Barto J. Otten - Concepedia

Author

Barto J. Otten

Radboud University Nijmegen

Also Known As

Barto J Otten, Barto J. Otten, Barto Otten

Publications

5.6K

Citations

H-Index

102

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center Leiden University Medical Center Erasmus University Rotterdam Hersenstichting

About

Barto J. Otten is an author at Radboud University Nijmegen specializing in medicine, endocrinology, and adrenal disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	22	1.8K
2	Health Sciences	6	6	328
3	Arts	2	2	169
4	Education	2	2	98
5	Public Health	2	2	389

Barto J. Otten

Publications

5.3K

Citations

H-Index

Page 1

	Year	Citations
Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation Dieter Kotzot, Silke Schmitt, Fabiana Bernasconi, Human Molecular Genetics	1995	302
High Prevalence of Testicular Adrenal Rest Tumors, Impaired Spermatogenesis, and Leydig Cell Failure in Adolescent and Adult Males with Congenital Adrenal Hyperplasia Nike Stikkelbroeck, Barto J. Otten, Arifa Pasic, The Journal of Clinical Endocrinology & Metabolism SpermatogenesisFertilityGynecologySemen AnalysisReproductive Biology	2001	294
Final Height in Girls with Turner Syndrome after Long-Term Growth Hormone Treatment in Three Dosages and Low Dose Estrogens Yvonne K. van Pareren, Sabine M.P.F. de Muinck Keizer‐Schrama, Theo Stijnen, The Journal of Clinical Endocrinology & Metabolism	2003	241
17β-Hydroxysteroid Dehydrogenase-3 Deficiency: Diagnosis, Phenotypic Variability, Population Genetics, and Worldwide Distribution of Ancient and de Novo Mutations1 Annemie L. M. Boehmer, Albert O. Brinkmann, Lodewijk A. Sandkuijl, The Journal of Clinical Endocrinology & Metabolism	1999	177
CYP21 Gene Mutation Analysis in 198 Patients with 21-Hydroxylase Deficiency in The Netherlands: Six Novel Mutations and a Specific Cluster of Four Mutations Nike Stikkelbroeck, Lies H. Hoefsloot, Ilse J. de Wijs, The Journal of Clinical Endocrinology & Metabolism Specific ClusterMendelian DisorderCongenital Adrenal HyperplasiaGenetic DisorderMedicine	2003	170
High Prevalence of Central Adrenal Insufficiency in Patients with Prader-Willi Syndrome Roderick F. A. de Lind van Wijngaarden, Barto J. Otten, Dederieke A. M. Festen, The Journal of Clinical Endocrinology & Metabolism	2008	163
Cosegregation of missense mutations of the luteinizing hormone receptor gene with familial male-limited precocious puberty Hannie Kremer, Edwin C.M. Mariman, Barto J. Otten, Human Molecular Genetics G Protein BindingMissense MutationsDevelopmental BiologyMendelian DisorderGenetic Disorder	1993	163
Normalization of Height in Girls with Turner Syndrome after Long-Term Growth Hormone Treatment: Results of a Randomized Dose-Response Trial<sup>1</sup> Theo Sas, Sabine M.P.F. de Muinck Keizer‐Schrama, Theo Stijnen, The Journal of Clinical Endocrinology & Metabolism	1999	151
Beneficial Effects of Growth Hormone Treatment on Cognition in Children with Prader-Willi Syndrome: A Randomized Controlled Trial and Longitudinal Study Elbrich P. C. Siemensma, Roderick F. A. Tummers-de Lind van Wijngaarden, Dederieke A. M. Festen, The Journal of Clinical Endocrinology & Metabolism	2012	140
Prevalence of testicular adrenal rest tumours in male children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency Hedi L. Claahsen‐van der Grinten, Fred C.G.J. Sweep, Johan G. Blickman, European Journal of Endocrinology	2007	140

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