| Clinical evaluation of R202Q alteration of MEFV genes in Turkish children E Comak, S Akman, M Koyun, CS Dogan, AU Gokceoglu, Y Arikan, ... Clinical rheumatology 33, 1765-1771, 2014 | 46 | 2014 |
| The association between intragenic SNP haplotypes and mutations of the beta globin gene in a Turkish population T Bilgen, Y Arikan, D Canatan, A Yeşilipek, I Keser Blood Cells, Molecules, and Diseases 46 (3), 226-229, 2011 | 30 | 2011 |
| The effect of HBB: c.*+ 96T> C (3'UTR+ 1570 T> C) on the mild [Beta]-thalassemia intermedia phenotype/HBB: c.*+ 96T> C (3'UTR+ 1570 T> C) mutasyonunun ilimli tip betatalasemi … T Bilgen, D Canatan, Y Arikan, A Yesilipek, İ Keser Turkish Journal of Haematology 28 (3), 219, 2011 | 10 | 2011 |
| The association between inherited thrombophilias and pregnancy-related hypertension recurrence I Mendilcioglu, T Bilgen, Y Arikan, I Keser, M Simsek, A Timuragaoglu Archives of gynecology and obstetrics 284, 837-841, 2011 | 9 | 2011 |
| C. 428_451 dup (24bp) mutation of the ARX gene detected in a Turkish family Y Arikan, T Bilgen, R Koken, S Turan, E Mihci, I Keser Genetic Counseling 23 (3), 367, 2012 | 6 | 2012 |
| Investigation of alpha globin gene mutations by complementary methods in Antalya I Keser, T Karaman MERCAN, T BILGEN, O KÜPESİZ, Y ARIKAN, ... Eastern Journal of Medicine 26 (1), 2021 | 1 | 2021 |
| Custom WES Panel Results in Patients with PCOS. Y Arıkan, T Onat Gazi Medical Journal 35, 2024 | | 2024 |
| INSR gene Exome Sequencing Results in patients with PCOS Y Arikan, T Onat MCBU SBED 10 (4), 411-419, 2023 | | 2023 |
| Polikistik Over Sendromu ve Genetik Çalışmalar Y ARIKAN Güncel Tıbbi Biyoloji ve Genetik Çalışmalar V, 115-136, 2023 | | 2023 |
| Fetal Hemoglobin Altering Effects of KLF1, BCL11A rs11886868 and XmnI-HBG2 on Transfusion Dependent Beta Thalassemia Patients: Preeliminary Study Y Arikan, BO Yolcular, E Kurtoğlu, ibrahim Keser Annals of Medical Research 30 (5), 598-603, 2023 | | 2023 |
| Erkek İnfertilitesinin Genetiği Y ARIKAN Güncel Tıbbi Biyoloji ve Genetik Çalışmalar IV, 19-40, 2023 | | 2023 |
| Evaluation of exonic copy numbers of SMN1 and SMN2 genes in SMA Y Arikan, SB Karauzum, H Uysal, E Mihci, B Nur, O Duman, S Haspolat, ... Gene 823, 146322, 2022 | | 2022 |
| FMR1 Gene Mutation Analysis and CGG Repeat Number Distribution from a Single Center Y ARIKAN, T Bilgen, E MIHÇI, Ö DUMAN, T Karaman, İ KESER Gazi Medical Journal 34 (4), 2022 | | 2022 |
| A Novel Mutation In The Control Group, What To Do Then? M Sultan Embel, T Karaman Mercan, Y Arikan, K Erdal Acta Medica 52 (Supp 3), 379-380, 2021 | | 2021 |
| Alterations of C9orf72, SOD1, TARDBP, FUS and UBQLN2 genes with amyotrophic lateral sclerosis V Ciftci, T Bilgen, S Darbas, Y Arikan, H Uysal, S Karauzum European Network to Cure ALS (ENCALS) 2018 1 (A02), 5, 2018 | | 2018 |
| Induction of fetal hemoglobin by modulation of epigenetic and genetic factors in beta thalassemia major patients İ Keser, Y Arikan, A Kupesiz, T Bilgen, E Kurtoglu European Journal of Human Genetics, 2018 | | 2018 |
| Antalya'da beta-talasemi minör/intermedia/majörlü hastaların beta-globin genindeki nadir delesyonel tıp mutasyonların MLPA yöntemiyle araştırılması D CANATAN, İ KESER, T BİLGEN, Y ARIKAN | | 2015 |
| FRI0535 Clinical Evaluation of R202Q Alteration of MEFV Genes in Turkish Children: is R202Q A Benign Polymorphism or A Disease-Causing Mutation? E Comak, S Akman, CS Dogan, AU Gokceoglu, Y Arikan, I Keser Annals of the Rheumatic Diseases 73 (Suppl 2), 580-580, 2014 | | 2014 |
| Complement Factor H Y403H Polymorphism in the Turkish Population A Yunus, B Turker, K Ibrahim Balkan Journal of Medical Genetics 13 (2), 41-45, 2011 | | 2011 |
| A RARE AND NEW SPLICE SITE MUTATION LEADING BETA-THALASSEMIA MAJOR: CODON 29 (C> T): I17 I Keser, T Bilgen, Y Arikan, Z Ozturk, P Kurt, A Yesilipek Clinical Genetics 78, 2010 | | 2010 |
