Leïla Lazaro

1.2k citations

9 papers · 411 indexed · h-index 8

Co-authors: Sylvie Odent Christèle Dubourg Martine Blayau Véronique David Laurent Pasquier Ana Ferreiro B. Estournet Pierre Quartier
Topics: Hedgehog Signaling Pathway Studies (2 papers)Muscle Physiology and Disorders (2 papers)Hereditary Neurological Disorders (2 papers)
Cited by: Genetics Developmental Biology Cellular and Molecular Neuroscience
Journals: Clinical Infectious Diseases Human Molecular Genetics Muscle & Nerve
Partner nations: France Chile Spain

In The Last Decade

Leïla Lazaro

9 papers receiving 408 citations

Peers

Countries citing papers authored by Leïla Lazaro

Since Specialization

Citations

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

Fields of papers citing papers by Leïla Lazaro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Leïla Lazaro

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

All Works

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9 of 9 papers shown

#	Work	Indexed citations
1	From Negative to Positive Diagnosis: Structural Variation Could Be the Second Mutation You Are Looking for in a Recessive Autosomal Gene 2022 ·Journal of Personalized Medicine ·(unknown),(unknown),Frédéric Favreau,Cyril Goizet,Leïla Lazaro,(unknown),(unknown),Franck Sturtz,Corinne Magdelaine,Anne‐Sophie Lia	5
2	The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease 2016 ·Human Molecular Genetics ·(unknown),Claire Chauveau,Cédric Julien,(unknown),Isabelle Duband‐Goulet,Éva Cabet,Brigitte Buendia,Alain Lilienbaum,John Rendu,(unknown),Agnès Guichet,Valérie Allamand,Nathalie Vadrot,Julien Fauré,Sylvie Odent,Leïla Lazaro,(unknown),Pascale Marcorelles,O. Dubourg,Ana Ferreiro	17
3	Whole‐body muscle magnetic resonance imaging in SEPN1‐related myopathy shows a homogeneous and recognizable pattern 2015 ·Muscle & Nerve ·Karolina Hankiewicz,Robert Carlier,Leïla Lazaro,(unknown),Christine Barnérias,David Gómez‐Andrés,Daniela Avila‐Smirnow,Ana Ferreiro,B. Estournet,Pascale Guicheney,Dominique P. Germain,Pascale Richard,(unknown),D. Mompoint,Susana Quijano‐Roy	37
4	5q12.1 deletion: Delineation of a phenotype including mental retardation and ocular defects 2011 ·American Journal of Medical Genetics Part A ·(unknown),Joris Andrieux,Ghislaine Plessis,Ana Cristina Victorino Krepischi,Josette Lucas,Véronique David,(unknown),Débora Romeo Bertola,Albert David,(unknown),Jean Mosser,Leïla Lazaro,Catherine Tréguier,Carla Rosenberg,Sylvie Odent,Christèle Dubourg	19
5	Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Type 2 Caused by Mitofusin 2 Mutations 2009 ·Archives of Neurology ·(unknown),Benoît Funalot,Robert Ouvrier,Leïla Lazaro,Annick Toutain,P. De Mas,P. Bouché,Brigitte Gilbert‐Dussardier,Marie‐Christine Arné‐Bes,(unknown),Hubert Journel,Marie-Christine Minot-Myhié,Claire Le Guillou,Karima Ghorab,Laurent Magy,Franck Sturtz,Jean‐Michel Vallat,Corinne Magdelaine	92
6	Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores 2008 ·Human Mutation ·Nicole Monnier,Isabelle Marty,Julien Fauré,Claudia Castiglioni,Claude Desnuelle,Sabrina Sacconi,B. Estournet,Ana Ferreiro,Norma B. Romero,Annie Laquerrière,Leïla Lazaro,Jean‐Jacques Martin,Éva Morava,Annick Rossi,Anneke J. van der Kooi,Marianne de Visser,(unknown),Joël Lunardi	75
7	Phenotypic and molecular variability of the holoprosencephalic spectrum 2004 ·American Journal of Medical Genetics Part A ·Leïla Lazaro,Christèle Dubourg,Laurent Pasquier,Franck Le Duff,Martine Blayau,(unknown),(unknown),(unknown),Véronique David,Sylvie Odent	53
8	Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations 2003 ·Human Genetics ·(unknown),Christèle Dubourg,Jocelyne Attia‐Sobol,Jacqueline Vigneron,Martine Blayau,Laurent Pasquier,Leïla Lazaro,Sylvie Odent,Véronique David	40
9	Enteroviral Meningoencephalitis after Anti‐CD20 (Rituximab) Treatment 2003 ·Clinical Infectious Diseases ·Pierre Quartier,Olivier Tournilhac,Christine Archimbaud,Leïla Lazaro,Carine Chaleteix,(unknown),H. Peigue‐Lafeuille,Stéphane Blanche,Alain Fischer,Jean‐Laurent Casanova,Philippe Travade,Marc Tardieu	73

About Leïla Lazaro

Leïla Lazaro is a scholar working on Cardiology and Cardiovascular Medicine, Cell Biology and Neurology, having authored 9 papers that have together received 411 indexed citations. Recurring topics across this work include Hedgehog Signaling Pathway Studies (2 papers), Muscle Physiology and Disorders (2 papers) and Hereditary Neurological Disorders (2 papers). The work is most often cited by research in Genetics (68 citations), Developmental Biology (12 citations) and Cellular and Molecular Neuroscience (96 citations). Leïla Lazaro has collaborated with scholars based in France, Chile and Spain. Frequent co-authors include Sylvie Odent, Christèle Dubourg, Martine Blayau, Véronique David, Laurent Pasquier, Ana Ferreiro, B. Estournet, Pierre Quartier, H. Peigue‐Lafeuille and Marc Tardieu. Their work appears in journals such as Clinical Infectious Diseases, Human Molecular Genetics and Muscle & Nerve.

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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