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H. K. Kurtulgan · SciRah

Researcher profile · Semantic Scholar

H. K. Kurtulgan

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H. K. Kurtulgan — researcher profile on SciRah

h-index: 9
Works: 30
Citations: 170

Most-cited papers

Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers
O. Ozdemır, I. Sezgin, H. K. Kurtulgan, F. Candan +10 more
2011Molecular Biology Reports39 citations
Semantic Scholar
Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia
M. Yıldırım, H. K. Kurtulgan, O. Ozdemır, H. Kilicgun +3 more
2019Annals of Saudi Medicine18 citations Open access
Semantic Scholar
The type and prevalence of chromosomal abnormalities in couples with recurrent first trimester abortions: A Turkish retrospective study.
M. Yıldırım, S. Karakuş, H. K. Kurtulgan, Burak Başer +1 more
2019Journal of Gynecology Obstetrics and Human Reproduction15 citations
Semantic Scholar
The Association of Plasminogen Activator Inhibitor Type 1 (PAI-1) Level and PAI-1 4G/5G Gene Polymorphism with the Formation and the Grade of Endometrial Cancer
M. Yıldırım, S. Karakuş, H. K. Kurtulgan, H. Kılıçgün +2 more
2017Biochemical Genetics15 citations
Semantic Scholar
CCR2 polymorphism in chronic renal failure patients requiring long-term hemodialysis.
I. Sezgin, Binnur Koksal, Gokhan Bagci, H. K. Kurtulgan +1 more
2011Internal medicine14 citations Open access
Semantic Scholar
Angiotensin-Converting Enzyme (ACE) I/D and Alpha-Adducin (ADD1) G460W Gene Polymorphisms in Turkish Patients with Severe Chronic Tinnitus.
Salim Yuce, E. Sancakdar, Gokhan Bagci, S. Koç +4 more
2016The journal of international advanced otology13 citations Open access
Semantic Scholar
Prevalence of Fabry Disease in Familial Mediterranean Fever Patients from Central Anatolia of Turkey
C. Huzmeli, F. Candan, Demet Alaygut, Gokhan Bagci +5 more
2016Biochemical Genetics13 citations
Semantic Scholar
Megacystis Microcolon Intestinal Hypoperistalsis Syndrome in Which a Different De Novo Actg2 Gene Mutation was Detected: A Case Report
E. Korğalı, A. Yavuz, Cemile Ece Çağlar Şimşek, Cengiz Güney +5 more
2018Fetal and Pediatric Pathology12 citations
Semantic Scholar
Ocular and Genetic Characteristics Observed in Two Cases of Fish-Eye Disease
Melih Ustaoglu, Nilgün Solmaz, Burak Başer, H. K. Kurtulgan +1 more
2018Cornea11 citations
Semantic Scholar
Bcıı—RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long-term hemodialysis
O. Ozdemır, M. Kayataş, S. Çetinkaya, M. Yıldırım +5 more
2015Renal Failure6 citations Open access
Semantic Scholar
PAI-1 4G/4G gene polymorphism is associated with higher serum lipid level in Turkish population.
N. Katrancioglu, O. Karahan, H. K. Kurtulgan, Umut Serhat Sanrı +1 more
2011\n Volume: 33, Issue: 3\n 307-311\n \n4 citations Open access
Semantic Scholar
Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion
H. K. Kurtulgan, L. Ozer, M. Yıldırım, Evrim Ünsal +4 more
2015Molecular Cytogenetics3 citations Open access
Semantic Scholar
MCP-1-2518 A>G and CCR2 V64I polymorphisms in Turkish patients with lung cancer
Binnur Bağcı, S. Arslan, H. K. Kurtulgan, I. Sezgin +2 more
20162 citations
Semantic Scholar
The Association of MCP-1 Level and MCP-1 -2518 A/G and CCR2 190 G/A Gene Polymorphisms with COPD and Pulmonary Hypertension
İlişkisi, M. Yıldırım, Serdar Berk, H. K. Kurtulgan +6 more
2021Gazi Medical Journal1 citations Open access
Semantic Scholar
Relationship Between Childhood Asthma and C3435T Multidrug Resistance 1 Gene
Fatma Duksal, H. K. Kurtulgan, Ömer Cevit, Binnur Koksah
