Florence Molinari

2.0k citations

30 papers · 1.4k · 1 hit paper · h-index 15

Impact in

Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases

Papers in

Molecular Biology 15
- Glycosylation and Glycoproteins Research 3
Genetics 11
- Genetics and Neurodevelopmental Disorders 9
- Genomic variations and chromosomal abnormalities 3
- Genomics and Rare Diseases 3

Co-authors: Laurence Colleaux (15 shared papers)Arnold Münnich (9 shared papers)Marlène Rio (7 shared papers)Noman Kadhom (2 shared papers)Sarah Boissel (2 shared papers)Michel Vekemans (4 shared papers)Luigi Palmieri (3 shared papers)Ferdinando Palmieri (3 shared papers)
Journals: The American Journal of Human Genetics (4 papers)Epilepsia (4 papers)Science (3 papers)Human Molecular Genetics (2 papers)Clinical Genetics (2 papers)
Partner nations: France Italy United Kingdom

In The Last Decade

Florence Molinari

29 papers receiving 1.4k citations

Florence Molinari's Hit Papers

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Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations 2009 · 298 citations

Peers

Countries citing papers authored by Florence Molinari

Since Specialization

Citations

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

Fields of papers citing papers by Florence Molinari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Florence Molinari, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Florence Molinari Line = papers co-authored together Florence Molinari links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 30 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations The American Journal of Human Genetics ·Sarah Boissel, Orit Reish, Karine Proulx, Hiroko Kawagoe-Takaki, Barbara Sedgwick, Giles S.H. Yeo, Stephen Eyre, Christelle Golzio, Florence Molinari, Noman Kadhom, Heather Etchevers, Vladimı́r Saudek, I. Sadaf Farooqi, Philippe Froguel, Tomas Lindahl, Stephen O’Rahilly, Arnold Münnich, Laurence Colleaux Hit paper breakdown →	2009	298
2	Truncating Neurotrypsin Mutation in Autosomal Recessive Nonsyndromic Mental Retardation Science ·Florence Molinari, Marlène Rio, Virginia Meskenaïte, Férechté Encha-Razavi, Joëlle Augé, Delphine Bacq, Sylvain Briault, Michel Vekemans, Arnold Münnich, Tania Attié‐Bitach, P. Sonderegger, Laurence Colleaux	2002	138
3	Association of a Functional Deficit of the BK _Ca Channel, a Synaptic Regulator of Neuronal Excitability, With Autism and Mental Retardation American Journal of Psychiatry ·Frédéric Laumonnier, Sébastien Roger, Pascaline Guérin, Florence Molinari, Ridha Mrad, Dominique Cahard, A. Belhadj, M.B. Halayem, Antonio M. Persico, Maurizio Elia, Valentino Romano, Sébastien Holbert, Christian Andrés, Habiba Chaâbouni, Laurence Colleaux, Jacques Constant, Jean-Yves Le Guennec, Sylvain Briault	2006	135
4	Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy The American Journal of Human Genetics ·Florence Molinari, Annick Raas‐Rothschild, Marlène Rio, Giuseppe Fiermonte, Férechté Encha‐Razavi, Luigi Palmieri, Ferdinando Palmieri, Ziva Ben‐Neriah, Noman Kadhom, Michel Vekemans, Tania Attié‐Bitach, Arnold Münnich, Pierre Rustin, Laurence Colleaux	2005	115
5	Oligosaccharyltransferase-Subunit Mutations in Nonsyndromic Mental Retardation The American Journal of Human Genetics ·Florence Molinari, François Foulquier, Patrick Tarpey, Willy Morelle, Sarah Boissel, Jon W. Teague, Sarah Edkins, P. Andrew Futreal, Michael R. Stratton, Gillian Turner, Gert Matthijs, Jozef Gécz, Arnold Münnich, Laurence Colleaux	2008	110
6	Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression bursts Clinical Genetics ·Florence Molinari, Anna Kamińska, Giuseppe Fiermonte, Nathalie Boddaert, Annick Raas‐Rothschild, P. Plouin, Luigi Palmieri, F Brunelle, Ferdinando Palmieri, Olivier Dulac, A Munnich, Laurence Colleaux	2009	95
7	Combination of Linkage Mapping and Microarray-Expression Analysis Identifies NF-κB Signaling Defect as a Cause of Autosomal-Recessive Mental Retardation The American Journal of Human Genetics ·Orianne Philippe, Marlène Rio, Astrid Carioux, Jean-Marc Plaza, Philippe Guigue, Florence Molinari, Nathalie Boddaert, Christine Bôle‐Feysot, Patrick Nitschké, Asma Smahi, Arnold Münnich, Laurence Colleaux	2009	74
8	Tequila, a Neurotrypsin Ortholog, Regulates Long-Term Memory Formation in Drosophila Science ·Gérard Didelot, Florence Molinari, P. Tchénio, Daniel Comas, Elodie Milhiet, Arnold Munnich, Laurence Colleaux, Thomas Préat	2006	67
9	Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation Journal of Medical Genetics ·Marlène Rio, Florence Molinari, S. Heuertz, Catherine Ozilou, Philippe Gosset, O Raoul, Valérie Cormier‐Daire, Aliza Amiel, Stanislas Lyonnet, L Le Merrer, C Turleau, (unknown), M Prieur, Serge Romana, Michel Vekemans, Arnold Münnich, Laurence Colleaux	2002	54
