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Ekim Taskiran
Ekim Taskiran
Verified email at hacettepe.edu.tr
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Cited by
Year
DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN
F Ozaltin, B Li, A Rauhauser, SW An, O Soylemezoglu, II Gonul, ...
Journal of the American Society of Nephrology 24 (3), 377-384, 2013
1722013
Disruption of PTPRO causes childhood-onset nephrotic syndrome
F Ozaltin, T Ibsirlioglu, EZ Taskiran, DE Baydar, F Kaymaz, M Buyukcelik, ...
The American Journal of Human Genetics 89 (1), 139-147, 2011
1432011
A case series of adenosine deaminase 2-deficient patients emphasizing treatment and genotype-phenotype correlations
ED Batu, O Karadag, EZ Taskiran, U Kalyoncu, I Aksentijevich, ...
The Journal of rheumatology 42 (8), 1532-1534, 2015
1192015
MEFV mutations in systemic onset juvenile idiopathic arthritis
NA Ayaz, S Özen, Y Bilginer, M Ergüven, E Taşkıran, E Yılmaz, N Beşbaş, ...
Rheumatology 48 (1), 23-25, 2009
1112009
A monogenic disease with a variety of phenotypes: deficiency of adenosine deaminase 2
S Özen, ED Batu, EZ Taşkıran, HA Özkara, Ş Ünal, N Güleray, A Erden, ...
The Journal of rheumatology 47 (1), 117-125, 2020
992020
Genotype and phenotype evaluation of patients with primary ciliary dyskinesia: first results from Turkey
N Emiralioğlu, EZ Taşkıran, C Koşukcu, E Bilgiç, P Atilla, B Kaya, ...
Pediatric pulmonology 55 (2), 383-393, 2020
652020
The effect of colchicine on pyrin and pyrin interacting proteins
EZ Taskiran, A Cetinkaya, B Balci‐Peynircioglu, YZ Akkaya, E Yilmaz
Journal of cellular biochemistry 113 (11), 3536-3546, 2012
632012
Mutations in ANKS6 cause a nephronophthisis-like phenotype with ESRD
EZ Taskiran, E Korkmaz, S Gucer, C Kosukcu, F Kaymaz, C Koyunlar, ...
Journal of the American Society of Nephrology 25 (8), 1653-1661, 2014
592014
Whole exome sequencing in early-onset systemic lupus erythematosus
ED Batu, C Koşukcu, E Taşkıran, S Sahin, S Akman, B Sözeri, E Ünsal, ...
The Journal of rheumatology 45 (12), 1671-1679, 2018
572018
HERC1 mutations in idiopathic intellectual disability
GE Utine, EZ Taşkıran, C Koşukcu, B Karaosmanoğlu, N Güleray, ...
European Journal of Medical Genetics 60 (5), 279-283, 2017
482017
The effect of boron-containing nano-hydroxyapatite on bone cells
M Gizer, S Köse, B Karaosmanoglu, EZ Taskiran, A Berkkan, M Timuçin, ...
Biological Trace Element Research 193, 364-376, 2020
452020
Expression of ASC in renal tissues of familial mediterranean fever patients with amyloidosis: postulating a role for ASC in AA type amyloid deposition
B Balci-Peynircioglu, AL Waite, P Schaner, ZE Taskiran, N Richards, ...
Experimental biology and medicine 233 (11), 1324-1333, 2008
442008
Human bone marrow mesenchymal stem cells secrete endocannabinoids that stimulate in vitro hematopoietic stem cell migration effectively comparable to beta-adrenergic stimulation
S Köse, F Aerts-Kaya, ÇZ Köprü, E Nemutlu, B Kuşkonmaz, ...
Experimental hematology 57, 30-41. e1, 2018
412018
TMCO1 deficiency causes autosomal recessive cerebrofaciothoracic dysplasia
Y Alanay, B Ergüner, E Utine, O Haçarız, POS Kiper, EZ Taşkıran, ...
American Journal of Medical Genetics Part A 164 (2), 291-304, 2014
352014
FARS1‐related disorders caused by bi‐allelic mutations in cytosolic phenylalanyl‐tRNA synthetase genes: Look beyond the lungs!
LA Schuch, M Forstner, CK Rapp, Y Li, DEC Smith, MI Mendes, ...
Clinical genetics 99 (6), 789-801, 2021
332021
Loss-of-function mutations in ELMO2 cause intraosseous vascular malformation by impeding RAC1 signaling
A Cetinkaya, JR Xiong, İ Vargel, K Kösemehmetoğlu, Hİ Canter, ...
The American Journal of Human Genetics 99 (2), 299-317, 2016
332016
Further expanding the mutational spectrum and investigation of genotype–phenotype correlation in 3M syndrome
PO Simsek‐Kiper, E Taskiran, C Kosukcu, UE Arslan, V Cormier‐Daire, ...
American Journal of Medical Genetics Part A 179 (7), 1157-1172, 2019
272019
Small cell lung cancer stem cells display mesenchymal properties and exploit immune checkpoint pathways in activated cytotoxic T lymphocytes
MA Kursunel, EZ Taskiran, E Tavukcuoglu, H Yanik, F Demirag, ...
Cancer Immunology, Immunotherapy, 1-15, 2022
232022
Diagnostic yield of whole‐exome sequencing in non‐syndromic intellectual disability
EZ Taşkıran, B Karaosmanoğlu, C Koşukcu, G Ürel‐Demir, ...
Journal of Intellectual Disability Research 65 (6), 577-588, 2021
232021
Whole exome sequencing in unclassified autoinflammatory diseases: more monogenic diseases in the pipeline?
C Kosukcu, EZ Taskiran, ED Batu, E Sag, Y Bilginer, M Alikasifoglu, ...
Rheumatology 60 (2), 607-616, 2021
212021
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