Linda Pons

460 total citations
14 papers, 89 citations indexed

About

Linda Pons is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Linda Pons has authored 14 papers receiving a total of 89 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Physiology. Recurrent topics in Linda Pons's work include Genetics and Neurodevelopmental Disorders (5 papers), RNA modifications and cancer (3 papers) and Congenital heart defects research (2 papers). Linda Pons is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), RNA modifications and cancer (3 papers) and Congenital heart defects research (2 papers). Linda Pons collaborates with scholars based in France, United States and Switzerland. Linda Pons's co-authors include Damien Sanlaville, Gaëtan Lesca, Audrey Labalme, Camille Louvrier, Caroline Schluth‐Bolard, Marianne Till, Patrick Edery, Vincent des Portes, Laurent Guibaud and Inès Harzallah and has published in prestigious journals such as PEDIATRICS, Clinical Genetics and Molecular Autism.

In The Last Decade

Linda Pons

9 papers receiving 87 citations

Peers

Countries citing papers authored by Linda Pons

Since Specialization

Citations

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

Fields of papers citing papers by Linda Pons

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Linda Pons

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

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	Serum Neurofilament Light Chain Correlates With Clinical Severity and Predicts Mortality in Anti-IgLON5 Disease 2025 ·Neurology Neuroimmunology & Neuroinflammation ·Antonio Farina, Macarena Villagrán‐García, (unknown), Marie Bénaiteau, E Bernard, Françoise Bouhour, Virginie Desestret, Bastien Joubert, Géraldine Picard, Anne‐Laurie Pinto, Linda Pons, (unknown), Stéphane Thobois, Sophie Trouillet‐Assant, Jérôme Honnorat	0
2	B‐cell immune deficiency in twin sisters expands the phenotype of MOPDI 2024 ·Clinical Genetics ·(unknown), Morgane Gossez, Christophe Malcus, Sébastien Viel, Guillaume Monneret, Rémy Bordonné, Linda Pons, (unknown), Marion Delous, Sylvie Mazoyer, Audrey Putoux, Patrick Edery	0
3	Chromosomal rearrangement in the 22q11.2 region: a critical locus for sociability and attentional skills 2023 ·Psychiatric Genetics ·(unknown), (unknown), Linda Pons, Caroline Schluth‐Bolard, Damien Sanlaville, Caroline Demily	0
4	A Novel Leptin Receptor LEPR Variant in a Toddler With Early-Onset Fatal Obesity 2023 ·PEDIATRICS ·(unknown), Linda Pons, (unknown), (unknown), Marc Nicolino	0
5	Disruption and deletion of the proximal part of TCF4 are associated with mild intellectual disability: About three new patients 2022 ·European Journal of Medical Genetics ·(unknown), Linda Pons, Tiffany Busa, Chantal Missirian, Matthew A. Lines, (unknown), (unknown), Pierre‐Antoine Rollat‐Farnier, Gaëtan Lesca, Damien Sanlaville, Caroline Schluth‐Bolard	3
6	Touch and olfaction/taste differentiate children carrying a 16p11.2 deletion from children with ASD 2021 ·Molecular Autism ·(unknown), Borja Rodríguez‐Herreros, David Romascano, (unknown), (unknown), Aurélie Pain, (unknown), (unknown), Bertrand Isidor, Lionel Van Maldergem, Linda Pons, Sabine Manificat, Nadia Chabane, (unknown), Anne Maillard	8
7	Intrafamilial Variability in <b><i>LPIN1</i></b>-Related Rhabdomyolysis 2020 ·Molecular Syndromology ·Linda Pons, Cécile Acquaviva, (unknown), (unknown), (unknown), Julie Steffann, Stéphanie Gobin, Pascale de Lonlay, Nathalie Guffon, Alain Fouilhoux	1
8	Novel truncating and missense variants extending the spectrum of EMC1-related phenotypes, causing autism spectrum disorder, severe global development delay and visual impairment 2020 ·European Journal of Medical Genetics ·(unknown), Gaëtan Lesca, Audrey Labalme, Vincent des Portes, Laurent Guibaud, Damien Sanlaville, Linda Pons	16
9	Intrauterine Growth Restriction and Hypertrophic Cardiomyopathy as Prenatal Ultrasound Findings in a Case of Leprechaunism 2020 ·Molecular Syndromology ·(unknown), Mona Massoud, (unknown), Olivier Lascols, Nicolas Pangaud, Carine Villanueva, Linda Pons	5
10	Multisystem disorders, severe developmental delay and seizures in two affected siblings, expanding the phenotype of PIGC deficiency 2020 ·European Journal of Medical Genetics ·Linda Pons, (unknown), Eudéline Alix, (unknown), Audrey Labalme, Damien Sanlaville, Gaëtan Lesca	0
11	Identification of TSC1 or TSC2 mutation limited to the tumor in three cases of solitary subependymal giant cell astrocytoma using next-generation sequencing technology 2020 ·Child s Nervous System ·Martine Fohlen, Inès Harzallah, Marc Polivka, Fabienne Giuliano, Linda Pons, Nathalie Streichenberger, Georg Dorfmüller, Renaud Touraine	10
12	Supravalvular Aortic Stenosis Caused by a Familial Chromosome 7 Inversion Disrupting the ELN Gene Uncovered by Whole-Genome Sequencing 2019 ·Molecular Syndromology ·Linda Pons, Patrice Bouvagnet, (unknown), Sylvie Di Filippo, Adrien Buisson, Nicolas Chatron, Audrey Jalabert, Olivier Metton, Julia Mitchell, (unknown), Pierre‐Antoine Rollat‐Farnier, Damien Sanlaville, Caroline Schluth‐Bolard	2
13	Neonatal tremor episodes and hyperekplexia‐like presentation at onset in a child with SCN8A developmental and epileptic encephalopathy 2018 ·Epileptic Disorders ·Linda Pons, Gaëtan Lesca, Damien Sanlaville, Nicolas Chatron, Audrey Labalme, Véronique Manel, Alexis Arzimanoglou, Julitta de Bellescize, Laurence Lion‐François	9
14	A new syndrome of intellectual disability with dysmorphism due to TBL1XR1 deletion 2014 ·American Journal of Medical Genetics Part A ·Linda Pons, (unknown), Audrey Labalme, Marianne Till, Camille Louvrier, Caroline Schluth‐Bolard, Gaëtan Lesca, Patrick Edery, Damien Sanlaville	35

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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