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M. Mert Sozen-PhD
M. Mert Sozen-PhD
İnönü Üniversitesi, Moleküler Biyoloji ve Genetik Bölümü
Verified email at inonu.edu.tr - Homepage
Title
Cited by
Cited by
Year
Mutations in GNA11 in Uveal Melanoma
CD Van Raamsdonk, KG Griewank, MB Crosby, MC Garrido, S Vemula, ...
New England Journal of Medicine 363 (23), 2191-2199, 2010
15872010
Genetic and molecular characterization of uveal melanoma cell lines
KG Griewank, X Yu, J Khalili, MM Sozen, K Stempke‐Hale, C Bernatchez, ...
Pigment cell & melanoma research 25 (2), 182-187, 2012
1402012
The molecular basis of familial hypercholesterolaemia in Turkish patients
MM Sözen, R Whittall, C Öner, A Tokatlı, HS Kalkanoğlu, A Dursun, ...
Atherosclerosis 180 (1), 63-71, 2005
612005
Multiplex ARMS analysis to detect 13 common mutations in familial hypercholesterolaemia
A Taylor, S Tabrah, D Wang, M Sozen, N Duxbury, R Whittall, ...
Clinical genetics 71 (6), 561-568, 2007
422007
The association between vitamin D receptor polymorphisms and multiple sclerosis in a Turkish population
O Kamisli, C Acar, M Sozen, M Tecellioglu, FE Yücel, D Vaizoglu, ...
Multiple sclerosis and related disorders 20, 78-81, 2018
232018
Analysis of vitamin D receptor polymorphisms in patients with familial multiple sclerosis
FE Yucel, O Kamıslı, C Acar, M Sozen, M Tecellioğlu, C Ozcan
Medical Archives 72 (1), 58, 2018
182018
Mutation detection in patients with familial hypercholesterolaemia using heteroduplex and single strand conformation polymorphism analysis by capillary electrophoresis
M Sozen, R Whittall, SE Humphries
Atherosclerosis Supplements 5 (5), 7-11, 2004
182004
Three novel mutations in the apolipoprotein E gene in a sample of individuals with type 2 diabetes mellitus
JW Stephens, MM Sozen, RA Whittall, MJ Caslake, D Bedford, J Acharya, ...
Clinical chemistry 51 (1), 119-124, 2005
132005
Lack of association between catechol-Omethyltransferase and schizophrenia in a Turkish population
C Acar, MM Sözen, H Gözükara, K Orman, Ş Kartalcı
Turkish Journal of Biochemistry 40 (3), 205-209, 2015
102015
Severe hemolytic anemia associated with Hb Volga [β27 (B9) Ala→ Asp]: GCC→ GAC at codon 27 in a Turkish family
M Sözen, C Karaaslan, R Öner, F Gümrük, MA Özdemir, C Altay, ...
American journal of hematology 76 (4), 378-382, 2004
92004
The novel synthesized pyridazinone derivates had the antiproliferative and apoptotic effects in SHSY5Y and HEP3B cancer cell line
O Ciftci, Z Ozdemir, C Acar, M Sozen, N Basak-Turkmen, I Ayhan, ...
Letters in Organic Chemistry 15 (4), 323-331, 2018
52018
β‐Thalassaemia intermedia in a Turkish girl: homozygosity for G→ A substitution at+ 22 relative to the β‐globin cap site
R Öner, C Öner, E Birben, M Sözen, F Gümrük, A Gürgey, C Altay
British journal of haematology 115 (1), 90-94, 2001
52001
Screening of three ERBB4 gene polymorphisms in a group of Turkish schizophrenia patients and controls/ERBB4 genindeki üç polimorfizmin bir Türk şizofreni hasta grubunda ve …
MM Sözen, Ş Kartalcı
Turkish Journal of Biochemistry 40 (6), 463-471, 2015
32015
Presence of a genetic association between NRG-3 SNP rs17101193 and schizophrenia
MM Sözen, C Acar, Ş Kartalcı
22020
Myelodysplastic syndrome (MDS) associated with increased hemoglobin F and trisomy 8: presentation of a patient
A Koc, R Öner, C Öner, D Aktas, M Sözen, E Tuncbilek, C Altay
Hematology and cell therapy 41, 187-189, 1999
21999
Association analysis of two polymorphisms in neuregulin-1 gene in a Turkish schizophrenia sample
A Saygili, S Kartalci, MM Sozen
12022
Lipoid proteinosis and epilepsy: Molecular analysis
M Tecellioglu, O Kamisli, C Acar, H Merge, M Sozen, T Karaduman, ...
12019
Association of a haplotype in the NRG1 gene with schizophrenia: a case-control study
MM Sözen, Ş Kartalcı
Turkish Journal of Biochemistry 48 (3), 246-256, 2023
2023
EVALUATION OF THE ASSOCIATION OF PLASMA PENTRAXIN-3 LEVELS WITH CAROTID INTIMA-MEDIA THICKNESS AND HIGH-SENSITIVE CRP IN PATIENTS WITH SUBCLINICAL HYPOTHYROIDISM
A Koç, I Guney, MC Kızılarslanoglu, G Gonulalan, CD Deniz, F Saçkan, ...
Acta Endocrinologica (Bucharest) 19 (3), 286, 2023
2023
Screening of ERBB4 SNP rs1026882 in a group of Schizophrenia patients and controls.
OT Yildirim, MM Sozen, S Kartalci
Medicine Science 11 (3), 2022
2022
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