Concepedia

Hakan Cangül

HC

Statistics

Publications

23

Citations

1.9K

H-Index

18

Active since

2002

Affiliations

University of Birmingham(Current)

Bursa Uludağ Üni̇versi̇tesi̇

University of Cambridge

University of Southampton

Bahçeşehir University

Hakan Cangül is an author at University of Birmingham specializing in human genetics, genetics, and medical genetics.

Publications per year

2002–2018

23

Publications

23

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 · 538 citations · Full text

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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 · 225 citations · Full text

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

Hakan Cangül · BMC Genetics · 2004 · 188 citations · Full text

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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 · 180 citations · Full text

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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 · 113 citations · Full text

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