| The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space J Klughammer, B Kiesel, T Roetzer, N Fortelny, A Nemc, KH Nenning, ... Nature medicine 24 (10), 1611-1624, 2018 | 282 | 2018 |
| Multimodal analysis of cell-free DNA whole-genome sequencing for pediatric cancers with low mutational burden P Peneder, AM Stütz, D Surdez, M Krumbholz, S Semper, M Chicard, ... Nature communications 12 (1), 3230, 2021 | 134 | 2021 |
| Mutation in MEOX1gene causes a recessive Klippel-Feil syndrome subtype F Bayrakli, B Guclu, C Yakicier, H Balaban, U Kartal, B Erguner, ... BMC genetics 14, 1-7, 2013 | 84 | 2013 |
| Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair GM Dal, B Ergüner, MS Sağıroğlu, B Yüksel, OE Onat, C Alkan, T Özçelik Journal of medical genetics 51 (7), 455-459, 2014 | 55 | 2014 |
| Comparative analysis of genome-scale, base-resolution DNA methylation profiles across 580 animal species J Klughammer, D Romanovskaia, A Nemc, A Posautz, CA Seid, ... Nature Communications 14 (1), 232, 2023 | 46 | 2023 |
| TMCO1 deficiency causes autosomal recessive cerebrofaciothoracic dysplasia Y Alanay, B Ergüner, E Utine, O Haçarız, POS Kiper, EZ Taşkıran, ... American Journal of Medical Genetics Part A 164 (2), 291-304, 2014 | 35 | 2014 |
| Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 gene F Bayrakli, HG Poyrazoglu, S Yuksel, C Yakicier, B Erguner, MS Sagiroglu, ... Journal of human genetics 60 (12), 763-768, 2015 | 28 | 2015 |
| Performance comparison of Next Generation sequencing platforms B Ergüner, D Üstek, MŞ Sağıroğlu 2015 37th Annual International Conference of the IEEE Engineering in …, 2015 | 21 | 2015 |
| GPR56 homozygous nonsense mutation p. R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria T Öncü-Öner, S Hız-Kurul, B Yüksel, B Ergüner, A Saraç, H Güleryüz, ... The Turkish Journal of Pediatrics 60 (3), 229-237, 2018 | 12 | 2018 |
| Myophosphorylase (PYGM) mutations determined by next generation sequencing in a cohort from Turkey with McArdle disease G Inal-Gültekin, B Toptaş-Hekimoğlu, Z Görmez, Ö Gelişin, H Durmuş, ... Neuromuscular Disorders 27 (11), 997-1008, 2017 | 12 | 2017 |
| Additively manufactured trapezoidal grooves for wideband and high gain Ku‐band antenna Y Asci, K Yegin International Journal of RF and Microwave Computer‐Aided Engineering 30 (3 …, 2020 | 10 | 2020 |
| Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsy Y Sahin, O Güngör, Z Gormez, H Demirci, B Ergüner, G Güngör, C Dilber Acta Neurologica Belgica 117 (1), 159-167, 2017 | 9 | 2017 |
| A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetus MB Mutlu, A Cetinkaya, N Koc, G Ceylaner, B Erguner, H Aydın, ... European Journal of Medical Genetics 59 (11), 604-606, 2016 | 9 | 2016 |
| Identifying disease-causing mutations with privacy protection M Akgün, AB Ünal, B Ergüner, N Pfeifer, O Kohlbacher Bioinformatics 36 (21), 5205-5213, 2020 | 8 | 2020 |
| Buffy coat signatures of breast cancer risk in a prospective cohort study FFL Chung, SG Maldonado, A Nemc, L Bouaoun, V Cahais, C Cuenin, ... Clinical epigenetics 15 (1), 102, 2023 | 7 | 2023 |
| Radiomic features define risk and are linked to DNA methylation attributes in primary CNS lymphoma KH Nenning, J Gesperger, J Furtner, A Nemc, T Roetzer-Pejrimovsky, ... Neuro-Oncology Advances 5 (1), vdad136, 2023 | 6 | 2023 |
| Prediction and classification for GPCR sequences based on ligand specific features B Ergüner, Ö Erdoğan, U Sezerman Computer and Information Sciences–ISCIS 2006: 21th International Symposium …, 2006 | 6 | 2006 |
| Finding underlying genetic mechanisms of two patients with autism spectrum disorder carrying familial apparently balanced chromosomal translocations B Toraman, SÇ Bilginer, ST Hesapçıoğlu, Z Göker, HO Soykam, ... The Journal of Gene Medicine 23 (4), e3322, 2021 | 5 | 2021 |
| Detection of allele frequencies of common c. 511C> T and c. 625G> A variants in the ACADS gene in the Turkish population M Kilic, B Erguner, C Koşukçu, R ÖZGÜL Turkish Journal of Pediatrics 62 (1), 2020 | 2 | 2020 |
| Human genome in a smart card M Akgün, B Ergüner, AO Bayrak, MŞ Sağıroğlu International Conference on Health Informatics 2, 310-316, 2014 | 2 | 2014 |
Mahmut Samil SagirogluCTO, ErlabVerified email at erlab.com.tr
