Christian Andrés

11.6k total citations · 1 hit paper
248 papers, 7.4k citations indexed

About

Christian Andrés is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Christian Andrés has authored 248 papers receiving a total of 7.4k indexed citations (citations by other indexed papers that have themselves been cited), including 89 papers in Neurology, 67 papers in Molecular Biology and 45 papers in Genetics. Recurrent topics in Christian Andrés's work include Amyotrophic Lateral Sclerosis Research (81 papers), Neurogenetic and Muscular Disorders Research (43 papers) and Autism Spectrum Disorder Research (23 papers). Christian Andrés is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (81 papers), Neurogenetic and Muscular Disorders Research (43 papers) and Autism Spectrum Disorder Research (23 papers). Christian Andrés collaborates with scholars based in France, Germany and United Kingdom. Christian Andrés's co-authors include Patrick Vourc’h, Hélène Blasco, Philippe Corcia, Patrick Emond, Lydie Nadal‐Desbarats, Catherine Barthélémy, Sylvie Chalon, Frédéric Laumonnier, Frédérique Bonnet‐Brilhault and Gordon Gilbert and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Christian Andrés

233 papers receiving 7.2k citations

Hit Papers

X-Linked Mental Retardati... 2004 2026 2011 2018 2004 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christian Andrés France 48 2.5k 1.6k 1.2k 1.2k 903 248 7.4k
Keun‐Hwa Jung South Korea 56 3.6k 1.4× 3.5k 2.1× 599 0.5× 804 0.7× 961 1.1× 438 12.5k
Serge Goldman Belgium 59 1.2k 0.5× 1.7k 1.0× 435 0.4× 2.7k 2.3× 2.1k 2.3× 387 11.5k
Paola Leone United States 49 4.2k 1.7× 610 0.4× 1.9k 1.6× 571 0.5× 611 0.7× 159 8.5k
Colin Smith United Kingdom 53 3.3k 1.3× 3.7k 2.3× 807 0.7× 449 0.4× 488 0.5× 210 11.0k
Hiroshi Abe Japan 64 6.4k 2.6× 3.1k 1.9× 586 0.5× 740 0.6× 1.1k 1.2× 646 17.5k
Piero Pavone Italy 41 1.6k 0.7× 841 0.5× 1.7k 1.4× 723 0.6× 241 0.3× 466 7.0k
Safa Al‐Sarraj United Kingdom 47 3.2k 1.3× 3.3k 2.0× 599 0.5× 300 0.3× 1.4k 1.6× 145 7.6k
Sanjeev Jain India 35 1.9k 0.8× 827 0.5× 1.7k 1.4× 1.1k 1.0× 202 0.2× 303 8.2k
Nigel Williams United Kingdom 49 2.9k 1.1× 944 0.6× 2.9k 2.5× 1.2k 1.1× 141 0.2× 246 8.3k
Lin Wang China 48 3.8k 1.5× 1.4k 0.8× 391 0.3× 388 0.3× 370 0.4× 427 9.1k

