Sylvie Forlani

5.7k total citations
37 papers, 1.6k citations indexed

About

Sylvie Forlani is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Sylvie Forlani has authored 37 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 20 papers in Cellular and Molecular Neuroscience and 7 papers in Neurology. Recurrent topics in Sylvie Forlani's work include Genetic Neurodegenerative Diseases (14 papers), Mitochondrial Function and Pathology (10 papers) and Neurological diseases and metabolism (7 papers). Sylvie Forlani is often cited by papers focused on Genetic Neurodegenerative Diseases (14 papers), Mitochondrial Function and Pathology (10 papers) and Neurological diseases and metabolism (7 papers). Sylvie Forlani collaborates with scholars based in France, United States and Germany. Sylvie Forlani's co-authors include Jacqueline Deschamps, Wim de Graaff, Kirstie A. Lawson, Alexis Brice, Alexandra Dürr, Eric van den Akker, Giovanni Stévanin, Felix Beck, Kallayanee Chawengsaksophak and Barbara I. Meyer and has published in prestigious journals such as Cell, Brain and Development.

In The Last Decade

Sylvie Forlani

37 papers receiving 1.6k citations

Peers

Countries citing papers authored by Sylvie Forlani

Since Specialization

Citations

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

Fields of papers citing papers by Sylvie Forlani

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sylvie Forlani

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	In vivo prime editing rescues alternating hemiplegia of childhood in mice 2025 ·Cell ·Alexander A. Sousa, (unknown), Hiroki Sakai, (unknown), Elena Arystarkhova, Natalia S. Morsci, Laura Anderson, Jun Xie, (unknown), Linda Laux, Emmanuel Roze, Sylvie Forlani, Guangping Gao, Simon D. W. Frost, Nikolaj Frost, Kathleen J. Sweadner, Alfred L. George, Cathleen Lutz, David R. Liu	5
2	Plasma microRNA signature in presymptomatic and symptomatic subjects with C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosis 2020 ·Journal of Neurology Neurosurgery & Psychiatry ·(unknown), Vincent Anquetil, Dario Saracino, Daisy Rinaldi, Agnès Camuzat, (unknown), Ludmila Jornéa, Sylvie Forlani, Philippe Couratier, David Wallon, Florence Pasquier, (unknown), Pierre de la Grange, Ivan Moszer, (unknown), Olivier Colliot, E. Becker	32
3	PolyQ-expanded ataxin-3 protein levels in peripheral blood mononuclear cells correlate with clinical parameters in SCA3: a pilot study 2020 ·Journal of Neurology ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Thomas Klockgether, Sylvie Forlani, Alexandra Dürr, Stefan Hauser, Tim W. Rattay, Matthis Synofzik, Holger Hengel, Lüdger Schöls, Olaf Rieß, Jeannette Hübener‐Schmid	10
4	The missense p.Trp7Arg mutation in GRN gene leads to progranulin haploinsufficiency 2019 ·Neurobiology of Aging ·Dario Saracino, Leila Sellami, Fabienne Clot, Agnès Camuzat, Foudil Lamari, Benoît Rucheton, (unknown), (unknown), Julien Lagarde, Marie Sarazin, Ludmila Jornéa, Sylvie Forlani, Éric Leguern, Bruno Dubois, Alexis Brice, Isabelle Le Ber	4
5	Novel VCP mutations expand the mutational spectrum of frontotemporal dementia 2018 ·Neurobiology of Aging ·Dario Saracino, Fabienne Clot, Agnès Camuzat, Vincent Anquetil, Didier Hannequin, Lucie Guyant‐Maréchal, Mira Didic, Léna Guillot‐Noël, Daisy Rinaldi, Morwena Latouche, Sylvie Forlani, (unknown), Cinzia Coppola, Giuseppe Di Iorio, (unknown), E. Le Guern, Alexis Brice, (unknown)	21
6	New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32 2013 ·JAMA Neurology ·Carmen Serrano, Marc Corral‐Juan, Giovanni Stévanin, (unknown), (unknown), (unknown), Berta Campos, (unknown), Carlos Morcillo-Suárez, Arcadi Navarro, Sylvie Forlani, Alexandra Dürr, Jaime Kulisevsky, Alexis Brice, Ivelisse Sánchez, Vı́ctor Volpini, Antoni Matilla‐Dueñas	29
7	The impact of single-nucleotide polymorphisms (SNPs) in OGG1 and XPC on the age at onset of Huntington disease 2013 ·Mutation Research/Genetic Toxicology and Environmental Mutagenesis ·Frédérique Berger, Laurence Vaslin, Lisa Belin, Bernard Asselain, Sylvie Forlani, Sandrine Humbert, Alexandra Dürr, Janet Hall	15
