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Kuyaş HEKİMLER ÖZTÜRK
Kuyaş HEKİMLER ÖZTÜRK
Verified email at sdu.edu.tr
Title
Cited by
Cited by
Year
A 10.46 Mb 12p11.1–12.1 interstitial deletion coincident with a 0.19 Mb NRXN1 deletion detected by array CGH in a girl with scoliosis and autism
Y Soysal, J Vermeesch, NA Davani, K Hekimler, N İmirzalıoğlu
American Journal of Medical Genetics Part A 155 (7), 1745-1752, 2011
212011
Genetic variations of DNA repair genes in breast cancer
A Özgöz, K Hekimler Öztürk, A Yükseltürk, H Şamlı, Z Başkan, ...
Pathology & Oncology Research 25, 107-114, 2019
202019
Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy
Y Soysal, S Balcı, K Hekimler, T Liehr, E Ewers, J Schoumans, TH Bui, ...
American Journal of Medical Genetics Part A 149 (12), 2782-2787, 2009
182009
An investigation of the effects of FGFR2 and B7-H4 polymorphisms in breast cancer
A Özgöz, H Şamlı, B Orhan, FM Içduygu, F Aktepe, N Imirzalioglu
Journal of Cancer Research and Therapeutics 9 (3), 370-375, 2013
152013
Evaluation of interleukin-23 receptor (IL-23R) gene polymorphisms and serum IL-23 levels in patients with psoriasis
B Filiz, M Yildirim, KH Öztürk, FB Şirin, S Çelik, I Erturan, S Korkmaz, ...
Turkish journal of medical sciences 49 (5), 1386-1394, 2019
132019
Low-penetrance susceptibility variants and postmenopausal oestrogen receptor positive breast cancer
A Özgöz, Fİ Mutlu İçduygu, A Yükseltürk, H ŞamlI, K Hekİmler Öztürk, ...
Journal of Genetics 99, 1-10, 2020
92020
SURGERY FOR ACUTE ABOOMEN AND MEFV MUTATIONS IN PATIENTS WITH FMF.
H ŞamIı, FM İçduygu, A Özgöz, G AkbuIut, K Hekimler, N İmirzalioğlu
Acta Reumatológica Portuguesa 34 (3), 2009
82009
Hypothalamic NR3C1 DNA methylation in rats exposed to prenatal stress
KH Öztürk, GÖ Ünal, DK Doğuç, VA Toğay, PA Koşar, M Sezik
Molecular biology reports 49 (8), 7921-7928, 2022
72022
Downregulation of plasma microRNA-29c-3p expression may be a new risk factor for diabetic retinopathy.
B Torus, H Korkmaz, KH Ozturk, FB Şİrİn, M Argun, KS Şevi, L TÖk
Minerva Endocrinologica, 2023
62023
Possibility of paclitaxel to induce the stemness-related characteristics of prostate cancer cells
FM Içduygu, H Şamlı, A Özgöz, B Vatansever, KH Öztürk, E Akgün
Wroclaw Medical Univ, 2021
62021
Molecular characterization of microduplication 22q11. 2 in a girl with hypernasal speech
Y Soysal, J Vermeesch, NA Davani, N Şensoy, K Hekimler, N İmirzalıoğlu
Genetics and Molecular Research 10 (3), 2148-2154, 2011
62011
Increased NLRP3 inflammasome expression in peripheral blood mononuclear cells of patients with schizophrenia: a case-control study
G Ozdamar Unal, K Hekimler Ozturk, HE Inci
International Journal of Psychiatry in Clinical Practice 27 (2), 111-117, 2023
52023
Maternal prenatal stress and depression‐like behavior associated with hippocampal and cortical neuroinflammation in the offspring: An experimental study
G Özdamar Ünal, K Hekimler Öztürk, G Erkılınç, F Dönmez, ...
International Journal of Developmental Neuroscience 82 (3), 231-242, 2022
42022
Circulating miR-29c-3p is downregulated in patients with acromegaly
H Korkmaz, KH Öztürk, B Torus
Turkish Journal of Medical Sciences 51 (4), 2080-2086, 2021
42021
Postmenopausal estrogen receptor positive breast cancer and obesity associated gene variants
A Özgöz, FM İçduygu, A Yükseltürk, H Samli, KH Öztürk, Z Baskan, ...
EXCLI journal 20, 1133, 2021
42021
New risk factors in diabetic nephropathy: microRNA-196-3p and microRNA-203.
I Eroglu, H Korkmaz, KH Ozturk, FB Sirin, S Sevik, B Afsar
Minerva Endocrinology 47 (3), 314-324, 2020
42020
A case with mosaic ring chromosome 18
H Şamlı, A Özgöz, FM İçduygu, K Hekimler, Y Sıvacı, N İmirzalıoğlu
Gazi Medical Journal 24 (3), 2013
42013
Novel splice‑site variants c. 393G> A, c. 278_2A> G in exon 2 and Q705K variant in exon 3 of NLRP3 gene are associated with bipolar I disorder
KH Öztürk, GÖ Ünal
Molecular Medicine Reports 26 (3), 1-9, 2022
32022
Is microRNA 1910-3p (miR-1910-3p) a really distinctive marker for psoriasis?
M Karabacak, I Erturan, KH Öztürk, HH Ayvaz, S Korkmaz, M Yildirim, ...
Turkish journal of medical sciences 51 (3), 1098-1105, 2021
32021
Prothrombotic gene polymorphisms in young patients with cerebrovascular accident
KH Öztürk, A Özgöz, FM Içduygu, Y Soysal, ÖY Küsbeci, N Imirzalioǧlu
Journal of Clinical and Analytical Medicine 4 (4), 2013
32013
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