Yayınlar & Eserler

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Oral microbiota and dental caries data from monozygotic and dizygotic twin children

Kasimoglu Y., Koruyucu M., Birant S., Karacan İ. , Topcuoglu N., Tuna E., et al.
SCIENTIFIC DATA, cilt.7, sa.1, 2020 (SCI İndekslerine Giren Dergi) identifier identifier

Geographical and temporal distribution of SARS-CoV-2 clades in the WHO European Region, January to June 2020

Alm E. , Broberg E. K. , Connor T., Hodcroft E. B. , Komissarov A. B. , Maurer-Stroh S., et al.
EUROSURVEILLANCE, cilt.25, sa.32, ss.7-14, 2020 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Diagnostic utility of a targeted next-generation sequencing gene panel in the clinical suspicion of systemic autoinflammatory diseases: a multi-center study.

Karacan İ. , Balamir A., Uğurlu S., Aydın A., Everest E., Zor S., et al.
Rheumatology international, cilt.39, ss.911-919, 2019 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Oral microbial dysbiosis in patients with Kostmann syndrome.

Topcuoglu N., Erdem A., Karacan I. , Kulekci G.
Journal of medical microbiology, cilt.68, ss.609-615, 2019 (SCI İndekslerine Giren Dergi) identifier identifier identifier

A Novel <i>ATP6V0A2</i> Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing

Karacan İ. , Diz K., KARAKUŞ F., SOLAKOĞLU S., TOLUN A., HANÇER V., et al.
Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.36, ss.29-36, 2019 (SCI Expanded İndekslerine Giren Dergi) Creative Commons License identifier identifier identifier

Detection of the unknown components of the oral microflora of teeth with periapical radiolucencies in a Turkish population using next-generation sequencing techniques.

İRIBOZ E., Arıcan Ö., KOLUKıRıK M., Karacan I. , Sazak Ö.
International endodontic journal, cilt.51, ss.1349-1357, 2018 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

<i>LACC1</i> Gene Defects in Familial Form of Juvenile Arthritis.

Karacan I. , Uğurlu S., Şahin S., Everest E., Kasapçopur Ö., Tolun A., et al.
The Journal of rheumatology, cilt.45, ss.726-728, 2018 (SCI Expanded İndekslerine Giren Dergi) Creative Commons License identifier identifier identifier

Other autoinflammatory disease genes in an FMF-prevalent population: a homozygous MVK mutation and a novel heterozygous TNFRSF1A mutation in two different Turkish families with clinical FMF.

Karacan İ. , Uğurlu S., Tolun A., Tahir T., Ozdogan H.
Clinical and experimental rheumatology, ss.75-81, 2017 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Diğer Dergilerde Yayınlanan Makaleler

SCREENING SLC2A1 GENE FOR SEQUENCE AND COPY NUMBER VARIATIONS ASSOCIATED WITH GLUT-1 DEFICIENCY SYNDROME

Ornek Erguzeloglu C., KARA B., Karacan İ. , Ozdemir O., Kesim Y., BEBEK N., et al.
JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, cilt.83, sa.3, ss.177-183, 2020 (ESCI İndekslerine Giren Dergi) identifier

The origin of SARS-CoV-2 in Istanbul: Sequencing findings from the epicenter of the pandemic in Turkey.

Karacan İ. , Akgun T., Agaoglu N., Irvem A., Alkurt G., Yildiz J., et al.
Northern clinics of Istanbul, cilt.7, ss.203-209, 2020 (ESCI İndekslerine Giren Dergi) identifier identifier