M. Tauber

9.4k total citations
174 papers, 4.6k citations indexed

About

M. Tauber is a scholar working on Genetics, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, M. Tauber has authored 174 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 107 papers in Genetics, 52 papers in Molecular Biology and 45 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in M. Tauber's work include Genetic Syndromes and Imprinting (84 papers), Genetics and Neurodevelopmental Disorders (40 papers) and Growth Hormone and Insulin-like Growth Factors (37 papers). M. Tauber is often cited by papers focused on Genetic Syndromes and Imprinting (84 papers), Genetics and Neurodevelopmental Disorders (40 papers) and Growth Hormone and Insulin-like Growth Factors (37 papers). M. Tauber collaborates with scholars based in France, United States and Germany. M. Tauber's co-authors include Gwénaëlle Diene, Catherine Molinas, Charlotte Höybye, Béatrice Jouret, P Rochiccioli, Jean‐Pierre Salles, Catherine Pienkowski, Denise Thuilleaux, Pierre Moulin and Cheri Deal and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Molecular and Cellular Biology.

In The Last Decade

M. Tauber

165 papers receiving 4.5k citations

Peers

M. Tauber

GENET

EDM

PPCH

SURGE

Peter C. Hindmarsh United Kingdom

Mohamad Maghnie Italy

Stenvert L. S. Drop Netherlands

Lucia Ghizzoni Italy

Antonino Crinò Italy

Juliane Léger France

R Stanhope United Kingdom

Erica A. Eugster United States

Peter A. Lee United States

Steven D. Chernausek United States

Peter C. Hindmarsh United Kingdom

M. Tauber

1.5k ×0.6

GENET

2.0k ×1.2

3.1k ×2.8

EDM

1.1k ×1.1

PPCH

719 ×1.0

SURGE

Citations per year, relative to M. Tauber M. Tauber (= 1×) peers Peter C. Hindmarsh

Countries citing papers authored by M. Tauber

Since Specialization

Citations

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

Fields of papers citing papers by M. Tauber

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Tauber

This figure shows the co-authorship network connecting the top 25 collaborators of M. Tauber. A scholar is included among the top collaborators of M. Tauber 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 M. Tauber. M. Tauber 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

Noor, Mohd Ismail, et al.. (2024). Management of food socialization for children with Prader-Willi Syndrome: An exploration study in Malaysia. PLoS ONE. 19(8). e0307874–e0307874.

Diene, Gwénaëlle, et al.. (2024). Cardiovascular autonomic dysfunction and sleep abnormalities in children with Prader–Willi syndrome. Clinical Autonomic Research. 35(2). 243–255. 1 indexed citations

Coutant, R., M. Tauber, Y. Brault, et al.. (2023). Treatment burden, adherence, and quality of life in children with daily GH treatment in France. Endocrine Connections. 12(4). 8 indexed citations

Strelnikov, Kuzma, et al.. (2023). Amygdala hyperactivation relates to eating behaviour: a potential indicator of food addiction in Prader–Willi syndrome. Brain Communications. 5(3). fcad138–fcad138. 5 indexed citations

Coupaye, Muriel, Héléna Mosbah, Graziella Pinto, et al.. (2021). Diabetes Mellitus in Prader-Willi Syndrome: Natural History during the Transition from Childhood to Adulthood in a Cohort of 39 Patients. Journal of Clinical Medicine. 10(22). 5310–5310. 8 indexed citations

Bellicha, Alice, Muriel Coupaye, Héléna Mosbah, et al.. (2021). Physical Activity in Patients with Prader-Willi Syndrome—A Systematic Review of Observational and Interventional Studies. Journal of Clinical Medicine. 10(11). 2528–2528. 8 indexed citations

Eddiry, Sanaa, Gwénaëlle Diene, Catherine Molinas, et al.. (2021). SNORD116 and growth hormone therapy impact IGFBP7 in Prader–Willi syndrome. Genetics in Medicine. 23(9). 1664–1672. 12 indexed citations

Mosbah, Héléna, Muriel Coupaye, M. Tauber, et al.. (2021). Effects of the COVID-19 pandemic and lockdown on the mental and physical health of adults with Prader-Willi syndrome. Orphanet Journal of Rare Diseases. 16(1). 202–202. 9 indexed citations

Capri, Yline, Catherine Pienkowski, Benoît Lepage, et al.. (2019). Gonadal Function of Female Patients with Noonan Syndrome. 92. 1 indexed citations

10.

Consoli, Angèle, Marie Raffin, Denise Thuilleaux, et al.. (2019). Effect of topiramate on eating behaviours in Prader-Willi syndrome: TOPRADER double-blind randomised placebo-controlled study. Translational Psychiatry. 9(1). 274–274. 34 indexed citations

11.

Allas, Soraya, Assumpta Caixàs, Christine Poitou, et al.. (2018). AZP-531, an unacylated ghrelin analog, improves food-related behavior in patients with Prader-Willi syndrome: A randomized placebo-controlled trial. PLoS ONE. 13(1). e0190849–e0190849. 69 indexed citations

12.

Burnett, Lisa C., Charles A. LeDuc, Carlos R. Sulsona, et al.. (2016). Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS. Stem Cell Research. 17(3). 526–530. 22 indexed citations

13.

Cadoudal, Thomas, Gwénaëlle Diene, Coralie Sengenès, et al.. (2014). Impairment of Adipose Tissue in Prader-Willi Syndrome Rescued by GH Treatment. 82. 1 indexed citations

14.

Creemers, John W.M., Hélène Choquet, Pieter Stijnen, et al.. (2011). Heterozygous Mutations Causing Partial Prohormone Convertase 1 Deficiency Contribute to Human Obesity. Diabetes. 61(2). 383–390. 82 indexed citations

15.

Pienkowski, Catherine, et al.. (2011). Syndrome de Klinefelter et syndrome de Turner : pour une meilleure prise en charge. Gynécologie Obstétrique & Fertilité. 39(9). 521–524. 1 indexed citations

16.

Ghoussaini, Maya, Fanny Stutzmann, Cyril Couturier, et al.. (2010). Analysis of the SIM1 Contribution to Polygenic Obesity in the French Population. Obesity. 18(8). 1670–1675. 14 indexed citations

17.

Gennero, Isabelle, Thomas Édouard, Mona M. Rashad, et al.. (2007). Identification of a Novel Mutation in the Human Growth Hormone Receptor Gene (GHR) in a Patient with Laron Syndrome. Journal of Pediatric Endocrinology and Metabolism. 20(7). 825–31. 9 indexed citations

18.

Tauber, M.. (2002). Prader-Willi syndrome: Update on treatment by growth hormone. Anales de Pediatría. 56. 12–16.

19.

Tauber, M., Catherine Pienkowski, & P Rochiccioli. (1998). Signes cliniques des syndromes turnériens. MTP. Médecine thérapeutique pédiatrie. 1(4). 315–318.

20.

Tauber, M., Pierre Moulin, Catherine Pienkowski, Béatrice Jouret, & P Rochiccioli. (1997). Growth Hormone (GH) Retesting and Auxological Data in 131 GH-Deficient Patients after Completion of Treatment. The Journal of Clinical Endocrinology & Metabolism. 82(2). 352–356. 149 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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