 papers), Blood properties and coagulation (75 papers) and Hemoglobinopathies and Related Disorders (59 papers). J. Delaunay collaborates with scholars based in France, United States and Italy. J. Delaunay's co-authors include Nicole Alloisio, Laurette Morlé, Achille Iolascon, G Schapira, Faouzi Baklouti, Gil Tchernia, D Dhermy, Silverio Perrotta, Gordon W. Stewart and Thérèse Cynober and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

J. Delaunay

335 papers receiving 7.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels

2013 266 citations J. Delaunay et al. profile →

Peers

Countries citing papers authored by J. Delaunay

Since Specialization

Citations

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

Fields of papers citing papers by J. Delaunay

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Delaunay

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	MRCK-Alpha and Its Effector Myosin II Regulatory Light Chain Bind ABCB4 and Regulate Its Membrane Expression 2022 ·Cells ·Alix Bruneau, J. Delaunay, Anne‐Marie Durand‐Schneider, Virginie Vauthier, (unknown), Lynda Aoudjehane, Haquima El Mourabit, Romain Morichon, Thomas Falguières, Jérémie Gautheron, Chantal Housset, Tounsia Aït‐Slimane	2
2	Molecular Regulation of Canalicular ABC Transporters 2021 ·International Journal of Molecular Sciences ·(unknown), Alix Bruneau, (unknown), Martine Lapalus, J. Delaunay, Emmanuel Gonzalès, Emmanuel Jacquemin, Tounsia Aït‐Slimane, Thomas Falguières	23
3	RAB10 Interacts with ABCB4 and Regulates Its Intracellular Traffic 2021 ·International Journal of Molecular Sciences ·(unknown), Virginie Vauthier, Martine Lapalus, (unknown), (unknown), Anne‐Marie Durand‐Schneider, Alix Bruneau, J. Delaunay, Emmanuel Gonzalès, Chantal Housset, Tounsia Aït‐Slimane, François Guillonneau, Emmanuel Jacquemin, Thomas Falguières	3
4	Effect of CFTR correctors on the traffic and the function of intracellularly retained ABCB4 variants 2021 ·Liver International ·(unknown), Virginie Vauthier, (unknown), (unknown), Anne‐Marie Durand‐Schneider, Alix Bruneau, J. Delaunay, Martine Lapalus, (unknown), Isabelle Garcin, Emmanuel Gonzalès, Chantal Housset, Tounsia Aït‐Slimane, Emmanuel Jacquemin, Florent Di Meo, Thomas Falguières	12
5	Functional rescue of an ABCB11 mutant by ivacaftor: A new targeted pharmacotherapy approach in bile salt export pump deficiency 2020 ·Liver International ·(unknown), Martine Lapalus, (unknown), (unknown), Tounsia Aït‐Slimane, J. Delaunay, (unknown), (unknown), Anne Spraul, Thomas Falguières, Isabelle Callebaut, Emmanuel Gonzalès, Emmanuel Jacquemin	30
6	Structural analogues of roscovitine rescue the intracellular traffic and the function of ER-retained ABCB4 variants in cell models 2019 ·Scientific Reports ·Virginie Vauthier, (unknown), (unknown), Nassima Oumata, Anne‐Marie Durand‐Schneider, Alix Bruneau, J. Delaunay, Chantal Housset, Tounsia Aït‐Slimane, Laurent Meijer, Thomas Falguières	15
7	Phosphorylation of ABCB4 impacts its function: Insights from disease-causing mutations 2014 ·Hepatology ·Julien Gautherot, Danièle Delautier, Marie-Anne Maubert, Tounsia Aït‐Slimane, Gérard Bolbach, J. Delaunay, Anne‐Marie Durand‐Schneider, Delphine Firrincieli, Véronique Barbu, Nicolas Chignard, Chantal Housset, Michèle Maurice, Thomas Falguières	40
8	Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome 2011 ·Blood ·Joanna F. Flatt, Hélène Guizouarn, Nicholas M. Burton, Franck Borgèse, Richard Tomlinson, Rob Forsyth, Stephen A. Baldwin, (unknown), Philippe Quittet, Patricia Aguilar‐Martinez, J. Delaunay, Gordon W. Stewart, Lesley J. Bruce	61
