M. Tauber

4.5k total citations
32 papers, 1.6k citations indexed

About

M. Tauber is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, M. Tauber has authored 32 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Genetics and 5 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in M. Tauber's work include Genetic Syndromes and Imprinting (7 papers), Child Nutrition and Feeding Issues (4 papers) and Sexual Differentiation and Disorders (4 papers). M. Tauber is often cited by papers focused on Genetic Syndromes and Imprinting (7 papers), Child Nutrition and Feeding Issues (4 papers) and Sexual Differentiation and Disorders (4 papers). M. Tauber collaborates with scholars based in France, United Kingdom and United States. M. Tauber's co-authors include Anita C. S. Hokken‐Koelega, Anthony P. Goldstone, B. P. Hauffa, Anthony Holland, Pierre Bougnères, Christine Dos Santos, Vincent Goffin, Cécile Teinturier, Laurent Essioux and John P. Monson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Journal of Neuroscience.

In The Last Decade

M. Tauber

31 papers receiving 1.6k citations

Peers

M. Tauber

GENET

EDM

PPCH

PHYSI

Carl‐Joachim Partsch Germany

M Vanderschueren‐Lodeweyckx Belgium

Inge François Belgium

Jesús Pozo Spain

H Wollmann Germany

Sonir Roberto Rauber Antonini Brazil

Heike Jung Germany

Gabriel Ángel Martos‐Moreno Spain

Melissa Smart United Kingdom

Urs Eiholzer Switzerland

Carl‐Joachim Partsch Germany

M. Tauber

637 ×0.8

GENET

1.1k ×1.6

1.0k ×2.0

EDM

231 ×0.7

PPCH

92 ×0.6

PHYSI

Citations per year, relative to M. Tauber M. Tauber (= 1×) peers Carl‐Joachim Partsch

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

Siegfried, Aurore, Claude Cancès, Marie Denuelle, et al.. (2017). Noonan syndrome, PTPN11 mutations, and brain tumors. A clinical report and review of the literature. American Journal of Medical Genetics Part A. 173(4). 1061–1065. 23 indexed citations

Dulac, Yves, M. Tauber, & Béatrice Jouret. (2012). Aortic or Carotid Intima-Media Thickness to Evaluate Children Born Small for Gestational Age?. Hormone Research in Paediatrics. 77(5). 340–340. 3 indexed citations

Barat, Pascal, et al.. (2012). Associations of glucocorticoid receptor and corticosteroid-binding globulin gene polymorphisms on fat mass and fat mass distribution in prepubertal obese children. Journal of Physiology and Biochemistry. 68(4). 645–650. 7 indexed citations

Copet, P., Virginie Laurier, Virginie Ehlinger, et al.. (2010). Cognitive profile in a large french cohort of adults with Prader–Willi syndrome: differences between genotypes. Journal of Intellectual Disability Research. 54(3). 204–215. 53 indexed citations

Paineau, Damien, François Beaufils, A Boulier, et al.. (2010). The cumulative effect of small dietary changes may significantly improve nutritional intakes in free-living children and adults. European Journal of Clinical Nutrition. 64(8). 782–791. 17 indexed citations

Zanella, Sébastien, M. Tauber, & Françoise Muscatelli. (2009). Breathing deficits of the Prader-Willi syndrome. Respiratory Physiology & Neurobiology. 168(1-2). 119–124. 24 indexed citations

Dulac, Yves, Catherine Pienkowski, Sylvia Abadir, M. Tauber, & Philippe Acar. (2008). Cardiovascular abnormalities in Turner's syndrome: What prevention?. Archives of cardiovascular diseases. 101(7-8). 485–490. 36 indexed citations

Zanella, Sébastien, Françoise Watrin, Saïda Mebarek, et al.. (2008). Necdin Plays a Role in the Serotonergic Modulation of the Mouse Respiratory Network: Implication for Prader-Willi Syndrome. Journal of Neuroscience. 28(7). 1745–1755. 67 indexed citations

Goldstone, Anthony P., Anthony Holland, B. P. Hauffa, Anita C. S. Hokken‐Koelega, & M. Tauber. (2008). Recommendations for the Diagnosis and Management of Prader-Willi Syndrome. The Journal of Clinical Endocrinology & Metabolism. 93(11). 4183–4197. 348 indexed citations

10.

Beaufils, François, A Boulier, J Chwalow, et al.. (2008). Family Dietary Coaching to Improve Nutritional Intakes and Body Weight Control. Archives of Pediatrics and Adolescent Medicine. 162(1). 34–34. 68 indexed citations

11.

Édouard, Thomas, Alexandra Montagner, Marie Dance, et al.. (2007). How do Shp2 mutations that oppositely influence its biochemical activity result in syndromes with overlapping symptoms?. Cellular and Molecular Life Sciences. 64(13). 1585–1590. 32 indexed citations

12.

Pienkowski, Catherine, et al.. (2007). Les troubles de la fertilité dans les affections endocriniennes. Archives de Pédiatrie. 14(6). 715–717.

13.

Bell, Christopher G., Stephen Eyre, Enrico Petretto, et al.. (2006). No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseases. European Journal of Human Genetics. 15(3). 320–327. 9 indexed citations

14.

Soriano-Guillén, Leandro, Joël Coste, Emmanuel Écosse, et al.. (2005). Adult Height and Pubertal Growth in Turner Syndrome after Treatment with Recombinant Growth Hormone. The Journal of Clinical Endocrinology & Metabolism. 90(9). 5197–5204. 100 indexed citations

15.

Ghoussaini, Maya, Stephen Eyre, Stéphane Lobbens, et al.. (2005). Implication of the Pro12Ala polymorphism of the PPAR-gamma 2gene in type 2 diabetes and obesity in the French population. BMC Medical Genetics. 6(1). 11–11. 91 indexed citations

16.

Clayton, Peter, Ross C. Cuneo, Anders Juul, et al.. (2005). Consensus statement on the management of the GH-treated adolescent in the transition to adult care. European Journal of Endocrinology. 152(2). 165–170. 179 indexed citations

17.

Santos, Christine Dos, Laurent Essioux, Cécile Teinturier, et al.. (2004). A common polymorphism of the growth hormone receptor is associated with increased responsiveness to growth hormone. Nature Genetics. 36(7). 720–724. 247 indexed citations

18.

Gennero, Isabelle, P. Moulin, Thomas Édouard, et al.. (2004). Métabolisme minéral osseux: données récentes et perspectives relatives à l’ostéogenèse. Archives de Pédiatrie. 11(12). 1473–1483. 5 indexed citations

19.

Tauber, M.. (2002). Âge normal de la puberté et explorations endocriniennes. Archives de Pédiatrie. 9. 229–230. 1 indexed citations

20.

Rochiccioli, P, et al.. (1992). School Achievement in Children with Hypothyroidism Detected at Birth and Search for Predictive Factors. Hormone Research. 38(5-6). 236–240. 25 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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