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  1. 2010

  2. Characterization of a novel loss-of-function mutation of PAX8 associated with congenital hypothyroidism

    Di Palma, T., Zampella, E., Filippone, M. G., Macchia, P. E., Ris-Stalpers, C., de Vroede, M. & Zannini, M., 2010, In: Clinical endocrinology. 73, 6, p. 808-814

    Research output: Contribution to journal › Article › Academic › peer-review

  3. Genetics and phenomics of hypothyroidism and goiter due to TPO mutations

    Ris-Stalpers, C. & Bikker, H., 2010, In: Molecular and cellular endocrinology. 322, 1-2, p. 38-43

    Research output: Contribution to journal › Review article › Academic › peer-review

  4. Initial Characterization of C16orf89, A Novel Thyroid-Specific Gene

    Afink, G. B., Veenboer, G., de Randamie, J., Keijser, R., Meischl, C., Niessen, H. & Ris-Stalpers, C., 2010, In: Thyroid. 20, 7, p. 811-821

    Research output: Contribution to journal › Article › Academic › peer-review

  5. Unique skin changes in a case of Albright hereditary osteodystrophy caused by a rare GNAS1 mutation

    Klaassens, M., Blom, E. W., Schrander, J. J. P., Ris-Stalpers, C., Nieuwenhuijzen Kruseman, A. C., van Steensel, M. A. M. & Schrander-Stumpel, C. T. R. M., 2010, In: British journal of dermatology. 162, 3, p. 690-694

    Research output: Contribution to journal › Article › Academic › peer-review

  6. 2008

  7. H9c2 cardiomyoblasts produce thyroid hormone

    Meischl, C., Buermans, H. P., Hazes, T., Zuidwijk, M. J., Musters, R. J. P., Boer, C., van Lingen, A., Simonides, W. S., Blankenstein, M. A., Dupuy, C., Paulus, W. J., Hack, C. E., Ris-Stalpers, C., Roos, D. & Niessen, H. W. M., 2008, In: American journal of physiology. Cell physiology. 294, 5, p. C1227-C1233

    Research output: Contribution to journal › Article › Academic › peer-review

  8. Molecular characterization of iodotyrosine dehalogenase deficiency in patients with hypothyroidism

    Afink, G., Kulik, W., Overmars, H., de Randamie, J., Veenboer, T., van Cruchten, A., Craen, M. & Ris-Stalpers, C., 2008, In: Journal of clinical endocrinology and metabolism. 93, 12, p. 4894-4901

    Research output: Contribution to journal › Article › Academic › peer-review

  9. Placental corticotrophin-releasing hormone mRNA and microparticles in maternal plasma are not measures of placental shedding of debris: a rebuttal

    Buimer, M., Lok, C. A. R., Nieuwland, R., Ris-Stalpers, C. & van der Post, J. A. M., 2008, In: Journal of thrombosis and haemostasis. 6, 10, p. 1837-8; author reply 1838-9

    Research output: Contribution to journal › Comment/Letter to the editor › Academic

  10. Seven placental transcripts characterize HELLP-syndrome

    Buimer, M., Keijser, R., Jebbink, J. M., Wehkamp, D., van Kampen, A. H. C., Boer, K., van der Post, J. A. M. & Ris-Stalpers, C., 2008, In: Placenta. 29, 5, p. 444-453

    Research output: Contribution to journal › Article › Academic › peer-review

  11. 2007

  12. Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis

    Tenenbaum-Rakover, Y., Mamanasiri, S., Ris-Stalpers, C., German, A., Sack, J., Allon-Shalev, S., Pohlenz, J. & Refetoff, S., 2007, In: Clinical endocrinology. 66, 5, p. 695-702

    Research output: Contribution to journal › Article › Academic › peer-review

  13. STOX1 is not imprinted and is not likely to be involved in preeclampsia

    Iglesias-Platas, I., Monk, D., Jebbink, J., Buimer, M., Boer, K., van der Post, J., Hills, F., Apostolidou, S., Ris-Stalpers, C., Stanier, P. & Moore, G. E., 2007, In: Nature genetics. 39, 3, p. 279-80; author reply 280-1

    Research output: Contribution to journal › Comment/Letter to the editor › Academic

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