Yayınlar & Eserler

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

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 , cilt.190, sa.10, ss.2136-2145, 2020 (SCI-Expanded) Creative Commons License identifier identifier identifier

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 , cilt.32, sa.9, ss.1768-1769, 2017 (SCI-Expanded) identifier

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 , cilt.59, ss.475-482, 2017 (SCI-Expanded) Creative Commons License identifier identifier identifier

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 , cilt.7, 2016 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

Chanarin-Dorfman syndrome: Genotype-Phenotype Correlation

NUR B., Gencpinar P., YÜZBAŞIOĞLU A., Emre S., MIHÇI E.
EUROPEAN JOURNAL OF MEDICAL GENETICS , cilt.58, sa.4, ss.238-242, 2015 (SCI-Expanded) identifier identifier identifier

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

YÜZBAŞIOĞLU A., Ozguc M.
NEW BIOTECHNOLOGY , cilt.30, sa.3, ss.339-342, 2013 (SCI-Expanded) identifier identifier identifier

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 , cilt.30, sa.1, ss.72-75, 2013 (SCI-Expanded) Creative Commons License identifier identifier

Novel mutations of the MLC1 gene in Turkish patients

YÜZBAŞIOĞLU A., TOPÇU M., KOCAEFE Y. Ç., ÖZGÜÇ M.
EUROPEAN JOURNAL OF MEDICAL GENETICS , cilt.54, sa.3, ss.281-283, 2011 (SCI-Expanded) identifier identifier identifier

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 , cilt.53, sa.3, ss.141-144, 2010 (SCI-Expanded) identifier identifier identifier

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 , cilt.29, sa.8, ss.1223-1231, 2009 (SCI-Expanded) identifier identifier identifier

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 , cilt.67, sa.4, ss.855-858, 2006 (SCI-Expanded) identifier identifier identifier

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

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, İspanya, 28 Eylül - 02 Ekim 2019, cilt.54 identifier

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, Türkiye, 10 - 14 Nisan 2019

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, Türkiye, 05 Eylül 2018, ss.46

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 Eylül 2017

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 Haziran 2017

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 Ekim 2016

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, Türkiye, 3 - 08 Eylül 2016, cilt.283, ss.31 identifier

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, Türkiye, 27 - 30 Ekim 2015

Rare Disease Biobanks For Personalized Medicine

YÜZBAŞIOĞLU A., ÖZGÜÇ M.
EPMA World Congress 2015, Bonn, Almanya, 3 - 05 Eylül 2015

Metrikler

Yayın

21

Atıf (WoS)

97

H-İndeks (WoS)

7

Atıf (Scopus)

122

H-İndeks (Scopus)

7

Proje

12

Açık Erişim

4
BM Sürdürülebilir Kalkınma Amaçları