Hakan Cangül
Istanbul Medipol University(TR)
Publications by Year
Research Areas
Thyroid Disorders and Treatments, RNA modifications and cancer, Congenital heart defects research, Ion channel regulation and function, Erythrocyte Function and Pathophysiology
Most-Cited Works
- → PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron(2006)537 cited
- → Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease(2010)222 cited
- → Hypoxia upregulates the expression of the NDRG1 gene leading to its overexpression in various human cancers(2004)184 cited
- → Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization(2010)178 cited
- → Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ(2016)110 cited
- → Molecular mechanisms of nickel carcinogenesis(2002)102 cited
- → Associations among genotype, clinical phenotype, and intracellular localization of trafficking proteins in ARC syndrome(2012)88 cited
- → Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism(2018)73 cited
- → Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community(2012)64 cited
- → Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism(2017)60 cited