Comparison of SUV(max) Values Obtained from F-18 FDG PET/CT and Cell-free DNA Levels Measured from Plasma in Oncology Patients

Tekijä Çelik, Fatmanur, Tan, Yusuf Ziya, Özdemir, Semra, Sılan, Fatma
Julkaisussa Mol Imaging Radionucl Ther (2019)

Contribution of the STAT4 rs7574865 gene polymorphism to the susceptibility to autoimmune thyroiditis in healthy Turk population and psoriatic subgroups

Tekijä Hiz, Meliha M., Kılıç, Sevilay, Işık, Selda, Ogretmen, Zerrin, Silan, Fatma
Julkaisussa Cent Eur J Immunol (2016)

Is there any increased risk of hypertension, diabetes and cardiac diseases in psoriatic patients with TNF-α G238A and G308A polymorphism?

Tekijä Işik, Selda, Hız, Meliha Merve, Kılıç, Sevilay, Öğretmen, Zerrin, Silan, Fatma
Julkaisussa Postepy Dermatol Alergol (2016)

Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism in psoriasis cases with hypertension

Tekijä Ogretmen, Zerrin, Hiz, Meliha Merve, Silan, Fatma, Uludag, Ahmet, Ozdemir, Ozturk
Julkaisussa Ann Saudi Med (2014)

Tumour necrosis factor alpha, ınterleukin 10 and ınterleukin 6 gene polymorphisms of ıschemic stroke patients ın south Marmara region of Turkey

Tekijä Ozkan, Adile, Sılan, Fatma, Uludağ, Ahmet, Degirmenci, Yıldız, Ozisik Karaman, Handan Isin
Julkaisussa Int J Clin Exp Pathol (2015)

Evaluation inflammatory markers of hemogram parameters in primary ovarian insufficiency

Tekijä Demir, Bülent, Sarıdaş Demir, Süreyya, Özkan Karacaer, Kübra, Paşa, Semir, Sılan, Fatma
Julkaisussa Turk J Obstet Gynecol (2020)

Endothelial function and germ-line ACE I/D, eNOS and PAI-1 gene profiles in patients with coronary slow flow in the Canakkale population: multiple thrombophilic gene profiles in co...

Tekijä Gazi, Emine, Temiz, Ahmet, Altun, Burak, Barutcu, Ahmet, Colkesen, Yucel, Silan, Fatma, Ozdemir, Ozturk
Julkaistu 2014

Fetal Vegf Genotype is More Important for Abortion Risk than Mother Genotype

Tekijä Yalcintepe, Sinem Atik, Silan, Fatma, Hacivelioglu, Servet Ozden, Uludag, Ahmet, Cosar, Emine, Ozdemir, Ozturk
Julkaistu 2014

Multiple Inherited Thrombophilic Gene Polymorphisms in Spontaneous Abortions in Turkish Population

Tekijä Yalcintepe, Sinem, Ozdemir, Ozturk, Hacivelioglu, Servet Ozden, Akurut, Cisem, Koc, Evrim, Uludag, Ahmet, Cosar, Emine, Silan, Fatma
Julkaisussa Int J Mol Cell Med (2015)

Intercellular Adhesion Molecule-1 K469E and Angiotensinogen T207M Polymorphisms in Coronary Slow Flow

Tekijä Gazi, Emine, Barutcu, Ahmet, Altun, Burak, Temiz, Ahmet, Bekler, Adem, Urfali, Mine, Silan, Fatma, Colkesen, Yucel, Ozdemir, Ozturk
Julkaisussa Med Princ Pract (2014)

MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss

Tekijä Bademci, Guney, Abad, Clemer, Incesulu, Armagan, Rad, Abolfazl, Alper, Ozgul, Kolb, Susanne M., Cengiz, Filiz B., Diaz-Horta, Oscar, Silan, Fatma, Mihci, Ercan, Ocak, Emre, Najafi, Maryam, Maroofian, Reza, Yilmaz, Elanur, Nur, Banu G., Duman, Duygu, Guo, Shengru, Sant, David W., Wang, Gaofeng, Monje, Paula V., Haaf, Thomas, Blanton, Susan H., Vona, Barbara, Walz, Katherina, Tekin, Mustafa
Julkaisussa Hum Genet (2018)

The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance

Tekijä Pehlivan, Davut, Bayram, Yavuz, Gunes, Nilay, Coban Akdemir, Zeynep, Shukla, Anju, Bierhals, Tatjana, Tabakci, Burcu, Sahin, Yavuz, Gezdirici, Alper, Fatih, Jawid M., Gulec, Elif Yilmaz, Yesil, Gozde, Punetha, Jaya, Ocak, Zeynep, Grochowski, Christopher M., Karaca, Ender, Albayrak, Hatice Mutlu, Radhakrishnan, Periyasamy, Erdem, Haktan Bagis, Sahin, Ibrahim, Yildirim, Timur, Bayhan, Ilhan A., Bursali, Aysegul, Elmas, Muhsin, Yuksel, Zafer, Ozdemir, Ozturk, Silan, Fatma, Yildiz, Onur, Yesilbas, Osman, Isikay, Sedat, Balta, Burhan, Gu, Shen, Jhangiani, Shalini N., Doddapaneni, Harsha, Hu, Jianhong, Muzny, Donna M., Boerwinkle, Eric, Gibbs, Richard A., Tsiakas, Konstantinos, Hempel, Maja, Girisha, Katta Mohan, Gul, Davut, Posey, Jennifer E., Elcioglu, Nursel H., Tuysuz, Beyhan, Lupski, James R.
Julkaisussa Am J Hum Genet (2019)