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1

Multi objective SNP selection using pareto optimality

Gumus, Ergun, Gormez, Zeliha, Kursun, Olcay

Journal:

Computational Biology and Chemistry

Year:

2013

Language:

english

File:

PDF, 724 KB

english, 2013

2

Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsy

Sahin, Yavuz, Güngör, Olcay, Gormez, Zeliha, Demirci, Huseyin, Ergüner, Bekir, Güngör, Gülay, Dilber, Cengiz

Journal:

Acta Neurologica Belgica

Year:

2017

Language:

english

File:

PDF, 2.84 MB

english, 2017

3

Myophosphorylase ( PYGM ) mutations determined by next generation sequencing in a cohort from turkey with McArdle disease

Inal-Gültekin, Güldal, Toptaş-Hekimoğlu, Bahar, Görmez, Zeliha, Gelişin, Özlem, Durmuş, Hacer, Ergüner, Bekir, Demirci, Hüseyin, Sağıroğlu, Mahmut Ş., Parman, Yeşim, Deymeer, Feza, Yılmaz-Aydoğan, Hül

Journal:

Neuromuscular Disorders

Year:

2017

Language:

english

File:

PDF, 1.07 MB

english, 2017

4

[IEEE 2013 35th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) - Osaka (2013.7.3-2013.7.7)] 2013 35th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) - Comparison of aggregators for multi-objective SNP selection

Gormez, Zeliha, Gumus, Ergun, Sertbas, Ahmet, Kursun, Olcay

Year:

2013

Language:

english

File:

PDF, 539 KB

english, 2013

5

The role of mediastinal adipose tissue 11β-hydroxysteroid d ehydrogenase type 1 and glucocorticoid expression in the development of coronary atherosclerosis in obese patients with ischemic heart disease

Fatmahan Atalar, Selcuk Gormez, Baris Caynak, Gokce Akan, Gamze Tanriverdi, Sema Bilgic-Gazioglu, Demet Gunay, Cihan Duran, Belhhan Akpinar, Ugur Ozbek, Ahmet Sevim Buyukdevrim, Zeliha Yazici

Journal:

Cardiovascular Diabetology

Year:

2012

Language:

english

File:

PDF, 554 KB

english, 2012

6

Coffin-Siris syndrome with café-au-lait spots, obesity and hyperinsulinism caused by a mutation in the ARID1B gene

Sonmez, Fatma Mujgan, Uctepe, Eyyup, Gunduz, Mehmet, Gormez, Zeliha, Erpolat, Seval, Oznur, Murat, Sagiroglu, Mahmut Samil, Demirci, Huseyin, Gunduz, Esra

Journal:

Intractable & Rare Diseases Research

Year:

2016

Language:

english

File:

PDF, 411 KB

english, 2016

7

FMFilter: A fast model based variant filtering tool

Akgün, Mete, Faruk Gerdan, Ö., Görmez, Zeliha, Demirci, Hüseyin

Journal:

Journal of Biomedical Informatics

Year:

2016

Language:

english

File:

PDF, 731 KB

english, 2016

8

A novel truncating mutation of dock7 gene with an early-onset non-encephalopathic epilepsy

Turkdogan, Dilsad, Turkyilmaz, Ayberk, Gormez, Zeliha, Sager, Gunes, Ekinci, Gazanfer

Journal:

Year:

2019

File:

PDF, 1.13 MB

2019

9

A further family of Stromme syndrome carrying CENPF mutation

Ozkinay, Ferda, Atik, Tahir, Isik, Esra, Gormez, Zeliha, Sagiroglu, Mahmut, Sahin, Ozlem Atan, Corduk, Nergul, Onay, Huseyin

Journal:

American Journal of Medical Genetics Part A

Year:

2017

Language:

english

File:

PDF, 1.31 MB

english, 2017

10

A novel truncating mutation of dock7 gene with an early-onset non-encephalopathic epilepsy

Turkdogan, Dilsad, Turkyilmaz, Ayberk, Gormez, Zeliha, Sager, Gunes, Ekinci, Gazanfer

Journal:

Year:

2019

Language:

english

File:

PDF, 1.13 MB

english, 2019

11

[IEEE 2009 2nd International Congress on Image and Signal Processing (CISP) - Tianjin, China (2009.10.17-2009.10.19)] 2009 2nd International Congress on Image and Signal Processing - Evaluation of the Concatenative Turkish Text-to-Speech System

Orhan, Zeynep, Gormez, Zeliha

Year:

2009

Language:

english

File:

PDF, 263 KB

english, 2009

12

[IEEE 2014 22nd Signal Processing and Communications Applications Conference (SIU) - Trabzon, Turkey (2014.4.23-2014.4.25)] 2014 22nd Signal Processing and Communications Applications Conference (SIU) - Hypertension prediction by multi-objective optimization methods

Gormez, Zeliha, Seker, Huseyin, Sertbas, Ahmet

Year:

2014

Language:

turkish

File:

PDF, 298 KB

turkish, 2014

13

A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous family

Tuncer, Feyza N., Gormez, Zeliha, Calik, Mustafa, Altiokka Uzun, Gunes, Sagiroglu, Mahmut S., Yuceturk, Betul, Yuksel, Bayram, Baykan, Betul, Bebek, Nerses, Iscan, Akin, Ugur Iseri, Sibel A., Ozbek, U

Journal:

Epilepsy Research

Year:

2015

Language:

english

File:

PDF, 1019 KB

english, 2015

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