9	Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian population 2011 ·American Journal of Hematology ·Roberta Russo, Antonella Gambale, Maria Rosaria Esposito, (unknown), (unknown), Ilaria Maggio, Mario Capasso, Lucio Luzzatto, J. Delaunay, Hannah Tamary, Achille Iolascon	19
10	The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein 2008 ·Blood ·Lesley J. Bruce, Hélène Guizouarn, Nicholas M. Burton, Nicole Gabillat, Joyce Poole, Joanna F. Flatt, R.L. Brady, Franck Borgèse, J. Delaunay, Gordon W. Stewart	84
11	Study of the effects of proteasome inhibitors on ribosomal protein S19 (RPS19) mutants, identified in patients with Diamond-Blackfan anemia 2008 ·Haematologica ·Aurore Crétien, Corinne Hurtaud, (unknown), Alexis Proust, Isabelle Marié, Orianne Wagner‐Ballon, Valérie Choesmel, Pierre‐Emmanuel Gleizes, Thierry Leblanc, J. Delaunay, Gil Tchernia, Narla Mohandas, Lydie Da Costa	15
12	Clinical and Laboratory Manifestations of Congenital Dyserythropoietic Anemia Type I in a Cohort of French Children 2005 ·Journal of Pediatric Hematology/Oncology ·Brigitte Bader‐Meunier, Guy Leverger, Gil Tchernia, Olivier Schischmanoff, Thérèse Cynober, Françoise Bernaudin, Thierry Leblanc, Martine Münzer, (unknown), (unknown), Isabelle Thuret, J. Delaunay	9
13	Heavy transfusions and presence of an anti-protein 4.2 antibody in 4. 2(-) hereditary spherocytosis (949delG). 2000 ·PubMed ·(unknown), Laurette Morlé, H U Lutz, P Stammler, (unknown), Rachel Petermann, Achille Iolascon, Silverio Perrotta, Thérèse Cynober, Gil Tchernia, J. Delaunay, Véronique Baudin‐Creuza	14
14	Le démembrement de la stomatocytose héréditaire : de la stomatine à Caenorhabditis elegans 1998 ·Hématologie ·J. Delaunay, Gil Tchernia	2
15	Protein 4.1 deficiency associated with an altered binding to the spectrin-actin complex of the red cell membrane skeleton. 1994 ·Journal of Clinical Investigation ·Felipe Lorenzo, Nicole Dalla Venezia, Laurette Morlé, Faouzi Baklouti, Nicole Alloisio, (unknown), (unknown), (unknown), J. Delaunay	29
16	Homozygous 4.1(-) hereditary elliptocytosis associated with a point mutation in the downstream initiation codon of protein 4.1 gene. 1992 ·Journal of Clinical Investigation ·Nicole Dalla Venezia, Florinda Gilsanz, Nicole Alloisio, (unknown), EJ Jr Benz, J. Delaunay	42
17	Two elliptocytogenic alpha I/74 variants of the spectrin alpha I domain. Spectrin Culoz (GGT----GTT; alpha I 40 Gly----Val) and spectrin Lyon (CTT----TTT; alpha I 43 Leu---Phe). 1990 ·Journal of Clinical Investigation ·Laurette Morlé, Anne‐Françoise Roux, Nicole Alloisio, B Pothier, Joëlle Starck, Luc Denoroy, François Morlé, R.-C. Rudigoz, BG Forget, J. Delaunay	36
18	The polyfluorenes: a family of versatile electroactive polymers. II: Poly(9,9-disubstituted fluorenes) existence of reversible p or n doping 1987 ·New Journal of Chemistry ·Joëlle Rault‐Berthelot, (unknown), J. Delaunay, Jacques Simonet	49
19	Absence of any detectable activity of the membrane marker enzyme 5'-nucleotidase in human red blood cells. 1978 ·Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·J. Delaunay, Siegmund Fischer, Marı́a Tortolero, (unknown), G Schapira	3
20	Activity of δ5-3 β-hydroxysteroid dehydrogenase in the adrenal cortex of the white rat deprived of vitamin A. 1966 ·(unknown), (unknown), J. Y. Le Gall, J. Delaunay, (unknown)	1

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