2015The Annals of Clinical and Analytical Medicine1 citations
Semantic Scholar
Vitamin D deficiency, myopathy and VDR gene polymorphism in a young woman
M. Yıldırım, H. K. Kurtulgan, A. Şahin
20151 citations Open access
Semantic Scholar
A Balanced Robertsonian Translocation (13;14) of a Male: A Case Report
F. Ozen, Z. Sağlam, H. K. Kurtulgan, Abdulah Ozen
20141 citations Open access
Semantic Scholar
Plazminojen aktivatör inhibitör-1 (PAI-1) 4G/4G polimorfizminin gebelik kayiplariyla ilişkisi The association of plasminogen activator inhibitor-1 (PAI-1) 4G/4G polymorphism with miscarriages
M. Yıldırım, H. K. Kurtulgan
20141 citations
Semantic Scholar
Methylation profile of CD247 and FOXP3 genes and frequency of certain HLA-DQ haplotypes in Celiac disease.
M. Yıldırım, H. Ataseven, H. K. Kurtulgan, Şeyma Taştemur +1 more
2025Clinics And Research in Hepatology and Gastroenterology0 citations
Semantic Scholar
A possible interaction of TIMP-1 and TSP-1 with familial mediterranean fever
M. Yıldırım, H. K. Kurtulgan, H. Kilicgun, D. Bakır +1 more
2019Journal of Clinical and Analytical Medicine0 citations
Semantic Scholar
Anti-inflammatory and apoptotic effects of quercetin and curcumin on chronic myeloid leukemia cancer cells
A. Dursun, L. Ozer, H. K. Kurtulgan, Burak Başer +5 more
20180 citations
Semantic Scholar
Hypermethylated promoter profiles for tumour supressor APC , p53, MSH6 and MGMT genes in CRC tumours
Ebru Sik, O. Ozdemır, H. K. Kurtulgan, Mine Urfali +2 more
20160 citations
Semantic Scholar
Relationship Between Childhood Asthma and C 3435 T Multidrug Resistance 1 Gene Çocukluk Astımı ve C 3435 T “ Multidrug Resistance 1 ” Geni
Fatma Duksal, H. K. Kurtulgan, Ömer Cevit, Binnur Köksal
20160 citations
Semantic Scholar
Prevalence of Fabry Disease in Familial Mediterranean Fever Patients from Central Anatolia of Turkey
C. Huzmeli, F. Candan, Demet Alaygut, Gokhan Bagci +5 more
2016Biochemical Genetics0 citations
Semantic Scholar
Role of MTHFR gene polymorphisms , serum tissue inhibitor of metalloproteinases-1 , thymus chemokine-1 and thrombospondin-1 in endometrial cancer
M. Yıldırım, H. Kılıçgün, H. K. Kurtulgan, S. Karakuş +3 more
20160 citations
Semantic Scholar
A female infant case with tetrasomy 18p Bir dişi infant tetrazomi 18p olgusu
M. Yıldırım, H. K. Kurtulgan, L. Ozer
20150 citations
Semantic Scholar
A female infant case with tetrasomy 18p
M. Yıldırım, H. K. Kurtulgan, L. Ozer, S. Karakuş +1 more
20150 citations Open access
Semantic Scholar
Vitamin D deficiency, myopathy and VDR gene polymorphism in a young woman Genç bayan hastada D vitamini eksikliği, miyopati ve VDR gen polimorfizmi
M. Yıldırım, H. K. Kurtulgan
20150 citations
Semantic Scholar
A neonate with Adams Oliver syndrome: A case report and review of the literature
H. K. Kurtulgan, F. Bolat, Gülseren Erkoca Göktolga, Nejmiye Akkuş +2 more
20130 citations
Semantic Scholar
PAI-1 4G/4G gene polymorphism is associated with higher serum lipid level in Turkish population. PAI-1 4G/4G gen polimorfizmi Türk popülasyonunda yüksek serum lipid düzeyleri ile ilişkilidir.
O. Karahan, H. K. Kurtulgan
20110 citations
Semantic Scholar

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Burak Başer×6
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Gokhan Bagci×6
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Binnur Bağcı×4

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L. Ozer — researcher profile on SciRah

Binnur Koksal×3

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H. Kılıçgün×3

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H. Kılıçgün — researcher profile on SciRah