Anne Lienhardt-Roussie

2.0k total citations
17 papers, 569 citations indexed

About

Anne Lienhardt-Roussie is a scholar working on Molecular Biology, Nephrology and Genetics. According to data from OpenAlex, Anne Lienhardt-Roussie has authored 17 papers receiving a total of 569 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Nephrology and 5 papers in Genetics. Recurrent topics in Anne Lienhardt-Roussie's work include Parathyroid Disorders and Treatments (5 papers), Sexual Differentiation and Disorders (4 papers) and Erythrocyte Function and Pathophysiology (3 papers). Anne Lienhardt-Roussie is often cited by papers focused on Parathyroid Disorders and Treatments (5 papers), Sexual Differentiation and Disorders (4 papers) and Erythrocyte Function and Pathophysiology (3 papers). Anne Lienhardt-Roussie collaborates with scholars based in France, Poland and Italy. Anne Lienhardt-Roussie's co-authors include Marc Delpech, Jacques Young, Catherine Dodé, Graeme Morgan, Arnaud Murat, Jean-Pierre Hardelin, Sławomir Wołczyński, Jacqueline Levilliers, Marie-Laure Kottler and James Lespinasse and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, PLoS Genetics and European Journal of Endocrinology.

In The Last Decade

Anne Lienhardt-Roussie

15 papers receiving 560 citations

Peers

Anne Lienhardt-Roussie

GENET

EDM

PPCH

Tokuo Mukai Japan

L Duprez Belgium

Dominique Langlois France

R. M. Gardner United States

Rachel E. Stamateris United States

Gökhan Özışık Türkiye

Nami Masumoto Japan

Mitsumori Kawaminami Japan

Nathalie Courtois‐Coutry France

Amiya Sinha Hikim United States

Tokuo Mukai Japan

Anne Lienhardt-Roussie

570 ×1.8

502 ×1.9

GENET

119 ×0.5

243 ×1.9

EDM

26 ×0.5

PPCH

Citations per year, relative to Anne Lienhardt-Roussie Anne Lienhardt-Roussie (= 1×) peers Tokuo Mukai

Countries citing papers authored by Anne Lienhardt-Roussie

Since Specialization

Citations

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

Fields of papers citing papers by Anne Lienhardt-Roussie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anne Lienhardt-Roussie. 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 Anne Lienhardt-Roussie. The network helps show where Anne Lienhardt-Roussie may publish in the future.

Co-authorship network of co-authors of Anne Lienhardt-Roussie

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

All Works

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17 of 17 papers shown

Bacchetta, Justine, Anya Rothenbühler, Anne Lienhardt-Roussie, et al.. (2020). Demographic Characteristics, Risk Factors, and Presenting Features of Children with Symptomatic Nutritional Rickets: A French Series. Hormone Research in Paediatrics. 93(5). 304–312. 7 indexed citations

Mallet, Delphine, Alexandre Janin, Rita Menassa, et al.. (2018). Aberrant Splicing Is the Pathogenicity Mechanism of the p.Glu314Lys Variant in CYP11A1 Gene. Frontiers in Endocrinology. 9. 491–491. 15 indexed citations

Habib, Walid Abi, Frédéric Brioude, Thomas Édouard, et al.. (2017). Genetic disruption of the oncogenic HMGA2–PLAG1–IGF2 pathway causes fetal growth restriction. Genetics in Medicine. 20(2). 250–258. 98 indexed citations

Erdeve, Şenay Savaş, Corinne Magdelaine, Anne Lienhardt-Roussie, et al.. (2016). Treatment Experience and Long-Term Follow-Up Data in Two Severe Neonatal Hyperparathyroidism Cases. 86. 2 indexed citations

Parween, Shaheena, Florence Roucher‐Boulez, Christa E. Flück, et al.. (2016). P450 Oxidoreductase Deficiency: Loss of Activity Caused by Protein Instability From a Novel L374H Mutation. The Journal of Clinical Endocrinology & Metabolism. 101(12). 4789–4798. 18 indexed citations

Erdeve, Şenay Savaş, Corinne Magdelaine, Anne Lienhardt-Roussie, et al.. (2016). Treatment experience and long-term follow-up data in two severe neonatal hyperparathyroidism cases. Journal of Pediatric Endocrinology and Metabolism. 29(9). 1103–10. 18 indexed citations

Gorduza, Daniela, Claire-Lise Gay, Pierre Chatelain, et al.. (2014). Late prenatal dexamethasone and phenotype variations in 46,XX CAH: Concerns about current protocols and benefits for surgical procedures. Journal of Pediatric Urology. 10(5). 941–947. 12 indexed citations

Kahveci̇oğlu, Dilek, Begüm Atasay, Merih Berberoğlu, et al.. (2014). A novel mutation in the calcium sensing receptor gene in a neonate with severe hyperparathyroidism. .. PubMed. 25(3). 331–5. 4 indexed citations

Laffargue, Fanny, Anne Lienhardt-Roussie, Didier Lacombe, & Marie‐Ange Delrue. (2013). Signes cliniques évocateurs d’un syndrome de Marfan chez l’enfant de moins de 10 ans. Archives de Pédiatrie. 20(11). 1193–1200. 7 indexed citations

10.

Lia-Baldini, Anne-Sophie, Corinne Magdelaine, Jean‐Pierre Salles, et al.. (2012). Two novel mutations of the calcium-sensing receptor gene affecting the same amino acid position lead to opposite phenotypes and reveal the importance of p.N802 on receptor activity. European Journal of Endocrinology. 168(2). K27–K34. 13 indexed citations

11.

Lienhardt-Roussie, Anne. (2012). Hypocalcémie et hypophosphatémie en période néonatale. Archives de Pédiatrie. 19(6). H178–H179.

12.

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

13.

Sainte‐Laudy, J., et al.. (2009). Évaluation de la cytomètrie en flux par rapport aux tests de provocation en simple insu pour le diagnostic de l’allergie alimentaire chez l’enfant. Revue française d'allergologie. 49(6). 454–461. 2 indexed citations

14.

Lienhardt-Roussie, Anne, et al.. (2008). Traitement des hypocalcémies chroniques de l’enfant. Archives de Pédiatrie. 15(5). 650–652.

15.

Ranger‐Rogez, Sylvie, et al.. (2008). O-05 Méningites et encéphalites à entérovirus diagnostiquées au CHU de Limoges : 2005-2006. Médecine et Maladies Infectieuses. 38. S174–S174. 1 indexed citations

16.

Dodé, Catherine, Luís Teixeira, Jacqueline Levilliers, et al.. (2006). Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2. PLoS Genetics. 2(10). e175–e175. 315 indexed citations

17.

Dodé, Catherine, Luís Augusto Teixeira, Jacqueline Levilliers, et al.. (2005). Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2. PLoS Genetics. preprint(2006). e175–e175. 5 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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