Wedell, Anna

Genotyping Is a Valuable Diagnostic Complement to Neonatal Screening for Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency1

Nordenström, A., Thilén, A., Hagenfeldt, L., Larsson, A., & Wedell, A. (1999) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 108

Epilepsy syndromes, etiologies, and the use of next‐generation sequencing in epilepsy presenting in the first 2 years of life: A population‐based study

Stödberg, T., Tomson, T., Barbaro, M., Stranneheim, H., Anderlid, B., Carlsson, S., Åmark, P., & Wedell, A. (2020) · Epilepsia

Epilepsy research and treatmentGenomics and Rare Diseases

Cited by 46

The mitochondrial methylation potential gates mitoribosome assembly

Glasgow, R. I. C., Singh, V., Peña-Pérez, L., Wilhalm, A., Moedas, M. F., Moore, D., Rosenberger, F. A., Li, X., Atanassov, I., Saba, M., et al. (2024) · Nature Communications

RNA and protein synthesis mechanismsRNA modifications and cancer

Cited by 14

The mitochondrial methylation potential gates mitoribosome assembly

Glasgow, R. I. C., Singh, V., Peña-Pérez, L., Wilhalm, A., Moedas, M. F., Moore, D., Rosenberger, F. A., Li, X., Atanassov, I., Saba, M., et al. (2025) · Nature Communications

RNA and protein synthesis mechanismsRNA modifications and cancer

Cited by 14