| The genomics of arthrogryposis, a complex trait: candidate genes and further evidence for oligogenic inheritance D Pehlivan, Y Bayram, N Gunes, ZC Akdemir, A Shukla, T Bierhals, ... The American Journal of Human Genetics 105 (1), 132-150, 2019 | 94 | 2019 |
| Correlation with platelet parameters and genetic markers of Thrombophilia Panel (Factor II g. 20210G> A, factor V leiden, MTHFR (C677T, A1298C), PAI-1, β-Fibrinogen, factor … S Tasdemir, HB Erdem, I Sahin, L Ozel, G Ozdemir, R Eroz, A Tatar Neuromolecular medicine 18, 170-176, 2016 | 26 | 2016 |
| Vici syndrome in siblings born to consanguineous parents S Tasdemir, I Sahin, A Cayır, I Yuce, S Ceylaner, A Tatar American Journal of Medical Genetics Part A 170 (1), 220-225, 2016 | 22 | 2016 |
| Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disorders AC Ceylan, S Citli, HB Erdem, I Sahin, E Acar Arslan, M Erdogan Molecular cytogenetics 11, 1-9, 2018 | 21 | 2018 |
| The Relationship Between Endothelial Nitric Oxide Synthase Gene (NOS3) Polymorphisms, NOS3 Expression, and Varicocele CY Kahraman, S Tasdemir, I Sahin, E Marzioglu Ozdemir, O Yaralı, ... Genetic testing and molecular biomarkers 20 (4), 191-196, 2016 | 16 | 2016 |
| SMN1 gene copy number analysis for spinal muscular atrophy (SMA) in a Turkish cohort by CODE-SEQ technology, an integrated solution for detection of SMN1 and SMN2 copy numbers … AC Ceylan, HB Erdem, İ Şahin, M Agarwal Neurological Sciences 41, 2575-2584, 2020 | 13 | 2020 |
| Myhre syndrome with novel findings: bilateral congenital cortical cataract, bilateral papilledema, accessory nipple, and adenoid hypertrophy HB Erdem, I Sahin, A Tatar Clinical Dysmorphology 27 (1), 12-14, 2018 | 11 | 2018 |
| Association Between Human Hair Loss and the Expression Levels of Nucleolin, Nucleophosmin, and UBTF Genes S Tasdemir, R Eroz, H Dogan, HB Erdem, I Sahin, M Kara, RI Engin, ... Genetic Testing and Molecular Biomarkers 20 (4), 197-202, 2016 | 10 | 2016 |
| Mitochondrial DNA deletions in patients with esophagitis, Barrett’s esophagus, esophageal adenocarcinoma and squamous cell carcinoma M Keles, I Sahin, A Kurt, C Bozoglu, G Simsek, E Kabalar, A Tatar African health sciences 19 (1), 1671-1676, 2019 | 9 | 2019 |
| An eight‐case 1q21 region series: novel aberrations and clinical variability with new features AC Ceylan, I Sahin, HB Erdem, G Kayhan, PO Simsek‐Kiper, GE Utine, ... Journal of Intellectual Disability Research 63 (6), 548-557, 2019 | 8 | 2019 |
| Becker’s myotonia: novel mutations and clinical variability in patients born to consanguineous parents I Sahin, HB Erdem, H Tan, A Tatar Acta Neurologica Belgica 118, 567-572, 2018 | 8 | 2018 |
| Holoprosencephaly: ZIC2 mutation in a case with panhypopituitarism S Tasdemir, I Sahin, A Cayır, H Doneray, BD Solomon, M Muenke, I Yuce, ... Journal of Pediatric Endocrinology and Metabolism 27 (7-8), 777-781, 2014 | 7 | 2014 |
| Positive correlation between platelet parameters and genetic markers of thrombophilia panel in recurrent pregnancy loss HB Erdem, AC Ceylan, A Kaya, T Bahsi, ZS Erdem, I Sahin, A Tatar Eurasian Journal of Family Medicine 7 (1), 19-28, 2018 | 6 | 2018 |
| Recurrent Rab3gap1 mutations in the Turkish population S Tasdemir, I Sahin, DJ Morris-Rosendahl, E Marzioglu, A Cayir, I Yuce, ... Genetic Counseling 26 (4), 415, 2015 | 6 | 2015 |
| A rare cause of dyspnea in emergency medicine: Keutel syndrome. A Bayramoğlu, M Saritemur, S Tasdemir, M Omeroglu, HB Erdem, I Sahin The American Journal of Emergency Medicine 34 (5), 935. e3-5, 2015 | 5 | 2015 |
| High expression of stem cell-related genes in polyps with villous features and high-grade dysplasia support malignant phenotype and colorectal carcinogenesis I Sahin, B Gündoğdu, AC Ceylan, HB Erdem, A Tatar Asian Pacific Journal of Cancer Prevention: APJCP 22 (8), 2429, 2021 | 4 | 2021 |
| Retrospective analysis of 1429 cases who underwent amniocentesis and cordocentesis. Ş Taşdemir, M Yılmaz, İ Şahin, HB Erdem, RA Al, M İngeç, A Tatar Perinatal Journal/Perinatoloji Dergisi 22 (3), 2014 | 4 | 2014 |
| Investigation of germline variants in Bahraini women with breast cancer using next-generation sequencing based-multigene panel G Al-Kafaji, G Jassim, A AlHajeri, AMT Alawadhi, M Fida, I Sahin, F Alali, ... Plos one 18 (9), e0291015, 2023 | 3 | 2023 |
| Hereditary spastic paraplegia: new insights into clinical variability and spasticity–ataxia phenotype, and novel mutations I Sahin, H Saat Acta Neurologica Belgica, 1-7, 2021 | 3 | 2021 |
| Mitochondrial DNA copy number alterations in familial mediterranean fever patients. HB Erdem, AC Ceylan, I Sahin, Z Sever-Erdem, S Citli, A Tatar Bratislavske Lekarske Listy 119 (7), 425-428, 2018 | 3 | 2018 |
Abdulgani TatarAtatürk Üniversitesi Tıp Fak. Tıbbi Genetik AD在 atauni.edu.tr 的电子邮件经过验证
