Kariyawasam, Dulanjalee

TUBB1 mutations cause thyroid dysgenesis associated with abnormal platelet physiology

Stoupa, A., Adam, F., Kariyawasam, D., Strassel, C., Gawade, S., Szinnai, G., Kauskot, A., Lasne, D., Janke, C., Natarajan, K., et al. (2018) · EMBO Molecular Medicine

Thyroid Disorders and TreatmentsGenetic and Kidney Cyst Diseases

Cited by 71

New genetics in congenital hypothyroidism

Stoupa, A., Kariyawasam, D., Muzza, M., de Filippis, T., Fugazzola, L., Polak, M., Persani, L., & Carré, A. (2021) · Endocrine

Thyroid Disorders and TreatmentsHead and Neck Anomalies

Cited by 59

Update of Thyroid Developmental Genes

Stoupa, A., Kariyawasam, D., Carré, A., & Polak, M. (2016) · Endocrinology and Metabolism Clinics of North America

Thyroid Disorders and TreatmentsHead and Neck Anomalies

Cited by 47

DYRK1A BAC Transgenic Mouse: A New Model of Thyroid Dysgenesis in Down Syndrome

Kariyawasam, D., Rachdi, L., Carré, A., Martin, M., Houlier, M., Janel, N., Delabar, J.-M., Scharfmann, R., & Polak, M. (2015) · Endocrinology

Thyroid Disorders and TreatmentsDown syndrome and intellectual disability research

Cited by 30

First case of fetal goitrous hypothyroidism due to SLC5A5/NIS mutations

Stoupa, A., Al Hage Chehade, G., Kariyawasam, D., Tohier, C., Bole-Feysot, C., Nitschke, P., Thibault, H., Jullie, M.-L., Polak, M., & Carré, A. (2020) · European Journal of Endocrinology

Thyroid Disorders and TreatmentsHead and Neck Anomalies

Cited by 16