Chantal Gendrot

520 total citations
15 papers, 301 citations indexed

About

Chantal Gendrot is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Chantal Gendrot has authored 15 papers receiving a total of 301 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Chantal Gendrot's work include Genetics and Neurodevelopmental Disorders (7 papers), RNA modifications and cancer (3 papers) and Drug Transport and Resistance Mechanisms (3 papers). Chantal Gendrot is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), RNA modifications and cancer (3 papers) and Drug Transport and Resistance Mechanisms (3 papers). Chantal Gendrot collaborates with scholars based in France, Germany and Poland. Chantal Gendrot's co-authors include Christian Andrés, Yannick Bacq, Martine Raynaud, Claude Moraine, Annick Toutain, Sylvain Briault, Nathalie Ronce, Patrick Vourc’h, Hélène Blasco and Marie‐Pierre Moizard and has published in prestigious journals such as BioMed Research International, Journal of the Neurological Sciences and Journal of Medical Genetics.

In The Last Decade

Chantal Gendrot

15 papers receiving 294 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chantal Gendrot France	11	91	82	78	68	52	15	301
I Suzuki Japan	10	69 0.8×	127 1.5×	59 0.8×	58 0.9×	35 0.7×	24	340
Ryogo Shobatake Japan	12	50 0.5×	54 0.7×	35 0.4×	62 0.9×	13 0.3×	24	333
Zifang Yin China	12	31 0.3×	70 0.9×	126 1.6×	134 2.0×	26 0.5×	19	456
Jaesung P. Choi Australia	11	30 0.3×	123 1.5×	25 0.3×	21 0.3×	84 1.6×	19	323
J. Juyn Netherlands	4	143 1.6×	88 1.1×	53 0.7×	55 0.8×	9 0.2×	4	296
Si Wu China	9	28 0.3×	126 1.5×	30 0.4×	12 0.2×	54 1.0×	19	344
Shu Song China	11	32 0.4×	122 1.5×	66 0.8×	22 0.3×	10 0.2×	22	288
Aki Murakami Japan	11	36 0.4×	98 1.2×	47 0.6×	16 0.2×	24 0.5×	23	491
Jessica Connor United States	9	59 0.6×	80 1.0×	68 0.9×	34 0.5×	4 0.1×	13	293
Mel Maranian United Kingdom	8	111 1.2×	107 1.3×	46 0.6×	9 0.1×	22 0.4×	12	389

Countries citing papers authored by Chantal Gendrot

Since Specialization

Citations

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

Fields of papers citing papers by Chantal Gendrot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chantal Gendrot

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

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

Barbet, Christelle, et al.. (2017). Stéatose hépatique aiguë gravidique et bêta-oxydation mitochondriale des acides gras : conséquences pour l’enfant. Archives de Pédiatrie. 24(8). 777–782. 3 indexed citations

Auvet, Adrien, Fabien Espitalier, Leslie Grammatico‐Guillon, et al.. (2016). Preanalytical conditions of point-of-care testing in the intensive care unit are decisive for analysis reliability. Annals of Intensive Care. 6(1). 57–57. 20 indexed citations

Bacq, Yannick, et al.. (2016). Ursodeoxycholic acid therapy in intrahepatic cholestasis of pregnancy: Results in real-world conditions and factors predictive of response to treatment. Digestive and Liver Disease. 49(1). 63–69. 32 indexed citations

Veyrat‐Durebex, Charlotte, Philippe Corcia, Cindy Mallet, et al.. (2014). Iron Metabolism Disturbance in a French Cohort of ALS Patients. BioMed Research International. 2014. 1–6. 54 indexed citations

Praline, Julien, Hélène Blasco, Patrick Vourc’h, et al.. (2012). Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis. Journal of the Neurological Sciences. 317(1-2). 58–61. 21 indexed citations

Guellec, Chantal Le, Isabelle Benz‐de Bretagne, A.‐P. Jonville‐Béra, et al.. (2012). A Case of Severe Toxicity During Coadministration of Vincristine and Piperacillin. Journal of Pediatric Hematology/Oncology. 34(8). e341–e343. 4 indexed citations

Bacq, Yannick, et al.. (2007). Stéatose hépatique aiguë gravidique récidivante. Gastroentérologie Clinique et Biologique. 31(12). 1135–1138. 23 indexed citations

Gomot, Marie, Chantal Gendrot, Alain Verloès, et al.. (2003). MECP2 gene mutations in non‐syndromic X‐linked mental retardation: Phenotype–genotype correlation. American Journal of Medical Genetics Part A. 123A(2). 129–139. 30 indexed citations

Gendrot, Chantal, et al.. (2003). A second heterozygous MDR3 nonsense mutation associated with intrahepatic cholestasis of pregnancy: Figure 1. Journal of Medical Genetics. 40(3). e32–e32. 49 indexed citations

10.

Raynaud, Martine, Marie‐Pierre Moizard, Sylvain Briault, et al.. (2000). Systematic analysis of X-inactivation in 19 XLMR families: extremely skewed profiles in carriers in three families. European Journal of Human Genetics. 8(4). 253–258. 17 indexed citations

11.

Gendrot, Chantal, Nathalie Ronce, Martine Raynaud, et al.. (1999). X‐linked nonspecific mental retardation (MRX16) mapping to distal Xq28: Linkage study and neuropsychological data in a large family. American Journal of Medical Genetics. 83(5). 411–418. 2 indexed citations

12.

Ronce, Nathalie, Martine Raynaud, Annick Toutain, et al.. (1999). Evidence for a new X-linked mental retardation gene in Xp21-Xp22: Clinical and molecular data in one family. American Journal of Medical Genetics. 83(2). 132–137. 10 indexed citations

13.

Gendrot, Chantal, Nathalie Ronce, Martine Raynaud, et al.. (1999). X-linked nonspecific mental retardation (MRX16) mapping to distal Xq28: Linkage study and neuropsychological data in a large family. American Journal of Medical Genetics. 83(5). 411–418. 10 indexed citations

14.

Raynaud, Martine, Chantal Gendrot, Anne Moncla, et al.. (1996). X-linked mental retardation with neonatal hypotonia in a French family (MRX15): Gene assignment to Xp11.22-Xp21.1. American Journal of Medical Genetics. 64(1). 97–106. 12 indexed citations

15.

Gendrot, Chantal, Nathalie Ronce, Annick Toutain, et al.. (1994). X‐linked mental retardation exhibiting linkage to DXS255 and PGKP1: a new MRX family (MRX14) with localization in the pericentromeric region. Clinical Genetics. 45(3). 145–153. 14 indexed citations

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