Hakan Cangül

PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron

Neil V. Morgan, Shawn K. Westaway, Jenny E.V. Morton et al. · Nature Genetics · 2006 · 535 citations · Full text

Neurodegenerative Diseases, Alzheimer's Disease, Biochemistry +12

Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease

Neil V. Morgan, Mark R. Morris, Hakan Cangül et al. · PLoS Genetics · 2010 · 222 citations · Full text

Genetics, Pathology, Molecular Genetics +16

Hypoxia upregulates the expression of the NDRG1 gene leading to its overexpression in various human cancers

Hakan Cangül · BMC Genetics · 2004 · 184 citations · Full text

Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization

Andrew R. Cullinane, Anna Straatman-Iwanowska, Andreas Zaucker et al. · Nature Genetics · 2010 · 178 citations · Full text

Urology, Autoimmune Disease, Cholestasis Syndrome Phenotype +13

Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ

Adeline K. Nicholas, Eva Serra, Hakan Cangül et al. · The Journal of Clinical Endocrinology & Metabolism · 2016 · 107 citations · Full text