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EISSN 2148-5607

TJG IS INDEXED IN WEB OF SCIENCE AND PUBMED IMPACT FACTOR: 1.2

Turkish Journal of Gastroenterology

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HIGHLY CITED ARTICLES

HBV and HCV are the risk factors in CCA

Tan et al.

Serum resolvin levels in irritable bowel syndrome

Karatay and Gül Utku

Microbial improvement after intervention

Qian et al.

18F-FDGPET/CT in gallbladder carcinoma

Arslan et al.

Bezoar in endoscopy

Gökbulut et al.

Effect of vitamin D on CD40L gene expression in UC

Sharifi et al.

ERCP for acute cholangitis

Khamaysi and Taha

Inborn metabolic causes of fatty liver disease

Yıldız and Sivri

Gastric and small intestinal TSA

Kiremitci et al.

COVID-19 in Hepatology and Liver transplantation

Kabaçam et al.

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Characterization of 23S rRNA gene mutation in primary and secondary clarithromycin-resistant Helicobacter pylori strains from East China

Zhu ZHEN-HUA, Huang DE-QIANG, Xie YONG, Liu LIN-LIN, Lu NONG-HUA

(Turk J Gastroenterol 2013; 24: 5-9) DOI: 10.4318/tjg.2013.0525

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The prevalence of primary hereditary hemochromatosis in central Anatolia

Halit KARACA, Kadri GÜVEN, Müge ÖNAL, Şebnem GÜRSOY, Mevlüt BAŞKOL, Yusuf ÖZKUL

(Turk J Gastroenterol 2013; 24: 43-50) DOI: 10.4318/tjg.2013.0579

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Two juvenile polyps, hereditary hemorrhagic telangiectasia and SMAD4 mutation

Oya BALCI, Figen ÖZÇAY

(Turk J Gastroenterol 2013; 24: 57-60) DOI: 10.4318/tjg.2013.0542

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Characterization of 23S rRNA gene mutation in primary and secondary clarithromycin-resistant Helicobacter pylori strains from East China

The prevalence of primary hereditary hemochromatosis in central Anatolia

Two juvenile polyps, hereditary hemorrhagic telangiectasia and SMAD4 mutation

Relationship between overexpression of ras p21 oncoprotein and K-ras codon 12 and 13 mutations in Turkish colorectal cancer patients

Definition of C282Y mutation in a hereditary hemochromatosis family from Turkey

A case of Budd-Chiari syndrome secondary to multiple thrombogenic conditions: A case report and review of literature*

Extra-gastrointestinal stromal tumor presenting as a surgical emergency

Diagnostic value of the JAK2 V617F mutation for latent chronic myeloproliferative disorders in patients with budd-chiari syndrome and/or portal vein thrombosis

Genotype-phenotype relationship in Iranian patients with cystic fibrosis

Mismatch repair gene expression in gastroesophageal cancers

Distribution of nucleotide variants in the DNA sequence of ERCC1 and XRCC1 genes and the effect of phenotype in patients with gastric cancer

A large Turkish pedigree with multiple endocrine neoplasia type 1 syndrome carrying a rare mutation: c.1680_1683 del TGAG

Comparison of Drug Resistance of Helicobacter pylori Between Children and Adults in Jilin, China

Molecular Characterization of Clarithromycin Resistance in Helicobacter pylori Strains

Predicting Duodenal Cancer Risk in Patients with Familial Adenomatous Polyposis Using Machine Learning Model