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Laurette Morlé

Université Claude Bernard Lyon 1 FR

90
Publications
2,468
Citations
30
H-Index
57
i10-Index
0
2yr Mean Cite
-
Cite/Paper
Data combined from OpenAlex + Semantic Scholar. OA = OpenAlex S2 = Semantic Scholar
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Publication & Citation Trends

Publications

90 total

RFX2 Is a Major Transcriptional Regulator of Spermiogenesis PDF

W. Stephen Kistler, Dominique Baas, Sylvain Lemeille, Marie Paschaki, Queralt Seguín-Estévez et al. - PLoS Genetics, 2015
Cited by 80 OpenAlex

The Ciliogenic Transcription Factor RFX3 Regulates Early Midline Distribution of Guidepost Neurons Required for Corpus Callosum Development PDF

Carine Benadiba, Dario Magnani, Mathieu Niquille, Laurette Morlé, Delphine Valloton et al. - PLoS Genetics, 2012
Cited by 80 OpenAlex

Transcriptional control of genes involved in ciliogenesis: a first step in making cilia PDF

J. Thomas, Laurette Morlé, Fabien Soulavie, Anne Laurençon, Sébastien Sagnol et al. - Biology of the Cell, 2010
Cited by 166 OpenAlex

RFX3 governs growth and beating efficiency of motile cilia in mouse and controls the expression of genes involved in human ciliopathies PDF

Loubna El Zein, Aouatef Ait‐Lounis, Laurette Morlé, J. Thomas, Brigitte Chhin et al. - Journal of Cell Science, 2009
Cited by 125 OpenAlex

Iconography : Transmission génétique de la cataracte congénitale

F. Beby, L. Morle, L. Michon, M. Bozon, P. Edery - Unknown Venue, 2008
Cited by 0 Semantic Scholar

Transmission génétique de la cataracte congénitale

F. Beby, L. Morle, L. Michon, M. Bozon, P. Edery - Unknown Venue, 2008
Cited by 5 Semantic Scholar

Les surdités génétiques : première cause de surdité de perception de l’enfant

G. Lina-granade, L. Morle, Nicole Alloisio, P. Edery, H. Plauchu - Unknown Venue, 2001
Cited by 4 Semantic Scholar

Apport de la génétique dans la prise en charge des surdités

G. Lina-granade, É. Truy, Nicole Alloisio, L. Morle, F. Disant - Unknown Venue, 2001
Cited by 0 Semantic Scholar

Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3. PDF

Letícia Ribeiro, Nicole Alloisio, Helena Almeida, Clara Gomes, Pascale Texier et al. - PubMed, 2000
Cited by 177 OpenAlex

Hereditary spherocytosis: from clinical to molecular defects.

Achille Iolascon, Emanuele Miraglia del Giudice, Silverio Perrotta, Nicole Alloisio, Laurette Morlé et al. - PubMed, 1998
Cited by 77 OpenAlex

Research Topics

Erythrocyte Function and Pathophysiology (60) Blood properties and coagulation (36) Hemoglobinopathies and Related Disorders (22) Blood groups and transfusion (13) Caveolin-1 and cellular processes (12)

Affiliations

Université Claude Bernard Lyon 1
FR 2020 - 1991
Hôpital Necker-Enfants Malades
FR 1985 - 1985
Centre National de la Recherche Scientifique
FR 2020 - 1986
Inserm
FR 2020 - 2016
Institut Pasteur
FR 1998 - 1992

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