Tara Hussein Tayeb

Germline CDKN1B loss-of-function variants cause pediatric Cushing's disease with or without an MEN4 phenotype.

F. Faucz, C. Stratakis, N. Pankratz, 2020, The Journal of clinical endocrinology and metabolism.

Congenital Hyperinsulinism Caused by Novel Homozygous KATP Channel Gene Variants May Be Linked to Unexplained Neonatal Deaths among Kurdish Consanguineous Families

P. Kučerová, S. Pruhova, J. Lebl, 2020, Hormone Research in Paediatrics.

Paediatric diabetes subtypes in a consanguineous population: a single-centre cohort study from Kurdistan, Iraq

E. De Franco, S. Pruhova, P. Dusatkova, 2023, Diabetologia.