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L. Morlé · SciRah

Researcher profile · Semantic Scholar

L. Morlé

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L. Morlé — researcher profile on SciRah

h-index: 31
Works: 99
Citations: 2,483

Most-cited papers

Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3.
M. Ribeiro, N. Alloisio, H. Almeida, C. Gomes +8 more
2000Blood182 citations
Semantic Scholar
Transcriptional control of genes involved in ciliogenesis: a first step in making cilia
Joëlle Thomas, L. Morlé, F. Soulavie, A. Laurençon +2 more
2010Biology of the Cell167 citations Open access
Semantic Scholar
RFX3 governs growth and beating efficiency of motile cilia in mouse and controls the expression of genes involved in human ciliopathies
L. El Zein, Aouatef Ait-Lounis, L. Morlé, Joëlle Thomas +4 more
2009Journal of Cell Science138 citations Open access
Semantic Scholar
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.
R. Wilmotte, J. Maréchal, L. Morlé, F. Baklouti +5 more
1993Journal of Clinical Investigation101 citations Open access
Semantic Scholar
The Ciliogenic Transcription Factor RFX3 Regulates Early Midline Distribution of Guidepost Neurons Required for Corpus Callosum Development
C. Benadiba, Dario Magnani, Mathieu Niquille, L. Morlé +9 more
2012PLoS Genetics90 citations Open access
Semantic Scholar
RFX2 Is a Major Transcriptional Regulator of Spermiogenesis
W. Kistler, D. Baas, S. Lemeille, M. Paschaki +7 more
2015PLoS Genetics78 citations Open access
Semantic Scholar
A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing loss
L. Morlé, M. Bozon, N. Alloisio, P. Latour +6 more
2000Journal of Medical Genetics73 citations Open access
Semantic Scholar
Hereditary spherocytosis: from clinical to molecular defects.
A. Iolascon, E. del Giudice, S. Perrotta, N. Alloisio +2 more
1998Haematologica72 citations
Semantic Scholar
Sp alpha V/41: a common spectrin polymorphism at the alpha IV-alpha V domain junction. Relevance to the expression level of hereditary elliptocytosis due to alpha-spectrin variants located in trans.
N. Alloisio, L. Morlé, J. Maréchal, A. Roux +7 more
1991Journal of Clinical Investigation59 citations Open access
Semantic Scholar
Mutation in the zonadhesin-like domain of α-tectorin associated with autosomal dominant non-syndromic hearing loss
N. Alloisio, L. Morlé, M. Bozon, J. Godet +6 more
1999European Journal of Human Genetics55 citations
Semantic Scholar
Interplay of RFX transcription factors 1, 2 and 3 in motile ciliogenesis
S. Lemeille, M. Paschaki, D. Baas, L. Morlé +11 more
2020Nucleic Acids Research52 citations Open access
Semantic Scholar
Modulation of clinical expression and band 3 deficiency in hereditary spherocytosis.
N. Alloisio, P. Texier, A. Vallier, M. Ribeiro +8 more
1997Blood51 citations
Semantic Scholar
A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15.
L. Morlé, M. Bozon, J. Zech, N. Alloisio +6 more
2000American Journal of Human Genetics45 citations Open access
Semantic Scholar
Molecular genetics of hereditary elliptocytosis and hereditary spherocytosis.
J. Delaunay, N. Alloisio, L. Morlé, F. Baklouti +3 more
1996Annales de Genetique45 citations
Semantic Scholar
High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis.
Emanuele Miraglia del Giudice, M. Francese, B. Nobili, L. Morlé +3 more
1998Jornal de Pediatria44 citations
Semantic Scholar
Red cell membrane sialoglycoptein β in homozygous and heterozygous 4.1(−) hereditary elliptocytosis
N. Alloisio, L. Morlé, D. Bachir, D. Guetarni +2 more
198544 citations
Semantic Scholar
Alterations of Globin Chain Synthesis and of Red Cell Membrane Proteins in Congenital Dyserythropoietic Anemia I and II
N. Alloisio, P. Jaccoud, E. Dorléac, L. Morlé +4 more
1982Pediatric Research44 citations
Semantic Scholar
Novel VCAN mutations and evidence for unbalanced alternative splicing in the pathogenesis of Wagner syndrome
B. Kloeckener-Gruissem, J. Neidhardt, I. Magyar, H. Plauchu +7 more
2012European Journal of Human Genetics43 citations Open access
Semantic Scholar
