Lect. PhD AYŞE YÜZBAŞIOĞLU

Publication Network

Articles 11

1. The Common miRNA Signatures Associated with Mitochondrial Dysfunction in Different Muscular Dystrophies

AKSU MENGEŞ E., Akkaya-Ulum Y. Z., DAYANGAÇ ERDEN D., Balci-Peynircioglu B., YÜZBAŞIOĞLU A., Topaloglu H., et al.

AMERICAN JOURNAL OF PATHOLOGY , vol.190, no.10, pp.2136-2145, 2020 (SCI-Expanded, Scopus)

2. CHARACTERIZATION OF POTENTIAL RISK MARKERS OF THE RENAL ARPKD PHENOTYPE

Ebner K., Feldkoetter M., Ariceta G., Bergmann C., Buettner R., Doyon A., et al.

PEDIATRIC NEPHROLOGY , vol.32, no.9, pp.1768-1769, 2017 (SCI-Expanded, Scopus)

3. Identification of two novel PNPLA1 mutations in Turkish families with autosomal recessive congenital ichthyosis.

Dökmeci-Emre S., TAŞKıRAN Z. E., YÜZBAŞıOĞLU A., ÖNAL G., AKARSU A. N., KARADUMAN A., et al.

The Turkish journal of pediatrics , vol.59, pp.475-482, 2017 (SCI-Expanded, Scopus, TRDizin)

4. Discovery of biomarkers in rare diseases: innovative approaches by predictive and personalized medicine

GÜLBAKAN B., ÖZGÜL R. K., YÜZBAŞIOĞLU A., Kohl M., Deigner H., ÖZGÜÇ M.

EPMA JOURNAL , vol.7, 2016 (SCI-Expanded, Scopus)

5. Chanarin-Dorfman syndrome: Genotype-Phenotype Correlation

NUR B., Gencpinar P., YÜZBAŞIOĞLU A., Emre S., MIHÇI E.

EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.58, no.4, pp.238-242, 2015 (SCI-Expanded, Scopus)

6. Biobanking: sample acquisition and quality assurance for 'omics' research

YÜZBAŞIOĞLU A., Ozguc M.

NEW BIOTECHNOLOGY , vol.30, no.3, pp.339-342, 2013 (SCI-Expanded, Scopus)

7. Chanarin-Dorfman Syndrome with Multi-System Involvement in Two Siblings

Camlar S. A., Gencpinar P., MAKAY B., YÜZBAŞIOĞLU A., ARSLAN N., DÖKMECİ S., et al.

TURKISH JOURNAL OF HEMATOLOGY , vol.30, no.1, pp.72-75, 2013 (SCI-Expanded, Scopus, TRDizin)

8. Novel mutations of the MLC1 gene in Turkish patients

YÜZBAŞIOĞLU A., TOPÇU M., KOCAEFE Y. Ç., ÖZGÜÇ M.

EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.54, no.3, pp.281-283, 2011 (SCI-Expanded, Scopus)

9. Molecular analysis of Chanarin-Dorfman syndrome (CDS) patients: Identification of novel mutations in the ABHD5 gene

EMRE S., Unver N., EVANS S., YÜZBAŞIOĞLU A., GÜRAKAN F., GÜMRÜK F., et al.

EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.53, no.3, pp.141-144, 2010 (SCI-Expanded, Scopus)

10. Changes in the expression of selenoproteins in mesial temporal lobe epilepsy patients

YÜZBAŞIOĞLU A., Karatas H., GURSOY-OZDEMIR Y., Saygi S., Akalan N., Soylemezoglu F., et al.

Cellular and Molecular Neurobiology , vol.29, no.8, pp.1223-1231, 2009 (SCI-Expanded, Scopus)

11. Androgen receptor immunostaining and androgen receptor messenger ribonucleic acid expression are increased in cremaster muscles associated with undescended testis

Tanyel F. C., Yuzbasioglu A., Kocaefe C., Orhan D., Ozguc M.

UROLOGY , vol.67, no.4, pp.855-858, 2006 (SCI-Expanded, Scopus)

Papers Presented at Peer-Reviewed Scientific Conferences 9

1. The Correlation Between Clinical Characteristics and Molecular Genetic Analysis Results of Primary Ciliary Dyskinesia Patients: Hacettepe University Experience

EMİRALİOĞLU N., Taskiran E., KOŞUKCU C., BİLGİÇ E., ATİLLA P., Kaya B., et al.

International Congress of the European-Respiratory-Society (ERS), Madrid, Spain, 28 September - 02 October 2019, vol.54, (Summary Text)

2. Primer Siliyer Diskinezi Tanısında Güncel Yöntemlerin Kullanımı: Hacettepe Deneyimi

EMİRALİOĞLU N., TAŞKIRAN Z. E., Kosukcu C., Bilgic E., Atilla P., Kaya B., et al.

Türk Toraks Derneği 22. Ulusal Kongresi, Antalya, Turkey, 10 - 14 April 2019, (Full Text)

3. Analysis of genetic background in Turkish early onset Parkinson’s disease patients

AKBABA T. H., ÖNAL G., YÜZBAŞIOĞLU A., YALÇIN ÇAKMAKLI G., PEYNİRCİOĞLU B., ÖZGÜÇ M., et al.

6th International Congress of the Molecular Biology Association of Turkey, İzmir, Turkey, 05 September 2018, pp.46, (Full Text)

4. Analysis of genomic rearrangements in aTurkish cohort of early onset Parkinson’sdisease

ÖNAL G., YÜZBAŞIOĞLU A., YALÇIN ÇAKMAKLI G., PEYNİRCİOĞLU B., DÖKMECİ S., ÖZGÜÇ M., et al.

42nd FEBS Congress, 10 - 14 September 2017, (Summary Text)

5. How common are the genomic rearrangements among possiblyautosomal recessive PD cases in Turkey?

YALÇIN ÇAKMAKLI G., YÜZBAŞIOĞLU A., ÖNAL G., PEYNİRCİOĞLU B., ÖZGÜÇ M., DÖKMECİ S., et al.

International Congress of Parkinson’xxs Disease and Movement Disorders, 4 - 08 June 2017, (Summary Text)

6. Analysis of Genomic Rearrangements in a Turkish cohort of early onset Pwarkinso s Disease

YÜZBAŞIOĞLU A., ÖNAL G., YALÇIN ÇAKMAKLI G., PEYNİRCİOĞLU B., ÖZGÜÇ M., ELİBOL B., et al.

^rd International Parkinson Disease Symposium, 6 - 08 October 2016, (Summary Text)

7. The role of PNPLA1 protein in lipophagy mediated regulation of lipid droplets

Onal G., Oral O., TASKIRAN E. Z., YÜZBAŞIOĞLU A., KARADUMAN A., Gozuacik D., et al.

41st FEBS Congress on Molecular and Systems Biology for a Better Life, Kusadasi, Turkey, 3 - 08 September 2016, vol.283, pp.31, (Summary Text)

8. Yağ Damlacıklarının Lipofaji Aracılı Regülasyonunda PNPLA1 Proteininin Rolü

ÖNAL G., ORAL Ö., TAŞKIRAN Z. E., YÜZBAŞIOĞLU A., KARADUMAN A., GÖZÜAÇIK D., et al.

XIV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 27 - 30 October 2015, (Full Text)

9. Rare Disease Biobanks For Personalized Medicine

YÜZBAŞIOĞLU A., ÖZGÜÇ M.

EPMA World Congress 2015, Bonn, Germany, 3 - 05 September 2015, (Full Text)

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