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H. Cangul · SciRah

Researcher profile · Semantic Scholar

H. Cangul

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H. Cangul — researcher profile on SciRah

h-index: 18
Works: 35
Citations: 1,738

Most-cited papers

PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron
N. Morgan, S. Westaway, J. Morton, A. Gregory +23 more
2006Nature Genetics551 citations Open access
Semantic Scholar
Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease
N. Morgan, M. Morris, H. Cangul, D. Gleeson +18 more
2010PLoS Genetics208 citations Open access
Semantic Scholar
Hypoxia upregulates the expression of the NDRG1 gene leading to its overexpression in various human cancers
H. Cangul
2004BMC Genetics180 citations Open access
Semantic Scholar
Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ
A. Nicholas, E. Serra, H. Cangul, S. Alyaarubi +33 more
2016Journal of Clinical Endocrinology and Metabolism106 citations Open access
Semantic Scholar
Associations Among Genotype, Clinical Phenotype, and Intracellular Localization of Trafficking Proteins in ARC Syndrome
Holly E. Smith, R. Galmes, E. Gogolina, A. Straatman-Iwanowska +20 more
2012Human Mutation85 citations Open access
Semantic Scholar
Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community
H. Cangul, Z. Aycan, Álvaro Olivera-Nappa, H. Sağlam +15 more
2013Clinical Endocrinology73 citations
Semantic Scholar
Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism
Z. Aycan, H. Cangul, M. Muzza, V. Baş +4 more
2017Journal of Clinical Endocrinology and Metabolism55 citations Open access
Semantic Scholar
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism.
H. Cangul, Xiao-Hui Liao, E. Schoenmakers, J. Kero +23 more
2018JCI Insight54 citations Open access
Semantic Scholar
Enhanced Expression of a Novel Protein in Human Cancer Cells: A Potential Aid to Cancer Diagnosis
H. Cangul, K. Salnikow, Herman Yee, D. Zagzag +2 more
2004Cell Biology and Toxicology53 citations
Semantic Scholar
Enhanced overexpression of an HIF-1/hypoxia-related protein in cancer cells.
H. Cangul, K. Salnikow, H. Yee, D. Zagzag +2 more
2002Environmental Health Perspectives46 citations Open access
Semantic Scholar
Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism
H. Cangul, N. Morgan, Julia R. Forman, H. Sağlam +19 more
2010Clinical Endocrinology43 citations
Semantic Scholar
TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis
H. Cangul, Z. Aycan, H. Sağlam, Julia R. Forman +19 more
2012Journal of Pediatric Endocrinology & Metabolism (JPEM)31 citations
Semantic Scholar
Novel truncating thyroglobulin gene mutations associated with congenital hypothyroidism
H. Cangul, K. Boelaert, M. Dogan, Y. Sağlam +3 more
2014Endocrine28 citations
Semantic Scholar
Nanoparticle growth and surface chemistry changes in cell-conditioned culture medium
M. Kendall, N. Hodges, Harry J. Whitwell, Jess Tyrrell +1 more
2015Philosophical Transactions of the Royal Society B: Biological Sciences22 citations Open access
Semantic Scholar
A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism
H. Cangul, Z. Aycan, Michael R. Kendall, V. Baş +3 more
2014Journal of Pediatric Endocrinology & Metabolism (JPEM)21 citations
Semantic Scholar
A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects
H. Cangul, V. Baş, Y. Sağlam, Michael R. Kendall +3 more
2014Journal of Pediatric Endocrinology & Metabolism (JPEM)19 citations
Semantic Scholar
Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation
V. Baş, H. Cangul, S. Ağladıoğlu, Michael R. Kendall +3 more
2012Journal of Pediatric Endocrinology & Metabolism (JPEM)18 citations
