Laurette Morlé

2.5k total citations
77 papers, 1.9k citations indexed

About

Laurette Morlé is a scholar working on Physiology, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Laurette Morlé has authored 77 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Physiology, 33 papers in Pulmonary and Respiratory Medicine and 24 papers in Molecular Biology. Recurrent topics in Laurette Morlé's work include Erythrocyte Function and Pathophysiology (52 papers), Blood properties and coagulation (33 papers) and Hemoglobinopathies and Related Disorders (18 papers). Laurette Morlé is often cited by papers focused on Erythrocyte Function and Pathophysiology (52 papers), Blood properties and coagulation (33 papers) and Hemoglobinopathies and Related Disorders (18 papers). Laurette Morlé collaborates with scholars based in France, United States and Algeria. Laurette Morlé's co-authors include Nicole Alloisio, J. Delaunay, Bénédicte Durand, B Pothier, Faouzi Baklouti, J. Thomas, Muriel Bozon, J Maréchal, R Kastally and R Wilmotte and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Investigation and SHILAP Revista de lepidopterología.

In The Last Decade

Laurette Morlé

74 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laurette Morlé France 28 1.1k 748 619 461 328 77 1.9k
Kim-Chew Lim United States 21 138 0.1× 1.3k 1.7× 187 0.3× 275 0.6× 208 0.6× 31 1.9k
M. Marin-Padilla United States 15 116 0.1× 930 1.2× 151 0.2× 261 0.6× 143 0.4× 24 1.6k
John R.W. Yates United Kingdom 19 522 0.5× 802 1.1× 135 0.2× 490 1.1× 52 0.2× 30 1.7k
Israela Lerer Israel 29 87 0.1× 1.2k 1.7× 343 0.6× 972 2.1× 161 0.5× 77 2.5k
Tomomasa Yokomizo Japan 24 210 0.2× 1.7k 2.3× 225 0.4× 176 0.4× 211 0.6× 48 2.8k
Anna Rajab Oman 23 142 0.1× 1.2k 1.6× 64 0.1× 628 1.4× 170 0.5× 58 1.9k
Georg C. Schwabe Germany 16 183 0.2× 1.2k 1.6× 342 0.6× 478 1.0× 157 0.5× 22 1.8k
Muriel Bozon France 19 184 0.2× 407 0.5× 109 0.2× 97 0.2× 145 0.4× 36 1.1k
David Geneviève France 24 88 0.1× 1.3k 1.8× 189 0.3× 1.1k 2.4× 168 0.5× 80 2.3k
R. J. M. Gardner New Zealand 18 241 0.2× 766 1.0× 90 0.1× 682 1.5× 101 0.3× 27 1.6k

