Véronique Tardy

1.7k total citations
34 papers, 1.1k citations indexed

About

Véronique Tardy is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Véronique Tardy has authored 34 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 23 papers in Endocrinology, Diabetes and Metabolism and 14 papers in Genetics. Recurrent topics in Véronique Tardy's work include Sexual Differentiation and Disorders (30 papers), Hormonal and reproductive studies (17 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers). Véronique Tardy is often cited by papers focused on Sexual Differentiation and Disorders (30 papers), Hormonal and reproductive studies (17 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers). Véronique Tardy collaborates with scholars based in France, Germany and Canada. Véronique Tardy's co-authors include Yves Morel, Raja Brauner, Christine Trivin, Anne Bachelot, L Billaud, Étienne Mornet, Philippe Touraine, Christine Bellanné‐Chantelot, Jean‐Louis Golmard and Marie-Béatrice Galand-Portier and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Endocrinology and Clinical Endocrinology.

In The Last Decade

Véronique Tardy

33 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Véronique Tardy France	17	975	776	421	208	168	34	1.1k
Guiomar Madureira Brazil	15	573 0.6×	432 0.6×	230 0.5×	138 0.7×	136 0.8×	27	677
F Lorenzen Germany	12	791 0.8×	721 0.9×	179 0.4×	231 1.1×	106 0.6×	17	1.1k
Lilia Baldazzi Italy	15	546 0.6×	393 0.5×	280 0.7×	102 0.5×	99 0.6×	28	669
Maria Szarras‐Czapnik Poland	15	538 0.6×	237 0.3×	331 0.8×	37 0.2×	125 0.7×	35	722
D. Levy United States	5	501 0.5×	472 0.6×	132 0.3×	123 0.6×	76 0.5×	7	738
Jérôme Dulon France	14	385 0.4×	271 0.3×	214 0.5×	71 0.3×	38 0.2×	28	737
Maria D. Urban United States	12	382 0.4×	296 0.4×	124 0.3×	68 0.3×	53 0.3×	25	503
Rafael Loch Batista Brazil	13	461 0.5×	310 0.4×	252 0.6×	14 0.1×	164 1.0×	44	668
María Sonia Baquedano Argentina	11	244 0.3×	200 0.3×	224 0.5×	12 0.1×	42 0.3×	19	462
Mark Leshin United States	14	386 0.4×	265 0.3×	191 0.5×	8 0.0×	137 0.8×	19	617

Countries citing papers authored by Véronique Tardy

Since Specialization

Citations

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

Fields of papers citing papers by Véronique Tardy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Véronique Tardy

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

All Works

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20 of 20 papers shown

Garabédian, Charles, Jeanne Sibiude, Olivia Anselem, et al.. (2024). Fetal death: Expert consensus of the French College of Obstetricians and Gynecologists. International Journal of Gynecology & Obstetrics. 168(3). 999–1008. 1 indexed citations

Garabédian, Charles, Jeanne Sibiude, Olivia Anselem, et al.. (2024). Mort fœtale : consensus formalisé d’experts du Collège national des gynécologues et obstétriciens français. Gynécologie Obstétrique Fertilité & Sénologie . 52(10). 549–611. 1 indexed citations

Tardy, Véronique, Neerja Gupta, Vandana Jain, et al.. (2017). Prenatal diagnosis of steroid 21-hydroxylase-deficient congenital adrenal hyperplasia. The Indian Journal of Medical Research. 145(2). 194–202. 9 indexed citations

Morel, Yves, et al.. (2016). Evolution of steroids during pregnancy: Maternal, placental and fetal synthesis. Annales d Endocrinologie. 77(2). 82–89. 83 indexed citations

Pierre, P., F Despert, François Tranquart, et al.. (2012). Adrenal rest tissue in gonads of patients with classical congenital adrenal hyperplasia: Multicenter study of 45 French male patients. Annales d Endocrinologie. 73(6). 515–522. 17 indexed citations

Bidet, Maud, Christine Bellanné‐Chantelot, Marie-Béatrice Galand-Portier, et al.. (2010). Fertility in Women with Nonclassical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency. The Journal of Clinical Endocrinology & Metabolism. 95(3). 1182–1190. 129 indexed citations