Countries citing papers authored by Christian Andrés

Since Specialization
Citations

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

Fields of papers citing papers by Christian Andrés

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christian Andrés

This figure shows the co-authorship network connecting the top 25 collaborators of Christian Andrés. A scholar is included among the top collaborators of Christian Andrés 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 Christian Andrés. Christian Andrés 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
4.
Richard, Élodie, Sylviane Marouillat, Céline Brulard, et al.. (2024). Post-Translational Variants of Major Proteins in Amyotrophic Lateral Sclerosis Provide New Insights into the Pathophysiology of the Disease. International Journal of Molecular Sciences. 25(16). 8664–8664. 5 indexed citations
5.
Morel, Julie, et al.. (2023). Evaluation of arterial blood gas parameters as prognostic markers in amyotrophic lateral sclerosis. European Journal of Neurology. 30(6). 1611–1618. 3 indexed citations
6.
Vourc’h, Patrick, Isabelle Benz‐de Bretagne, Éric Piver, et al.. (2023). Implication of Central Nervous System Barrier Impairment in Amyotrophic Lateral Sclerosis: Gender-Related Difference in Patients. International Journal of Molecular Sciences. 24(13). 11196–11196. 7 indexed citations
7.
Vallet, Nicolas, Charlotte Veyrat‐Durebex, Louis Bernard, et al.. (2022). Specific Changes of Erythroid Regulators and Hepcidin in Patients Infected by SARS-COV-2. Journal of Investigative Medicine. 70(4). 934–938. 7 indexed citations
8.
Lanznaster, Débora, Clément Bruno, Jérôme Bourgeais, et al.. (2022). Metabolic Profile and Pathological Alterations in the Muscle of Patients with Early-Stage Amyotrophic Lateral Sclerosis. Biomedicines. 10(6). 1307–1307. 11 indexed citations
9.
Lanznaster, Débora, Jean‐Michel Escoffre, Philippe Corcia, et al.. (2022). Taking Advantages of Blood–Brain or Spinal Cord Barrier Alterations or Restoring Them to Optimize Therapy in ALS?. Journal of Personalized Medicine. 12(7). 1071–1071. 10 indexed citations
10.
Lagrue, Emmanuelle, Christian Andrés, Patrick Emond, et al.. (2018). Cerebrospinal fluid metabolomics in West Syndrome: central role of the serine metabolic pathway. Journal of Translational Science. 4(4). 1 indexed citations
11.
Marouillat, Sylviane, Joëlle Malvy, Annick Toutain, et al.. (2015). Mutation screening of the ubiquitin ligase gene RNF135 in French patients with autism. Psychiatric Genetics. 25(6). 263–267. 18 indexed citations
12.
El‐Hage, Wissam, Patrick Vourc’h, Philippe Gaillard, et al.. (2014). The BDNF Val66Met polymorphism is associated with escitalopram response in depressed patients. Psychopharmacology. 232(3). 575–581. 22 indexed citations
13.
Charon, Céline, Audrey Guilmatre, Patrick Vourc’h, et al.. (2013). Xq27 FRAXA Locus is a Strong Candidate for Dyslexia: Evidence from a Genome-Wide Scan in French Families. Behavior Genetics. 43(2). 132–140. 7 indexed citations
14.
Andrés, Christian, Jan Gutermuth, Johannes Ring, et al.. (2012). Lymphangitic carcinomatosis of colon carcinoma: a sign of poor prognosis. Clinical and Experimental Dermatology. 37(8). 937–939. 1 indexed citations
15.
Prut, L., Françoise Saurini, Yann S. Mineur, et al.. (2012). Gabra5-gene haplotype block associated with behavioral properties of the full agonist benzodiazepine chlordiazepoxide. Behavioural Brain Research. 233(2). 474–482. 3 indexed citations
16.
Andrés, Christian, et al.. (2011). Superimposed segmental manifestation of cherry angiomas. European Journal of Dermatology. 21(6). 864–865. 2 indexed citations
17.
Blasco, Hélène, Philippe Corcia, Caroline Moreau, et al.. (2010). Correction:1H-NMR-Based Metabolomic Profiling of CSF in Early Amyotrophic Lateral Sclerosis. PLoS ONE. 5(11). 26 indexed citations
18.
Eberlein, Bernadette, et al.. (2009). UVA-1-phototherapy in the treatment of circumscripted scleroderma - a retrospective and prospective study. mediaTUM (Technical University of Munich). 1 indexed citations
19.
Andrés, Christian. (2005). A propósito de historia clásica y de historia natural en "La Dragontea". Anuario Lope de Vega. 29–40.
20.
Laumonnier, Frédéric, Frédérique Bonnet‐Brilhault, Marie Gomot, et al.. (2004). X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family. The American Journal of Human Genetics. 74(3). 552–557. 553 indexed citations breakdown →

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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