Countries citing papers authored by Laurette Morlé

Since Specialization
Citations

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

Fields of papers citing papers by Laurette Morlé

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laurette Morlé

This figure shows the co-authorship network connecting the top 25 collaborators of Laurette Morlé. A scholar is included among the top collaborators of Laurette Morlé 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 Laurette Morlé. Laurette Morlé 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.
Tebbe, Lars, C. R. Weber, Nadia Messaddeq, et al.. (2015). A novel function of Huntingtin in the cilium and retinal ciliopathy in Huntington's disease mice. Neurobiology of Disease. 80. 15–28. 26 indexed citations
2.
Kistler, W. Stephen, Dominique Baas, Sylvain Lemeille, et al.. (2015). RFX2 Is a Major Transcriptional Regulator of Spermiogenesis. PLoS Genetics. 11(7). e1005368–e1005368. 46 indexed citations
3.
Magnani, Dario, Laurette Morlé, Kerstin Hasenpusch‐Theil, et al.. (2015). The ciliogenic transcription factor Rfx3 is required for the formation of the thalamocortical tract by regulating the patterning of prethalamus and ventral telencephalon. Human Molecular Genetics. 24(9). 2578–2593. 19 indexed citations
4.
Benadiba, Carine, Dario Magnani, Mathieu Niquille, et al.. (2012). The Ciliogenic Transcription Factor RFX3 Regulates Early Midline Distribution of Guidepost Neurons Required for Corpus Callosum Development. PLoS Genetics. 8(3). e1002606–e1002606. 55 indexed citations
5.
Thomas, J., et al.. (2010). Transcriptional control of genes involved in ciliogenesis: a first step in making cilia. Biology of the Cell. 102(9). 499–513. 125 indexed citations
6.
Zein, Loubna El, Aouatef Ait‐Lounis, Laurette Morlé, et al.. (2009). RFX3 governs growth and beating efficiency of motile cilia in mouse and controls the expression of genes involved in human ciliopathies. Journal of Cell Science. 122(17). 3180–3189. 90 indexed citations
7.
Vérot, Lucie, Nicole Alloisio, Laurette Morlé, et al.. (2003). Localization of a non‐syndromic X‐linked mental retardation gene (MRX80) to Xq22‐q24. American Journal of Medical Genetics Part A. 122A(1). 37–41. 5 indexed citations
8.
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
9.
Morlé, Laurette, Muriel Bozon, Jean‐Christophe Zech, et al.. (2000). A Locus for Autosomal Dominant Colobomatous Microphthalmia Maps to Chromosome 15q12-q15. The American Journal of Human Genetics. 67(6). 1592–1597. 35 indexed citations
10.
Alloisio, Nicole, Laurette Morlé, Muriel Bozon, et al.. (1999). Mutation in the zonadhesin-like domain of α-tectorin associated with autosomal dominant non-syndromic hearing loss. European Journal of Human Genetics. 7(2). 255–258. 39 indexed citations
11.
Iolascon, Achille, Emanuele Miraglia del Giudice, Silverio Perrotta, et al.. (1998). Hereditary spherocytosis: from clinical to molecular defects.. PubMed. 83(3). 240–57. 43 indexed citations
12.
Morlé, Laurette, Muriel Bozon, Nicole Alloisio, et al.. (1997). Ankyrin Bugey: A de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosis. American Journal of Hematology. 54(3). 242–248. 17 indexed citations
13.
Randon, Jacques, Emanuele Miraglia del Giudice, Muriel Bozon, et al.. (1997). Frequent de novo mutations of the ANK1 gene mimic a recessive mode of transmission in hereditary spherocytosis: three new ANK1 variants: ankyrins Bari, Napoli II and Anzio. British Journal of Haematology. 96(3). 500–506. 21 indexed citations
14.
Delaunay, J., Nicole Alloisio, & Laurette Morlé. (1996). Molecular genetics of hereditary spherocytosis. Cellular & Molecular Biology Letters. 1(1). 9 indexed citations
15.
Delaunay, J., et al.. (1995). La sphérocytose héréditaire en 1995 : l'apport de la génétique moléculaire. Hématologie. 1(2). 3 indexed citations
16.
Lorenzo, Felipe, Nicole Dalla Venezia, Laurette Morlé, et al.. (1994). Protein 4.1 deficiency associated with an altered binding to the spectrin-actin complex of the red cell membrane skeleton.. Journal of Clinical Investigation. 94(4). 1651–1656. 29 indexed citations
17.
Wilmotte, R, J Maréchal, Laurette Morlé, et al.. (1993). Low expression allele alpha LELY of red cell spectrin is associated with mutations in exon 40 (alpha V/41 polymorphism) and intron 45 and with partial skipping of exon 46.. Journal of Clinical Investigation. 91(5). 2091–2096. 80 indexed citations
18.
Morlé, Laurette, Anne‐Françoise Roux, Nicole Alloisio, et al.. (1990). 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).. Journal of Clinical Investigation. 86(2). 548–554. 36 indexed citations
19.
Pothier, B, J Maréchal, Laurette Morlé, et al.. (1990). A haemolytic syndrome associated with the complete absence of red cell membrane protein 4.2 in two Tunisian siblings. British Journal of Haematology. 75(3). 414–420. 34 indexed citations
20.
Pothier, B, et al.. (1989). Two distinct variants of erythrocyte spectrin ?IV domain. Human Genetics. 83(4). 373–376. 3 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 Kim-Chew Lim Breakdown of academic impact, for papers by M. Marin-Padilla Breakdown of academic impact, for papers by John R.W. Yates Breakdown of academic impact, for papers by Israela Lerer Breakdown of academic impact, for papers by Tomomasa Yokomizo Breakdown of academic impact, for papers by Anna Rajab Breakdown of academic impact, for papers by Georg C. Schwabe Breakdown of academic impact, for papers by Muriel Bozon Breakdown of academic impact, for papers by David Geneviève Breakdown of academic impact, for papers by R. J. M. Gardner
Rankless by CCL
2026