Young, Jacques, Véronique Tardy, Aude Brac de la Perrière, Anne Bachelot, & Yves Morel. (2010). Detection and management of late-onset 21-hydroxylase deficiency in women with hyperandrogenism. Annales d Endocrinologie. 71(1). 14–18. 15 indexed citations

Paris, Françoise, et al.. (2010). Premature pubarche in Mediterranean girls: high prevalence of heterozygous CYP21 mutation carriers. Gynecological Endocrinology. 26(5). 319–324. 17 indexed citations

Skordis, Nicos, Andreas Kyriakou, Véronique Tardy, et al.. (2010). Molecular Defects of the <i>CYP21A2</i> Gene in Greek-Cypriot Patients with Congenital Adrenal Hyperplasia. Hormone Research in Paediatrics. 75(3). 180–186. 22 indexed citations

10.

Tardy, Véronique, Rita Menassa, V. Sulmont, et al.. (2010). Phenotype-Genotype Correlations of 13 Rare CYP21A2 Mutations Detected in 46 Patients Affected with 21-Hydroxylase Deficiency and in One Carrier. The Journal of Clinical Endocrinology & Metabolism. 95(3). 1288–1300. 52 indexed citations

11.

Bidet, Maud, Christine Bellanné‐Chantelot, Marie-Béatrice Galand-Portier, et al.. (2009). Clinical and Molecular Characterization of a Cohort of 161 Unrelated Women with Nonclassical Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency and 330 Family Members. The Journal of Clinical Endocrinology & Metabolism. 94(5). 1570–1578. 140 indexed citations

12.

Cavarzere, Paolo, Dinane Samara‐Boustani, Isabelle Flechtner, et al.. (2009). Transient hyper-17-hydroxyprogesteronemia: a clinical subgroup of patients diagnosed at neonatal screening for congenital adrenal hyperplasia. European Journal of Endocrinology. 161(2). 285–292. 29 indexed citations

13.

Chevalier, Nicolas, A Chevallier, Karl‐Heinz Wagner, et al.. (2009). Adrenocortical incidentaloma with uncertain prognosis associated with an inadequately treated congenital adrenal hyperplasia. Annales d Endocrinologie. 71(1). 56–59. 4 indexed citations

14.

Tardy, Véronique, et al.. (2008). CYP21A2 gene mutation analysis in Moroccan patients with classic form of 21-hydroxylase deficiency: high regional prevalence of p.Q318X mutation and identification of a novel p.L353R mutation. Clinical Chemistry and Laboratory Medicine (CCLM). 46(12). 1707–13. 13 indexed citations

15.

Menassa, Rita, et al.. (2008). p.H62L, a Rare Mutation of the CYP21 Gene Identified in Two Forms of 21-Hydroxylase Deficiency. The Journal of Clinical Endocrinology & Metabolism. 93(5). 1901–1908. 29 indexed citations

16.

Forest, Maguelone G., Véronique Tardy, Marc Nicolino, M David, & Yves Morel. (2005). 21-hydroxylase deficiency: an exemplary model of the contribution of molecular biology in the understanding and management of the disease. Annales d Endocrinologie. 66(3). 225–232. 21 indexed citations

17.

Tardy, Véronique & Yves Morel. (2004). Conseil génétique et conduite à tenir avant, pendant et après la grossesse en cas de bloc surrénalien en 21-hydroxylase. 6(5). 281–286. 2 indexed citations

18.

Kharrat, Maher, Véronique Tardy, Ridha Mrad, et al.. (2004). Molecular Genetic Analysis of Tunisian Patients with a Classic Form of 21-Hydroxylase Deficiency: Identification of Four Novel Mutations and High Prevalence of Q318X Mutation. The Journal of Clinical Endocrinology & Metabolism. 89(1). 368–374. 74 indexed citations

19.

Pinto, Graziella, Véronique Tardy, Christine Trivin, et al.. (2003). Follow-Up of 68 Children with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Relevance of Genotype for Management. The Journal of Clinical Endocrinology & Metabolism. 88(6). 2624–2633. 86 indexed citations

20.

Delague, Valérie, Eliane Khallouf, Véronique Tardy, et al.. (2000). Mutational Analysis in Lebanese Patients with Congenital Adrenal Hyperplasia due to a Deficit in 21-Hydroxylase. Hormone Research in Paediatrics. 53(2). 77–82. 11 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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