New phenotype associated with an Arg116Cys mutation in the CRYAA gene: nuclear cataract, iris coloboma, and microphthalmia.
F. Béby, C. Commeaux, M. Bozon, P. Denis +2 more
2007A M A Archives of Ophthalmology43 citations
Semantic Scholar
Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosis
P. Maillet, N. Alloisio, L. Morlé, J. Delaunay
1996Human Mutation43 citations Open access
Semantic Scholar
The heterozygous form of 4.1(-) hereditary elliptocytosis [the 4.1(-) trait].
N. Alloisio, L. Morlé, E. Dorléac, O. Gentilhomme +6 more
1985Blood43 citations Open access
Semantic Scholar
A deletional frameshift mutation in protein 4.2 gene (allele 4.2 Lisboa) associated with hereditary hemolytic anemia.
S. Hayette, D. Dhermy, Meliisa Gonçales dos Santos, M. Bozon +5 more
1995Blood41 citations
Semantic Scholar
The red cell skeleton and its genetic disorders.
J. Delaunay, N. Alloisio, L. Morlé, B. Pothier
1990Molecular Aspects of Medicine39 citations
Semantic Scholar
Elliptocytogenic alpha I/36 spectrin Sfax lacks nine amino acids in helix 3 of repeat 4. Evidence for the activation of a cryptic 5'-splice site in exon 8 of spectrin alpha-gene.
F. Baklouti, J. Maréchal, R. Wilmotte, N. Alloisio +7 more
1992Blood38 citations
Semantic Scholar
A novel function of Huntingtin in the cilium and retinal ciliopathy in Huntington's disease mice.
A. Karam, Lars Tebbe, C. Weber, N. Messaddeq +4 more
2015Neurobiology of Disease36 citations Open access
Semantic Scholar
Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain.
L. Morlé, F. Morlé, A. Roux, J. Godet +6 more
1989Blood35 citations Open access
Semantic Scholar
Reduction of membrane band 7 and activation of volume stimulated (K+, Cl−)‐cotransport in a case of congenital stomatocytosis
L. Morlé, B. Pothier, N. Alloisio, C. Féo +3 more
1989British Journal of Haematology35 citations
Semantic Scholar
Spα1/65 hereditary elliptocytosis in North Africa
N. Alloisio, D. Guetarni, L. Morlé, B. Pothier +6 more
198635 citations
Semantic Scholar
The ciliogenic transcription factor Rfx3 is required for the formation of the thalamocortical tract by regulating the patterning of prethalamus and ventral telencephalon.
Dario Magnani, L. Morlé, K. Hasenpusch-Theil, M. Paschaki +4 more
2015Human Molecular Genetics34 citations Open access
Semantic Scholar
A haemolytic syndrome associated with the complete absence of red cell membrane protein 4.2 in two Tunisian siblings
A. Ghanem, B. Pothier, J. Maréchal, M. T. Ducluzeau +6 more
1990British Journal of Haematology34 citations
Semantic Scholar
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
J. Randon, E. del Giudice, M. Bozon, S. Perrotta +4 more
1997British Journal of Haematology32 citations
Semantic Scholar
Protein 4.1 deficiency associated with an altered binding to the spectrin-actin complex of the red cell membrane skeleton.
F. Lorenzo, N. Venezia, L. Morlé, F. Baklouti +5 more
1994Journal of Clinical Investigation31 citations Open access
Semantic Scholar
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).
L. Morlé, A. Roux, N. Alloisio, B. Pothier +6 more
1990Journal of Clinical Investigation29 citations Open access
Semantic Scholar
A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemia
S. Hayette, L. Morlé, M. Bozon, A. Ghanem +6 more
1995British Journal of Haematology28 citations
Semantic Scholar
Total absence of protein 4.2 and partial deficiency of band 3 in hereditary spherocytosis
A. Kanzaki, S. Hayette, L. Morlé, Fumihide Inoue +8 more
1997British Journal of Haematology27 citations
Semantic Scholar
Homozygous hemoglobin Knossos (alpha 2 beta 227(B9) Ala----Ser): a new variety of beta+-thalassemia intermedia associated with delta degree- thalassemia
F. Baklouti, E. Dorléac, L. Morlé, P. Laselve +4 more
198627 citations Open access
Semantic Scholar
Ankyrin Napoli: a de novo deletional frameshift mutation in exon 16 of ankyrin gene (ANK1) associated with spherocytosis
E. Giudice, S. Hayette, M. Bozon, S. Perrotta +5 more
1996British Journal of Haematology26 citations
Semantic Scholar
