Morwena Latouche

2.5k total citations · 1 hit paper
16 papers, 1.9k citations indexed

About

Morwena Latouche is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Morwena Latouche has authored 16 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 8 papers in Neurology. Recurrent topics in Morwena Latouche's work include Amyotrophic Lateral Sclerosis Research (7 papers), Parkinson's Disease Mechanisms and Treatments (5 papers) and Genetic Neurodegenerative Diseases (4 papers). Morwena Latouche is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (7 papers), Parkinson's Disease Mechanisms and Treatments (5 papers) and Genetic Neurodegenerative Diseases (4 papers). Morwena Latouche collaborates with scholars based in France, United Kingdom and United States. Morwena Latouche's co-authors include Alexis Brice, Gennadij Raivich, Rhona Mirsky, Axel Behrens, Kristján R. Jessen, Edor Kabashi, Serena Lattante, Isabelle Le Ber, Richard Mitter and Peter Arthur‐Farraj and has published in prestigious journals such as Neuron, Journal of Neuroscience and The Journal of Cell Biology.

In The Last Decade

Morwena Latouche

16 papers receiving 1.8k citations

Hit Papers

align trajectories

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.

c-Jun Reprograms Schwann Cells of Injured Nerves to Generate a Repair Cell Essential for Regeneration

2012 632 citations Peter Arthur‐Farraj, Morwena Latouche et al. Neuron profile →

Peers

Countries citing papers authored by Morwena Latouche

Since Specialization

Citations

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

Fields of papers citing papers by Morwena Latouche

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Morwena Latouche

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	MicroRNAsignatures in genetic frontotemporal dementia and amyotrophic lateral sclerosis 2022 ·Annals of Clinical and Translational Neurology ·(unknown), Morwena Latouche, Dario Saracino, Daisy Rinaldi, Agnès Camuzat, (unknown), (unknown), Olivier Colliot, E. Becker	9
2	C9ORF72: What It Is, What It Does, and Why It Matters 2021 ·Frontiers in Cellular Neuroscience ·(unknown), (unknown), Morwena Latouche	91
3	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
4	New Antibody-Free Mass Spectrometry-Based Quantification Reveals That C9ORF72 Long Protein Isoform Is Reduced in the Frontal Cortex of Hexanucleotide-Repeat Expansion Carriers 2018 ·Frontiers in Neuroscience ·Arthur Viodé, Clémence Fournier, Agnès Camuzat, François Fenaille, (unknown), Morwena Latouche, Fanny M. Elahi, (unknown), Christophe Junot, Foudil Lamari, Vincent Anquetil, (unknown)	23
5	The Gastric Myoelectrical Activity Response To Emotional Stimuli 2018 ·(unknown), (unknown), (unknown), Vincent Navarro, Sami Abboud, Morwena Latouche	2
6	hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes 2013 ·Neurobiology of Aging ·Isabelle Le Ber, (unknown), Gaël Nicolas, (unknown), Agnès Camuzat, David Wallon, Anne de Septenville, Morwena Latouche, Serena Lattante, Edor Kabashi, Ludmila Jornéa, Didier Hannequin, Alexis Brice	51
7	Interferon beta induces clearance of mutant ataxin 7 and improves locomotion in SCA7 knock-in mice 2013 ·Brain ·(unknown), Sandro Alves, Martina Marinello, (unknown), (unknown), Christelle Tesson, Morwena Latouche, Darren P. Baker, Martine Barkats, Khalid Hamid El Hachimi, Merle Ruberg, Alexandre Janer, Giovanni Stévanin, Alexis Brice, Annie Sittler	59
8	Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis 2013 ·Annals of Neurology ·Sorana Ciura, Serena Lattante, Isabelle Le Ber, Morwena Latouche, Hervé Tostivint, Alexis Brice, Edor Kabashi	245
9	c-Jun Reprograms Schwann Cells of Injured Nerves to Generate a Repair Cell Essential for Regeneration breakdown → 2012 ·Neuron ·Peter Arthur‐Farraj, Morwena Latouche, Daniel K. Wilton, Susanne Quintes, E Chabrol, (unknown), Ashwin Woodhoo, (unknown), (unknown), Mark Turmaine, Grzegorz Wicher, Richard Mitter, Linda Greensmith, Axel Behrens, Gennadij Raivich, Rhona Mirsky, Kristján R. Jessen	632
10	c-Jun in Schwann cells promotes axonal regeneration and motoneuron survival via paracrine signaling 2012 ·The Journal of Cell Biology ·Xavier Fontana, Mariya Hristova, Clive Da Costa, Smriti Patodia, Laura Thei, Milan Makwana, Bradley Spencer‐Dene, Morwena Latouche, Rhona Mirsky, Kristján R. Jessen, Rüdiger Klein, Gennadij Raivich, Axel Behrens	210
11	Mistargeting of SH3TC2 away from the recycling endosome causes Charcot–Marie–Tooth disease type 4C 2009 ·Human Molecular Genetics ·Rhys Roberts, Andrew A. Peden, Folma Buß, Nicholas A. Bright, Morwena Latouche, Mary M. Reilly, John Kendrick‐Jones, J. Paul Luzio	68
12	A Conditional Pan-NeuronalDrosophilaModel of Spinocerebellar Ataxia 7 with a Reversible Adult Phenotype Suitable for Identifying Modifier Genes 2007 ·Journal of Neuroscience ·Morwena Latouche, Christelle Lasbleiz, Elodie Martin, Véronique Monnier, Thomas Debeir, Annick Mouatt‐Prigent, Marie‐Paule Muriel, Lydie Morel, Merle Ruberg, Alexis Brice, Giovanni Stévanin, Hervé Tricoire	70
13	Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesis 2007 ·Molecular and Cellular Neuroscience ·Michito Namekawa, (unknown), Alexandre Janer, Morwena Latouche, Aurélien Dauphin, Thomas Debeir, Elodie Martin, Charles Duyckaerts, A.F. Prigent, Christel Depienne, Annie Sittler, Alexis Brice, Merle Ruberg	58
14	PML clastosomes prevent nuclear accumulation of mutant ataxin-7 and other polyglutamine proteins 2006 ·The Journal of Cell Biology ·Alexandre Janer, Elodie Martin, Marie‐Paule Muriel, Morwena Latouche, Hiroto Fujigasaki, Merle Ruberg, Alexis Brice, Yvon Trottier, Annie Sittler	72
15	Polyglutamine and polyalanine expansions in ataxin7 result in different types of aggregation and levels of toxicity 2005 ·Molecular and Cellular Neuroscience ·Morwena Latouche, (unknown), Elodie Martin, Khalid Hamid El Hachimi, Cecilia Zander, Annie Sittler, Merle Ruberg, Alexis Brice, Giovanni Stévanin	19
16	Parkin mutations are frequent in patients with isolated early‐onset parkinsonism 2003 ·Brain ·Magali Periquet, Morwena Latouche, Ebba Lohmann, Nina Rawal, Giuseppe De Michele, Sylvain Ricard, Hélio Afonso Ghizoni Teive, Valérie Fraix, Marie Vidailhet, David Nicholl, Paolo Barone, Nicholas Wood, Salmo Raskin, Jean‐François Deleuze, Yves Agid, Alexandra Dürr, Alexis Brice	224

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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