8	A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42) 2010 ·European Journal of Human Genetics ·Nina Schlipf, Christian Beetz, Rebecca Schüle, Giovanni Stévanin, Anne Kjersti Erichsen, Sylvie Forlani, Cécile Zaros, Kathrin N. Karle, Stephan Klebe, Sven Klimpe, Alexandra Dürr, Susanne Otto, Chantal Tallaksen, Olaf Rieß, Alexis Brice, Peter Bauer, Lüdger Schöls	16
9	Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds 2010 ·Journal of Neurology Neurosurgery & Psychiatry ·Peter Bauer, Giovanni Stévanin, Christian Beetz, Matthis Synofzik, Tanja Schmitz‐Hübsch, Ullrich Wüllner, Erwin Berthier, Elisabeth Ollagnon‐Roman, (unknown), Sylvie Forlani, Emeline Mundwiller, A. Dürr, Lüdger Schöls, Alexis Brice	36
10	KCNC3: phenotype, mutations, channel biophysics-a study of 260 familial ataxia patients 2009 ·Human Mutation ·Karla P. Figueroa, Natali A. Minassian, Giovanni Stévanin, Michael D. Waters, (unknown), Sylvie Forlani, Adam Strzelczyk, Katrin Bürk, Alexis Brice, Alexandra Dürr, Diane M. Papazian, Stefan M. Pulst	67
11	Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome 2008 ·The American Journal of Human Genetics ·Sylvain Hanein, Elodie Martin, Amir Boukhris, P. Byrne, Cyril Goizet, Abdelmadjid Hamri, Ali Benomar, Alexander Lossos, Paola S. Denora, José Carlos Fernández Fernández, Nizar Elleuch, Sylvie Forlani, Alexandra Dürr, Imed Feki, Michael Hutchinson, Filippo M. Santorelli, Chokri Mhiri, Alexis Brice, Giovanni Stévanin	148
12	Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10 2008 ·Human Mutation ·Cyril Goizet, Amir Boukhris, Emeline Mundwiller, Chantal Tallaksen, Sylvie Forlani, Annick Toutain, (unknown), (unknown), Christel Depienne, Alexandra Dürr, Giovanni Stévanin, Alexis Brice	95
13	Composite cerebellar functional severity score: validation of a quantitative score of cerebellar impairment 2008 ·Brain ·Sophie Tézenas du Montcel, Perrine Charles, Pascale Ribaı̈, Cyril Goizet, (unknown), Pierre Labauge, Lucie Guyant‐Maréchal, Sylvie Forlani, C Jauffret, N. Vandenberghe, Karine Nguyen, Isabelle Le Ber, David Devos, (unknown), Mario‐Ubaldo Manto, François Tison, Didier Hannequin, Merle Ruberg, Alexis Brice, Alexandra Dürr	67
14	Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description 2007 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Stephan Klebe, Alexandra Dürr, Naïma Bouslam, Djamel Grid, Caroline Paternotte, Christel Depienne, Sylvain Hanein, Ahmed Bouhouche, Nizar Elleuch, Hamid Azzedine, Sandrine Poëa‐Guyon, Sylvie Forlani, (unknown), Céline Charon, Jamïlé Hazan, Alexis Brice, Giovanni Stévanin	14
15	A novel locus for autosomal dominant “uncomplicated” hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3 2007 ·Human Genetics ·Sylvain Hanein, Alexandra Dürr, Pascale Ribaı̈, Sylvie Forlani, Anne‐Louise Leutenegger, Isabelle Nelson, Marie‐Claude Babron, Nizar Elleuch, Christel Depienne, Céline Charon, Alexis Brice, Giovanni Stévanin	18
16	Glypicans are differentially expressed during patterning and neurogenesis of early mouse brain 2006 ·Biochemical and Biophysical Research Communications ·Guillaume Luxardi, Antonella Galli, Sylvie Forlani, Kirstie A. Lawson, Flavio Maina, Rosanna Dono	29
17	Hox cluster polarity in early transcriptional availability: a high order regulatory level of clustered Hox genes in the mouse 2002 ·Mechanisms of Development ·Bernard A.J. Roelen, Wim de Graaff, Sylvie Forlani, Jacqueline Deschamps	38
18	LagoZ et LagZ, deux gènes appauvris en dinucléotides CpG dérivés du gène LacZ pour l'étude des contrôles épigénétiques 1999 ·Comptes Rendus de l Académie des Sciences - Series III - Sciences de la Vie ·Isabelle Henry, Sylvie Forlani, (unknown), John Muschler, André Choulika, Jean‐François Nicolas	6
19	Quantification of minute levels of β galactosidase in individual 2- to 16-cell-stage mouse embryos 1996 ·Trends in Genetics ·Sylvie Forlani, Jean‐François Nicolas	5
20	A regulatory function for K10 in the establishment of dorsoventral polarity in the Drosophila egg and embryo 1993 ·Mechanisms of Development ·Sylvie Forlani, Dominique Ferrandon, (unknown), Eliane Mohier	12

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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