Semantic Scholar
Puberty, stress, and sudden death.
Metin Guclu, Lin Lin, E. Erturk, J. Achermann +1 more
2010The Lancet18 citations
Semantic Scholar
A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect
V. Baş, Z. Aycan, H. Cangul, Michael R. Kendall +3 more
2014Journal of Pediatric Endocrinology & Metabolism (JPEM)17 citations
Semantic Scholar
Association of urokinase gene 3′-UTR T/C polymorphism with calcium oxalate urolithiasis in children
M. Ozturk, Y. Kordan, H. Cangul, H. Doğan +3 more
2008International Urology and Nephrology17 citations
Semantic Scholar
A deletion including exon 2 of the TSHR gene is associated with thyroid dysgenesis and severe congenital hypothyroidism
H. Cangul, N. Schoenmakers, H. Sağlam, Durmus Doganlar +7 more
2014Journal of Pediatric Endocrinology & Metabolism (JPEM)12 citations
Semantic Scholar
Molecular mechanisms of nickel carcinogenesis.
H. Cangul, Limor Broday, K. Salnikow, Jessica E. Sutherland +6 more
2002Toxicology Letters12 citations
Semantic Scholar
A comprehensive next generation sequencing-based strategy for genetic diagnosis in congenital hypothyroidism
N. Schoenmakers, H. Cangul, A. Nicholas, E. Schoenmakers +13 more
201311 citations
Semantic Scholar
Erratum: Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type
N. Morgan, S. Westaway, J. Morton, A. Gregory +23 more
2006Nature Genetics11 citations Open access
Semantic Scholar
A truncating TPO mutation (Y55X) in patients with hypothyroidism and total iodide organification defect
H. Cangul, F. Darendeliler, Y. Sağlam, B. Kucukemre +4 more
2015Endocrine Research10 citations
Semantic Scholar
An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesis
H. Cangul, H. Sağlam, Y. Sağlam, E. Eren +5 more
2014Journal of Pediatric Endocrinology & Metabolism (JPEM)10 citations
Semantic Scholar
Duplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD
S. Temel, H. Cangul
2013Journal of Pediatric Endocrinology & Metabolism (JPEM)8 citations
Semantic Scholar
A Homozygous TPO Gene Duplication (c.1184_1187dup4) Causes Congenital Hypothyroidism in Three Siblings Born to a Consanguineous Family
H. Cangul, B. Aydin, F. Baş
2015Journal of Pediatric Genetics5 citations Open access
Semantic Scholar
Investigating the genetic architecture of gland-in-situ congenital hypothyroidism by comprehensive screening of eight known causative genes
A. Nicholas, E. Serra, H. Cangul, Saif Al-Yaarubi +16 more
20153 citations
Semantic Scholar
Novel TSHR mutations in a large cohort of consanguineous families with congenital non-goitrous hypothyroidism
H. Cangul, Z. Aycan, H. Sağlam, T. Yakut +16 more
20103 citations
Semantic Scholar
Infantile Systemic Hyalinosis with Early Thyroid Dysfunction
O. Pirgon, M. Atabek, Hasan Esen, H. Cangul
2007Journal of Pediatric Endocrinology & Metabolism (JPEM)3 citations
Semantic Scholar
The calcium-independent phospholipase A2 gene, PLA2G6, is mutated in a spectrum of childhood neurodegenerative disorders with high brain iron
N. Morgan, S. Westaway, J. Morton, A. Gregory +23 more
20063 citations
Semantic Scholar
Strong Similarities in Turkish and European Patients Diagnosed with APECED Syndrome
Metin Guclu, H. Cangul, C. Ersoy
20152 citations Open access
Semantic Scholar
Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization
A. Cullinane, A. Straatman-Iwanowska, A. Zaucker, Y. Wakabayashi +21 more
2010Nature Genetics2 citations Open access
Semantic Scholar
Turkish perspective of Jervell and Lange-Nielsen syndrome
S. Temel, O. Bostan, H. Cangul, E. Cil
2013Annals of Indian Academy of Neurology1 citations Open access
Semantic Scholar

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