Florence Molinari

2.0k total citations · 1 hit paper
30 papers, 1.4k citations indexed

About

Florence Molinari is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Florence Molinari has authored 30 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 13 papers in Cellular and Molecular Neuroscience and 13 papers in Genetics. Recurrent topics in Florence Molinari's work include Genetics and Neurodevelopmental Disorders (11 papers), Neuroscience and Neuropharmacology Research (8 papers) and Metabolism and Genetic Disorders (4 papers). Florence Molinari is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Neuroscience and Neuropharmacology Research (8 papers) and Metabolism and Genetic Disorders (4 papers). Florence Molinari collaborates with scholars based in France, Italy and Finland. Florence Molinari's co-authors include Laurence Colleaux, Arnold Münnich, Marlène Rio, Noman Kadhom, Sarah Boissel, Michel Vekemans, Ferdinando Palmieri, Tania Attié‐Bitach, Luigi Palmieri and Sylvain Briault and has published in prestigious journals such as Science, American Journal of Psychiatry and Brain.

In The Last Decade

Florence Molinari

28 papers receiving 1.3k citations

Hit Papers

Loss-of-Function Mutation in the Dioxygenase-Encoding FTO... 2009 2026 2014 2020 2009 50 100 150 200 250
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations
    2009 294 citations Sarah Boissel, Florence Molinari et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Florence Molinari France 15 824 515 257 141 138 30 1.4k
Koen L.I. van Gassen Netherlands 22 564 0.7× 407 0.8× 319 1.2× 68 0.5× 96 0.7× 42 1.3k
Kimberly A. Burton United States 16 940 1.1× 400 0.8× 794 3.1× 132 0.9× 42 0.3× 21 2.1k
Paymaan Jafar‐Nejad United States 23 1.6k 2.0× 320 0.6× 920 3.6× 71 0.5× 46 0.3× 55 2.3k
Daniel P. Seeburg United States 16 1.4k 1.7× 380 0.7× 570 2.2× 408 2.9× 93 0.7× 26 2.2k
Guillermo López‐Doménech United Kingdom 18 1.1k 1.3× 172 0.3× 366 1.4× 63 0.4× 143 1.0× 21 1.5k
Yi‐Shuian Huang Taiwan 25 1.7k 2.1× 219 0.4× 463 1.8× 209 1.5× 93 0.7× 69 2.3k
Byoung-Il Bae United States 13 1.5k 1.9× 289 0.6× 477 1.9× 120 0.9× 64 0.5× 17 2.0k
Ning Huang China 21 913 1.1× 184 0.4× 331 1.3× 141 1.0× 49 0.4× 54 1.8k
Yonatan Perez Israel 14 728 0.9× 248 0.5× 86 0.3× 73 0.5× 28 0.2× 27 1.1k
Haijun Chen United States 16 863 1.0× 294 0.6× 396 1.5× 21 0.1× 39 0.3× 27 1.2k

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-authorship network of co-authors of Florence Molinari