Altered GLI3 and FGF8 signaling underlies acrocallosal syndrome phenotypes in Kif7 depleted mice
A. Putoux, D. Baas, M. Paschaki, L. Morlé +4 more
2018Human Molecular Genetics23 citations
Semantic Scholar
Molecular analysis of hereditary elliptocytosis with reduced protein 4.1 in the French Northern Alps.
S. Feddal, G. Brunet, L. Roda, S. Chabanis +8 more
1991Blood23 citations
Semantic Scholar
The association of hemoglobin Knossos and hemoglobin Lepore in an Algerian patient.
L. Morlé, F. Morlé, E. Dorléac, Faouzi Baklouti +3 more
1984Hemoglobin21 citations
Semantic Scholar
Spa V / 41 : a Common Spectrin Polymorphism at the alV-aV Domain Junction Relevance to the Expression Level of Hereditary Elliptocytosis Due to a-Spectrin Variants Located in trans
N. Alloisio, L. Morlé, J. Maréchal, A. Roux +7 more
21 citations
Semantic Scholar
Spectrin Nice (beta 220/216): a shortened beta-chain variant associated with an increase of the alpha I/74 fragment in a case of elliptocytosis.
B. Pothier, L. Morlé, N. Alloisio, MT Ducluzeau +6 more
1987Blood20 citations Open access
Semantic Scholar
The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1.
L. Morlé, M. Garbarz, Nicole Alloisio, Robert Girot +3 more
1985Blood20 citations Open access
Semantic Scholar
Two distinct truncated variants of ankyrin associated with hereditary spherocytosis
S. Hayette, G. Carré, M. Bozon, N. Alloisio +8 more
1998American journal of hematology/oncology19 citations Open access
Semantic Scholar
Spectrin Oran (alpha II/21), a new spectrin variant concerning the alpha II domain and causing severe elliptocytosis in the homozygous state.
N. Alloisio, L. Morlé, B. Pothier, A. Roux +4 more
1988Blood19 citations Open access
Semantic Scholar
Heavy transfusions and presence of an anti-protein 4 . 2 antibody in 4 . 2 ( – ) hereditary spherocytosis ( 949 delG )
A. Beauchamp‐Nicoud, L. Morlé, H. Lutz, Rachel PETERMANN-KHDER +5 more
199918 citations
Semantic Scholar
Ankyrin Bugey: A de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosis
L. Morlé, M. Bozon, N. Alloisio, A. Vallier +6 more
1997American journal of hematology/oncology18 citations Open access
Semantic Scholar
Wagner vitreoretinal degeneration with genetic linkage refinement on chromosome 5q13-q14
J. Zech, L. Morlé, P. Vincent, N. Alloisio +7 more
1999Graefe's Archive for Clinical and Experimental Ophthalmology17 citations
Semantic Scholar
Severe poikilocytosis associated with a de novoα28 Arg→Cys mutation in spectrin
F. Lorenzo, E. M. Giudice, N. Alloisio, L. Morlé +5 more
199317 citations
Semantic Scholar
Spectrin Jendouba: an alpha II/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self-association site.
N. Alloisio, R. Wilmotte, L. Morlé, F. Baklouti +7 more
1992Blood17 citations Open access
Semantic Scholar

Frequent co-authors

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N. Alloisio×32
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N. Alloisio — researcher profile on SciRah
J. Delaunay×24
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J. Delaunay — researcher profile on SciRah
M. Bozon×12
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M. Bozon — researcher profile on SciRah
F. Baklouti×9
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F. Baklouti — researcher profile on SciRah

×9

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B. Pothier — researcher profile on SciRah

J. Maréchal×8

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J. Maréchal — researcher profile on SciRah

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B. Durand — researcher profile on SciRah

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R. Kastally — researcher profile on SciRah

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J. Godet — researcher profile on SciRah

M. Ducluzeau×6

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M. Ducluzeau — researcher profile on SciRah

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R. Wilmotte — researcher profile on SciRah

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J. Delaunay — researcher profile on SciRah