Publications & Works

Articles Published in Journals That Entered SCI, SSCI and AHCI Indexes

Loss of mechanosensitivity causes skeletal muscle degeneration in LGMD2R

FEBS OPEN BIO, vol.9, pp.199-200, 2019 (Journal Indexed in SCI) identifier

Proinflammatory effect of AbetaPP induced ST6GAL1 secretion from C2C12 myogenic cell line

TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI, vol.40, no.1, pp.31-36, 2015 (Journal Indexed in SCI) identifier identifier

Response (to Sewry and Goebel).

Neuromuscular disorders : NMD, vol.24, pp.1122, 2014 (Journal Indexed in SCI Expanded) identifier identifier

Linkage Analysis in a Large Primary Osteoporosis Family

TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI, vol.33, no.4, pp.215-222, 2008 (Journal Indexed in SCI) identifier

Calpain-3 mutations in Turkey

EUROPEAN JOURNAL OF PEDIATRICS, vol.165, no.5, pp.293-298, 2006 (Journal Indexed in SCI) identifier identifier identifier

A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families

JOURNAL OF MEDICAL GENETICS, vol.37, no.5, pp.361-367, 2000 (Journal Indexed in SCI) identifier

DNA diagnostic tests in Xp21 dystrophy families for prenatal diagnosis.

The Turkish journal of pediatrics, vol.40, pp.347-55, 1998 (Journal Indexed in SCI Expanded) identifier identifier identifier

Calpain-3 deficiency causes a mild muscular dystrophy in childhood

NEUROPEDIATRICS, vol.28, no.4, pp.212-216, 1997 (Journal Indexed in SCI) identifier identifier identifier

An unusual case of Duchenne muscular dystrophy.

Brain & development, vol.15, pp.313-5, 1993 (Journal Indexed in SCI) identifier identifier identifier

Articles Published in Other Journals

Could autosomal dominant TGFBI-related corneal dystrophies be modelled in zebrafish by using CRISPR/Cas9: Challenges and Possibilities

World Journal of Ophthalmology and Vision Research, vol.1, no.3, pp.1-13, 2019 (Refereed Journals of Other Institutions) Creative Commons License

Genome Editing Technologies: From Bench Side to Bedside

Acta Medica, vol.49, no.3, pp.30-40, 2018 (National Refreed University Journal)

INHERITANCE OF ACQUIRED EPIGENETIC MODIFICATIONS AND ITS ROLE IN DISEASE SUSCEPTIBILITY

İstanbul Tıp Fakültesi Dergisi, vol.80, no.1, pp.45-53, 2017 (National Refreed University Journal)

INHERITANCE OF ACQUIRED EPIGENETIC MODIFICATIONS AND ITS ROLE IN DISEASE SUSCEPTIBILITY

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, vol.80, no.1, pp.45-53, 2017 (Journal Indexed in ESCI) identifier

Exome Sequencing for The Identification of Mendelian Disease Genes

ERCIYES MEDICAL JOURNAL, vol.36, no.4, pp.139-143, 2014 (Journal Indexed in ESCI) identifier identifier

Next-Generation DNA Sequencing Technologies

ERCIYES MEDICAL JOURNAL, vol.36, no.3, pp.99-103, 2014 (Journal Indexed in ESCI) identifier identifier

The new era in therapeutic approaches: Non-coding RNAs and diseases

MARMARA MEDICAL JOURNAL, vol.26, no.1, pp.5-10, 2013 (Journal Indexed in ESCI) identifier identifier

Pitfall of identifying a disease locus by using low-resolution SNP arrays.

Journal of molecular and genetic medicine : an international journal of biomedical research, vol.5, pp.264-5, 2010 (Refereed Journals of Other Institutions) identifier

Beta-sarcoglycan gene mutations in Turkey.

Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, vol.23, pp.154-8, 2004 (Refereed Journals of Other Institutions) identifier identifier

Refereed Congress / Symposium Publications in Proceedings

Defining the role of mechanotransduction in limb-girdle muscular dystrophy type 2R

Mechanical Forces in Biology (EMBO-EMBL Symposia), Heidelberg, Germany, 12 - 15 July 2017

Effect of MST1/2 kinase inhibitor on LGMD2R phenotype

14. Ulusal Tıbbi Genetik Kongresi, Ankara, Turkey, 20 - 22 November 2020, pp.56

Cells lacking LAP1B are defective in withdrawal from the cell cycle during myogenic differentiation.

