| Psoriasis: An Immunogenetic Perspective A Kocaaga, M Kocaaga Glob Med Genet 9 (1), 1-55, 2022 | 12 | 2022 |
| Identification of novel gene variants in children with drug-resistant epilepsy: expanding the genetic spectrum A Kocaaga, S Yimenicioglu Pediatric Neurology 139, 7-12, 2023 | 5 | 2023 |
| Association Between IL28B, IL29 Gene Polymorphisms and Clinical Manifestations of Behçet’s Disease G Cakmak Genc, S Karakas Celık, A Kocaaga, R Koca, A Dursun Immunological Investigations 50 (8), 906-913, 2021 | 5 | 2021 |
| First report of tethered cord syndrome in a patient with Verheij syndrome A Kocaaga, S Yimenicioglu, Y Ö Atikel, Ö O Yavuz Ophthalmic Genetics, 1-5, 2022 | 4 | 2022 |
| Association of NOD1, NOD2, PYDC1 and PYDC2 genes with Behcet’s disease susceptibility and clinical manifestations A Kocaaga, G Cakmak Genc, S Karakas Celık, R Koca, A Dursun Ophthalmic Genetics 42 (6), 691-697, 2021 | 3 | 2021 |
| Identification of novel variants in retinitis pigmentosa genes by whole-exome sequencing A Kocaaga, İÖ Aköz, NU Demir, B Paksoy Revista da Associação Médica Brasileira 69 (5), 2023 | 2 | 2023 |
| The pattern of chromosomal abnormalities in recurrent miscarriages: a single center retrospective study A Kocaaga, H Kılıc, S Gülec Annals of Saudi Medicine 42 (6), 2022 | 2 | 2022 |
| Diagnosis and Genetic Analysis of Polycythemia In Children and a Novel EPAS1 Gene Mutation MH Cakmak, Ö Kartal, A Kocaağa, Y Bildirici Pediatrics & Neonatology, 2022 | 2 | 2022 |
| Novel NR2F1 variant identified by whole-exome sequencing in a patient with Bosch–Boonstra–Schaaf optic atrophy syndrome A Kocaaga, S Yimenicioglu, HH Gürsoy Indian Journal of Ophthalmology 70 (7), 2022 | 2 | 2022 |
| Genetics of Behçet’s Disease A Kocaaga Rare Diseases - Recent Advances [Working Title], 2021 | 2 | 2021 |
| Evaluation of molecular and clinical findings in children with Neurofibromatosis type 1: Identification of 15 novel variants Y Bildirici, A Kocaaga, CN Karademir-Arslan, S Yimenicioglu Pediatric Neurology 149, 2023 | 1 | 2023 |
| Incidence and spectrum of thrombophilia in women with recurrent pregnancy loss: a retrospective study A KOCAAĞA, H KILIÇ, S GÜLEÇ Eskisehir Medical Journal 4 (2), 2023 | 1 | 2023 |
| A p.Val412Serfs pathogenic variant associated with Wolfram-like syndrome and leukodystrophy A Kocaaga, S Yimenicioglu, M Bayav The Egyptian Journal of Neurology, Psychiatry and Neurosurgery 59 (6), 2023 | 1 | 2023 |
| Case report the novel homozygous ADCY6 c. 413G> A; p. R138H gene variant associated with lethal congenital contracture syndrome 8 in a female patient with epilepsy and pachygyria S Yimenicioğlu, A Kocaağa, B Paksoy Hong Kong J Paediatr 28 (1), 36-40, 2023 | 1 | 2023 |
| Association of NOD1 and NOD2 Polymorphisms With Susceptibility to Subacute Sclerosing Panencephalitis A Kocaaga, G Cakmak Genc, S Karakas Celik, İ E. Piskin, M Calik, ... Journal of Child Neurology, 2022 | 1 | 2022 |
| An immunogenetic perspective of ANCA-associated vasculitides A Kocaaga, M Kocaaga Egyptian Rheumatology and Rehabilitation 49 (1), 2022 | 1 | 2022 |
| Presentation of an Infant with Chromosome 18p Deletion Syndrome and Asymmetric Septal Hypertrophy A Kocaaga, S Yimenicioglu Glob Med Genet 9 (1), 1-55, 2022 | 1 | 2022 |
| The immunogenetics of subacute sclerosing panencephalitis: A comprehensive review A Kocaaga Karnataka Paediatric Journal 36 (4), 151-154, 2022 | 1 | 2022 |
| Case report: Pai syndrome with multiple ventricular septal defect and without cleft palate A Kocaaga, Y Bildirici, S Yimenicioglu, NC Karademir-Arslan, C Vural, ... Clinical Neurology and Neurosurgery 236, 108045, 2024 | | 2024 |
| The genetic spectrum of polycystic kidney disease in children A Kocaaga, OY Atikel, M Sak, K Taner Revista da Associação Médica Brasileira 11 (69), 2023 | | 2023 |
Sevgi YimenicioğluSağlık Bilimleri Üniversitesi Sağlık Uygulama ve Araştırma Merkezi Eskişehir Şehir Hastanesi在 sbu.edu.tr 的电子邮件经过验证
