Léna Damaj

1.7k total citations
19 papers, 479 citations indexed

About

Léna Damaj is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Léna Damaj has authored 19 papers receiving a total of 479 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 5 papers in Physiology. Recurrent topics in Léna Damaj's work include Metabolism and Genetic Disorders (7 papers), Mitochondrial Function and Pathology (3 papers) and Lysosomal Storage Disorders Research (3 papers). Léna Damaj is often cited by papers focused on Metabolism and Genetic Disorders (7 papers), Mitochondrial Function and Pathology (3 papers) and Lysosomal Storage Disorders Research (3 papers). Léna Damaj collaborates with scholars based in France, Switzerland and Italy. Léna Damaj's co-authors include Alexis Lupien‐Meilleur, Louise Gagnon, Émilie Riou, Elsa Rossignol, Anne Lortie, Luis H. Ospina, Pascale de Lonlay, Laurence Hubert, Sylvie Odent and Serge Romana and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, PEDIATRICS and International Journal of Molecular Sciences.

In The Last Decade

Léna Damaj

19 papers receiving 468 citations

Peers

Léna Damaj

EDM

GENET

PPCH

Sau Cheung Tiu China

Kristin Barañano United States

Joerg Klepper Germany

Bilge Volkan Salancı Türkiye

Rosario Berardi Italy

Angel On-Kei Chan China

Mónica George Spain

Takehiko Inui Japan

Hiroko Iwamoto Japan

Tessa Wassenberg Netherlands

Sau Cheung Tiu China

Léna Damaj

204 ×1.1

158 ×1.3

EDM

101 ×0.9

GENET

30 ×0.3

49 ×0.6

PPCH

Citations per year, relative to Léna Damaj Léna Damaj (= 1×) peers Sau Cheung Tiu

Countries citing papers authored by Léna Damaj

Since Specialization

Citations

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

Fields of papers citing papers by Léna Damaj

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Léna Damaj

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

All Works

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19 of 19 papers shown

Leclerc, Delphine, Sylvie Jaillard, Léna Damaj, et al.. (2023). Gene Editing Corrects In Vitro a G > A GLB1 Transition from a GM1 Gangliosidosis Patient. The CRISPR Journal. 6(1). 17–31. 2 indexed citations

Labarthe, François, Caroline Moreau, Jean‐Baptiste Arnoux, et al.. (2023). Newborn Screening of Primary Carnitine Deficiency: An Overview of Worldwide Practices and Pitfalls to Define an Algorithm before Expansion of Newborn Screening in France. International Journal of Neonatal Screening. 9(1). 6–6. 9 indexed citations

Denamur, Sophie, Guy Touati, Léna Damaj, et al.. (2022). Recommended respiratory tests are not routinely performed for mucopolysaccharidosis patients. ERJ Open Research. 8(1). 567–2021. 2 indexed citations

Lebigot, Élise, Emmanuel Roze, Claude Cancés, et al.. (2022). Movement disorders in valine métabolism diseases caused by HIBCH and ECHS1 deficiencies. European Journal of Neurology. 29(11). 3229–3242. 11 indexed citations

Damaj, Léna, et al.. (2020). Immunoassay Disruption by High-Dose Biotin Therapy: Fair Warning for Neonatal Care Physicians. Pediatric Neurology. 112. 8–9. 2 indexed citations

Dubourg, Christèle, Samia Pichard, Virginie Gandemer, et al.. (2020). Incidental diagnosis of mucopolysaccharidosis type I in an infant with chronic intestinal pseudoobstruction by exome sequencing. Molecular Genetics and Metabolism Reports. 24. 100621–100621. 3 indexed citations

Peoc’h, Katell, Léna Damaj, Romain Pelletier, et al.. (2020). Early care of N-acetyl glutamate synthase (NAGS) deficiency in three infants from an inbred family. Molecular Genetics and Metabolism Reports. 22. 100558–100558. 4 indexed citations

Peoc’h, Katell, Maëla Le Lous, Guillaume Bouzillé, et al.. (2020). Maternal and neonatal outcomes and prognostic factors in acute fatty liver of pregnancy. European Journal of Obstetrics & Gynecology and Reproductive Biology. 252. 198–205. 17 indexed citations

Girard, M, Claire Douillard, Dominique Debray, et al.. (2020). Long term outcome of MPI‐CDG patients on D‐mannose therapy. Journal of Inherited Metabolic Disease. 43(6). 1360–1369. 18 indexed citations

10.

Moreau, Caroline, Katell Peoc’h, Edouard Bardou‐Jacquet, et al.. (2019). Pregnancy in metabolic diseases with hepatic expression: what risks for the mother and the child?. Annales de biologie clinique. 77(6). 605–618. 2 indexed citations

11.

Pasquier, Laurent, David Cohen, Mélanie Fradin, et al.. (2017). Role of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy. International Journal of Molecular Sciences. 18(3). 618–618. 22 indexed citations

12.

Padidela, Raja, Bing Han, Adam Stevens, et al.. (2016). mTOR Inhibitors for the Treatment of Severe Congenital Hyperinsulinism: Perspectives on Limited Therapeutic Success. The Journal of Clinical Endocrinology & Metabolism. 101(12). 4719–4729. 38 indexed citations

13.

Mazzuca, Michel, Marie-Anne Maubert, Léna Damaj, et al.. (2015). Combined Sepiapterin Reductase and Methylmalonyl-CoA Epimerase Deficiency in a Second Patient: Cerebrospinal Fluid Polyunsaturated Fatty Acid Level and Follow-Up Under l-DOPA, 5-HTP and BH4 Trials. JIMD Reports. 22. 47–55. 10 indexed citations

14.

Damaj, Léna, Alexis Lupien‐Meilleur, Anne Lortie, et al.. (2015). CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms. European Journal of Human Genetics. 23(11). 1505–1512. 144 indexed citations

15.

Damaj, Léna, Valérie Serre, Laurence Hubert, et al.. (2013). Aromatic L-Amino Acid Decarboxylase Deficiency Is a Cause of Long-Fasting Hypoglycemia. The Journal of Clinical Endocrinology & Metabolism. 98(11). 4279–4284. 22 indexed citations

16.

Keil, Stefanie, Francjan J. van Spronsen, Nilo Lambruschini, et al.. (2013). Long-term Follow-up and Outcome of Phenylketonuria Patients on Sapropterin: A Retrospective Study. PEDIATRICS. 131(6). e1881–e1888. 61 indexed citations

17.

Gataullina, Svetlana, Pascale de Lonlay, Georges Dellatolas, et al.. (2012). Topography of brain damage in metabolic hypoglycaemia is determined by age at which hypoglycaemia occurred. Developmental Medicine & Child Neurology. 55(2). 162–166. 27 indexed citations

18.

Damaj, Léna, Bertrand Bruneau, M.L. Moutard, et al.. (2010). Pediatric outcome of children with the prenatal diagnosis of isolated septal agenesis. Prenatal Diagnosis. 30(12-13). 1143–1150. 26 indexed citations

19.

Damaj, Léna, Marc Le Lorc’h, Virginie Verkarre, et al.. (2008). Chromosome 11p15 Paternal Isodisomy in Focal Forms of Neonatal Hyperinsulinism. The Journal of Clinical Endocrinology & Metabolism. 93(12). 4941–4947. 59 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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