Hasan Doğan

Dr. Hasan Doğan

orcid

Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 2015 in Gene
Verified
Journal Article
Closed access
HDHasan Doğan
Hasan Doğan
OBOmer Faruk Bayrak
Omer Faruk Bayrak
MEMucahit Emet
Mucahit Emet
MKMustafa Keles
Mustafa Keles
SGSukru Gulluoglu
Sukru Gulluoglu
IPIbrahim Pirim
Ibrahim Pirim

1 May 2007
Verified
Journal Article
Closed access
FGFuat Gündogdu
Fuat Gündogdu
YIYahya Islamoglu
Yahya Islamoglu
IPIbrahim Pirim
Ibrahim Pirim
YGYekta Gurlertop
Yekta Gurlertop
HDHasan Doğan
Hasan Doğan
HSHuseyin Senocak
Huseyin Senocak

1 July 2014 in BMC Medical Genetics
Verified
Journal Article
Open access
PDF file
HDHasan Doğan
Hasan Doğan
FAFatih Akdemir
Fatih Akdemir
STSener Tasdemir
Sener Tasdemir
OAOmer Atis
Omer Atis
EDEda Diyarbakir
Eda Diyarbakir
MIMevlit Ikbal
Mevlit Ikbal
Familial Mediterranean Fever (FMF), characterized by recurrent fever and inflammation of serous membranes, is an autosomal recessive disease caused by mutations in the Mediterranean fever (MEFV) gene. Around 296 mutations have been reported to date.

19 March 2014 in Multidisciplinary Respiratory Medicine
Verified
Journal Article
Open access
PDF file
HDHasan Doğan
Hasan Doğan
MAMetin Akgün
Metin Akgün
OAOmer Araz
Omer Araz
EUElif Yilmazel Ucar
Elif Yilmazel Ucar
OYOzgur Yoruk
Ozgur Yoruk
IPIbrahim Pirim
Ibrahim Pirim
Denim sandblasting may cause silicosis as a result of free crystalline silica inhalation. Its pathogenesis remains unclear, but autoimmunity may play a role in the development of silicosis. The present study aimed to investigate the relationships between human leukocyte antigen (HLA) and the severity and latency period of silicosis.

1 February 2013 in Transfusion and Apheresis Science
Verified
Journal Article
Closed access
RYRahsan Yildirim
Rahsan Yildirim
MGMEHMET ALI GÜNDOGDU
MEHMET ALI GÜNDOGDU
AOAysu Ozbıcer
Aysu Ozbıcer
IKIlhami Kiki
Ilhami Kiki
FEFuat Erdem
Fuat Erdem
HDHasan Doğan
Hasan Doğan

Verified
Journal Article
Open access
PDF file
HDHasan Doğan
Hasan Doğan
AKAslı Kara
Aslı Kara
EÇerdem çankaya
erdem çankaya
EBEDA BALKAN
EDA BALKAN
MGMuhammet Ali Gürbüz
Muhammet Ali Gürbüz
MAMerve Aykaç
Merve Aykaç
This prospective cross-sectional study aimed to evaluate leukocyte DNA damage in coronavirus disease (COVID-19) patients. In this study, 50 COVID-19-positive patients attending the Erzurum City Hospital Internal Medicine Outpatient Clinic and 42 control group patients were included. DNA damage was detected in living cells through leukocyte isolation in 50 COVID-19-positive patients using the comet assay method. DNA tail/head (olive) moments were evaluated and compared. White blood cells (WBC), red blood cells (RBC), hemoglobin (HGB), neutrophils (NEU), lymphocytes (LYM), eosinophils (EO), monocytes (MONO), basophils (BASO), platelets (PLT), and the neutrophil/lymphocyte ratio (NLR) were analyzed. The RBC, lymphocyte, eosinophil, and monocyte means were significantly higher in the control group (p < 0.05), whereas the HGB and neutrophile means were significantly higher in the study group (p < 0.05). There were significant negative correlations between COVID-19 and RBC (r = −0.863), LYM (r = −0.542), EO (r = −0.686), and MONO (r = −0.385). Meanwhile, there were significant positive correlations between COVID-19 and HGB (r = 0.863), NEU (r = 0.307), tail moment (r = 0.598), and olive moment (r = 0.582). Both the tail and olive moment mean differences were significantly higher in the study group, with higher ranges (p < 0.05). COVID-19 infection caused statistically significant increases in both the tail and olive damage percentage in patients, causing DNA damage. Lastly, the NLR rate was associated with the presence and progression of COVID-19.