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Bekir Ergüner
Bekir Ergüner
Senior Computational Scientist, Exscientia
Verifierad e-postadress på exscientia.co.uk
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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
2542018
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
1042021
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
782013
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
522014
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
312014
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
262015
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
222023
Performance comparison of Next Generation sequencing platforms
B Ergüner, D Üstek, MŞ Sağıroğlu
2015 37th Annual International Conference of the IEEE Engineering in …, 2015
212015
GPR56 homozygous nonsense mutation p. R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria
T Oncu-Oner, A Unalp, İ Porsuk-Doru, S Agilkaya, H Güleryüz Uçar, ...
Turkish Journal of Pediatrics 60 (3), 2018
112018
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
112017
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
82020
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
82017
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
82016
Identifying disease-causing mutations with privacy protection
M Akgün, AB Ünal, B Ergüner, N Pfeifer, O Kohlbacher
Bioinformatics 36 (21), 5205-5213, 2020
72020
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
62006
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
32023
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
32021
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
22020
Human genome in a smart card
M Akgün, B Ergüner, AO Bayrak, MŞ Sağıroğlu
International Conference on Health Informatics 2, 310-316, 2014
22014
Mutational and inflammatory microenvironment characteristics in primary and matched local recurrent non-small cell lung cancer brain metastases
AS Berghoff, B Erguener, MR Schuster, U Rajky, G Ricken, JM Frischer, ...
Annals of Oncology 29, viii122, 2018
12018
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