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Cangul, Hakan
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1

Computational analysis of missense filamin-A variants, incl..:

Gerlevik, Umut ; Saygı, Ceren ; Cangül, Hakan...
PLOS ONE.  17 (2022)  5 - p. e0265400 , 2022
Link: https://doi.org/10.1371/..
 
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2

Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital ..:

Aycan, Zehra ; Cangul, Hakan ; Muzza, Marina...
The Journal of Clinical Endocrinology & Metabolism.  102 (2017)  9 - p. 3085-3090 , 2017
Link: https://doi.org/10.1210/..
 
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3

Comprehensive Screening of Eight Known Causative Genes in C..:

Nicholas, Adeline K. ; Serra, Eva G. ; Cangul, Hakan...
The Journal of Clinical Endocrinology & Metabolism.  101 (2016)  12 - p. 4521-4531 , 2016
Link: https://doi.org/10.1210/..
 
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4

Nanoparticle growth and surface chemistry changes in cell-c..:

Kendall, Michaela ; Hodges, Nikolas J. ; Whitwell, Harry..
Philosophical Transactions: Biological Sciences.  370 (2015)  1661 - p. 1-9 , 2015
Link: http://www.jstor.org/sta..
 
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5

Thyroid dyshormonogenesis is mainly caused byTPOmutations i..:

Cangul, Hakan ; Aycan, Zehra ; Olivera-Nappa, Alvaro...
Clinical Endocrinology.  79 (2013)  2 - p. 275-281 , 2013
Link: https://doi.org/10.1111/..
 
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6

Jervell and Lange–Nielsen Syndrome: Homozygous Missense Mut..:

Bostan, Ozlem ; Temel, Şehime G. ; Cangül, Hakan..
Pediatric Cardiology.  34 (2013)  8 - p. 2063-2067 , 2013
Link: https://doi.org/10.1007/..
 
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7

Novel truncating thyroglobulin gene mutations associated wi..:

Cangul, Hakan ; Boelaert, Kristien ; Dogan, Murat...
Endocrine.  45 (2013)  2 - p. 206-212 , 2013
Link: https://doi.org/10.1007/..
 
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8

Turkish perspective of Jervell and Lange-Nielsen syndrome:

Temel, SehimeG ; Bostan, OzlemM ; Cangul, Hakan.
Annals of Indian Academy of Neurology.  16 (2013)  1 - p. 129 , 2013
Link: https://doi.org/10.4103/..
 
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9

Duplication of SOX9 is not a common cause of 46,XX testicul..:

Temel, Sehime G. ; Cangul, Hakan
Journal of Pediatric Endocrinology and Metabolism.  26 (2013)  1-2 - p. , 2013
Link: https://doi.org/10.1515/..
 
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10

TSHR is the main causative locus in autosomal recessively i..:

Cangul, Hakan ; Aycan, Zehra ; Saglam, Halil...
Journal of Pediatric Endocrinology and Metabolism.  25 (2012)  5-6 - p. , 2012
Link: https://doi.org/10.1515/..
 
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11

Mild and severe congenital primary hypothyroidism in two pa..:

Baş, Veysel Nijat ; Cangul, Hakan ; Agladioglu, Sebahat Yilmaz...
Journal of Pediatric Endocrinology and Metabolism.  25 (2012)  11-12 - p. , 2012
Link: https://doi.org/10.1515/..
 
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12

Erratum: Corrigendum: Mutations in VIPAR cause an arthrogry..:

Cullinane, Andrew R ; Straatman-Iwanowska, Anna ; Zaucker, Andreas...
Nature Genetics.  43 (2011)  3 - p. 277-277 , 2011
Link: https://doi.org/10.1038/..
 
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13

Novel TSHR mutations in consanguineous families with congen..:

Cangul, Hakan ; Morgan, Neil V. ; Forman, Julia R....
Clinical Endocrinology.  73 (2010)  5 - p. 671-677 , 2010
Link: https://doi.org/10.1111/..
 
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14

Mutations in SLC29A3, Encoding an Equilibrative Nucleoside ..:

Morgan, Neil V. ; Morris, Mark R. ; Cangul, Hakan...
PLoS Genetics.  6 (2010)  2 - p. e1000833 , 2010
Link: https://doi.org/10.1371/..
 
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15

Mutations in VIPAR cause an arthrogryposis, renal dysfuncti..:

Cullinane, Andrew R ; Straatman-Iwanowska, Anna ; Zaucker, Andreas...
Nature Genetics.  42 (2010)  4 - p. 303-312 , 2010
Link: https://doi.org/10.1038/..
 
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