Oostdijk, Wilma
Leiden University Medical Center
10 papers on CoChatORCID 0000-0003-0180-2470
Most cited papers
- Verified
Pubertal development in The Netherlands 1965–1997
Mul, D., Fredriks, A. M., van Buuren, S., Oostdijk, W., Verloove-Vanhorick, S. P., & Wit, J. M. (2001) · Pediatric Research
Hypothalamic control of reproductive hormonesHuman Health and Disease
Cited by 313
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Genotype Versus Phenotype in Families with Androgen Insensitivity Syndrome
Boehmer, A. L. M., Brüggenwirth, H., van Assendelft, C., Otten, B. J., Verleun-Mooijman, M. C. T., Niermeijer, M. F., Brunner, H. G., Rouwé, C. W., Waelkens, J. J., Oostdijk, W., et al. (2001) · The Journal of Clinical Endocrinology & Metabolism
Sexual Differentiation and DisordersGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Cited by 290
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Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement
Sun, Y., Bak, B., Schoenmakers, N., van Trotsenburg, A. S. P., Oostdijk, W., Voshol, P., Cambridge, E., White, J. K., le Tissier, P., Gharavy, S. N. M., et al. (2012) · Nature Genetics
Thyroid Disorders and TreatmentsHypothalamic control of reproductive hormones
Cited by 217
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Mutations in TBL1X Are Associated With Central Hypothyroidism
Heinen, C. A., Losekoot, M., Sun, Y., Watson, P. J., Fairall, L., Joustra, S. D., Zwaveling-Soonawala, N., Oostdijk, W., van den Akker, E. L. T., Alders, M., et al. (2016) · The Journal of Clinical Endocrinology & Metabolism
Thyroid Disorders and TreatmentsGenomics and Rare Diseases
Cited by 92
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IGSF1 Deficiency: Lessons From an Extensive Case Series and Recommendations for Clinical Management
Joustra, S. D., Heinen, C. A., Schoenmakers, N., Bonomi, M., Ballieux, B. E. P. B., Turgeon, M.-O., Bernard, D. J., Fliers, E., van Trotsenburg, A. S. P., Losekoot, M., et al. (2016) · The Journal of Clinical Endocrinology & Metabolism
Immunodeficiency and Autoimmune DisordersThyroid Disorders and Treatments
Cited by 91
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PAPSS2 deficiency causes androgen excess via impaired DHEA sulfation–in vitro and in vivo studies in a family harboring two novel PAPSS2 mutations
Oostdijk, W., Idkowiak, J., Mueller, J. W., House, P. J., Taylor, A. E., O'Reilly, M. W., Hughes, B. A., de Vries, M. C., Kant, S. G., Santen, G. W. E., et al. (2015) · The Journal of Clinical Endocrinology & Metabolism
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 81
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New reference charts for testicular volume in Dutch children and adolescents allow the calculation of standard deviation scores
Joustra, S. D., van der Plas, E. M., Goede, J., Oostdijk, W., Delemarre‐van de Waal, H. A., Hack, W. W. M., van Buuren, S., & Wit, J. M. (2015) · Acta Paediatrica
Hypothalamic control of reproductive hormonesTesticular diseases and treatments
Cited by 75
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Relation between Early Over- and Undertreatment and Behavioural Problems in Preadolescent Children with Congenital Hypothyroidism
Bongers-Schokking, J. J., Resing, W. C. M., Oostdijk, W., de Rijke, Y. B., & de Muinck Keizer-Schrama, S. M. P. F. (2018) · Hormone Research in Paediatrics
Thyroid Disorders and TreatmentsThyroid and Parathyroid Surgery
Cited by 39
- Verified
Mild deficits in attentional control in patients with the IGSF 1 deficiency syndrome
Joustra, S. D., Andela, C. D., Oostdijk, W., van Trotsenburg, A. S. P., Fliers, E., Wit, J. M., Pereira, A. M., Middelkoop, H. A. M., & Biermasz, N. R. (2016) · Clinical Endocrinology
Thyroid Disorders and TreatmentsImmunodeficiency and Autoimmune Disorders
Cited by 21
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Heterozygotes for 17α-hydroxylase deficiency can be detected with a short ACTH test
WIT, J. M., VAN ROERMUND, H. P. C., OOSTDIJK, W., BENRAAD, T. H. J., THIJSSEN, J. H. H., BOER, P., JANSEN, M., SPIT, M., & VAN DEN BRANDE, J. L. (1988) · Clinical Endocrinology
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 18
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