Nadia Coudray

590 total citations
15 papers, 413 citations indexed

About

Nadia Coudray is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Nadia Coudray has authored 15 papers receiving a total of 413 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Nadia Coudray's work include Genetic Syndromes and Imprinting (5 papers), Vitamin D Research Studies (4 papers) and Epigenetics and DNA Methylation (4 papers). Nadia Coudray is often cited by papers focused on Genetic Syndromes and Imprinting (5 papers), Vitamin D Research Studies (4 papers) and Epigenetics and DNA Methylation (4 papers). Nadia Coudray collaborates with scholars based in France, Canada and United States. Nadia Coudray's co-authors include Nicolas Richard, Marie‐Laure Kottler, Arnaud Molin, Hervé Mittre, Yves Lecarpentier, D. S. Chemla, Harald Jüppner, Nicolas Gruchy, P. Cathébras and Glenville Jones and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, European Heart Journal and Journal of Pharmacology and Experimental Therapeutics.

In The Last Decade

Nadia Coudray

15 papers receiving 402 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nadia Coudray France	10	168	156	147	67	61	15	413
Kenjiro Honda Japan	11	98 0.6×	99 0.6×	79 0.5×	73 1.1×	257 4.2×	28	510
Linda Xu United States	5	87 0.5×	207 1.3×	49 0.3×	12 0.2×	222 3.6×	10	422
Raiz Ahmad Misgar India	12	54 0.3×	116 0.7×	28 0.2×	24 0.4×	68 1.1×	35	427
María Luisa González‐Casaus Spain	11	64 0.4×	49 0.3×	200 1.4×	41 0.6×	241 4.0×	36	474
Ronen Levi Israel	8	119 0.7×	156 1.0×	111 0.8×	13 0.2×	281 4.6×	13	439
E Aganna United Kingdom	6	125 0.7×	124 0.8×	199 1.4×	5 0.1×	28 0.5×	7	446
Bülend Yüksel United Kingdom	6	84 0.5×	77 0.5×	28 0.2×	18 0.3×	132 2.2×	7	433
Peter Jackuliak Slovakia	10	52 0.3×	131 0.8×	80 0.5×	7 0.1×	42 0.7×	53	448
Anna Kepley United States	12	33 0.2×	56 0.4×	130 0.9×	9 0.1×	197 3.2×	17	463
Dominika Januś Poland	10	73 0.4×	150 1.0×	75 0.5×	16 0.2×	72 1.2×	50	413

Countries citing papers authored by Nadia Coudray

Since Specialization

Citations

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

Fields of papers citing papers by Nadia Coudray

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nadia Coudray

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

All Works

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15 of 15 papers shown

Molin, Arnaud, Sandrine Lemoine, Martin Kaufmann, et al.. (2021). Overlapping Phenotypes Associated With CYP24A1, SLC34A1, and SLC34A3 Mutations: A Cohort Study of Patients With Hypersensitivity to Vitamin D. Frontiers in Endocrinology. 12. 736240–736240. 15 indexed citations

Colson, Cindy, Matthieu Décamp, Nicolas Gruchy, et al.. (2019). High frequency of paternal iso or heterodisomy at chromosome 20 associated with sporadic pseudohypoparathyroidism 1B. Bone. 123. 145–152. 18 indexed citations

Molin, Arnaud, Cindy Colson, Nadia Coudray, et al.. (2019). Maternal Transmission Ratio Distortion of GNAS Loss-of-Function Mutations. Journal of Bone and Mineral Research. 35(5). 913–919. 9 indexed citations

Molin, Arnaud, Nadia Coudray, Hervé Mittre, et al.. (2018). Molecular characterization of a recurrent 10.9 kb CYP24A1 deletion in Idiopathic Infantile Hypercalcemia. European Journal of Medical Genetics. 62(11). 103577–103577. 5 indexed citations

Molin, Arnaud, Arnaud Wiedemann, Martin Kaufmann, et al.. (2017). Vitamin D–Dependent Rickets Type 1B (25-Hydroxylase Deficiency): A Rare Condition or a Misdiagnosed Condition?. Journal of Bone and Mineral Research. 32(9). 1893–1899. 45 indexed citations

Molin, Arnaud, Martin Kaufmann, J.-C. Souberbielle, et al.. (2015). CYP24A1Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive Trait. The Journal of Clinical Endocrinology & Metabolism. 100(10). E1343–E1352. 97 indexed citations

Richard, Nicolas, et al.. (2013). PaternalGNASMutations Lead to Severe Intrauterine Growth Retardation (IUGR) and Provide Evidence for a Role of XLαs in Fetal Development. The Journal of Clinical Endocrinology & Metabolism. 98(9). E1549–E1556. 56 indexed citations

Richard, Nicolas, Nadia Coudray, Hervé Mittre, et al.. (2012). A New Deletion Ablating NESP55 Causes Loss of Maternal Imprint of A/BGNASand Autosomal Dominant Pseudohypoparathyroidism Type Ib. The Journal of Clinical Endocrinology & Metabolism. 97(5). E863–E867. 71 indexed citations

Richard, Nicolas, et al.. (2009). Épigénétique et pseudohypoparathyroïdies. Pathologie Biologie. 58(5). 367–371. 2 indexed citations

10.

Coudray, Nadia, D. De Zuttère, Gilles Force, et al.. (1995). Left ventricular diastolic function in asymptomatic and symptomatic human immunodeficiency virus carriers: an echocardiographic study. European Heart Journal. 16(1). 61–67. 43 indexed citations

11.

Coudray, Nadia, D. De Zuttère, O Blétry, et al.. (1995). M mode and Doppler echocardiographic assessment of left ventricular diastolic function in primary antiphospholipid syndrome.. Heart. 74(5). 531–535. 19 indexed citations

12.

Coudray, Nadia, D. De Zuttère, O Blétry, et al.. (1993). Altération de la fonction ventriculaire gauche diastolique au cours du syndrome primitif des anticorps antiphospholipides. La Revue de Médecine Interne. 14(10). 938–938. 1 indexed citations

13.

Coudray, Nadia, Jean-Paul Bérégi, Yves Lecarpentier, & D. S. Chemla. (1993). Effects of isoproterenol on myocardial relaxation rate: influence of the level of load. American Journal of Physiology-Heart and Circulatory Physiology. 265(5). H1645–H1653. 21 indexed citations

14.

Bérégi, Jean-Paul, D. F. Escande, Nadia Coudray, et al.. (1992). Positive inotropic effects of RP 62719, a new pure class III antiarrhythmic agent, on guinea pig myocardium.. Journal of Pharmacology and Experimental Therapeutics. 263(3). 1369–1376. 10 indexed citations

15.

Gouge, P. Donzeau, et al.. (1987). [Metastatic tumor of the right atrium responsible for a superior caval syndrome and congestive cardiac insufficiency: surgical excision].. PubMed. 138(8). 672–4. 1 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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