10	Inhibition of the Mitochondrial Glutamate Carrier SLC25A22 in Astrocytes Leads to Intracellular Glutamate Accumulation Frontiers in Cellular Neuroscience ·Emmanuelle Goubert, Yanina Mircheva, Francesco M. Lasorsa, Christophe Melon, Emanuela Profilo, Julie Sutera, Hélène Becq, Ferdinando Palmieri, Luigi Palmieri, Laurent Aniksztejn, Florence Molinari	2017	45
11	A Kv7.2 mutation associated with early onset epileptic encephalopathy with suppression‐burst enhances Kv7/M channel activity Epilepsia ·Jérôme Devaux, Affef Abidi, Agathe Roubertie, Florence Molinari, Hélène Becq, Caroline Lacoste, Laurent Villard, Mathieu Milh, Laurent Aniksztejn	2016	36
12	High-intensity interval training is superior to moderate intensity training on aerobic capacity in rats: Impact on hippocampal plasticity markers Behavioural Brain Research ·Annabelle Constans, Caroline Pin-Barre, Florence Molinari, Jean-Jacques Temprado, Thomas Brioche, Christophe Pellegrino, Jérôme Laurin	2020	36
13	Extracellular proteases and their inhibitors ingenetic diseases of the central nervous system Human Molecular Genetics ·Florence Molinari, V. Meskanaite, Arnold Münnich, P. Sonderegger, Laurence Colleaux	2003	29
14	A knock‐in mouse model for KCNQ2‐related epileptic encephalopathy displays spontaneous generalized seizures and cognitive impairment Epilepsia ·Mathieu Milh, Pierre L. Roubertoux, Najoua Biba, Julie Chavany, Adeline Ghata, Camille Fulachier, Stephan C. Collins, Christel Wagner, Jean‐Christophe Roux, Binnaz Yalcin, Marie‐Solenne Félix, Florence Molinari, Pierre‐Pascal Lenck‐Santini, Laurent Villard	2020	27
15	The conversion of glutamate by glutamine synthase in neocortical astrocytes from juvenile rat is important to limit glutamate spillover and peri/extrasynaptic activation of NMDA receptors Glia ·Mohamed Trabelsi, Mohamed Amri, Hélène Becq, Florence Molinari, Laurent Aniksztejn	2016	27
16	Glutamate transporters control metabotropic glutamate receptors activation to prevent the genesis of paroxysmal burst in the developing hippocampus Neuroscience ·Florence Molinari, Adriano Cattani, Julius Baya Mdzomba, Laurent Aniksztejn	2012	13
17	Response to Comment on "Tequila, a Neurotrypsin Ortholog, Regulates Long-Term Memory Formation in Drosophila " Science ·Thomas Préat, Jean‐Luc Da Lage, Laurence Colleaux, Gérard Didelot, Florence Molinari, P. Tchénio, Elodie Milhiet, Arnold Munnich, Marie‐Louise Cariou	2007	12
18	Mitochondria and neonatal epileptic encephalopathies with suppression burst Journal of Bioenergetics and Biomembranes ·Florence Molinari	2010	11
19	Bumetanide induces post-traumatic microglia–interneuron contact to promote neurogenesis and recovery Brain ·M. Tessier, Marta Saez Garcia, Emmanuelle Goubert, Edith Blasco, Amandine Consumi, Benoît Dehapiot, (unknown), Florence Molinari, Jérôme Laurin, François Guillemot, Christian A. Hübner, Christophe Pellegrino, Claudio Rivera	2023	10
20	A possible link between KCNQ2‐ and STXBP1‐related encephalopathies: STXBP1 reduces the inhibitory impact of syntaxin‐1A on M current Epilepsia ·Jérôme Devaux, Sandra Dhifallah, Michela De Maria, Geoffrey Stuart‐Lopez, Hélène Becq, Mathieu Milh, Florence Molinari, Laurent Aniksztejn	2017	9

About Florence Molinari

Florence Molinari is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Clinical Biochemistry and Cell Biology, having authored 30 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (9 papers), Neuroscience and Neuropharmacology Research (6 papers), Metabolism and Genetic Disorders (4 papers), Glycosylation and Glycoproteins Research (3 papers), Cellular transport and secretion (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (3 papers) and Epilepsy research and treatment (3 papers). The work is most often cited by research in Clinical Biochemistry (128 citations), Genetics (461 citations), Cellular and Molecular Neuroscience (234 citations), Developmental Neuroscience (43 citations) and Molecular Biology (760 citations). Florence Molinari has collaborated with scholars based in France, Italy and United Kingdom. Frequent co-authors include Laurence Colleaux, Arnold Münnich, Marlène Rio, Noman Kadhom, Sarah Boissel, Michel Vekemans, Luigi Palmieri, Ferdinando Palmieri, Tania Attié‐Bitach and Sylvain Briault. Their work appears in journals such as The American Journal of Human Genetics, Epilepsia, Science, Human Molecular Genetics and Clinical Genetics.

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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Florence Molinari

Florence Molinari's Hit Papers

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