| Concepts of double hit and triple hit disease in multiple myeloma, entity and prognostic significance M Baysal, U Demirci, E Umit, HO Kirkizlar, EI Atli, H Gurkan, SK Gulsaran, ... Scientific Reports 10 (1), 5991, 2020 | 45 | 2020 |
| IDH1 mutations is prognostic marker for primary glioblastoma multiforme but MGMT hypermethylation is not prognostic for primary glioblastoma multiforme R Kalkan, Eİ Atli, M Özdemir, E Çiftçi, HE Aydin, S Artan, A Arslantaş Gene 554 (1), 81-86, 2015 | 35 | 2015 |
| FOXF2 is required for cochlear development in humans and mice G Bademci, C Abad, A Incesulu, F Elian, A Reyahi, O Diaz-Horta, ... Human molecular genetics 28 (8), 1286-1297, 2019 | 27 | 2019 |
| The impacts of miRNAs in glioblastoma progression R Kalkan, Eİ Atli Critical Reviews™ in Eukaryotic Gene Expression 26 (2), 2016 | 18 | 2016 |
| Wiedemann-Steiner syndrome as a differential diagnosis of Cornelia de Lange syndrome using targeted next-generation sequencing: a case report S Demir, H Gürkan, V Öz, S Yalçıntepe, Eİ Atlı, E Atlı Molecular Syndromology 12 (1), 46-51, 2021 | 17 | 2021 |
| Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development G Bademci, C Abad, FB Cengiz, S Seyhan, A Incesulu, S Guo, S Fitoz, ... The Journal of clinical investigation 130 (8), 4213-4217, 2020 | 16 | 2020 |
| The application of next generation sequencing maturity onset diabetes of the young gene panel in Turkish patients from Trakya region S Yalçıntepe, FÖ Çömlek, H Gürkan, S Demir, Eİ Atlı, E Atlı, D Eker, ... Journal of Clinical Research in Pediatric Endocrinology 13 (3), 320, 2021 | 14 | 2021 |
| Genetic screening results of individuals with high risk BRCA-related breast/ovarian cancer in Trakya region of Turkey S Demir, H Tozkir, H Gurkan, EI Atli, S Yalcintepe, E Atli, YA Sezer, D Eker, ... J buon 25 (3), 1337-1347, 2020 | 14 | 2020 |
| Schizencephaly accompanied by occipital encephalocele and deletion of chromosome 22q13. 32: a case report C Inan, NC Sayin, H Gurkan, E Atli, S Gursoy Erzincan, I Uzun, H Sutcu, ... Fetal and pediatric pathology 38 (6), 496-502, 2019 | 12 | 2019 |
| Chromosomal microarray analysis in Turkish patients with unexplained developmental delay and intellectual developmental disorders H Gürkan, EI Atli, E Atli, L Bozatli, MA Altay, S Yalcintepe, Y Özen, D Eker, ... Archives of Neuropsychiatry 57 (3), 177, 2020 | 9 | 2020 |
| Clinical implications of chromosome 16 copy number variation EI Atli, S Yalcintepe, E Atli, S Demir, C Mail, H Gurkan Molecular Syndromology 13 (3), 184-192, 2022 | 8 | 2022 |
| Investigation on the effects of modifying genes on the spinal muscular atrophy phenotype D Zhuri, H Gurkan, D Eker, Y Karal, S Yalcintepe, E Atli, S Demir, EI Atli Global Medical Genetics 9 (03), 226-236, 2022 | 7 | 2022 |
| Customised targeted massively parallel sequencing enables more precise diagnosis of patients with epilepsy EI Atli, E Atli, S Yalcintepe, S Demir, R Kalkan, D Eker, H Gurkan Internal medicine journal 52 (7), 1174-1184, 2022 | 7 | 2022 |
| The importance of multiple gene analysis for diagnosis and differential diagnosis in Charcot Marie Tooth disease S Yalçıntepe, H Gürkan, İG Doğan, S Demir, ŞÖ Sağ, ZM Kabayeğit, ... Turkish Neurosurgical, 2021 | 7 | 2021 |
| Pros and cons for fluorescent hybridization, karyotyping and next generation sequencing for diagnosis and follow-up of multiple myeloma EI Atli, H Gurkan, HO Kirkizlar, E Atli, S Demir, S Yalcintepe, R Kalkan, ... Balkan Journal of Medical Genetics 23 (2), 59-64, 2020 | 7 | 2020 |
| Prenatal diagnosis of chromosomal polymorphisms: most commonly observed polymorphism on Chromosome 9 have associations with low PAPP-A values C Inan, NC Sayin, ZN Dolgun, H Gurkan, SG Erzincan, I Uzun, H Sutcu, ... The Journal of Maternal-Fetal & Neonatal Medicine 32 (10), 1688-1695, 2019 | 7 | 2019 |
| Identification of a novel homozygous TBC1D24 mutation in a Turkish family with DOORS syndrome E Atli, H Gurkan, S Ulusal, Y Karal, EI Atli, H Tozkir Clinical Dysmorphology 27 (1), 1-3, 2018 | 7 | 2018 |
| The importance of targeted next-generation sequencing usage in cytogenetically normal myeloid malignancies EI Atli, H Gurkan, E Atli, HO Kirkizlar, S Yalcintepe, S Demir, U Demirci, ... Mediterranean Journal of Hematology and Infectious Diseases 13 (1), 2021 | 6 | 2021 |
| A case with Emanuel syndrome: extra derivative 22 chromosome inherited from the mother Eİ Atli, H Gürkan, Ü Vatansever, S Ulusal, H Tozkir Balkan Journal of Medical Genetics 18 (2), 77-82, 2015 | 6 | 2015 |
| The evaluation of risk factors leading to early deaths in patients with acute promyelocytic leukemia: a retrospective study M Baysal, V Gürsoy, FC Hunutlu, B Erkan, U Demirci, V Bas, SK Gulsaran, ... Annals of hematology 101 (5), 1049-1057, 2022 | 5 | 2022 |
Rasime KALKANProf. of Medical Genetics, European University of Lefke在 eul.edu.tr 的电子邮件经过验证
Rasime KALKANProf. of Medical Genetics, European University of Lefke在 eul.edu.tr 的电子邮件经过验证