Mahmut Samil Sagiroglu
Mahmut Samil Sagiroglu
CTO, Erlab
Verified email at
Cited by
Cited by
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction
N Akizu, V Cantagrel, MS Zaki, L Al-Gazali, X Wang, RO Rosti, E Dikoglu, ...
Nature genetics 47 (5), 528-534, 2015
The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome
PJ van der Sluijs, S Jansen, SA Vergano, M Adachi-Fukuda, Y Alanay, ...
Genetics in Medicine 21 (6), 1295-1307, 2019
A texture based matching approach for automated assembly of puzzles
MS Sagiroglu, A Erçil
18th International Conference on Pattern Recognition (ICPR'06) 3, 1036-1041, 2006
Privacy preserving processing of genomic data: A survey
M Akgün, AO Bayrak, B Ozer, MŞ Sağıroğlu
Journal of biomedical informatics 56, 103-111, 2015
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
HomSI: a homozygous stretch identifier from next-generation sequencing data
Z Görmez, B Bakir-Gungor, MŞ Sağıroğlu
Bioinformatics 30 (3), 445-447, 2014
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
Design and characterisation of a thin-film electrode array with shared reference/counter electrodes for electrochemical detection
Y Uludag, Z Olcer, MS Sagiroglu
Biosensors and Bioelectronics 57, 85-90, 2014
A texture based approach to reconstruction of archaeological finds
MŞ Sağıroğlu, A Erçil
Eurographics, 2005
Generating a detailed protein profile of Fasciola hepatica during the chronic stage of infection in cattle
O Haçarız, AT Baykal, M Akgün, P Kavak, MŞ Sağıroğlu, GP Sayers
Proteomics 14 (12), 1519-1530, 2014
Novel POC1A mutation in primordial dwarfism reveals new insights for centriole biogenesis
A Koparir, OF Karatas, B Yuceturk, B Yuksel, AO Bayrak, OF Gerdan, ...
Human Molecular Genetics 24 (19), 5378-5387, 2015
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
A probable new syndrome with the storage disease phenotype caused by the VPS33A gene mutation
A Dursun, D Yalnizoglu, OF Gerdan, D Yucel-Yilmaz, MS Sagiroglu, ...
Clinical dysmorphology 26 (1), 1-12, 2017
Loss-of-function mutations in ELMO2 cause intraosseous vascular malformation by impeding RAC1 signaling
A Cetinkaya, JR Xiong, İ Vargel, K Kösemehmetoğlu, Hİ Canter, ...
The American Journal of Human Genetics 99 (2), 299-317, 2016
Comparative transcriptome profiling approach to glean virulence and immunomodulation-related genes of Fasciola hepatica
O Haçarız, M Akgün, P Kavak, B Yüksel, MŞ Sağıroğlu
BMC genomics 16, 1-22, 2015
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
Performance comparison of Next Generation sequencing platforms
B Ergüner, D Üstek, MŞ Sağıroğlu
2015 37th Annual International Conference of the IEEE Engineering in …, 2015
A patient with mitochondrial disorder due to a novel mutation in MRPS22
M Kılıç, KK Oğuz, E Kılıç, D Yüksel, H Demirci, MŞ Sağıroğlu, ...
Metabolic Brain Disease 32, 1389-1393, 2017
Coffin-Siris syndrome with cafe-au-lait spots, obesity and hyperinsulinism caused by a mutation in the ARID1B gene
FM Sonmez, E Uctepe, M Gunduz, Z Gormez, S Erpolat, M Oznur, ...
Intractable & Rare Diseases Research 5 (3), 222-226, 2016
Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span
D Yücel-Yılmaz, E Yücesan, D Yalnızoğlu, KK Oğuz, MŞ Sağıroğlu, ...
Brain and Development 40 (6), 458-464, 2018
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