This figure shows the co-authorship network connecting the top 25 collaborators of Florence Molinari. A scholar is included among the top collaborators of Florence Molinari 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 Florence Molinari. Florence Molinari 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.
Mignon‐Ravix, Cécile, Géraldine Daquin, Pierre Cacciagli, et al.. (2023). NAPB and developmental and epileptic encephalopathy: Description of the electroclinical profile associated with a novel pathogenic variant. Epilepsia. 64(6). e127–e134. 5 indexed citations
2.
Mignon‐Ravix, Cécile, Pierre Cacciagli, Béatrice Desnous, et al.. (2023). Loss of NDST1 N-sulfotransferase activity is associated with autosomal recessive intellectual disability. Human Molecular Genetics. 33(6). 520–529.
3.
Dehapiot, Benoît, Li Tian, Florence Molinari, et al.. (2023). Bumetanide induces post-traumatic microglia–interneuron contact to promote neurogenesis and recovery. Brain. 146(10). 4247–4261. 10 indexed citations
4.
Pin-Barre, Caroline, Florence Molinari, Jean-Jacques Temprado, et al.. (2020). High-intensity interval training is superior to moderate intensity training on aerobic capacity in rats: Impact on hippocampal plasticity markers. Behavioural Brain Research. 398. 112977–112977. 33 indexed citations
5.
Ludwig, Anastasia, T. E. Sukhanova, Florence Molinari, et al.. (2020). Novel carbon film induces precocious calcium oscillation to promote neuronal cell maturation. Scientific Reports. 10(1). 17661–17661. 1 indexed citations
6.
Khirug, Stanislav, Liang Zhou, Natalia Kulesskaya, et al.. (2020). Protective Role of Low Ethanol Administration Following Ischemic Stroke via Recovery of KCC2 and p75NTR Expression. Molecular Neurobiology. 58(3). 1145–1161. 7 indexed citations
7.
Lasorsa, Francesco M., Christophe Melon, Hélène Becq, et al.. (2017). Inhibition of the Mitochondrial Glutamate Carrier SLC25A22 in Astrocytes Leads to Intracellular Glutamate Accumulation. Frontiers in Cellular Neuroscience. 11. 149–149. 45 indexed citations
8.
Devaux, Jérôme, Agathe Roubertie, Florence Molinari, et al.. (2016). A Kv7.2 mutation associated with early onset epileptic encephalopathy with suppression‐burst enhances Kv7/M channel activity. Epilepsia. 57(5). e87–93. 35 indexed citations
9.
Rio, Marlène, Jean-Marc Plaza, Philippe Guigue, et al.. (2009). 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. 85(6). 903–908. 73 indexed citations
10.
Molinari, Florence, Anna Kamińska, Giuseppe Fiermonte, et al.. (2009). Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression bursts. Clinical Genetics. 76(2). 188–194. 95 indexed citations
11.
Molinari, Florence, François Foulquier, Patrick Tarpey, et al.. (2008). Oligosaccharyltransferase-Subunit Mutations in Nonsyndromic Mental Retardation. The American Journal of Human Genetics. 82(5). 1150–1157. 110 indexed citations
12.
Molinari, Florence, S. Romano, François Foulquier, et al.. (2007). Oligosaccharyltransferase subunits mutations in non-syndromic mental retardation. European Journal of Human Genetics. 16. 25. 4 indexed citations
13.
Didelot, Gérard, Florence Molinari, P. Tchénio, et al.. (2006). Tequila, a Neurotrypsin Ortholog, Regulates Long-Term Memory Formation in Drosophila. Science. 313(5788). 851–853. 67 indexed citations
14.
Laumonnier, Frédéric, Sébastien Roger, Pascaline Guérin, et al.. (2006). 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. 163(9). 1622–1629. 135 indexed citations
15.
Molinari, Florence, Annick Raas‐Rothschild, Marlène Rio, et al.. (2005). Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy. The American Journal of Human Genetics. 76(2). 334–339. 115 indexed citations
16.
Rio, Marlène, Laurence Colleaux, Damien Sanlaville, et al.. (2004). Approche diagnostique du sujet présentant un retard mental sévère et syndromique. Archives de Pédiatrie. 11(6). 566–568. 1 indexed citations
17.
Borck, Guntram, Marlène Rio, Damien Sanlaville, et al.. (2004). Genome‐wide screening using automated fluorescent genotyping to detect cryptic cytogenetic abnormalities in children with idiopathic syndromic mental retardation. Clinical Genetics. 66(2). 122–127. 6 indexed citations
18.
Molinari, Florence, et al.. (2003). Extracellular proteases and their inhibitors ingenetic diseases of the central nervous system. Human Molecular Genetics. 12(suppl 2). R195–R200. 29 indexed citations
19.
Colleaux, Laurence, S. Heuertz, Florence Molinari, & Marlène Rio. (2003). Fluorescence Genotyping for Screening Cryptic Telomeric Rearrangements. Molecular Cytogenetics. 204. 181–190. 5 indexed citations
20.
Rio, Marlène, Florence Molinari, S. Heuertz, et al.. (2002). Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation. Journal of Medical Genetics. 39(4). 266–270. 54 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.

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