XVI. Congress of the Medical Biology and Genetics Society of Turkey, Muğla, Turkey, 27 October 2019, pp.5

Intramuscular drug application in zebrafish

Moleküler Biyoloji Derneği 7.Uluslararası Kongresi, İstanbul, Turkey, 27 September 2019

Analysing the expression profiles of human DES orthologous desma and desmb by using knockout zebrafish models

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.618 identifier

Modeling of a unique desmin mutation in zebrafish by using genome editing brings new insights into desmin function

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.427 identifier

Myogenic Differentiation and Fusion Defects in Myoblasts Lacking LAP1B

6th International Congress of the Molecular Biology Association of Turkey, İzmir, Turkey, 05 September 2018, vol.1, pp.162

Disease Modeling in Zebrafish: Limb-Girdle MuscularDystrophy 2R

6th International Congress of the Molecular Biology Association of Turkey, Turkey, 5 - 08 September 2018, pp.5-6

Rare disease modeling by genome editing tools in zebrafish

15. Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 27 October 2017, pp.149

LGMD2R disease modeling in zebrafish by genome editing tools

Mammalian Genetics and Genomics: From Molecular Mechanisms to Translational Applications, Heidelberg, Germany, 24 - 27 October 2017

In vivo targeted mutagenesis via CRISPR/Cas9 and TALEN in zebrafish enables rapid screening of candidate rare diseases genes

42nd Congress of the Federation-of-European-Biochemical-Societies (FEBS) on From Molecules to Cells and Back, Jerusalem, Israel, 10 - 14 September 2017, vol.284, pp.171 identifier

Co-expression Network of a Rare Disease: Significant Genes in Dysferlinopathy and Functional Prediction of TOR1AIP1

Rare and Undiagnosed Diseases: Discovery and Models of Precision Therapy (Keystone Symposia), Massachusetts, United States Of America, 3 - 08 May 2017

Hacettepe University Zebrafish Research Laboratory: zebrafish disease modeling by genome editing tools

41st FEBS Congress on Molecular and Systems Biology for a Better Life, Kusadasi, Turkey, 3 - 08 September 2016, vol.283, pp.116 identifier

Çekirdek zarfı hastalıkları ile ilişkili yeni bir gen: TOR1AIP1 ve kas distrofisi

14. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 27 October 2015, pp.23

A Novel Nuclear Envelopathy-Related Gene: Mutation İn Tor1aip1 Encoding Lap1b Causes Muscular Dystrophy

Türkiye Moleküler Biyoloji Derneği 3. Uluslararasi Kongresi, İzmir, Turkey, 11 September 2014, pp.15

Reduction of LARGE expression in different types of muscular dystrophies other than dystroglycanopathy

18th International Congress of the World-Muscle-Society (WMS), California, United States Of America, 1 - 05 October 2013, vol.23, pp.780 identifier

A novel desmin mutation causes autosomal recessive limb girdle muscular dystrophy without features of myofibrillar myopathy

18th International Congress of the World-Muscle-Society (WMS), California, United States Of America, 1 - 05 October 2013, vol.23, pp.851-852 identifier

Inflammatory effect of AbetaPP induced ST6Gal1 secretion from myogenic cell line

16th International Congress of the World-Muscle-Society, Algarve, Portugal, 18 - 22 October 2011, vol.21, pp.746 identifier

Mutation screening of CAPN3 gene in 13 Turkish LGMD2A patients

12th International Congress of the World-Muscle-Society, Giardini Naxos, Italy, 17 - 20 October 2007, vol.17, pp.791 identifier

Limb-girdle muscular dystrophy and mental retardation (LGMD2M) has a heterogeneous background

11th International Congress of the World-Muscle-Society, Bruges, Belgium, 4 - 07 October 2006, vol.16, pp.679-680 identifier

The first successful prenatal diagnosis in two different forms of muscular dystrophies: MEB and LGMD2M

11th International Congress of the World-Muscle-Society, Bruges, Belgium, 4 - 07 October 2006, vol.16, pp.678-679 identifier

Autosomal recessive limb-girdle muscular dystrophies (LGMD2s) in Turkey

11th International Congress on Neuromuscular Diseases, İstanbul, Turkey, 2 - 07 July 2006, vol.16 identifier

Consanguinity and neuromuscular disorders in Turkey

11th International Congress on Neuromuscular Diseases, İstanbul, Turkey, 2 - 07 July 2006, vol.16 identifier

The first prenatal diagnosis in Muscle-Eye-Brain Disease

11th International Congress on Neuromuscular Diseases, İstanbul, Turkey, 2 - 07 July 2006, vol.16 identifier

Muscle pathology in childhood cases of calpainopathy

9th International Congress of the World-Muscle-Society, Goteborg, Sweden, 1 - 04 September 2004, vol.14, pp.605 identifier

Books & Book Chapters